| ID: 127897126 | OCT4-NANOG hESC enhancer GRCh37_chrX:7154725-7155349 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (7236684..7237308) | | |
| ID: 127897125 | H3K4me1 hESC enhancer GRCh37_chrX:7034397-7034896 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (7116356..7116855) | | |
| ID: 127897124 | H3K4me1 hESC enhancer GRCh37_chrX:7033895-7034396 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (7115854..7116355) | | |
| ID: 127897123 | H3K4me1 hESC enhancer GRCh37_chrX:7000681-7001181 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (7082640..7083140) | | |
| ID: 127897122 | H3K4me1 hESC enhancer GRCh37_chrX:7000180-7000680 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (7082139..7082639) | | |
| ID: 127897121 | H3K4me1 hESC enhancer GRCh37_chrX:6986912-6987412 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (7068871..7069371) | | |
| ID: 127897120 | H3K4me1 hESC enhancer GRCh37_chrX:6975911-6976411 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (7057870..7058370) | | |
| ID: 127897119 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chrX:6884751-6885264 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (6966710..6967223) | | |
| ID: 127897118 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chrX:6877453-6878076 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (6959412..6960035) | | |
| ID: 127897117 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chrX:6876827-6877452 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (6958786..6959411) | | |
| ID: 127897116 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chrX:6850622-6851287 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (6932581..6933246) | | |
| ID: 127897115 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chrX:6849955-6850621 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (6931914..6932580) | | |
| ID: 127897114 | OCT4-NANOG hESC enhancer GRCh37_chrX:6610973-6611531 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (6692932..6693490) | | |
| ID: 127897113 | OCT4-NANOG hESC enhancer GRCh37_chrX:6582190-6583002 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (6664149..6664961) | | |
| ID: 113875037 | Sharpr-MPRA regulatory region 5189 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (7245588..7245882) | | |
| ID: 107987331 | uncharacterized LOC107987331 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (7012499..7026870) | | |
| ID: 100616467 | microRNA 4767 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (7147860..7147937) | mir-4767 | |
| ID: 392425 | RPS27A pseudogene 17 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (6989329..6990021) | RPS27A_9_1763 | |
| ID: 8226 | pseudouridine 5'-phosphatase [Homo sapiens (human)] | Chromosome X, NC_000023.11 (6705838..7148153, complement) | DXF68S1E, FAM16AX, GS1, HDHD1, HDHD1A | 306480 |
| ID: 412 | steroid sulfatase [Homo sapiens (human)] | Chromosome X, NC_000023.11 (7147290..7354641) | ARSC, ARSC1, ASC, ES, SSDD, XLI | 300747 |