Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 8910 |
| ensemblid | ENSG00000127990.19 |
| hgncid | 10808 |
| symbol | SGCE |
| name | sarcoglycan epsilon |
| refseq_nuc | NM_003919.3 |
| refseq_prot | NP_003910.1 |
| ensembl_nuc | ENST00000648936.2 |
| ensembl_prot | ENSP00000497130.1 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 94584980 |
| end | 94656133 |
| strand | - |
| ver | v1.2 |
| region | chr7:94584980-94656133 |
| region5000 | chr7:94579980-94661133 |
| regionname0 | SGCE_chr7_94584980_94656133 |
| regionname5000 | SGCE_chr7_94579980_94661133 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 437 | 388 | 81 | 58 | 199 | 8 | 40 | 161 | SGCE_chr7_94579980_94661133 | SGCE | MQLPR others(432): Show |
chr7 | 94579980 | 94661133 |
| a0002 | 0/0 | 437 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | MQLPR others(432): Show |
chr7 | 94579980 | 94661133 |
| a0003 | 0/0 | 437 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SGCE_chr7_94579980_94661133 | SGCE | MQLPR others(432): Show |
chr7 | 94579980 | 94661133 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1311 | 386 | 80 | 58 | 199 | 8 | 39 | SGCE_chr7_94579980_94661133 | SGCE | ATGCA others(1306): Show |
chr7 | 94579980 | 94661133 | ||
| a0001c0004 | 0/0 | 1311 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | ATGCA others(1306): Show |
chr7 | 94579980 | 94661133 | ||
| a0001c0005 | 0/0 | 1311 | 1 | 0 | 0 | 0 | 0 | 1 | SGCE_chr7_94579980_94661133 | SGCE | ATGCA others(1306): Show |
chr7 | 94579980 | 94661133 | ||
| a0002c0003 | 0/0 | 1311 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | ATGCA others(1306): Show |
chr7 | 94579980 | 94661133 | ||
| a0003c0002 | 0/0 | 1311 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | ATGCA others(1306): Show |
chr7 | 94579980 | 94661133 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1868 | 379 | 80 | 58 | 192 | 8 | 39 | SGCE_chr7_94579980_94661133 | SGCE | GAGAA others(1863): Show |
chr7 | 94579980 | 94661133 |
| a0001c0001t0002 | 0/0 | 1868 | 7 | 0 | 0 | 7 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | GAGAA others(1863): Show |
chr7 | 94579980 | 94661133 |
| a0001c0004t0001 | 0/0 | 1868 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | GAGAA others(1863): Show |
chr7 | 94579980 | 94661133 |
| a0001c0005t0001 | 0/0 | 1868 | 1 | 0 | 0 | 0 | 0 | 1 | SGCE_chr7_94579980_94661133 | SGCE | GAGAA others(1863): Show |
chr7 | 94579980 | 94661133 |
| a0002c0003t0001 | 0/0 | 1868 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | GAGAA others(1863): Show |
chr7 | 94579980 | 94661133 |
| a0003c0002t0001 | 0/0 | 1868 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | GAGAA others(1863): Show |
chr7 | 94579980 | 94661133 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0027 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0205 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0002g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0004t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0001c0005t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0002c0003t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| a0003c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0270 | EUR | FIN | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0206 | EUR | FIN | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | CHS | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | CHS | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | CHS | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | CHS | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | CHS | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | CHS | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0288 | AMR | PUR | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | CLM | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | CLM | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0279 | AMR | CLM | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | CLM | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0036 | EUR | IBS | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0198 | EUR | IBS | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0036 | EUR | IBS | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | ACB | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | ACB | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | PEL | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PEL | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | PEL | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | PEL | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | KHV | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | ACB | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02145 | hp1 | a0002 | c0003 | t0001 | g0238 | AFR | ACB | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | CDX | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | CDX | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | ACB | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0304 | AFR | ACB | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | ACB | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0318 | AMR | PEL | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0309 | AFR | ACB | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | KHV | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0317 | AFR | GWD | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | GWD | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | GWD | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | GWD | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0322 | AFR | GWD | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02630 | hp2 | a0001 | c0004 | t0001 | g0230 | AFR | GWD | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0319 | SAS | PJL | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0306 | AFR | GWD | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0313 | AFR | GWD | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | GWD | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0321 | AFR | GWD | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0295 | AFR | GWD | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0316 | AFR | GWD | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | GWD | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | GWD | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0301 | AFR | GWD | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0291 | AFR | GWD | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0308 | AFR | ESN | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0315 | AFR | ESN | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | ESN | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | ESN | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | MSL | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | MSL | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | ESN | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0292 | AFR | ESN | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0314 | AFR | ESN | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | ESN | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0311 | AFR | ESN | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | MSL | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | MSL | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0305 | AFR | MSL | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | MSL | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | MSL | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0320 | AFR | MSL | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0249 | SAS | PJL | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0298 | AFR | ESN | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | ESN | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0307 | AFR | GWD | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG03654 | hp2 | a0001 | c0005 | t0001 | g0074 | SAS | PJL | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | STU | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0269 | SAS | STU | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | BEB | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | BEB | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | BEB | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0268 | SAS | BEB | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | STU | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0267 | SAS | STU | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | BEB | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | BEB | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | STU | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | STU | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | STU | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | STU | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | STU | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0259 | SAS | STU | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | YRI | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | YRI | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | CHB | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | CHB | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0303 | AFR | YRI | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | YRI | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19011 | hp1 | a0003 | c0002 | t0001 | g0148 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | LWK | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | LWK | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | LWK | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0302 | AFR | LWK | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0294 | AFR | YRI | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | YRI | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | ASW | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ASW | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0207 | EUR | TSI | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0056 | EUR | TSI | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | CLM | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | CLM | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | ACB | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | ACB | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | ACB | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | USA | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | USA | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | USA | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | USA | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | LWK | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | LWK | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0205 | REF | REF | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0027 | REF | REF | SGCE_chr7_94579980_94661133 | SGCE | chr7 | 94579980 | 94661133 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:94598802 | G | A | 1 | a0003 | 1 | NA19011.hp1 | missense_variant | MODERATE | c.1226C>T | p.Thr409Ile | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 9/11 | 1261/1868 | 1226/1314 | 409/437 | chr7 | 94598802 | |||
| chr7:94603346 | T | G | 1 | a0002 | 1 | HG02145.hp1 | missense_variant | MODERATE | c.769A>C | p.Thr257Pro | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 6/11 | 804/1868 | 769/1314 | 257/437 | chr7 | 94603346 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:94618814 | T | C | 1 | a0001c0004 | 1 | HG02630.hp2 | synonymous_variant | LOW | c.606A>G | p.Thr202Thr | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/11 | 641/1868 | 606/1314 | 202/437 | chr7 | 94618814 | |||
| chr7:94618829 | G | A | 1 | a0001c0005 | 1 | HG03654.hp2 | synonymous_variant | LOW | c.591C>T | p.Asn197Asn | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/11 | 626/1868 | 591/1314 | 197/437 | chr7 | 94618829 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:94585200 | T | G | 1 | a0001c0001t0002 | 7 | HG00621.hp2 NA18944.hp2 NA18954.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*299A>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 11/11 | 299 | chr7 | 94585200 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:94585957 | G | A | 3 | a0001c0001t0001g0032 a0001c0001t0001g0137 a0001c0001t0001g0139 |
4 | HG02717.hp1 HG02976.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1298-442C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 10/10 | chr7 | 94585957 | |||||||
| chr7:94586061 | G | GA | 139 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(136): Show |
167 | HG00597.hp1 HG00597.hp2 HG00609.hp1 others(164): Show |
intron_variant | MODIFIER | c.1298-547dupT | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 10/10 | chr7 | 94586061 | |||||||
| chr7:94586061 | G | GAA | 56 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(53): Show |
69 | HG00544.hp1 HG01069.hp2 HG01070.hp1 others(66): Show |
intron_variant | MODIFIER | c.1298-548_1298-547d others(4): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 10/10 | chr7 | 94586061 | |||||||
| chr7:94586061 | G | GAAA | 6 | a0001c0001t0001g0096 a0001c0001t0001g0142 a0001c0001t0001g0156 others(3): Show |
6 | HG00438.hp2 HG00735.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1298-549_1298-547d others(5): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 10/10 | chr7 | 94586061 | |||||||
| chr7:94586061 | GA | G | 33 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0017 others(30): Show |
40 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.1298-547delT | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 10/10 | chr7 | 94586061 | |||||||
| chr7:94586088 | C | A | 6 | a0001c0001t0001g0002 a0001c0001t0001g0091 a0001c0001t0001g0092 others(3): Show |
9 | HG01884.hp2 HG02015.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1298-573G>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 10/10 | chr7 | 94586088 | |||||||
| chr7:94586133 | A | G | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1298-618T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 10/10 | chr7 | 94586133 | |||||||
| chr7:94586218 | G | A | 1 | a0001c0001t0001g0242 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1298-703C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 10/10 | chr7 | 94586218 | |||||||
| chr7:94586328 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1298-813G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 10/10 | chr7 | 94586328 | |||||||
| chr7:94586377 | A | G | 1 | a0001c0001t0001g0234 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1298-862T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 10/10 | chr7 | 94586377 | |||||||
| chr7:94586502 | T | C | 1 | a0001c0001t0001g0152 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1298-987A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 10/10 | chr7 | 94586502 | |||||||
| chr7:94586582 | C | A | 1 | a0001c0001t0001g0102 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1298-1067G>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 10/10 | chr7 | 94586582 | |||||||
| chr7:94586587 | C | T | 2 | a0001c0001t0001g0245 a0001c0001t0001g0256 |
2 | NA19010.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1298-1072G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 10/10 | chr7 | 94586587 | |||||||
| chr7:94586666 | A | AT | 41 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(38): Show |
45 | HG01243.hp2 HG01884.hp1 HG01891.hp2 others(42): Show |
intron_variant | MODIFIER | c.1298-1152dupA | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 10/10 | chr7 | 94586666 | |||||||
| chr7:94586798 | A | G | 105 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(102): Show |
118 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(115): Show |
intron_variant | MODIFIER | c.1298-1283T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 10/10 | chr7 | 94586798 | |||||||
| chr7:94586956 | C | CTG | 41 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(38): Show |
45 | HG01243.hp2 HG01884.hp1 HG01891.hp2 others(42): Show |
intron_variant | MODIFIER | c.1298-1443_1298-144 others(6): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 10/10 | chr7 | 94586956 | |||||||
| chr7:94587105 | T | C | 5 | a0001c0001t0001g0029 a0001c0001t0001g0105 a0001c0001t0001g0106 others(2): Show |
6 | HG00639.hp2 HG01884.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.1297+1584A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 10/10 | chr7 | 94587105 | |||||||
| chr7:94587115 | T | G | 4 | a0001c0001t0001g0011 a0001c0001t0001g0182 a0001c0001t0001g0183 others(1): Show |
