Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:48233281-48233473 | Common:2; Rare:65 | ||||
chr13:48303674-48303721 | Rare:19; Clinvar (pathogenic):1 | ||||
chr13:48492747-48492795 | Common:1; Rare:7 | ||||
chr13:48533050-48533288 | Common:1; Rare:69 | ||||
chr13:48975780-48976051 | Common:1; Rare:85 | ||||
chr13:48976313-48976698 | Common:3; Rare:125 | ||||
chr13:49110228-49110396 | Common:2; Rare:47 | ||||
chr13:49247807-49247976 | Rare:48 | ||||
chr13:49443996-49444136 | Common:1; Rare:52 | ||||
chr13:49444143-49444175 | Rare:12 | ||||
chr13:49444215-49444476 | Rare:81 | ||||
chr13:49585527-49585620 | Common:1; Rare:29 | ||||
chr13:49792520-49792804 | Common:5; Rare:111 | ||||
chr13:49936222-49936592 | Common:1; Rare:115 | ||||
chr13:50081980-50082267 | Common:1; Rare:79 |