| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:123739700-123739974 | Common:2; Rare:48; Clinvar (benign):2 | ||||
| chr3:123951357-123951495 | Common:1; Rare:21 | ||||
| chr3:125497917-125498064 | Rare:38 | ||||
| chr3:125990519-125990575 | Common:2; Rare:18 | ||||
| chr3:139373390-139373678 | Rare:53 | ||||
| chr3:142416772-142417010 | Common:1; Rare:52 | ||||
| chr3:143023980-143024151 | Rare:33 | ||||
| chr3:150408836-150408988 | Rare:46 | ||||
| chr3:153163779-153164056 | Rare:47 | ||||
| chr3:155116494-155116755 | Common:1; Rare:71; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr3:160423688-160423782 | Rare:30 | ||||
| chr3:160515221-160515471 | Common:1; Rare:50 | ||||
| chr3:177038137-177038396 | Rare:38; Clinvar:1 | ||||
| chr3:177047303-177047505 | Common:1; Rare:42; Clinvar (benign):3 | ||||
| chr3:184323517-184323794 | Common:3; Rare:74 |