| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:89657644-89658053 | Common:3; Rare:213 | ||||
| chr16:89686567-89686702 | Common:6; Rare:59 | ||||
| chr16:89720865-89720974 | Common:1; Rare:29 | ||||
| chr16:89873482-89873678 | Common:1; Rare:94 | ||||
| chr16:89923156-89923425 | Rare:115 | ||||
| chr16:89948701-89948803 | Common:2; Rare:21 | ||||
| chr16:89972521-89972614 | Rare:30 | ||||
| chr16:90022529-90022691 | Rare:62 | ||||
| chr17:714782-714901 | Common:2; Rare:41 | ||||
| chr17:752146-752347 | Common:2; Rare:78 | ||||
| chr17:1078950-1079085 | Rare:44 | ||||
| chr17:1400048-1400311 | Common:2; Rare:102 | ||||
| chr17:1516590-1516945 | Common:1; Rare:120 | ||||
| chr17:1684794-1685038 | Common:2; Rare:80; Clinvar:4; Clinvar (benign):1 | ||||
| chr17:1761766-1762003 | Rare:50; Clinvar:1 |