Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:105015093-105015196 | Rare:22 | ||||
chr7:105107100-105107222 | Rare:37 | ||||
chr7:106217063-106217328 | Common:2; Rare:54 | ||||
chr7:106219356-106219519 | Common:2; Rare:41 | ||||
chr7:106278230-106278358 | Rare:28 | ||||
chr7:106281600-106281878 | Rare:55 | ||||
chr7:106281937-106282169 | Common:2; Rare:44 | ||||
chr7:106419877-106420079 | Rare:35 | ||||
chr7:106421060-106421291 | Common:4; Rare:51 | ||||
chr7:106422164-106422480 | Common:6; Rare:53 | ||||
chr7:106425109-106425296 | Rare:41 | ||||
chr7:106444189-106444489 | Common:1; Rare:53 | ||||
chr7:107167816-107168129 | Common:2; Rare:62 | ||||
chr7:107926262-107926507 | Common:1; Rare:79; Clinvar (benign):2 | ||||
chr7:107951226-107951575 | Common:3; Rare:86; Clinvar (benign):2 |