| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:126303961-126304100 | Rare:81 | ||||
| chr11:126355531-126355755 | Common:1; Rare:61 | ||||
| chr11:128693803-128694078 | Common:2; Rare:48 | ||||
| chr11:130314427-130314465 | Rare:12 | ||||
| chr11:134253298-134253586 | Common:2; Rare:94; Clinvar (benign):1 | ||||
| chr12:991109-991278 | Common:1; Rare:67 | ||||
| chr12:2876997-2877268 | Rare:85 | ||||
| chr12:2959843-2959920 | Common:1; Rare:18 | ||||
| chr12:3077211-3077428 | Common:6; Rare:91 | ||||
| chr12:3873355-3873514 | Common:1; Rare:36 | ||||
| chr12:4320949-4321260 | Common:5; Rare:118 | ||||
| chr12:4538444-4538940 | Common:3; Rare:112 | ||||
| chr12:4649026-4649158 | Common:1; Rare:50; Clinvar (benign):2 | ||||
| chr12:6200005-6200467 | Common:4; Rare:135 | ||||
| chr12:6493140-6493503 | Common:8; Rare:113 |