| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:75560921-75561035 | Rare:27 | ||||
| chr2:75710669-75710761 | Common:1; Rare:38 | ||||
| chr2:75710872-75710986 | Common:1; Rare:42 | ||||
| chr2:84459228-84459593 | Common:3; Rare:92; Clinvar:4; Clinvar (benign):4 | ||||
| chr2:84516145-84516544 | Common:2; Rare:102 | ||||
| chr2:84881004-84881215 | Common:1; Rare:57 | ||||
| chr2:84881314-84881507 | Rare:29 | ||||
| chr2:84905506-84905937 | Common:1; Rare:130 | ||||
| chr2:84906997-84907264 | Common:1; Rare:46 | ||||
| chr2:85327936-85328080 | Common:2; Rare:67 | ||||
| chr2:85354526-85354792 | Common:1; Rare:85 | ||||
| chr2:85413994-85414076 | Common:1; Rare:21 | ||||
| chr2:85539068-85539188 | Common:2; Rare:50 | ||||
| chr2:85561425-85561571 | Rare:53; Clinvar:4 | ||||
| chr2:85577496-85577627 | Common:1; Rare:37 |