Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:576382-576555 | Rare:67 | ||||
chr11:613618-613807 | Common:11; Rare:72; Clinvar:1 | ||||
chr11:615546-615747 | Rare:65 | ||||
chr11:615852-616315 | Common:2; Rare:131 | ||||
chr11:616323-616338 | Rare:4 | ||||
chr11:695002-695417 | Common:1; Rare:100 | ||||
chr11:695584-695676 | Common:1; Rare:19 | ||||
chr11:695696-696107 | Common:6; Rare:120 | ||||
chr11:696203-696726 | Common:7; Rare:104 | ||||
chr11:726321-726490 | Rare:64 | ||||
chr11:747141-747515 | Rare:134; Clinvar:2; Clinvar (benign):1 | ||||
chr11:776421-776802 | Common:4; Rare:95 | ||||
chr11:777035-777182 | Common:1; Rare:43 | ||||
chr11:777403-777675 | Common:2; Rare:125 | ||||
chr11:790098-790153 | Common:1; Rare:8 |