| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:12664075-12664300 | Common:1; Rare:61; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:14124728-14125179 | Common:4; Rare:128; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178569-14178870 | Common:2; Rare:155; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14402437-14402628 | Rare:47 | ||||
| chr3:14947365-14947551 | Common:3; Rare:87 | ||||
| chr3:15427459-15427623 | Common:1; Rare:61 | ||||
| chr3:15601556-15601804 | Common:3; Rare:92; Clinvar:1 | ||||
| chr3:16264881-16265220 | Common:2; Rare:109 | ||||
| chr3:17742596-17742952 | Common:4; Rare:124 | ||||
| chr3:19946974-19947436 | Common:7; Rare:171 | ||||
| chr3:20186192-20186415 | Common:2; Rare:70 | ||||
| chr3:23202926-23203130 | Common:1; Rare:76 | ||||
| chr3:23916898-23917181 | Rare:110 | ||||
| chr3:25428107-25428275 | Rare:33 | ||||
| chr3:25783388-25783640 | Common:2; Rare:80; Clinvar (benign):3 |