| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:95843037-95843146 | Common:1; Rare:22 | ||||
| chr2:95937007-95937283 | Rare:4 | ||||
| chr2:96010450-96010621 | Rare:43 | ||||
| chr2:96019004-96019260 | Common:2; Rare:45 | ||||
| chr2:96267391-96267649 | Common:2; Rare:73 | ||||
| chr2:96297436-96297708 | Common:1; Rare:69; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:97158483-97158611 | Rare:27 | ||||
| chr2:98771879-98772017 | Common:1; Rare:23 | ||||
| chr2:99404614-99404875 | Common:1; Rare:57 | ||||
| chr2:99703729-99703795 | Rare:9 | ||||
| chr2:100320718-100321022 | Common:1; Rare:49 | ||||
| chr2:100818551-100818598 | Rare:12 | ||||
| chr2:100818675-100818737 | Rare:10 | ||||
| chr2:101003918-101004268 | Rare:78 | ||||
| chr2:101008096-101008532 | Common:2; Rare:138 |