Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:6745312-6745379 | Rare:10 | ||||
chr19:6749878-6749995 | Common:1; Rare:43 | ||||
chr19:7561224-7561485 | Common:1; Rare:80; Clinvar:2; Clinvar (benign):1 | ||||
chr19:7619812-7619984 | Common:1; Rare:67 | ||||
chr19:7853147-7853332 | Common:1; Rare:52 | ||||
chr19:8388524-8388555 | Rare:5 | ||||
chr19:8473678-8473967 | Common:2; Rare:54 | ||||
chr19:9428076-9428229 | Rare:29 | ||||
chr19:9658074-9658208 | Rare:44 | ||||
chr19:9683388-9683582 | Rare:39 | ||||
chr19:9749706-9749918 | Common:1; Rare:38 | ||||
chr19:9945544-9945837 | Common:4; Rare:58 | ||||
chr19:10118620-10118721 | Rare:32 | ||||
chr19:10284497-10284870 | Common:5; Rare:110 | ||||
chr19:10561057-10561223 | Common:3; Rare:61 |