| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:144755467-144755685 | Common:1; Rare:72 | ||||
| chr8:144792289-144792585 | Common:3; Rare:110 | ||||
| chr8:144798781-144798923 | Common:1; Rare:46 | ||||
| chr8:144852974-144853164 | Rare:70 | ||||
| chr8:144950816-144950911 | Common:1; Rare:32 | ||||
| chr8:145052153-145052504 | Common:11; Rare:91 | ||||
| chr9:470136-470371 | Common:16; Rare:102 | ||||
| chr9:2014992-2015387 | Common:3; Rare:122 | ||||
| chr9:2017561-2017694 | Rare:36 | ||||
| chr9:2621860-2622207 | Common:6; Rare:123; Clinvar:8; Clinvar (benign):3 | ||||
| chr9:2844047-2844329 | Common:5; Rare:104 | ||||
| chr9:3525763-3526119 | Common:1; Rare:133 | ||||
| chr9:3526414-3526512 | Common:4; Rare:51 | ||||
| chr9:4679437-4679838 | Common:1; Rare:177 | ||||
| chr9:4792633-4793030 | Common:2; Rare:146 |