Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:229271027-229271315 | Rare:95 | ||||
chr1:229342554-229342661 | Rare:33 | ||||
chr1:229508291-229508429 | Common:1; Rare:55 | ||||
chr1:229625950-229626274 | Rare:109 | ||||
chr1:230714117-230714333 | Common:3; Rare:42; Clinvar:4; Clinvar (benign):3 | ||||
chr1:230978742-230979108 | Common:2; Rare:139 | ||||
chr1:231241112-231241257 | Rare:79; Clinvar:2 | ||||
chr1:231337830-231338049 | Common:2; Rare:81 | ||||
chr1:231528540-231528728 | Common:2; Rare:71 | ||||
chr1:232805318-232805425 | Common:2; Rare:61 | ||||
chr1:232950488-232950664 | Common:3; Rare:59 | ||||
chr1:234373388-234373775 | Common:1; Rare:177; Clinvar (benign):7 | ||||
chr1:234608194-234608318 | Rare:42 | ||||
chr1:235128767-235129041 | Rare:110 | ||||
chr1:235328227-235328606 | Common:3; Rare:100 |