| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:89819724-89819863 | Rare:49 | ||||
| chr6:89829607-89829965 | Common:1; Rare:91 | ||||
| chr6:95577407-95577597 | Common:5; Rare:55 | ||||
| chr6:96521687-96521856 | Common:6; Rare:79 | ||||
| chr6:96897780-96898057 | Common:4; Rare:104; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:97283154-97283416 | Common:3; Rare:79 | ||||
| chr6:99425250-99425527 | Common:2; Rare:75 | ||||
| chr6:100881077-100881501 | Common:7; Rare:138 | ||||
| chr6:105137155-105137264 | Rare:45 | ||||
| chr6:105179879-105180090 | Common:4; Rare:61 | ||||
| chr6:105403041-105403207 | Common:2; Rare:58 | ||||
| chr6:106325538-106325892 | Common:1; Rare:115 | ||||
| chr6:106629454-106629676 | Common:4; Rare:54 | ||||
| chr6:107957251-107957419 | Rare:36 | ||||
| chr6:107958059-107958383 | Common:2; Rare:97; Clinvar:2; Clinvar (benign):3 |