| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:184248875-184249026 | Rare:79; Clinvar:5; Clinvar (benign):2 | ||||
| chr3:184249531-184249697 | Rare:48 | ||||
| chr3:184298957-184299330 | Common:5; Rare:113 | ||||
| chr3:184335852-184335977 | Rare:46 | ||||
| chr3:185282861-185283006 | Common:1; Rare:37 | ||||
| chr3:185586000-185586334 | Common:1; Rare:73 | ||||
| chr3:185821122-185821325 | Rare:37 | ||||
| chr3:186567289-186567520 | Common:3; Rare:62 | ||||
| chr3:186783270-186783598 | Common:1; Rare:123 | ||||
| chr3:186806426-186806577 | Rare:53 | ||||
| chr3:188153835-188153892 | Common:1; Rare:13 | ||||
| chr3:188154046-188154216 | Rare:51 | ||||
| chr3:190322394-190322566 | Common:2; Rare:45 | ||||
| chr3:191329288-191329702 | Common:4; Rare:122 | ||||
| chr3:192917830-192918023 | Common:2; Rare:86 |