Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:66533916-66534182 | Common:1; Rare:63 | ||||
chr1:66924820-66925024 | Rare:89 | ||||
chr1:66925182-66925514 | Common:2; Rare:106 | ||||
chr1:66929991-66930385 | Rare:130 | ||||
chr1:67430247-67430552 | Rare:111 | ||||
chr1:67833342-67833527 | Common:2; Rare:73 | ||||
chr1:68232464-68232631 | Rare:38 | ||||
chr1:69568523-69568800 | Common:2; Rare:83 | ||||
chr1:70205529-70205764 | Rare:82 | ||||
chr1:70221276-70221530 | Rare:108 | ||||
chr1:70354659-70354871 | Rare:67 | ||||
chr1:70411078-70411279 | Common:1; Rare:49; Clinvar:1; Clinvar (benign):1 | ||||
chr1:71080963-71081392 | Rare:119 | ||||
chr1:74198141-74198340 | Common:2; Rare:112 | ||||
chr1:74733019-74733314 | Common:6; Rare:104 |