| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:91779133-91779476 | Common:2; Rare:60 | ||||
| chrX:93673546-93673773 | Common:1; Rare:37 | ||||
| chrX:93673910-93674259 | Rare:39 | ||||
| chrX:96684664-96684678 | Rare:4 | ||||
| chrX:96684683-96684977 | Rare:54 | ||||
| chrX:96684992-96685046 | Rare:9 | ||||
| chrX:100644032-100644284 | Common:1; Rare:31 | ||||
| chrX:100820226-100820428 | Common:2; Rare:49 | ||||
| chrX:101051786-101052291 | Common:2; Rare:80 | ||||
| chrX:101097894-101098248 | Common:1; Rare:69 | ||||
| chrX:101348636-101348801 | Common:4; Rare:28; Clinvar:1; Clinvar (benign):3 | ||||
| chrX:101390877-101391124 | Rare:86 | ||||
| chrX:101391222-101391563 | Common:2; Rare:45 | ||||
| chrX:101407708-101408487 | Common:5; Rare:140; Clinvar:3; Clinvar (benign):14 | ||||
| chrX:101622990-101623209 | Common:1; Rare:38 |