Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:31713818-31713988 | Common:1; Rare:32 | ||||
chr6:31721628-31721877 | Rare:45 | ||||
chr6:31815330-31815550 | Common:1; Rare:67 | ||||
chr6:31827526-31827941 | Common:8; Rare:183 | ||||
chr6:31897670-31897783 | Rare:22 | ||||
chr6:31958899-31959195 | Rare:98; Clinvar:8 | ||||
chr6:32130186-32130389 | Common:2; Rare:38 | ||||
chr6:32153326-32153598 | Rare:47 | ||||
chr6:32178084-32178497 | Common:3; Rare:69 | ||||
chr6:32190127-32190345 | Rare:44 | ||||
chr6:32843979-32844115 | Rare:32; Clinvar:1 | ||||
chr6:32844319-32844843 | Common:1; Rare:115 | ||||
chr6:32853221-32853541 | Rare:98; Clinvar:4; Clinvar (benign):3 | ||||
chr6:32853664-32854209 | Common:4; Rare:162; Clinvar:2; Clinvar (benign):3 | ||||
chr6:32968812-32968924 | Common:4; Rare:39 |