| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:18801429-18801830 | Common:4; Rare:140; Clinvar:1 | ||||
| chr16:18925743-18925914 | Common:2; Rare:55 | ||||
| chr16:19067455-19067702 | Common:5; Rare:104; Clinvar:1 | ||||
| chr16:19067808-19067911 | Common:2; Rare:25 | ||||
| chr16:19555494-19555729 | Common:1; Rare:110 | ||||
| chr16:20806349-20806663 | Rare:102 | ||||
| chr16:20900748-20900914 | Common:1; Rare:50 | ||||
| chr16:21953003-21953419 | Common:1; Rare:105; Clinvar (benign):3 | ||||
| chr16:22436936-22437071 | Rare:52 | ||||
| chr16:22437184-22437302 | Rare:38 | ||||
| chr16:22437512-22437579 | Rare:21 | ||||
| chr16:23453154-23453242 | Rare:22 | ||||
| chr16:23557315-23557550 | Common:2; Rare:93; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:23641247-23641536 | Common:2; Rare:83; Clinvar:1; Clinvar (benign):3 | ||||
| chr16:23678666-23678951 | Common:5; Rare:87 |