| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:85413978-85414136 | Common:2; Rare:33 | ||||
| chr2:85539054-85539373 | Common:3; Rare:153; Clinvar (benign):7 | ||||
| chr2:85540946-85541169 | Common:1; Rare:57; Clinvar (benign):1 | ||||
| chr2:85561421-85561562 | Rare:53; Clinvar:4 | ||||
| chr2:85595543-85595867 | Common:2; Rare:106 | ||||
| chr2:85602631-85602924 | Rare:77 | ||||
| chr2:85612009-85612147 | Rare:43 | ||||
| chr2:85753622-85753863 | Common:2; Rare:70 | ||||
| chr2:85888817-85889280 | Common:5; Rare:138; Clinvar:3; Clinvar (benign):3 | ||||
| chr2:86105792-86106330 | Common:4; Rare:187 | ||||
| chr2:86195338-86195658 | Common:5; Rare:108 | ||||
| chr2:86199414-86199493 | Common:1; Rare:32 | ||||
| chr2:88055628-88055692 | Rare:19 | ||||
| chr2:88055723-88055923 | Rare:74 | ||||
| chr2:88627400-88627916 | Common:3; Rare:142; Clinvar:4; Clinvar (benign):1 |