Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:2649522-2649546 | Rare:5 | ||||
chr11:2650324-2650580 | Rare:59 | ||||
chr11:3018460-3018635 | Rare:53 | ||||
chr11:6646708-6646963 | Common:1; Rare:48 | ||||
chr11:9437898-9438131 | Common:13; Rare:88 | ||||
chr11:9808074-9808292 | Rare:37; Clinvar (benign):2 | ||||
chr11:12287951-12287959 | Rare:2 | ||||
chr11:12676419-12676708 | Common:1; Rare:58 | ||||
chr11:14480840-14481037 | Rare:44 | ||||
chr11:14498912-14499106 | Common:2; Rare:57 | ||||
chr11:27685507-27685671 | Rare:25 | ||||
chr11:46312328-46312912 | Common:1; Rare:140 | ||||
chr11:47750927-47751145 | Common:1; Rare:63 | ||||
chr11:57332249-57332456 | Rare:52 | ||||
chr11:59639167-59639318 | Rare:47 |