ID: 129660127 | ReSE screen-validated silencer GRCh37_chr1:18979869-18980025 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (18653375..18653531) | | |
ID: 127267849 | H3K4me1 hESC enhancer GRCh37_chr1:19066201-19066702 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (18739707..18740208) | | |
ID: 127267848 | H3K4me1 hESC enhancer GRCh37_chr1:19064839-19065345 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (18738345..18738851) | | |
ID: 127267847 | H3K4me1 hESC enhancer GRCh37_chr1:19064331-19064838 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (18737837..18738344) | | |
ID: 127267846 | H3K4me1 hESC enhancer GRCh37_chr1:19018361-19018860 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (18691867..18692366) | | |
ID: 127267845 | OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chr1:18978097-18978886 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (18651603..18652392) | | |
ID: 127267844 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:18976025-18976654 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (18649531..18650160) | | |
ID: 127267843 | H3K4me1 hESC enhancer GRCh37_chr1:18967445-18967966 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (18640951..18641472) | | |
ID: 127267842 | H3K4me1 hESC enhancer GRCh37_chr1:18963679-18964296 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (18637185..18637802) | | |
ID: 127267841 | H3K4me1 hESC enhancer GRCh37_chr1:18963062-18963678 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (18636568..18637184) | | |
ID: 127267840 | H3K4me1 hESC enhancer GRCh37_chr1:18962444-18963061 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (18635950..18636567) | | |
ID: 122056776 | Sharpr-MPRA regulatory region 1855 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (18653975..18654269) | | |
ID: 108254694 | PAX7 promoter region [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (18630530..18631629) | | |
ID: 108175348 | PAX7 intron homotypic clusters of transcription factor binding sites enhancer [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (18632169..18633790) | | |
ID: 5081 | paired box 7 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (18630846..18748866) | CMYO19, CMYP19, HUP1, MYOSCOB, RMS2, PAX7 | 167410 |