| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:144503287-144503621 | Common:2; Rare:79 | ||||
| chr8:144504045-144504163 | Rare:22 | ||||
| chr8:144755461-144755637 | Common:1; Rare:62 | ||||
| chr8:144792335-144792562 | Common:3; Rare:85 | ||||
| chr8:144827235-144827604 | Common:2; Rare:95 | ||||
| chr8:144852974-144853078 | Rare:40 | ||||
| chr8:144901416-144901708 | Common:1; Rare:83 | ||||
| chr8:145052106-145052504 | Common:11; Rare:101 | ||||
| chr9:214426-214889 | Common:7; Rare:248; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:215004-215215 | Common:5; Rare:128; Clinvar:3; Clinvar (benign):2 | ||||
| chr9:470139-470320 | Common:15; Rare:73 | ||||
| chr9:707063-707245 | Common:4; Rare:66 | ||||
| chr9:2015763-2016090 | Common:1; Rare:104 | ||||
| chr9:2017464-2017694 | Common:2; Rare:71 | ||||
| chr9:2844025-2844359 | Common:5; Rare:133 |