| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:136116612-136116725 | Common:1; Rare:22 | ||||
| chr2:136117965-136118336 | Rare:99 | ||||
| chr2:137964092-137964508 | Common:2; Rare:67 | ||||
| chr2:138501675-138501949 | Common:2; Rare:97 | ||||
| chr2:142877511-142877711 | Common:1; Rare:31 | ||||
| chr2:144332444-144332752 | Common:1; Rare:122 | ||||
| chr2:144513688-144513959 | Rare:77 | ||||
| chr2:144517307-144517727 | Common:5; Rare:131; Clinvar:3; Clinvar (benign):5 | ||||
| chr2:144520032-144520543 | Common:4; Rare:100; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:144524536-144524657 | Common:3; Rare:36 | ||||
| chr2:148020682-148021019 | Common:2; Rare:71 | ||||
| chr2:148021510-148021675 | Rare:33 | ||||
| chr2:152717911-152718055 | Rare:51 | ||||
| chr2:152718501-152718650 | Rare:57 | ||||
| chr2:156332670-156332870 | Rare:63; Clinvar:3 |