| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:2047724-2048043 | Rare:155; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:2205681-2205881 | Common:4; Rare:94 | ||||
| chr16:2268066-2268174 | Common:1; Rare:54 | ||||
| chr16:2520163-2520449 | Common:8; Rare:165 | ||||
| chr16:3134835-3135149 | Common:3; Rare:85 | ||||
| chr16:3305325-3305514 | Common:3; Rare:63 | ||||
| chr16:3400965-3401232 | Common:6; Rare:99 | ||||
| chr16:3443460-3443729 | Common:3; Rare:91 | ||||
| chr16:4425757-4425888 | Common:1; Rare:61 | ||||
| chr16:4476270-4476466 | Common:3; Rare:73 | ||||
| chr16:4734190-4734537 | Common:1; Rare:114 | ||||
| chr16:4847265-4847442 | Common:1; Rare:76 | ||||
| chr16:5033920-5033955 | Rare:14 | ||||
| chr16:8797621-8797885 | Rare:105; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:11976615-11976763 | Common:2; Rare:55 |