Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:45341040-45341508 | Common:4; Rare:224 | ||||
chr13:45418340-45418578 | Rare:71 | ||||
chr13:46052709-46052856 | Common:2; Rare:39 | ||||
chr13:48001265-48001410 | Common:1; Rare:67; Clinvar:3; Clinvar (benign):2 | ||||
chr13:48975811-48975923 | Rare:41 | ||||
chr13:49247823-49247967 | Rare:43 | ||||
chr13:49444002-49444328 | Common:1; Rare:108 | ||||
chr13:49495942-49496041 | Rare:27 | ||||
chr13:49585567-49585612 | Rare:10 | ||||
chr13:49792523-49792712 | Common:4; Rare:75 | ||||
chr13:49936240-49936586 | Common:1; Rare:104 | ||||
chr13:50081992-50082275 | Common:1; Rare:80 | ||||
chr13:51453013-51453377 | Rare:138 | ||||
chr13:51804149-51804244 | Rare:26 | ||||
chr13:52011946-52012428 | Common:2; Rare:154; Clinvar:1; Clinvar (pathogenic):1 |