| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:157174857-157175322 | Common:3; Rare:195 | ||||
| chr3:159763077-159763141 | Rare:17 | ||||
| chr3:161068730-161068924 | Rare:45 | ||||
| chr3:164451228-164451413 | Common:3; Rare:26 | ||||
| chr3:169764847-169765222 | Common:1; Rare:140; Clinvar:17; Clinvar (pathogenic):6 | ||||
| chr3:171167177-171167451 | Common:1; Rare:43 | ||||
| chr3:172104536-172104739 | Rare:29 | ||||
| chr3:175718673-175718814 | Common:1; Rare:26 | ||||
| chr3:177026370-177026636 | Rare:46; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:177035475-177035507 | Rare:6 | ||||
| chr3:177300256-177300539 | Common:1; Rare:59 | ||||
| chr3:180962729-180963090 | Rare:92 | ||||
| chr3:184015637-184015832 | Rare:24 | ||||
| chr3:184322700-184322948 | Rare:63 | ||||
| chr3:184323079-184323593 | Common:2; Rare:144 |