Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:96053336-96053594 | Common:2; Rare:111 | ||||
chr13:97222154-97222402 | Rare:43 | ||||
chr13:98977981-98978174 | Common:2; Rare:38 | ||||
chr13:98978336-98978605 | Common:3; Rare:39 | ||||
chr13:99200652-99200924 | Common:7; Rare:126 | ||||
chr13:100088901-100089117 | Rare:77; Clinvar:1; Clinvar (benign):2 | ||||
chr13:100674754-100675055 | Common:3; Rare:121 | ||||
chr13:102596785-102597059 | Common:1; Rare:127; Clinvar (benign):1 | ||||
chr13:102773716-102773842 | Rare:59 | ||||
chr13:102798922-102799202 | Common:1; Rare:58 | ||||
chr13:102845689-102846129 | Common:9; Rare:120; Clinvar:3; Clinvar (benign):4 | ||||
chr13:106567805-106568267 | Rare:127 | ||||
chr13:108215495-108215580 | Rare:23 | ||||
chr13:108218339-108218532 | Rare:74 | ||||
chr13:110307154-110307397 | Common:4; Rare:82; Clinvar (benign):4 |