| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:4734199-4734522 | Common:1; Rare:104 | ||||
| chr16:5033933-5033962 | Rare:9 | ||||
| chr16:8797624-8797883 | Rare:102; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:8868973-8869312 | Common:6; Rare:152 | ||||
| chr16:10580581-10580749 | Rare:52 | ||||
| chr16:10944309-10944599 | Common:1; Rare:89 | ||||
| chr16:11915889-11916229 | Common:2; Rare:138 | ||||
| chr16:11976648-11976777 | Rare:52 | ||||
| chr16:14630195-14630498 | Rare:113 | ||||
| chr16:14632722-14632990 | Common:1; Rare:90 | ||||
| chr16:15094229-15094409 | Common:1; Rare:90 | ||||
| chr16:18801536-18801888 | Common:4; Rare:104 | ||||
| chr16:19067455-19067717 | Common:6; Rare:111; Clinvar:1 | ||||
| chr16:19067817-19067920 | Common:1; Rare:25 | ||||
| chr16:19555405-19555729 | Common:1; Rare:142 |