Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:186680283-186680670 | Common:3; Rare:91 | ||||
chr1:192808809-192809070 | Common:4; Rare:111 | ||||
chr1:193059308-193059710 | Rare:190 | ||||
chr1:193105378-193105515 | Common:2; Rare:56 | ||||
chr1:193121617-193122237 | Common:3; Rare:218; Clinvar:5; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
chr1:193186554-193186683 | Rare:22 | ||||
chr1:201171545-201171620 | Rare:13 | ||||
chr1:201377610-201378008 | Common:4; Rare:85; Clinvar:1; Clinvar (benign):4 | ||||
chr1:201888420-201888688 | Common:2; Rare:59 | ||||
chr1:201946448-201946793 | Common:2; Rare:55 | ||||
chr1:201955369-201955551 | Common:1; Rare:57 | ||||
chr1:203007246-203007442 | Common:2; Rare:77 | ||||
chr1:203128208-203128332 | Rare:37 | ||||
chr1:203305265-203305720 | Common:3; Rare:131 | ||||
chr1:203351051-203351496 | Common:5; Rare:94 |