Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:150293749-150293920 | Common:1; Rare:58 | ||||
chr1:150321421-150321590 | Rare:54; Clinvar:3; Clinvar (benign):1 | ||||
chr1:150363968-150364225 | Common:3; Rare:92 | ||||
chr1:150364572-150364717 | Common:1; Rare:51 | ||||
chr1:150578578-150578748 | Rare:38 | ||||
chr1:150579126-150579271 | Rare:62 | ||||
chr1:150579593-150579830 | Common:9; Rare:77 | ||||
chr1:150629522-150629825 | Rare:60 | ||||
chr1:150876569-150876980 | Common:5; Rare:141 | ||||
chr1:150926177-150926327 | Rare:43 | ||||
chr1:150926337-150926464 | Rare:40 | ||||
chr1:150974617-150974908 | Common:2; Rare:87 | ||||
chr1:151008373-151008564 | Common:1; Rare:59 | ||||
chr1:151060246-151060519 | Rare:50 | ||||
chr1:151165851-151166166 | Common:3; Rare:90 |