| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:161100994-161101239 | Rare:64 | ||||
| chr3:161104370-161104770 | Common:7; Rare:145 | ||||
| chr3:161104840-161105820 | Common:12; Rare:436 | ||||
| chr3:161221138-161221820 | Common:9; Rare:376 | ||||
| chr3:161221812-161222212 | Common:18; Rare:234 | ||||
| chr3:161371103-161372253 | Common:15; Rare:443 | ||||
| chr3:161372263-161372586 | Common:5; Rare:86 | ||||
| chr3:161372703-161373285 | Common:7; Rare:296 | ||||
| chr3:167734817-167735308 | Common:13; Rare:428; Clinvar:3; Clinvar (benign):3 | ||||
| chr3:167735516-167735796 | Rare:155; Clinvar:1 | ||||
| chr3:168095524-168096286 | Common:10; Rare:374 | ||||
| chr3:169662756-169663203 | Common:3; Rare:277 | ||||
| chr3:169663160-169663960 | Common:9; Rare:358 | ||||
| chr3:169769293-169769804 | Common:5; Rare:306 | ||||
| chr3:169772682-169772868 | Common:2; Rare:100 |