Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:38557238-38557257 | Rare:5 | ||||
chr5:39074381-39074516 | Common:1; Rare:58 | ||||
chr5:39425106-39425405 | Common:3; Rare:66 | ||||
chr5:40755876-40756114 | Rare:64 | ||||
chr5:40798161-40798461 | Common:2; Rare:114 | ||||
chr5:41870364-41870437 | Rare:35; Clinvar:1 | ||||
chr5:41903985-41904377 | Common:2; Rare:118 | ||||
chr5:43064958-43065134 | Rare:48 | ||||
chr5:43067348-43067499 | Rare:21 | ||||
chr5:43121410-43121655 | Common:1; Rare:93 | ||||
chr5:43313393-43313503 | Common:3; Rare:34 | ||||
chr5:43483831-43483926 | Common:1; Rare:35 | ||||
chr5:43603082-43603259 | Rare:42 | ||||
chr5:44388364-44388425 | Rare:13; Clinvar (benign):1 | ||||
chr5:44808761-44808965 | Common:2; Rare:64 |