Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:28399710-28399872 | Common:1; Rare:31 | ||||
chr6:30061149-30061306 | Rare:33 | ||||
chr6:30066902-30067291 | Common:2; Rare:66 | ||||
chr6:30326374-30326525 | Common:1; Rare:26 | ||||
chr6:30326844-30326929 | Rare:22 | ||||
chr6:30556074-30556348 | Rare:97 | ||||
chr6:30571257-30571489 | Common:1; Rare:78 | ||||
chr6:30686628-30686779 | Common:1; Rare:28 | ||||
chr6:30720128-30720436 | Common:1; Rare:78 | ||||
chr6:30742616-30742906 | Common:2; Rare:75 | ||||
chr6:31620383-31620762 | Common:1; Rare:117 | ||||
chr6:31665832-31666119 | Common:3; Rare:77 | ||||
chr6:31958885-31959191 | Rare:100; Clinvar:8 | ||||
chr6:32844002-32844115 | Rare:25; Clinvar:1 | ||||
chr6:32853690-32853923 | Rare:88; Clinvar:1; Clinvar (benign):2 |