Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:153727786-153728088 | Common:1; Rare:86 | ||||
chr1:153963493-153963745 | Common:2; Rare:70 | ||||
chr1:154182987-154183290 | Rare:97 | ||||
chr1:154220498-154220984 | Common:1; Rare:164 | ||||
chr1:154956097-154956224 | Rare:36 | ||||
chr1:154970701-154970869 | Rare:32 | ||||
chr1:154974312-154974730 | Rare:106 | ||||
chr1:154983050-154983392 | Common:2; Rare:68; Clinvar (benign):1 | ||||
chr1:155051144-155051368 | Common:2; Rare:76 | ||||
chr1:155135705-155135886 | Common:2; Rare:79 | ||||
chr1:155173160-155173383 | Common:3; Rare:105 | ||||
chr1:155173829-155173905 | Rare:12 | ||||
chr1:155209102-155209254 | Rare:68 | ||||
chr1:155244606-155244894 | Common:3; Rare:81 | ||||
chr1:155255450-155255575 | Common:1; Rare:26 |