| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:138780350-138780536 | Rare:60 | ||||
| chr2:142130731-142130929 | Common:2; Rare:71 | ||||
| chr2:142130948-142131031 | Rare:23 | ||||
| chr2:144332449-144332648 | Rare:79 | ||||
| chr2:144513791-144513954 | Rare:43 | ||||
| chr2:144517324-144517627 | Common:5; Rare:82; Clinvar:3; Clinvar (benign):4 | ||||
| chr2:144518134-144518203 | Common:1; Rare:14 | ||||
| chr2:144520068-144520570 | Common:5; Rare:89; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:148020681-148021480 | Common:2; Rare:188; Clinvar (benign):2 | ||||
| chr2:148021520-148021552 | Rare:6 | ||||
| chr2:148021571-148021666 | Rare:18 | ||||
| chr2:148021782-148021814 | Rare:6 | ||||
| chr2:148875554-148875639 | Common:2; Rare:32; Clinvar (benign):3 | ||||
| chr2:149587326-149587415 | Common:1; Rare:20 | ||||
| chr2:149587669-149587814 | Common:1; Rare:42; Clinvar:2 |