Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:36464276-36464503 | Common:3; Rare:66 | ||||
chr1:37474405-37474582 | Rare:69 | ||||
chr1:37692231-37692564 | Common:4; Rare:74 | ||||
chr1:37859596-37859804 | Common:4; Rare:69 | ||||
chr1:38873306-38873554 | Common:3; Rare:85 | ||||
chr1:39026246-39026397 | Common:1; Rare:41 | ||||
chr1:39883456-39883570 | Common:1; Rare:46; Clinvar (pathogenic):1 | ||||
chr1:40040444-40040788 | Common:3; Rare:102 | ||||
chr1:40097231-40097316 | Rare:35; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr1:40257928-40258282 | Common:4; Rare:94; Clinvar:7; Clinvar (benign):1 | ||||
chr1:40691504-40691830 | Common:2; Rare:155 | ||||
chr1:42335165-42335346 | Common:3; Rare:95 | ||||
chr1:42456446-42456626 | Common:1; Rare:80 | ||||
chr1:42658320-42658452 | Rare:39 | ||||
chr1:42767030-42767293 | Common:3; Rare:74 |