Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:70237439-70237758 | Common:1; Rare:57 | ||||
chr1:70246816-70247076 | Rare:53 | ||||
chr1:70354681-70354856 | Rare:62 | ||||
chr1:71080988-71081396 | Rare:112 | ||||
chr1:74198145-74198343 | Common:2; Rare:113 | ||||
chr1:74732815-74733360 | Common:6; Rare:170 | ||||
chr1:75786754-75787082 | Common:2; Rare:69 | ||||
chr1:75791073-75791484 | Common:1; Rare:85 | ||||
chr1:77219384-77219528 | Rare:67 | ||||
chr1:77888437-77888506 | Common:1; Rare:16 | ||||
chr1:77926600-77926885 | Common:1; Rare:90; Clinvar:8; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
chr1:77947072-77947124 | Common:1; Rare:11 | ||||
chr1:77947464-77947815 | Rare:52 | ||||
chr1:77948221-77948548 | Rare:48 | ||||
chr1:77960183-77960478 | Rare:73; Clinvar:1 |