Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:66924800-66925083 | Rare:115 | ||||
chr1:66925182-66925518 | Common:2; Rare:107 | ||||
chr1:67053925-67054059 | Rare:67 | ||||
chr1:67054083-67054259 | Common:2; Rare:37 | ||||
chr1:67424855-67425225 | Rare:91 | ||||
chr1:67429989-67430449 | Rare:177 | ||||
chr1:67833332-67833527 | Common:2; Rare:77 | ||||
chr1:70205542-70205775 | Rare:73 | ||||
chr1:70221312-70221682 | Rare:144 | ||||
chr1:70354671-70354865 | Rare:65 | ||||
chr1:70411069-70411285 | Common:2; Rare:55; Clinvar:1; Clinvar (benign):1 | ||||
chr1:71080950-71081379 | Rare:113 | ||||
chr1:74198117-74198332 | Common:3; Rare:120 | ||||
chr1:74732994-74733273 | Common:5; Rare:88 | ||||
chr1:75724634-75724816 | Common:2; Rare:88; Clinvar:4; Clinvar (benign):2 |