| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:167734472-167734605 | Rare:31 | ||||
| chr3:167734825-167735254 | Common:5; Rare:136; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:167735563-167735763 | Rare:50 | ||||
| chr3:168095205-168095434 | Rare:77 | ||||
| chr3:168095862-168096205 | Common:1; Rare:114 | ||||
| chr3:169769581-169769643 | Rare:19 | ||||
| chr3:169772693-169772825 | Common:1; Rare:34 | ||||
| chr3:169773331-169773425 | Rare:30 | ||||
| chr3:169966610-169966851 | Common:2; Rare:89 | ||||
| chr3:170222315-170222572 | Common:2; Rare:86 | ||||
| chr3:170358205-170358574 | Common:4; Rare:124 | ||||
| chr3:170870157-170870239 | Rare:54 | ||||
| chr3:171810102-171810309 | Common:1; Rare:36 | ||||
| chr3:172039489-172039785 | Common:2; Rare:92 | ||||
| chr3:172040238-172040587 | Common:3; Rare:88 |