| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:111883913-111883989 | Rare:23 | ||||
| chr2:111884012-111884283 | Common:2; Rare:71 | ||||
| chr2:111898300-111898632 | Common:2; Rare:73 | ||||
| chr2:112254307-112254610 | Common:1; Rare:58 | ||||
| chr2:112254988-112255169 | Common:1; Rare:79 | ||||
| chr2:112275384-112275637 | Common:1; Rare:89 | ||||
| chr2:112481954-112482314 | Common:3; Rare:125 | ||||
| chr2:112542148-112542504 | Common:2; Rare:111 | ||||
| chr2:112584346-112584657 | Common:1; Rare:89 | ||||
| chr2:112584770-112584892 | Rare:28 | ||||
| chr2:112645665-112645964 | Common:2; Rare:110 | ||||
| chr2:112646105-112646395 | Common:2; Rare:91 | ||||
| chr2:112763876-112764216 | Common:4; Rare:104 | ||||
| chr2:112764575-112764859 | Common:2; Rare:96; Clinvar (pathogenic):1 | ||||
| chr2:112784453-112784537 | Rare:16 |