| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:86575808-86576573 | Common:8; Rare:238 | ||||
| chr16:87317241-87317594 | Common:14; Rare:225 | ||||
| chr16:87383707-87383986 | Common:2; Rare:202 | ||||
| chr16:87765843-87766085 | Common:2; Rare:183 | ||||
| chr16:87869056-87869656 | Common:5; Rare:414 | ||||
| chr16:87950830-87951190 | Common:6; Rare:155 | ||||
| chr16:87951334-87951573 | Rare:173 | ||||
| chr16:88453040-88453344 | Common:2; Rare:124 | ||||
| chr16:88570110-88570503 | Common:4; Rare:278 | ||||
| chr16:88650949-88651220 | Common:2; Rare:179; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr16:88651390-88651722 | Common:5; Rare:127 | ||||
| chr16:88663034-88663407 | Common:18; Rare:306 | ||||
| chr16:88706325-88706560 | Common:9; Rare:227 | ||||
| chr16:88785074-88785290 | Common:3; Rare:121 | ||||
| chr16:88803578-88803944 | Common:10; Rare:266; Clinvar (benign):2 |