Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:150872961-150873136 | Common:1; Rare:21 | ||||
chrX:150873137-150873189 | Rare:6 | ||||
chrX:153705436-153705567 | Rare:23 | ||||
chrX:154366127-154366370 | Common:3; Rare:72; Clinvar:8; Clinvar (benign):9 | ||||
chrY:3002658-3002940 | Rare:1 | ||||
chrY:12662221-12662506 | Rare:3 | ||||
chrY:19075996-19076207 | Rare:2 |