| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:52536360-52536703 | Common:2; Rare:108 | ||||
| chr3:52685912-52686043 | Common:1; Rare:43 | ||||
| chr3:52705570-52706167 | Common:4; Rare:184 | ||||
| chr3:52770913-52771044 | Common:2; Rare:31 | ||||
| chr3:53130427-53130565 | Common:1; Rare:38; Clinvar (benign):1 | ||||
| chr3:53347525-53347669 | Common:1; Rare:41 | ||||
| chr3:53891816-53892021 | Common:2; Rare:63 | ||||
| chr3:55487637-55487698 | Common:3; Rare:11 | ||||
| chr3:56557086-56557228 | Common:2; Rare:54 | ||||
| chr3:56801938-56802084 | Common:1; Rare:47 | ||||
| chr3:57227585-57227886 | Common:3; Rare:104 | ||||
| chr3:57556032-57556307 | Rare:67 | ||||
| chr3:57597338-57597551 | Common:4; Rare:68 | ||||
| chr3:58433632-58434043 | Common:2; Rare:149; Clinvar:3; Clinvar (benign):4 | ||||
| chr3:61251363-61251586 | Common:4; Rare:53 |