| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:23916905-23917196 | Rare:111 | ||||
| chr3:25428107-25428392 | Rare:64 | ||||
| chr3:25783380-25783627 | Common:2; Rare:82; Clinvar (benign):3 | ||||
| chr3:25790008-25790118 | Common:3; Rare:42 | ||||
| chr3:27369366-27369568 | Rare:44 | ||||
| chr3:28348644-28348736 | Rare:20 | ||||
| chr3:28348768-28349196 | Common:4; Rare:139 | ||||
| chr3:29280837-29281076 | Common:3; Rare:48 | ||||
| chr3:30894624-30894744 | Common:2; Rare:35 | ||||
| chr3:31532380-31532728 | Common:4; Rare:105 | ||||
| chr3:32106431-32106714 | Common:3; Rare:74; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:32570673-32570962 | Common:1; Rare:125 | ||||
| chr3:33277313-33277476 | Common:1; Rare:41 | ||||
| chr3:33798537-33798697 | Common:2; Rare:62 | ||||
| chr3:33799014-33799029 | Rare:6 |