Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:185156885-185157300 | Common:2; Rare:118 | ||||
chr1:185317212-185317495 | Common:2; Rare:83 | ||||
chr1:185734231-185734392 | Common:3; Rare:38 | ||||
chr1:186375126-186375398 | Rare:76 | ||||
chr1:186375609-186375941 | Common:1; Rare:96 | ||||
chr1:186679949-186680637 | Common:9; Rare:245 | ||||
chr1:190478030-190478390 | Common:1; Rare:91 | ||||
chr1:190478490-190478990 | Common:8; Rare:111 | ||||
chr1:192808800-192809111 | Common:4; Rare:136 | ||||
chr1:193059325-193059672 | Rare:162 | ||||
chr1:193060059-193060221 | Rare:45 | ||||
chr1:193105339-193105714 | Common:3; Rare:151 | ||||
chr1:193121737-193122182 | Common:2; Rare:158; Clinvar:5; Clinvar (benign):1 | ||||
chr1:193186077-193186477 | Rare:124 | ||||
chr1:196608230-196608690 | Common:2; Rare:103 |