| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:144078450-144078718 | Common:1; Rare:83 | ||||
| chr8:144082491-144082745 | Common:2; Rare:77 | ||||
| chr8:144095977-144096348 | Common:1; Rare:149; Clinvar (benign):4 | ||||
| chr8:144103671-144103875 | Common:1; Rare:71 | ||||
| chr8:144104141-144104510 | Common:3; Rare:119 | ||||
| chr8:144104596-144104856 | Common:1; Rare:73 | ||||
| chr8:144104886-144105098 | Rare:72 | ||||
| chr8:144106200-144106345 | Rare:51 | ||||
| chr8:144137621-144137821 | Common:2; Rare:58 | ||||
| chr8:144147802-144148061 | Common:2; Rare:60 | ||||
| chr8:144291273-144291668 | Common:1; Rare:125 | ||||
| chr8:144313318-144313613 | Rare:111 | ||||
| chr8:144317589-144317827 | Common:2; Rare:79; Clinvar (pathogenic):1 | ||||
| chr8:144396431-144396732 | Common:1; Rare:134 | ||||
| chr8:144409137-144409410 | Rare:89 |