| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:3379608-3379808 | Common:2; Rare:81 | ||||
| chr2:3519478-3519660 | Common:2; Rare:57 | ||||
| chr2:3558244-3558715 | Common:6; Rare:174 | ||||
| chr2:3575107-3575358 | Common:2; Rare:73; Clinvar:3; Clinvar (benign):5 | ||||
| chr2:6865647-6865799 | Common:1; Rare:46 | ||||
| chr2:6866531-6866558 | Rare:5 | ||||
| chr2:9423169-9423720 | Common:1; Rare:156 | ||||
| chr2:9474500-9474630 | Common:6; Rare:62 | ||||
| chr2:9555627-9556065 | Common:3; Rare:145 | ||||
| chr2:9843273-9843371 | Common:1; Rare:28 | ||||
| chr2:9843392-9843553 | Common:5; Rare:45 | ||||
| chr2:10043393-10043735 | Common:4; Rare:155; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:10302439-10302549 | Rare:38 | ||||
| chr2:10302721-10302915 | Common:3; Rare:69 | ||||
| chr2:10419637-10419799 | Rare:43 |