ID: 127402158 | H3K4me1 hESC enhancer GRCh37_chr5:181876-182376 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (181761..182261) | | |
ID: 127402157 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr5:171359-171872 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (171244..171757) | | |
ID: 127402156 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr5:170845-171358 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (170730..171243) | | |
ID: 127402155 | H3K27ac hESC enhancer GRCh37_chr5:160287-160787 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (160172..160672) | | |
ID: 127402154 | H3K27ac hESC enhancer GRCh37_chr5:159786-160286 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (159671..160171) | | |
ID: 127402153 | H3K4me1 hESC enhancer GRCh37_chr5:137535-138040 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (137420..137925) | | |
ID: 127402152 | NANOG hESC enhancer GRCh37_chr5:99879-100414 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (99764..100299) | | |
ID: 127402151 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr5:90483-91322 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (90368..91207) | | |
ID: 126807280 | MED14-independent group 3 enhancer GRCh37_chr5:169157-170356 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (169042..170241) | | |
ID: 124900929 | uncharacterized LOC124900929 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (192728..194727, complement) | | |
ID: 123493257 | Sharpr-MPRA regulatory region 15179 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (186094..186388) | | |
ID: 123493256 | Sharpr-MPRA regulatory region 259 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (82614..82908) | | |
ID: 121725197 | Sharpr-MPRA regulatory region 11960 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (188614..188908) | | |
ID: 100128803 | Spi-C transcription factor pseudogene 4 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (58175..59069) | | |
ID: 389257 | leucine rich repeat containing 14B [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (191495..196334) | | |
ID: 153478 | pleckstrin homology and RhoGEF domain containing G4B [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (92168..189966) | ARHGEF48 | 620665 |
ID: 133957 | coiled-coil domain containing 127 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (196868..218153, complement) | | |