| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:49079772-49080005 | Rare:50 | ||||
| chrX:49100858-49101415 | Common:5; Rare:158; Clinvar (benign):2 | ||||
| chrX:49123653-49123772 | Common:1; Rare:39 | ||||
| chrX:49163650-49164110 | Common:4; Rare:171 | ||||
| chrX:49164160-49164338 | Common:1; Rare:28 | ||||
| chrX:49171721-49172094 | Common:8; Rare:109 | ||||
| chrX:49172340-49172840 | Common:2; Rare:111 | ||||
| chrX:49184810-49185290 | Common:3; Rare:89 | ||||
| chrX:49186273-49186493 | Common:2; Rare:71 | ||||
| chrX:49200183-49200358 | Rare:93 | ||||
| chrX:49235323-49235577 | Common:2; Rare:47 | ||||
| chrX:49235600-49235890 | Common:8; Rare:91 | ||||
| chrX:49269100-49269480 | Common:1; Rare:61 | ||||
| chrX:49269579-49269870 | Rare:125 | ||||
| chrX:49879210-49879710 | Common:1; Rare:153 |