| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:52534288-52535302 | Common:12; Rare:401 | ||||
| chr3:52536251-52537358 | Common:15; Rare:781 | ||||
| chr3:52679556-52680260 | Rare:312 | ||||
| chr3:52685437-52686241 | Common:14; Rare:986 | ||||
| chr3:52705126-52705235 | Rare:22 | ||||
| chr3:52705618-52706247 | Common:16; Rare:1023 | ||||
| chr3:52770447-52770847 | Common:2; Rare:120 | ||||
| chr3:52770780-52771300 | Common:27; Rare:581 | ||||
| chr3:52830340-52830955 | Common:9; Rare:220 | ||||
| chr3:52897340-52897850 | Rare:307 | ||||
| chr3:53045146-53045697 | Common:8; Rare:413 | ||||
| chr3:53045800-53046200 | Common:8; Rare:209 | ||||
| chr3:53130351-53130785 | Common:7; Rare:538; Clinvar:7; Clinvar (benign):20 | ||||
| chr3:53161020-53161255 | Common:17; Rare:181 | ||||
| chr3:53236078-53236478 | Common:6; Rare:71 |