Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:46387203-46387352 | Rare:37 | ||||
chr13:46797094-46797357 | Common:3; Rare:88 | ||||
chr13:48001225-48001405 | Common:1; Rare:82; Clinvar:3; Clinvar (benign):6 | ||||
chr13:48037481-48037769 | Rare:108 | ||||
chr13:48233053-48233475 | Common:3; Rare:146 | ||||
chr13:48533044-48533094 | Common:1; Rare:16 | ||||
chr13:48975800-48975967 | Rare:61 | ||||
chr13:48976500-48976666 | Common:2; Rare:56 | ||||
chr13:49247830-49247994 | Rare:52 | ||||
chr13:49443996-49444476 | Common:1; Rare:156 | ||||
chr13:49585499-49585658 | Common:1; Rare:58 | ||||
chr13:49936257-49936578 | Common:1; Rare:97 | ||||
chr13:49996748-49997092 | Common:1; Rare:70 | ||||
chr13:50081969-50082229 | Common:1; Rare:73 | ||||
chr13:50910013-50910074 | Rare:15 |