| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:180951230-180951377 | Rare:32 | ||||
| chr3:180989659-180989786 | Rare:54; Clinvar:1 | ||||
| chr3:183253039-183253293 | Common:3; Rare:75 | ||||
| chr3:183555695-183556010 | Common:2; Rare:53 | ||||
| chr3:183884842-183884981 | Rare:52 | ||||
| chr3:184135221-184135398 | Common:2; Rare:55; Clinvar:5 | ||||
| chr3:184142105-184142368 | Common:1; Rare:70; Clinvar (benign):1 | ||||
| chr3:184185888-184186215 | Common:4; Rare:122 | ||||
| chr3:184249463-184249689 | Rare:54 | ||||
| chr3:184298964-184299320 | Common:3; Rare:108 | ||||
| chr3:184325283-184325622 | Common:1; Rare:88 | ||||
| chr3:184337356-184337616 | Rare:42 | ||||
| chr3:184362142-184362263 | Common:1; Rare:18 | ||||
| chr3:184711943-184712267 | Common:1; Rare:108 | ||||
| chr3:185282838-185283006 | Common:1; Rare:45 |