Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:693345-693551 | Rare:44 | ||||
chr11:694586-694637 | Rare:14 | ||||
chr11:694639-694737 | Rare:34 | ||||
chr11:694814-695442 | Common:1; Rare:222; Clinvar:3; Clinvar (benign):4 | ||||
chr11:695574-696030 | Common:5; Rare:124 | ||||
chr11:696128-696290 | Rare:34 | ||||
chr11:696294-696699 | Common:2; Rare:83 | ||||
chr11:702992-703105 | Rare:44 | ||||
chr11:705813-706287 | Common:3; Rare:145 | ||||
chr11:706460-706788 | Common:2; Rare:63 | ||||
chr11:706924-707106 | Common:1; Rare:47 | ||||
chr11:726321-726579 | Common:1; Rare:105 | ||||
chr11:726592-726753 | Rare:71 | ||||
chr11:746695-746872 | Rare:39 | ||||
chr11:747200-747581 | Rare:150; Clinvar:5; Clinvar (benign):1 |