| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:190880644-190880862 | Common:4; Rare:78 | ||||
| chr2:191678565-191678663 | Rare:41 | ||||
| chr2:192194923-192195034 | Rare:16 | ||||
| chr2:197434976-197435183 | Rare:70 | ||||
| chr2:197453244-197453558 | Rare:107 | ||||
| chr2:197499817-197500435 | Common:1; Rare:240; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:197675707-197675820 | Rare:14 | ||||
| chr2:200306767-200306918 | Rare:46 | ||||
| chr2:200509922-200510263 | Common:2; Rare:115 | ||||
| chr2:200811804-200811973 | Rare:73 | ||||
| chr2:200889005-200889464 | Common:3; Rare:149 | ||||
| chr2:200963611-200963884 | Common:1; Rare:69 | ||||
| chr2:201071609-201072006 | Rare:83 | ||||
| chr2:201258311-201258378 | Rare:26 | ||||
| chr2:201451426-201451767 | Common:1; Rare:78 |