| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:101407929-101408272 | Common:3; Rare:57; Clinvar (benign):5 | ||||
| chrX:103356244-103356572 | Common:3; Rare:48 | ||||
| chrX:103686720-103686913 | Common:1; Rare:32 | ||||
| chrX:108091504-108091774 | Rare:71 | ||||
| chrX:109733224-109733480 | Common:1; Rare:56 | ||||
| chrX:119470133-119470452 | Rare:67 | ||||
| chrX:119574352-119574589 | Rare:53 | ||||
| chrX:119871733-119871884 | Common:1; Rare:37; Clinvar (benign):2 | ||||
| chrX:120604005-120604188 | Rare:33 | ||||
| chrX:120604632-120604769 | Rare:15 | ||||
| chrX:123733025-123733211 | Rare:34 | ||||
| chrX:130110495-130110677 | Common:1; Rare:39 | ||||
| chrX:135052104-135052280 | Common:2; Rare:49 | ||||
| chrX:149540718-149541021 | Common:4; Rare:58 | ||||
| chrX:152830712-152831112 | Common:2; Rare:71 |