Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:36346270-36346509 | Common:3; Rare:66; Clinvar:3; Clinvar (benign):2 | ||||
chr13:36999281-36999468 | Rare:75 | ||||
chr13:37000757-37000804 | Rare:23 | ||||
chr13:37059603-37059731 | Common:1; Rare:44 | ||||
chr13:39038053-39038456 | Common:1; Rare:98 | ||||
chr13:41060957-41061598 | Common:5; Rare:223 | ||||
chr13:43879467-43879614 | Rare:41 | ||||
chr13:43879616-43879788 | Common:6; Rare:35 | ||||
chr13:44989456-44989607 | Rare:53 | ||||
chr13:45120358-45120523 | Common:2; Rare:46 | ||||
chr13:45341109-45341570 | Common:4; Rare:220 | ||||
chr13:46052718-46052819 | Common:2; Rare:29 | ||||
chr13:48037628-48037730 | Rare:36 | ||||
chr13:49247830-49247982 | Rare:47 | ||||
chr13:49443996-49444281 | Common:1; Rare:99 |