| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:19067385-19067702 | Common:5; Rare:121; Clinvar:1 | ||||
| chr16:19067808-19068020 | Common:2; Rare:53 | ||||
| chr16:20806343-20806533 | Rare:70 | ||||
| chr16:20900226-20900873 | Common:4; Rare:154 | ||||
| chr16:21953038-21953456 | Common:1; Rare:108; Clinvar (benign):3 | ||||
| chr16:21957245-21957565 | Rare:107; Clinvar (benign):1 | ||||
| chr16:22436934-22437063 | Rare:48 | ||||
| chr16:22437175-22437313 | Rare:40 | ||||
| chr16:22437513-22437676 | Common:2; Rare:40 | ||||
| chr16:23557336-23557551 | Common:1; Rare:83; Clinvar:1; Clinvar (benign):1 | ||||
| chr16:23641266-23641526 | Common:2; Rare:73; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:24540385-24540727 | Rare:90 | ||||
| chr16:24729604-24729829 | Common:7; Rare:96 | ||||
| chr16:25015296-25015457 | Common:2; Rare:60 | ||||
| chr16:25111472-25111802 | Common:2; Rare:89 |