Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:154936668-154936770 | Common:2; Rare:35 | ||||
chr1:154961455-154961547 | Rare:26 | ||||
chr1:154970703-154970874 | Rare:32 | ||||
chr1:154970957-154971285 | Common:1; Rare:66 | ||||
chr1:154974313-154974803 | Rare:124 | ||||
chr1:154983097-154983392 | Common:2; Rare:57; Clinvar (benign):1 | ||||
chr1:155051150-155051384 | Common:2; Rare:79 | ||||
chr1:155135707-155135920 | Common:3; Rare:92 | ||||
chr1:155173152-155173388 | Common:3; Rare:107 | ||||
chr1:155173751-155173861 | Rare:32 | ||||
chr1:155209111-155209274 | Rare:75 | ||||
chr1:155244625-155244917 | Common:3; Rare:82 | ||||
chr1:155255427-155255528 | Rare:21 | ||||
chr1:155262177-155262502 | Common:2; Rare:95 | ||||
chr1:155273465-155273606 | Rare:45 |