| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:99424874-99424929 | Rare:21 | ||||
| chr6:99425253-99425490 | Common:2; Rare:66 | ||||
| chr6:99515400-99515580 | Common:1; Rare:59 | ||||
| chr6:100881189-100881501 | Common:6; Rare:111 | ||||
| chr6:105136716-105136838 | Common:2; Rare:26 | ||||
| chr6:105136968-105137324 | Common:3; Rare:116 | ||||
| chr6:105179873-105180085 | Common:4; Rare:60 | ||||
| chr6:106325538-106325892 | Common:1; Rare:115 | ||||
| chr6:106629435-106629665 | Common:3; Rare:57 | ||||
| chr6:107028096-107028407 | Common:2; Rare:101 | ||||
| chr6:107459485-107459708 | Common:1; Rare:55; Clinvar:1 | ||||
| chr6:107958015-107958428 | Common:2; Rare:129; Clinvar:2; Clinvar (benign):3 | ||||
| chr6:108074668-108074928 | Common:1; Rare:90; Clinvar:1 | ||||
| chr6:108260765-108260812 | Rare:13 | ||||
| chr6:108260879-108261155 | Rare:117 |