Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:70205531-70205775 | Rare:81 | ||||
chr1:70221303-70221519 | Rare:94 | ||||
chr1:70354687-70354856 | Rare:62 | ||||
chr1:71080962-71081394 | Rare:120 | ||||
chr1:72282868-72282974 | Common:3; Rare:45 | ||||
chr1:74198126-74198348 | Common:3; Rare:119 | ||||
chr1:74732988-74733273 | Common:5; Rare:89 | ||||
chr1:75724371-75724778 | Common:5; Rare:143; Clinvar:7; Clinvar (benign):5 | ||||
chr1:77219375-77219520 | Rare:71 | ||||
chr1:77371078-77371301 | Common:1; Rare:35 | ||||
chr1:77683322-77683577 | Common:1; Rare:82 | ||||
chr1:77888430-77888646 | Common:1; Rare:45; Clinvar:2 | ||||
chr1:77979020-77979185 | Common:2; Rare:58 | ||||
chr1:77979468-77979537 | Common:1; Rare:20 | ||||
chr1:78004552-78004873 | Common:3; Rare:80 |