Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:14644838-14644928 | Rare:35 | ||||
chr11:14644934-14644986 | Rare:19 | ||||
chr11:16604275-16604443 | Rare:35 | ||||
chr11:16606951-16607075 | Common:1; Rare:31 | ||||
chr11:16793107-16793354 | Rare:36 | ||||
chr11:16996397-16996668 | Rare:52 | ||||
chr11:18269031-18269315 | Common:3; Rare:63; Clinvar:1 | ||||
chr11:19380486-19380733 | Rare:49 | ||||
chr11:19397803-19398113 | Common:2; Rare:65 | ||||
chr11:19398937-19398944 | Rare:1 | ||||
chr11:26188643-26188813 | Rare:31 | ||||
chr11:33061385-33061681 | Rare:64 | ||||
chr11:34910112-34910346 | Common:2; Rare:39 | ||||
chr11:35169071-35169115 | Rare:10 | ||||
chr11:35663496-35663633 | Rare:42; Clinvar (pathogenic):1 |