| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:95682510-95682900 | Common:3; Rare:174 | ||||
| chr2:95686343-95687016 | Common:3; Rare:276 | ||||
| chr2:95992790-95993110 | Common:2; Rare:69 | ||||
| chr2:96010251-96010608 | Rare:103 | ||||
| chr2:96108927-96109036 | Rare:22 | ||||
| chr2:96116990-96117350 | Common:1; Rare:120 | ||||
| chr2:96147010-96147390 | Common:6; Rare:183 | ||||
| chr2:96298549-96299523 | Common:4; Rare:453; Clinvar:5; Clinvar (benign):5 | ||||
| chr2:96680553-96680885 | Common:3; Rare:59 | ||||
| chr2:96714550-96714920 | Rare:54 | ||||
| chr2:96737890-96738326 | Rare:187 | ||||
| chr2:96762952-96763159 | Rare:41 | ||||
| chr2:96769937-96770306 | Common:1; Rare:61 | ||||
| chr2:96771818-96772324 | Common:2; Rare:165 | ||||
| chr2:96773908-96774814 | Common:3; Rare:282 |