| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:93973790-93974360 | Common:1; Rare:185; Clinvar:8 | ||||
| chr3:93979913-93980288 | Common:12; Rare:364; Clinvar:4; Clinvar (benign):6 | ||||
| chr3:94028199-94028940 | Rare:200 | ||||
| chr3:94062708-94063152 | Common:4; Rare:242 | ||||
| chr3:94063160-94063440 | Rare:100 | ||||
| chr3:96813983-96814098 | Rare:26 | ||||
| chr3:96814118-96814240 | Common:1; Rare:32 | ||||
| chr3:96814349-96814771 | Rare:289 | ||||
| chr3:97764346-97764821 | Common:3; Rare:256; Clinvar:2; Clinvar (benign):3 | ||||
| chr3:97821841-97822125 | Common:1; Rare:164 | ||||
| chr3:97971910-97972270 | Common:1; Rare:118 | ||||
| chr3:97972337-97972549 | Common:6; Rare:134 | ||||
| chr3:98522582-98522798 | Rare:55 | ||||
| chr3:98522821-98523006 | Common:1; Rare:105 | ||||
| chr3:98593060-98593540 | Common:3; Rare:236; Clinvar:10; Clinvar (benign):9; Clinvar (pathogenic):3 |