6 | HG00609.hp1 HG02074.hp2 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.1297+1574A>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 10/10 | chr7 | 94587115 | |||||||
| chr7:94587426 | A | T | 1 | a0001c0001t0001g0311 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1297+1263T>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 10/10 | chr7 | 94587426 | |||||||
| chr7:94587878 | A | T | 103 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(100): Show |
116 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(113): Show |
intron_variant | MODIFIER | c.1297+811T>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 10/10 | chr7 | 94587878 | |||||||
| chr7:94587942 | C | A | 1 | a0001c0001t0001g0266 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1297+747G>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 10/10 | chr7 | 94587942 | |||||||
| chr7:94588191 | C | T | 2 | a0001c0001t0001g0040 a0001c0001t0001g0234 |
3 | NA18971.hp1 NA18975.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1297+498G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 10/10 | chr7 | 94588191 | |||||||
| chr7:94588229 | T | C | 1 | a0001c0004t0001g0230 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1297+460A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 10/10 | chr7 | 94588229 | |||||||
| chr7:94588587 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1297+102A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 10/10 | chr7 | 94588587 | |||||||
| chr7:94588764 | GT | G | 7 | a0001c0001t0001g0017 a0001c0001t0001g0058 a0001c0001t0001g0060 others(4): Show |
8 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(5): Show |
intron_variant | MODIFIER | c.1254-33delA | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 9/10 | chr7 | 94588764 | |||||||
| chr7:94588818 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1254-86G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 9/10 | chr7 | 94588818 | |||||||
| chr7:94588953 | G | A | 2 | a0001c0001t0001g0044 a0001c0001t0001g0251 |
3 | NA18969.hp1 NA19058.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1254-221C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 9/10 | chr7 | 94588953 | |||||||
| chr7:94589318 | C | T | 25 | a0001c0001t0001g0048 a0001c0001t0001g0286 a0001c0001t0001g0287 others(22): Show |
26 | HG01243.hp2 HG01891.hp2 HG02258.hp2 others(23): Show |
intron_variant | MODIFIER | c.1254-586G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 9/10 | chr7 | 94589318 | |||||||
| chr7:94589324 | G | T | 25 | a0001c0001t0001g0048 a0001c0001t0001g0286 a0001c0001t0001g0287 others(22): Show |
26 | HG01243.hp2 HG01891.hp2 HG02258.hp2 others(23): Show |
intron_variant | MODIFIER | c.1254-592C>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 9/10 | chr7 | 94589324 | |||||||
| chr7:94589635 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1254-903G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 9/10 | chr7 | 94589635 | |||||||
| chr7:94590782 | C | T | 1 | a0001c0001t0001g0285 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1254-2050G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 9/10 | chr7 | 94590782 | |||||||
| chr7:94590875 | T | G | 1 | a0001c0001t0001g0017 | 2 | NA18991.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1254-2143A>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 9/10 | chr7 | 94590875 | |||||||
| chr7:94590963 | G | C | 1 | a0001c0001t0001g0233 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1254-2231C>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 9/10 | chr7 | 94590963 | |||||||
| chr7:94591057 | G | A | 3 | a0001c0001t0001g0163 a0001c0001t0001g0241 a0001c0001t0001g0255 |
3 | NA18952.hp1 NA18994.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1254-2325C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 9/10 | chr7 | 94591057 | |||||||
| chr7:94591130 | T | C | 4 | a0001c0001t0001g0029 a0001c0001t0001g0105 a0001c0001t0001g0106 others(1): Show |
5 | HG00639.hp2 HG02055.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1254-2398A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 9/10 | chr7 | 94591130 | |||||||
| chr7:94591218 | A | G | 2 | a0001c0001t0001g0276 a0001c0001t0001g0277 |
2 | HG02886.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1254-2486T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 9/10 | chr7 | 94591218 | |||||||
| chr7:94591279 | A | T | 1 | a0001c0005t0001g0074 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1254-2547T>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 9/10 | chr7 | 94591279 | |||||||
| chr7:94591470 | C | T | 1 | a0001c0001t0001g0176 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1254-2738G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 9/10 | chr7 | 94591470 | |||||||
| chr7:94591622 | G | GC | 64 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(61): Show |
76 | HG00323.hp2 HG00609.hp1 HG00735.hp2 others(73): Show |
intron_variant | MODIFIER | c.1254-2891dupG | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 9/10 | chr7 | 94591622 | |||||||
| chr7:94591645 | C | T | 2 | a0001c0001t0001g0050 a0001c0001t0001g0166 |
2 | HG00438.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.1254-2913G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 9/10 | chr7 | 94591645 | |||||||
| chr7:94591730 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1254-2998C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 9/10 | chr7 | 94591730 | |||||||
| chr7:94592032 | G | A | 1 | a0001c0001t0001g0277 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1254-3300C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 9/10 | chr7 | 94592032 | |||||||
| chr7:94592691 | C | G | 1 | a0001c0001t0001g0193 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1254-3959G>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 9/10 | chr7 | 94592691 | |||||||
| chr7:94593035 | T | C | 2 | a0001c0001t0001g0052 a0001c0001t0001g0068 |
2 | HG03017.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.1254-4303A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 9/10 | chr7 | 94593035 | |||||||
| chr7:94593109 | A | G | 1 | a0001c0001t0001g0138 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1254-4377T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 9/10 | chr7 | 94593109 | |||||||
| chr7:94593140 | A | C | 1 | a0001c0001t0001g0132 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1254-4408T>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 9/10 | chr7 | 94593140 | |||||||
| chr7:94593174 | T | G | 1 | a0001c0001t0001g0243 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1254-4442A>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 9/10 | chr7 | 94593174 | |||||||
| chr7:94593412 | T | C | 55 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(52): Show |
64 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.1254-4680A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 9/10 | chr7 | 94593412 | |||||||
| chr7:94593690 | G | C | 2 | a0001c0001t0001g0144 a0001c0001t0001g0170 |
2 | HG02155.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.1254-4958C>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 9/10 | chr7 | 94593690 | |||||||
| chr7:94594068 | C | T | 29 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0038 others(26): Show |
37 | HG01123.hp2 HG01261.hp2 HG01358.hp2 others(34): Show |
intron_variant | MODIFIER | c.1253+4707G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 9/10 | chr7 | 94594068 | |||||||
| chr7:94594155 | G | A | 2 | a0001c0001t0001g0049 a0001c0001t0001g0054 |
2 | HG01167.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.1253+4620C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 9/10 | chr7 | 94594155 | |||||||
| chr7:94594303 | A | G | 4 | a0001c0001t0001g0029 a0001c0001t0001g0105 a0001c0001t0001g0106 others(1): Show |
5 | HG00639.hp2 HG02055.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1253+4472T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 9/10 | chr7 | 94594303 | |||||||
| chr7:94594534 | C | T | 1 | a0001c0001t0001g0314 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1253+4241G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 9/10 | chr7 | 94594534 | |||||||
| chr7:94594625 | C | T | 1 | a0001c0001t0001g0231 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1253+4150G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 9/10 | chr7 | 94594625 | |||||||
| chr7:94594964 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1253+3811G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 9/10 | chr7 | 94594964 | |||||||
| chr7:94595020 | C | T | 4 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(1): Show |
4 | HG00738.hp2 HG02486.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1253+3755G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 9/10 | chr7 | 94595020 | |||||||
| chr7:94595215 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1253+3560A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 9/10 | chr7 | 94595215 | |||||||
| chr7:94595330 | G | A | 1 | a0001c0001t0001g0312 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1253+3445C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 9/10 | chr7 | 94595330 | |||||||
| chr7:94595480 | G | T | 1 | a0001c0001t0001g0105 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1253+3295C>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 9/10 | chr7 | 94595480 | |||||||
| chr7:94595529 | T | G | 1 | a0001c0001t0001g0100 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1253+3246A>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 9/10 | chr7 | 94595529 | |||||||
| chr7:94595539 | A | G | 62 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(59): Show |
71 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.1253+3236T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 9/10 | chr7 | 94595539 | |||||||
| chr7:94595556 | T | C | 4 | a0001c0001t0001g0009 a0001c0001t0001g0036 a0001c0001t0001g0155 others(1): Show |
7 | HG00735.hp1 HG01069.hp2 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.1253+3219A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 9/10 | chr7 | 94595556 | |||||||
| chr7:94595602 | A | G | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1253+3173T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 9/10 | chr7 | 94595602 | |||||||
| chr7:94596028 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1253+2747C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 9/10 | chr7 | 94596028 | |||||||
| chr7:94596039 | A | G | 1 | a0001c0001t0001g0197 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1253+2736T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 9/10 | chr7 | 94596039 | |||||||
| chr7:94596243 | A | G | 38 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0042 others(35): Show |
45 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.1253+2532T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 9/10 | chr7 | 94596243 | |||||||
| chr7:94596668 | T | G | 1 | a0001c0001t0001g0226 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1253+2107A>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 9/10 | chr7 | 94596668 | |||||||
| chr7:94596693 | G | C | 1 | a0001c0001t0001g0147 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1253+2082C>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 9/10 | chr7 | 94596693 | |||||||
| chr7:94596803 | A | G | 31 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0030 others(28): Show |
37 | HG00597.hp2 HG01257.hp2 HG01433.hp2 others(34): Show |
intron_variant | MODIFIER | c.1253+1972T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 9/10 | chr7 | 94596803 | |||||||
| chr7:94596994 | T | G | 1 | a0001c0001t0001g0231 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1253+1781A>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 9/10 | chr7 | 94596994 | |||||||
| chr7:94597231 | A | C | 1 | a0001c0001t0001g0321 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1253+1544T>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 9/10 | chr7 | 94597231 | |||||||
| chr7:94597357 | G | T | 2 | a0001c0001t0001g0109 a0001c0001t0001g0110 |
2 | HG01884.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1253+1418C>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 9/10 | chr7 | 94597357 | |||||||
| chr7:94597403 | T | G | 2 | a0001c0001t0001g0171 a0001c0001t0001g0217 |
2 | HG02145.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1253+1372A>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 9/10 | chr7 | 94597403 | |||||||
| chr7:94597503 | T | C | 15 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(12): Show |
18 | HG01884.hp1 HG02109.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.1253+1272A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 9/10 | chr7 | 94597503 | |||||||
| chr7:94597552 | TGA | T | 35 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0029 others(32): Show |
42 | HG00597.hp2 HG00639.hp2 HG01257.hp2 others(39): Show |
intron_variant | MODIFIER | c.1253+1221_1253+122 others(6): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 9/10 | chr7 | 94597552 | |||||||
| chr7:94597641 | G | A | 2 | a0001c0001t0001g0109 a0001c0001t0001g0110 |
2 | HG01884.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1253+1134C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 9/10 | chr7 | 94597641 | |||||||
| chr7:94597961 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1253+814G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 9/10 | chr7 | 94597961 | |||||||
| chr7:94597963 | C | T | 3 | a0001c0001t0001g0197 a0001c0001t0001g0204 a0001c0001t0001g0213 |
3 | HG00735.hp2 HG01069.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1253+812G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 9/10 | chr7 | 94597963 | |||||||
| chr7:94597964 | T | G | 251 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(248): Show |
293 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(290): Show |
intron_variant | MODIFIER | c.1253+811A>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 9/10 | chr7 | 94597964 | |||||||
| chr7:94598197 | G | A | 251 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(248): Show |
293 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(290): Show |
intron_variant | MODIFIER | c.1253+578C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 9/10 | chr7 | 94598197 | |||||||
| chr7:94598223 | C | A | 2 | a0001c0001t0001g0259 a0001c0001t0001g0267 |
2 | HG04115.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1253+552G>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 9/10 | chr7 | 94598223 | |||||||
| chr7:94598503 | T | C | 55 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(52): Show |
64 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.1253+272A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 9/10 | chr7 | 94598503 | |||||||
| chr7:94598534 | T | C | 5 | a0001c0001t0001g0313 a0001c0001t0001g0314 a0001c0001t0001g0315 others(2): Show |
5 | HG02572.hp1 HG02723.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1253+241A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 9/10 | chr7 | 94598534 | |||||||
| chr7:94599005 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1065-42T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 8/10 | chr7 | 94599005 | |||||||
| chr7:94599900 | G | A | 1 | a0001c0001t0001g0249 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1038-177C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 7/10 | chr7 | 94599900 | |||||||
| chr7:94599959 | G | A | 43 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0033 others(40): Show |
52 | HG00438.hp2 HG00544.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.1038-236C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 7/10 | chr7 | 94599959 | |||||||
| chr7:94599968 | G | A | 43 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0033 others(40): Show |
52 | HG00438.hp2 HG00544.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.1038-245C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 7/10 | chr7 | 94599968 | |||||||
| chr7:94599980 | A | G | 1 | a0001c0001t0001g0311 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1038-257T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 7/10 | chr7 | 94599980 | |||||||
| chr7:94599987 | A | G | 1 | a0001c0001t0001g0116 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1038-264T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 7/10 | chr7 | 94599987 | |||||||
| chr7:94600313 | C | T | 3 | a0001c0001t0001g0032 a0001c0001t0001g0137 a0001c0001t0001g0139 |
