| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74421562-74421768 | Rare:68 | ||||
| chr2:74454916-74455130 | Rare:64 | ||||
| chr2:74458146-74458486 | Common:1; Rare:104 | ||||
| chr2:74465360-74465455 | Common:1; Rare:25 | ||||
| chr2:74482916-74483098 | Common:1; Rare:60 | ||||
| chr2:74507371-74507545 | Rare:52 | ||||
| chr2:74507669-74507799 | Rare:27 | ||||
| chr2:74529639-74530031 | Rare:124; Clinvar:4; Clinvar (benign):1 | ||||
| chr2:74833876-74834147 | Rare:80 | ||||
| chr2:74958502-74958697 | Common:3; Rare:72 | ||||
| chr2:74958872-74959038 | Rare:62 | ||||
| chr2:75646739-75646836 | Rare:35 | ||||
| chr2:75710648-75711011 | Common:3; Rare:156 | ||||
| chr2:84459231-84459593 | Common:3; Rare:91; Clinvar:4; Clinvar (benign):4 | ||||
| chr2:84894960-84894993 | Rare:5 |