| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:155121739-155122147 | Rare:141 | ||||
| chr6:155216670-155217060 | Common:1; Rare:67 | ||||
| chr6:155314426-155314898 | Common:15; Rare:157 | ||||
| chr6:156777079-156777350 | Common:3; Rare:72 | ||||
| chr6:156777490-156777980 | Common:3; Rare:169; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:156778323-156778479 | Common:1; Rare:64; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:156778760-156779030 | Common:4; Rare:108; Clinvar:8; Clinvar (benign):15 | ||||
| chr6:157323120-157323317 | Rare:35 | ||||
| chr6:157323460-157323665 | Common:3; Rare:73 | ||||
| chr6:157324035-157324232 | Common:2; Rare:34 | ||||
| chr6:157381018-157381231 | Common:1; Rare:69 | ||||
| chr6:157823034-157823285 | Common:3; Rare:101 | ||||
| chr6:157823452-157823852 | Common:3; Rare:132 | ||||
| chr6:157981430-157981900 | Common:4; Rare:115 | ||||
| chr6:158167579-158167979 | Common:2; Rare:107 |