| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:288831-289250 | Rare:88 | ||||
| chr2:676665-677085 | Common:6; Rare:153 | ||||
| chr2:677355-677598 | Common:2; Rare:170 | ||||
| chr2:3377655-3378009 | Common:2; Rare:178 | ||||
| chr2:3379577-3379861 | Common:5; Rare:195 | ||||
| chr2:3518918-3519275 | Common:2; Rare:100 | ||||
| chr2:3519371-3519695 | Common:5; Rare:150 | ||||
| chr2:3558208-3558731 | Common:12; Rare:377 | ||||
| chr2:3575087-3575407 | Common:4; Rare:179; Clinvar:6; Clinvar (benign):12 | ||||
| chr2:3594919-3595164 | Rare:159 | ||||
| chr2:3605251-3605785 | Common:18; Rare:187 | ||||
| chr2:8678676-8679090 | Common:11; Rare:314 | ||||
| chr2:8679110-8679290 | Rare:120 | ||||
| chr2:8681463-8682344 | Common:14; Rare:537 | ||||
| chr2:9206500-9206897 | Rare:268 |