Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:86800303-86800604 | Common:2; Rare:110 | ||||
chr11:86955372-86955660 | Common:1; Rare:92 | ||||
chr11:87037767-87038043 | Common:3; Rare:129 | ||||
chr11:88337725-88337881 | Common:3; Rare:72; Clinvar:1; Clinvar (benign):2 | ||||
chr11:89491318-89491485 | Rare:39 | ||||
chr11:90222998-90223120 | Common:1; Rare:48 | ||||
chr11:93741403-93741702 | Common:7; Rare:122 | ||||
chr11:93784189-93784362 | Common:3; Rare:55 | ||||
chr11:93784832-93785130 | Common:1; Rare:62 | ||||
chr11:94493791-94494031 | Common:3; Rare:68; Clinvar (benign):1 | ||||
chr11:94973542-94973722 | Rare:51 | ||||
chr11:95067448-95067573 | Rare:45 | ||||
chr11:95089681-95089981 | Common:3; Rare:123 | ||||
chr11:95789764-95789998 | Common:3; Rare:82 | ||||
chr11:95790372-95790565 | Rare:72 |