| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:85595562-85595764 | Common:1; Rare:65 | ||||
| chr2:85611983-85612113 | Rare:55 | ||||
| chr2:85616002-85616193 | Rare:70 | ||||
| chr2:85663344-85663853 | Common:4; Rare:154; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr2:85753621-85753844 | Common:2; Rare:66 | ||||
| chr2:85888838-85889157 | Common:3; Rare:102; Clinvar:2; Clinvar (benign):3 | ||||
| chr2:86036999-86037212 | Common:3; Rare:36 | ||||
| chr2:86105843-86106254 | Common:3; Rare:113 | ||||
| chr2:86195391-86195666 | Common:5; Rare:91 | ||||
| chr2:88691462-88691673 | Common:2; Rare:62 | ||||
| chr2:95165651-95165828 | Rare:54 | ||||
| chr2:95207435-95207549 | Rare:42 | ||||
| chr2:95402600-95402757 | Rare:55 | ||||
| chr2:96208258-96208407 | Rare:76 | ||||
| chr2:96208805-96208950 | Common:3; Rare:56 |