| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:169773341-169773410 | Rare:19 | ||||
| chr3:170870168-170870264 | Rare:51 | ||||
| chr3:172750352-172750794 | Common:4; Rare:100 | ||||
| chr3:179347595-179347761 | Common:1; Rare:38 | ||||
| chr3:179604591-179604852 | Common:3; Rare:102 | ||||
| chr3:180602020-180602232 | Common:1; Rare:68 | ||||
| chr3:180989659-180989790 | Rare:56; Clinvar:1 | ||||
| chr3:183099475-183099758 | Common:2; Rare:80; Clinvar:2; Clinvar (benign):3 | ||||
| chr3:184135221-184135403 | Common:2; Rare:56; Clinvar:5 | ||||
| chr3:184185863-184186203 | Common:5; Rare:126 | ||||
| chr3:184249487-184249777 | Common:1; Rare:89 | ||||
| chr3:184298979-184299320 | Common:3; Rare:102 | ||||
| chr3:184711972-184712119 | Rare:54 | ||||
| chr3:185282844-185283003 | Common:1; Rare:40 | ||||
| chr3:185585987-185586241 | Common:1; Rare:62 |