Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:6740619-6740935 | Common:1; Rare:73 | ||||
chr19:7395057-7395203 | Common:3; Rare:48 | ||||
chr19:7489006-7489059 | Rare:25 | ||||
chr19:7535414-7535785 | Common:3; Rare:119; Clinvar:2 | ||||
chr19:7629531-7629848 | Common:5; Rare:113; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr19:7903526-7903904 | Common:1; Rare:116 | ||||
chr19:7943630-7943967 | Rare:92 | ||||
chr19:8005504-8005822 | Common:1; Rare:111 | ||||
chr19:8321324-8321703 | Common:2; Rare:153 | ||||
chr19:8364034-8364158 | Common:1; Rare:34 | ||||
chr19:8390032-8390412 | Common:1; Rare:106 | ||||
chr19:8444791-8445040 | Common:4; Rare:112 | ||||
chr19:8514144-8514222 | Common:1; Rare:23 | ||||
chr19:9140311-9140446 | Common:1; Rare:39 | ||||
chr19:9435512-9435605 | Rare:39 |