| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:135876377-135876641 | Common:1; Rare:73 | ||||
| chr2:136118144-136118266 | Rare:37 | ||||
| chr2:142130853-142131022 | Rare:47 | ||||
| chr2:144513791-144513955 | Rare:44 | ||||
| chr2:144517426-144517816 | Common:6; Rare:96 | ||||
| chr2:144517888-144518203 | Common:2; Rare:52 | ||||
| chr2:144518386-144518506 | Rare:27 | ||||
| chr2:144520136-144520569 | Common:5; Rare:75; Clinvar (benign):1 | ||||
| chr2:148020681-148021113 | Common:2; Rare:99; Clinvar (benign):2 | ||||
| chr2:149330354-149330605 | Common:1; Rare:109 | ||||
| chr2:149587681-149587822 | Common:1; Rare:39; Clinvar:1 | ||||
| chr2:151289611-151289745 | Common:1; Rare:33 | ||||
| chr2:151828463-151828793 | Common:2; Rare:95 | ||||
| chr2:152335013-152335174 | Common:1; Rare:57 | ||||
| chr2:152717829-152717985 | Rare:66 |