| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:17600649-17601049 | Common:33; Rare:214 | ||||
| chr6:17706377-17706516 | Rare:64 | ||||
| chr6:17706599-17706945 | Common:1; Rare:140 | ||||
| chr6:17706856-17707077 | Common:1; Rare:103 | ||||
| chr6:17986700-17987070 | Common:2; Rare:141 | ||||
| chr6:17987445-17987691 | Common:1; Rare:103 | ||||
| chr6:18155026-18155565 | Common:22; Rare:269; Clinvar:3 | ||||
| chr6:18264467-18264789 | Rare:221 | ||||
| chr6:18387110-18387355 | Rare:59 | ||||
| chr6:18387278-18387503 | Common:2; Rare:76 | ||||
| chr6:20401541-20401936 | Common:6; Rare:199 | ||||
| chr6:20403363-20403772 | Common:2; Rare:151 | ||||
| chr6:24357739-24358156 | Common:4; Rare:181 | ||||
| chr6:24402702-24403006 | Common:4; Rare:70 | ||||
| chr6:24494521-24495010 | Common:15; Rare:177; Clinvar (benign):2 |