| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:109733185-109733490 | Common:1; Rare:71 | ||||
| chrX:119468209-119468496 | Common:3; Rare:96 | ||||
| chrX:119574384-119574586 | Rare:43 | ||||
| chrX:119791588-119791978 | Common:2; Rare:104 | ||||
| chrX:119871638-119871914 | Common:1; Rare:60; Clinvar (benign):3 | ||||
| chrX:120559865-120560247 | Rare:58 | ||||
| chrX:120560468-120560860 | Rare:62; Clinvar:2 | ||||
| chrX:120561428-120561710 | Common:1; Rare:38 | ||||
| chrX:120630013-120630266 | Common:3; Rare:51 | ||||
| chrX:123961202-123961432 | Common:2; Rare:31 | ||||
| chrX:129905939-129906173 | Rare:61 | ||||
| chrX:135344590-135344824 | Common:2; Rare:42 | ||||
| chrX:135973707-135973858 | Rare:52 | ||||
| chrX:139933025-139933211 | Rare:37 | ||||
| chrX:141177020-141177325 | Common:1; Rare:46 |