Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:134312332-134312355 | Rare:5 | ||||
chr3:136987134-136987288 | Common:1; Rare:35 | ||||
chr3:139538892-139539004 | Rare:40 | ||||
chr3:150408849-150409035 | Rare:55 | ||||
chr3:150761883-150761943 | Common:1; Rare:7 | ||||
chr3:153161215-153161472 | Rare:64 | ||||
chr3:156784143-156784395 | Common:1; Rare:47 | ||||
chr3:156816980-156817248 | Rare:85 | ||||
chr3:157174935-157175223 | Common:3; Rare:126 | ||||
chr3:169765033-169765200 | Rare:75; Clinvar:2; Clinvar (pathogenic):2 | ||||
chr3:171797238-171797535 | Common:1; Rare:38 | ||||
chr3:183447501-183447680 | Common:1; Rare:46 | ||||
chr3:185727999-185728211 | Common:1; Rare:43 | ||||
chr3:194583872-194584020 | Common:10; Rare:55 | ||||
chr3:195657970-195658120 | Common:9; Rare:26 |