4 | HG02717.hp1 HG02976.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1037+333G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 7/10 | chr7 | 94600313 | |||||||
| chr7:94600938 | AT | A | 5 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0123 others(2): Show |
5 | HG00597.hp2 NA18612.hp2 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.826-82delA | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 6/10 | chr7 | 94600938 | |||||||
| chr7:94601122 | G | A | 1 | a0002c0003t0001g0238 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.826-265C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 6/10 | chr7 | 94601122 | |||||||
| chr7:94601321 | G | A | 2 | a0001c0001t0001g0171 a0001c0001t0001g0217 |
2 | HG02145.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.826-464C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 6/10 | chr7 | 94601321 | |||||||
| chr7:94601323 | C | G | 64 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(61): Show |
76 | HG00323.hp2 HG00609.hp1 HG00735.hp2 others(73): Show |
intron_variant | MODIFIER | c.826-466G>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 6/10 | chr7 | 94601323 | |||||||
| chr7:94601443 | C | CA | 18 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0023 others(15): Show |
23 | HG00621.hp1 HG00673.hp2 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.826-587dupT | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 6/10 | chr7 | 94601443 | |||||||
| chr7:94601443 | C | CAAA | 10 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0030 others(7): Show |
15 | HG02896.hp1 HG02922.hp1 HG03239.hp2 others(12): Show |
intron_variant | MODIFIER | c.826-589_826-587dup others(3): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 6/10 | chr7 | 94601443 | |||||||
| chr7:94601443 | C | CAAAA | 24 | a0001c0001t0001g0031 a0001c0001t0001g0048 a0001c0001t0001g0111 others(21): Show |
26 | HG01257.hp2 HG01433.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.826-590_826-587dup others(4): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 6/10 | chr7 | 94601443 | |||||||
| chr7:94601443 | C | CAAAAA | 18 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0049 others(15): Show |
20 | HG00597.hp2 HG02109.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.826-591_826-587dup others(5): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 6/10 | chr7 | 94601443 | |||||||
| chr7:94601443 | C | CAAAAAA | 19 | a0001c0001t0001g0008 a0001c0001t0001g0046 a0001c0001t0001g0096 others(16): Show |
22 | HG01243.hp2 HG01884.hp2 HG02155.hp1 others(19): Show |
intron_variant | MODIFIER | c.826-592_826-587dup others(6): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 6/10 | chr7 | 94601443 | |||||||
| chr7:94601443 | C | CAAAAAAA | 20 | a0001c0001t0001g0009 a0001c0001t0001g0037 a0001c0001t0001g0110 others(17): Show |
23 | HG00438.hp2 HG00544.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.826-593_826-587dup others(7): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 6/10 | chr7 | 94601443 | |||||||
| chr7:94601443 | C | CAAAAAAA others(1): Show |
12 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(9): Show |
16 | HG01516.hp1 HG01517.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.826-594_826-587dup others(8): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 6/10 | chr7 | 94601443 | |||||||
| chr7:94601443 | C | CAAAAAAA others(3): Show |
2 | a0001c0001t0001g0159 a0001c0001t0001g0165 |
2 | NA19064.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.826-596_826-587dup others(10): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 6/10 | chr7 | 94601443 | |||||||
| chr7:94601443 | C | CAAAAAAA others(4): Show |
1 | a0001c0001t0001g0155 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.826-597_826-587dup others(11): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 6/10 | chr7 | 94601443 | |||||||
| chr7:94601443 | C | CAAAAAAA others(8): Show |
1 | a0001c0001t0001g0137 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.826-601_826-587dup others(15): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 6/10 | chr7 | 94601443 | |||||||
| chr7:94601443 | C | CAAAAAAA others(9): Show |
1 | a0001c0001t0001g0139 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.826-602_826-587dup others(16): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 6/10 | chr7 | 94601443 | |||||||
| chr7:94601443 | CA | C | 18 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0052 others(15): Show |
25 | HG00621.hp2 HG01106.hp2 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.826-587delT | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 6/10 | chr7 | 94601443 | |||||||
| chr7:94601443 | CAAA | C | 20 | a0001c0001t0001g0016 a0001c0001t0001g0226 a0001c0001t0001g0227 others(17): Show |
22 | HG01074.hp2 HG01106.hp1 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.826-589_826-587del others(3): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 6/10 | chr7 | 94601443 | |||||||
| chr7:94601443 | CAAAA | C | 37 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0042 others(34): Show |
44 | HG00323.hp1 HG00438.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.826-590_826-587del others(4): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 6/10 | chr7 | 94601443 | |||||||
| chr7:94601443 | CAAAAAAA others(1): Show |
C | 5 | a0001c0001t0001g0029 a0001c0001t0001g0065 a0001c0001t0001g0105 others(2): Show |
6 | HG00639.hp2 HG02055.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.826-594_826-587del others(8): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 6/10 | chr7 | 94601443 | |||||||
| chr7:94601443 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0311 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.826-596_826-587del others(10): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 6/10 | chr7 | 94601443 | |||||||
| chr7:94601443 | CAAAAAAA others(10): Show |
C | 1 | a0001c0001t0001g0116 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.826-603_826-587del others(17): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 6/10 | chr7 | 94601443 | |||||||
| chr7:94601443 | CAAAAAAA others(11): Show |
C | 1 | a0001c0001t0001g0190 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.826-604_826-587del others(18): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 6/10 | chr7 | 94601443 | |||||||
| chr7:94601443 | CAAAAAAA others(12): Show |
C | 59 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(56): Show |
71 | HG00323.hp2 HG00609.hp1 HG00735.hp2 others(68): Show |
intron_variant | MODIFIER | c.826-605_826-587del others(19): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 6/10 | chr7 | 94601443 | |||||||
| chr7:94601484 | A | G | 2 | a0001c0001t0001g0011 a0001c0001t0001g0183 |
4 | HG00609.hp1 HG02074.hp2 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.826-627T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 6/10 | chr7 | 94601484 | |||||||
| chr7:94601555 | G | A | 1 | a0001c0001t0001g0049 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.826-698C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 6/10 | chr7 | 94601555 | |||||||
| chr7:94601568 | G | A | 1 | a0001c0001t0001g0108 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.826-711C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 6/10 | chr7 | 94601568 | |||||||
| chr7:94601608 | T | G | 1 | a0001c0001t0001g0233 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.826-751A>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 6/10 | chr7 | 94601608 | |||||||
| chr7:94601771 | T | C | 2 | a0001c0001t0001g0252 a0001c0001t0001g0260 |
2 | NA18947.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.826-914A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 6/10 | chr7 | 94601771 | |||||||
| chr7:94601807 | G | T | 1 | a0001c0001t0001g0193 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.826-950C>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 6/10 | chr7 | 94601807 | |||||||
| chr7:94601836 | T | G | 1 | a0001c0001t0001g0286 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.826-979A>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 6/10 | chr7 | 94601836 | |||||||
| chr7:94601991 | A | G | 1 | a0001c0001t0001g0221 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.826-1134T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 6/10 | chr7 | 94601991 | |||||||
| chr7:94602006 | A | C | 1 | a0001c0001t0001g0087 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.826-1149T>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 6/10 | chr7 | 94602006 | |||||||
| chr7:94602088 | A | G | 1 | a0001c0001t0001g0087 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.825+1202T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 6/10 | chr7 | 94602088 | |||||||
| chr7:94602111 | A | C | 1 | a0001c0001t0001g0087 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.825+1179T>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 6/10 | chr7 | 94602111 | |||||||
| chr7:94602209 | G | A | 1 | a0001c0001t0001g0159 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.825+1081C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 6/10 | chr7 | 94602209 | |||||||
| chr7:94602222 | T | C | 1 | a0001c0001t0001g0083 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.825+1068A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 6/10 | chr7 | 94602222 | |||||||
| chr7:94602231 | T | C | 2 | a0001c0001t0001g0241 a0001c0001t0001g0255 |
2 | NA18952.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.825+1059A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 6/10 | chr7 | 94602231 | |||||||
| chr7:94602283 | T | G | 1 | a0001c0001t0001g0248 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.825+1007A>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 6/10 | chr7 | 94602283 | |||||||
| chr7:94602337 | A | C | 41 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(38): Show |
45 | HG01243.hp2 HG01884.hp1 HG01891.hp2 others(42): Show |
intron_variant | MODIFIER | c.825+953T>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 6/10 | chr7 | 94602337 | |||||||
| chr7:94602394 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.825+896A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 6/10 | chr7 | 94602394 | |||||||
| chr7:94602426 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.825+864T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 6/10 | chr7 | 94602426 | |||||||
| chr7:94602539 | A | T | 1 | a0001c0001t0001g0277 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.825+751T>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 6/10 | chr7 | 94602539 | |||||||
| chr7:94602580 | T | A | 1 | a0001c0001t0001g0154 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.825+710A>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 6/10 | chr7 | 94602580 | |||||||
| chr7:94602779 | A | G | 2 | a0001c0001t0001g0276 a0001c0001t0001g0277 |
2 | HG02886.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.825+511T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 6/10 | chr7 | 94602779 | |||||||
| chr7:94603027 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.825+263G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 6/10 | chr7 | 94603027 | |||||||
| chr7:94603582 | C | T | 1 | a0001c0001t0001g0277 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.663-130G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94603582 | |||||||
| chr7:94603756 | G | GATTACTA others(9): Show |
1 | a0001c0001t0001g0310 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.663-320_663-305dup others(16): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94603756 | |||||||
| chr7:94603772 | A | T | 25 | a0001c0001t0001g0048 a0001c0001t0001g0286 a0001c0001t0001g0287 others(22): Show |
26 | HG01243.hp2 HG01891.hp2 HG02258.hp2 others(23): Show |
intron_variant | MODIFIER | c.663-320T>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94603772 | |||||||
| chr7:94603857 | A | G | 1 | a0001c0005t0001g0074 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.663-405T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94603857 | |||||||
| chr7:94603993 | G | T | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.663-541C>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94603993 | |||||||
| chr7:94604123 | T | G | 4 | a0001c0001t0001g0029 a0001c0001t0001g0105 a0001c0001t0001g0106 others(1): Show |
5 | HG00639.hp2 HG02055.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.663-671A>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94604123 | |||||||
| chr7:94604413 | T | TAC | 3 | a0001c0001t0001g0067 a0001c0001t0001g0122 a0001c0001t0001g0249 |
3 | HG01192.hp1 HG03492.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.663-963_663-962dup others(2): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94604413 | |||||||
| chr7:94604413 | T | TACAC | 45 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0032 others(42): Show |
55 | HG00438.hp2 HG00544.hp1 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.663-965_663-962dup others(4): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94604413 | |||||||
| chr7:94604689 | TGTCCTAC others(213): Show |
T | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG03710.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.663-1457_663-1238d others(2): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94604689 | |||||||
| chr7:94604693 | C | G | 2 | a0001c0001t0001g0268 a0001c0001t0001g0269 |
2 | HG03688.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.663-1241G>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94604693 | |||||||
| chr7:94604705 | G | A | 1 | a0001c0001t0001g0268 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.663-1253C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94604705 | |||||||
| chr7:94604806 | A | AAT | 22 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0022 others(19): Show |
23 | HG01099.hp1 HG01256.hp2 HG01258.hp2 others(20): Show |
intron_variant | MODIFIER | c.663-1356_663-1355d others(4): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94604806 | |||||||
| chr7:94604806 | A | AATAT | 14 | a0001c0001t0001g0006 a0001c0001t0001g0038 a0001c0001t0001g0061 others(11): Show |
14 | HG00558.hp1 HG01192.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.663-1358_663-1355d others(6): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94604806 | |||||||
| chr7:94604806 | A | AATATAT | 19 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0009 others(16): Show |
20 | HG01069.hp2 HG01070.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.663-1360_663-1355d others(8): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94604806 | |||||||
| chr7:94604806 | A | AATATATA others(1): Show |
9 | a0001c0001t0001g0012 a0001c0001t0001g0021 a0001c0001t0001g0038 others(6): Show |
9 | HG01361.hp1 HG02155.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.663-1362_663-1355d others(10): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94604806 | |||||||
| chr7:94604806 | A | AATATATA others(3): Show |
12 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0037 others(9): Show |
13 | HG01081.hp2 HG01257.hp1 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.663-1364_663-1355d others(12): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94604806 | |||||||
| chr7:94604806 | A | AATATATA others(5): Show |
4 | a0001c0001t0001g0052 a0001c0001t0001g0155 a0001c0001t0001g0197 others(1): Show |
4 | HG01069.hp1 HG01192.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.663-1366_663-1355d others(14): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94604806 | |||||||
| chr7:94604806 | A | AATATATA others(7): Show |
2 | a0001c0001t0001g0025 a0001c0001t0001g0216 |
2 | HG01123.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.663-1368_663-1355d others(16): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94604806 | |||||||
| chr7:94604806 | AAT | A | 33 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0013 others(30): Show |
35 | HG00438.hp2 HG00639.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.663-1356_663-1355d others(4): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94604806 | |||||||
| chr7:94604806 | AATAT | A | 19 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0036 others(16): Show |
22 | HG00673.hp2 HG01358.hp2 HG01516.hp1 others(19): Show |
intron_variant | MODIFIER | c.663-1358_663-1355d others(6): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94604806 | |||||||
| chr7:94604806 | AATATAT | A | 19 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(16): Show |
21 | HG00323.hp2 HG00558.hp2 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.663-1360_663-1355d others(8): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94604806 | |||||||
