Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:112645688-112645947 | Common:1; Rare:94 | ||||
chr2:112764594-112764765 | Common:1; Rare:54; Clinvar (pathogenic):1 | ||||
chr2:113627070-113627312 | Common:4; Rare:68 | ||||
chr2:113756566-113756791 | Common:3; Rare:79 | ||||
chr2:113889766-113890165 | Common:8; Rare:128 | ||||
chr2:118014056-118014214 | Common:2; Rare:91 | ||||
chr2:119366778-119367068 | Common:1; Rare:90 | ||||
chr2:119679102-119679219 | Common:3; Rare:33 | ||||
chr2:120012973-120013074 | Common:1; Rare:40 | ||||
chr2:121530574-121530884 | Common:7; Rare:131 | ||||
chr2:121736824-121737229 | Common:5; Rare:157 | ||||
chr2:126655778-126656214 | Common:1; Rare:115 | ||||
chr2:127294119-127294246 | Common:2; Rare:47; Clinvar (benign):2 | ||||
chr2:127526421-127526612 | Common:2; Rare:64 | ||||
chr2:127811139-127811259 | Rare:37 |