| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:18926381-18926627 | Common:2; Rare:101 | ||||
| chr16:19067441-19067702 | Common:5; Rare:108; Clinvar:1 | ||||
| chr16:19067808-19067925 | Common:2; Rare:31 | ||||
| chr16:20806349-20806530 | Rare:68 | ||||
| chr16:20900226-20900892 | Common:4; Rare:156 | ||||
| chr16:21953038-21953456 | Common:1; Rare:108; Clinvar (benign):3 | ||||
| chr16:21957257-21957566 | Rare:104; Clinvar (benign):1 | ||||
| chr16:22436927-22437067 | Rare:51 | ||||
| chr16:22437189-22437308 | Rare:36 | ||||
| chr16:23453163-23453211 | Rare:14 | ||||
| chr16:23557325-23557557 | Common:2; Rare:89; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:23641247-23641536 | Common:2; Rare:83; Clinvar:1; Clinvar (benign):3 | ||||
| chr16:24729531-24729745 | Common:6; Rare:100 | ||||
| chr16:25015251-25015437 | Common:1; Rare:64 | ||||
| chr16:25111472-25111834 | Common:2; Rare:104 |