| chr7:94604806 | AATATATA others(1): Show |
A | 24 | a0001c0001t0001g0017 a0001c0001t0001g0046 a0001c0001t0001g0047 others(21): Show |
24 | HG00597.hp2 HG00738.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.663-1362_663-1355d others(10): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94604806 | |||||||
| chr7:94604806 | AATATATA others(3): Show |
A | 28 | a0001c0001t0001g0011 a0001c0001t0001g0030 a0001c0001t0001g0033 others(25): Show |
29 | HG00609.hp1 HG01934.hp1 HG01978.hp1 others(26): Show |
intron_variant | MODIFIER | c.663-1364_663-1355d others(12): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94604806 | |||||||
| chr7:94604806 | AATATATA others(5): Show |
A | 6 | a0001c0001t0001g0034 a0001c0001t0001g0108 a0001c0001t0001g0118 others(3): Show |
6 | HG02074.hp1 HG02135.hp2 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.663-1366_663-1355d others(14): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94604806 | |||||||
| chr7:94604806 | AATATATA others(7): Show |
A | 16 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(13): Show |
18 | HG01167.hp2 HG02135.hp1 HG02818.hp2 others(15): Show |
intron_variant | MODIFIER | c.663-1368_663-1355d others(16): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94604806 | |||||||
| chr7:94604806 | AATATATA others(9): Show |
A | 9 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0096 others(6): Show |
11 | HG00544.hp1 HG02074.hp2 HG02132.hp2 others(8): Show |
intron_variant | MODIFIER | c.663-1370_663-1355d others(18): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94604806 | |||||||
| chr7:94604806 | AATATATA others(11): Show |
A | 5 | a0001c0001t0001g0077 a0001c0001t0001g0115 a0001c0001t0001g0157 others(2): Show |
5 | HG01361.hp2 HG01891.hp2 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.663-1372_663-1355d others(20): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94604806 | |||||||
| chr7:94604806 | AATATATA others(13): Show |
A | 1 | a0001c0001t0001g0317 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.663-1374_663-1355d others(22): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94604806 | |||||||
| chr7:94604806 | AATATATA others(15): Show |
A | 2 | a0001c0001t0001g0032 a0002c0003t0001g0238 |
3 | HG02145.hp1 HG02976.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.663-1376_663-1355d others(24): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94604806 | |||||||
| chr7:94604806 | AATATATA others(19): Show |
A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0231 a0001c0001t0001g0314 |
3 | HG03139.hp2 NA19005.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.663-1380_663-1355d others(28): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94604806 | |||||||
| chr7:94604806 | AATATATA others(21): Show |
A | 1 | a0001c0001t0001g0220 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.663-1382_663-1355d others(30): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94604806 | |||||||
| chr7:94604806 | AATATATA others(23): Show |
A | 1 | a0001c0001t0001g0098 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.663-1384_663-1355d others(32): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94604806 | |||||||
| chr7:94604806 | AATATATA others(27): Show |
A | 3 | a0001c0001t0001g0040 a0001c0001t0001g0247 a0001c0001t0001g0250 |
3 | HG00438.hp1 NA18975.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.663-1388_663-1355d others(36): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94604806 | |||||||
| chr7:94604806 | AATATATA others(29): Show |
A | 55 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(52): Show |
64 | HG00323.hp1 HG00597.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.663-1390_663-1355d others(38): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94604806 | |||||||
| chr7:94604806 | AATATATA others(33): Show |
A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0179 a0001c0001t0001g0194 |
5 | NA18943.hp2 NA18949.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.663-1394_663-1355d others(42): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94604806 | |||||||
| chr7:94604844 | TATATATA others(8): Show |
T | 1 | a0001c0001t0001g0070 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.663-1407_663-1393d others(17): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94604844 | |||||||
| chr7:94604851 | A | ATATT | 2 | a0001c0001t0002g0001 a0001c0001t0002g0019 |
3 | NA18954.hp1 NA18988.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.663-1400_663-1399i others(6): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94604851 | |||||||
| chr7:94604858 | T | A | 4 | a0001c0001t0001g0028 a0001c0001t0001g0062 a0001c0001t0001g0247 others(1): Show |
5 | HG00438.hp1 HG02698.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.663-1406A>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94604858 | |||||||
| chr7:94604910 | G | A | 2 | a0001c0001t0001g0231 a0001c0004t0001g0230 |
2 | HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.663-1458C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94604910 | |||||||
| chr7:94604991 | A | T | 1 | a0001c0001t0001g0193 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.663-1539T>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94604991 | |||||||
| chr7:94605084 | A | G | 81 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(78): Show |
98 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.663-1632T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94605084 | |||||||
| chr7:94605165 | C | G | 1 | a0001c0001t0001g0115 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.663-1713G>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94605165 | |||||||
| chr7:94605417 | T | C | 29 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0017 others(26): Show |
37 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.663-1965A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94605417 | |||||||
| chr7:94605787 | C | A | 62 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(59): Show |
71 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.663-2335G>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94605787 | |||||||
| chr7:94605809 | A | G | 3 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0312 |
3 | HG02976.hp1 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.663-2357T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94605809 | |||||||
| chr7:94605989 | C | G | 60 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(57): Show |
69 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.663-2537G>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94605989 | |||||||
| chr7:94606109 | G | A | 3 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0312 |
3 | HG02976.hp1 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.663-2657C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94606109 | |||||||
| chr7:94606453 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.663-3001G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94606453 | |||||||
| chr7:94606836 | A | G | 64 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(61): Show |
73 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.663-3384T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94606836 | |||||||
| chr7:94607104 | A | C | 1 | a0001c0001t0001g0193 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.663-3652T>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94607104 | |||||||
| chr7:94607562 | T | G | 251 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(248): Show |
293 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(290): Show |
intron_variant | MODIFIER | c.663-4110A>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94607562 | |||||||
| chr7:94607662 | C | T | 5 | a0001c0001t0001g0035 a0001c0001t0001g0133 a0001c0001t0001g0154 others(2): Show |
6 | NA18941.hp2 NA18968.hp2 NA18987.hp2 others(3): Show |
intron_variant | MODIFIER | c.663-4210G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94607662 | |||||||
| chr7:94608365 | A | G | 41 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(38): Show |
45 | HG01243.hp2 HG01884.hp1 HG01891.hp2 others(42): Show |
intron_variant | MODIFIER | c.663-4913T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94608365 | |||||||
| chr7:94608453 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.663-5001A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94608453 | |||||||
| chr7:94608751 | A | G | 4 | a0001c0001t0001g0020 a0001c0001t0001g0051 a0001c0001t0001g0058 others(1): Show |
5 | HG00558.hp2 NA18939.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.663-5299T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94608751 | |||||||
| chr7:94609554 | C | T | 1 | a0001c0005t0001g0074 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.663-6102G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94609554 | |||||||
| chr7:94609591 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.663-6139G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94609591 | |||||||
| chr7:94609672 | A | G | 55 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(52): Show |
64 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.663-6220T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94609672 | |||||||
| chr7:94609968 | G | A | 2 | a0001c0001t0001g0276 a0001c0001t0001g0277 |
2 | HG02886.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.663-6516C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94609968 | |||||||
| chr7:94610009 | G | C | 1 | a0001c0001t0001g0232 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.663-6557C>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94610009 | |||||||
| chr7:94610584 | A | G | 1 | a0001c0001t0001g0151 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.663-7132T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94610584 | |||||||
| chr7:94611101 | G | A | 8 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0291 others(5): Show |
10 | HG02258.hp1 HG02451.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.663-7649C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94611101 | |||||||
| chr7:94611169 | T | C | 2 | a0001c0001t0001g0276 a0001c0001t0001g0277 |
2 | HG02886.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.662+7589A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94611169 | |||||||
| chr7:94611192 | A | G | 1 | a0001c0001t0001g0183 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.662+7566T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94611192 | |||||||
| chr7:94611518 | C | T | 1 | a0001c0001t0001g0295 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.662+7240G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94611518 | |||||||
| chr7:94611531 | G | T | 1 | a0001c0001t0001g0182 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.662+7227C>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94611531 | |||||||
| chr7:94611777 | C | T | 9 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0285 others(6): Show |
11 | HG02258.hp1 HG02451.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.662+6981G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94611777 | |||||||
| chr7:94611869 | A | G | 1 | a0001c0001t0001g0316 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.662+6889T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94611869 | |||||||
| chr7:94611920 | A | G | 1 | a0001c0001t0001g0231 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.662+6838T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94611920 | |||||||
| chr7:94611946 | A | G | 2 | a0001c0001t0001g0227 a0001c0001t0001g0228 |
2 | HG02486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.662+6812T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94611946 | |||||||
| chr7:94612063 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.662+6695G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94612063 | |||||||
| chr7:94612129 | C | G | 5 | a0001c0001t0001g0042 a0001c0001t0001g0103 a0001c0001t0001g0253 others(2): Show |
6 | NA18939.hp1 NA18980.hp2 NA18981.hp2 others(3): Show |
intron_variant | MODIFIER | c.662+6629G>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94612129 | |||||||
| chr7:94612283 | A | G | 1 | a0001c0001t0001g0234 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.662+6475T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94612283 | |||||||
| chr7:94612436 | C | A | 1 | a0001c0001t0001g0073 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.662+6322G>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94612436 | |||||||
| chr7:94612463 | G | C | 1 | a0001c0001t0001g0287 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.662+6295C>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94612463 | |||||||
| chr7:94613128 | G | A | 1 | a0001c0001t0001g0304 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.662+5630C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94613128 | |||||||
| chr7:94613236 | A | G | 62 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(59): Show |
71 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.662+5522T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94613236 | |||||||
| chr7:94613238 | T | A | 43 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0033 others(40): Show |
52 | HG00438.hp2 HG00544.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.662+5520A>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94613238 | |||||||
| chr7:94613253 | T | C | 1 | a0002c0003t0001g0238 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.662+5505A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94613253 | |||||||
| chr7:94613272 | A | G | 60 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(57): Show |
69 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.662+5486T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94613272 | |||||||
| chr7:94613417 | T | A | 1 | a0001c0001t0001g0088 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.662+5341A>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94613417 | |||||||
| chr7:94613433 | G | A | 1 | a0001c0001t0001g0123 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.662+5325C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94613433 | |||||||
| chr7:94613500 | T | TG | 2 | a0001c0001t0001g0013 a0001c0001t0001g0209 |
4 | HG01074.hp1 HG01167.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.662+5257dupC | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94613500 | |||||||
| chr7:94613528 | T | C | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.662+5230A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94613528 | |||||||
| chr7:94613569 | C | A | 1 | a0001c0001t0001g0226 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.662+5189G>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94613569 | |||||||
| chr7:94613618 | C | A | 1 | a0001c0001t0001g0204 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.662+5140G>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94613618 | |||||||
| chr7:94613623 | C | G | 62 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(59): Show |
71 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.662+5135G>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94613623 | |||||||
| chr7:94613919 | C | A | 2 | a0001c0001t0001g0171 a0001c0001t0001g0217 |
2 | HG02145.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.662+4839G>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94613919 | |||||||
| chr7:94614106 | T | TA | 3 | a0001c0001t0001g0175 a0001c0001t0001g0185 a0001c0001t0001g0186 |
3 | NA19000.hp1 NA19012.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.662+4651_662+4652i others(3): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94614106 | |||||||
| chr7:94614106 | TC | T | 8 | a0001c0001t0001g0013 a0001c0001t0001g0174 a0001c0001t0001g0180 others(5): Show |
10 | HG01074.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.662+4651delG | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94614106 | |||||||
| chr7:94614107 | C | A | 52 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(49): Show |
61 | HG00323.hp2 HG00609.hp1 HG00735.hp2 others(58): Show |
intron_variant | MODIFIER | c.662+4651G>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94614107 | |||||||
| chr7:94614107 | C | CA | 70 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(67): Show |
75 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.662+4650dupT | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94614107 | |||||||
| chr7:94614107 | C | CAA | 6 | a0001c0001t0001g0014 a0001c0001t0001g0043 a0001c0001t0001g0232 others(3): Show |
