Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79585 |
| ensemblid | ENSG00000262246.6 |
| hgncid | 26161 |
| symbol | CORO7 |
| name | coronin 7 |
| refseq_nuc | NM_024535.5 |
| refseq_prot | NP_078811.3 |
| ensembl_nuc | ENST00000251166.9 |
| ensembl_prot | ENSP00000251166.4 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 4354542 |
| end | 4416596 |
| strand | - |
| ver | v1.2 |
| region | chr16:4354542-4416596 |
| region5000 | chr16:4349542-4421596 |
| regionname0 | CORO7_chr16_4354542_4416596 |
| regionname5000 | CORO7_chr16_4349542_4421596 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 925 | 133 | 53 | 26 | 34 | 5 | 14 | 23 | CORO7_chr16_4349542_4421596 | CORO7 | MNRFR others(920): Show |
chr16 | 4349542 | 4421596 |
| a0002 | 0/0 | 925 | 127 | 14 | 32 | 54 | 7 | 20 | 37 | CORO7_chr16_4349542_4421596 | CORO7 | MNRFR others(920): Show |
chr16 | 4349542 | 4421596 |
| a0003 | 0/0 | 925 | 17 | 17 | 0 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | MNRFR others(920): Show |
chr16 | 4349542 | 4421596 |
| a0004 | 0/0 | 925 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | MNRFR others(920): Show |
chr16 | 4349542 | 4421596 |
| a0005 | 0/0 | 925 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | MNRFR others(920): Show |
chr16 | 4349542 | 4421596 |
| a0006 | 0/0 | 925 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | MNRFR others(920): Show |
chr16 | 4349542 | 4421596 |
| a0007 | 0/0 | 925 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | MNRFR others(920): Show |
chr16 | 4349542 | 4421596 |
| a0008 | 0/0 | 925 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | MNRFR others(920): Show |
chr16 | 4349542 | 4421596 |
| a0009 | 0/0 | 925 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | MNRFR others(920): Show |
chr16 | 4349542 | 4421596 |
| a0010 | 0/0 | 925 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | MNRFR others(920): Show |
chr16 | 4349542 | 4421596 |
| a0011 | 0/0 | 925 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | MNRFR others(920): Show |
chr16 | 4349542 | 4421596 |
| a0012 | 0/0 | 925 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | MNRFR others(920): Show |
chr16 | 4349542 | 4421596 |
| a0013 | 0/0 | 925 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | MNRFR others(920): Show |
chr16 | 4349542 | 4421596 |
| a0014 | 0/0 | 925 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | MNRFR others(920): Show |
chr16 | 4349542 | 4421596 |
| a0015 | 0/0 | 925 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | MNRFR others(920): Show |
chr16 | 4349542 | 4421596 |
| a0016 | 0/0 | 925 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | MNRFR others(920): Show |
chr16 | 4349542 | 4421596 |
| a0017 | 0/0 | 925 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | MNRFR others(920): Show |
chr16 | 4349542 | 4421596 |
| a0018 | 0/0 | 925 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | MNRFR others(920): Show |
chr16 | 4349542 | 4421596 |
| a0019 | 0/0 | 925 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | MNRFR others(920): Show |
chr16 | 4349542 | 4421596 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 0/1 | 2775 | 118 | 38 | 26 | 34 | 5 | 14 | CORO7_chr16_4349542_4421596 | CORO7 | ATGAA others(2770): Show |
chr16 | 4349542 | 4421596 | ||
| a0001c0004 | 0/0 | 2775 | 13 | 13 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | ATGAA others(2770): Show |
chr16 | 4349542 | 4421596 | ||
| a0001c0014 | 0/0 | 2775 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | ATGAA others(2770): Show |
chr16 | 4349542 | 4421596 | ||
| a0001c0023 | 0/0 | 2775 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | ATGAA others(2770): Show |
chr16 | 4349542 | 4421596 | ||
| a0002c0001 | 0/0 | 2775 | 123 | 14 | 29 | 53 | 7 | 20 | CORO7_chr16_4349542_4421596 | CORO7 | ATGAA others(2770): Show |
chr16 | 4349542 | 4421596 | ||
| a0002c0006 | 0/0 | 2775 | 3 | 0 | 3 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | ATGAA others(2770): Show |
chr16 | 4349542 | 4421596 | ||
| a0002c0013 | 0/0 | 2775 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | ATGAA others(2770): Show |
chr16 | 4349542 | 4421596 | ||
| a0003c0003 | 0/0 | 2775 | 15 | 15 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | ATGAA others(2770): Show |
chr16 | 4349542 | 4421596 | ||
| a0003c0018 | 0/0 | 2775 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | ATGAA others(2770): Show |
chr16 | 4349542 | 4421596 | ||
| a0003c0019 | 0/0 | 2775 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | ATGAA others(2770): Show |
chr16 | 4349542 | 4421596 | ||
| a0004c0005 | 0/0 | 2775 | 4 | 4 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | ATGAA others(2770): Show |
chr16 | 4349542 | 4421596 | ||
| a0005c0007 | 0/0 | 2775 | 2 | 2 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | ATGAA others(2770): Show |
chr16 | 4349542 | 4421596 | ||
| a0006c0009 | 0/0 | 2775 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | ATGAA others(2770): Show |
chr16 | 4349542 | 4421596 | ||
| a0007c0021 | 0/0 | 2775 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | ATGAA others(2770): Show |
chr16 | 4349542 | 4421596 | ||
| a0008c0022 | 0/0 | 2775 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | ATGAA others(2770): Show |
chr16 | 4349542 | 4421596 | ||
| a0009c0017 | 0/0 | 2775 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | ATGAA others(2770): Show |
chr16 | 4349542 | 4421596 | ||
| a0010c0012 | 0/0 | 2775 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | ATGAA others(2770): Show |
chr16 | 4349542 | 4421596 | ||
| a0011c0011 | 0/0 | 2775 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | ATGAA others(2770): Show |
chr16 | 4349542 | 4421596 | ||
| a0012c0024 | 0/0 | 2775 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | ATGAA others(2770): Show |
chr16 | 4349542 | 4421596 | ||
| a0013c0015 | 0/0 | 2775 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | ATGAA others(2770): Show |
chr16 | 4349542 | 4421596 | ||
| a0014c0025 | 0/0 | 2775 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | ATGAA others(2770): Show |
chr16 | 4349542 | 4421596 | ||
| a0015c0010 | 0/0 | 2775 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | ATGAA others(2770): Show |
chr16 | 4349542 | 4421596 | ||
| a0016c0026 | 0/0 | 2775 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | ATGAA others(2770): Show |
chr16 | 4349542 | 4421596 | ||
| a0017c0008 | 0/0 | 2775 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | ATGAA others(2770): Show |
chr16 | 4349542 | 4421596 | ||
| a0018c0016 | 0/0 | 2775 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | ATGAA others(2770): Show |
chr16 | 4349542 | 4421596 | ||
| a0019c0020 | 0/0 | 2775 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | ATGAA others(2770): Show |
chr16 | 4349542 | 4421596 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001 | 0/1 | 3472 | 72 | 19 | 20 | 19 | 3 | 10 | CORO7_chr16_4349542_4421596 | CORO7 | AGTCG others(3467): Show |
chr16 | 4349542 | 4421596 |
| a0001c0002t0002 | 0/0 | 3472 | 46 | 19 | 6 | 15 | 2 | 4 | CORO7_chr16_4349542_4421596 | CORO7 | AGTCG others(3467): Show |
chr16 | 4349542 | 4421596 |
| a0001c0004t0001 | 0/0 | 3472 | 13 | 13 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | AGTCG others(3467): Show |
chr16 | 4349542 | 4421596 |
| a0001c0014t0001 | 0/0 | 3472 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | AGTCG others(3467): Show |
chr16 | 4349542 | 4421596 |
| a0001c0023t0001 | 0/0 | 3472 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | AGTCG others(3467): Show |
chr16 | 4349542 | 4421596 |
| a0002c0001t0001 | 0/0 | 3472 | 121 | 14 | 28 | 52 | 7 | 20 | CORO7_chr16_4349542_4421596 | CORO7 | AGTCG others(3467): Show |
chr16 | 4349542 | 4421596 |
| a0002c0001t0002 | 0/0 | 3472 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | AGTCG others(3467): Show |
chr16 | 4349542 | 4421596 |
| a0002c0001t0004 | 0/0 | 3472 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | AGTCG others(3467): Show |
chr16 | 4349542 | 4421596 |
| a0002c0006t0001 | 0/0 | 3472 | 3 | 0 | 3 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | AGTCG others(3467): Show |
chr16 | 4349542 | 4421596 |
| a0002c0013t0001 | 0/0 | 3472 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | AGTCG others(3467): Show |
chr16 | 4349542 | 4421596 |
| a0003c0003t0001 | 0/0 | 3472 | 15 | 15 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | AGTCG others(3467): Show |
chr16 | 4349542 | 4421596 |
| a0003c0018t0001 | 0/0 | 3472 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | AGTCG others(3467): Show |
chr16 | 4349542 | 4421596 |
| a0003c0019t0001 | 0/0 | 3472 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | AGTCG others(3467): Show |
chr16 | 4349542 | 4421596 |
| a0004c0005t0001 | 0/0 | 3472 | 3 | 3 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | AGTCG others(3467): Show |
chr16 | 4349542 | 4421596 |
| a0004c0005t0002 | 0/0 | 3472 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | AGTCG others(3467): Show |
chr16 | 4349542 | 4421596 |
| a0005c0007t0001 | 0/0 | 3472 | 2 | 2 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | AGTCG others(3467): Show |
chr16 | 4349542 | 4421596 |
| a0006c0009t0001 | 0/0 | 3472 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | AGTCG others(3467): Show |
chr16 | 4349542 | 4421596 |
| a0007c0021t0001 | 0/0 | 3472 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | AGTCG others(3467): Show |
chr16 | 4349542 | 4421596 |
| a0008c0022t0001 | 0/0 | 3472 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | AGTCG others(3467): Show |
chr16 | 4349542 | 4421596 |
| a0009c0017t0001 | 0/0 | 3472 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | AGTCG others(3467): Show |
chr16 | 4349542 | 4421596 |
| a0010c0012t0001 | 0/0 | 3472 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | AGTCG others(3467): Show |
chr16 | 4349542 | 4421596 |
| a0011c0011t0001 | 0/0 | 3472 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | AGTCG others(3467): Show |
chr16 | 4349542 | 4421596 |
| a0012c0024t0005 | 0/0 | 3472 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | AGTCG others(3467): Show |
chr16 | 4349542 | 4421596 |
| a0013c0015t0001 | 0/0 | 3472 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | AGTCG others(3467): Show |
chr16 | 4349542 | 4421596 |
| a0014c0025t0001 | 0/0 | 3472 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | AGTCG others(3467): Show |
chr16 | 4349542 | 4421596 |
| a0015c0010t0001 | 0/0 | 3472 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | AGTCG others(3467): Show |
chr16 | 4349542 | 4421596 |
| a0016c0026t0001 | 0/0 | 3472 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | AGTCG others(3467): Show |
chr16 | 4349542 | 4421596 |
| a0017c0008t0002 | 0/0 | 3472 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | AGTCG others(3467): Show |
chr16 | 4349542 | 4421596 |
| a0018c0016t0003 | 0/0 | 3472 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | AGTCG others(3467): Show |
chr16 | 4349542 | 4421596 |
| a0019c0020t0002 | 0/0 | 3472 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | AGTCG others(3467): Show |
chr16 | 4349542 | 4421596 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0027 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0002g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0002g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0002g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0002g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0002t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0004t0001g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0004t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0004t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0004t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0004t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0004t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0004t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0004t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0004t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0004t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0014t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0001c0023t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0012 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0001t0004g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0006t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0006t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0002c0013t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0003c0003t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0003c0003t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0003c0003t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0003c0003t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0003c0003t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0003c0003t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0003c0003t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0003c0003t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0003c0003t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0003c0003t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0003c0003t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0003c0003t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0003c0003t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0003c0003t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0003c0018t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0003c0019t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0004c0005t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0004c0005t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0004c0005t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0004c0005t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0005c0007t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0005c0007t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0006c0009t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0007c0021t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0008c0022t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0009c0017t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0010c0012t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0011c0011t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0012c0024t0005g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0013c0015t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0014c0025t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0015c0010t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0016c0026t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0017c0008t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0018c0016t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| a0019c0020t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0001 | t0001 | g0089 | EUR | GBR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG00099 | hp2 | a0002 | c0001 | t0001 | g0012 | EUR | GBR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG00140 | hp1 | a0002 | c0001 | t0001 | g0047 | EUR | GBR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0106 | EUR | GBR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG00280 | hp1 | a0002 | c0001 | t0001 | g0011 | EUR | FIN | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG00280 | hp2 | a0002 | c0001 | t0001 | g0224 | EUR | FIN | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0102 | EAS | CHS | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG00423 | hp2 | a0002 | c0001 | t0001 | g0212 | EAS | CHS | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG00544 | hp1 | a0001 | c0002 | t0002 | g0067 | EAS | CHS | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG00544 | hp2 | a0002 | c0001 | t0001 | g0247 | EAS | CHS | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG00597 | hp1 | a0002 | c0001 | t0001 | g0192 | EAS | CHS | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG00597 | hp2 | a0001 | c0002 | t0002 | g0070 | EAS | CHS | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG00639 | hp1 | a0002 | c0001 | t0001 | g0012 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG00639 | hp2 | a0002 | c0001 | t0001 | g0191 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0030 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG00642 | hp2 | a0002 | c0001 | t0001 | g0199 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0101 | EAS | CHS | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG00673 | hp2 | a0002 | c0001 | t0001 | g0178 | EAS | CHS | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG00733 | hp1 | a0006 | c0009 | t0001 | g0246 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0198 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0201 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0153 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG00738 | hp2 | a0002 | c0001 | t0001 | g0004 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG00741 | hp1 | a0002 | c0001 | t0001 | g0184 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0059 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0010 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG01069 | hp2 | a0002 | c0001 | t0001 | g0200 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0025 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG01070 | hp2 | a0002 | c0001 | t0001 | g0211 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0024 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0010 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG01074 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0147 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG01081 | hp1 | a0002 | c0001 | t0001 | g0209 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG01099 | hp1 | a0007 | c0021 | t0001 | g0034 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG01099 | hp2 | a0008 | c0022 | t0001 | g0125 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG01106 | hp1 | a0002 | c0006 | t0001 | g0245 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG01106 | hp2 | a0002 | c0001 | t0001 | g0165 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG01109 | hp1 | a0002 | c0001 | t0001 | g0203 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG01109 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG01168 | hp1 | a0002 | c0001 | t0001 | g0013 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG01168 | hp2 | a0002 | c0001 | t0001 | g0164 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG01243 | hp1 | a0002 | c0001 | t0001 | g0168 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0140 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG01255 | hp1 | a0002 | c0001 | t0001 | g0035 | AMR | CLM | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0095 | AMR | CLM | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG01257 | hp1 | a0002 | c0001 | t0001 | g0166 | AMR | CLM | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG01257 | hp2 | a0002 | c0006 | t0001 | g0015 | AMR | CLM | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG01258 | hp1 | a0002 | c0006 | t0001 | g0015 | AMR | CLM | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG01258 | hp2 | a0002 | c0001 | t0001 | g0202 | AMR | CLM | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG01261 | hp1 | a0002 | c0001 | t0004 | g0189 | AMR | CLM | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0084 | AMR | CLM | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG01346 | hp1 | a0002 | c0001 | t0001 | g0156 | AMR | CLM | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG01346 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | CLM | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG01361 | hp1 | a0002 | c0001 | t0001 | g0155 | AMR | CLM | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0023 | AMR | CLM | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG01496 | hp1 | a0009 | c0017 | t0001 | g0079 | AMR | CLM | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG01496 | hp2 | a0002 | c0001 | t0001 | g0177 | AMR | CLM | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0078 | EUR | IBS | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG01515 | hp2 | a0001 | c0002 | t0002 | g0094 | EUR | IBS | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG01516 | hp1 | a0002 | c0001 | t0001 | g0167 | EUR | IBS | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG01516 | hp2 | a0001 | c0002 | t0002 | g0072 | EUR | IBS | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG01884 | hp1 | a0002 | c0001 | t0001 | g0250 | AFR | ACB | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG01884 | hp2 | a0001 | c0002 | t0002 | g0039 | AFR | ACB | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0029 | AFR | ACB | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG01891 | hp2 | a0001 | c0004 | t0001 | g0139 | AFR | ACB | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG01928 | hp1 | a0002 | c0001 | t0001 | g0207 | AMR | PEL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0120 | AMR | PEL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG01934 | hp1 | a0002 | c0001 | t0001 | g0160 | AMR | PEL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG01934 | hp2 | a0001 | c0002 | t0002 | g0057 | AMR | PEL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG01943 | hp1 | a0002 | c0001 | t0001 | g0206 | AMR | PEL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG01943 | hp2 | a0001 | c0002 | t0002 | g0077 | AMR | PEL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG01952 | hp1 | a0001 | c0002 | t0002 | g0056 | AMR | PEL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG01952 | hp2 | a0002 | c0001 | t0001 | g0004 | AMR | PEL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0119 | AMR | PEL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG01975 | hp2 | a0002 | c0001 | t0001 | g0004 | AMR | PEL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02015 | hp1 | a0002 | c0001 | t0001 | g0233 | EAS | KHV | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02015 | hp2 | a0002 | c0001 | t0001 | g0197 | EAS | KHV | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02027 | hp1 | a0001 | c0002 | t0002 | g0083 | EAS | KHV | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02027 | hp2 | a0002 | c0001 | t0001 | g0018 | EAS | KHV | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02040 | hp1 | a0002 | c0001 | t0001 | g0219 | EAS | KHV | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02040 | hp2 | a0002 | c0001 | t0001 | g0063 | EAS | KHV | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02055 | hp1 | a0001 | c0002 | t0002 | g0091 | AFR | ACB | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02055 | hp2 | a0002 | c0001 | t0001 | g0121 | AFR | ACB | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02056 | hp1 | a0002 | c0001 | t0001 | g0225 | EAS | KHV | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02056 | hp2 | a0002 | c0001 | t0001 | g0232 | EAS | KHV | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02071 | hp1 | a0002 | c0001 | t0001 | g0220 | EAS | KHV | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0054 | EAS | KHV | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02080 | hp1 | a0002 | c0001 | t0001 | g0234 | EAS | KHV | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02080 | hp2 | a0002 | c0001 | t0001 | g0154 | EAS | KHV | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0115 | EAS | KHV | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02083 | hp2 | a0002 | c0001 | t0001 | g0196 | EAS | KHV | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02145 | hp1 | a0002 | c0001 | t0001 | g0208 | AFR | ACB | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02145 | hp2 | a0001 | c0002 | t0002 | g0002 | AFR | ACB | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02148 | hp1 | a0002 | c0001 | t0001 | g0097 | AMR | PEL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02148 | hp2 | a0002 | c0001 | t0001 | g0185 | AMR | PEL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0104 | EAS | CDX | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02155 | hp2 | a0002 | c0001 | t0001 | g0221 | EAS | CDX | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02258 | hp1 | a0002 | c0001 | t0001 | g0122 | AFR | ACB | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0092 | AFR | ACB | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0103 | AMR | PEL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02273 | hp2 | a0002 | c0001 | t0001 | g0187 | AMR | PEL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02280 | hp1 | a0003 | c0003 | t0001 | g0260 | AFR | ACB | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02280 | hp2 | a0001 | c0004 | t0001 | g0138 | AFR | ACB | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02451 | hp1 | a0003 | c0003 | t0001 | g0016 | AFR | ACB | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02451 | hp2 | a0001 | c0002 | t0002 | g0265 | AFR | ACB | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0055 | EAS | KHV | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0129 | EAS | KHV | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02572 | hp1 | a0001 | c0002 | t0002 | g0243 | AFR | GWD | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02572 | hp2 | a0001 | c0002 | t0001 | g0133 | AFR | GWD | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02602 | hp1 | a0002 | c0001 | t0001 | g0171 | SAS | PJL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02602 | hp2 | a0010 | c0012 | t0001 | g0194 | SAS | PJL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02615 | hp1 | a0003 | c0003 | t0001 | g0263 | AFR | GWD | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02615 | hp2 | a0001 | c0002 | t0002 | g0002 | AFR | GWD | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02622 | hp1 | a0002 | c0001 | t0001 | g0134 | AFR | GWD | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02622 | hp2 | a0001 | c0004 | t0001 | g0242 | AFR | GWD | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0088 | AFR | GWD | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02630 | hp2 | a0001 | c0002 | t0002 | g0124 | AFR | GWD | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02698 | hp1 | a0002 | c0001 | t0001 | g0163 | SAS | PJL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02698 | hp2 | a0002 | c0001 | t0001 | g0183 | SAS | PJL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02717 | hp1 | a0001 | c0002 | t0002 | g0050 | AFR | GWD | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0090 | AFR | GWD | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02723 | hp1 | a0002 | c0001 | t0001 | g0204 | AFR | GWD | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02723 | hp2 | a0001 | c0014 | t0001 | g0028 | AFR | GWD | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02735 | hp1 | a0002 | c0001 | t0001 | g0190 | SAS | PJL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0098 | SAS | PJL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02738 | hp1 | a0002 | c0001 | t0001 | g0170 | SAS | PJL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02738 | hp2 | a0011 | c0011 | t0001 | g0223 | SAS | PJL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02809 | hp1 | a0003 | c0003 | t0001 | g0272 | AFR | GWD | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02809 | hp2 | a0002 | c0001 | t0001 | g0038 | AFR | GWD | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02818 | hp1 | a0001 | c0002 | t0002 | g0244 | AFR | GWD | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02818 | hp2 | a0002 | c0001 | t0001 | g0146 | AFR | GWD | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02886 | hp1 | a0001 | c0004 | t0001 | g0008 | AFR | GWD | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02886 | hp2 | a0003 | c0003 | t0001 | g0016 | AFR | GWD | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02895 | hp1 | a0002 | c0001 | t0001 | g0143 | AFR | GWD | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02895 | hp2 | a0004 | c0005 | t0001 | g0256 | AFR | GWD | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02896 | hp1 | a0002 | c0001 | t0001 | g0149 | AFR | GWD | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02896 | hp2 | a0003 | c0003 | t0001 | g0274 | AFR | GWD | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02897 | hp1 | a0004 | c0005 | t0001 | g0254 | AFR | GWD | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02897 | hp2 | a0003 | c0018 | t0001 | g0275 | AFR | GWD | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02922 | hp1 | a0012 | c0024 | t0005 | g0277 | AFR | ESN | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02922 | hp2 | a0001 | c0023 | t0001 | g0042 | AFR | ESN | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0150 | AFR | ESN | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02965 | hp2 | a0001 | c0004 | t0001 | g0043 | AFR | ESN | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02970 | hp1 | a0003 | c0003 | t0001 | g0262 | AFR | ESN | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02970 | hp2 | a0002 | c0001 | t0001 | g0210 | AFR | ESN | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02976 | hp1 | a0001 | c0002 | t0002 | g0161 | AFR | ESN | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02976 | hp2 | a0003 | c0003 | t0001 | g0271 | AFR | ESN | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0099 | SAS | PJL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG03017 | hp2 | a0002 | c0001 | t0001 | g0230 | SAS | PJL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG03041 | hp1 | a0005 | c0007 | t0001 | g0044 | AFR | GWD | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG03041 | hp2 | a0003 | c0003 | t0001 | g0264 | AFR | GWD | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG03098 | hp1 | a0003 | c0003 | t0001 | g0261 | AFR | MSL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0053 | AFR | MSL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0151 | AFR | ESN | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG03130 | hp2 | a0004 | c0005 | t0002 | g0258 | AFR | ESN | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0132 | AFR | ESN | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG03139 | hp2 | a0004 | c0005 | t0001 | g0255 | AFR | ESN | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0021 | AFR | ESN | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG03195 | hp2 | a0001 | c0004 | t0001 | g0058 | AFR | ESN | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG03209 | hp1 | a0003 | c0003 | t0001 | g0266 | AFR | MSL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG03209 | hp2 | a0001 | c0002 | t0002 | g0006 | AFR | MSL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG03239 | hp1 | a0001 | c0002 | t0002 | g0096 | SAS | PJL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG03239 | hp2 | a0002 | c0001 | t0001 | g0162 | SAS | PJL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG03453 | hp1 | a0001 | c0004 | t0001 | g0008 | AFR | MSL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG03453 | hp2 | a0001 | c0002 | t0002 | g0006 | AFR | MSL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG03486 | hp1 | a0005 | c0007 | t0001 | g0045 | AFR | MSL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG03486 | hp2 | a0001 | c0002 | t0002 | g0123 | AFR | MSL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG03490 | hp1 | a0002 | c0001 | t0001 | g0144 | SAS | PJL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0108 | SAS | PJL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0109 | SAS | PJL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG03491 | hp2 | a0002 | c0001 | t0001 | g0186 | SAS | PJL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0040 | AFR | ESN | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG03516 | hp2 | a0003 | c0019 | t0001 | g0270 | AFR | ESN | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG03540 | hp1 | a0003 | c0003 | t0001 | g0268 | AFR | GWD | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0087 | AFR | GWD | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0032 | AFR | MSL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0152 | AFR | MSL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0127 | SAS | PJL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG03654 | hp2 | a0002 | c0001 | t0001 | g0112 | SAS | PJL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG03688 | hp1 | a0002 | c0001 | t0001 | g0014 | SAS | STU | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0128 | SAS | STU | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG03704 | hp1 | a0002 | c0001 | t0001 | g0014 | SAS | PJL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG03704 | hp2 | a0002 | c0001 | t0001 | g0251 | SAS | PJL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG03710 | hp1 | a0002 | c0001 | t0001 | g0158 | SAS | PJL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG03710 | hp2 | a0001 | c0002 | t0002 | g0086 | SAS | PJL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG03834 | hp1 | a0013 | c0015 | t0001 | g0126 | SAS | BEB | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG03834 | hp2 | a0002 | c0001 | t0001 | g0228 | SAS | BEB | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG03927 | hp1 | a0002 | c0001 | t0001 | g0159 | SAS | BEB | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0060 | SAS | BEB | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG03942 | hp1 | a0002 | c0001 | t0001 | g0231 | SAS | BEB | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0248 | SAS | BEB | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG04184 | hp1 | a0002 | c0001 | t0001 | g0172 | SAS | BEB | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG04184 | hp2 | a0014 | c0025 | t0001 | g0241 | SAS | BEB | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG04199 | hp1 | a0001 | c0002 | t0002 | g0031 | SAS | STU | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG04199 | hp2 | a0002 | c0001 | t0001 | g0174 | SAS | STU | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG04228 | hp1 | a0001 | c0002 | t0002 | g0085 | SAS | STU | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0169 | SAS | STU | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA18522 | hp1 | a0002 | c0001 | t0001 | g0180 | AFR | YRI | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA18522 | hp2 | a0003 | c0003 | t0001 | g0267 | AFR | YRI | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA18612 | hp1 | a0002 | c0001 | t0001 | g0188 | EAS | CHB | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA18612 | hp2 | a0001 | c0002 | t0002 | g0229 | EAS | CHB | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA18906 | hp1 | a0001 | c0004 | t0001 | g0135 | AFR | YRI | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA18906 | hp2 | a0001 | c0002 | t0002 | g0118 | AFR | YRI | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA18939 | hp1 | a0015 | c0010 | t0001 | g0179 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA18939 | hp2 | a0002 | c0001 | t0001 | g0217 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA18942 | hp2 | a0002 | c0001 | t0001 | g0237 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA18943 | hp1 | a0016 | c0026 | t0001 | g0131 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA18943 | hp2 | a0002 | c0001 | t0002 | g0276 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA18944 | hp1 | a0002 | c0001 | t0001 | g0222 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA18944 | hp2 | a0001 | c0002 | t0002 | g0074 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA18946 | hp1 | a0001 | c0002 | t0002 | g0069 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA18946 | hp2 | a0002 | c0001 | t0001 | g0065 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0113 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA18948 | hp2 | a0002 | c0001 | t0001 | g0175 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA18960 | hp1 | a0002 | c0001 | t0001 | g0240 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA18960 | hp2 | a0002 | c0001 | t0001 | g0145 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA18962 | hp2 | a0002 | c0013 | t0001 | g0205 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA18966 | hp1 | a0002 | c0001 | t0001 | g0216 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA18966 | hp2 | a0002 | c0001 | t0001 | g0066 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA18969 | hp1 | a0002 | c0001 | t0001 | g0020 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA18969 | hp2 | a0002 | c0001 | t0001 | g0181 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA18977 | hp1 | a0001 | c0002 | t0002 | g0049 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA18977 | hp2 | a0002 | c0001 | t0001 | g0182 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA18978 | hp1 | a0002 | c0001 | t0001 | g0227 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA18978 | hp2 | a0001 | c0002 | t0002 | g0064 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA18979 | hp1 | a0002 | c0001 | t0001 | g0215 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA18980 | hp1 | a0001 | c0002 | t0002 | g0249 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA18980 | hp2 | a0002 | c0001 | t0001 | g0238 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA18981 | hp1 | a0002 | c0001 | t0001 | g0193 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA18981 | hp2 | a0001 | c0002 | t0002 | g0037 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA18982 | hp1 | a0002 | c0001 | t0001 | g0253 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0107 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA18997 | hp1 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA18997 | hp2 | a0002 | c0001 | t0001 | g0173 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA18998 | hp2 | a0002 | c0001 | t0001 | g0142 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA19000 | hp1 | a0002 | c0001 | t0001 | g0235 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA19000 | hp2 | a0002 | c0001 | t0001 | g0009 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA19007 | hp1 | a0002 | c0001 | t0001 | g0213 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA19007 | hp2 | a0002 | c0001 | t0001 | g0226 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA19010 | hp1 | a0001 | c0002 | t0002 | g0117 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA19010 | hp2 | a0002 | c0001 | t0001 | g0019 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA19030 | hp1 | a0017 | c0008 | t0002 | g0061 | AFR | LWK | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0116 | AFR | LWK | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA19043 | hp1 | a0001 | c0004 | t0001 | g0001 | AFR | LWK | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA19043 | hp2 | a0003 | c0003 | t0001 | g0259 | AFR | LWK | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA19054 | hp1 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA19054 | hp2 | a0002 | c0001 | t0001 | g0239 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA19055 | hp1 | a0002 | c0001 | t0001 | g0176 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA19055 | hp2 | a0001 | c0002 | t0001 | g0105 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA19066 | hp1 | a0001 | c0002 | t0002 | g0052 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA19066 | hp2 | a0002 | c0001 | t0001 | g0236 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA19068 | hp1 | a0002 | c0001 | t0001 | g0071 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA19068 | hp2 | a0002 | c0001 | t0001 | g0252 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA19079 | hp1 | a0002 | c0001 | t0001 | g0009 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA19079 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA19080 | hp1 | a0001 | c0002 | t0002 | g0082 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA19080 | hp2 | a0002 | c0001 | t0001 | g0157 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA19084 | hp2 | a0002 | c0001 | t0001 | g0130 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA19087 | hp1 | a0002 | c0001 | t0001 | g0214 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA19087 | hp2 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA19088 | hp1 | a0002 | c0001 | t0001 | g0017 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA19088 | hp2 | a0001 | c0002 | t0002 | g0080 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA19089 | hp1 | a0002 | c0001 | t0001 | g0218 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA19089 | hp2 | a0001 | c0002 | t0002 | g0081 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0033 | AFR | YRI | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0041 | AFR | YRI | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0036 | AFR | ASW | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA20129 | hp2 | a0018 | c0016 | t0003 | g0257 | AFR | ASW | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0022 | EUR | TSI | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA20805 | hp2 | a0002 | c0001 | t0001 | g0073 | EUR | TSI | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA20905 | hp1 | a0002 | c0001 | t0001 | g0011 | SAS | GIH | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0062 | SAS | GIH | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0046 | AMR | CLM | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG01123 | hp2 | a0002 | c0001 | t0001 | g0195 | AMR | CLM | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02109 | hp1 | a0001 | c0002 | t0002 | g0002 | AFR | ACB | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0148 | AFR | ACB | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02486 | hp1 | a0001 | c0004 | t0001 | g0001 | AFR | ACB | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02486 | hp2 | a0001 | c0004 | t0001 | g0136 | AFR | ACB | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02559 | hp1 | a0001 | c0002 | t0002 | g0076 | AFR | ACB | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG02559 | hp2 | a0003 | c0003 | t0001 | g0269 | AFR | ACB | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0273 | AFR | MSL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG03471 | hp2 | a0001 | c0004 | t0001 | g0001 | AFR | MSL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG06807 | hp1 | a0001 | c0004 | t0001 | g0137 | AFR | USA | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| HG06807 | hp2 | a0002 | c0001 | t0001 | g0141 | AFR | USA | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA20300 | hp1 | a0001 | c0002 | t0002 | g0114 | AFR | USA | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA20300 | hp2 | a0002 | c0001 | t0001 | g0013 | AFR | USA | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA21309 | hp1 | a0019 | c0020 | t0002 | g0048 | AFR | LWK | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| NA21309 | hp2 | a0001 | c0002 | t0002 | g0093 | AFR | LWK | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0027 | REF | REF | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:4355303 | C | G | 1 | a0011 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.2755G>C | p.Val919Leu | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 27/28 | 2833/3472 | 2755/2778 | 919/925 | chr16 | 4355303 | |||
| chr16:4355347 | A | G | 1 | a0015 | 1 | NA18939.hp1 | missense_variant | MODERATE | c.2711T>C | p.Leu904Pro | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 27/28 | 2789/3472 | 2711/2778 | 904/925 | chr16 | 4355347 | |||
| chr16:4357176 | T | C | 1 | a0010 | 1 | HG02602.hp2 | missense_variant | MODERATE | c.2677A>G | p.Lys893Glu | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 26/28 | 2755/3472 | 2677/2778 | 893/925 | chr16 | 4357176 | |||
| chr16:4358001 | G | A | 1 | a0007 | 1 | HG01099.hp1 | missense_variant | MODERATE | c.2560C>T | p.Leu854Phe | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 25/28 | 2638/3472 | 2560/2778 | 854/925 | chr16 | 4358001 | |||
| chr16:4359512 | G | A | 1 | a0018 | 1 | NA20129.hp2 | missense_variant | MODERATE | c.2218C>T | p.Pro740Ser | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 22/28 | 2296/3472 | 2218/2778 | 740/925 | chr16 | 4359512 | |||
| chr16:4360314 | C | T | 1 | a0008 | 1 | HG01099.hp2 | missense_variant | MODERATE | c.2072G>A | p.Cys691Tyr | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 21/28 | 2150/3472 | 2072/2778 | 691/925 | chr16 | 4360314 | |||
| chr16:4360356 | G | C | 1 | a0005 | 2 | HG03041.hp1 HG03486.hp1 |
missense_variant | MODERATE | c.2030C>G | p.Pro677Arg | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 21/28 | 2108/3472 | 2030/2778 | 677/925 | chr16 | 4360356 | |||
| chr16:4360975 | C | G | 1 | a0006 | 1 | HG00733.hp1 | missense_variant | MODERATE | c.1885G>C | p.Asp629His | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 19/28 | 1963/3472 | 1885/2778 | 629/925 | chr16 | 4360975 | |||
| chr16:4361382 | C | T | 1 | a0019 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.1666G>A | p.Asp556Asn | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 17/28 | 1744/3472 | 1666/2778 | 556/925 | chr16 | 4361382 | |||
| chr16:4364344 | C | T | 2 | a0003 a0018 |
18 | HG02280.hp1 HG02451.hp1 HG02559.hp2 others(15): Show |
missense_variant | MODERATE | c.1207G>A | p.Ala403Thr | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 14/28 | 1285/3472 | 1207/2778 | 403/925 | chr16 | 4364344 | |||
| chr16:4364887 | C | T | 1 | a0009 | 1 | HG01496.hp1 | missense_variant | MODERATE | c.932G>A | p.Gly311Glu | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 12/28 | 1010/3472 | 932/2778 | 311/925 | chr16 | 4364887 | |||
| chr16:4388001 | A | G | 2 | a0004 a0018 |
5 | HG02895.hp2 HG02897.hp1 HG03130.hp2 others(2): Show |
missense_variant | MODERATE | c.770T>C | p.Leu257Ser | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/28 | 848/3472 | 770/2778 | 257/925 | chr16 | 4388001 | |||
| chr16:4388056 | C | T | 1 | a0013 | 1 | HG03834.hp1 | missense_variant | MODERATE | c.715G>A | p.Glu239Lys | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/28 | 793/3472 | 715/2778 | 239/925 | chr16 | 4388056 | |||
| chr16:4395326 | C | T | 5 | a0002 a0006 a0010 others(2): Show |
131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
missense_variant | MODERATE | c.578G>A | p.Arg193Gln | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/28 | 656/3472 | 578/2778 | 193/925 | chr16 | 4395326 | |||
| chr16:4405522 | C | T | 1 | a0017 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.533G>A | p.Arg178Gln | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/28 | 611/3472 | 533/2778 | 178/925 | chr16 | 4405522 | |||
| chr16:4405534 | G | A | 1 | a0012 | 1 | HG02922.hp1 | missense_variant | MODERATE | c.521C>T | p.Ala174Val | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/28 | 599/3472 | 521/2778 | 174/925 | chr16 | 4405534 | |||
| chr16:4405552 | C | G | 1 | a0012 | 1 | HG02922.hp1 | missense_variant | MODERATE | c.503G>C | p.Gly168Ala | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/28 | 581/3472 | 503/2778 | 168/925 | chr16 | 4405552 | |||
| chr16:4408182 | G | A | 1 | a0014 | 1 | HG04184.hp2 | missense_variant&splice_region_variant | MODERATE | c.302C>T | p.Thr101Met | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 4/28 | 380/3472 | 302/2778 | 101/925 | chr16 | 4408182 | |||
| chr16:4413314 | G | A | 1 | a0016 | 1 | NA18943.hp1 | missense_variant | MODERATE | c.151C>T | p.Arg51Cys | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 2/28 | 229/3472 | 151/2778 | 51/925 | chr16 | 4413314 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:4357186 | G | A | 1 | a0002c0013 | 1 | NA18962.hp2 | synonymous_variant | LOW | c.2667C>T | p.Asp889Asp | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 26/28 | 2745/3472 | 2667/2778 | 889/925 | chr16 | 4357186 | |||
| chr16:4361223 | C | T | 2 | a0001c0004 a0007c0021 |
14 | HG01099.hp1 HG01891.hp2 HG02280.hp2 others(11): Show |
synonymous_variant | LOW | c.1713G>A | p.Leu571Leu | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 18/28 | 1791/3472 | 1713/2778 | 571/925 | chr16 | 4361223 | |||
| chr16:4362006 | C | T | 2 | a0002c0006 a0006c0009 |
4 | HG00733.hp1 HG01106.hp1 HG01257.hp2 others(1): Show |
synonymous_variant | LOW | c.1557G>A | p.Gly519Gly | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 16/28 | 1635/3472 | 1557/2778 | 519/925 | chr16 | 4362006 | |||
| chr16:4362018 | C | G | 1 | a0003c0019 | 1 | HG03516.hp2 | synonymous_variant | LOW | c.1545G>C | p.Leu515Leu | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 16/28 | 1623/3472 | 1545/2778 | 515/925 | chr16 | 4362018 | |||
| chr16:4362694 | C | T | 1 | a0005c0007 | 2 | HG03041.hp1 HG03486.hp1 |
synonymous_variant | LOW | c.1320G>A | p.Thr440Thr | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 15/28 | 1398/3472 | 1320/2778 | 440/925 | chr16 | 4362694 | |||
| chr16:4364327 | G | A | 1 | a0001c0023 | 1 | HG02922.hp2 | synonymous_variant | LOW | c.1224C>T | p.Asp408Asp | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 14/28 | 1302/3472 | 1224/2778 | 408/925 | chr16 | 4364327 | |||
| chr16:4364372 | C | G | 1 | a0003c0018 | 1 | HG02897.hp2 | synonymous_variant | LOW | c.1179G>C | p.Pro393Pro | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 14/28 | 1257/3472 | 1179/2778 | 393/925 | chr16 | 4364372 | |||
| chr16:4395301 | C | G | 1 | a0001c0014 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.603G>C | p.Pro201Pro | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/28 | 681/3472 | 603/2778 | 201/925 | chr16 | 4395301 | |||
| chr16:4407594 | G | A | 1 | a0012c0024 | 1 | HG02922.hp1 | synonymous_variant | LOW | c.394C>T | p.Leu132Leu | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/28 | 472/3472 | 394/2778 | 132/925 | chr16 | 4407594 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:4354619 | C | T | 6 | a0001c0002t0002 a0002c0001t0002 a0004c0005t0002 others(3): Show |
51 | HG00544.hp1 HG00597.hp2 HG01074.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*539G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 28/28 | 539 | chr16 | 4354619 | ||||||
| chr16:4354728 | G | A | 1 | a0018c0016t0003 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*430C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 28/28 | 430 | chr16 | 4354728 | ||||||
| chr16:4354856 | G | A | 6 | a0001c0002t0002 a0002c0001t0002 a0004c0005t0002 others(3): Show |
51 | HG00544.hp1 HG00597.hp2 HG01074.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*302C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 28/28 | 302 | chr16 | 4354856 | ||||||
| chr16:4355017 | G | A | 1 | a0002c0001t0004 | 1 | HG01261.hp1 | 3_prime_UTR_variant | MODIFIER | c.*141C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 28/28 | 141 | chr16 | 4355017 | ||||||
| chr16:4416560 | G | C | 1 | a0012c0024t0005 | 1 | HG02922.hp1 | 5_prime_UTR_variant | MODIFIER | c.-42C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/28 | 42 | chr16 | 4416560 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:4355237 | T | G | 16 | a0003c0003t0001g0016 a0003c0003t0001g0259 a0003c0003t0001g0260 others(13): Show |
17 | HG02280.hp1 HG02451.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.2772+49A>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 27/27 | chr16 | 4355237 | |||||||
| chr16:4355270 | G | A | 3 | a0001c0002t0001g0090 a0001c0002t0001g0092 a0001c0002t0001g0132 |
3 | HG02258.hp2 HG02717.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2772+16C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 27/27 | chr16 | 4355270 | |||||||
| chr16:4355468 | CT | C | 6 | a0002c0001t0001g0020 a0002c0001t0001g0175 a0002c0001t0001g0227 others(3): Show |
6 | HG02897.hp2 HG03041.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2686-97delA | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 26/27 | chr16 | 4355468 | |||||||
| chr16:4355489 | G | T | 39 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0031 others(36): Show |
43 | HG00544.hp1 HG00597.hp2 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.2686-117C>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 26/27 | chr16 | 4355489 | |||||||
| chr16:4355537 | C | T | 1 | a0018c0016t0003g0257 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2686-165G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 26/27 | chr16 | 4355537 | |||||||
| chr16:4355538 | G | A | 1 | a0001c0002t0001g0273 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2686-166C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 26/27 | chr16 | 4355538 | |||||||
| chr16:4355636 | T | G | 16 | a0003c0003t0001g0016 a0003c0003t0001g0259 a0003c0003t0001g0260 others(13): Show |
17 | HG02280.hp1 HG02451.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.2686-264A>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 26/27 | chr16 | 4355636 | |||||||
| chr16:4355659 | G | C | 10 | a0001c0002t0001g0005 a0001c0002t0001g0022 a0001c0002t0001g0023 others(7): Show |
11 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.2686-287C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 26/27 | chr16 | 4355659 | |||||||
| chr16:4355761 | G | A | 3 | a0001c0002t0001g0040 a0001c0002t0001g0041 a0001c0023t0001g0042 |
3 | HG02922.hp2 HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2686-389C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 26/27 | chr16 | 4355761 | |||||||
| chr16:4355778 | G | A | 1 | a0001c0002t0001g0078 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2686-406C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 26/27 | chr16 | 4355778 | |||||||
| chr16:4355849 | C | G | 1 | a0002c0001t0001g0143 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2686-477G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 26/27 | chr16 | 4355849 | |||||||
| chr16:4355858 | G | A | 2 | a0002c0001t0001g0226 a0002c0001t0001g0227 |
2 | NA18978.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.2686-486C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 26/27 | chr16 | 4355858 | |||||||
| chr16:4356006 | T | G | 1 | a0019c0020t0002g0048 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2686-634A>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 26/27 | chr16 | 4356006 | |||||||
| chr16:4356223 | G | A | 16 | a0003c0003t0001g0016 a0003c0003t0001g0259 a0003c0003t0001g0260 others(13): Show |
17 | HG02280.hp1 HG02451.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.2686-851C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 26/27 | chr16 | 4356223 | |||||||
| chr16:4356273 | A | T | 1 | a0002c0001t0001g0186 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2685+895T>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 26/27 | chr16 | 4356273 | |||||||
| chr16:4356286 | G | C | 2 | a0005c0007t0001g0044 a0005c0007t0001g0045 |
2 | HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2685+882C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 26/27 | chr16 | 4356286 | |||||||
| chr16:4356409 | ATTTTATT others(5): Show |
