| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:143939459-143939846 | Common:8; Rare:181 | ||||
| chr8:143942595-143942807 | Common:4; Rare:108 | ||||
| chr8:143943980-143944340 | Common:2; Rare:243 | ||||
| chr8:143953773-143954030 | Common:6; Rare:124 | ||||
| chr8:143976702-143976847 | Rare:67 | ||||
| chr8:143989935-143990196 | Common:2; Rare:170 | ||||
| chr8:144060674-144060846 | Rare:93 | ||||
| chr8:144078461-144078827 | Common:2; Rare:176 | ||||
| chr8:144082484-144082744 | Common:2; Rare:79 | ||||
| chr8:144094960-144095108 | Rare:48 | ||||
| chr8:144095960-144096400 | Common:2; Rare:283; Clinvar (benign):7 | ||||
| chr8:144103652-144103910 | Common:3; Rare:145 | ||||
| chr8:144104096-144104618 | Common:8; Rare:326 | ||||
| chr8:144137600-144137836 | Common:4; Rare:127 | ||||
| chr8:144147710-144148086 | Common:4; Rare:172 |