| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:119574410-119574603 | Rare:43 | ||||
| chrX:119605801-119606078 | Rare:38 | ||||
| chrX:119606380-119606517 | Rare:24 | ||||
| chrX:119693095-119693265 | Common:1; Rare:45 | ||||
| chrX:119693394-119693621 | Common:1; Rare:28 | ||||
| chrX:119791577-119791994 | Common:2; Rare:112 | ||||
| chrX:119852932-119853233 | Common:3; Rare:49; Clinvar (benign):3 | ||||
| chrX:119871614-119871973 | Common:2; Rare:71; Clinvar (benign):3 | ||||
| chrX:119895983-119896226 | Rare:20 | ||||
| chrX:120250592-120250960 | Common:4; Rare:59 | ||||
| chrX:120560488-120560859 | Rare:58; Clinvar:2 | ||||
| chrX:120603860-120604162 | Rare:60 | ||||
| chrX:120604289-120604780 | Rare:71 | ||||
| chrX:120629932-120630150 | Common:1; Rare:39 | ||||
| chrX:123732991-123733152 | Rare:30; Clinvar (benign):1 |