Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:42567939-42568118 | Rare:41 | ||||
chr2:42792543-42792826 | Common:3; Rare:81 | ||||
chr2:43595946-43596205 | Common:1; Rare:94 | ||||
chr2:44361479-44362007 | Common:3; Rare:165 | ||||
chr2:46297653-46297857 | Common:1; Rare:76; Clinvar:5; Clinvar (benign):2 | ||||
chr2:46544067-46544296 | Rare:62 | ||||
chr2:46617019-46617273 | Common:7; Rare:112 | ||||
chr2:46698772-46698942 | Common:1; Rare:52 | ||||
chr2:46915722-46915950 | Common:2; Rare:76; Clinvar:2; Clinvar (benign):1 | ||||
chr2:46916007-46916173 | Common:2; Rare:55 | ||||
chr2:47176434-47176927 | Common:5; Rare:225; Clinvar (benign):5 | ||||
chr2:47782861-47783198 | Common:3; Rare:140; Clinvar:4; Clinvar (benign):7 | ||||
chr2:48440619-48440956 | Common:8; Rare:148 | ||||
chr2:53767559-53767865 | Common:4; Rare:106 | ||||
chr2:53786842-53787164 | Rare:119 |