| ID: 127898085 | H3K4me1 hESC enhancer GRCh37_chrX:109844205-109844705 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (110600977..110601477) | | |
| ID: 127898084 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chrX:109763200-109764196 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (110519972..110520968) | | |
| ID: 127898083 | NANOG hESC enhancer GRCh37_chrX:109670142-109670791 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (110426914..110427563) | | |
| ID: 127898082 | H3K4me1 hESC enhancer GRCh37_chrX:109661556-109662056 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (110418328..110418828) | | |
| ID: 127898081 | NANOG hESC enhancer GRCh37_chrX:109488243-109488792 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (110245015..110245564) | | |
| ID: 127898080 | H3K27ac hESC enhancer GRCh37_chrX:109403823-109404356 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (110160595..110161128) | | |
| ID: 124905230 | uncharacterized LOC124905230 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (110175773..110177788) | | |
| ID: 105373312 | uncharacterized LOC105373312 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (110318252..110333992) | | |
| ID: 100616491 | microRNA 3978 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (110082118..110082218) | | |
| ID: 692226 | small nucleolar RNA, C/D box 96B [Homo sapiens (human)] | Chromosome X, NC_000023.11 (110224989..110225060, complement) | U96b | |
| ID: 347687 | G protein subunit gamma 5B [Homo sapiens (human)] | Chromosome X, NC_000023.11 (110346454..110346973, complement) | GNG5P2, GNG5ps, HG3L1, HG3L3, dJ364I1.1 | |
| ID: 84187 | transmembrane protein 164 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (110002369..110184251) | bB360B22.3 | |
| ID: 57529 | retrotransposon Gag like 9 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (110358848..110456334) | MAR9, MART9, RGAG1, SIRH10 | 300965 |
| ID: 9949 | AMMECR nuclear protein 1 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (110194186..110440233, complement) | AMMERC1, MFHIEN | 300195 |
| ID: 6998 | cripto, EGF-CFC family member 3 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (110520896..110523021) | CR-3, CRIPTO, CRIPTO-3, TDGF1P3, TDGF2, TDGF3 | |