| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:4734232-4734298 | Rare:19 | ||||
| chr16:5033920-5033964 | Rare:17 | ||||
| chr16:5097735-5098025 | Common:4; Rare:102 | ||||
| chr16:7332641-7332936 | Common:2; Rare:93 | ||||
| chr16:7333035-7333082 | Rare:27; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr16:8797621-8797866 | Rare:93; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:9092160-9092215 | Rare:21 | ||||
| chr16:10580569-10580756 | Rare:58 | ||||
| chr16:10944327-10944622 | Common:1; Rare:89 | ||||
| chr16:11851406-11851637 | Common:1; Rare:118 | ||||
| chr16:11915889-11916150 | Common:2; Rare:120 | ||||
| chr16:11976636-11976766 | Rare:47 | ||||
| chr16:14632722-14632989 | Common:1; Rare:89 | ||||
| chr16:15395923-15396021 | Rare:37 | ||||
| chr16:15643031-15643267 | Rare:73 |