Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:149928223-149928247 | Rare:5 | ||||
chr1:150067646-150067852 | Rare:60 | ||||
chr1:150150177-150150286 | Common:2; Rare:41 | ||||
chr1:150235904-150236171 | Common:1; Rare:62 | ||||
chr1:150268279-150268434 | Rare:27 | ||||
chr1:150293834-150293913 | Rare:26 | ||||
chr1:150321371-150321618 | Rare:77; Clinvar:3; Clinvar (benign):1 | ||||
chr1:150487311-150487473 | Common:3; Rare:49; Clinvar (benign):3 | ||||
chr1:150578985-150579099 | Common:1; Rare:50 | ||||
chr1:150579595-150579917 | Common:11; Rare:94 | ||||
chr1:150629116-150629407 | Common:1; Rare:89 | ||||
chr1:150629541-150629853 | Common:1; Rare:67 | ||||
chr1:150876560-150876869 | Common:5; Rare:115 | ||||
chr1:150926342-150926446 | Rare:32 | ||||
chr1:151005979-151006136 | Common:1; Rare:25 |