Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:145964554-145964749 | Rare:48 | ||||
chr1:145996503-145996869 | Common:1; Rare:148 | ||||
chr1:146938265-146938343 | Rare:32 | ||||
chr1:147172351-147172769 | Common:1; Rare:114 | ||||
chr1:147541189-147541653 | Common:5; Rare:76 | ||||
chr1:147928268-147928486 | Common:2; Rare:80 | ||||
chr1:148951927-148952166 | Common:3; Rare:60 | ||||
chr1:148952259-148952642 | Common:5; Rare:104 | ||||
chr1:149812358-149812570 | Rare:62 | ||||
chr1:149842748-149842962 | Rare:3 | ||||
chr1:149850812-149851068 | Rare:3 | ||||
chr1:149886628-149887166 | Common:3; Rare:213 | ||||
chr1:149887915-149888221 | Rare:91 | ||||
chr1:149917743-149917993 | Common:2; Rare:66 | ||||
chr1:149927751-149927968 | Common:1; Rare:89; Clinvar (benign):5 |