Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:190476065-190476288 | Common:2; Rare:62 | ||||
chr1:190477531-190477753 | Common:2; Rare:57 | ||||
chr1:190477847-190478534 | Common:1; Rare:149 | ||||
chr1:190478550-190478989 | Common:7; Rare:103 | ||||
chr1:192808918-192809105 | Common:2; Rare:85 | ||||
chr1:193059280-193059440 | Rare:70 | ||||
chr1:193059443-193059677 | Rare:121 | ||||
chr1:193105384-193105533 | Common:2; Rare:61 | ||||
chr1:193121680-193122229 | Common:3; Rare:198; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
chr1:193186388-193186668 | Common:3; Rare:51 | ||||
chr1:196608863-196609189 | Common:2; Rare:61 | ||||
chr1:197902516-197902659 | Common:1; Rare:49 | ||||
chr1:197916847-197917093 | Rare:41 | ||||
chr1:197917095-197917449 | Common:6; Rare:105 | ||||
chr1:200410005-200410165 | Rare:49 |