Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:97972403-97972679 | Common:8; Rare:61 | ||||
chr3:99638389-99638616 | Common:1; Rare:56 | ||||
chr3:99817558-99817938 | Rare:118 | ||||
chr3:100260733-100261021 | Rare:74 | ||||
chr3:100334658-100334780 | Common:1; Rare:55 | ||||
chr3:100492282-100492619 | Common:2; Rare:105 | ||||
chr3:100709234-100709644 | Common:6; Rare:134; Clinvar (benign):1 | ||||
chr3:101574003-101574225 | Rare:77 | ||||
chr3:101686677-101686870 | Common:2; Rare:81 | ||||
chr3:105366614-105366919 | Common:3; Rare:80 | ||||
chr3:108589422-108589704 | Common:3; Rare:69 | ||||
chr3:112561615-112561716 | Rare:32 | ||||
chr3:112990900-112990996 | Common:1; Rare:36 | ||||
chr3:113515129-113515250 | Rare:36 | ||||
chr3:119468837-119468996 | Rare:57 |