| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:85799513-85799803 | Common:2; Rare:88 | ||||
| chr16:87317361-87317493 | Common:4; Rare:45 | ||||
| chr16:87383707-87383949 | Common:1; Rare:98 | ||||
| chr16:87765942-87766022 | Rare:29 | ||||
| chr16:88570179-88570433 | Common:1; Rare:94 | ||||
| chr16:88663041-88663371 | Common:8; Rare:138 | ||||
| chr16:88706347-88706555 | Common:3; Rare:101 | ||||
| chr16:88856918-88857166 | Common:4; Rare:116; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:89217627-89217710 | Common:1; Rare:33 | ||||
| chr16:89562385-89562471 | Common:2; Rare:35 | ||||
| chr16:89657637-89658091 | Common:3; Rare:238 | ||||
| chr16:89720833-89720996 | Common:1; Rare:42 | ||||
| chr16:89972458-89972661 | Common:1; Rare:73 | ||||
| chr16:90019850-90019908 | Rare:15 | ||||
| chr17:714722-714955 | Common:4; Rare:80; Clinvar (benign):1 |