| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:96897803-96898083 | Common:4; Rare:104; Clinvar:3; Clinvar (benign):1 | ||||
| chr6:97283128-97283399 | Common:3; Rare:73 | ||||
| chr6:99425245-99425452 | Common:2; Rare:56 | ||||
| chr6:100881073-100881483 | Common:7; Rare:134 | ||||
| chr6:105137091-105137270 | Common:1; Rare:68 | ||||
| chr6:106325544-106325859 | Common:1; Rare:100 | ||||
| chr6:106629476-106629639 | Common:3; Rare:33 | ||||
| chr6:107459522-107459713 | Common:1; Rare:43 | ||||
| chr6:107958103-107958429 | Common:1; Rare:101; Clinvar:2; Clinvar (benign):2 | ||||
| chr6:108294791-108295071 | Common:1; Rare:75 | ||||
| chr6:109382209-109382235 | Rare:10 | ||||
| chr6:109382239-109382556 | Common:4; Rare:139; Clinvar (benign):2 | ||||
| chr6:109691158-109691339 | Common:3; Rare:42; Clinvar:4; Clinvar (benign):3 | ||||
| chr6:110179616-110179720 | Rare:42 | ||||
| chr6:110874633-110874798 | Common:4; Rare:54 |