| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:57079235-57079382 | Common:2; Rare:49 | ||||
| chr3:57227600-57227913 | Common:3; Rare:107 | ||||
| chr3:57556012-57556307 | Rare:70 | ||||
| chr3:57597278-57597576 | Common:4; Rare:92 | ||||
| chr3:57889876-57890100 | Rare:50; Clinvar (benign):2 | ||||
| chr3:58433799-58433944 | Rare:57; Clinvar (benign):3 | ||||
| chr3:61251391-61251597 | Common:4; Rare:52 | ||||
| chr3:62318888-62319080 | Rare:80 | ||||
| chr3:63863774-63864132 | Common:7; Rare:119 | ||||
| chr3:64687605-64687738 | Rare:34 | ||||
| chr3:64687996-64688164 | Common:1; Rare:49 | ||||
| chr3:67654566-67654727 | Common:1; Rare:63 | ||||
| chr3:69013197-69013384 | Rare:53 | ||||
| chr3:71130539-71130692 | Common:1; Rare:61; Clinvar:2 | ||||
| chr3:81761513-81761846 | Common:8; Rare:110; Clinvar:1; Clinvar (benign):1 |