| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:3400955-3401241 | Common:6; Rare:108 | ||||
| chr16:3443450-3443725 | Common:3; Rare:90 | ||||
| chr16:3457932-3458124 | Common:2; Rare:92 | ||||
| chr16:3577387-3577478 | Common:1; Rare:21 | ||||
| chr16:3611567-3611784 | Rare:94; Clinvar:1 | ||||
| chr16:4371671-4371872 | Common:1; Rare:73 | ||||
| chr16:4425494-4425998 | Common:3; Rare:211 | ||||
| chr16:4476271-4476487 | Common:3; Rare:80 | ||||
| chr16:4614832-4615047 | Common:1; Rare:60 | ||||
| chr16:4664658-4664775 | Common:1; Rare:49 | ||||
| chr16:4734199-4734494 | Common:1; Rare:91 | ||||
| chr16:4767153-4767360 | Common:1; Rare:65 | ||||
| chr16:5033920-5033976 | Rare:23 | ||||
| chr16:5071776-5071861 | Rare:40; Clinvar (benign):1 | ||||
| chr16:8621608-8621749 | Common:1; Rare:53 |