Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:101698196-101698371 | Common:1; Rare:42 | ||||
chr2:102736811-102736965 | Common:1; Rare:78 | ||||
chr2:105037832-105038169 | Common:4; Rare:120 | ||||
chr2:105337187-105337659 | Common:6; Rare:157 | ||||
chr2:105398993-105399258 | Common:1; Rare:92 | ||||
chr2:106194210-106194543 | Common:6; Rare:143 | ||||
chr2:106886778-106886897 | Common:1; Rare:39 | ||||
chr2:106887161-106887261 | Rare:30 | ||||
chr2:108449070-108449277 | Rare:87 | ||||
chr2:108534199-108534438 | Common:7; Rare:99 | ||||
chr2:108719344-108719635 | Common:3; Rare:131; Clinvar (benign):2 | ||||
chr2:108719738-108719816 | Rare:22 | ||||
chr2:109613885-109614089 | Common:2; Rare:72 | ||||
chr2:110204934-110205064 | Common:1; Rare:58; Clinvar:1; Clinvar (benign):1 | ||||
chr2:110678014-110678259 | Rare:79 |