| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:155805662-155806288 | Common:4; Rare:146 | ||||
| chr3:155806212-155806486 | Common:2; Rare:116 | ||||
| chr3:155853161-155854060 | Common:5; Rare:533; Clinvar:11; Clinvar (benign):18; Clinvar (pathogenic):3 | ||||
| chr3:155854287-155855222 | Common:2; Rare:951; Clinvar (benign):2 | ||||
| chr3:155870160-155870827 | Common:15; Rare:958 | ||||
| chr3:155870764-155871384 | Common:3; Rare:193 | ||||
| chr3:156455749-156456149 | Common:2; Rare:100 | ||||
| chr3:156456680-156456934 | Common:5; Rare:77 | ||||
| chr3:156553641-156554336 | Common:10; Rare:257 | ||||
| chr3:156554735-156555444 | Common:12; Rare:804 | ||||
| chr3:156673899-156674696 | Common:31; Rare:790 | ||||
| chr3:156675396-156675796 | Common:7; Rare:210 | ||||
| chr3:156825393-156826510 | Common:29; Rare:795 | ||||
| chr3:156826510-156826760 | Common:4; Rare:174 | ||||
| chr3:156826730-156827310 | Common:12; Rare:230 |