Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:207381-207720 | Common:7; Rare:99 | ||||
chr11:208688-208847 | Rare:63 | ||||
chr11:236333-236513 | Common:6; Rare:52 | ||||
chr11:236909-237047 | Common:1; Rare:55 | ||||
chr11:407083-407407 | Common:8; Rare:105 | ||||
chr11:506737-506966 | Common:3; Rare:81 | ||||
chr11:560710-561016 | Common:5; Rare:142 | ||||
chr11:576438-576531 | Rare:40 | ||||
chr11:615948-616033 | Common:1; Rare:27 | ||||
chr11:695742-695817 | Rare:27 | ||||
chr11:747292-747504 | Rare:91; Clinvar:2; Clinvar (benign):1 | ||||
chr11:777460-777598 | Common:1; Rare:61 | ||||
chr11:832826-833014 | Common:7; Rare:62 | ||||
chr11:842468-842895 | Common:7; Rare:176 | ||||
chr11:3057363-3057553 | Rare:69 |