Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:48303712-48303880 | Rare:50; Clinvar:3; Clinvar (pathogenic):1 | ||||
chr13:48975659-48975923 | Common:2; Rare:82 | ||||
chr13:48976540-48976670 | Common:1; Rare:46 | ||||
chr13:49247830-49247990 | Rare:50 | ||||
chr13:49444005-49444476 | Common:1; Rare:152 | ||||
chr13:49495907-49496041 | Rare:28 | ||||
chr13:49585491-49585633 | Common:1; Rare:48 | ||||
chr13:49936222-49936543 | Common:1; Rare:101 | ||||
chr13:49996715-49997053 | Common:1; Rare:67 | ||||
chr13:50081980-50082262 | Common:1; Rare:78 | ||||
chr13:51453019-51453388 | Rare:143 | ||||
chr13:51804102-51804187 | Common:2; Rare:30 | ||||
chr13:52012062-52012428 | Common:2; Rare:120; Clinvar:1 | ||||
chr13:52406132-52406414 | Common:2; Rare:80 | ||||
chr13:52455344-52455523 | Common:3; Rare:63 |