Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:89829614-89829909 | Rare:69 | ||||
chr6:90587022-90587370 | Common:4; Rare:93 | ||||
chr6:93419535-93419824 | Common:1; Rare:77 | ||||
chr6:95577414-95577553 | Common:3; Rare:39 | ||||
chr6:96521646-96521871 | Common:9; Rare:108 | ||||
chr6:96897796-96898061 | Common:4; Rare:98; Clinvar:4; Clinvar (benign):1 | ||||
chr6:99425259-99425494 | Common:2; Rare:66 | ||||
chr6:100881265-100881498 | Common:5; Rare:94 | ||||
chr6:106086226-106086339 | Rare:23 | ||||
chr6:106325577-106325856 | Rare:95 | ||||
chr6:106629462-106629588 | Common:1; Rare:25 | ||||
chr6:107958126-107958399 | Common:1; Rare:82; Clinvar:2; Clinvar (benign):2 | ||||
chr6:108074677-108074871 | Common:1; Rare:63; Clinvar:1 | ||||
chr6:109382308-109382560 | Common:4; Rare:110; Clinvar (benign):2 | ||||
chr6:109455726-109456031 | Common:1; Rare:75 |