Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:45311708-45311820 | Rare:29 | ||||
chr20:45312352-45312515 | Rare:50 | ||||
chr20:45765117-45765130 | Rare:3 | ||||
chr20:45765329-45765393 | Rare:3 | ||||
chr20:45765451-45765699 | Common:1; Rare:47 | ||||
chr20:45815719-45815911 | Rare:59 | ||||
chr20:45824188-45824285 | Common:2; Rare:28 | ||||
chr20:46011733-46011932 | Common:2; Rare:60; Clinvar (benign):1 | ||||
chr20:46363684-46363812 | Rare:25 | ||||
chr20:47357800-47357986 | Rare:31 | ||||
chr20:47369056-47369316 | Rare:55 | ||||
chr20:47369365-47369399 | Rare:4 | ||||
chr20:49071996-49072309 | Common:1; Rare:77 | ||||
chr20:49279106-49279228 | Common:3; Rare:38 | ||||
chr20:49280868-49280965 | Rare:23 |