Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:91906164-91906564 | Common:1; Rare:172 | ||||
chr1:92080100-92080978 | Common:13; Rare:681 | ||||
chr1:92298280-92299260 | Common:9; Rare:816; Clinvar:10; Clinvar (benign):10 | ||||
chr1:92299303-92299703 | Common:3; Rare:81 | ||||
chr1:92485768-92486400 | Common:2; Rare:215 | ||||
chr1:92784867-92785710 | Common:34; Rare:873 | ||||
chr1:92791872-92792643 | Common:4; Rare:223 | ||||
chr1:92831762-92832162 | Common:9; Rare:722; Clinvar:40; Clinvar (benign):36 | ||||
chr1:92832243-92832346 | Rare:31 | ||||
chr1:92832447-92832969 | Common:3; Rare:355 | ||||
chr1:92836187-92836390 | Rare:48; Clinvar:1; Clinvar (benign):2 | ||||
chr1:92961274-92961674 | Common:3; Rare:369 | ||||
chr1:92961670-92962490 | Common:9; Rare:240 | ||||
chr1:93078694-93079521 | Common:24; Rare:821 | ||||
chr1:93079657-93080079 | Rare:236 |