| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:81761515-81761773 | Common:8; Rare:89; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:87227235-87227477 | Common:2; Rare:64; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:88058631-88058723 | Common:1; Rare:34 | ||||
| chr3:88058917-88059319 | Common:3; Rare:155 | ||||
| chr3:88149606-88149750 | Common:1; Rare:34 | ||||
| chr3:88149798-88150049 | Common:5; Rare:86 | ||||
| chr3:93980182-93980192 | Common:1; Rare:4; Clinvar (benign):1 | ||||
| chr3:94028414-94028675 | Rare:39 | ||||
| chr3:94062904-94063121 | Rare:54 | ||||
| chr3:97764448-97764804 | Common:1; Rare:85; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:97821890-97822209 | Common:2; Rare:108 | ||||
| chr3:99638374-99638624 | Common:1; Rare:60 | ||||
| chr3:99817568-99817900 | Rare:95 | ||||
| chr3:99876116-99876262 | Rare:36 | ||||
| chr3:100260704-100261061 | Rare:107 |