Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:22174661-22174818 | Common:1; Rare:21 | ||||
chr18:22174934-22175047 | Rare:22 | ||||
chr18:22175806-22175998 | Common:2; Rare:36 | ||||
chr18:22180849-22181102 | Common:1; Rare:48 | ||||
chr18:22183012-22183079 | Common:1; Rare:20; Clinvar (benign):3 | ||||
chr18:22189037-22189181 | Rare:22 | ||||
chr18:22194233-22194407 | Rare:39 | ||||
chr18:22267625-22268065 | Common:1; Rare:87 | ||||
chr18:22268066-22268181 | Common:2; Rare:22 | ||||
chr18:22277735-22278062 | Rare:77 | ||||
chr18:22559889-22560231 | Rare:69 | ||||
chr18:24987631-24987806 | Rare:31 | ||||
chr18:28175105-28175240 | Common:1; Rare:33 | ||||
chr18:31724625-31724680 | Rare:7 | ||||
chr18:36468281-36468499 | Common:2; Rare:46 |