| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:52692924-52693349 | Common:1; Rare:140 | ||||
| chr3:52693432-52694197 | Common:6; Rare:229 | ||||
| chr3:52705447-52706231 | Common:5; Rare:234 | ||||
| chr3:52770916-52771120 | Common:3; Rare:67 | ||||
| chr3:53229081-53229436 | Common:3; Rare:104 | ||||
| chr3:53255836-53256076 | Common:1; Rare:82 | ||||
| chr3:53347486-53347749 | Common:2; Rare:90 | ||||
| chr3:53891789-53892063 | Common:3; Rare:88 | ||||
| chr3:55487301-55487704 | Common:3; Rare:85; Clinvar:6; Clinvar (benign):1 | ||||
| chr3:56557086-56557241 | Common:2; Rare:61 | ||||
| chr3:57079266-57079566 | Common:2; Rare:88 | ||||
| chr3:57227574-57227925 | Common:4; Rare:119 | ||||
| chr3:57556032-57556329 | Rare:73 | ||||
| chr3:57597239-57597744 | Common:5; Rare:151 | ||||
| chr3:58306461-58306559 | Common:1; Rare:38 |