Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:507114-507537 | Common:4; Rare:138 | ||||
chr11:560686-561024 | Common:6; Rare:160 | ||||
chr11:575808-576189 | Common:4; Rare:88 | ||||
chr11:576398-576582 | Rare:76 | ||||
chr11:695030-695376 | Common:1; Rare:79 | ||||
chr11:695596-695830 | Common:1; Rare:61 | ||||
chr11:705934-706267 | Common:2; Rare:102 | ||||
chr11:706516-706660 | Rare:27 | ||||
chr11:747329-747521 | Rare:81; Clinvar:2; Clinvar (benign):1 | ||||
chr11:777418-777638 | Common:1; Rare:104 | ||||
chr11:790063-790426 | Common:5; Rare:91 | ||||
chr11:797973-798044 | Rare:14 | ||||
chr11:798221-798486 | Common:2; Rare:91 | ||||
chr11:809210-809401 | Common:2; Rare:45 | ||||
chr11:809493-809654 | Common:2; Rare:45 |