Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:160343157-160343391 | Rare:92 | ||||
chr1:161045878-161046064 | Common:1; Rare:48 | ||||
chr1:161118022-161118141 | Rare:59 | ||||
chr1:161132426-161132700 | Common:1; Rare:94 | ||||
chr1:161166222-161166511 | Common:2; Rare:77; Clinvar:3; Clinvar (benign):1 | ||||
chr1:161215159-161215334 | Common:2; Rare:55 | ||||
chr1:161314212-161314405 | Common:3; Rare:66; Clinvar:2; Clinvar (benign):2 | ||||
chr1:161766163-161766382 | Common:3; Rare:70 | ||||
chr1:162023318-162023575 | Common:3; Rare:73; Clinvar (pathogenic):1 | ||||
chr1:162023625-162023921 | Common:1; Rare:80 | ||||
chr1:163321733-163322007 | Common:1; Rare:75 | ||||
chr1:165698510-165698759 | Common:5; Rare:97 | ||||
chr1:165768823-165768933 | Common:1; Rare:50 | ||||
chr1:166839322-166839514 | Rare:53 | ||||
chr1:167630063-167630336 | Common:5; Rare:46 |