| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:190322382-190322552 | Common:2; Rare:44 | ||||
| chr3:191329310-191329672 | Common:3; Rare:113 | ||||
| chr3:192917836-192918003 | Common:2; Rare:76 | ||||
| chr3:193593090-193593402 | Rare:97; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:194486970-194487146 | Common:4; Rare:88 | ||||
| chr3:195543189-195543364 | Common:3; Rare:65 | ||||
| chr3:195583915-195584192 | Common:9; Rare:62 | ||||
| chr3:196287681-196287831 | Common:1; Rare:46 | ||||
| chr3:196318156-196318346 | Common:1; Rare:85 | ||||
| chr3:196503697-196503945 | Common:4; Rare:86 | ||||
| chr3:196639581-196639805 | Common:2; Rare:55 | ||||
| chr3:196712190-196712582 | Common:6; Rare:129 | ||||
| chr3:196942375-196942650 | Common:1; Rare:113 | ||||
| chr3:197736851-197737133 | Common:3; Rare:86 | ||||
| chr3:197749826-197750007 | Rare:70 |