A | 1 | a0002c0001t0001g0184 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2685+747_2685+758d others(14): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 26/27 | chr16 | 4356409 | |||||||
| chr16:4356501 | C | T | 2 | a0002c0001t0001g0226 a0002c0001t0001g0227 |
2 | NA18978.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.2685+667G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 26/27 | chr16 | 4356501 | |||||||
| chr16:4356502 | G | A | 1 | a0001c0004t0001g0136 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2685+666C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 26/27 | chr16 | 4356502 | |||||||
| chr16:4356622 | G | A | 2 | a0005c0007t0001g0044 a0005c0007t0001g0045 |
2 | HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2685+546C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 26/27 | chr16 | 4356622 | |||||||
| chr16:4356633 | G | A | 10 | a0001c0002t0001g0005 a0001c0002t0001g0022 a0001c0002t0001g0023 others(7): Show |
11 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.2685+535C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 26/27 | chr16 | 4356633 | |||||||
| chr16:4356693 | A | G | 1 | a0001c0002t0002g0037 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2685+475T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 26/27 | chr16 | 4356693 | |||||||
| chr16:4356784 | G | A | 1 | a0001c0004t0001g0139 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2685+384C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 26/27 | chr16 | 4356784 | |||||||
| chr16:4356984 | C | A | 1 | a0001c0002t0001g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2685+184G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 26/27 | chr16 | 4356984 | |||||||
| chr16:4356984 | C | T | 1 | a0004c0005t0002g0258 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2685+184G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 26/27 | chr16 | 4356984 | |||||||
| chr16:4356992 | G | A | 1 | a0001c0002t0001g0153 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2685+176C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 26/27 | chr16 | 4356992 | |||||||
| chr16:4357108 | C | T | 1 | a0001c0004t0001g0139 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2685+60G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 26/27 | chr16 | 4357108 | |||||||
| chr16:4357292 | C | A | 1 | a0001c0004t0001g0136 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2594-33G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 25/27 | chr16 | 4357292 | |||||||
| chr16:4357346 | T | C | 1 | a0001c0002t0002g0243 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2594-87A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 25/27 | chr16 | 4357346 | |||||||
| chr16:4357347 | C | T | 1 | a0001c0002t0002g0243 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2594-88G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 25/27 | chr16 | 4357347 | |||||||
| chr16:4357351 | CTTTCT | C | 48 | a0001c0002t0001g0041 a0001c0002t0001g0088 a0001c0002t0001g0273 others(45): Show |
52 | HG00544.hp1 HG00597.hp2 HG01074.hp1 others(49): Show |
intron_variant | MODIFIER | c.2594-97_2594-93del others(5): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 25/27 | chr16 | 4357351 | |||||||
| chr16:4357355 | CT | C | 88 | a0001c0002t0001g0005 a0001c0002t0001g0007 a0001c0002t0001g0010 others(85): Show |
95 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.2594-97delA | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 25/27 | chr16 | 4357355 | |||||||
| chr16:4357355 | CTT | C | 7 | a0001c0002t0001g0100 a0001c0002t0001g0108 a0001c0002t0001g0111 others(4): Show |
7 | HG02895.hp1 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.2594-98_2594-97del others(2): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 25/27 | chr16 | 4357355 | |||||||
| chr16:4357360 | T | C | 4 | a0003c0003t0001g0264 a0003c0003t0001g0266 a0003c0003t0001g0267 others(1): Show |
4 | HG02809.hp1 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2594-101A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 25/27 | chr16 | 4357360 | |||||||
| chr16:4357463 | G | A | 1 | a0001c0002t0002g0093 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2594-204C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 25/27 | chr16 | 4357463 | |||||||
| chr16:4357505 | G | A | 1 | a0002c0001t0001g0192 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2594-246C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 25/27 | chr16 | 4357505 | |||||||
| chr16:4357513 | C | T | 1 | a0001c0002t0001g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2594-254G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 25/27 | chr16 | 4357513 | |||||||
| chr16:4357602 | C | T | 1 | a0002c0001t0001g0130 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2594-343G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 25/27 | chr16 | 4357602 | |||||||
| chr16:4357647 | C | T | 3 | a0001c0002t0001g0110 a0002c0001t0001g0219 a0002c0001t0001g0240 |
3 | HG02040.hp1 NA18960.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.2593+321G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 25/27 | chr16 | 4357647 | |||||||
| chr16:4357743 | C | G | 94 | a0001c0002t0001g0005 a0001c0002t0001g0010 a0001c0002t0001g0021 others(91): Show |
104 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(101): Show |
intron_variant | MODIFIER | c.2593+225G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 25/27 | chr16 | 4357743 | |||||||
| chr16:4357752 | C | CGT | 18 | a0001c0002t0002g0003 a0003c0003t0001g0016 a0003c0003t0001g0259 others(15): Show |
21 | HG01074.hp1 HG01109.hp2 HG01346.hp2 others(18): Show |
intron_variant | MODIFIER | c.2593+214_2593+215d others(4): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 25/27 | chr16 | 4357752 | |||||||
| chr16:4357802 | G | A | 1 | a0001c0004t0001g0058 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2593+166C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 25/27 | chr16 | 4357802 | |||||||
| chr16:4358266 | A | G | 25 | a0001c0002t0001g0005 a0001c0002t0001g0022 a0001c0002t0001g0023 others(22): Show |
29 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.2457+101T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 24/27 | chr16 | 4358266 | |||||||
| chr16:4358324 | C | T | 7 | a0001c0004t0001g0001 a0001c0004t0001g0008 a0001c0004t0001g0043 others(4): Show |
10 | HG02280.hp2 HG02486.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.2457+43G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 24/27 | chr16 | 4358324 | |||||||
| chr16:4358587 | C | T | 10 | a0001c0002t0001g0005 a0001c0002t0001g0022 a0001c0002t0001g0023 others(7): Show |
11 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.2341-104G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 23/27 | chr16 | 4358587 | |||||||
| chr16:4358590 | G | A | 1 | a0001c0002t0002g0070 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2341-107C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 23/27 | chr16 | 4358590 | |||||||
| chr16:4358591 | G | A | 1 | a0001c0002t0002g0070 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2341-108C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 23/27 | chr16 | 4358591 | |||||||
| chr16:4358940 | C | T | 89 | a0001c0002t0001g0005 a0001c0002t0001g0022 a0001c0002t0001g0023 others(86): Show |
98 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(95): Show |
intron_variant | MODIFIER | c.2340+356G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 23/27 | chr16 | 4358940 | |||||||
| chr16:4359067 | G | A | 3 | a0004c0005t0001g0254 a0004c0005t0001g0255 a0004c0005t0001g0256 |
3 | HG02895.hp2 HG02897.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2340+229C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 23/27 | chr16 | 4359067 | |||||||
| chr16:4359095 | T | C | 2 | a0001c0002t0002g0077 a0001c0002t0002g0094 |
2 | HG01515.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.2340+201A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 23/27 | chr16 | 4359095 | |||||||
| chr16:4359275 | G | A | 1 | a0001c0002t0001g0273 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2340+21C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 23/27 | chr16 | 4359275 | |||||||
| chr16:4359438 | C | A | 1 | a0001c0002t0001g0030 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2250+42G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 22/27 | chr16 | 4359438 | |||||||
| chr16:4359750 | A | T | 1 | a0001c0002t0001g0273 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2109-129T>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 21/27 | chr16 | 4359750 | |||||||
| chr16:4359878 | T | G | 25 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0087 others(22): Show |
31 | HG01099.hp1 HG01891.hp2 HG02055.hp2 others(28): Show |
intron_variant | MODIFIER | c.2109-257A>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 21/27 | chr16 | 4359878 | |||||||
| chr16:4359894 | T | TATCTCCC others(91): Show |
3 | a0001c0002t0002g0050 a0001c0002t0002g0123 a0003c0003t0001g0274 |
3 | HG02717.hp1 HG02896.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2108+286_2109-274d others(100): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 21/27 | chr16 | 4359894 | |||||||
| chr16:4359968 | A | ACCCCCCT others(92): Show |
1 | a0003c0018t0001g0275 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2108+309_2108+310i others(101): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 21/27 | chr16 | 4359968 | |||||||
| chr16:4359968 | A | G | 4 | a0003c0003t0001g0259 a0004c0005t0001g0254 a0004c0005t0001g0255 others(1): Show |
4 | HG02895.hp2 HG02897.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2108+310T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 21/27 | chr16 | 4359968 | |||||||
| chr16:4360034 | C | A | 1 | a0002c0001t0001g0193 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2108+244G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 21/27 | chr16 | 4360034 | |||||||
| chr16:4360242 | T | G | 34 | a0001c0002t0001g0005 a0001c0002t0001g0021 a0001c0002t0001g0022 others(31): Show |
36 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.2108+36A>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 21/27 | chr16 | 4360242 | |||||||
| chr16:4360373 | T | C | 11 | a0001c0002t0001g0005 a0001c0002t0001g0022 a0001c0002t0001g0023 others(8): Show |
12 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.2023-10A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 20/27 | chr16 | 4360373 | |||||||
| chr16:4360398 | C | T | 3 | a0001c0002t0001g0090 a0001c0002t0001g0092 a0001c0002t0001g0132 |
3 | HG02258.hp2 HG02717.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2023-35G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 20/27 | chr16 | 4360398 | |||||||
| chr16:4360415 | A | G | 1 | a0001c0002t0001g0273 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2022+29T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 20/27 | chr16 | 4360415 | |||||||
| chr16:4360429 | C | T | 2 | a0001c0002t0001g0054 a0001c0002t0001g0055 |
2 | HG02071.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.2022+15G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 20/27 | chr16 | 4360429 | |||||||
| chr16:4360658 | T | TC | 3 | a0002c0001t0001g0207 a0003c0003t0001g0261 a0017c0008t0002g0061 |
3 | HG01928.hp1 HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1918-111dupG | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 19/27 | chr16 | 4360658 | |||||||
| chr16:4360684 | GCCTCTCC others(14): Show |
G | 1 | a0002c0001t0001g0184 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1918-157_1918-137d others(23): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 19/27 | chr16 | 4360684 | |||||||
| chr16:4360696 | T | G | 1 | a0001c0004t0001g0058 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1918-148A>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 19/27 | chr16 | 4360696 | |||||||
| chr16:4360866 | TCACTGCT others(15): Show |
T | 108 | a0001c0002t0001g0010 a0001c0002t0001g0021 a0001c0002t0001g0029 others(105): Show |
116 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.1917+55_1917+76del others(22): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 19/27 | chr16 | 4360866 | |||||||
| chr16:4360880 | A | G | 1 | a0002c0001t0001g0012 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1917+63T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 19/27 | chr16 | 4360880 | |||||||
| chr16:4360880 | ACCTCTCC others(15): Show |
A | 1 | a0001c0002t0001g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1917+41_1917+62del others(22): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 19/27 | chr16 | 4360880 | |||||||
| chr16:4361505 | A | G | 28 | a0001c0002t0001g0005 a0001c0002t0001g0022 a0001c0002t0001g0023 others(25): Show |
30 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.1579-36T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 16/27 | chr16 | 4361505 | |||||||
| chr16:4361647 | A | G | 10 | a0001c0004t0001g0001 a0001c0004t0001g0008 a0001c0004t0001g0043 others(7): Show |
13 | HG01891.hp2 HG02280.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.1579-178T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 16/27 | chr16 | 4361647 | |||||||
| chr16:4361696 | C | T | 2 | a0001c0002t0001g0127 a0002c0001t0001g0230 |
2 | HG03017.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1579-227G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 16/27 | chr16 | 4361696 | |||||||
| chr16:4361700 | G | A | 1 | a0002c0001t0001g0234 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1579-231C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 16/27 | chr16 | 4361700 | |||||||
| chr16:4361911 | G | A | 2 | a0001c0002t0001g0103 a0002c0001t0001g0035 |
2 | HG01255.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.1578+74C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 16/27 | chr16 | 4361911 | |||||||
| chr16:4362478 | T | C | 2 | a0005c0007t0001g0044 a0005c0007t0001g0045 |
2 | HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1402+134A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 15/27 | chr16 | 4362478 | |||||||
| chr16:4362493 | G | C | 1 | a0001c0002t0001g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1402+119C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 15/27 | chr16 | 4362493 | |||||||
| chr16:4362596 | C | T | 1 | a0001c0002t0002g0118 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1402+16G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 15/27 | chr16 | 4362596 | |||||||
| chr16:4362597 | G | A | 16 | a0003c0003t0001g0016 a0003c0003t0001g0259 a0003c0003t0001g0260 others(13): Show |
17 | HG02280.hp1 HG02451.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.1402+15C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 15/27 | chr16 | 4362597 | |||||||
| chr16:4362805 | C | T | 8 | a0001c0004t0001g0008 a0001c0004t0001g0058 a0001c0004t0001g0135 others(5): Show |
9 | HG01099.hp1 HG01891.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1276-67G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 14/27 | chr16 | 4362805 | |||||||
| chr16:4362843 | G | A | 1 | a0001c0002t0002g0006 | 2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1276-105C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 14/27 | chr16 | 4362843 | |||||||
| chr16:4362867 | C | G | 139 | a0001c0002t0001g0021 a0001c0002t0001g0029 a0001c0002t0001g0032 others(136): Show |
150 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.1276-129G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 14/27 | chr16 | 4362867 | |||||||
| chr16:4362880 | G | A | 3 | a0001c0002t0001g0273 a0005c0007t0001g0044 a0005c0007t0001g0045 |
3 | HG03041.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1276-142C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 14/27 | chr16 | 4362880 | |||||||
| chr16:4362920 | C | T | 17 | a0003c0003t0001g0016 a0003c0003t0001g0259 a0003c0003t0001g0260 others(14): Show |
18 | HG02280.hp1 HG02451.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.1276-182G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 14/27 | chr16 | 4362920 | |||||||
| chr16:4362939 | A | G | 1 | a0007c0021t0001g0034 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1276-201T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 14/27 | chr16 | 4362939 | |||||||
| chr16:4363081 | A | G | 1 | a0002c0001t0001g0219 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1276-343T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 14/27 | chr16 | 4363081 | |||||||
| chr16:4363179 | C | T | 16 | a0003c0003t0001g0016 a0003c0003t0001g0259 a0003c0003t0001g0260 others(13): Show |
17 | HG02280.hp1 HG02451.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.1276-441G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 14/27 | chr16 | 4363179 | |||||||
| chr16:4363328 | A | G | 1 | a0001c0002t0002g0085 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1276-590T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 14/27 | chr16 | 4363328 | |||||||
| chr16:4363432 | C | T | 6 | a0001c0002t0001g0021 a0001c0002t0001g0040 a0001c0002t0001g0041 others(3): Show |
8 | HG02486.hp1 HG02922.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1276-694G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 14/27 | chr16 | 4363432 | |||||||
| chr16:4363515 | G | GCCAACAT others(9): Show |
1 | a0003c0018t0001g0275 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1275+745_1275+760d others(18): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 14/27 | chr16 | 4363515 | |||||||
| chr16:4363573 | G | A | 1 | a0002c0001t0001g0175 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1275+703C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 14/27 | chr16 | 4363573 | |||||||
| chr16:4363729 | A | C | 1 | a0003c0018t0001g0275 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1275+547T>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 14/27 | chr16 | 4363729 | |||||||
| chr16:4363780 | A | G | 1 | a0003c0018t0001g0275 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1275+496T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 14/27 | chr16 | 4363780 | |||||||
| chr16:4363781 | G | C | 1 | a0003c0018t0001g0275 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1275+495C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 14/27 | chr16 | 4363781 | |||||||
| chr16:4363817 | G | A | 109 | a0001c0002t0001g0021 a0001c0002t0001g0029 a0001c0002t0001g0032 others(106): Show |
118 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.1275+459C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 14/27 | chr16 | 4363817 | |||||||
| chr16:4363837 | G | A | 1 | a0019c0020t0002g0048 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1275+439C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 14/27 | chr16 | 4363837 | |||||||
| chr16:4363866 | A | G | 1 | a0001c0004t0001g0242 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1275+410T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 14/27 | chr16 | 4363866 | |||||||
| chr16:4364072 | G | A | 1 | a0001c0002t0001g0273 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1275+204C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 14/27 | chr16 | 4364072 | |||||||
| chr16:4364132 | G | A | 1 | a0004c0005t0001g0255 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1275+144C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 14/27 | chr16 | 4364132 | |||||||
| chr16:4364414 | C | G | 1 | a0001c0002t0001g0092 | 1 | HG02258.hp2 | splice_acceptor_variant&intron_variant | HIGH | c.1138-1G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 13/27 | chr16 | 4364414 | |||||||
| chr16:4364465 | A | G | 1 | a0003c0018t0001g0275 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1138-52T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 13/27 | chr16 | 4364465 | |||||||
| chr16:4364466 | G | A | 1 | a0003c0018t0001g0275 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1138-53C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 13/27 | chr16 | 4364466 | |||||||
| chr16:4364542 | C | T | 4 | a0001c0004t0001g0008 a0001c0004t0001g0135 a0001c0004t0001g0137 others(1): Show |
5 | HG02280.hp2 HG02886.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1137+55G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 13/27 | chr16 | 4364542 | |||||||
| chr16:4364691 | T | A | 1 | a0002c0013t0001g0205 | 1 | NA18962.hp2 | splice_acceptor_variant&intron_variant | HIGH | c.1045-2A>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 12/27 | chr16 | 4364691 | |||||||
| chr16:4364693 | G | T | 1 | a0003c0018t0001g0275 | 1 | HG02897.hp2 | splice_region_variant&intron_variant | LOW | c.1045-4C>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 12/27 | chr16 | 4364693 | |||||||
| chr16:4364726 | G | A | 110 | a0001c0002t0001g0021 a0001c0002t0001g0029 a0001c0002t0001g0032 others(107): Show |
118 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.1045-37C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 12/27 | chr16 | 4364726 | |||||||
| chr16:4364747 | C | G | 1 | a0002c0001t0001g0163 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1044+28G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 12/27 | chr16 | 4364747 | |||||||
| chr16:4364773 | A | C | 1 | a0001c0002t0001g0127 | 1 | HG03654.hp1 | splice_donor_variant&intron_variant | HIGH | c.1044+2T>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 12/27 | chr16 | 4364773 | |||||||
| chr16:4364965 | G | T | 1 | a0003c0018t0001g0275 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.898+38C>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 11/27 | chr16 | 4364965 | |||||||
| chr16:4364986 | G | A | 102 | a0001c0002t0001g0029 a0001c0002t0001g0032 a0001c0002t0001g0068 others(99): Show |
109 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.898+17C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 11/27 | chr16 | 4364986 | |||||||
| chr16:4365085 | C | T | 1 | a0018c0016t0003g0257 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.841-25G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 10/27 | chr16 | 4365085 | |||||||
| chr16:4365268 | C | G | 1 | a0003c0018t0001g0275 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.841-208G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 10/27 | chr16 | 4365268 | |||||||
| chr16:4365268 | C | T | 6 | a0001c0002t0001g0021 a0001c0002t0001g0040 a0001c0002t0001g0041 others(3): Show |
8 | HG02486.hp1 HG02922.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.841-208G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 10/27 | chr16 | 4365268 | |||||||
| chr16:4365269 | G | A | 1 | a0001c0002t0001g0273 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.841-209C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 10/27 | chr16 | 4365269 | |||||||
| chr16:4365272 | G | T | 1 | a0003c0018t0001g0275 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.841-212C>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 10/27 | chr16 | 4365272 | |||||||
| chr16:4365310 | G | A | 1 | a0001c0004t0001g0058 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.840+181C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 10/27 | chr16 | 4365310 | |||||||
| chr16:4365376 | G | C | 1 | a0001c0002t0002g0086 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.840+115C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 10/27 | chr16 | 4365376 | |||||||
| chr16:4365409 | G | T | 137 | a0001c0002t0001g0021 a0001c0002t0001g0029 a0001c0002t0001g0032 others(134): Show |
148 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.840+82C>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 10/27 | chr16 | 4365409 | |||||||
| chr16:4365454 | C | G | 141 | a0001c0002t0001g0021 a0001c0002t0001g0029 a0001c0002t0001g0032 others(138): Show |
151 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.840+37G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 10/27 | chr16 | 4365454 | |||||||
| chr16:4365466 | G | C | 1 | a0001c0002t0002g0070 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.840+25C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 10/27 | chr16 | 4365466 | |||||||
| chr16:4365474 | C | A | 3 | a0001c0002t0001g0053 a0001c0002t0001g0133 a0001c0002t0001g0140 |
3 | HG01243.hp2 HG02572.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.840+17G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 10/27 | chr16 | 4365474 | |||||||
| chr16:4365695 | C | G | 132 | a0001c0002t0001g0029 a0001c0002t0001g0032 a0001c0002t0001g0051 others(129): Show |
140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.786-150G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4365695 | |||||||
| chr16:4365726 | C | T | 3 | a0002c0001t0001g0164 a0002c0001t0001g0165 a0002c0001t0001g0166 |
3 | HG01106.hp2 HG01168.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.786-181G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4365726 | |||||||
| chr16:4365755 | G | C | 17 | a0003c0003t0001g0016 a0003c0003t0001g0259 a0003c0003t0001g0260 others(14): Show |
18 | HG02280.hp1 HG02451.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.786-210C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4365755 | |||||||
| chr16:4365774 | C | T | 2 | a0003c0003t0001g0269 a0003c0003t0001g0271 |
2 | HG02559.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.786-229G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4365774 | |||||||
| chr16:4365918 | G | A | 5 | a0002c0001t0001g0009 a0002c0001t0001g0142 a0002c0001t0001g0175 others(2): Show |
6 | HG00423.hp2 HG00597.hp1 NA18948.hp2 others(3): Show |
intron_variant | MODIFIER | c.786-373C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4365918 | |||||||
| chr16:4366054 | C | T | 1 | a0003c0018t0001g0275 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.786-509G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4366054 | |||||||
| chr16:4366100 | C | T | 17 | a0003c0003t0001g0016 a0003c0003t0001g0259 a0003c0003t0001g0260 others(14): Show |
18 | HG02280.hp1 HG02451.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.786-555G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4366100 | |||||||
| chr16:4366138 | C | T | 1 | a0002c0001t0001g0222 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.786-593G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4366138 | |||||||
| chr16:4366140 | C | G | 18 | a0001c0002t0001g0036 a0003c0003t0001g0016 a0003c0003t0001g0259 others(15): Show |
19 | HG02280.hp1 HG02451.hp1 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.786-595G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4366140 | |||||||
| chr16:4366211 | G | A | 3 | a0001c0002t0001g0053 a0001c0002t0001g0133 a0001c0002t0001g0140 |
3 | HG01243.hp2 HG02572.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.786-666C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4366211 | |||||||
| chr16:4366228 | T | C | 1 | a0003c0018t0001g0275 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.786-683A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4366228 | |||||||
| chr16:4366229 | C | T | 1 | a0003c0018t0001g0275 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.786-684G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4366229 | |||||||
| chr16:4366316 | G | A | 9 | a0001c0004t0001g0008 a0001c0004t0001g0058 a0001c0004t0001g0135 others(6): Show |
10 | HG01099.hp1 HG01891.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.786-771C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4366316 | |||||||
| chr16:4366362 | C | CA | 28 | a0001c0002t0001g0005 a0001c0002t0001g0022 a0001c0002t0001g0023 others(25): Show |
