Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:154607932-154608332 | Common:1; Rare:202; Clinvar (benign):2 | ||||
chr1:154608660-154609000 | Common:15; Rare:99 | ||||
chr1:154627042-154627483 | Common:11; Rare:248 | ||||
chr1:154627408-154628370 | Common:23; Rare:609 | ||||
chr1:154859980-154860640 | Common:5; Rare:232 | ||||
chr1:154870152-154870552 | Rare:169 | ||||
chr1:154936340-154937462 | Common:19; Rare:975 | ||||
chr1:154937476-154937876 | Common:5; Rare:67 | ||||
chr1:154954972-154955997 | Common:4; Rare:205 | ||||
chr1:154955982-154956382 | Common:4; Rare:281 | ||||
chr1:154961260-154961671 | Rare:517 | ||||
chr1:154961645-154962110 | Common:6; Rare:565 | ||||
chr1:154970607-154971007 | Common:3; Rare:219 | ||||
chr1:154973590-154974345 | Common:7; Rare:473 | ||||
chr1:154974282-154974792 | Rare:684 |