Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:54317240-54317310 | Common:7; Rare:39 | ||||
chr19:54369802-54369974 | Rare:40 | ||||
chr19:54387936-54388111 | Common:2; Rare:28 | ||||
chr19:54600507-54600927 | Common:2; Rare:133 | ||||
chr19:54602659-54602777 | Rare:28 | ||||
chr19:54871814-54872004 | Rare:36 | ||||
chr19:54875590-54875766 | Rare:32 | ||||
chr19:54878329-54878412 | Common:1; Rare:16 | ||||
chr19:54878429-54878537 | Common:1; Rare:20 | ||||
chr19:55636168-55636312 | Rare:25 | ||||
chr2:9543191-9543472 | Common:1; Rare:61; Clinvar (benign):1 | ||||
chr2:16555073-16555260 | Rare:34 | ||||
chr2:16656887-16656960 | Rare:10 | ||||
chr2:16658214-16658376 | Common:1; Rare:23 | ||||
chr2:20037305-20037593 | Rare:81 |