6 | NA18522.hp2 NA18940.hp2 NA18972.hp2 others(3): Show |
intron_variant | MODIFIER | c.662+4649_662+4650d others(4): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94614107 | |||||||
| chr7:94614107 | CA | C | 13 | a0001c0001t0001g0009 a0001c0001t0001g0035 a0001c0001t0001g0058 others(10): Show |
14 | HG00558.hp2 HG00673.hp2 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.662+4650delT | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94614107 | |||||||
| chr7:94614163 | A | T | 1 | a0001c0001t0001g0157 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.662+4595T>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94614163 | |||||||
| chr7:94614223 | G | T | 2 | a0001c0001t0001g0171 a0001c0001t0001g0217 |
2 | HG02145.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.662+4535C>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94614223 | |||||||
| chr7:94614288 | T | C | 1 | a0001c0001t0001g0130 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.662+4470A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94614288 | |||||||
| chr7:94614314 | A | G | 1 | a0001c0001t0001g0177 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.662+4444T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94614314 | |||||||
| chr7:94614504 | T | C | 2 | a0001c0001t0001g0096 a0001c0001t0001g0157 |
2 | NA19065.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.662+4254A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94614504 | |||||||
| chr7:94614552 | C | T | 25 | a0001c0001t0001g0048 a0001c0001t0001g0286 a0001c0001t0001g0287 others(22): Show |
26 | HG01243.hp2 HG01891.hp2 HG02258.hp2 others(23): Show |
intron_variant | MODIFIER | c.662+4206G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94614552 | |||||||
| chr7:94614558 | T | C | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.662+4200A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94614558 | |||||||
| chr7:94614730 | A | G | 1 | a0001c0001t0001g0032 | 2 | HG02976.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.662+4028T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94614730 | |||||||
| chr7:94614835 | C | T | 2 | a0001c0001t0001g0062 a0001c0001t0001g0063 |
2 | HG02698.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.662+3923G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94614835 | |||||||
| chr7:94614883 | A | G | 2 | a0001c0001t0001g0241 a0001c0001t0001g0255 |
2 | NA18952.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.662+3875T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94614883 | |||||||
| chr7:94614916 | G | A | 1 | a0002c0003t0001g0238 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.662+3842C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94614916 | |||||||
| chr7:94615365 | AATAG | A | 135 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(132): Show |
150 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(147): Show |
intron_variant | MODIFIER | c.662+3389_662+3392d others(6): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94615365 | |||||||
| chr7:94615365 | AATAGATA others(1): Show |
A | 91 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(88): Show |
103 | HG00323.hp1 HG00323.hp2 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.662+3385_662+3392d others(10): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94615365 | |||||||
| chr7:94615365 | AATAGATA others(5): Show |
A | 69 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(66): Show |
77 | HG00544.hp2 HG00558.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.662+3381_662+3392d others(14): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94615365 | |||||||
| chr7:94615365 | AATAGATA others(9): Show |
A | 11 | a0001c0001t0001g0024 a0001c0001t0001g0048 a0001c0001t0001g0075 others(8): Show |
12 | HG00438.hp2 HG01081.hp2 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.662+3377_662+3392d others(18): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94615365 | |||||||
| chr7:94615365 | AATAGATA others(13): Show |
A | 6 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0100 others(3): Show |
10 | HG03492.hp2 NA18948.hp1 NA18957.hp1 others(7): Show |
intron_variant | MODIFIER | c.662+3373_662+3392d others(22): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94615365 | |||||||
| chr7:94615365 | AATAGATA others(17): Show |
A | 2 | a0001c0001t0001g0045 a0001c0001t0001g0306 |
2 | HG02451.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.662+3369_662+3392d others(26): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94615365 | |||||||
| chr7:94615409 | GATAGATA others(9): Show |
G | 1 | a0001c0001t0001g0064 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.662+3333_662+3348d others(18): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94615409 | |||||||
| chr7:94615413 | GATAGATA others(5): Show |
G | 1 | a0001c0001t0001g0018 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.662+3333_662+3344d others(14): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94615413 | |||||||
| chr7:94615425 | A | G | 1 | a0001c0001t0001g0063 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.662+3333T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94615425 | |||||||
| chr7:94616117 | C | T | 3 | a0001c0001t0002g0001 a0001c0001t0002g0019 a0001c0001t0002g0136 |
7 | HG00621.hp2 NA18944.hp2 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.662+2641G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94616117 | |||||||
| chr7:94616200 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.662+2558C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94616200 | |||||||
| chr7:94616687 | T | A | 1 | a0001c0001t0001g0083 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.662+2071A>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94616687 | |||||||
| chr7:94616828 | T | C | 1 | a0001c0001t0001g0226 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.662+1930A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94616828 | |||||||
| chr7:94616842 | A | G | 1 | a0001c0001t0001g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.662+1916T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94616842 | |||||||
| chr7:94616917 | T | C | 1 | a0001c0001t0001g0233 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.662+1841A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94616917 | |||||||
| chr7:94616964 | A | G | 22 | a0001c0001t0001g0048 a0001c0001t0001g0288 a0001c0001t0001g0290 others(19): Show |
23 | HG01243.hp2 HG01891.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.662+1794T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94616964 | |||||||
| chr7:94617044 | G | T | 1 | a0001c0001t0001g0268 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.662+1714C>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94617044 | |||||||
| chr7:94617333 | C | T | 2 | a0001c0001t0001g0097 a0001c0001t0001g0198 |
2 | HG01517.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.662+1425G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94617333 | |||||||
| chr7:94617358 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.662+1400C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94617358 | |||||||
| chr7:94617581 | T | C | 1 | a0001c0001t0001g0208 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.662+1177A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94617581 | |||||||
| chr7:94617783 | C | G | 1 | a0001c0001t0001g0218 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.662+975G>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94617783 | |||||||
| chr7:94617796 | A | ACT | 251 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(248): Show |
293 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(290): Show |
intron_variant | MODIFIER | c.662+961_662+962ins others(2): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94617796 | |||||||
| chr7:94617951 | T | C | 1 | a0001c0001t0001g0211 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.662+807A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94617951 | |||||||
| chr7:94617992 | T | C | 1 | a0001c0001t0001g0097 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.662+766A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94617992 | |||||||
| chr7:94618276 | A | T | 1 | a0001c0001t0001g0112 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.662+482T>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94618276 | |||||||
| chr7:94618366 | T | C | 4 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0001c0001t0001g0114 others(1): Show |
6 | HG01257.hp2 HG01433.hp2 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.662+392A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94618366 | |||||||
| chr7:94618659 | C | A | 251 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(248): Show |
293 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(290): Show |
intron_variant | MODIFIER | c.662+99G>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 5/10 | chr7 | 94618659 | |||||||
| chr7:94619556 | A | G | 1 | a0001c0001t0001g0286 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.464-600T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 4/10 | chr7 | 94619556 | |||||||
| chr7:94619566 | A | G | 28 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0030 others(25): Show |
34 | HG00597.hp2 HG01257.hp2 HG01433.hp2 others(31): Show |
intron_variant | MODIFIER | c.464-610T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 4/10 | chr7 | 94619566 | |||||||
| chr7:94619621 | T | A | 1 | a0001c0001t0001g0156 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.464-665A>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 4/10 | chr7 | 94619621 | |||||||
| chr7:94619666 | T | C | 1 | a0001c0001t0001g0287 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.464-710A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 4/10 | chr7 | 94619666 | |||||||
| chr7:94620038 | C | T | 3 | a0001c0001t0001g0320 a0001c0001t0001g0321 a0001c0001t0001g0322 |
3 | HG02630.hp1 HG02809.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.464-1082G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 4/10 | chr7 | 94620038 | |||||||
| chr7:94620402 | G | T | 2 | a0001c0001t0001g0231 a0001c0004t0001g0230 |
2 | HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.464-1446C>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 4/10 | chr7 | 94620402 | |||||||
| chr7:94620403 | C | T | 2 | a0001c0001t0001g0231 a0001c0004t0001g0230 |
2 | HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.464-1447G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 4/10 | chr7 | 94620403 | |||||||
| chr7:94620505 | C | T | 2 | a0001c0001t0001g0231 a0001c0004t0001g0230 |
2 | HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.464-1549G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 4/10 | chr7 | 94620505 | |||||||
| chr7:94620513 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.464-1557A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 4/10 | chr7 | 94620513 | |||||||
| chr7:94620672 | A | C | 1 | a0001c0001t0001g0268 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.464-1716T>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 4/10 | chr7 | 94620672 | |||||||
| chr7:94620873 | C | T | 2 | a0001c0001t0001g0171 a0001c0001t0001g0217 |
2 | HG02145.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.464-1917G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 4/10 | chr7 | 94620873 | |||||||
| chr7:94620925 | A | G | 1 | a0001c0001t0001g0068 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.464-1969T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 4/10 | chr7 | 94620925 | |||||||
| chr7:94620957 | T | C | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | HG01993.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.464-2001A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 4/10 | chr7 | 94620957 | |||||||
| chr7:94621073 | A | G | 3 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0002c0003t0001g0238 |
3 | HG02145.hp1 HG02886.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.464-2117T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 4/10 | chr7 | 94621073 | |||||||
| chr7:94621324 | G | A | 1 | a0001c0001t0001g0316 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.463+2001C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 4/10 | chr7 | 94621324 | |||||||
| chr7:94621392 | C | T | 2 | a0001c0001t0001g0252 a0001c0001t0001g0260 |
2 | NA18947.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.463+1933G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 4/10 | chr7 | 94621392 | |||||||
| chr7:94621491 | C | T | 2 | a0001c0001t0001g0171 a0001c0001t0001g0217 |
2 | HG02145.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.463+1834G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 4/10 | chr7 | 94621491 | |||||||
| chr7:94621492 | G | A | 4 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(1): Show |
4 | HG00738.hp2 HG02486.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.463+1833C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 4/10 | chr7 | 94621492 | |||||||
| chr7:94621626 | G | A | 2 | a0001c0001t0001g0156 a0001c0001t0001g0233 |
2 | HG00735.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.463+1699C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 4/10 | chr7 | 94621626 | |||||||
| chr7:94621714 | G | A | 2 | a0001c0001t0001g0277 a0002c0003t0001g0238 |
2 | HG02145.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.463+1611C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 4/10 | chr7 | 94621714 | |||||||
| chr7:94621815 | C | T | 2 | a0001c0001t0001g0231 a0001c0004t0001g0230 |
2 | HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.463+1510G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 4/10 | chr7 | 94621815 | |||||||
| chr7:94621922 | G | A | 3 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0002c0003t0001g0238 |
3 | HG02145.hp1 HG02886.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.463+1403C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 4/10 | chr7 | 94621922 | |||||||
| chr7:94621991 | A | G | 1 | a0001c0001t0001g0139 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.463+1334T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 4/10 | chr7 | 94621991 | |||||||
| chr7:94622021 | G | T | 1 | a0001c0001t0001g0114 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.463+1304C>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 4/10 | chr7 | 94622021 | |||||||
| chr7:94622052 | C | CAT | 251 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(248): Show |
293 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(290): Show |
intron_variant | MODIFIER | c.463+1272_463+1273i others(4): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 4/10 | chr7 | 94622052 | |||||||
| chr7:94622414 | A | G | 65 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(62): Show |
74 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.463+911T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 4/10 | chr7 | 94622414 | |||||||
| chr7:94622461 | C | G | 1 | a0001c0001t0001g0311 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.463+864G>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 4/10 | chr7 | 94622461 | |||||||
| chr7:94622626 | T | A | 3 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0002c0003t0001g0238 |
3 | HG02145.hp1 HG02886.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.463+699A>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 4/10 | chr7 | 94622626 | |||||||
| chr7:94622869 | T | G | 2 | a0001c0001t0001g0191 a0001c0001t0001g0192 |
2 | HG02647.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.463+456A>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 4/10 | chr7 | 94622869 | |||||||
| chr7:94623059 | A | G | 54 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(51): Show |
63 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.463+266T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 4/10 | chr7 | 94623059 | |||||||
| chr7:94623400 | A | G | 24 | a0001c0001t0001g0048 a0001c0001t0001g0286 a0001c0001t0001g0287 others(21): Show |
25 | HG01243.hp2 HG01891.hp2 HG02258.hp2 others(22): Show |
splice_region_variant&intron_variant | LOW | c.391-3T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 3/10 | chr7 | 94623400 | |||||||
| chr7:94623440 | T | G | 54 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(51): Show |
63 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.391-43A>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 3/10 | chr7 | 94623440 | |||||||
| chr7:94623476 | C | A | 1 | a0001c0001t0001g0124 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.391-79G>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 3/10 | chr7 | 94623476 | |||||||
