| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:6228825-6229074 | Common:2; Rare:43 | ||||
| chrX:7148109-7148304 | Common:1; Rare:58 | ||||
| chrX:7927371-7927770 | Common:2; Rare:91 | ||||
| chrX:9912926-9913109 | Common:2; Rare:48 | ||||
| chrX:10156724-10156891 | Common:2; Rare:17 | ||||
| chrX:10620495-10620688 | Common:1; Rare:26 | ||||
| chrX:11111147-11111368 | Common:3; Rare:46 | ||||
| chrX:11759528-11759665 | Rare:18 | ||||
| chrX:12138612-12138895 | Rare:65 | ||||
| chrX:12791283-12791459 | Rare:32 | ||||
| chrX:12974964-12975265 | Common:2; Rare:72 | ||||
| chrX:12975801-12976361 | Common:4; Rare:104 | ||||
| chrX:13652983-13653312 | Common:2; Rare:76 | ||||
| chrX:13688969-13689207 | Common:1; Rare:64 | ||||
| chrX:13734529-13734832 | Common:3; Rare:94; Clinvar (benign):1 |