| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:4797760-4798120 | Common:2; Rare:186; Clinvar:9; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr16:4885870-4886204 | Common:4; Rare:118 | ||||
| chr16:4889018-4889186 | Common:2; Rare:51 | ||||
| chr16:8894701-8894811 | Common:1; Rare:33 | ||||
| chr16:15023047-15023380 | Common:1; Rare:36 | ||||
| chr16:15029873-15030051 | Common:1; Rare:44 | ||||
| chr16:15701290-15701494 | Rare:45 | ||||
| chr16:17457851-17457942 | Rare:22 | ||||
| chr16:17471856-17471982 | Common:1; Rare:23 | ||||
| chr16:17803691-17804059 | Common:2; Rare:60 | ||||
| chr16:18854987-18855206 | Common:1; Rare:35 | ||||
| chr16:19572834-19573198 | Common:3; Rare:80 | ||||
| chr16:19717460-19717506 | Rare:7 | ||||
| chr16:21627044-21627243 | Common:1; Rare:36 | ||||
| chr16:21820388-21820465 | Rare:16 |