Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:40548970-40549184 | Rare:61 | ||||
chr17:40549187-40549443 | Common:2; Rare:44 | ||||
chr17:41938754-41938919 | Rare:39 | ||||
chr17:42122587-42122726 | Rare:23 | ||||
chr17:42320063-42320216 | Rare:24 | ||||
chr17:42865718-42865944 | Common:1; Rare:43 | ||||
chr17:43315634-43315920 | Common:7; Rare:121 | ||||
chr17:43388310-43388443 | Rare:29 | ||||
chr17:44005391-44005523 | Rare:21 | ||||
chr17:44250494-44250730 | Common:1; Rare:54; Clinvar:1; Clinvar (benign):1 | ||||
chr17:44251142-44251556 | Common:2; Rare:113; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):5 | ||||
chr17:44257705-44258172 | Common:3; Rare:136; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr17:44259321-44259579 | Common:1; Rare:67; Clinvar:2; Clinvar (pathogenic):1 | ||||
chr17:44260386-44260694 | Common:1; Rare:87; Clinvar:1; Clinvar (pathogenic):2 | ||||
chr17:44268840-44268968 | Rare:25 |