| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:130356446-130356599 | Common:2; Rare:30 | ||||
| chr2:130372962-130373229 | Common:3; Rare:55 | ||||
| chr2:131093405-131093569 | Rare:73 | ||||
| chr2:131492762-131493106 | Common:8; Rare:105 | ||||
| chr2:132416413-132416654 | Common:1; Rare:62 | ||||
| chr2:134918591-134918898 | Common:1; Rare:129 | ||||
| chr2:135531195-135531508 | Common:1; Rare:57 | ||||
| chr2:135985429-135985648 | Common:4; Rare:105; Clinvar (benign):1 | ||||
| chr2:135985653-135985932 | Common:2; Rare:71 | ||||
| chr2:136118139-136118247 | Rare:36 | ||||
| chr2:137964154-137964515 | Common:2; Rare:64 | ||||
| chr2:138501649-138501969 | Common:4; Rare:121 | ||||
| chr2:144332457-144332706 | Rare:95 | ||||
| chr2:148020688-148021096 | Common:2; Rare:95; Clinvar (benign):2 | ||||
| chr2:148021571-148021658 | Rare:18 |