| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:9749980-9750312 | Common:2; Rare:100 | ||||
| chr3:9792384-9792590 | Rare:56 | ||||
| chr3:9792705-9793123 | Common:3; Rare:148 | ||||
| chr3:9917023-9917319 | Common:3; Rare:63 | ||||
| chr3:9933497-9933870 | Common:2; Rare:149; Clinvar:3 | ||||
| chr3:10026335-10026411 | Rare:23 | ||||
| chr3:11719432-11719577 | Rare:45 | ||||
| chr3:12287733-12287995 | Common:7; Rare:52 | ||||
| chr3:12663821-12663931 | Rare:29; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:12664064-12664277 | Common:2; Rare:56; Clinvar:1; Clinvar (benign):4 | ||||
| chr3:13480040-13480339 | Common:2; Rare:70 | ||||
| chr3:13548983-13549181 | Common:1; Rare:66 | ||||
| chr3:14124685-14125179 | Common:4; Rare:145; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178564-14178881 | Common:2; Rare:166; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:14402379-14402716 | Common:1; Rare:84 |