| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:40309486-40309851 | Common:9; Rare:125 | ||||
| chr3:40457204-40457470 | Common:6; Rare:123 | ||||
| chr3:42581903-42582106 | Common:2; Rare:66 | ||||
| chr3:42600285-42600720 | Common:3; Rare:169 | ||||
| chr3:42804427-42804663 | Common:2; Rare:71 | ||||
| chr3:43286471-43286645 | Common:2; Rare:78 | ||||
| chr3:43690622-43690967 | Common:4; Rare:133; Clinvar:6; Clinvar (benign):1 | ||||
| chr3:44477641-44477739 | Common:1; Rare:20 | ||||
| chr3:44624767-44625033 | Common:1; Rare:54 | ||||
| chr3:44761577-44761804 | Common:3; Rare:87 | ||||
| chr3:44861811-44861927 | Common:2; Rare:56 | ||||
| chr3:44976028-44976320 | Common:5; Rare:116 | ||||
| chr3:45003743-45004040 | Common:1; Rare:58 | ||||
| chr3:45146301-45146504 | Common:1; Rare:72 | ||||
| chr3:45689156-45689459 | Common:2; Rare:103 |