| ID: 127898437 | H3K4me1 hESC enhancer GRCh37_chrX:148228505-148229004 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (149146975..149147474) | | |
| ID: 127898436 | H3K4me1 hESC enhancer GRCh37_chrX:148228003-148228504 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (149146473..149146974) | | |
| ID: 127898435 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chrX:147582797-147583674 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (148501277..148502154) | | |
| ID: 126863341 | MED14-independent group 3 enhancer GRCh37_chrX:147636485-147637684 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (148554964..148556163) | | |
| ID: 109461475 | fragile site, folic acid type, rare, fra(X)(q28) E [Homo sapiens (human)] | Chromosome X, NC_000023.11 (148500602..148500743) | FMR2 | |
| ID: 107048984 | origin of replication in 5' region of AFF2/FMR2 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (148500443..148500606) | | |
| ID: 106480478 | RN7SK pseudogene 267 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (148822164..148822448, complement) | | |
| ID: 347509 | RPL7L1 pseudogene 11 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (148464669..148465581) | | |
| ID: 2334 | ALF transcription elongation factor 2 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (148500617..149000663) | FMR2, FMR2P, FRAXE, MRX2, OX19, XLID109 | 300806 |