ID: 127459835 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr8:82632569-82633513 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (81720334..81721278) | | |
ID: 127459834 | H3K27ac hESC enhancer GRCh37_chr8:82598306-82598806 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (81686071..81686571) | | |
ID: 124174284 | Sharpr-MPRA regulatory region 11945 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (81630754..81631048) | | |
ID: 100631269 | SLC10A5 pseudogene 1 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (81634324..81635442, complement) | | |
ID: 100271114 | ribosomal protein S26 pseudogene 34 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (81627247..81627799) | RPS26_9_922 | |
ID: 650747 | inositol monophosphatase 1 pseudogene 1 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (81603884..81631277, complement) | IMPA1P | |
ID: 347051 | solute carrier family 10 member 5 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (81693631..81695058, complement) | P5 | 618582 |
ID: 79752 | zinc finger AN1-type containing 1 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (81701331..81721304, complement) | | |
ID: 3612 | inositol monophosphatase 1 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (81656914..81686325, complement) | IMP, IMPA, MRT59 | 602064 |