Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:6235922-6236106 | Common:2; Rare:68 | ||||
chr1:7961482-7961787 | Common:3; Rare:97; Clinvar:2; Clinvar (benign):3 | ||||
chr1:8423707-8423913 | Rare:98 | ||||
chr1:8878582-8878860 | Rare:146 | ||||
chr1:9943357-9943489 | Common:2; Rare:28 | ||||
chr1:10398788-10399114 | Common:2; Rare:129 | ||||
chr1:11654336-11654501 | Rare:47 | ||||
chr1:11654669-11654909 | Common:4; Rare:68 | ||||
chr1:11805900-11806191 | Common:2; Rare:80; Clinvar:1 | ||||
chr1:11934500-11934739 | Common:3; Rare:78; Clinvar:4 | ||||
chr1:12019242-12019540 | Common:5; Rare:103 | ||||
chr1:12617294-12617344 | Rare:9 | ||||
chr1:12618175-12618433 | Common:2; Rare:54 | ||||
chr1:13583717-13583877 | Common:1; Rare:75 | ||||
chr1:16156035-16156287 | Rare:56; Clinvar:1 |