| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:137964355-137964481 | Common:1; Rare:20 | ||||
| chr2:138501631-138502046 | Common:4; Rare:153 | ||||
| chr2:144332449-144332672 | Rare:90 | ||||
| chr2:144517324-144517576 | Rare:75; Clinvar:3; Clinvar (benign):4 | ||||
| chr2:144518386-144518532 | Rare:31 | ||||
| chr2:147844159-147844507 | Common:5; Rare:111 | ||||
| chr2:148020673-148021109 | Common:2; Rare:101; Clinvar (benign):2 | ||||
| chr2:148021374-148021671 | Rare:77 | ||||
| chr2:149330344-149330703 | Common:2; Rare:139 | ||||
| chr2:149587321-149587371 | Rare:10 | ||||
| chr2:149587669-149587892 | Common:1; Rare:64; Clinvar:2 | ||||
| chr2:151828446-151828604 | Common:2; Rare:37 | ||||
| chr2:152099014-152099134 | Rare:56; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:152175679-152176073 | Common:2; Rare:111 | ||||
| chr2:152717829-152718045 | Rare:86 |