Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:185156681-185156835 | Common:1; Rare:56 | ||||
chr1:185156900-185157297 | Common:2; Rare:109 | ||||
chr1:185157439-185157523 | Common:1; Rare:29 | ||||
chr1:185317165-185317468 | Common:1; Rare:88 | ||||
chr1:186375099-186375974 | Common:1; Rare:240 | ||||
chr1:186680301-186680681 | Common:3; Rare:88 | ||||
chr1:192808603-192809235 | Common:5; Rare:221; Clinvar:1 | ||||
chr1:193059183-193059774 | Common:1; Rare:254 | ||||
chr1:193105270-193105533 | Common:4; Rare:118 | ||||
chr1:193121764-193122210 | Common:2; Rare:158; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr1:193122359-193122484 | Rare:50 | ||||
chr1:196608407-196608674 | Common:1; Rare:59 | ||||
chr1:197146279-197146827 | Common:1; Rare:170; Clinvar:8; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
chr1:197902535-197902659 | Common:1; Rare:41 | ||||
chr1:197902876-197903020 | Common:1; Rare:75 |