| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:144827248-144827609 | Common:1; Rare:95 | ||||
| chr8:144852982-144853164 | Rare:65 | ||||
| chr8:144901386-144901734 | Common:1; Rare:98 | ||||
| chr8:144902185-144902509 | Common:3; Rare:86 | ||||
| chr8:145052198-145052530 | Common:10; Rare:104 | ||||
| chr9:178898-179311 | Common:9; Rare:81 | ||||
| chr9:214665-214889 | Common:5; Rare:130; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:215081-215237 | Common:2; Rare:86 | ||||
| chr9:470139-470343 | Common:16; Rare:86 | ||||
| chr9:504393-504742 | Common:4; Rare:168 | ||||
| chr9:706772-707187 | Common:3; Rare:139 | ||||
| chr9:977122-977388 | Common:2; Rare:104 | ||||
| chr9:2015050-2015390 | Common:3; Rare:100 | ||||
| chr9:2016655-2017071 | Common:2; Rare:111 | ||||
| chr9:2017483-2017725 | Rare:73 |