| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:85561411-85561581 | Rare:63; Clinvar:4 | ||||
| chr2:85595502-85595868 | Common:2; Rare:121 | ||||
| chr2:85602654-85602920 | Rare:65 | ||||
| chr2:85611930-85612203 | Rare:108 | ||||
| chr2:85888837-85889282 | Common:5; Rare:135; Clinvar:2; Clinvar (benign):3 | ||||
| chr2:86105803-86106323 | Common:4; Rare:181 | ||||
| chr2:86195341-86195522 | Common:3; Rare:64 | ||||
| chr2:86195528-86195627 | Common:1; Rare:30 | ||||
| chr2:88055628-88055700 | Rare:20 | ||||
| chr2:88055726-88055958 | Common:1; Rare:88 | ||||
| chr2:88627430-88627765 | Common:3; Rare:83; Clinvar:4; Clinvar (benign):1 | ||||
| chr2:88691415-88691726 | Common:3; Rare:113 | ||||
| chr2:95165652-95165830 | Rare:54 | ||||
| chr2:95207445-95207584 | Rare:55 | ||||
| chr2:95402617-95402867 | Rare:67 |