| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:89711610-89711909 | Common:3; Rare:113 | ||||
| chr16:89720787-89721004 | Common:1; Rare:65 | ||||
| chr16:89721322-89721554 | Common:1; Rare:103 | ||||
| chr16:89816613-89816760 | Common:2; Rare:74; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr16:89873482-89873844 | Common:3; Rare:164 | ||||
| chr16:89921658-89922009 | Common:1; Rare:92 | ||||
| chr16:89972462-89972595 | Common:1; Rare:40 | ||||
| chr16:90019403-90019643 | Common:4; Rare:74 | ||||
| chr16:90022443-90022716 | Common:2; Rare:92 | ||||
| chr17:714697-714955 | Common:4; Rare:90; Clinvar (benign):1 | ||||
| chr17:752155-752366 | Common:2; Rare:83 | ||||
| chr17:782685-782985 | Common:1; Rare:71 | ||||
| chr17:1109037-1109437 | Common:1; Rare:115 | ||||
| chr17:1361042-1361162 | Rare:31 | ||||
| chr17:1361272-1361358 | Common:1; Rare:28 |