| ID: 127138852 | H3K4me1 hESC enhancer GRCh37_chrY:644837-645338 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (734102..734603); Chromosome Y, NC_000024.10 (734102..734603) | | |
| ID: 127138851 | H3K4me1 hESC enhancer GRCh37_chrY:639405-639905 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (728670..729170); Chromosome Y, NC_000024.10 (728670..729170) | | |
| ID: 127138850 | OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chrY:534047-534914 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (623312..624179); Chromosome Y, NC_000024.10 (623312..624179) | | |
| ID: 108353832 | CNE-2 enhancer upstream of SHOX [Homo sapiens (human)] | Chromosome X, NC_000023.11 (555875..556494); Chromosome Y, NC_000024.10 (555875..556494) | | |
| ID: 107652445 | meiotic recombination hotspot SHOX [Homo sapiens (human)] | Chromosome X, NC_000023.11 (633053..636275); Chromosome Y, NC_000024.10 (633053..636275) | | |
| ID: 106480712 | fatty acid binding protein 5 pseudogene 13 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (523741..524101, complement); Chromosome Y, NC_000024.10 (523741..524101, complement) | FABP5L13 | |
| ID: 106478925 | keratin 18 pseudogene 53 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (545236..545352, complement); Chromosome Y, NC_000024.10 (545236..545352, complement) | | |
| ID: 6473 | SHOX homeobox [Homo sapiens (human)] | Chromosome X, NC_000023.11 (624344..659411); Chromosome Y, NC_000024.10 (624344..659411) | GCFX, PHOG1, SHOXY, SS, SHOX | 312865, 400020 |