| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:135531172-135531520 | Common:1; Rare:74 | ||||
| chr2:135985404-135985642 | Common:4; Rare:111; Clinvar (benign):1 | ||||
| chr2:135985645-135985720 | Rare:20 | ||||
| chr2:136118117-136118319 | Rare:49 | ||||
| chr2:137964095-137964628 | Common:2; Rare:99 | ||||
| chr2:138501652-138502010 | Common:3; Rare:129 | ||||
| chr2:143129026-143129447 | Common:2; Rare:91 | ||||
| chr2:144513775-144513954 | Rare:47 | ||||
| chr2:144514820-144514910 | Rare:13 | ||||
| chr2:144517277-144517742 | Common:6; Rare:140; Clinvar:3; Clinvar (benign):5 | ||||
| chr2:144518134-144518205 | Common:1; Rare:16 | ||||
| chr2:144519947-144520563 | Common:4; Rare:121; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:148020692-148021096 | Common:2; Rare:94; Clinvar (benign):2 | ||||
| chr2:148021331-148021447 | Rare:21 | ||||
| chr2:148021544-148021625 | Rare:17 |