| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:87227032-87227417 | Common:2; Rare:112; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:88058917-88059322 | Common:3; Rare:156 | ||||
| chr3:88149617-88149768 | Rare:36 | ||||
| chr3:88149856-88150049 | Common:5; Rare:77 | ||||
| chr3:93973762-93973981 | Rare:70; Clinvar:5 | ||||
| chr3:93979898-93980211 | Common:4; Rare:113; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:94062860-94063097 | Rare:60 | ||||
| chr3:97764439-97764844 | Common:1; Rare:95; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:97821866-97822107 | Rare:87 | ||||
| chr3:98732219-98732412 | Rare:36 | ||||
| chr3:98732421-98732521 | Rare:18 | ||||
| chr3:98732587-98732742 | Rare:28 | ||||
| chr3:98733097-98733241 | Common:2; Rare:26 | ||||
| chr3:98733536-98733707 | Rare:32 | ||||
| chr3:98901699-98902014 | Common:1; Rare:109 |