| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:120560475-120560845 | Rare:57; Clinvar:2 | ||||
| chrX:120561420-120561745 | Common:1; Rare:48 | ||||
| chrX:120604009-120604171 | Rare:32 | ||||
| chrX:120629927-120630319 | Common:4; Rare:76 | ||||
| chrX:123733025-123733152 | Rare:20 | ||||
| chrX:123859684-123860109 | Common:2; Rare:62 | ||||
| chrX:123960350-123960745 | Rare:28 | ||||
| chrX:123961270-123961435 | Common:2; Rare:22 | ||||
| chrX:123961561-123961850 | Rare:39 | ||||
| chrX:129523290-129523677 | Common:4; Rare:80 | ||||
| chrX:129843794-129844034 | Common:1; Rare:31 | ||||
| chrX:129905957-129906213 | Rare:66 | ||||
| chrX:130165689-130165920 | Rare:45; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chrX:130171817-130171979 | Common:1; Rare:42 | ||||
| chrX:130339818-130339962 | Rare:21 |