| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:70114115-70114409 | Common:3; Rare:101 | ||||
| chr16:70289387-70289565 | Common:1; Rare:71; Clinvar:1; Clinvar (benign):4 | ||||
| chr16:70299147-70299239 | Rare:22 | ||||
| chr16:70346751-70346994 | Common:2; Rare:119 | ||||
| chr16:70454324-70454638 | Common:2; Rare:85 | ||||
| chr16:70523517-70523892 | Common:3; Rare:125; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr16:71289205-71289483 | Common:2; Rare:77 | ||||
| chr16:71564894-71565015 | Common:1; Rare:42 | ||||
| chr16:71723806-71724052 | Common:5; Rare:88 | ||||
| chr16:71808745-71808875 | Common:1; Rare:68 | ||||
| chr16:71809024-71809339 | Common:3; Rare:100 | ||||
| chr16:71845920-71846035 | Common:1; Rare:36 | ||||
| chr16:71884010-71884280 | Common:1; Rare:87 | ||||
| chr16:71895330-71895578 | Common:1; Rare:84 | ||||
| chr16:71922235-71922555 | Rare:119 |