| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:99425570-99425820 | Common:2; Rare:87 | ||||
| chr6:99515362-99515654 | Common:2; Rare:165 | ||||
| chr6:100881050-100881538 | Common:12; Rare:261 | ||||
| chr6:104859785-104860010 | Common:1; Rare:121 | ||||
| chr6:105403010-105403195 | Common:3; Rare:108 | ||||
| chr6:106086197-106086389 | Rare:93 | ||||
| chr6:106325547-106325908 | Common:2; Rare:217 | ||||
| chr6:106629410-106629713 | Common:9; Rare:142 | ||||
| chr6:106975291-106975534 | Common:1; Rare:106 | ||||
| chr6:107028072-107028397 | Common:3; Rare:160 | ||||
| chr6:107115092-107115327 | Rare:79 | ||||
| chr6:107115439-107115544 | Rare:26 | ||||
| chr6:107459429-107459743 | Common:4; Rare:127; Clinvar:1 | ||||
| chr6:107957030-107957510 | Common:4; Rare:154 | ||||
| chr6:107957910-107958438 | Common:4; Rare:306; Clinvar:4; Clinvar (benign):6 |