| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:9917023-9917191 | Common:2; Rare:31 | ||||
| chr3:9933673-9933919 | Common:2; Rare:88 | ||||
| chr3:10026299-10026480 | Rare:60 | ||||
| chr3:10115545-10115748 | Common:3; Rare:77 | ||||
| chr3:10141660-10142012 | Common:1; Rare:164; Clinvar:40; Clinvar (benign):34 | ||||
| chr3:10321048-10321257 | Common:2; Rare:90 | ||||
| chr3:11154361-11154502 | Common:3; Rare:39 | ||||
| chr3:11272233-11272423 | Common:1; Rare:42 | ||||
| chr3:11582332-11582439 | Rare:30 | ||||
| chr3:11643755-11644074 | Common:2; Rare:87 | ||||
| chr3:11719425-11719577 | Rare:48 | ||||
| chr3:12004240-12004402 | Common:2; Rare:49 | ||||
| chr3:12158844-12159021 | Rare:58 | ||||
| chr3:12484165-12484554 | Common:5; Rare:115; Clinvar:3; Clinvar (benign):2 | ||||
| chr3:12664081-12664330 | Common:1; Rare:68; Clinvar:1; Clinvar (benign):3 |