| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74482937-74483124 | Common:1; Rare:75 | ||||
| chr2:74483240-74483402 | Common:2; Rare:62 | ||||
| chr2:74507282-74507473 | Rare:52 | ||||
| chr2:74507592-74507795 | Rare:51 | ||||
| chr2:74529653-74530041 | Rare:120; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:74530434-74530650 | Common:2; Rare:64; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:74548931-74549133 | Rare:55 | ||||
| chr2:74554395-74554755 | Common:2; Rare:107 | ||||
| chr2:74654103-74654394 | Common:1; Rare:102 | ||||
| chr2:74833772-74834166 | Common:1; Rare:119 | ||||
| chr2:74835132-74835316 | Rare:46 | ||||
| chr2:74958538-74958677 | Common:3; Rare:49 | ||||
| chr2:74958872-74959076 | Rare:73 | ||||
| chr2:75647021-75647168 | Common:1; Rare:40 | ||||
| chr2:75710606-75711013 | Common:3; Rare:166 |