Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:66925207-66925525 | Common:2; Rare:99 | ||||
chr1:67430151-67430670 | Rare:196 | ||||
chr1:67833366-67833776 | Common:4; Rare:139 | ||||
chr1:70205542-70205759 | Rare:69 | ||||
chr1:70221302-70221506 | Rare:87 | ||||
chr1:70354659-70354846 | Rare:63 | ||||
chr1:70411094-70411268 | Rare:39; Clinvar:1 | ||||
chr1:71081003-71081364 | Rare:93 | ||||
chr1:74198152-74198292 | Common:1; Rare:78 | ||||
chr1:74733019-74733245 | Common:5; Rare:69 | ||||
chr1:75724308-75724784 | Common:6; Rare:166; Clinvar:7; Clinvar (benign):5 | ||||
chr1:77219398-77219520 | Rare:54 | ||||
chr1:77888378-77888730 | Common:2; Rare:81; Clinvar:2 | ||||
chr1:77979020-77979291 | Common:2; Rare:92 | ||||
chr1:78004552-78004951 | Common:4; Rare:91 |