30 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.786-818_786-817ins others(1): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4366362 | |||||||
| chr16:4366497 | C | T | 11 | a0001c0002t0001g0005 a0001c0002t0001g0022 a0001c0002t0001g0023 others(8): Show |
12 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.786-952G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4366497 | |||||||
| chr16:4366535 | C | CT | 18 | a0001c0002t0001g0036 a0001c0002t0001g0109 a0001c0002t0001g0110 others(15): Show |
20 | HG01099.hp1 HG02055.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.786-991dupA | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4366535 | |||||||
| chr16:4366535 | C | CTT | 26 | a0001c0002t0001g0005 a0001c0002t0001g0022 a0001c0002t0001g0023 others(23): Show |
28 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.786-992_786-991dup others(2): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4366535 | |||||||
| chr16:4366535 | CT | C | 18 | a0001c0002t0001g0105 a0001c0002t0001g0108 a0001c0002t0001g0113 others(15): Show |
18 | HG01070.hp2 HG01099.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.786-991delA | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4366535 | |||||||
| chr16:4366697 | T | G | 2 | a0001c0002t0002g0086 a0003c0018t0001g0275 |
2 | HG02897.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.786-1152A>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4366697 | |||||||
| chr16:4366857 | C | G | 11 | a0001c0002t0001g0005 a0001c0002t0001g0022 a0001c0002t0001g0023 others(8): Show |
12 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.786-1312G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4366857 | |||||||
| chr16:4366872 | C | T | 1 | a0003c0018t0001g0275 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.786-1327G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4366872 | |||||||
| chr16:4366873 | T | G | 1 | a0003c0018t0001g0275 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.786-1328A>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4366873 | |||||||
| chr16:4366916 | C | T | 16 | a0003c0003t0001g0016 a0003c0003t0001g0259 a0003c0003t0001g0260 others(13): Show |
17 | HG02280.hp1 HG02451.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.786-1371G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4366916 | |||||||
| chr16:4366921 | C | T | 11 | a0001c0002t0001g0005 a0001c0002t0001g0022 a0001c0002t0001g0023 others(8): Show |
12 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.786-1376G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4366921 | |||||||
| chr16:4366981 | C | T | 1 | a0001c0002t0002g0093 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.786-1436G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4366981 | |||||||
| chr16:4367159 | G | C | 28 | a0001c0002t0001g0005 a0001c0002t0001g0022 a0001c0002t0001g0023 others(25): Show |
30 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.786-1614C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4367159 | |||||||
| chr16:4367179 | C | A | 28 | a0001c0002t0001g0005 a0001c0002t0001g0022 a0001c0002t0001g0023 others(25): Show |
30 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.786-1634G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4367179 | |||||||
| chr16:4367252 | A | T | 28 | a0001c0002t0001g0005 a0001c0002t0001g0022 a0001c0002t0001g0023 others(25): Show |
30 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.786-1707T>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4367252 | |||||||
| chr16:4367261 | C | T | 1 | a0001c0002t0001g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.786-1716G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4367261 | |||||||
| chr16:4367337 | T | C | 28 | a0001c0002t0001g0005 a0001c0002t0001g0022 a0001c0002t0001g0023 others(25): Show |
30 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.786-1792A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4367337 | |||||||
| chr16:4367390 | C | T | 2 | a0001c0002t0002g0056 a0001c0002t0002g0057 |
2 | HG01934.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.786-1845G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4367390 | |||||||
| chr16:4367418 | G | A | 1 | a0018c0016t0003g0257 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.786-1873C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4367418 | |||||||
| chr16:4367627 | C | A | 1 | a0001c0002t0002g0006 | 2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.786-2082G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4367627 | |||||||
| chr16:4367796 | A | C | 28 | a0001c0002t0001g0005 a0001c0002t0001g0022 a0001c0002t0001g0023 others(25): Show |
30 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.786-2251T>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4367796 | |||||||
| chr16:4367887 | C | T | 1 | a0001c0002t0001g0119 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.786-2342G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4367887 | |||||||
| chr16:4367981 | T | C | 1 | a0002c0001t0001g0159 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.786-2436A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4367981 | |||||||
| chr16:4368067 | C | T | 1 | a0001c0002t0001g0021 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.786-2522G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4368067 | |||||||
| chr16:4368146 | A | C | 2 | a0002c0001t0001g0226 a0002c0001t0001g0227 |
2 | NA18978.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.786-2601T>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4368146 | |||||||
| chr16:4368238 | T | C | 1 | a0001c0002t0002g0070 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.786-2693A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4368238 | |||||||
| chr16:4368284 | T | C | 18 | a0001c0002t0001g0053 a0001c0002t0001g0133 a0003c0003t0001g0016 others(15): Show |
19 | HG02280.hp1 HG02451.hp1 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.786-2739A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4368284 | |||||||
| chr16:4368308 | A | G | 1 | a0001c0004t0001g0139 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.786-2763T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4368308 | |||||||
| chr16:4368406 | G | A | 1 | a0002c0001t0001g0193 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.786-2861C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4368406 | |||||||
| chr16:4368412 | C | G | 1 | a0002c0001t0001g0202 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.786-2867G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4368412 | |||||||
| chr16:4368650 | A | G | 1 | a0001c0004t0001g0058 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.786-3105T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4368650 | |||||||
| chr16:4368653 | C | T | 1 | a0001c0002t0002g0067 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.786-3108G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4368653 | |||||||
| chr16:4368747 | C | CA | 13 | a0001c0002t0001g0036 a0001c0002t0001g0040 a0001c0002t0001g0055 others(10): Show |
13 | HG01099.hp1 HG01884.hp1 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.786-3203dupT | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4368747 | |||||||
| chr16:4368747 | C | CAA | 8 | a0001c0002t0002g0081 a0001c0004t0001g0008 a0001c0004t0001g0058 others(5): Show |
9 | HG01891.hp2 HG02280.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.786-3204_786-3203d others(4): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4368747 | |||||||
| chr16:4368747 | C | CAAA | 11 | a0001c0002t0001g0005 a0001c0002t0001g0022 a0001c0002t0001g0023 others(8): Show |
12 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.786-3205_786-3203d others(5): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4368747 | |||||||
| chr16:4368747 | CA | C | 9 | a0001c0002t0002g0064 a0001c0002t0002g0086 a0002c0001t0001g0164 others(6): Show |
9 | HG00673.hp2 HG01069.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.786-3203delT | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4368747 | |||||||
| chr16:4368781 | G | A | 1 | a0002c0001t0001g0224 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.786-3236C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4368781 | |||||||
| chr16:4368834 | C | T | 11 | a0001c0002t0001g0090 a0001c0002t0001g0092 a0001c0002t0001g0116 others(8): Show |
12 | HG01074.hp2 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.786-3289G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4368834 | |||||||
| chr16:4368996 | T | C | 1 | a0001c0002t0002g0091 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.786-3451A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4368996 | |||||||
| chr16:4369021 | C | T | 1 | a0002c0001t0001g0226 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.786-3476G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4369021 | |||||||
| chr16:4369034 | G | T | 1 | a0002c0001t0001g0219 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.786-3489C>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4369034 | |||||||
| chr16:4369120 | T | G | 29 | a0001c0002t0001g0005 a0001c0002t0001g0022 a0001c0002t0001g0023 others(26): Show |
31 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.786-3575A>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4369120 | |||||||
| chr16:4369206 | T | A | 7 | a0001c0002t0001g0005 a0001c0002t0001g0022 a0001c0002t0001g0023 others(4): Show |
8 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.786-3661A>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4369206 | |||||||
| chr16:4369314 | G | A | 10 | a0001c0002t0001g0005 a0001c0002t0001g0022 a0001c0002t0001g0023 others(7): Show |
11 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.786-3769C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4369314 | |||||||
| chr16:4369323 | G | C | 16 | a0003c0003t0001g0016 a0003c0003t0001g0259 a0003c0003t0001g0260 others(13): Show |
17 | HG02280.hp1 HG02451.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.786-3778C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4369323 | |||||||
| chr16:4369344 | T | C | 33 | a0001c0002t0001g0005 a0001c0002t0001g0022 a0001c0002t0001g0023 others(30): Show |
35 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.786-3799A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4369344 | |||||||
| chr16:4369463 | G | A | 2 | a0001c0002t0002g0081 a0002c0001t0002g0276 |
2 | NA18943.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.786-3918C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4369463 | |||||||
| chr16:4369511 | G | C | 1 | a0001c0002t0001g0026 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.786-3966C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4369511 | |||||||
| chr16:4369557 | C | T | 1 | a0004c0005t0002g0258 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.786-4012G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4369557 | |||||||
| chr16:4369614 | C | A | 11 | a0001c0002t0001g0090 a0001c0002t0001g0092 a0001c0002t0001g0116 others(8): Show |
12 | HG01074.hp2 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.786-4069G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4369614 | |||||||
| chr16:4369853 | C | T | 2 | a0002c0001t0001g0159 a0002c0001t0001g0228 |
2 | HG03834.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.786-4308G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4369853 | |||||||
| chr16:4370280 | G | C | 16 | a0003c0003t0001g0016 a0003c0003t0001g0259 a0003c0003t0001g0260 others(13): Show |
17 | HG02280.hp1 HG02451.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.786-4735C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4370280 | |||||||
| chr16:4370372 | T | C | 2 | a0002c0001t0001g0196 a0002c0001t0001g0197 |
2 | HG02015.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.786-4827A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4370372 | |||||||
| chr16:4370645 | A | G | 1 | a0002c0001t0001g0253 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.786-5100T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4370645 | |||||||
| chr16:4370646 | G | A | 1 | a0002c0001t0001g0253 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.786-5101C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4370646 | |||||||
| chr16:4370647 | A | T | 1 | a0002c0001t0001g0253 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.786-5102T>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4370647 | |||||||
| chr16:4370694 | C | T | 2 | a0005c0007t0001g0044 a0005c0007t0001g0045 |
2 | HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.786-5149G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4370694 | |||||||
| chr16:4370786 | T | C | 148 | a0001c0002t0001g0010 a0001c0002t0001g0029 a0001c0002t0001g0032 others(145): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.786-5241A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4370786 | |||||||
| chr16:4370816 | G | GC | 120 | a0001c0002t0001g0051 a0001c0002t0001g0054 a0001c0002t0001g0055 others(117): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.786-5272dupG | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4370816 | |||||||
| chr16:4370874 | G | C | 4 | a0002c0001t0001g0183 a0002c0001t0001g0184 a0002c0001t0001g0185 others(1): Show |
4 | HG00741.hp1 HG01123.hp2 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.786-5329C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4370874 | |||||||
| chr16:4370954 | A | G | 16 | a0003c0003t0001g0016 a0003c0003t0001g0259 a0003c0003t0001g0260 others(13): Show |
17 | HG02280.hp1 HG02451.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.786-5409T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4370954 | |||||||
| chr16:4370957 | G | A | 1 | a0001c0002t0001g0273 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.786-5412C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4370957 | |||||||
| chr16:4371026 | G | A | 4 | a0001c0002t0001g0273 a0005c0007t0001g0044 a0005c0007t0001g0045 others(1): Show |
4 | HG03041.hp1 HG03471.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.786-5481C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4371026 | |||||||
| chr16:4371124 | T | A | 2 | a0001c0002t0001g0051 a0002c0001t0001g0216 |
2 | NA18966.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.786-5579A>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4371124 | |||||||
| chr16:4371125 | C | G | 6 | a0001c0002t0001g0021 a0001c0002t0001g0040 a0001c0002t0001g0041 others(3): Show |
8 | HG02486.hp1 HG02922.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.786-5580G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4371125 | |||||||
| chr16:4371189 | C | T | 1 | a0001c0002t0001g0273 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.786-5644G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4371189 | |||||||
| chr16:4371233 | T | G | 13 | a0001c0002t0001g0273 a0001c0004t0001g0008 a0001c0004t0001g0058 others(10): Show |
14 | HG01099.hp1 HG01891.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.786-5688A>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4371233 | |||||||
| chr16:4371315 | A | G | 1 | a0002c0001t0004g0189 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.786-5770T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4371315 | |||||||
| chr16:4371602 | C | CTGTAAAA others(6): Show |
1 | a0001c0002t0001g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.786-6058_786-6057i others(15): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4371602 | |||||||
| chr16:4371603 | G | C | 1 | a0001c0002t0001g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.786-6058C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4371603 | |||||||
| chr16:4371685 | G | A | 1 | a0018c0016t0003g0257 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.786-6140C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4371685 | |||||||
| chr16:4371822 | A | G | 1 | a0002c0001t0001g0181 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.786-6277T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4371822 | |||||||
| chr16:4371931 | C | G | 4 | a0001c0002t0001g0273 a0005c0007t0001g0044 a0005c0007t0001g0045 others(1): Show |
4 | HG03041.hp1 HG03471.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.786-6386G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4371931 | |||||||
| chr16:4372121 | A | G | 194 | a0001c0002t0001g0005 a0001c0002t0001g0010 a0001c0002t0001g0021 others(191): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.786-6576T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4372121 | |||||||
| chr16:4372124 | C | G | 1 | a0018c0016t0003g0257 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.786-6579G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4372124 | |||||||
| chr16:4372192 | G | A | 1 | a0002c0001t0001g0168 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.786-6647C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4372192 | |||||||
| chr16:4372304 | G | A | 150 | a0001c0002t0001g0010 a0001c0002t0001g0021 a0001c0002t0001g0029 others(147): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.786-6759C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4372304 | |||||||
| chr16:4372385 | C | T | 6 | a0001c0002t0001g0021 a0001c0002t0001g0040 a0001c0002t0001g0041 others(3): Show |
8 | HG02486.hp1 HG02922.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.786-6840G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4372385 | |||||||
| chr16:4372515 | C | T | 1 | a0001c0002t0002g0123 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.786-6970G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4372515 | |||||||
| chr16:4372606 | G | T | 150 | a0001c0002t0001g0010 a0001c0002t0001g0021 a0001c0002t0001g0029 others(147): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.786-7061C>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4372606 | |||||||
| chr16:4372646 | G | C | 2 | a0001c0002t0001g0119 a0001c0002t0001g0120 |
2 | HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.786-7101C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4372646 | |||||||
| chr16:4372743 | A | G | 31 | a0001c0002t0001g0005 a0001c0002t0001g0022 a0001c0002t0001g0023 others(28): Show |
33 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.786-7198T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4372743 | |||||||
| chr16:4372759 | C | A | 1 | a0002c0001t0001g0018 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.786-7214G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4372759 | |||||||
| chr16:4372825 | G | A | 20 | a0002c0001t0001g0013 a0002c0001t0001g0073 a0002c0001t0001g0089 others(17): Show |
21 | HG00099.hp1 HG00642.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.786-7280C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4372825 | |||||||
| chr16:4372911 | G | C | 33 | a0001c0002t0001g0005 a0001c0002t0001g0022 a0001c0002t0001g0023 others(30): Show |
35 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.786-7366C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4372911 | |||||||
| chr16:4373020 | G | A | 1 | a0001c0002t0002g0118 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.786-7475C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4373020 | |||||||
| chr16:4373282 | C | T | 1 | a0001c0002t0001g0106 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.786-7737G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4373282 | |||||||
| chr16:4373314 | C | A | 2 | a0001c0002t0001g0273 a0018c0016t0003g0257 |
2 | HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.786-7769G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4373314 | |||||||
| chr16:4373367 | T | C | 193 | a0001c0002t0001g0005 a0001c0002t0001g0010 a0001c0002t0001g0021 others(190): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.786-7822A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4373367 | |||||||
| chr16:4373577 | G | C | 1 | a0002c0001t0001g0175 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.786-8032C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4373577 | |||||||
| chr16:4373613 | G | A | 1 | a0002c0001t0001g0225 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.786-8068C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4373613 | |||||||
| chr16:4373632 | G | A | 2 | a0001c0002t0002g0243 a0001c0002t0002g0244 |
2 | HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.786-8087C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4373632 | |||||||
| chr16:4373643 | C | T | 10 | a0001c0002t0001g0005 a0001c0002t0001g0022 a0001c0002t0001g0023 others(7): Show |
11 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.786-8098G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4373643 | |||||||
| chr16:4373685 | A | G | 1 | a0001c0002t0001g0150 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.786-8140T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4373685 | |||||||
| chr16:4373703 | A | T | 1 | a0009c0017t0001g0079 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.786-8158T>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4373703 | |||||||
| chr16:4373801 | C | T | 2 | a0002c0001t0001g0238 a0002c0001t0001g0239 |
2 | NA18980.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.786-8256G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4373801 | |||||||
| chr16:4373863 | C | T | 1 | a0002c0001t0001g0209 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.786-8318G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4373863 | |||||||
| chr16:4373892 | C | G | 1 | a0001c0002t0001g0140 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.786-8347G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4373892 | |||||||
| chr16:4373982 | C | T | 8 | a0001c0004t0001g0008 a0001c0004t0001g0135 a0001c0004t0001g0136 others(5): Show |
9 | HG01099.hp1 HG01891.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.786-8437G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4373982 | |||||||
| chr16:4373995 | T | C | 1 | a0001c0002t0001g0140 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.786-8450A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4373995 | |||||||
| chr16:4374086 | C | CGT | 30 | a0001c0002t0001g0005 a0001c0002t0001g0022 a0001c0002t0001g0023 others(27): Show |
33 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.786-8543_786-8542d others(4): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4374086 | |||||||
| chr16:4374086 | C | CGTGTGTG others(13): Show |
2 | a0001c0002t0001g0273 a0018c0016t0003g0257 |
2 | HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.786-8561_786-8542d others(22): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4374086 | |||||||
| chr16:4374142 | G | A | 1 | a0002c0001t0001g0173 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.786-8597C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4374142 | |||||||
| chr16:4374260 | C | T | 1 | a0001c0002t0001g0101 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.786-8715G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4374260 | |||||||
| chr16:4374300 | C | T | 1 | a0002c0001t0001g0250 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.786-8755G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4374300 | |||||||
| chr16:4374321 | C | T | 1 | a0019c0020t0002g0048 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.786-8776G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4374321 | |||||||
| chr16:4374387 | C | A | 1 | a0013c0015t0001g0126 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.786-8842G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4374387 | |||||||
| chr16:4374449 | C | T | 1 | a0001c0002t0002g0096 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.786-8904G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4374449 | |||||||
| chr16:4374540 | G | A | 2 | a0001c0002t0002g0039 a0001c0002t0002g0118 |
2 | HG01884.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.786-8995C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4374540 | |||||||
| chr16:4374551 | G | T | 1 | a0004c0005t0001g0255 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.786-9006C>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4374551 | |||||||
| chr16:4374680 | C | G | 1 | a0002c0001t0001g0175 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.786-9135G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4374680 | |||||||
| chr16:4374910 | G | C | 1 | a0001c0002t0002g0086 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.786-9365C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4374910 | |||||||
| chr16:4374915 | T | G | 1 | a0001c0002t0001g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.786-9370A>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4374915 | |||||||
| chr16:4374995 | C | G | 2 | a0001c0002t0001g0105 a0002c0001t0001g0176 |
2 | NA19055.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.786-9450G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4374995 | |||||||
| chr16:4375010 | G | A | 1 | a0002c0001t0001g0252 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.786-9465C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4375010 | |||||||
| chr16:4375073 | C | T | 1 | a0001c0002t0002g0057 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.786-9528G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4375073 | |||||||
| chr16:4375121 | C | T | 1 | a0001c0002t0002g0118 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.786-9576G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4375121 | |||||||
| chr16:4375440 | G | A | 1 | a0001c0002t0001g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.786-9895C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4375440 | |||||||
| chr16:4375491 | ATTC | A | 9 | a0001c0002t0001g0005 a0001c0002t0001g0022 a0001c0002t0001g0023 others(6): Show |
10 | HG00642.hp1 HG00738.hp1 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.786-9949_786-9947d others(5): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4375491 | |||||||
| chr16:4375527 | A | G | 188 | a0001c0002t0001g0005 a0001c0002t0001g0010 a0001c0002t0001g0021 others(185): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.786-9982T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4375527 | |||||||
| chr16:4375729 | C | T | 1 | a0001c0002t0002g0082 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.786-10184G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4375729 | |||||||
| chr16:4375730 | G | A | 2 | a0002c0001t0001g0195 a0002c0001t0002g0276 |
2 | HG01123.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.786-10185C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4375730 | |||||||
| chr16:4375783 | C | T | 1 | a0001c0002t0002g0067 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.786-10238G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4375783 | |||||||
| chr16:4376072 | C | T | 1 | a0002c0001t0001g0144 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.786-10527G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4376072 | |||||||
| chr16:4376107 | A | G | 1 | a0001c0002t0001g0029 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.786-10562T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4376107 | |||||||
| chr16:4376114 | G | A | 1 | a0001c0004t0001g0058 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.786-10569C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4376114 | |||||||
| chr16:4376188 | C | T | 1 | a0001c0002t0001g0273 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.786-10643G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4376188 | |||||||
| chr16:4376408 | C | T | 11 | a0001c0002t0001g0053 a0001c0004t0001g0008 a0001c0004t0001g0135 others(8): Show |