| chr7:94623644 | T | C | 3 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0002c0003t0001g0238 |
3 | HG02145.hp1 HG02886.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.391-247A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 3/10 | chr7 | 94623644 | |||||||
| chr7:94623714 | T | C | 1 | a0001c0001t0001g0193 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.391-317A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 3/10 | chr7 | 94623714 | |||||||
| chr7:94623874 | T | C | 1 | a0001c0001t0001g0233 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.391-477A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 3/10 | chr7 | 94623874 | |||||||
| chr7:94624087 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.391-690C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 3/10 | chr7 | 94624087 | |||||||
| chr7:94624159 | C | T | 4 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(1): Show |
4 | NA18951.hp1 NA18974.hp2 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.391-762G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 3/10 | chr7 | 94624159 | |||||||
| chr7:94624162 | CA | C | 240 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(237): Show |
282 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(279): Show |
intron_variant | MODIFIER | c.391-766delT | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 3/10 | chr7 | 94624162 | |||||||
| chr7:94624206 | T | C | 1 | a0001c0001t0001g0053 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.391-809A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 3/10 | chr7 | 94624206 | |||||||
| chr7:94624305 | A | G | 60 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(57): Show |
72 | HG00323.hp2 HG00609.hp1 HG00735.hp2 others(69): Show |
intron_variant | MODIFIER | c.391-908T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 3/10 | chr7 | 94624305 | |||||||
| chr7:94624307 | T | C | 3 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0002c0003t0001g0238 |
3 | HG02145.hp1 HG02886.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.391-910A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 3/10 | chr7 | 94624307 | |||||||
| chr7:94624344 | T | C | 3 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0002c0003t0001g0238 |
3 | HG02145.hp1 HG02886.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.391-947A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 3/10 | chr7 | 94624344 | |||||||
| chr7:94624744 | C | T | 1 | a0001c0001t0001g0268 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.391-1347G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 3/10 | chr7 | 94624744 | |||||||
| chr7:94624964 | C | G | 35 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0029 others(32): Show |
42 | HG00597.hp2 HG00639.hp2 HG01257.hp2 others(39): Show |
intron_variant | MODIFIER | c.391-1567G>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 3/10 | chr7 | 94624964 | |||||||
| chr7:94625078 | C | T | 1 | a0001c0001t0001g0039 | 2 | NA18957.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.391-1681G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 3/10 | chr7 | 94625078 | |||||||
| chr7:94625223 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.391-1826T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 3/10 | chr7 | 94625223 | |||||||
| chr7:94625391 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.391-1994G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 3/10 | chr7 | 94625391 | |||||||
| chr7:94625393 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.391-1996A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 3/10 | chr7 | 94625393 | |||||||
| chr7:94625396 | T | A | 1 | a0001c0001t0001g0114 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.391-1999A>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 3/10 | chr7 | 94625396 | |||||||
| chr7:94625398 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.391-2001T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 3/10 | chr7 | 94625398 | |||||||
| chr7:94625455 | T | C | 2 | a0001c0001t0001g0206 a0001c0001t0001g0207 |
2 | HG00323.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.391-2058A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 3/10 | chr7 | 94625455 | |||||||
| chr7:94625643 | T | G | 3 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0002c0003t0001g0238 |
3 | HG02145.hp1 HG02886.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.391-2246A>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 3/10 | chr7 | 94625643 | |||||||
| chr7:94625825 | G | A | 2 | a0001c0001t0001g0268 a0001c0001t0001g0269 |
2 | HG03688.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.390+2377C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 3/10 | chr7 | 94625825 | |||||||
| chr7:94625865 | C | A | 3 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0002c0003t0001g0238 |
3 | HG02145.hp1 HG02886.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.390+2337G>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 3/10 | chr7 | 94625865 | |||||||
| chr7:94626005 | T | C | 1 | a0001c0001t0001g0125 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.390+2197A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 3/10 | chr7 | 94626005 | |||||||
| chr7:94626292 | T | A | 3 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0002c0003t0001g0238 |
3 | HG02145.hp1 HG02886.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.390+1910A>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 3/10 | chr7 | 94626292 | |||||||
| chr7:94626554 | A | G | 3 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0002c0003t0001g0238 |
3 | HG02145.hp1 HG02886.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.390+1648T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 3/10 | chr7 | 94626554 | |||||||
| chr7:94626897 | G | T | 1 | a0001c0001t0001g0138 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.390+1305C>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 3/10 | chr7 | 94626897 | |||||||
| chr7:94627005 | T | C | 5 | a0001c0001t0001g0035 a0001c0001t0001g0133 a0001c0001t0001g0154 others(2): Show |
6 | NA18941.hp2 NA18968.hp2 NA18987.hp2 others(3): Show |
intron_variant | MODIFIER | c.390+1197A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 3/10 | chr7 | 94627005 | |||||||
| chr7:94627039 | T | C | 1 | a0001c0001t0001g0208 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.390+1163A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 3/10 | chr7 | 94627039 | |||||||
| chr7:94627049 | G | A | 1 | a0001c0001t0001g0234 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.390+1153C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 3/10 | chr7 | 94627049 | |||||||
| chr7:94627231 | T | C | 1 | a0001c0001t0001g0126 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.390+971A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 3/10 | chr7 | 94627231 | |||||||
| chr7:94627306 | T | C | 1 | a0001c0001t0001g0129 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.390+896A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 3/10 | chr7 | 94627306 | |||||||
| chr7:94627339 | T | C | 62 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(59): Show |
71 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.390+863A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 3/10 | chr7 | 94627339 | |||||||
| chr7:94627358 | T | C | 1 | a0001c0001t0001g0108 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.390+844A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 3/10 | chr7 | 94627358 | |||||||
| chr7:94627577 | C | T | 1 | a0001c0001t0001g0304 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.390+625G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 3/10 | chr7 | 94627577 | |||||||
| chr7:94627675 | G | A | 1 | a0001c0001t0001g0036 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.390+527C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 3/10 | chr7 | 94627675 | |||||||
| chr7:94627787 | A | G | 1 | a0001c0001t0001g0114 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.390+415T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 3/10 | chr7 | 94627787 | |||||||
| chr7:94627850 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.390+352G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 3/10 | chr7 | 94627850 | |||||||
| chr7:94627959 | G | A | 65 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(62): Show |
74 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.390+243C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 3/10 | chr7 | 94627959 | |||||||
| chr7:94628002 | A | G | 2 | a0001c0001t0001g0276 a0001c0001t0001g0277 |
2 | HG02886.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.390+200T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 3/10 | chr7 | 94628002 | |||||||
| chr7:94628137 | T | TAC | 72 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(69): Show |
86 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.390+63_390+64dupGT | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 3/10 | chr7 | 94628137 | |||||||
| chr7:94628137 | T | TACAC | 12 | a0001c0001t0001g0017 a0001c0001t0001g0036 a0001c0001t0001g0038 others(9): Show |
15 | HG01081.hp1 HG01243.hp1 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.390+61_390+64dupGT others(2): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 3/10 | chr7 | 94628137 | |||||||
| chr7:94628137 | T | TACACAC | 3 | a0001c0001t0001g0009 a0001c0001t0001g0155 a0001c0001t0001g0156 |
5 | HG00735.hp1 HG01069.hp2 HG01070.hp1 others(2): Show |
intron_variant | MODIFIER | c.390+59_390+64dupGT others(4): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 3/10 | chr7 | 94628137 | |||||||
| chr7:94628137 | TAC | T | 8 | a0001c0001t0001g0220 a0001c0001t0001g0226 a0001c0001t0001g0227 others(5): Show |
8 | HG00738.hp2 HG02486.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.390+63_390+64delGT | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 3/10 | chr7 | 94628137 | |||||||
| chr7:94628684 | A | G | 251 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(248): Show |
293 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(290): Show |
intron_variant | MODIFIER | c.233-325T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 2/10 | chr7 | 94628684 | |||||||
| chr7:94628809 | G | A | 3 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0002c0003t0001g0238 |
3 | HG02145.hp1 HG02886.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.233-450C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 2/10 | chr7 | 94628809 | |||||||
| chr7:94628834 | C | A | 1 | a0001c0001t0001g0303 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.233-475G>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 2/10 | chr7 | 94628834 | |||||||
| chr7:94629195 | A | T | 1 | a0001c0001t0001g0234 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.232+524T>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 2/10 | chr7 | 94629195 | |||||||
| chr7:94629260 | T | C | 1 | a0001c0001t0001g0170 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.232+459A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 2/10 | chr7 | 94629260 | |||||||
| chr7:94629369 | T | G | 1 | a0001c0001t0001g0168 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.232+350A>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 2/10 | chr7 | 94629369 | |||||||
| chr7:94629387 | T | G | 1 | a0001c0001t0001g0220 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.232+332A>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 2/10 | chr7 | 94629387 | |||||||
| chr7:94629428 | A | C | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.232+291T>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 2/10 | chr7 | 94629428 | |||||||
| chr7:94629585 | C | T | 60 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(57): Show |
69 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.232+134G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 2/10 | chr7 | 94629585 | |||||||
| chr7:94629892 | G | A | 2 | a0001c0001t0001g0171 a0001c0001t0001g0217 |
2 | HG02145.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.110-51C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94629892 | |||||||
| chr7:94630275 | T | C | 2 | a0001c0001t0001g0044 a0001c0001t0001g0251 |
3 | NA18969.hp1 NA19058.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.110-434A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94630275 | |||||||
| chr7:94630296 | T | C | 1 | a0001c0001t0001g0234 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.110-455A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94630296 | |||||||
| chr7:94630360 | G | C | 4 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(1): Show |
4 | HG00738.hp2 HG02486.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.110-519C>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94630360 | |||||||
| chr7:94630971 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.110-1130G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94630971 | |||||||
| chr7:94630972 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.110-1131C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94630972 | |||||||
| chr7:94630996 | G | T | 1 | a0001c0001t0001g0299 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.110-1155C>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94630996 | |||||||
| chr7:94631061 | T | C | 1 | a0002c0003t0001g0238 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.110-1220A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94631061 | |||||||
| chr7:94631137 | C | G | 2 | a0001c0001t0001g0109 a0001c0001t0001g0110 |
2 | HG01884.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.110-1296G>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94631137 | |||||||
| chr7:94631148 | T | TGTACTA | 60 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(57): Show |
69 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.110-1313_110-1308d others(8): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94631148 | |||||||
| chr7:94631163 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.110-1322T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94631163 | |||||||
| chr7:94631247 | G | A | 31 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0030 others(28): Show |
37 | HG00597.hp2 HG01257.hp2 HG01433.hp2 others(34): Show |
intron_variant | MODIFIER | c.110-1406C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94631247 | |||||||
| chr7:94631298 | C | CT | 34 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0029 others(31): Show |
41 | HG00597.hp2 HG00639.hp2 HG01257.hp2 others(38): Show |
intron_variant | MODIFIER | c.110-1458dupA | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94631298 | |||||||
| chr7:94631402 | C | T | 2 | a0001c0001t0001g0196 a0001c0001t0001g0201 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.110-1561G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94631402 | |||||||
| chr7:94631706 | G | A | 3 | a0001c0001t0001g0032 a0001c0001t0001g0137 a0001c0001t0001g0139 |
4 | HG02717.hp1 HG02976.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.110-1865C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94631706 | |||||||
| chr7:94631773 | G | C | 2 | a0001c0001t0001g0302 a0001c0001t0001g0303 |
2 | NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.110-1932C>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94631773 | |||||||
| chr7:94631895 | C | A | 12 | a0001c0001t0001g0037 a0001c0001t0001g0050 a0001c0001t0001g0141 others(9): Show |
13 | HG00438.hp2 NA18944.hp1 NA18954.hp2 others(10): Show |
intron_variant | MODIFIER | c.110-2054G>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94631895 | |||||||
| chr7:94632151 | C | T | 2 | a0001c0001t0001g0051 a0001c0001t0001g0066 |
2 | NA18967.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.110-2310G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94632151 | |||||||
| chr7:94632332 | A | G | 21 | a0001c0001t0001g0048 a0001c0001t0001g0288 a0001c0001t0001g0297 others(18): Show |
22 | HG01243.hp2 HG01891.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.110-2491T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94632332 | |||||||
| chr7:94632706 | C | G | 1 | a0001c0001t0001g0174 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.110-2865G>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94632706 | |||||||
| chr7:94632755 | G | T | 251 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(248): Show |
293 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(290): Show |
