ID: 127888080 | H3K4me1 hESC enhancer GRCh37_chr17:75275663-75276310 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (77279581..77280228) | | |
ID: 127888079 | H3K4me1 hESC enhancer GRCh37_chr17:75262565-75263064 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (77266483..77266982) | | |
ID: 127888078 | H3K4me1 hESC enhancer GRCh37_chr17:75262063-75262564 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (77265981..77266482) | | |
ID: 127888077 | H3K4me1 hESC enhancer GRCh37_chr17:75254313-75254968 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (77258231..77258886) | | |
ID: 127888076 | H3K4me1 hESC enhancer GRCh37_chr17:75253655-75254312 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (77257573..77258230) | | |
ID: 127888075 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:75243257-75244107 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (77247114..77248025) | | |
ID: 127888074 | H3K27ac hESC enhancer GRCh37_chr17:75217629-75218128 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (77221547..77222046) | | |
ID: 126862651 | MED14-independent group 3 enhancer GRCh37_chr17:75281897-75283096 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (77285448..77287014) | | |
ID: 126862650 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr17:75250208-75251407 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (77254126..77255325) | | |
ID: 126862649 | BRD4-independent group 4 enhancer GRCh37_chr17:75229305-75230504 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (77233223..77234422) | | |
ID: 121627812 | Sharpr-MPRA regulatory region 14112 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (77235547..77235841) | | |
ID: 107984143 | uncharacterized LOC107984143 [Homo sapiens (human)] | | | |
ID: 105371907 | SEPTIN9 divergent transcript [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (77273784..77281897, complement) | | |
ID: 105371906 | lung adenocarcinoma-associated transcript 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (77253814..77259345) | | |
ID: 10801 | septin 9 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (77281499..77500596) | AF17q25, MSF, MSF1, NAPB, PNUTL4, SEPT9, SINT1, SeptD1 | 604061 |