| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:94823145-94823343 | Common:2; Rare:111 | ||||
| chr8:94895119-94895381 | Common:1; Rare:140 | ||||
| chr8:94895611-94895911 | Common:7; Rare:145 | ||||
| chr8:95024902-95025131 | Common:3; Rare:171; Clinvar:4; Clinvar (benign):16; Clinvar (pathogenic):2 | ||||
| chr8:95133351-95134055 | Common:6; Rare:285 | ||||
| chr8:95268687-95268876 | Common:17; Rare:91 | ||||
| chr8:95269181-95269320 | Common:10; Rare:105; Clinvar:2 | ||||
| chr8:96235512-96235652 | Common:2; Rare:131; Clinvar (benign):4 | ||||
| chr8:96261512-96262062 | Common:12; Rare:330 | ||||
| chr8:97643808-97644340 | Common:20; Rare:265 | ||||
| chr8:97644600-97644986 | Common:1; Rare:168 | ||||
| chr8:97645244-97645504 | Common:1; Rare:61 | ||||
| chr8:97775587-97776011 | Common:10; Rare:307; Clinvar (benign):1 | ||||
| chr8:98045260-98045679 | Common:9; Rare:246 | ||||
| chr8:98116965-98117389 | Common:8; Rare:239 |