| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:186784134-186784251 | Common:1; Rare:49 | ||||
| chr3:187291679-187291877 | Common:1; Rare:70 | ||||
| chr3:187291948-187292309 | Common:19; Rare:73 | ||||
| chr3:188153763-188153982 | Common:1; Rare:40 | ||||
| chr3:190120319-190120526 | Common:1; Rare:82; Clinvar (pathogenic):1 | ||||
| chr3:190321984-190322216 | Common:1; Rare:80; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr3:190322404-190322538 | Common:2; Rare:35 | ||||
| chr3:190513903-190514101 | Common:2; Rare:55 | ||||
| chr3:192917838-192918014 | Common:2; Rare:80 | ||||
| chr3:193593107-193593303 | Rare:58; Clinvar:1 | ||||
| chr3:194136416-194136650 | Rare:77 | ||||
| chr3:195542940-195542978 | Rare:15 | ||||
| chr3:195543283-195543439 | Common:2; Rare:60 | ||||
| chr3:195584081-195584408 | Common:12; Rare:64 | ||||
| chr3:195811779-195812066 | Common:6; Rare:81 |