Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:560693-561021 | Common:6; Rare:152 | ||||
chr11:695567-695821 | Common:1; Rare:65 | ||||
chr11:706516-706629 | Rare:17 | ||||
chr11:747292-747574 | Rare:121; Clinvar:5; Clinvar (benign):1 | ||||
chr11:777461-777593 | Common:1; Rare:56 | ||||
chr11:809498-809595 | Rare:30 | ||||
chr11:809872-810047 | Common:2; Rare:82 | ||||
chr11:842453-842978 | Common:8; Rare:218 | ||||
chr11:1309554-1309836 | Common:2; Rare:118 | ||||
chr11:1834216-1834495 | Rare:61 | ||||
chr11:1871049-1871346 | Common:4; Rare:92 | ||||
chr11:2270969-2271173 | Common:3; Rare:53 | ||||
chr11:3057363-3057545 | Rare:65 | ||||
chr11:3379089-3379332 | Common:4; Rare:65 | ||||
chr11:3840905-3841082 | Rare:77 |