12 | HG01099.hp1 HG01891.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.786-10863G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4376408 | |||||||
| chr16:4376563 | T | G | 186 | a0001c0002t0001g0005 a0001c0002t0001g0010 a0001c0002t0001g0021 others(183): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.786-11018A>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4376563 | |||||||
| chr16:4376573 | G | A | 1 | a0002c0001t0001g0157 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.786-11028C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4376573 | |||||||
| chr16:4376761 | C | T | 1 | a0001c0002t0001g0026 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.786-11216G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4376761 | |||||||
| chr16:4377009 | G | C | 158 | a0001c0002t0001g0010 a0001c0002t0001g0021 a0001c0002t0001g0036 others(155): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.785+10977C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4377009 | |||||||
| chr16:4377142 | C | T | 11 | a0001c0002t0001g0053 a0001c0004t0001g0008 a0001c0004t0001g0135 others(8): Show |
12 | HG01099.hp1 HG01891.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.785+10844G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4377142 | |||||||
| chr16:4377214 | C | T | 1 | a0018c0016t0003g0257 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.785+10772G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4377214 | |||||||
| chr16:4377234 | T | A | 1 | a0004c0005t0002g0258 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.785+10752A>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4377234 | |||||||
| chr16:4377235 | C | A | 1 | a0004c0005t0002g0258 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.785+10751G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4377235 | |||||||
| chr16:4377429 | C | G | 9 | a0001c0002t0001g0021 a0001c0002t0001g0040 a0001c0002t0001g0041 others(6): Show |
11 | HG02280.hp1 HG02486.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.785+10557G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4377429 | |||||||
| chr16:4377443 | G | A | 13 | a0003c0003t0001g0016 a0003c0003t0001g0262 a0003c0003t0001g0263 others(10): Show |
14 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.785+10543C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4377443 | |||||||
| chr16:4377618 | G | A | 1 | a0001c0004t0001g0139 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.785+10368C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4377618 | |||||||
| chr16:4377736 | T | C | 1 | a0007c0021t0001g0034 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.785+10250A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4377736 | |||||||
| chr16:4377782 | A | C | 180 | a0001c0002t0001g0005 a0001c0002t0001g0021 a0001c0002t0001g0022 others(177): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.785+10204T>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4377782 | |||||||
| chr16:4377793 | G | A | 1 | a0001c0004t0001g0136 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.785+10193C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4377793 | |||||||
| chr16:4377796 | T | C | 2 | a0001c0002t0002g0082 a0001c0002t0002g0083 |
2 | HG02027.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.785+10190A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4377796 | |||||||
| chr16:4377824 | A | C | 1 | a0001c0002t0001g0059 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.785+10162T>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4377824 | |||||||
| chr16:4377860 | C | T | 9 | a0001c0002t0001g0053 a0001c0004t0001g0008 a0001c0004t0001g0135 others(6): Show |
10 | HG01099.hp1 HG01891.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.785+10126G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4377860 | |||||||
| chr16:4377929 | G | A | 1 | a0001c0004t0001g0138 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.785+10057C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4377929 | |||||||
| chr16:4377958 | C | T | 4 | a0001c0002t0001g0005 a0001c0002t0001g0023 a0001c0002t0001g0024 others(1): Show |
5 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.785+10028G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4377958 | |||||||
| chr16:4378132 | C | T | 1 | a0002c0001t0001g0163 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.785+9854G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4378132 | |||||||
| chr16:4378250 | G | A | 24 | a0001c0002t0001g0005 a0001c0002t0001g0022 a0001c0002t0001g0023 others(21): Show |
26 | HG00642.hp1 HG00738.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.785+9736C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4378250 | |||||||
| chr16:4378309 | C | T | 1 | a0003c0003t0001g0263 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.785+9677G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4378309 | |||||||
| chr16:4378328 | C | CGGCCACA others(23): Show |
2 | a0001c0002t0001g0147 a0001c0002t0001g0148 |
2 | HG01074.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.785+9628_785+9657d others(32): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4378328 | |||||||
| chr16:4378494 | T | C | 8 | a0002c0001t0001g0121 a0002c0001t0001g0122 a0002c0001t0001g0134 others(5): Show |
8 | HG02055.hp2 HG02258.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.785+9492A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4378494 | |||||||
| chr16:4378555 | C | T | 1 | a0001c0002t0001g0022 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.785+9431G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4378555 | |||||||
| chr16:4378652 | G | A | 1 | a0002c0001t0004g0189 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.785+9334C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4378652 | |||||||
| chr16:4378883 | G | A | 139 | a0001c0002t0001g0005 a0001c0002t0001g0007 a0001c0002t0001g0022 others(136): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.785+9103C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4378883 | |||||||
| chr16:4378961 | C | T | 2 | a0001c0002t0002g0049 a0001c0002t0002g0249 |
2 | NA18977.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.785+9025G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4378961 | |||||||
| chr16:4379106 | C | T | 133 | a0001c0002t0001g0021 a0001c0002t0001g0041 a0001c0002t0001g0051 others(130): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.785+8880G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4379106 | |||||||
| chr16:4379320 | T | G | 2 | a0001c0002t0001g0054 a0001c0002t0001g0055 |
2 | HG02071.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.785+8666A>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4379320 | |||||||
| chr16:4379324 | G | A | 2 | a0001c0002t0002g0050 a0001c0002t0002g0123 |
2 | HG02717.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.785+8662C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4379324 | |||||||
| chr16:4379392 | C | G | 176 | a0001c0002t0001g0005 a0001c0002t0001g0021 a0001c0002t0001g0022 others(173): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.785+8594G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4379392 | |||||||
| chr16:4379711 | C | T | 1 | a0002c0001t0001g0163 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.785+8275G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4379711 | |||||||
| chr16:4379730 | C | A | 1 | a0001c0002t0001g0078 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.785+8256G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4379730 | |||||||
| chr16:4379880 | T | TA | 140 | a0001c0002t0001g0010 a0001c0002t0001g0021 a0001c0002t0001g0040 others(137): Show |
151 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.785+8105dupT | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4379880 | |||||||
| chr16:4379880 | TA | T | 10 | a0001c0002t0001g0053 a0001c0002t0001g0107 a0001c0002t0001g0109 others(7): Show |
10 | HG01884.hp2 HG02622.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.785+8105delT | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4379880 | |||||||
| chr16:4379882 | A | C | 2 | a0001c0002t0001g0054 a0001c0002t0001g0055 |
2 | HG02071.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.785+8104T>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4379882 | |||||||
| chr16:4379901 | T | A | 1 | a0001c0002t0001g0273 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.785+8085A>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4379901 | |||||||
| chr16:4379916 | TGCATGGT others(5): Show |
T | 141 | a0001c0002t0001g0010 a0001c0002t0001g0021 a0001c0002t0001g0040 others(138): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.785+8058_785+8069d others(14): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4379916 | |||||||
| chr16:4380057 | C | CA | 8 | a0001c0002t0001g0055 a0001c0002t0001g0060 a0001c0002t0001g0107 others(5): Show |
9 | HG00280.hp2 HG01099.hp1 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.785+7928dupT | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4380057 | |||||||
| chr16:4380172 | C | G | 11 | a0001c0002t0001g0005 a0001c0002t0001g0022 a0001c0002t0001g0023 others(8): Show |
12 | HG00642.hp1 HG00738.hp1 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.785+7814G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4380172 | |||||||
| chr16:4380368 | C | T | 1 | a0001c0002t0001g0101 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.785+7618G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4380368 | |||||||
| chr16:4380369 | G | A | 1 | a0001c0002t0001g0169 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.785+7617C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4380369 | |||||||
| chr16:4380395 | G | A | 2 | a0002c0001t0001g0158 a0002c0001t0001g0190 |
2 | HG02735.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.785+7591C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4380395 | |||||||
| chr16:4380421 | C | T | 1 | a0001c0002t0001g0273 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.785+7565G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4380421 | |||||||
| chr16:4380480 | C | G | 11 | a0001c0002t0001g0005 a0001c0002t0001g0022 a0001c0002t0001g0023 others(8): Show |
12 | HG00642.hp1 HG00738.hp1 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.785+7506G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4380480 | |||||||
| chr16:4380630 | C | T | 1 | a0001c0002t0001g0101 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.785+7356G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4380630 | |||||||
| chr16:4380660 | C | T | 4 | a0001c0004t0001g0008 a0001c0004t0001g0135 a0001c0004t0001g0137 others(1): Show |
5 | HG02280.hp2 HG02886.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.785+7326G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4380660 | |||||||
| chr16:4380727 | C | T | 4 | a0001c0002t0001g0005 a0001c0002t0001g0023 a0001c0002t0001g0024 others(1): Show |
5 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.785+7259G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4380727 | |||||||
| chr16:4380909 | T | C | 1 | a0002c0001t0001g0221 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.785+7077A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4380909 | |||||||
| chr16:4380917 | C | T | 1 | a0002c0001t0001g0221 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.785+7069G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4380917 | |||||||
| chr16:4380955 | C | T | 1 | a0001c0002t0001g0169 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.785+7031G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4380955 | |||||||
| chr16:4381025 | G | T | 1 | a0001c0002t0001g0140 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.785+6961C>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4381025 | |||||||
| chr16:4381201 | A | G | 181 | a0001c0002t0001g0005 a0001c0002t0001g0010 a0001c0002t0001g0021 others(178): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.785+6785T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4381201 | |||||||
| chr16:4381255 | C | T | 1 | a0001c0002t0002g0057 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.785+6731G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4381255 | |||||||
| chr16:4381264 | C | T | 1 | a0002c0001t0001g0038 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.785+6722G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4381264 | |||||||
| chr16:4381359 | G | A | 6 | a0002c0001t0001g0162 a0002c0001t0001g0164 a0002c0001t0001g0165 others(3): Show |
6 | HG01106.hp2 HG01168.hp2 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.785+6627C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4381359 | |||||||
| chr16:4381372 | G | C | 4 | a0002c0001t0001g0047 a0002c0001t0001g0191 a0002c0001t0001g0208 others(1): Show |
4 | HG00140.hp1 HG00639.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.785+6614C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4381372 | |||||||
| chr16:4381464 | C | T | 1 | a0001c0002t0001g0108 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.785+6522G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4381464 | |||||||
| chr16:4381582 | C | T | 3 | a0001c0002t0001g0029 a0001c0002t0001g0032 a0001c0014t0001g0028 |
3 | HG01891.hp1 HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.785+6404G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4381582 | |||||||
| chr16:4381879 | C | T | 6 | a0001c0002t0001g0021 a0001c0002t0001g0040 a0001c0002t0001g0041 others(3): Show |
8 | HG02486.hp1 HG02922.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.785+6107G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4381879 | |||||||
| chr16:4381909 | C | T | 1 | a0002c0001t0001g0142 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.785+6077G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4381909 | |||||||
| chr16:4382028 | A | C | 181 | a0001c0002t0001g0005 a0001c0002t0001g0010 a0001c0002t0001g0021 others(178): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.785+5958T>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4382028 | |||||||
| chr16:4382163 | C | T | 1 | a0001c0002t0001g0100 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.785+5823G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4382163 | |||||||
| chr16:4382234 | C | G | 1 | a0002c0001t0001g0219 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.785+5752G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4382234 | |||||||
| chr16:4382467 | T | C | 2 | a0005c0007t0001g0044 a0005c0007t0001g0045 |
2 | HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.785+5519A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4382467 | |||||||
| chr16:4382506 | G | A | 1 | a0001c0002t0001g0273 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.785+5480C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4382506 | |||||||
| chr16:4382569 | C | T | 1 | a0001c0004t0001g0136 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.785+5417G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4382569 | |||||||
| chr16:4382643 | C | T | 1 | a0004c0005t0002g0258 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.785+5343G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4382643 | |||||||
| chr16:4382664 | C | T | 1 | a0002c0001t0001g0252 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.785+5322G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4382664 | |||||||
| chr16:4383015 | G | A | 17 | a0001c0002t0002g0265 a0003c0003t0001g0016 a0003c0003t0001g0259 others(14): Show |
18 | HG02280.hp1 HG02451.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.785+4971C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4383015 | |||||||
| chr16:4383170 | C | T | 1 | a0001c0002t0001g0053 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.785+4816G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4383170 | |||||||
| chr16:4383497 | T | C | 1 | a0001c0004t0001g0058 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.785+4489A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4383497 | |||||||
| chr16:4383602 | CA | C | 40 | a0001c0002t0001g0005 a0001c0002t0001g0022 a0001c0002t0001g0023 others(37): Show |
43 | HG00642.hp1 HG00738.hp1 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.785+4383delT | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4383602 | |||||||
| chr16:4383606 | GC | G | 147 | a0001c0002t0001g0010 a0001c0002t0001g0021 a0001c0002t0001g0040 others(144): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.785+4379delG | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4383606 | |||||||
| chr16:4383607 | C | G | 40 | a0001c0002t0001g0005 a0001c0002t0001g0022 a0001c0002t0001g0023 others(37): Show |
43 | HG00642.hp1 HG00738.hp1 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.785+4379G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4383607 | |||||||
| chr16:4383734 | A | G | 275 | a0001c0002t0001g0005 a0001c0002t0001g0007 a0001c0002t0001g0010 others(272): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.785+4252T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4383734 | |||||||
| chr16:4383779 | G | T | 7 | a0001c0002t0001g0198 a0002c0001t0001g0011 a0002c0001t0001g0012 others(4): Show |
9 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(6): Show |
intron_variant | MODIFIER | c.785+4207C>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4383779 | |||||||
| chr16:4383918 | G | C | 1 | a0001c0002t0002g0229 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.785+4068C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4383918 | |||||||
| chr16:4384197 | T | C | 187 | a0001c0002t0001g0005 a0001c0002t0001g0010 a0001c0002t0001g0021 others(184): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.785+3789A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4384197 | |||||||
| chr16:4384373 | G | A | 187 | a0001c0002t0001g0005 a0001c0002t0001g0010 a0001c0002t0001g0021 others(184): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.785+3613C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4384373 | |||||||
| chr16:4384475 | A | C | 5 | a0004c0005t0001g0254 a0004c0005t0001g0255 a0004c0005t0001g0256 others(2): Show |
5 | HG02895.hp2 HG02897.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.785+3511T>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4384475 | |||||||
| chr16:4384600 | G | A | 1 | a0002c0001t0001g0035 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.785+3386C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4384600 | |||||||
| chr16:4384694 | G | C | 5 | a0001c0002t0001g0090 a0001c0002t0001g0092 a0001c0002t0001g0132 others(2): Show |
5 | HG02258.hp2 HG02630.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.785+3292C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4384694 | |||||||
| chr16:4384706 | C | T | 1 | a0001c0002t0001g0140 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.785+3280G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4384706 | |||||||
| chr16:4384732 | T | A | 1 | a0001c0002t0001g0148 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.785+3254A>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4384732 | |||||||
| chr16:4384810 | C | T | 1 | a0002c0001t0001g0174 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.785+3176G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4384810 | |||||||
| chr16:4384871 | G | A | 1 | a0001c0002t0001g0273 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.785+3115C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4384871 | |||||||
| chr16:4385107 | C | T | 2 | a0001c0002t0002g0049 a0001c0002t0002g0249 |
2 | NA18977.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.785+2879G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4385107 | |||||||
| chr16:4385162 | G | C | 134 | a0001c0002t0001g0010 a0001c0002t0001g0051 a0001c0002t0001g0084 others(131): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.785+2824C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4385162 | |||||||
| chr16:4385356 | G | A | 2 | a0005c0007t0001g0044 a0005c0007t0001g0045 |
2 | HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.785+2630C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4385356 | |||||||
| chr16:4385379 | T | A | 1 | a0001c0002t0001g0103 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.785+2607A>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4385379 | |||||||
| chr16:4385556 | TG | T | 6 | a0001c0002t0001g0010 a0001c0002t0001g0147 a0001c0002t0001g0148 others(3): Show |
7 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.785+2429delC | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4385556 | |||||||
| chr16:4386278 | T | G | 1 | a0001c0002t0002g0076 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.785+1708A>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4386278 | |||||||
| chr16:4386380 | C | A | 1 | a0001c0002t0001g0092 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.785+1606G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4386380 | |||||||
| chr16:4386444 | A | G | 247 | a0001c0002t0001g0005 a0001c0002t0001g0007 a0001c0002t0001g0010 others(244): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.785+1542T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4386444 | |||||||
| chr16:4386551 | G | A | 5 | a0001c0002t0001g0104 a0001c0002t0001g0105 a0001c0002t0001g0111 others(2): Show |
7 | HG01074.hp1 HG01109.hp2 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.785+1435C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4386551 | |||||||
| chr16:4386577 | G | A | 19 | a0001c0002t0001g0005 a0001c0002t0001g0022 a0001c0002t0001g0023 others(16): Show |
21 | HG00642.hp1 HG00738.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.785+1409C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4386577 | |||||||
| chr16:4386706 | C | A | 5 | a0001c0002t0001g0090 a0001c0002t0001g0092 a0001c0002t0001g0132 others(2): Show |
5 | HG02258.hp2 HG02630.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.785+1280G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4386706 | |||||||
| chr16:4386780 | G | A | 1 | a0001c0002t0001g0033 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.785+1206C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4386780 | |||||||
| chr16:4386840 | G | A | 1 | a0001c0002t0001g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.785+1146C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4386840 | |||||||
| chr16:4386840 | G | C | 7 | a0001c0002t0001g0010 a0001c0002t0001g0147 a0001c0002t0001g0148 others(4): Show |
8 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.785+1146C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4386840 | |||||||
| chr16:4386902 | G | A | 1 | a0002c0001t0001g0178 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.785+1084C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4386902 | |||||||
| chr16:4387003 | A | G | 1 | a0001c0002t0001g0116 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.785+983T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4387003 | |||||||
| chr16:4387153 | C | T | 3 | a0001c0002t0002g0050 a0001c0002t0002g0123 a0001c0002t0002g0161 |
3 | HG02717.hp1 HG02976.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.785+833G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4387153 | |||||||
| chr16:4387253 | G | A | 2 | a0001c0002t0002g0085 a0001c0002t0002g0086 |
2 | HG03710.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.785+733C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4387253 | |||||||
| chr16:4387419 | G | A | 1 | a0002c0001t0001g0197 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.785+567C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4387419 | |||||||
| chr16:4387491 | G | A | 1 | a0001c0002t0001g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.785+495C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4387491 | |||||||
| chr16:4387523 | CCCACCTC others(5): Show |
C | 1 | a0002c0001t0001g0252 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.785+451_785+462del others(12): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4387523 | |||||||
| chr16:4387539 | C | T | 1 | a0001c0002t0001g0248 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.785+447G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4387539 | |||||||
| chr16:4387725 | C | T | 5 | a0004c0005t0001g0254 a0004c0005t0001g0255 a0004c0005t0001g0256 others(2): Show |
5 | HG02895.hp2 HG02897.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.785+261G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4387725 | |||||||
| chr16:4387824 | G | T | 20 | a0001c0002t0001g0088 a0001c0002t0002g0265 a0003c0003t0001g0016 others(17): Show |
21 | HG02280.hp1 HG02451.hp1 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.785+162C>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4387824 | |||||||
| chr16:4387830 | G | A | 4 | a0002c0001t0001g0181 a0002c0001t0001g0182 a0002c0001t0001g0226 others(1): Show |
4 | NA18969.hp2 NA18977.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.785+156C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4387830 | |||||||
| chr16:4387869 | G | T | 4 | a0001c0002t0001g0036 a0001c0002t0001g0053 a0001c0004t0001g0242 others(1): Show |
4 | HG01099.hp1 HG02622.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.785+117C>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4387869 | |||||||
| chr16:4388082 | G | A | 1 | a0002c0001t0001g0175 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.703-14C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 8/27 | chr16 | 4388082 | |||||||
| chr16:4388121 | C | T | 7 | a0001c0002t0001g0010 a0001c0002t0001g0147 a0001c0002t0001g0148 others(4): Show |
8 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.703-53G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 8/27 | chr16 | 4388121 | |||||||
| chr16:4388127 | G | C | 1 | a0002c0001t0001g0163 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.703-59C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 8/27 | chr16 | 4388127 | |||||||
| chr16:4388199 | G | A | 39 | a0001c0002t0001g0005 a0001c0002t0001g0022 a0001c0002t0001g0023 others(36): Show |
42 | HG00642.hp1 HG00738.hp1 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.703-131C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 8/27 | chr16 | 4388199 | |||||||
| chr16:4388201 | G | A | 5 | a0001c0002t0002g0265 a0003c0003t0001g0264 a0003c0003t0001g0266 others(2): Show |
5 | HG02451.hp2 HG02809.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.703-133C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 8/27 | chr16 | 4388201 | |||||||
| chr16:4388290 | C | T | 1 | a0001c0004t0001g0136 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.703-222G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 8/27 | chr16 | 4388290 | |||||||
| chr16:4388459 | C | G | 3 | a0001c0002t0001g0029 a0001c0002t0001g0032 a0001c0014t0001g0028 |
3 | HG01891.hp1 HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.702+86G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 8/27 | chr16 | 4388459 | |||||||
| chr16:4388460 | G | T | 3 | a0001c0002t0001g0029 a0001c0002t0001g0032 a0001c0014t0001g0028 |
3 | HG01891.hp1 HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.702+85C>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 8/27 | chr16 | 4388460 | |||||||
| chr16:4388785 | G | A | 1 | a0001c0002t0001g0106 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.616-154C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4388785 | |||||||
