| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74503307-74503501 | Rare:52 | ||||
| chr2:74507635-74507823 | Rare:46 | ||||
| chr2:74529653-74530044 | Rare:121; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:74530434-74530620 | Common:2; Rare:57; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:74554406-74554757 | Common:2; Rare:104 | ||||
| chr2:74555623-74555798 | Common:1; Rare:51 | ||||
| chr2:74654112-74654280 | Rare:42 | ||||
| chr2:74833854-74834204 | Rare:103 | ||||
| chr2:74834891-74835026 | Rare:32 | ||||
| chr2:74835132-74835343 | Common:1; Rare:51 | ||||
| chr2:74958494-74958791 | Common:5; Rare:120 | ||||
| chr2:74958876-74959076 | Rare:71 | ||||
| chr2:75199513-75199629 | Rare:23 | ||||
| chr2:75560929-75561170 | Common:2; Rare:66 | ||||
| chr2:84459219-84459587 | Common:3; Rare:93; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 |