| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:154374527-154374673 | Common:2; Rare:57 | ||||
| chrX:154378660-154379350 | Rare:205 | ||||
| chrX:154398490-154398730 | Common:2; Rare:100; Clinvar (benign):2 | ||||
| chrX:154398753-154399029 | Common:7; Rare:110 | ||||
| chrX:154409182-154409437 | Rare:78 | ||||
| chrX:154411430-154411691 | Rare:95 | ||||
| chrX:154428446-154428708 | Common:4; Rare:91 | ||||
| chrX:154443993-154444243 | Common:12; Rare:129 | ||||
| chrX:154446310-154446740 | Rare:113 | ||||
| chrX:154478749-154479075 | Common:5; Rare:139 | ||||
| chrX:154479188-154479344 | Rare:58 | ||||
| chrX:154486532-154486815 | Common:1; Rare:72 | ||||
| chrX:154490589-154490854 | Common:4; Rare:109 | ||||
| chrX:154516120-154516565 | Common:7; Rare:157 | ||||
| chrX:154540870-154541328 | Rare:112 |