intron_variant | MODIFIER | c.110-2914C>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94632755 | |||||||
| chr7:94632760 | G | A | 251 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(248): Show |
293 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(290): Show |
intron_variant | MODIFIER | c.110-2919C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94632760 | |||||||
| chr7:94632863 | A | G | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.110-3022T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94632863 | |||||||
| chr7:94632893 | C | T | 3 | a0001c0001t0001g0030 a0001c0001t0001g0112 a0001c0001t0001g0113 |
4 | NA18974.hp1 NA18977.hp1 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.110-3052G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94632893 | |||||||
| chr7:94633074 | G | A | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.110-3233C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94633074 | |||||||
| chr7:94633176 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.110-3335G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94633176 | |||||||
| chr7:94633446 | C | T | 1 | a0001c0001t0001g0233 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.110-3605G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94633446 | |||||||
| chr7:94633781 | A | C | 2 | a0001c0001t0001g0038 a0001c0001t0001g0180 |
3 | NA18612.hp1 NA18940.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.110-3940T>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94633781 | |||||||
| chr7:94633868 | G | A | 65 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(62): Show |
74 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.110-4027C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94633868 | |||||||
| chr7:94633985 | A | G | 1 | a0001c0001t0001g0233 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.110-4144T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94633985 | |||||||
| chr7:94634077 | T | C | 3 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0002c0003t0001g0238 |
3 | HG02145.hp1 HG02886.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.110-4236A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94634077 | |||||||
| chr7:94634155 | T | C | 1 | a0001c0001t0001g0168 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.110-4314A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94634155 | |||||||
| chr7:94634519 | T | C | 1 | a0001c0001t0001g0129 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.110-4678A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94634519 | |||||||
| chr7:94634565 | C | T | 1 | a0001c0001t0001g0226 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.110-4724G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94634565 | |||||||
| chr7:94634736 | A | G | 210 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(207): Show |
248 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(245): Show |
intron_variant | MODIFIER | c.110-4895T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94634736 | |||||||
| chr7:94634899 | G | A | 3 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0002c0003t0001g0238 |
3 | HG02145.hp1 HG02886.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.110-5058C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94634899 | |||||||
| chr7:94634986 | C | T | 2 | a0001c0001t0001g0241 a0001c0001t0001g0255 |
2 | NA18952.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.110-5145G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94634986 | |||||||
| chr7:94635180 | G | A | 2 | a0001c0001t0001g0075 a0001c0001t0001g0076 |
2 | NA18975.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.110-5339C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94635180 | |||||||
| chr7:94635338 | T | A | 46 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0032 others(43): Show |
56 | HG00438.hp2 HG00544.hp1 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.110-5497A>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94635338 | |||||||
| chr7:94635395 | C | A | 4 | a0001c0001t0001g0029 a0001c0001t0001g0105 a0001c0001t0001g0106 others(1): Show |
5 | HG00639.hp2 HG02055.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.110-5554G>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94635395 | |||||||
| chr7:94635483 | C | T | 1 | a0001c0001t0001g0220 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.110-5642G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94635483 | |||||||
| chr7:94635484 | G | A | 2 | a0001c0001t0001g0252 a0001c0001t0001g0260 |
2 | NA18947.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.110-5643C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94635484 | |||||||
| chr7:94635521 | T | C | 1 | a0001c0001t0001g0276 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.110-5680A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94635521 | |||||||
| chr7:94635539 | T | G | 2 | a0001c0001t0001g0171 a0001c0001t0001g0217 |
2 | HG02145.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.110-5698A>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94635539 | |||||||
| chr7:94635541 | T | C | 1 | a0001c0001t0001g0210 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.110-5700A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94635541 | |||||||
| chr7:94635600 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.110-5759G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94635600 | |||||||
| chr7:94635712 | T | C | 3 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0002c0003t0001g0238 |
3 | HG02145.hp1 HG02886.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.110-5871A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94635712 | |||||||
| chr7:94635737 | C | G | 4 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(1): Show |
4 | HG00738.hp2 HG02486.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.110-5896G>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94635737 | |||||||
| chr7:94635805 | A | C | 81 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(78): Show |
98 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.110-5964T>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94635805 | |||||||
| chr7:94635812 | C | A | 1 | a0001c0001t0001g0232 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.110-5971G>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94635812 | |||||||
| chr7:94636027 | T | G | 1 | a0001c0001t0001g0170 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.110-6186A>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94636027 | |||||||
| chr7:94636073 | A | G | 2 | a0001c0001t0001g0062 a0001c0001t0001g0063 |
2 | HG02698.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.110-6232T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94636073 | |||||||
| chr7:94636123 | A | T | 1 | a0001c0001t0001g0101 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.110-6282T>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94636123 | |||||||
| chr7:94636316 | A | G | 4 | a0001c0001t0001g0297 a0001c0001t0001g0298 a0001c0001t0001g0308 others(1): Show |
4 | HG01891.hp2 HG02451.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.110-6475T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94636316 | |||||||
| chr7:94636355 | T | C | 4 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0084 others(1): Show |
6 | NA18946.hp2 NA18959.hp2 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.110-6514A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94636355 | |||||||
| chr7:94636407 | T | G | 1 | a0001c0001t0001g0157 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.110-6566A>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94636407 | |||||||
| chr7:94636721 | A | G | 3 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0002c0003t0001g0238 |
3 | HG02145.hp1 HG02886.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.110-6880T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94636721 | |||||||
| chr7:94636753 | C | A | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | NA18987.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.110-6912G>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94636753 | |||||||
| chr7:94636776 | A | C | 1 | a0001c0001t0001g0233 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.110-6935T>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94636776 | |||||||
| chr7:94636925 | C | T | 63 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(60): Show |
72 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.110-7084G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94636925 | |||||||
| chr7:94636984 | G | T | 1 | a0001c0001t0001g0289 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.110-7143C>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94636984 | |||||||
| chr7:94637164 | G | A | 62 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(59): Show |
71 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.110-7323C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94637164 | |||||||
| chr7:94637177 | G | C | 3 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0002c0003t0001g0238 |
3 | HG02145.hp1 HG02886.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.110-7336C>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94637177 | |||||||
| chr7:94637322 | A | G | 1 | a0001c0001t0001g0100 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.110-7481T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94637322 | |||||||
| chr7:94637493 | C | T | 2 | a0001c0001t0001g0231 a0001c0004t0001g0230 |
2 | HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.110-7652G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94637493 | |||||||
| chr7:94637611 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.110-7770C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94637611 | |||||||
| chr7:94637961 | T | C | 1 | a0001c0001t0001g0130 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.110-8120A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94637961 | |||||||
| chr7:94638122 | G | T | 15 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(12): Show |
18 | HG01884.hp1 HG02109.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.110-8281C>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94638122 | |||||||
| chr7:94638183 | G | A | 1 | a0001c0004t0001g0230 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.110-8342C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94638183 | |||||||
| chr7:94638452 | A | G | 3 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0002c0003t0001g0238 |
3 | HG02145.hp1 HG02886.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.110-8611T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94638452 | |||||||
| chr7:94638550 | T | C | 60 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(57): Show |
69 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.110-8709A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94638550 | |||||||
| chr7:94638584 | C | T | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.110-8743G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94638584 | |||||||
| chr7:94638639 | C | CA | 7 | a0001c0001t0001g0132 a0001c0001t0001g0160 a0001c0001t0001g0224 others(4): Show |
7 | HG01261.hp2 HG02083.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.110-8799dupT | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94638639 | |||||||
| chr7:94638639 | CA | C | 41 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(38): Show |
45 | HG01243.hp2 HG01884.hp1 HG01891.hp2 others(42): Show |
intron_variant | MODIFIER | c.110-8799delT | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94638639 | |||||||
| chr7:94638883 | A | G | 2 | a0001c0001t0001g0075 a0001c0001t0001g0076 |
2 | NA18975.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.110-9042T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94638883 | |||||||
| chr7:94638903 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.110-9062C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94638903 | |||||||
| chr7:94638941 | T | G | 21 | a0001c0001t0001g0048 a0001c0001t0001g0288 a0001c0001t0001g0297 others(18): Show |
22 | HG01243.hp2 HG01891.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.110-9100A>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94638941 | |||||||
| chr7:94639472 | C | A | 2 | a0001c0001t0001g0306 a0001c0001t0001g0307 |
2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.110-9631G>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94639472 | |||||||
| chr7:94639489 | T | C | 3 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0002c0003t0001g0238 |
3 | HG02145.hp1 HG02886.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.110-9648A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94639489 | |||||||
| chr7:94639565 | T | A | 1 | a0001c0001t0001g0139 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.110-9724A>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94639565 | |||||||
| chr7:94639636 | G | A | 46 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0032 others(43): Show |
56 | HG00438.hp2 HG00544.hp1 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.110-9795C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94639636 | |||||||
| chr7:94639706 | A | G | 3 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0002c0003t0001g0238 |
3 | HG02145.hp1 HG02886.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.110-9865T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94639706 | |||||||
| chr7:94640009 | A | G | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.110-10168T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94640009 | |||||||
| chr7:94640146 | C | A | 1 | a0001c0001t0001g0177 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.110-10305G>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94640146 | |||||||
| chr7:94640646 | T | TTTTTTG | 3 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0002c0003t0001g0238 |
3 | HG02145.hp1 HG02886.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.110-10811_110-1080 others(10): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94640646 | |||||||
| chr7:94640840 | G | A | 54 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(51): Show |
63 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.110-10999C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94640840 | |||||||
| chr7:94640847 | T | C | 319 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(316): Show |
386 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(383): Show |
intron_variant | MODIFIER | c.110-11006A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94640847 | |||||||
| chr7:94640891 | G | A | 4 | a0001c0001t0001g0211 a0001c0001t0001g0276 a0001c0001t0001g0277 others(1): Show |
4 | HG02145.hp1 HG02886.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.110-11050C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94640891 | |||||||
| chr7:94640943 | C | T | 3 | a0001c0001t0001g0320 a0001c0001t0001g0321 a0001c0001t0001g0322 |
3 | HG02630.hp1 HG02809.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.110-11102G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94640943 | |||||||
| chr7:94641316 | T | C | 1 | a0001c0001t0001g0049 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.110-11475A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94641316 | |||||||
| chr7:94641399 | G | T | 2 | a0001c0001t0001g0171 a0001c0001t0001g0217 |
2 | HG02145.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.110-11558C>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94641399 | |||||||
| chr7:94641400 | C | G | 1 | a0001c0001t0001g0287 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.110-11559G>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94641400 | |||||||
| chr7:94641456 | A | G | 5 | a0001c0001t0001g0313 a0001c0001t0001g0314 a0001c0001t0001g0315 others(2): Show |
5 | HG02572.hp1 HG02723.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.110-11615T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94641456 | |||||||
| chr7:94641499 | A | T | 10 | a0001c0001t0001g0042 a0001c0001t0001g0103 a0001c0001t0001g0253 others(7): Show |
11 | HG00597.hp1 NA18939.hp1 NA18951.hp1 others(8): Show |
intron_variant | MODIFIER | c.110-11658T>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94641499 | |||||||
| chr7:94641602 | G | A | 1 | a0001c0001t0001g0277 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.110-11761C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94641602 | |||||||
| chr7:94641755 | C | CA | 54 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(51): Show |
