Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:109548507-109548642 | Common:1; Rare:46 | ||||
chr1:110339204-110339473 | Rare:85 | ||||
chr1:110407616-110407795 | Common:2; Rare:82 | ||||
chr1:111140056-111140259 | Common:1; Rare:70 | ||||
chr1:112619101-112619182 | Rare:32 | ||||
chr1:112956193-112956433 | Common:4; Rare:108; Clinvar:8; Clinvar (benign):3 | ||||
chr1:119140648-119140724 | Rare:20 | ||||
chr1:145918695-145919022 | Common:2; Rare:69 | ||||
chr1:145927430-145927644 | Common:1; Rare:62; Clinvar (pathogenic):1 | ||||
chr1:145964484-145964743 | Rare:60 | ||||
chr1:149886552-149887004 | Common:2; Rare:174 | ||||
chr1:149887938-149888215 | Rare:67 | ||||
chr1:150629541-150629792 | Rare:52 | ||||
chr1:151165872-151166181 | Common:3; Rare:94 | ||||
chr1:153535962-153536178 | Common:2; Rare:48 |