| chr16:4388793 | G | C | 4 | a0002c0001t0001g0181 a0002c0001t0001g0182 a0002c0001t0001g0226 others(1): Show |
4 | NA18969.hp2 NA18977.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.616-162C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4388793 | |||||||
| chr16:4388827 | G | A | 2 | a0001c0002t0001g0107 a0001c0002t0001g0113 |
2 | NA18948.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.616-196C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4388827 | |||||||
| chr16:4388948 | C | T | 1 | a0001c0002t0001g0129 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.616-317G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4388948 | |||||||
| chr16:4388949 | G | A | 1 | a0003c0003t0001g0266 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.616-318C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4388949 | |||||||
| chr16:4389010 | C | T | 1 | a0001c0002t0001g0116 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.616-379G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4389010 | |||||||
| chr16:4389028 | C | A | 1 | a0001c0002t0001g0023 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.616-397G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4389028 | |||||||
| chr16:4389057 | G | A | 1 | a0002c0001t0001g0219 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.616-426C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4389057 | |||||||
| chr16:4389130 | C | T | 181 | a0001c0002t0001g0005 a0001c0002t0001g0010 a0001c0002t0001g0021 others(178): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.616-499G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4389130 | |||||||
| chr16:4389208 | G | A | 131 | a0001c0002t0001g0010 a0001c0002t0001g0021 a0001c0002t0001g0040 others(128): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.616-577C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4389208 | |||||||
| chr16:4389542 | G | A | 5 | a0004c0005t0001g0254 a0004c0005t0001g0255 a0004c0005t0001g0256 others(2): Show |
5 | HG02895.hp2 HG02897.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.616-911C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4389542 | |||||||
| chr16:4389677 | G | T | 2 | a0005c0007t0001g0044 a0005c0007t0001g0045 |
2 | HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.616-1046C>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4389677 | |||||||
| chr16:4389760 | C | T | 1 | a0001c0002t0001g0099 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.616-1129G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4389760 | |||||||
| chr16:4389772 | C | G | 2 | a0002c0001t0001g0164 a0002c0001t0001g0165 |
2 | HG01106.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.616-1141G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4389772 | |||||||
| chr16:4389957 | G | T | 2 | a0001c0002t0001g0078 a0001c0002t0002g0077 |
2 | HG01515.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.616-1326C>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4389957 | |||||||
| chr16:4390054 | A | C | 1 | a0001c0002t0001g0053 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.616-1423T>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4390054 | |||||||
| chr16:4390071 | T | C | 13 | a0002c0001t0001g0009 a0002c0001t0001g0063 a0002c0001t0001g0065 others(10): Show |
14 | HG00423.hp2 HG00597.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.616-1440A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4390071 | |||||||
| chr16:4390284 | A | G | 2 | a0001c0002t0001g0054 a0001c0002t0001g0055 |
2 | HG02071.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.616-1653T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4390284 | |||||||
| chr16:4390396 | G | C | 130 | a0001c0002t0001g0010 a0001c0002t0001g0051 a0001c0002t0001g0147 others(127): Show |
139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.616-1765C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4390396 | |||||||
| chr16:4390425 | C | G | 186 | a0001c0002t0001g0005 a0001c0002t0001g0010 a0001c0002t0001g0021 others(183): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.616-1794G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4390425 | |||||||
| chr16:4390526 | A | G | 11 | a0001c0002t0001g0005 a0001c0002t0001g0022 a0001c0002t0001g0023 others(8): Show |
12 | HG00642.hp1 HG00738.hp1 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.616-1895T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4390526 | |||||||
| chr16:4390592 | C | T | 185 | a0001c0002t0001g0005 a0001c0002t0001g0010 a0001c0002t0001g0021 others(182): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.616-1961G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4390592 | |||||||
| chr16:4390670 | A | C | 1 | a0002c0001t0001g0065 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.616-2039T>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4390670 | |||||||
| chr16:4390744 | C | G | 51 | a0001c0002t0001g0005 a0001c0002t0001g0021 a0001c0002t0001g0022 others(48): Show |
56 | HG00642.hp1 HG00738.hp1 HG01070.hp1 others(53): Show |
intron_variant | MODIFIER | c.616-2113G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4390744 | |||||||
| chr16:4390810 | C | T | 2 | a0001c0002t0001g0273 a0001c0002t0002g0076 |
2 | HG02559.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.616-2179G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4390810 | |||||||
| chr16:4390827 | G | A | 6 | a0001c0002t0001g0021 a0001c0002t0001g0040 a0001c0002t0001g0041 others(3): Show |
8 | HG02486.hp1 HG02922.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.616-2196C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4390827 | |||||||
| chr16:4391031 | T | G | 11 | a0001c0002t0001g0005 a0001c0002t0001g0022 a0001c0002t0001g0023 others(8): Show |
12 | HG00642.hp1 HG00738.hp1 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.616-2400A>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4391031 | |||||||
| chr16:4391081 | C | T | 14 | a0001c0002t0001g0021 a0001c0002t0001g0040 a0001c0002t0001g0041 others(11): Show |
16 | HG02486.hp1 HG02895.hp2 HG02897.hp1 others(13): Show |
intron_variant | MODIFIER | c.616-2450G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4391081 | |||||||
| chr16:4391143 | G | C | 2 | a0005c0007t0001g0044 a0005c0007t0001g0045 |
2 | HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.616-2512C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4391143 | |||||||
| chr16:4391201 | C | T | 1 | a0003c0003t0001g0268 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.616-2570G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4391201 | |||||||
| chr16:4391507 | G | C | 1 | a0001c0002t0001g0150 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.616-2876C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4391507 | |||||||
| chr16:4391616 | A | C | 154 | a0001c0002t0001g0005 a0001c0002t0001g0010 a0001c0002t0001g0022 others(151): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.616-2985T>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4391616 | |||||||
| chr16:4391680 | G | A | 1 | a0010c0012t0001g0194 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.616-3049C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4391680 | |||||||
| chr16:4391710 | G | A | 1 | a0001c0002t0001g0273 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.616-3079C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4391710 | |||||||
| chr16:4391769 | C | A | 1 | a0006c0009t0001g0246 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.616-3138G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4391769 | |||||||
| chr16:4391916 | A | G | 1 | a0001c0002t0002g0074 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.616-3285T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4391916 | |||||||
| chr16:4391937 | G | A | 2 | a0001c0002t0001g0053 a0001c0004t0001g0242 |
2 | HG02622.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.616-3306C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4391937 | |||||||
| chr16:4391963 | C | A | 5 | a0004c0005t0001g0254 a0004c0005t0001g0255 a0004c0005t0001g0256 others(2): Show |
5 | HG02895.hp2 HG02897.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.615+3326G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4391963 | |||||||
| chr16:4392117 | C | A | 1 | a0002c0001t0001g0020 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.615+3172G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4392117 | |||||||
| chr16:4392147 | G | A | 14 | a0001c0002t0002g0265 a0003c0003t0001g0016 a0003c0003t0001g0262 others(11): Show |
15 | HG02451.hp1 HG02451.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.615+3142C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4392147 | |||||||
| chr16:4392260 | G | A | 2 | a0005c0007t0001g0044 a0005c0007t0001g0045 |
2 | HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.615+3029C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4392260 | |||||||
| chr16:4392526 | C | T | 123 | a0001c0002t0001g0198 a0002c0001t0001g0004 a0002c0001t0001g0009 others(120): Show |
131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.615+2763G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4392526 | |||||||
| chr16:4392625 | C | T | 1 | a0001c0002t0001g0098 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.615+2664G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4392625 | |||||||
| chr16:4392710 | C | T | 1 | a0002c0001t0001g0204 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.615+2579G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4392710 | |||||||
| chr16:4392950 | A | G | 3 | a0001c0002t0001g0053 a0001c0004t0001g0242 a0007c0021t0001g0034 |
3 | HG01099.hp1 HG02622.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.615+2339T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4392950 | |||||||
| chr16:4392974 | C | T | 1 | a0007c0021t0001g0034 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.615+2315G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4392974 | |||||||
| chr16:4393050 | A | C | 1 | a0017c0008t0002g0061 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.615+2239T>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4393050 | |||||||
| chr16:4393058 | G | A | 3 | a0001c0002t0001g0053 a0001c0004t0001g0242 a0007c0021t0001g0034 |
3 | HG01099.hp1 HG02622.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.615+2231C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4393058 | |||||||
| chr16:4393064 | G | C | 1 | a0002c0001t0001g0122 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.615+2225C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4393064 | |||||||
| chr16:4393164 | C | A | 6 | a0001c0002t0001g0010 a0001c0002t0001g0147 a0001c0002t0001g0148 others(3): Show |
7 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.615+2125G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4393164 | |||||||
| chr16:4393168 | A | G | 1 | a0001c0002t0001g0110 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.615+2121T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4393168 | |||||||
| chr16:4393249 | T | C | 186 | a0001c0002t0001g0005 a0001c0002t0001g0010 a0001c0002t0001g0021 others(183): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.615+2040A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4393249 | |||||||
| chr16:4393372 | T | C | 2 | a0001c0002t0001g0053 a0001c0004t0001g0242 |
2 | HG02622.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.615+1917A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4393372 | |||||||
| chr16:4393491 | G | C | 4 | a0002c0001t0001g0181 a0002c0001t0001g0182 a0002c0001t0001g0226 others(1): Show |
4 | NA18969.hp2 NA18977.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.615+1798C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4393491 | |||||||
| chr16:4393541 | C | T | 37 | a0001c0002t0001g0005 a0001c0002t0001g0022 a0001c0002t0001g0023 others(34): Show |
40 | HG00642.hp1 HG00738.hp1 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.615+1748G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4393541 | |||||||
| chr16:4393567 | C | A | 2 | a0005c0007t0001g0044 a0005c0007t0001g0045 |
2 | HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.615+1722G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4393567 | |||||||
| chr16:4393626 | T | A | 2 | a0001c0002t0001g0053 a0001c0004t0001g0242 |
2 | HG02622.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.615+1663A>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4393626 | |||||||
| chr16:4393829 | G | A | 1 | a0002c0001t0001g0233 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.615+1460C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4393829 | |||||||
| chr16:4393915 | A | G | 1 | a0001c0002t0001g0140 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.615+1374T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4393915 | |||||||
| chr16:4393925 | C | A | 1 | a0001c0002t0001g0030 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.615+1364G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4393925 | |||||||
| chr16:4393928 | G | A | 14 | a0001c0002t0002g0265 a0003c0003t0001g0016 a0003c0003t0001g0262 others(11): Show |
15 | HG02451.hp1 HG02451.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.615+1361C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4393928 | |||||||
| chr16:4393966 | T | C | 5 | a0001c0002t0002g0002 a0001c0002t0002g0087 a0001c0002t0002g0243 others(2): Show |
7 | HG02109.hp1 HG02145.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.615+1323A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4393966 | |||||||
| chr16:4394032 | C | T | 2 | a0001c0002t0001g0147 a0001c0002t0001g0148 |
2 | HG01074.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.615+1257G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4394032 | |||||||
| chr16:4394043 | G | T | 1 | a0001c0002t0001g0273 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.615+1246C>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4394043 | |||||||
| chr16:4394134 | C | T | 1 | a0001c0002t0002g0002 | 3 | HG02109.hp1 HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.615+1155G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4394134 | |||||||
| chr16:4394155 | C | T | 1 | a0002c0001t0001g0020 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.615+1134G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4394155 | |||||||
| chr16:4394217 | G | A | 19 | a0001c0002t0001g0005 a0001c0002t0001g0022 a0001c0002t0001g0023 others(16): Show |
21 | HG00642.hp1 HG00738.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.615+1072C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4394217 | |||||||
| chr16:4394238 | G | A | 5 | a0004c0005t0001g0254 a0004c0005t0001g0255 a0004c0005t0001g0256 others(2): Show |
5 | HG02895.hp2 HG02897.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.615+1051C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4394238 | |||||||
| chr16:4394242 | G | A | 8 | a0001c0002t0001g0021 a0001c0002t0001g0040 a0001c0004t0001g0001 others(5): Show |
10 | HG02280.hp1 HG02486.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.615+1047C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4394242 | |||||||
| chr16:4394247 | C | T | 1 | a0001c0002t0001g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.615+1042G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4394247 | |||||||
| chr16:4394317 | C | T | 1 | a0001c0002t0001g0062 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.615+972G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4394317 | |||||||
| chr16:4394318 | G | A | 1 | a0001c0002t0002g0069 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.615+971C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4394318 | |||||||
| chr16:4394380 | C | T | 5 | a0004c0005t0001g0254 a0004c0005t0001g0255 a0004c0005t0001g0256 others(2): Show |
5 | HG02895.hp2 HG02897.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.615+909G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4394380 | |||||||
| chr16:4394435 | C | T | 3 | a0001c0002t0001g0075 a0001c0002t0002g0052 a0001c0002t0002g0074 |
3 | NA18944.hp2 NA18998.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.615+854G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4394435 | |||||||
| chr16:4394448 | C | CA | 25 | a0001c0002t0001g0095 a0001c0002t0001g0108 a0001c0002t0001g0109 others(22): Show |
26 | HG00597.hp2 HG00735.hp2 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.615+840dupT | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4394448 | |||||||
| chr16:4394448 | CA | C | 8 | a0001c0002t0002g0124 a0002c0001t0001g0073 a0002c0001t0001g0149 others(5): Show |
8 | HG02630.hp2 HG02895.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.615+840delT | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4394448 | |||||||
| chr16:4394465 | A | C | 5 | a0003c0003t0001g0016 a0003c0003t0001g0268 a0003c0003t0001g0269 others(2): Show |
6 | HG02451.hp1 HG02559.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.615+824T>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4394465 | |||||||
| chr16:4395024 | T | C | 1 | a0001c0002t0001g0054 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.615+265A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4395024 | |||||||
| chr16:4395218 | C | T | 1 | a0001c0002t0002g0006 | 2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.615+71G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4395218 | |||||||
| chr16:4395452 | C | T | 2 | a0001c0002t0002g0056 a0001c0002t0002g0057 |
2 | HG01934.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.565-113G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4395452 | |||||||
| chr16:4395477 | G | C | 2 | a0005c0007t0001g0044 a0005c0007t0001g0045 |
2 | HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.565-138C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4395477 | |||||||
| chr16:4395485 | C | T | 1 | a0001c0002t0001g0088 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.565-146G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4395485 | |||||||
| chr16:4395587 | T | C | 1 | a0001c0002t0001g0273 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.565-248A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4395587 | |||||||
| chr16:4395795 | C | T | 1 | a0001c0002t0001g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.565-456G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4395795 | |||||||
| chr16:4395908 | A | C | 1 | a0007c0021t0001g0034 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.565-569T>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4395908 | |||||||
| chr16:4395927 | C | T | 1 | a0001c0002t0001g0140 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.565-588G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4395927 | |||||||
| chr16:4395975 | A | ATGTG | 186 | a0001c0002t0001g0005 a0001c0002t0001g0010 a0001c0002t0001g0021 others(183): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.565-640_565-637dup others(4): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4395975 | |||||||
| chr16:4395995 | G | A | 3 | a0002c0001t0001g0009 a0002c0001t0001g0142 a0002c0001t0001g0212 |
4 | HG00423.hp2 NA18998.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.565-656C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4395995 | |||||||
| chr16:4395996 | T | TGTGTG | 8 | a0001c0002t0001g0133 a0001c0002t0001g0140 a0001c0004t0001g0008 others(5): Show |
9 | HG01243.hp2 HG01891.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.565-658_565-657ins others(5): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4395996 | |||||||
| chr16:4395996 | T | TGTGTGTG others(2): Show |
15 | a0001c0002t0001g0005 a0001c0002t0001g0022 a0001c0002t0001g0023 others(12): Show |
16 | HG00642.hp1 HG00738.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.565-658_565-657ins others(9): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4395996 | |||||||
| chr16:4395996 | T | TGTGTGTG others(4): Show |
10 | a0001c0002t0001g0041 a0001c0004t0001g0001 a0001c0004t0001g0043 others(7): Show |
12 | HG01099.hp1 HG01243.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.565-658_565-657ins others(11): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4395996 | |||||||
| chr16:4395996 | T | TGTGTGTG others(6): Show |
137 | a0001c0002t0001g0010 a0001c0002t0001g0021 a0001c0002t0001g0036 others(134): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.565-658_565-657ins others(13): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4395996 | |||||||
| chr16:4395996 | T | TGTGTGTG others(8): Show |
13 | a0002c0001t0001g0071 a0002c0001t0001g0121 a0002c0001t0001g0122 others(10): Show |
13 | HG01258.hp2 HG02055.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.565-658_565-657ins others(15): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4395996 | |||||||
| chr16:4395996 | T | TGTGTGTG others(10): Show |
1 | a0004c0005t0002g0258 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.565-658_565-657ins others(17): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4395996 | |||||||
| chr16:4395996 | T | TGTGTGTG others(14): Show |
1 | a0002c0001t0001g0214 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.565-658_565-657ins others(21): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4395996 | |||||||
| chr16:4395996 | T | TGTGTGTG others(16): Show |
1 | a0001c0002t0001g0273 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.565-658_565-657ins others(23): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4395996 | |||||||
| chr16:4396011 | T | TAC | 7 | a0001c0002t0001g0021 a0001c0002t0001g0040 a0001c0002t0001g0041 others(4): Show |
9 | HG02486.hp1 HG02922.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.565-674_565-673dup others(2): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4396011 | |||||||
| chr16:4396225 | G | T | 1 | a0001c0002t0002g0243 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.565-886C>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4396225 | |||||||
| chr16:4396468 | T | G | 1 | a0012c0024t0005g0277 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.565-1129A>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4396468 | |||||||
| chr16:4396552 | G | A | 7 | a0001c0002t0001g0021 a0001c0002t0001g0040 a0001c0002t0001g0041 others(4): Show |
9 | HG02486.hp1 HG02922.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.565-1213C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4396552 | |||||||
| chr16:4396634 | C | T | 1 | a0001c0002t0001g0113 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.565-1295G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4396634 | |||||||
| chr16:4396775 | C | T | 1 | a0001c0002t0002g0031 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.565-1436G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4396775 | |||||||
| chr16:4396894 | T | A | 11 | a0001c0002t0001g0005 a0001c0002t0001g0022 a0001c0002t0001g0023 others(8): Show |
12 | HG00642.hp1 HG00738.hp1 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.565-1555A>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4396894 | |||||||
| chr16:4396915 | C | T | 1 | a0001c0002t0001g0248 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.565-1576G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4396915 | |||||||
| chr16:4397015 | C | CA | 24 | a0001c0002t0001g0053 a0001c0002t0001g0111 a0001c0002t0002g0003 others(21): Show |
27 | HG00642.hp2 HG01074.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.565-1677dupT | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4397015 | |||||||
| chr16:4397030 | AG | A | 7 | a0001c0002t0001g0025 a0001c0004t0001g0043 a0002c0001t0001g0141 others(4): Show |
7 | HG01069.hp2 HG01070.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.565-1692delC | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4397030 | |||||||
| chr16:4397031 | G | A | 177 | a0001c0002t0001g0005 a0001c0002t0001g0010 a0001c0002t0001g0021 others(174): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.565-1692C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4397031 | |||||||
| chr16:4397215 | G | A | 17 | a0001c0002t0002g0265 a0003c0003t0001g0016 a0003c0003t0001g0259 others(14): Show |
18 | HG02280.hp1 HG02451.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.565-1876C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4397215 | |||||||
| chr16:4397300 | G | A | 1 | a0007c0021t0001g0034 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.565-1961C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4397300 | |||||||
| chr16:4397336 | G | A | 1 | a0001c0002t0001g0273 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.565-1997C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4397336 | |||||||
| chr16:4397476 | G | A | 186 | a0001c0002t0001g0005 a0001c0002t0001g0010 a0001c0002t0001g0021 others(183): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.565-2137C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4397476 | |||||||
| chr16:4397551 | C | A | 188 | a0001c0002t0001g0005 a0001c0002t0001g0010 a0001c0002t0001g0021 others(185): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.565-2212G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4397551 | |||||||
| chr16:4397567 | C | T | 1 | a0001c0002t0001g0273 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.565-2228G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4397567 | |||||||
| chr16:4397578 | C | T | 4 | a0001c0002t0001g0053 a0001c0004t0001g0242 a0007c0021t0001g0034 others(1): Show |
4 | HG01099.hp1 HG02622.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.565-2239G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4397578 | |||||||
| chr16:4397582 | A | G | 1 | a0001c0002t0001g0273 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.565-2243T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4397582 | |||||||
| chr16:4397677 | G | A | 17 | a0001c0002t0002g0265 a0003c0003t0001g0016 a0003c0003t0001g0259 others(14): Show |
18 | HG02280.hp1 HG02451.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.565-2338C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4397677 | |||||||
| chr16:4397683 | G | A | 1 | a0001c0002t0001g0033 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.565-2344C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4397683 | |||||||
| chr16:4397738 | C | A | 1 | a0001c0002t0001g0273 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.565-2399G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4397738 | |||||||
| chr16:4397770 | C | T | 136 | a0001c0002t0001g0010 a0001c0002t0001g0021 a0001c0002t0001g0040 others(133): Show |
147 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.565-2431G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4397770 | |||||||
| chr16:4397939 | CAG | C | 3 | a0001c0002t0001g0053 a0001c0004t0001g0242 a0007c0021t0001g0034 |
3 | HG01099.hp1 HG02622.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.565-2602_565-2601d others(4): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4397939 | |||||||
| chr16:4397947 | C | T | 1 | a0001c0002t0002g0052 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.565-2608G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4397947 | |||||||
| chr16:4397956 | G | A | 4 | a0002c0001t0001g0156 a0002c0001t0001g0202 a0002c0001t0001g0206 others(1): Show |
4 | HG01258.hp2 HG01346.hp1 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.565-2617C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4397956 | |||||||
