| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:187291684-187291864 | Common:1; Rare:65 | ||||
| chr3:190322423-190322552 | Common:1; Rare:36 | ||||
| chr3:193593097-193593338 | Rare:75; Clinvar:1 | ||||
| chr3:195543203-195543475 | Common:3; Rare:102 | ||||
| chr3:196287610-196287782 | Common:1; Rare:53 | ||||
| chr3:196318174-196318346 | Common:1; Rare:73 | ||||
| chr3:196503686-196503949 | Common:5; Rare:90 | ||||
| chr3:196568526-196568643 | Common:1; Rare:29 | ||||
| chr3:196712228-196712344 | Common:2; Rare:37 | ||||
| chr3:196867738-196867931 | Rare:59 | ||||
| chr3:196941873-196941966 | Rare:31 | ||||
| chr3:196942375-196942679 | Common:1; Rare:127 | ||||
| chr3:197736833-197737193 | Common:3; Rare:119 | ||||
| chr3:197749777-197749962 | Common:1; Rare:71 | ||||
| chr3:197949890-197950235 | Common:4; Rare:106; Clinvar (benign):1 |