| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:88627282-88627948 | Common:3; Rare:192; Clinvar:5; Clinvar (benign):1 | ||||
| chr2:88628051-88628337 | Rare:55 | ||||
| chr2:88690756-88691199 | Common:2; Rare:87 | ||||
| chr2:88691365-88691918 | Common:3; Rare:205; Clinvar:2 | ||||
| chr2:95121722-95121879 | Common:1; Rare:72 | ||||
| chr2:95121899-95122135 | Rare:74 | ||||
| chr2:95159556-95159945 | Common:4; Rare:116 | ||||
| chr2:95165184-95165280 | Rare:18 | ||||
| chr2:95165370-95165490 | Rare:19 | ||||
| chr2:95165584-95165882 | Common:1; Rare:93 | ||||
| chr2:95207366-95207623 | Rare:96 | ||||
| chr2:95402553-95402788 | Rare:76 | ||||
| chr2:95402932-95402974 | Rare:11 | ||||
| chr2:95403272-95403380 | Rare:24 | ||||
| chr2:95991530-95991574 | Rare:12 |