| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:96837370-96837480 | Common:2; Rare:39 | ||||
| chr6:96897391-96897492 | Rare:32 | ||||
| chr6:96897791-96898106 | Common:4; Rare:114; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:96924337-96924608 | Common:4; Rare:71 | ||||
| chr6:97283203-97283478 | Common:3; Rare:68 | ||||
| chr6:98834214-98834356 | Common:2; Rare:44 | ||||
| chr6:98834709-98835479 | Common:2; Rare:272 | ||||
| chr6:98947596-98947790 | Common:1; Rare:57 | ||||
| chr6:98947840-98948200 | Rare:99 | ||||
| chr6:99349324-99349653 | Common:3; Rare:126 | ||||
| chr6:99393876-99394088 | Common:1; Rare:92 | ||||
| chr6:99424864-99424990 | Rare:48 | ||||
| chr6:99425245-99425496 | Common:2; Rare:71 | ||||
| chr6:99515371-99515649 | Common:1; Rare:86 | ||||
| chr6:99568597-99568932 | Common:2; Rare:106 |