Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:121184846-121185067 | Rare:81 | ||||
chr1:145823937-145824261 | Rare:115 | ||||
chr1:145927404-145927648 | Common:1; Rare:67; Clinvar (pathogenic):1 | ||||
chr1:145964542-145964748 | Rare:53 | ||||
chr1:147172427-147172779 | Common:1; Rare:91 | ||||
chr1:149103511-149103570 | Common:2; Rare:22 | ||||
chr1:149842746-149842947 | Rare:3 | ||||
chr1:149850826-149851064 | Rare:1 | ||||
chr1:149886664-149887059 | Common:2; Rare:140 | ||||
chr1:149887885-149888214 | Rare:101 | ||||
chr1:150010679-150010837 | Common:1; Rare:37 | ||||
chr1:150067680-150067866 | Rare:59 | ||||
chr1:150282279-150282572 | Common:3; Rare:55 | ||||
chr1:150293753-150293909 | Rare:52 | ||||
chr1:150364584-150364717 | Rare:47 |