Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:243572950-243573195 | Rare:54; Clinvar (benign):1 | ||||
chr1:243624960-243625116 | Rare:27 | ||||
chr1:243749369-243749523 | Rare:20 | ||||
chr1:243759987-243760272 | Common:1; Rare:51 | ||||
chr1:243769887-243770027 | Rare:16 | ||||
chr1:243795059-243795449 | Common:1; Rare:75 | ||||
chr1:243797860-243797881 | Rare:7 | ||||
chr1:243805446-243805492 | Rare:9 | ||||
chr1:243805936-243806122 | Common:1; Rare:39 | ||||
chr1:243831784-243832090 | Common:4; Rare:51 | ||||
chr1:243833745-243834078 | Common:1; Rare:61 | ||||
chr1:243839891-243840211 | Common:1; Rare:58 | ||||
chr1:243849016-243849161 | Common:2; Rare:31 | ||||
chr1:243849473-243849567 | Rare:30 | ||||
chr1:243917514-243917746 | Common:1; Rare:33 |