Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:75549426-75549834 | Common:8; Rare:107 | ||||
chr13:75635747-75635861 | Common:1; Rare:30 | ||||
chr13:75635913-75636397 | Common:2; Rare:126 | ||||
chr13:79405797-79405907 | Rare:36 | ||||
chr13:94601568-94601924 | Common:4; Rare:106 | ||||
chr13:95676937-95677213 | Common:3; Rare:91 | ||||
chr13:96053353-96053602 | Common:2; Rare:101 | ||||
chr13:99200668-99200903 | Common:6; Rare:111 | ||||
chr13:100088921-100089117 | Rare:69; Clinvar:1; Clinvar (benign):2 | ||||
chr13:102596801-102597035 | Common:1; Rare:112 | ||||
chr13:102773726-102773879 | Rare:66 | ||||
chr13:102798939-102799130 | Common:1; Rare:40 | ||||
chr13:106568091-106568267 | Rare:56 | ||||
chr13:108218313-108218520 | Rare:80 | ||||
chr13:110307155-110307442 | Common:5; Rare:92; Clinvar (benign):5 |