| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:72848398-72848531 | Rare:40 | ||||
| chr3:87227186-87227395 | Common:1; Rare:72; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:88058923-88059338 | Common:3; Rare:156 | ||||
| chr3:88149617-88150033 | Common:2; Rare:117 | ||||
| chr3:93979918-93980195 | Common:4; Rare:99; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:94028503-94028718 | Rare:33 | ||||
| chr3:94062930-94063090 | Rare:37 | ||||
| chr3:97764706-97764813 | Common:1; Rare:24; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:97821892-97822074 | Rare:66 | ||||
| chr3:98732445-98732512 | Rare:13 | ||||
| chr3:98801187-98801305 | Common:1; Rare:24 | ||||
| chr3:99638505-99638624 | Common:1; Rare:25 | ||||
| chr3:99817558-99817920 | Rare:106 | ||||
| chr3:99876126-99876278 | Common:1; Rare:38 | ||||
| chr3:100260701-100261028 | Rare:86 |