| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:53891760-53892040 | Common:2; Rare:90 | ||||
| chr3:55487258-55487635 | Rare:81; Clinvar:7; Clinvar (benign):1 | ||||
| chr3:56557076-56557238 | Common:2; Rare:63 | ||||
| chr3:56683010-56683355 | Common:4; Rare:119 | ||||
| chr3:57079252-57079389 | Common:2; Rare:45 | ||||
| chr3:57227591-57227930 | Common:4; Rare:114 | ||||
| chr3:57556009-57556321 | Rare:75 | ||||
| chr3:57597314-57597682 | Common:4; Rare:114 | ||||
| chr3:57692998-57693221 | Common:1; Rare:68 | ||||
| chr3:58008259-58008449 | Common:2; Rare:75; Clinvar:1 | ||||
| chr3:58306483-58306581 | Common:3; Rare:38 | ||||
| chr3:58332800-58332978 | Common:3; Rare:51 | ||||
| chr3:58433766-58434022 | Common:1; Rare:103; Clinvar:2; Clinvar (benign):3 | ||||
| chr3:61251370-61251594 | Common:4; Rare:55 | ||||
| chr3:61561412-61561581 | Common:1; Rare:65 |