Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:119366801-119367070 | Common:1; Rare:80 | ||||
chr2:119759740-119759928 | Common:1; Rare:51 | ||||
chr2:121530596-121530880 | Common:7; Rare:113 | ||||
chr2:121736851-121737105 | Common:4; Rare:88 | ||||
chr2:121755405-121755737 | Common:2; Rare:107 | ||||
chr2:127106956-127107385 | Common:5; Rare:126; Clinvar:8; Clinvar (benign):2 | ||||
chr2:127294133-127294206 | Common:2; Rare:20; Clinvar (benign):2 | ||||
chr2:127811153-127811267 | Rare:33 | ||||
chr2:127885950-127885975 | Rare:3 | ||||
chr2:130181549-130181714 | Common:1; Rare:64 | ||||
chr2:130182096-130182388 | Common:2; Rare:112 | ||||
chr2:130342642-130342938 | Common:5; Rare:94 | ||||
chr2:130355747-130356062 | Common:3; Rare:86 | ||||
chr2:130372584-130372782 | Common:1; Rare:58 | ||||
chr2:131105247-131105356 | Common:1; Rare:51 |