| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:138780203-138780455 | Rare:66 | ||||
| chr2:142130734-142131044 | Common:2; Rare:100 | ||||
| chr2:144430770-144431051 | Rare:46 | ||||
| chr2:144513791-144513958 | Rare:44 | ||||
| chr2:144517324-144517579 | Rare:75; Clinvar:3; Clinvar (benign):4 | ||||
| chr2:144517745-144518104 | Common:2; Rare:55 | ||||
| chr2:144518134-144518203 | Common:1; Rare:14 | ||||
| chr2:144518374-144518503 | Rare:29 | ||||
| chr2:144519999-144520561 | Common:4; Rare:111; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:144524431-144524627 | Common:4; Rare:51 | ||||
| chr2:147845203-147845412 | Common:1; Rare:59 | ||||
| chr2:148020665-148021109 | Common:2; Rare:102; Clinvar (benign):2 | ||||
| chr2:148021332-148021541 | Rare:63 | ||||
| chr2:148021544-148021673 | Rare:23 | ||||
| chr2:148875554-148875680 | Common:2; Rare:40; Clinvar (benign):3 |