Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:197146521-197146817 | Common:1; Rare:65; Clinvar:4; Clinvar (benign):1 | ||||
chr1:197268113-197268295 | Rare:32; Clinvar:1; Clinvar (benign):1 | ||||
chr1:197902560-197902647 | Rare:29 | ||||
chr1:197902886-197903034 | Common:1; Rare:77 | ||||
chr1:200409977-200410356 | Rare:106 | ||||
chr1:200669846-200670136 | Common:12; Rare:96 | ||||
chr1:201154438-201154642 | Common:2; Rare:55 | ||||
chr1:201377641-201377982 | Common:4; Rare:71; Clinvar (benign):2 | ||||
chr1:201829554-201829622 | Common:2; Rare:8 | ||||
chr1:201955281-201955529 | Common:1; Rare:70 | ||||
chr1:201983334-201983391 | Rare:10 | ||||
chr1:202341884-202342204 | Common:1; Rare:82 | ||||
chr1:202348549-202348720 | Common:1; Rare:38 | ||||
chr1:202889100-202889284 | Common:2; Rare:69 | ||||
chr1:202927121-202927337 | Common:4; Rare:96 |