| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:179572929-179572966 | Rare:6 | ||||
| chr3:179604525-179604848 | Common:3; Rare:127 | ||||
| chr3:180602104-180602288 | Common:1; Rare:65 | ||||
| chr3:180912367-180912730 | Common:4; Rare:121 | ||||
| chr3:180989647-180989790 | Rare:62; Clinvar:1 | ||||
| chr3:180989804-180990125 | Rare:69 | ||||
| chr3:182793362-182793710 | Common:3; Rare:97 | ||||
| chr3:183099463-183099780 | Common:2; Rare:90; Clinvar:2; Clinvar (benign):4 | ||||
| chr3:183697680-183697917 | Common:2; Rare:105 | ||||
| chr3:183884726-183884972 | Rare:102 | ||||
| chr3:183983652-183983781 | Rare:22 | ||||
| chr3:184135221-184135400 | Common:2; Rare:55; Clinvar:5 | ||||
| chr3:184155297-184155501 | Rare:62 | ||||
| chr3:184164124-184164374 | Common:2; Rare:61 | ||||
| chr3:184174620-184174969 | Common:3; Rare:94 |