| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:188154058-188154216 | Rare:47 | ||||
| chr3:190120254-190120682 | Common:1; Rare:184; Clinvar (pathogenic):1 | ||||
| chr3:190120783-190121137 | Rare:96 | ||||
| chr3:190322415-190322552 | Common:2; Rare:36 | ||||
| chr3:191329331-191329660 | Common:3; Rare:100 | ||||
| chr3:192917784-192918008 | Common:2; Rare:103 | ||||
| chr3:193593078-193593380 | Rare:97; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:194135911-194136120 | Rare:51 | ||||
| chr3:194136134-194136365 | Common:2; Rare:56 | ||||
| chr3:194425498-194425776 | Rare:61 | ||||
| chr3:194632812-194633010 | Rare:36 | ||||
| chr3:194633650-194633774 | Common:1; Rare:25 | ||||
| chr3:194633827-194633936 | Rare:15 | ||||
| chr3:194686205-194686452 | Common:5; Rare:53 | ||||
| chr3:195271063-195271309 | Common:1; Rare:99 |