Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr21:44034357-44034547 | Common:1; Rare:43 | ||||
chr21:44485351-44485602 | Common:2; Rare:82 | ||||
chr21:44505540-44505565 | Rare:1 | ||||
chr21:44520345-44520528 | Rare:45 | ||||
chr21:44598217-44598402 | Rare:39 | ||||
chr21:44704125-44704463 | Common:7; Rare:80 | ||||
chr21:44748790-44748936 | Rare:29 | ||||
chr21:45405918-45406052 | Rare:21 | ||||
chr21:45530332-45530342 | Rare:4 | ||||
chr21:45590534-45590801 | Common:6; Rare:88 | ||||
chr21:45953168-45953356 | Common:2; Rare:37 | ||||
chr21:45976819-45977077 | Common:3; Rare:49 | ||||
chr21:45977184-45977346 | Common:3; Rare:27 | ||||
chr21:45977632-45977865 | Common:5; Rare:31 | ||||
chr21:45992051-45992215 | Common:1; Rare:64; Clinvar:9; Clinvar (benign):3 |