| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:89508305-89508428 | Common:1; Rare:62; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr16:89560541-89560717 | Rare:73 | ||||
| chr16:89657647-89658089 | Common:3; Rare:233 | ||||
| chr16:89686631-89686723 | Common:7; Rare:59 | ||||
| chr16:89816625-89816933 | Common:6; Rare:146; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:89873485-89873715 | Common:1; Rare:103 | ||||
| chr16:89921783-89921940 | Rare:51 | ||||
| chr16:89923185-89923348 | Rare:60 | ||||
| chr16:89948560-89948814 | Common:3; Rare:75 | ||||
| chr16:89972521-89972635 | Rare:43 | ||||
| chr17:732345-732677 | Common:2; Rare:114 | ||||
| chr17:752229-752360 | Common:2; Rare:48 | ||||
| chr17:752794-752895 | Rare:24 | ||||
| chr17:1516588-1516969 | Common:2; Rare:133 | ||||
| chr17:1684802-1685038 | Common:2; Rare:77; Clinvar:3; Clinvar (benign):1 |