| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:143553358-143553685 | Common:4; Rare:54 | ||||
| chr8:143558267-143558595 | Common:2; Rare:132 | ||||
| chr8:143617479-143617727 | Common:1; Rare:95 | ||||
| chr8:143829275-143829532 | Rare:100 | ||||
| chr8:144078512-144078718 | Common:1; Rare:64 | ||||
| chr8:144082496-144082674 | Common:2; Rare:61 | ||||
| chr8:144103678-144103870 | Common:1; Rare:68 | ||||
| chr8:144104243-144104509 | Common:1; Rare:84 | ||||
| chr8:144104895-144105045 | Rare:54 | ||||
| chr8:144148583-144148676 | Rare:18 | ||||
| chr8:144291373-144291651 | Common:1; Rare:92 | ||||
| chr8:144428495-144428666 | Common:2; Rare:67 | ||||
| chr8:144509002-144509131 | Rare:43 | ||||
| chr8:144517739-144518033 | Common:1; Rare:106; Clinvar:8; Clinvar (benign):1 | ||||
| chr8:144827207-144827602 | Common:2; Rare:111 |