| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:167734827-167735071 | Common:2; Rare:84; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:169663620-169663846 | Common:2; Rare:59 | ||||
| chr3:169773341-169773424 | Rare:25 | ||||
| chr3:171460320-171460607 | Rare:69 | ||||
| chr3:172039485-172039656 | Common:1; Rare:56 | ||||
| chr3:172750552-172750794 | Common:3; Rare:69 | ||||
| chr3:172750949-172751026 | Rare:23 | ||||
| chr3:179604620-179604877 | Common:2; Rare:100 | ||||
| chr3:180601960-180602258 | Common:1; Rare:94 | ||||
| chr3:180989618-180989790 | Rare:76; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:182793385-182793630 | Common:3; Rare:53 | ||||
| chr3:183099443-183099742 | Common:2; Rare:96; Clinvar:3; Clinvar (benign):5 | ||||
| chr3:183635473-183635687 | Common:3; Rare:70 | ||||
| chr3:184135209-184135400 | Common:2; Rare:57; Clinvar:5 | ||||
| chr3:184176574-184176874 | Common:4; Rare:56 |