Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:6603542-6603876 | Common:4; Rare:96; Clinvar (benign):3 | ||||
chr11:6683267-6683458 | Common:4; Rare:96 | ||||
chr11:6926254-6926463 | Common:4; Rare:57 | ||||
chr11:7020311-7020510 | Rare:70 | ||||
chr11:7513626-7513948 | Common:5; Rare:93 | ||||
chr11:7673448-7673567 | Common:1; Rare:40 | ||||
chr11:8168970-8169089 | Common:2; Rare:40 | ||||
chr11:8594145-8594293 | Rare:55 | ||||
chr11:8682628-8683041 | Common:2; Rare:172 | ||||
chr11:8910935-8911265 | Common:6; Rare:90 | ||||
chr11:8964354-8964602 | Common:4; Rare:87 | ||||
chr11:9314519-9314903 | Common:5; Rare:118 | ||||
chr11:9384335-9384729 | Common:3; Rare:113 | ||||
chr11:9460627-9461050 | Common:4; Rare:109 | ||||
chr11:9575480-9575790 | Common:1; Rare:58 |