| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:52693487-52694112 | Common:4; Rare:189 | ||||
| chr3:52705444-52706252 | Common:5; Rare:247 | ||||
| chr3:52706354-52706704 | Common:1; Rare:93 | ||||
| chr3:52770913-52771015 | Common:2; Rare:24 | ||||
| chr3:53229007-53229434 | Common:3; Rare:122 | ||||
| chr3:53347488-53347699 | Common:2; Rare:66 | ||||
| chr3:55480833-55480982 | Rare:42; Clinvar (benign):1 | ||||
| chr3:55480983-55481448 | Common:1; Rare:105 | ||||
| chr3:55487297-55487682 | Rare:81; Clinvar:6; Clinvar (benign):1 | ||||
| chr3:56557075-56557239 | Common:2; Rare:65 | ||||
| chr3:57227582-57227925 | Common:4; Rare:115 | ||||
| chr3:57556003-57556343 | Rare:87 | ||||
| chr3:57597250-57597732 | Common:4; Rare:147 | ||||
| chr3:58008313-58008553 | Common:1; Rare:91; Clinvar:5; Clinvar (benign):1 | ||||
| chr3:58306473-58306658 | Common:3; Rare:70 |