| chr16:4397969 | C | T | 275 | a0001c0002t0001g0005 a0001c0002t0001g0007 a0001c0002t0001g0010 others(272): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.565-2630G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4397969 | |||||||
| chr16:4397985 | C | T | 1 | a0002c0001t0001g0220 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.565-2646G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4397985 | |||||||
| chr16:4398074 | C | T | 1 | a0001c0002t0002g0074 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.565-2735G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4398074 | |||||||
| chr16:4398247 | T | C | 1 | a0002c0001t0001g0230 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.565-2908A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4398247 | |||||||
| chr16:4398266 | T | A | 1 | a0002c0001t0001g0203 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.565-2927A>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4398266 | |||||||
| chr16:4398389 | C | T | 3 | a0001c0002t0001g0029 a0001c0002t0001g0032 a0001c0014t0001g0028 |
3 | HG01891.hp1 HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.565-3050G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4398389 | |||||||
| chr16:4398436 | G | C | 1 | a0002c0001t0001g0204 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.565-3097C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4398436 | |||||||
| chr16:4398495 | G | A | 31 | a0001c0002t0001g0007 a0001c0002t0001g0051 a0001c0002t0001g0059 others(28): Show |
34 | HG00140.hp2 HG00423.hp1 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.565-3156C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4398495 | |||||||
| chr16:4398526 | C | T | 1 | a0012c0024t0005g0277 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.565-3187G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4398526 | |||||||
| chr16:4398561 | G | A | 7 | a0001c0002t0001g0133 a0001c0002t0001g0140 a0001c0004t0001g0008 others(4): Show |
8 | HG01243.hp2 HG02280.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.565-3222C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4398561 | |||||||
| chr16:4398652 | C | T | 36 | a0001c0002t0001g0005 a0001c0002t0001g0022 a0001c0002t0001g0023 others(33): Show |
39 | HG00642.hp1 HG00738.hp1 HG01070.hp1 others(36): Show |
intron_variant | MODIFIER | c.565-3313G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4398652 | |||||||
| chr16:4398665 | G | GA | 6 | a0001c0002t0001g0059 a0001c0002t0001g0095 a0001c0002t0001g0110 others(3): Show |
6 | HG00544.hp2 HG00741.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.565-3327dupT | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4398665 | |||||||
| chr16:4398665 | GA | G | 7 | a0001c0002t0001g0036 a0001c0002t0002g0064 a0001c0004t0001g0139 others(4): Show |
7 | HG00673.hp2 HG01891.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.565-3327delT | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4398665 | |||||||
| chr16:4398697 | T | TGGTGGCT others(136): Show |
1 | a0007c0021t0001g0034 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.565-3359_565-3358i others(145): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4398697 | |||||||
| chr16:4398727 | G | T | 4 | a0001c0002t0001g0053 a0001c0004t0001g0242 a0007c0021t0001g0034 others(1): Show |
4 | HG01099.hp1 HG02622.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.565-3388C>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4398727 | |||||||
| chr16:4398925 | A | G | 1 | a0012c0024t0005g0277 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.565-3586T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4398925 | |||||||
| chr16:4398967 | C | CA | 13 | a0001c0002t0001g0036 a0001c0002t0001g0053 a0001c0002t0002g0049 others(10): Show |
13 | HG01934.hp2 HG02615.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.565-3629dupT | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4398967 | |||||||
| chr16:4399021 | C | T | 1 | a0002c0001t0001g0176 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.565-3682G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4399021 | |||||||
| chr16:4399132 | C | T | 1 | a0018c0016t0003g0257 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.565-3793G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4399132 | |||||||
| chr16:4399321 | G | A | 5 | a0001c0002t0002g0118 a0004c0005t0001g0254 a0004c0005t0001g0255 others(2): Show |
5 | HG02895.hp2 HG02897.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.565-3982C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4399321 | |||||||
| chr16:4399489 | C | T | 2 | a0001c0002t0002g0114 a0001c0002t0002g0118 |
2 | NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.565-4150G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4399489 | |||||||
| chr16:4399723 | G | A | 1 | a0012c0024t0005g0277 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.565-4384C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4399723 | |||||||
| chr16:4399884 | C | A | 1 | a0001c0002t0002g0093 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.565-4545G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4399884 | |||||||
| chr16:4399902 | G | T | 2 | a0004c0005t0002g0258 a0018c0016t0003g0257 |
2 | HG03130.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.565-4563C>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4399902 | |||||||
| chr16:4400008 | C | T | 1 | a0012c0024t0005g0277 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.565-4669G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4400008 | |||||||
| chr16:4400033 | C | T | 1 | a0001c0002t0001g0248 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.565-4694G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4400033 | |||||||
| chr16:4400145 | C | T | 1 | a0002c0001t0001g0230 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.565-4806G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4400145 | |||||||
| chr16:4400420 | T | G | 178 | a0001c0002t0001g0005 a0001c0002t0001g0010 a0001c0002t0001g0021 others(175): Show |
192 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.564+5071A>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4400420 | |||||||
| chr16:4400519 | G | A | 37 | a0001c0002t0001g0005 a0001c0002t0001g0022 a0001c0002t0001g0023 others(34): Show |
40 | HG00642.hp1 HG00738.hp1 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.564+4972C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4400519 | |||||||
| chr16:4400632 | TCAAAAAC others(5): Show |
T | 1 | a0001c0002t0002g0039 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.564+4847_564+4858d others(14): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4400632 | |||||||
| chr16:4400665 | C | CA | 39 | a0001c0002t0001g0005 a0001c0002t0001g0022 a0001c0002t0001g0023 others(36): Show |
42 | HG00642.hp1 HG00738.hp1 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.564+4825dupT | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4400665 | |||||||
| chr16:4400679 | G | C | 2 | a0001c0002t0001g0111 a0001c0002t0002g0003 |
4 | HG01074.hp1 HG01109.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.564+4812C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4400679 | |||||||
| chr16:4400757 | T | C | 2 | a0001c0002t0001g0036 a0001c0002t0001g0053 |
2 | HG03098.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.564+4734A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4400757 | |||||||
| chr16:4400797 | C | CAAT | 25 | a0001c0002t0001g0029 a0001c0002t0001g0032 a0001c0002t0002g0049 others(22): Show |
25 | HG00423.hp2 HG01516.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.564+4691_564+4693d others(5): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4400797 | |||||||
| chr16:4400797 | C | CAATAAT | 23 | a0001c0002t0001g0010 a0001c0002t0001g0152 a0001c0002t0001g0153 others(20): Show |
25 | HG00099.hp2 HG00639.hp1 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.564+4688_564+4693d others(8): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4400797 | |||||||
| chr16:4400797 | C | CAATAATA others(2): Show |
96 | a0001c0002t0001g0005 a0001c0002t0001g0021 a0001c0002t0001g0040 others(93): Show |
105 | HG00280.hp1 HG00597.hp1 HG00639.hp2 others(102): Show |
intron_variant | MODIFIER | c.564+4685_564+4693d others(11): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4400797 | |||||||
| chr16:4400797 | C | CAATAATA others(5): Show |
33 | a0001c0002t0001g0024 a0001c0002t0001g0025 a0001c0002t0001g0026 others(30): Show |
35 | HG00280.hp2 HG00544.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.564+4682_564+4693d others(14): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4400797 | |||||||
| chr16:4400797 | C | CAATAATA others(8): Show |
8 | a0001c0002t0001g0022 a0001c0002t0001g0023 a0001c0002t0001g0030 others(5): Show |
9 | HG00642.hp1 HG01074.hp2 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.564+4679_564+4693d others(17): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4400797 | |||||||
| chr16:4400797 | C | CAATAATA others(11): Show |
2 | a0003c0003t0001g0262 a0003c0003t0001g0263 |
2 | HG02615.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.564+4676_564+4693d others(20): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4400797 | |||||||
| chr16:4400999 | C | T | 1 | a0012c0024t0005g0277 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.564+4492G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4400999 | |||||||
| chr16:4401023 | C | T | 1 | a0001c0002t0001g0090 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.564+4468G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4401023 | |||||||
| chr16:4401026 | A | C | 1 | a0012c0024t0005g0277 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.564+4465T>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4401026 | |||||||
| chr16:4401039 | T | G | 1 | a0002c0001t0001g0208 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.564+4452A>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4401039 | |||||||
| chr16:4401079 | G | A | 1 | a0001c0002t0002g0039 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.564+4412C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4401079 | |||||||
| chr16:4401140 | C | T | 1 | a0001c0002t0001g0119 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.564+4351G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4401140 | |||||||
| chr16:4401154 | T | C | 1 | a0001c0002t0001g0021 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.564+4337A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4401154 | |||||||
| chr16:4401228 | G | A | 1 | a0002c0001t0001g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.564+4263C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4401228 | |||||||
| chr16:4401298 | G | A | 2 | a0001c0002t0001g0036 a0001c0002t0001g0053 |
2 | HG03098.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.564+4193C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4401298 | |||||||
| chr16:4401319 | C | T | 1 | a0001c0002t0001g0029 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.564+4172G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4401319 | |||||||
| chr16:4401337 | T | C | 1 | a0001c0002t0001g0113 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.564+4154A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4401337 | |||||||
| chr16:4401664 | C | T | 2 | a0002c0001t0001g0176 a0012c0024t0005g0277 |
2 | HG02922.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.564+3827G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4401664 | |||||||
| chr16:4401734 | G | C | 1 | a0001c0002t0002g0039 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.564+3757C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4401734 | |||||||
| chr16:4401911 | C | CT | 43 | a0001c0002t0001g0005 a0001c0002t0001g0022 a0001c0002t0001g0023 others(40): Show |
47 | HG00544.hp1 HG00597.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.564+3579dupA | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4401911 | |||||||
| chr16:4402063 | C | T | 1 | a0014c0025t0001g0241 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.564+3428G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4402063 | |||||||
| chr16:4402140 | T | C | 2 | a0005c0007t0001g0044 a0005c0007t0001g0045 |
2 | HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.564+3351A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4402140 | |||||||
| chr16:4402241 | TTTGTTGT others(2): Show |
T | 22 | a0001c0002t0001g0005 a0001c0002t0001g0022 a0001c0002t0001g0023 others(19): Show |
24 | HG00642.hp1 HG00738.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.564+3241_564+3249d others(11): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4402241 | |||||||
| chr16:4402256 | G | C | 1 | a0012c0024t0005g0277 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.564+3235C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4402256 | |||||||
| chr16:4402265 | G | T | 1 | a0013c0015t0001g0126 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.564+3226C>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4402265 | |||||||
| chr16:4402321 | T | C | 2 | a0005c0007t0001g0044 a0005c0007t0001g0045 |
2 | HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.564+3170A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4402321 | |||||||
| chr16:4402327 | C | T | 1 | a0001c0002t0001g0147 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.564+3164G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4402327 | |||||||
| chr16:4402392 | G | A | 1 | a0001c0002t0001g0148 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.564+3099C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4402392 | |||||||
| chr16:4402482 | A | T | 1 | a0001c0002t0001g0062 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.564+3009T>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4402482 | |||||||
| chr16:4402528 | T | A | 1 | a0012c0024t0005g0277 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.564+2963A>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4402528 | |||||||
| chr16:4402583 | G | A | 89 | a0001c0002t0001g0198 a0001c0002t0001g0201 a0002c0001t0001g0004 others(86): Show |
95 | HG00280.hp2 HG00423.hp2 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.564+2908C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4402583 | |||||||
| chr16:4402598 | G | C | 2 | a0001c0002t0001g0151 a0001c0002t0001g0152 |
2 | HG03130.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.564+2893C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4402598 | |||||||
| chr16:4402757 | G | A | 1 | a0002c0001t0001g0209 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.564+2734C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4402757 | |||||||
| chr16:4402790 | C | T | 7 | a0002c0001t0001g0162 a0002c0001t0001g0163 a0002c0001t0001g0164 others(4): Show |
7 | HG01106.hp2 HG01168.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.564+2701G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4402790 | |||||||
| chr16:4402835 | G | A | 2 | a0002c0001t0001g0210 a0002c0001t0001g0250 |
2 | HG01884.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.564+2656C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4402835 | |||||||
| chr16:4402865 | T | A | 1 | a0007c0021t0001g0034 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.564+2626A>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4402865 | |||||||
| chr16:4403000 | T | C | 1 | a0001c0002t0002g0039 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.564+2491A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4403000 | |||||||
| chr16:4403065 | C | A | 6 | a0001c0002t0001g0090 a0001c0002t0001g0092 a0001c0002t0001g0132 others(3): Show |
6 | HG02055.hp1 HG02258.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.564+2426G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4403065 | |||||||
| chr16:4403087 | C | T | 2 | a0005c0007t0001g0044 a0005c0007t0001g0045 |
2 | HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.564+2404G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4403087 | |||||||
| chr16:4403096 | T | C | 2 | a0005c0007t0001g0044 a0005c0007t0001g0045 |
2 | HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.564+2395A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4403096 | |||||||
| chr16:4403253 | C | T | 1 | a0012c0024t0005g0277 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.564+2238G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4403253 | |||||||
| chr16:4403278 | G | A | 1 | a0002c0001t0001g0211 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.564+2213C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4403278 | |||||||
| chr16:4403285 | T | A | 2 | a0001c0002t0001g0024 a0001c0002t0001g0025 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.564+2206A>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4403285 | |||||||
| chr16:4403308 | G | A | 1 | a0001c0002t0001g0140 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.564+2183C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4403308 | |||||||
| chr16:4403318 | C | G | 99 | a0001c0002t0001g0059 a0001c0002t0001g0169 a0001c0002t0001g0198 others(96): Show |
107 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.564+2173G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4403318 | |||||||
| chr16:4403351 | G | C | 130 | a0001c0002t0001g0005 a0001c0002t0001g0010 a0001c0002t0001g0022 others(127): Show |
141 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.564+2140C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4403351 | |||||||
| chr16:4403363 | C | T | 2 | a0001c0002t0001g0095 a0001c0002t0002g0094 |
2 | HG01255.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.564+2128G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4403363 | |||||||
| chr16:4403436 | C | G | 5 | a0004c0005t0001g0254 a0004c0005t0001g0255 a0004c0005t0001g0256 others(2): Show |
5 | HG02895.hp2 HG02897.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.564+2055G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4403436 | |||||||
| chr16:4403526 | G | C | 1 | a0007c0021t0001g0034 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.564+1965C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4403526 | |||||||
| chr16:4403595 | G | C | 1 | a0002c0001t0001g0212 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.564+1896C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4403595 | |||||||
| chr16:4403713 | T | C | 10 | a0001c0002t0001g0022 a0001c0002t0001g0023 a0001c0002t0001g0024 others(7): Show |
10 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.564+1778A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4403713 | |||||||
| chr16:4403715 | G | A | 14 | a0001c0002t0002g0265 a0003c0003t0001g0016 a0003c0003t0001g0262 others(11): Show |
15 | HG02451.hp1 HG02451.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.564+1776C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4403715 | |||||||
| chr16:4403805 | G | C | 1 | a0001c0002t0002g0039 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.564+1686C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4403805 | |||||||
| chr16:4403941 | G | A | 15 | a0002c0001t0001g0213 a0002c0001t0001g0214 a0002c0001t0001g0215 others(12): Show |
15 | HG00544.hp2 HG02040.hp1 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.564+1550C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4403941 | |||||||
| chr16:4404135 | A | G | 2 | a0005c0007t0001g0044 a0005c0007t0001g0045 |
2 | HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.564+1356T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4404135 | |||||||
| chr16:4404167 | G | A | 1 | a0002c0001t0001g0143 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.564+1324C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4404167 | |||||||
| chr16:4404169 | A | G | 176 | a0001c0002t0001g0005 a0001c0002t0001g0010 a0001c0002t0001g0021 others(173): Show |
190 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.564+1322T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4404169 | |||||||
| chr16:4404443 | C | A | 1 | a0012c0024t0005g0277 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.564+1048G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4404443 | |||||||
| chr16:4404758 | C | T | 2 | a0004c0005t0001g0254 a0004c0005t0001g0256 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.564+733G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4404758 | |||||||
| chr16:4404813 | G | A | 1 | a0002c0001t0001g0221 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.564+678C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4404813 | |||||||
| chr16:4404911 | T | G | 1 | a0001c0002t0002g0093 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.564+580A>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4404911 | |||||||
| chr16:4405049 | A | T | 1 | a0012c0024t0005g0277 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.564+442T>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4405049 | |||||||
| chr16:4405107 | G | A | 37 | a0001c0002t0001g0007 a0001c0002t0001g0051 a0001c0002t0001g0059 others(34): Show |
40 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(37): Show |
intron_variant | MODIFIER | c.564+384C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4405107 | |||||||
| chr16:4405425 | C | A | 1 | a0002c0001t0001g0222 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.564+66G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4405425 | |||||||
| chr16:4405435 | C | T | 4 | a0001c0002t0001g0010 a0001c0002t0001g0147 a0001c0002t0001g0148 others(1): Show |
5 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.564+56G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4405435 | |||||||
| chr16:4405444 | G | A | 1 | a0001c0002t0002g0114 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.564+47C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4405444 | |||||||
| chr16:4405596 | C | T | 5 | a0001c0002t0001g0005 a0001c0002t0001g0022 a0001c0002t0001g0023 others(2): Show |
6 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.488-29G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4405596 | |||||||
| chr16:4405625 | G | T | 1 | a0012c0024t0005g0277 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.488-58C>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4405625 | |||||||
| chr16:4405646 | G | A | 2 | a0001c0002t0001g0036 a0001c0002t0001g0053 |
2 | HG03098.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.488-79C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4405646 | |||||||
| chr16:4405673 | C | A | 1 | a0012c0024t0005g0277 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.488-106G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4405673 | |||||||
| chr16:4405674 | G | A | 175 | a0001c0002t0001g0005 a0001c0002t0001g0010 a0001c0002t0001g0021 others(172): Show |
189 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.488-107C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4405674 | |||||||
| chr16:4405777 | ATCACTCA others(24): Show |
A | 3 | a0002c0001t0001g0014 a0002c0001t0001g0224 a0011c0011t0001g0223 |
4 | HG00280.hp2 HG02738.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.488-241_488-211del others(31): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4405777 | |||||||
| chr16:4405809 | C | A | 3 | a0002c0001t0001g0014 a0002c0001t0001g0224 a0011c0011t0001g0223 |
4 | HG00280.hp2 HG02738.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.488-242G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4405809 | |||||||
| chr16:4405812 | GCCT | G | 3 | a0002c0001t0001g0014 a0002c0001t0001g0224 a0011c0011t0001g0223 |
4 | HG00280.hp2 HG02738.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.488-248_488-246del others(3): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4405812 | |||||||
| chr16:4405816 | G | T | 3 | a0002c0001t0001g0014 a0002c0001t0001g0224 a0011c0011t0001g0223 |
4 | HG00280.hp2 HG02738.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.488-249C>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4405816 | |||||||
| chr16:4405819 | T | C | 3 | a0002c0001t0001g0014 a0002c0001t0001g0224 a0011c0011t0001g0223 |
4 | HG00280.hp2 HG02738.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.488-252A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4405819 | |||||||
| chr16:4405820 | C | A | 3 | a0002c0001t0001g0014 a0002c0001t0001g0224 a0011c0011t0001g0223 |
4 | HG00280.hp2 HG02738.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.488-253G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4405820 | |||||||
| chr16:4406085 | C | T | 1 | a0001c0002t0001g0060 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.488-518G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4406085 | |||||||
| chr16:4406116 | C | T | 1 | a0001c0002t0001g0273 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.488-549G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4406116 | |||||||
| chr16:4406117 | G | A | 1 | a0012c0024t0005g0277 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.488-550C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4406117 | |||||||
| chr16:4406188 | C | T | 1 | a0001c0002t0001g0059 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.488-621G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4406188 | |||||||
| chr16:4406189 | G | A | 20 | a0001c0002t0001g0273 a0001c0002t0002g0265 a0003c0003t0001g0016 others(17): Show |
21 | HG02451.hp1 HG02451.hp2 HG02559.hp2 others(18): Show |
intron_variant | MODIFIER | c.488-622C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4406189 | |||||||
| chr16:4406320 | G | A | 1 | a0001c0002t0001g0115 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.488-753C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4406320 | |||||||
| chr16:4406328 | C | T | 1 | a0002c0001t0001g0160 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.488-761G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4406328 | |||||||
| chr16:4406552 | G | T | 4 | a0004c0005t0001g0254 a0004c0005t0001g0256 a0004c0005t0002g0258 others(1): Show |
4 | HG02895.hp2 HG02897.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.487+949C>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4406552 | |||||||
| chr16:4406651 | A | T | 1 | a0012c0024t0005g0277 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.487+850T>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4406651 | |||||||
| chr16:4406689 | C | T | 1 | a0001c0014t0001g0028 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.487+812G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4406689 | |||||||
| chr16:4406700 | C | T | 2 | a0001c0002t0002g0049 a0001c0002t0002g0249 |
2 | NA18977.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.487+801G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4406700 | |||||||
| chr16:4406751 | T | C | 1 | a0012c0024t0005g0277 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.487+750A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4406751 | |||||||
| chr16:4406830 | G | A | 6 | a0001c0004t0001g0008 a0001c0004t0001g0135 a0001c0004t0001g0136 others(3): Show |
7 | HG02280.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.487+671C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4406830 | |||||||
| chr16:4406831 | C | T | 11 | a0001c0002t0001g0005 a0001c0002t0001g0022 a0001c0002t0001g0023 others(8): Show |
12 | HG00642.hp1 HG00738.hp1 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.487+670G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4406831 | |||||||
| chr16:4406832 | G | A | 1 | a0002c0001t0001g0225 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.487+669C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4406832 | |||||||
