Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:154970645-154970869 | Rare:39 | ||||
chr1:154974322-154974738 | Rare:108 | ||||
chr1:154983097-154983392 | Common:2; Rare:57; Clinvar (benign):1 | ||||
chr1:155051144-155051389 | Common:2; Rare:84 | ||||
chr1:155127747-155127918 | Common:1; Rare:36 | ||||
chr1:155173125-155173389 | Common:3; Rare:114 | ||||
chr1:155173824-155173881 | Rare:10 | ||||
chr1:155209040-155209254 | Rare:89 | ||||
chr1:155254549-155254651 | Common:1; Rare:30 | ||||
chr1:155262177-155262502 | Common:2; Rare:95 | ||||
chr1:155308596-155308965 | Common:1; Rare:85 | ||||
chr1:155324360-155324536 | Common:2; Rare:79 | ||||
chr1:155562770-155562979 | Common:1; Rare:115 | ||||
chr1:155563090-155563246 | Rare:65 | ||||
chr1:155688312-155688467 | Rare:72 |