| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:219178103-219178470 | Common:6; Rare:149 | ||||
| chr2:219206665-219206885 | Rare:86 | ||||
| chr2:219229303-219229400 | Rare:31 | ||||
| chr2:219229553-219229958 | Common:3; Rare:120 | ||||
| chr2:219245442-219245531 | Rare:29 | ||||
| chr2:219253851-219254056 | Common:1; Rare:63 | ||||
| chr2:219279201-219279545 | Common:3; Rare:105; Clinvar (benign):1 | ||||
| chr2:219387768-219387804 | Rare:15 | ||||
| chr2:219498691-219498911 | Common:2; Rare:44 | ||||
| chr2:219597751-219597901 | Common:1; Rare:56 | ||||
| chr2:221572204-221572448 | Common:2; Rare:85 | ||||
| chr2:221573963-221574149 | Common:1; Rare:34 | ||||
| chr2:222298990-222299177 | Rare:34 | ||||
| chr2:226835918-226836117 | Common:1; Rare:80 | ||||
| chr2:227325195-227325425 | Common:5; Rare:79 |