Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:49996795-49997092 | Common:1; Rare:53 | ||||
chr13:50081980-50082354 | Common:1; Rare:105 | ||||
chr13:50715485-50715697 | Rare:47 | ||||
chr13:50909732-50910074 | Common:1; Rare:77; Clinvar:5; Clinvar (benign):1 | ||||
chr13:51453005-51453389 | Rare:150 | ||||
chr13:51804082-51804234 | Common:2; Rare:45 | ||||
chr13:52011919-52011975 | Rare:22 | ||||
chr13:52011991-52012431 | Common:2; Rare:144; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr13:52159550-52159628 | Common:1; Rare:17 | ||||
chr13:52406132-52406397 | Common:2; Rare:74 | ||||
chr13:52450576-52450689 | Rare:34 | ||||
chr13:52455335-52455507 | Common:3; Rare:56 | ||||
chr13:52652361-52652817 | Common:2; Rare:117 | ||||
chr13:60163887-60164080 | Common:1; Rare:48 | ||||
chr13:72727598-72727934 | Common:4; Rare:119 |