Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:184249489-184249678 | Rare:46 | ||||
chr3:184314421-184314654 | Common:3; Rare:71 | ||||
chr3:184362450-184362609 | Rare:35 | ||||
chr3:184381345-184381409 | Rare:21 | ||||
chr3:185499033-185499157 | Rare:33 | ||||
chr3:186567335-186567370 | Rare:10 | ||||
chr3:188154016-188154209 | Rare:50 | ||||
chr3:195271083-195271277 | Common:1; Rare:79 | ||||
chr3:195583924-195584158 | Common:2; Rare:50 | ||||
chr3:196287628-196287812 | Common:1; Rare:58 | ||||
chr3:196503685-196503952 | Common:5; Rare:92 | ||||
chr3:196867764-196867934 | Rare:58 | ||||
chr3:196942375-196942677 | Common:1; Rare:127 | ||||
chr3:197749733-197749957 | Common:1; Rare:81 | ||||
chr3:197949885-197950230 | Common:4; Rare:101; Clinvar (benign):1 |