| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:196568512-196568679 | Common:6; Rare:91 | ||||
| chr3:196712240-196712425 | Common:8; Rare:127 | ||||
| chr3:196867747-196868012 | Rare:161 | ||||
| chr3:196942337-196942719 | Common:2; Rare:326 | ||||
| chr3:196968000-196968630 | Common:4; Rare:234 | ||||
| chr3:196968785-196968956 | Common:2; Rare:106 | ||||
| chr3:197029800-197029945 | Common:1; Rare:45 | ||||
| chr3:197297841-197298176 | Rare:188 | ||||
| chr3:197298531-197298731 | Rare:112 | ||||
| chr3:197299270-197299480 | Rare:56 | ||||
| chr3:197573167-197573484 | Common:2; Rare:102 | ||||
| chr3:197736784-197737227 | Common:6; Rare:261 | ||||
| chr3:197749693-197749998 | Common:2; Rare:170 | ||||
| chr3:197949882-197950281 | Common:8; Rare:232; Clinvar (benign):4 | ||||
| chr3:197959983-197960245 | Common:2; Rare:176 |