| chr16:4406923 | G | A | 1 | a0002c0001t0001g0234 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.487+578C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4406923 | |||||||
| chr16:4407016 | C | T | 23 | a0001c0002t0001g0273 a0001c0002t0002g0265 a0003c0003t0001g0016 others(20): Show |
24 | HG02280.hp1 HG02451.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.487+485G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4407016 | |||||||
| chr16:4407018 | G | C | 2 | a0002c0001t0001g0226 a0002c0001t0001g0227 |
2 | NA18978.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.487+483C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4407018 | |||||||
| chr16:4407099 | C | T | 22 | a0001c0002t0002g0265 a0003c0003t0001g0016 a0003c0003t0001g0259 others(19): Show |
23 | HG02280.hp1 HG02451.hp1 HG02451.hp2 others(20): Show |
intron_variant | MODIFIER | c.487+402G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4407099 | |||||||
| chr16:4407101 | C | T | 11 | a0001c0002t0001g0010 a0001c0002t0001g0147 a0001c0002t0001g0148 others(8): Show |
12 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.487+400G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4407101 | |||||||
| chr16:4407110 | G | T | 1 | a0002c0001t0001g0155 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.487+391C>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4407110 | |||||||
| chr16:4407275 | C | T | 1 | a0016c0026t0001g0131 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.487+226G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4407275 | |||||||
| chr16:4407277 | G | GA | 33 | a0001c0002t0001g0040 a0001c0002t0001g0041 a0001c0002t0001g0055 others(30): Show |
36 | HG00735.hp2 HG01099.hp1 HG02280.hp1 others(33): Show |
intron_variant | MODIFIER | c.487+223dupT | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4407277 | |||||||
| chr16:4407288 | A | G | 1 | a0001c0002t0001g0026 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.487+213T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4407288 | |||||||
| chr16:4407289 | A | T | 1 | a0001c0002t0001g0026 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.487+212T>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4407289 | |||||||
| chr16:4407291 | C | A | 1 | a0001c0002t0001g0026 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.487+210G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4407291 | |||||||
| chr16:4407292 | A | G | 1 | a0001c0002t0001g0129 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.487+209T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4407292 | |||||||
| chr16:4407711 | A | G | 1 | a0001c0002t0001g0273 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.304-27T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 4/27 | chr16 | 4407711 | |||||||
| chr16:4407743 | C | G | 1 | a0001c0004t0001g0058 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.304-59G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 4/27 | chr16 | 4407743 | |||||||
| chr16:4407744 | T | G | 1 | a0001c0002t0001g0116 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.304-60A>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 4/27 | chr16 | 4407744 | |||||||
| chr16:4407772 | G | A | 3 | a0002c0006t0001g0015 a0002c0006t0001g0245 a0006c0009t0001g0246 |
4 | HG00733.hp1 HG01106.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.304-88C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 4/27 | chr16 | 4407772 | |||||||
| chr16:4407906 | C | G | 178 | a0001c0002t0001g0005 a0001c0002t0001g0010 a0001c0002t0001g0021 others(175): Show |
192 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.304-222G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 4/27 | chr16 | 4407906 | |||||||
| chr16:4407953 | A | G | 1 | a0012c0024t0005g0277 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.303+228T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 4/27 | chr16 | 4407953 | |||||||
| chr16:4408070 | G | A | 1 | a0001c0002t0002g0117 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.303+111C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 4/27 | chr16 | 4408070 | |||||||
| chr16:4408077 | T | C | 1 | a0001c0002t0002g0039 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.303+104A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 4/27 | chr16 | 4408077 | |||||||
| chr16:4408139 | G | A | 2 | a0001c0002t0001g0054 a0001c0002t0001g0055 |
2 | HG02071.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.303+42C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 4/27 | chr16 | 4408139 | |||||||
| chr16:4408326 | C | T | 1 | a0012c0024t0005g0277 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.233-75G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4408326 | |||||||
| chr16:4408329 | G | A | 5 | a0004c0005t0001g0254 a0004c0005t0001g0255 a0004c0005t0001g0256 others(2): Show |
5 | HG02895.hp2 HG02897.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.233-78C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4408329 | |||||||
| chr16:4408388 | C | T | 6 | a0001c0002t0001g0021 a0001c0002t0001g0040 a0001c0002t0001g0041 others(3): Show |
8 | HG02486.hp1 HG02922.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.233-137G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4408388 | |||||||
| chr16:4408505 | C | T | 2 | a0005c0007t0001g0044 a0005c0007t0001g0045 |
2 | HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.233-254G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4408505 | |||||||
| chr16:4408559 | G | C | 1 | a0012c0024t0005g0277 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.233-308C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4408559 | |||||||
| chr16:4408590 | G | A | 1 | a0001c0002t0001g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.233-339C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4408590 | |||||||
| chr16:4408733 | T | C | 1 | a0012c0024t0005g0277 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.233-482A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4408733 | |||||||
| chr16:4408738 | A | G | 1 | a0012c0024t0005g0277 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.233-487T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4408738 | |||||||
| chr16:4409092 | A | T | 1 | a0001c0002t0001g0140 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.233-841T>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4409092 | |||||||
| chr16:4409108 | G | A | 1 | a0001c0002t0002g0039 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.233-857C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4409108 | |||||||
| chr16:4409111 | G | T | 2 | a0001c0002t0002g0056 a0001c0002t0002g0057 |
2 | HG01934.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.233-860C>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4409111 | |||||||
| chr16:4409145 | G | T | 1 | a0002c0001t0001g0159 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.233-894C>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4409145 | |||||||
| chr16:4409154 | G | A | 1 | a0012c0024t0005g0277 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.233-903C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4409154 | |||||||
| chr16:4409161 | T | A | 2 | a0002c0001t0001g0231 a0002c0001t0001g0251 |
2 | HG03704.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.233-910A>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4409161 | |||||||
| chr16:4409198 | G | A | 1 | a0002c0001t0001g0020 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.233-947C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4409198 | |||||||
| chr16:4409209 | G | A | 1 | a0001c0002t0001g0053 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.233-958C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4409209 | |||||||
| chr16:4409242 | G | A | 1 | a0001c0002t0002g0118 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.233-991C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4409242 | |||||||
| chr16:4409267 | C | T | 6 | a0001c0002t0001g0005 a0001c0002t0001g0022 a0001c0002t0001g0023 others(3): Show |
7 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-1016G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4409267 | |||||||
| chr16:4409341 | T | C | 1 | a0001c0004t0001g0139 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.233-1090A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4409341 | |||||||
| chr16:4409413 | G | A | 2 | a0005c0007t0001g0044 a0005c0007t0001g0045 |
2 | HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.233-1162C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4409413 | |||||||
| chr16:4409434 | G | A | 1 | a0001c0002t0001g0140 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.233-1183C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4409434 | |||||||
| chr16:4409496 | G | A | 14 | a0001c0002t0002g0265 a0003c0003t0001g0016 a0003c0003t0001g0262 others(11): Show |
15 | HG02451.hp1 HG02451.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.233-1245C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4409496 | |||||||
| chr16:4409589 | C | T | 1 | a0002c0001t0001g0158 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.233-1338G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4409589 | |||||||
| chr16:4409613 | A | G | 1 | a0001c0002t0001g0051 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.233-1362T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4409613 | |||||||
| chr16:4409664 | T | A | 1 | a0012c0024t0005g0277 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.233-1413A>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4409664 | |||||||
| chr16:4409699 | C | A | 2 | a0001c0002t0001g0119 a0001c0002t0001g0120 |
2 | HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.233-1448G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4409699 | |||||||
| chr16:4409756 | T | A | 1 | a0001c0002t0001g0051 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.233-1505A>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4409756 | |||||||
| chr16:4409776 | G | A | 3 | a0002c0001t0001g0232 a0002c0001t0001g0233 a0002c0001t0001g0234 |
3 | HG02015.hp1 HG02056.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.233-1525C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4409776 | |||||||
| chr16:4409815 | G | C | 1 | a0001c0002t0001g0051 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.233-1564C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4409815 | |||||||
| chr16:4409833 | A | G | 184 | a0001c0002t0001g0005 a0001c0002t0001g0010 a0001c0002t0001g0021 others(181): Show |
198 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.233-1582T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4409833 | |||||||
| chr16:4409904 | T | G | 1 | a0001c0002t0001g0051 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.233-1653A>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4409904 | |||||||
| chr16:4410048 | A | G | 182 | a0001c0002t0001g0005 a0001c0002t0001g0010 a0001c0002t0001g0021 others(179): Show |
196 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.233-1797T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4410048 | |||||||
| chr16:4410097 | G | T | 1 | a0006c0009t0001g0246 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.233-1846C>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4410097 | |||||||
| chr16:4410113 | A | G | 184 | a0001c0002t0001g0005 a0001c0002t0001g0010 a0001c0002t0001g0021 others(181): Show |
198 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.233-1862T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4410113 | |||||||
| chr16:4410132 | G | A | 182 | a0001c0002t0001g0005 a0001c0002t0001g0010 a0001c0002t0001g0021 others(179): Show |
196 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.233-1881C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4410132 | |||||||
| chr16:4410155 | T | G | 1 | a0001c0002t0001g0273 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.233-1904A>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4410155 | |||||||
| chr16:4410579 | T | G | 1 | a0012c0024t0005g0277 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.232+1777A>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4410579 | |||||||
| chr16:4410771 | T | C | 4 | a0002c0001t0001g0157 a0002c0001t0001g0235 a0002c0001t0001g0236 others(1): Show |
4 | NA18942.hp2 NA19000.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.232+1585A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4410771 | |||||||
| chr16:4410818 | T | C | 1 | a0019c0020t0002g0048 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.232+1538A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4410818 | |||||||
| chr16:4410842 | T | C | 1 | a0001c0002t0002g0124 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.232+1514A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4410842 | |||||||
| chr16:4410886 | T | C | 1 | a0008c0022t0001g0125 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.232+1470A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4410886 | |||||||
| chr16:4410917 | G | A | 1 | a0012c0024t0005g0277 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.232+1439C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4410917 | |||||||
| chr16:4410919 | G | A | 1 | a0002c0001t0001g0247 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.232+1437C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4410919 | |||||||
| chr16:4411001 | G | C | 3 | a0001c0002t0001g0127 a0001c0002t0001g0128 a0013c0015t0001g0126 |
3 | HG03654.hp1 HG03688.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.232+1355C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4411001 | |||||||
| chr16:4411018 | C | T | 1 | a0001c0002t0001g0129 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.232+1338G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4411018 | |||||||
| chr16:4411020 | T | G | 1 | a0001c0002t0001g0129 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.232+1336A>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4411020 | |||||||
| chr16:4411048 | G | A | 13 | a0001c0002t0001g0005 a0001c0002t0001g0022 a0001c0002t0001g0023 others(10): Show |
14 | HG00642.hp1 HG00738.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.232+1308C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4411048 | |||||||
| chr16:4411088 | T | C | 1 | a0001c0002t0001g0033 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.232+1268A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4411088 | |||||||
| chr16:4411132 | G | C | 1 | a0012c0024t0005g0277 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.232+1224C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4411132 | |||||||
| chr16:4411559 | A | T | 6 | a0001c0002t0001g0054 a0001c0002t0001g0055 a0002c0001t0001g0155 others(3): Show |
6 | HG01346.hp1 HG01361.hp1 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.232+797T>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4411559 | |||||||
| chr16:4411597 | G | C | 1 | a0012c0024t0005g0277 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.232+759C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4411597 | |||||||
| chr16:4411650 | A | G | 5 | a0004c0005t0001g0254 a0004c0005t0001g0255 a0004c0005t0001g0256 others(2): Show |
5 | HG02895.hp2 HG02897.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.232+706T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4411650 | |||||||
| chr16:4411683 | C | T | 2 | a0005c0007t0001g0044 a0005c0007t0001g0045 |
2 | HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.232+673G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4411683 | |||||||
| chr16:4411721 | C | G | 1 | a0012c0024t0005g0277 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.232+635G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4411721 | |||||||
| chr16:4411860 | A | G | 179 | a0001c0002t0001g0005 a0001c0002t0001g0010 a0001c0002t0001g0021 others(176): Show |
193 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.232+496T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4411860 | |||||||
| chr16:4411996 | G | A | 1 | a0001c0002t0001g0051 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.232+360C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4411996 | |||||||
| chr16:4411997 | A | G | 1 | a0001c0002t0001g0051 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.232+359T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4411997 | |||||||
| chr16:4412025 | C | G | 1 | a0001c0002t0002g0050 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.232+331G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4412025 | |||||||
| chr16:4412033 | G | A | 1 | a0012c0024t0005g0277 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.232+323C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4412033 | |||||||
| chr16:4412053 | A | C | 1 | a0002c0001t0001g0154 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.232+303T>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4412053 | |||||||
| chr16:4412066 | G | A | 4 | a0004c0005t0001g0254 a0004c0005t0001g0256 a0004c0005t0002g0258 others(1): Show |
4 | HG02895.hp2 HG02897.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.232+290C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4412066 | |||||||
| chr16:4412469 | C | T | 2 | a0001c0002t0002g0049 a0001c0002t0002g0249 |
2 | NA18977.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.158-39G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 2/27 | chr16 | 4412469 | |||||||
| chr16:4412618 | A | G | 123 | a0001c0002t0001g0010 a0001c0002t0001g0147 a0001c0002t0001g0148 others(120): Show |
132 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.158-188T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 2/27 | chr16 | 4412618 | |||||||
| chr16:4412623 | T | C | 1 | a0002c0001t0001g0146 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.158-193A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 2/27 | chr16 | 4412623 | |||||||
| chr16:4412735 | T | A | 1 | a0002c0001t0001g0240 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.158-305A>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 2/27 | chr16 | 4412735 | |||||||
| chr16:4412795 | A | G | 2 | a0001c0002t0002g0039 a0002c0001t0001g0038 |
2 | HG01884.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.158-365T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 2/27 | chr16 | 4412795 | |||||||
| chr16:4412831 | C | T | 178 | a0001c0002t0001g0005 a0001c0002t0001g0010 a0001c0002t0001g0021 others(175): Show |
192 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.158-401G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 2/27 | chr16 | 4412831 | |||||||
| chr16:4412835 | G | A | 122 | a0001c0002t0001g0010 a0001c0002t0001g0147 a0001c0002t0001g0148 others(119): Show |
131 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.158-405C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 2/27 | chr16 | 4412835 | |||||||
| chr16:4412896 | C | A | 112 | a0001c0002t0001g0169 a0001c0002t0001g0198 a0001c0002t0001g0201 others(109): Show |
120 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.157+412G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 2/27 | chr16 | 4412896 | |||||||
| chr16:4412926 | A | T | 1 | a0001c0002t0002g0049 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.157+382T>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 2/27 | chr16 | 4412926 | |||||||
| chr16:4413045 | C | T | 1 | a0002c0001t0001g0038 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.157+263G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 2/27 | chr16 | 4413045 | |||||||
| chr16:4413217 | A | G | 2 | a0001c0002t0002g0006 a0019c0020t0002g0048 |
3 | HG03209.hp2 HG03453.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.157+91T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 2/27 | chr16 | 4413217 | |||||||
| chr16:4413283 | A | C | 1 | a0012c0024t0005g0277 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.157+25T>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 2/27 | chr16 | 4413283 | |||||||
| chr16:4413425 | A | C | 1 | a0002c0001t0001g0047 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.61-21T>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4413425 | |||||||
| chr16:4413763 | C | G | 2 | a0001c0002t0002g0039 a0002c0001t0001g0038 |
2 | HG01884.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.61-359G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4413763 | |||||||
| chr16:4413767 | G | A | 1 | a0001c0002t0001g0132 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.61-363C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4413767 | |||||||
| chr16:4413845 | G | A | 155 | a0001c0002t0001g0010 a0001c0002t0001g0021 a0001c0002t0001g0040 others(152): Show |
167 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.61-441C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4413845 | |||||||
| chr16:4413914 | G | C | 1 | a0012c0024t0005g0277 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.61-510C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4413914 | |||||||
| chr16:4413999 | C | T | 1 | a0001c0002t0001g0046 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.61-595G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4413999 | |||||||
| chr16:4414014 | T | C | 177 | a0001c0002t0001g0005 a0001c0002t0001g0010 a0001c0002t0001g0021 others(174): Show |
191 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.61-610A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4414014 | |||||||
| chr16:4414190 | CA | C | 151 | a0001c0002t0001g0010 a0001c0002t0001g0021 a0001c0002t0001g0040 others(148): Show |
163 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.61-787delT | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4414190 | |||||||
| chr16:4414190 | CAA | C | 7 | a0002c0001t0001g0035 a0002c0001t0001g0143 a0002c0001t0001g0144 others(4): Show |
7 | HG01255.hp1 HG02895.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.61-788_61-787delTT | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4414190 | |||||||
| chr16:4414304 | C | T | 2 | a0002c0001t0001g0009 a0002c0001t0001g0142 |
3 | NA18998.hp2 NA19000.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.61-900G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4414304 | |||||||
| chr16:4414372 | G | A | 1 | a0001c0004t0001g0242 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.61-968C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4414372 | |||||||
| chr16:4414545 | A | G | 1 | a0002c0001t0001g0141 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.61-1141T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4414545 | |||||||
| chr16:4414616 | T | C | 125 | a0001c0002t0001g0010 a0001c0002t0001g0147 a0001c0002t0001g0148 others(122): Show |
134 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.61-1212A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4414616 | |||||||
| chr16:4414689 | A | G | 1 | a0001c0002t0001g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.61-1285T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4414689 | |||||||
| chr16:4414692 | G | C | 2 | a0001c0002t0002g0243 a0001c0002t0002g0244 |
2 | HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.61-1288C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4414692 | |||||||
| chr16:4414815 | C | T | 1 | a0002c0001t0001g0035 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.61-1411G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4414815 | |||||||
| chr16:4414931 | G | A | 3 | a0002c0006t0001g0015 a0002c0006t0001g0245 a0006c0009t0001g0246 |
4 | HG00733.hp1 HG01106.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.61-1527C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4414931 | |||||||
| chr16:4414955 | C | G | 1 | a0012c0024t0005g0277 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.60+1504G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4414955 | |||||||
| chr16:4414956 | G | A | 12 | a0001c0002t0001g0005 a0001c0002t0001g0022 a0001c0002t0001g0023 others(9): Show |
13 | HG00544.hp2 HG00642.hp1 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.60+1503C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4414956 | |||||||
| chr16:4415116 | A | T | 1 | a0007c0021t0001g0034 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.60+1343T>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4415116 | |||||||
| chr16:4415212 | G | A | 1 | a0001c0002t0001g0248 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.60+1247C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4415212 | |||||||
| chr16:4415253 | T | G | 1 | a0012c0024t0005g0277 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.60+1206A>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4415253 | |||||||
| chr16:4415329 | C | T | 4 | a0002c0001t0001g0017 a0002c0001t0001g0018 a0002c0001t0001g0019 others(1): Show |
4 | HG02027.hp2 NA18969.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.60+1130G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4415329 | |||||||
| chr16:4415389 | T | A | 1 | a0001c0002t0002g0249 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.60+1070A>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4415389 | |||||||
| chr16:4415390 | A | C | 1 | a0001c0002t0001g0033 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.60+1069T>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4415390 | |||||||
| chr16:4415692 | C | A | 1 | a0012c0024t0005g0277 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.60+767G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4415692 | |||||||
| chr16:4415713 | A | T | 11 | a0001c0002t0001g0005 a0001c0002t0001g0022 a0001c0002t0001g0023 others(8): Show |
12 | HG00642.hp1 HG00738.hp1 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.60+746T>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4415713 | |||||||
| chr16:4415849 | C | G | 1 | a0001c0002t0001g0021 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.60+610G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4415849 | |||||||
| chr16:4415869 | C | G | 5 | a0004c0005t0001g0254 a0004c0005t0001g0255 a0004c0005t0001g0256 others(2): Show |
5 | HG02895.hp2 HG02897.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.60+590G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4415869 | |||||||
| chr16:4415962 | G | A | 1 | a0002c0001t0001g0250 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.60+497C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4415962 | |||||||
| chr16:4416185 | G | A | 1 | a0002c0001t0001g0251 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.60+274C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4416185 | |||||||
| chr16:4416235 | G | C | 2 | a0002c0001t0001g0252 a0002c0001t0001g0253 |
2 | NA18982.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.60+224C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4416235 | |||||||
| chr16:4416306 | C | G | 4 | a0002c0001t0001g0017 a0002c0001t0001g0018 a0002c0001t0001g0019 others(1): Show |
4 | HG02027.hp2 NA18969.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.60+153G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4416306 | |||||||
| chr16:4416429 | G | A | 23 | a0001c0002t0001g0273 a0001c0002t0002g0265 a0003c0003t0001g0016 others(20): Show |
24 | HG02280.hp1 HG02451.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.60+30C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4416429 | |||||||
| chr16:4416440 | G | C | 1 | a0002c0001t0002g0276 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.60+19C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4416440 |