Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:129906051-129906213 | Rare:43 | ||||
chrX:130165826-130165975 | Rare:31; Clinvar (benign):1 | ||||
chrX:135022468-135022560 | Rare:32 | ||||
chrX:135051887-135051987 | Common:1; Rare:18 | ||||
chrX:135344016-135344227 | Common:1; Rare:38 | ||||
chrX:135344595-135344821 | Common:2; Rare:40 | ||||
chrX:135973687-135973825 | Rare:51 | ||||
chrX:139204989-139205155 | Rare:25 | ||||
chrX:139933005-139933183 | Rare:35 | ||||
chrX:141177026-141177330 | Common:1; Rare:50 | ||||
chrX:149938440-149938632 | Common:1; Rare:50 | ||||
chrX:151397033-151397300 | Common:5; Rare:129 | ||||
chrX:152830706-152831094 | Common:2; Rare:69 | ||||
chrX:152941639-152941701 | Common:1; Rare:19 | ||||
chrX:153599060-153599402 | Common:14; Rare:75 |