Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:193593090-193593402 | Rare:97; Clinvar:2; Clinvar (benign):2 | ||||
chr3:195543244-195543475 | Common:3; Rare:90 | ||||
chr3:196287664-196287952 | Common:2; Rare:88 | ||||
chr3:196318174-196318350 | Common:1; Rare:74 | ||||
chr3:196503689-196503934 | Common:5; Rare:83 | ||||
chr3:196568527-196568848 | Common:5; Rare:98 | ||||
chr3:196639578-196639793 | Common:2; Rare:54 | ||||
chr3:196942375-196942650 | Common:1; Rare:113 | ||||
chr3:197949903-197950250 | Common:3; Rare:105; Clinvar (benign):2 | ||||
chr3:197950912-197951212 | Rare:101; Clinvar:1; Clinvar (benign):2 | ||||
chr3:197959985-197960242 | Common:1; Rare:91 | ||||
chr4:337480-337858 | Common:1; Rare:108 | ||||
chr4:499123-499285 | Common:3; Rare:60 | ||||
chr4:663595-663714 | Rare:37 | ||||
chr4:674238-674626 | Common:3; Rare:178 |