| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:135742124-135742898 | Common:1; Rare:243 | ||||
| chr2:135876305-135876681 | Common:2; Rare:165 | ||||
| chr2:135985026-135985243 | Common:1; Rare:97 | ||||
| chr2:135985365-135985766 | Common:15; Rare:410; Clinvar (benign):3 | ||||
| chr2:136118067-136118332 | Rare:166 | ||||
| chr2:137964030-137964599 | Common:11; Rare:215 | ||||
| chr2:138501514-138502366 | Common:10; Rare:604 | ||||
| chr2:142130488-142131174 | Common:4; Rare:236 | ||||
| chr2:142131234-142131677 | Common:11; Rare:183 | ||||
| chr2:142877220-142877790 | Common:9; Rare:157 | ||||
| chr2:144332123-144332400 | Common:6; Rare:266 | ||||
| chr2:144332414-144332789 | Common:2; Rare:374 | ||||
| chr2:147844198-147844866 | Common:17; Rare:527 | ||||
| chr2:148020565-148021285 | Common:6; Rare:372; Clinvar (benign):6 | ||||
| chr2:148021290-148022046 | Rare:393; Clinvar (benign):3 |