| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:58471330-58471670 | Common:2; Rare:91 | ||||
| chr3:75435021-75435339 | Common:7; Rare:214 | ||||
| chr3:75672105-75672302 | Common:26; Rare:11 | ||||
| chr3:81760850-81761420 | Common:2; Rare:215; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr3:86951280-86951610 | Rare:100 | ||||
| chr3:101676191-101676507 | Common:7; Rare:183 | ||||
| chr3:107240525-107240980 | Rare:185 | ||||
| chr3:107241397-107241690 | Rare:93 | ||||
| chr3:107431365-107431770 | Common:10; Rare:209 | ||||
| chr3:107431790-107432250 | Common:4; Rare:194 | ||||
| chr3:110971315-110971493 | Common:2; Rare:65 | ||||
| chr3:115147840-115148100 | Rare:88 | ||||
| chr3:115783840-115785012 | Common:11; Rare:433 | ||||
| chr3:115790690-115791102 | Common:4; Rare:124 | ||||
| chr3:115792603-115793021 | Common:1; Rare:119 |