ID: 129664043 | ReSE screen-validated silencer GRCh37_chr17:39300532-39300634 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41144280..41144382) | | |
ID: 127886828 | H3K4me1 hESC enhancer GRCh37_chr17:39567789-39568290 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41411537..41412038) | | |
ID: 127886827 | H3K4me1 hESC enhancer GRCh37_chr17:39550287-39550786 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41394035..41394534) | | |
ID: 127886826 | H3K4me1 hESC enhancer GRCh37_chr17:39549785-39550286 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41393533..41394034) | | |
ID: 127886825 | H3K4me1 hESC enhancer GRCh37_chr17:39520859-39521360 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41364607..41365108) | | |
ID: 127886824 | H3K4me1 hESC enhancer GRCh37_chr17:39503213-39503713 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41346961..41347461) | | |
ID: 127886823 | H3K4me1 hESC enhancer GRCh37_chr17:39502712-39503212 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41346460..41346960) | | |
ID: 127886822 | H3K4me1 hESC enhancer GRCh37_chr17:39485793-39486362 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41329541..41330110) | | |
ID: 127886821 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:39405666-39406220 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41249414..41249968) | | |
ID: 127886820 | H3K4me1 hESC enhancer GRCh37_chr17:39295928-39296440 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41139676..41140188) | | |
ID: 127886819 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:39279561-39280114 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41123309..41123862) | | |
ID: 127886818 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:39240697-39241226 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41084445..41084974) | | |
ID: 127886817 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:39221865-39222401 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41065613..41066149) | | |
ID: 127886816 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:39221327-39221864 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41065075..41065612) | | |
ID: 127886815 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:39216111-39216685 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41059859..41060433) | | |
ID: 127886814 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:39215536-39216110 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41059284..41059858) | | |
ID: 126862564 | BRD4-independent group 4 enhancer GRCh37_chr17:39559942-39561141 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41403690..41404889) | | |
ID: 126862563 | BRD4-independent group 4 enhancer GRCh37_chr17:39537551-39538750 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41381299..41382498) | | |
ID: 125177474 | Sharpr-MPRA regulatory region 10866 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41421117..41421411) | | |
ID: 112296190 | keratin associated protein 4-17, pseudogene [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41186344..41187736, complement) | KRTAP4p3 | |