| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:109455605-109455860 | Common:7; Rare:123 | ||||
| chr6:109691139-109691344 | Common:6; Rare:92; Clinvar:8; Clinvar (benign):6 | ||||
| chr6:110179580-110179740 | Rare:92 | ||||
| chr6:110179922-110180194 | Common:4; Rare:145 | ||||
| chr6:110415450-110415740 | Rare:119 | ||||
| chr6:110814336-110814671 | Common:2; Rare:110 | ||||
| chr6:110815338-110815770 | Common:7; Rare:212 | ||||
| chr6:110815843-110816106 | Common:4; Rare:125 | ||||
| chr6:110874609-110874925 | Common:8; Rare:151 | ||||
| chr6:110958621-110958806 | Common:5; Rare:140 | ||||
| chr6:110958830-110959080 | Common:5; Rare:60 | ||||
| chr6:110981951-110982119 | Common:4; Rare:171 | ||||
| chr6:111259178-111259402 | Common:3; Rare:81 | ||||
| chr6:111483089-111483544 | Common:2; Rare:225 | ||||
| chr6:111483599-111483922 | Common:2; Rare:248 |