| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:143734161-143734192 | Rare:6 | ||||
| chr8:143829039-143829138 | Rare:37 | ||||
| chr8:143829310-143829510 | Rare:78 | ||||
| chr8:143939541-143939678 | Common:2; Rare:49 | ||||
| chr8:143943918-143944122 | Rare:77 | ||||
| chr8:143953790-143954152 | Common:3; Rare:100 | ||||
| chr8:143989904-143990144 | Common:1; Rare:87 | ||||
| chr8:143992550-143992703 | Common:1; Rare:47 | ||||
| chr8:144060678-144060799 | Rare:30 | ||||
| chr8:144063956-144064056 | Common:3; Rare:21 | ||||
| chr8:144078501-144078752 | Common:1; Rare:79 | ||||
| chr8:144082530-144082677 | Common:1; Rare:52 | ||||
| chr8:144096060-144096375 | Common:1; Rare:121; Clinvar (benign):3 | ||||
| chr8:144103686-144103875 | Common:1; Rare:68 | ||||
| chr8:144104163-144104530 | Common:3; Rare:126 |