| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:119943708-119943857 | Rare:26 | ||||
| chrX:120559914-120560120 | Rare:32 | ||||
| chrX:120560528-120560865 | Rare:55; Clinvar:1 | ||||
| chrX:120560951-120561143 | Rare:32 | ||||
| chrX:120604035-120604154 | Rare:25 | ||||
| chrX:123733025-123733152 | Rare:20 | ||||
| chrX:123960373-123960735 | Rare:23 | ||||
| chrX:123961283-123961432 | Common:2; Rare:21 | ||||
| chrX:123961458-123961819 | Rare:48 | ||||
| chrX:129738910-129739249 | Common:2; Rare:58 | ||||
| chrX:129843800-129844066 | Common:1; Rare:34 | ||||
| chrX:129906052-129906213 | Rare:43 | ||||
| chrX:130110413-130110613 | Rare:47 | ||||
| chrX:130165703-130165961 | Rare:54; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chrX:132023152-132023305 | Rare:39 |