63 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.110-11915dupT | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94641755 | |||||||
| chr7:94641768 | G | T | 1 | a0001c0001t0001g0090 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.110-11927C>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94641768 | |||||||
| chr7:94641798 | T | G | 1 | a0001c0001t0001g0261 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.110-11957A>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94641798 | |||||||
| chr7:94641801 | T | G | 96 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(93): Show |
113 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.110-11960A>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94641801 | |||||||
| chr7:94641804 | G | T | 45 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0018 others(42): Show |
55 | HG00544.hp1 HG00735.hp1 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.110-11963C>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94641804 | |||||||
| chr7:94641843 | T | C | 57 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(54): Show |
66 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.110-12002A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94641843 | |||||||
| chr7:94641945 | G | A | 57 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(54): Show |
66 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.110-12104C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94641945 | |||||||
| chr7:94642271 | G | A | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.110-12430C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94642271 | |||||||
| chr7:94642344 | C | T | 56 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(53): Show |
65 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.110-12503G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94642344 | |||||||
| chr7:94642353 | T | A | 1 | a0001c0001t0001g0225 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.110-12512A>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94642353 | |||||||
| chr7:94642686 | G | A | 57 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(54): Show |
66 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.110-12845C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94642686 | |||||||
| chr7:94642799 | T | C | 57 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(54): Show |
66 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.110-12958A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94642799 | |||||||
| chr7:94643047 | G | A | 36 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0029 others(33): Show |
43 | HG00597.hp2 HG00639.hp2 HG01257.hp2 others(40): Show |
intron_variant | MODIFIER | c.109+12943C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94643047 | |||||||
| chr7:94643073 | C | T | 3 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0200 |
3 | HG01496.hp1 HG01517.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.109+12917G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94643073 | |||||||
| chr7:94643172 | C | G | 1 | a0001c0001t0001g0111 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.109+12818G>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94643172 | |||||||
| chr7:94643864 | T | C | 1 | a0001c0001t0001g0270 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.109+12126A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94643864 | |||||||
| chr7:94643869 | C | T | 57 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(54): Show |
66 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.109+12121G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94643869 | |||||||
| chr7:94643899 | G | T | 57 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(54): Show |
66 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.109+12091C>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94643899 | |||||||
| chr7:94643913 | A | G | 8 | a0001c0001t0001g0017 a0001c0001t0001g0057 a0001c0001t0001g0058 others(5): Show |
9 | HG00544.hp2 HG00558.hp2 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.109+12077T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94643913 | |||||||
| chr7:94643922 | G | A | 57 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(54): Show |
66 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.109+12068C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94643922 | |||||||
| chr7:94643951 | A | G | 2 | a0001c0001t0001g0231 a0001c0004t0001g0230 |
2 | HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.109+12039T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94643951 | |||||||
| chr7:94644063 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.109+11927G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94644063 | |||||||
| chr7:94644326 | T | C | 57 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(54): Show |
66 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.109+11664A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94644326 | |||||||
| chr7:94644441 | C | T | 1 | a0001c0001t0001g0056 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.109+11549G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94644441 | |||||||
| chr7:94644578 | T | C | 1 | a0001c0001t0001g0131 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.109+11412A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94644578 | |||||||
| chr7:94644635 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.109+11355C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94644635 | |||||||
| chr7:94644682 | A | G | 65 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(62): Show |
74 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.109+11308T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94644682 | |||||||
| chr7:94644720 | T | C | 57 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(54): Show |
66 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.109+11270A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94644720 | |||||||
| chr7:94644742 | C | T | 1 | a0001c0001t0001g0218 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.109+11248G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94644742 | |||||||
| chr7:94644955 | T | A | 6 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(3): Show |
6 | HG00738.hp2 HG02486.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.109+11035A>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94644955 | |||||||
| chr7:94645049 | T | G | 57 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(54): Show |
66 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.109+10941A>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94645049 | |||||||
| chr7:94645113 | G | A | 61 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(58): Show |
71 | HG00323.hp2 HG00609.hp1 HG00735.hp2 others(68): Show |
intron_variant | MODIFIER | c.109+10877C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94645113 | |||||||
| chr7:94645142 | C | A | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.109+10848G>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94645142 | |||||||
| chr7:94645239 | G | T | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.109+10751C>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94645239 | |||||||
| chr7:94645296 | T | G | 57 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(54): Show |
66 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.109+10694A>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94645296 | |||||||
| chr7:94645363 | T | C | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.109+10627A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94645363 | |||||||
| chr7:94645521 | G | T | 1 | a0001c0001t0001g0288 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.109+10469C>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94645521 | |||||||
| chr7:94645622 | C | G | 1 | a0001c0001t0001g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.109+10368G>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94645622 | |||||||
| chr7:94645703 | T | G | 1 | a0001c0001t0001g0086 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.109+10287A>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94645703 | |||||||
| chr7:94645710 | G | T | 1 | a0002c0003t0001g0238 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.109+10280C>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94645710 | |||||||
| chr7:94645954 | T | C | 12 | a0001c0001t0001g0037 a0001c0001t0001g0050 a0001c0001t0001g0141 others(9): Show |
13 | HG00438.hp2 NA18944.hp1 NA18954.hp2 others(10): Show |
intron_variant | MODIFIER | c.109+10036A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94645954 | |||||||
| chr7:94646258 | A | G | 2 | a0001c0001t0001g0109 a0001c0001t0001g0110 |
2 | HG01884.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.109+9732T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94646258 | |||||||
| chr7:94646480 | A | T | 1 | a0001c0001t0001g0032 | 2 | HG02976.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.109+9510T>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94646480 | |||||||
| chr7:94646625 | C | A | 1 | a0001c0001t0001g0219 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.109+9365G>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94646625 | |||||||
| chr7:94646673 | TA | T | 57 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(54): Show |
66 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.109+9316delT | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94646673 | |||||||
| chr7:94646730 | C | T | 2 | a0001c0001t0001g0231 a0001c0004t0001g0230 |
2 | HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.109+9260G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94646730 | |||||||
| chr7:94647068 | T | C | 1 | a0001c0001t0001g0234 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.109+8922A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94647068 | |||||||
| chr7:94647073 | A | C | 3 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0312 |
3 | HG02976.hp1 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.109+8917T>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94647073 | |||||||
| chr7:94647284 | G | C | 1 | a0001c0001t0001g0139 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.109+8706C>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94647284 | |||||||
| chr7:94647443 | G | C | 1 | a0001c0001t0001g0229 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.109+8547C>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94647443 | |||||||
| chr7:94647484 | C | A | 1 | a0001c0001t0001g0194 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.109+8506G>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94647484 | |||||||
| chr7:94647509 | C | T | 1 | a0001c0001t0001g0277 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.109+8481G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94647509 | |||||||
| chr7:94647540 | T | C | 1 | a0001c0001t0001g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.109+8450A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94647540 | |||||||
| chr7:94647686 | G | T | 57 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(54): Show |
66 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.109+8304C>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94647686 | |||||||
| chr7:94647772 | T | C | 57 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(54): Show |
66 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.109+8218A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94647772 | |||||||
| chr7:94647776 | G | A | 1 | a0001c0001t0001g0261 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.109+8214C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94647776 | |||||||
| chr7:94647961 | A | T | 1 | a0001c0001t0001g0219 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.109+8029T>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94647961 | |||||||
| chr7:94648054 | T | A | 1 | a0001c0001t0001g0087 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.109+7936A>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94648054 | |||||||
| chr7:94648123 | A | G | 1 | a0001c0001t0001g0177 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.109+7867T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94648123 | |||||||
| chr7:94648132 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.109+7858C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94648132 | |||||||
| chr7:94648144 | G | T | 1 | a0001c0001t0001g0142 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.109+7846C>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94648144 | |||||||
| chr7:94648201 | C | T | 81 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(78): Show |
98 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.109+7789G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94648201 | |||||||
| chr7:94648244 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.109+7746C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94648244 | |||||||
| chr7:94648299 | C | T | 2 | a0001c0001t0001g0231 a0001c0004t0001g0230 |
2 | HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.109+7691G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94648299 | |||||||
| chr7:94648376 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0277 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.109+7604_109+7613d others(12): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94648376 | |||||||
| chr7:94648376 | C | CAAAAAAA others(4): Show |
1 | a0001c0001t0001g0240 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.109+7603_109+7613d others(13): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94648376 | |||||||
| chr7:94648376 | C | CAAAAAAA others(5): Show |
17 | a0001c0001t0001g0014 a0001c0001t0001g0042 a0001c0001t0001g0103 others(14): Show |
20 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.109+7602_109+7613d others(14): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94648376 | |||||||
| chr7:94648376 | C | CAAAAAAA others(6): Show |
17 | a0001c0001t0001g0015 a0001c0001t0001g0043 a0001c0001t0001g0044 others(14): Show |
21 | HG00597.hp1 HG00673.hp1 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.109+7601_109+7613d others(15): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94648376 | |||||||
| chr7:94648376 | C | CAAAAAAA others(7): Show |
14 | a0001c0001t0001g0016 a0001c0001t0001g0237 a0001c0001t0001g0262 others(11): Show |
16 | HG00323.hp1 HG01074.hp2 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.109+7600_109+7613d others(16): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94648376 | |||||||
| chr7:94648376 | C | CAAAAAAA others(8): Show |
4 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0275 others(1): Show |
4 | HG01169.hp1 HG02300.hp2 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.109+7599_109+7613d others(17): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94648376 | |||||||
| chr7:94648376 | CA | C | 187 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(184): Show |
220 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(217): Show |
intron_variant | MODIFIER | c.109+7613delT | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94648376 | |||||||
| chr7:94648376 | CAA | C | 7 | a0001c0001t0001g0141 a0001c0001t0001g0172 a0001c0001t0001g0174 others(4): Show |
7 | HG01069.hp1 HG01256.hp2 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.109+7612_109+7613d others(4): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94648376 | |||||||
| chr7:94648515 | A | G | 1 | a0001c0001t0001g0108 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.109+7475T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94648515 | |||||||
| chr7:94648584 | C | T | 1 | a0001c0001t0001g0285 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.109+7406G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94648584 | |||||||
| chr7:94648673 | A | T | 1 | a0001c0001t0001g0052 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.109+7317T>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94648673 | |||||||
| chr7:94648714 | A | G | 43 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0033 others(40): Show |
52 | HG00438.hp2 HG00544.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.109+7276T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94648714 | |||||||
| chr7:94648835 | T | C | 4 | a0001c0001t0001g0029 a0001c0001t0001g0105 a0001c0001t0001g0106 others(1): Show |
5 | HG00639.hp2 HG02055.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.109+7155A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94648835 | |||||||
| chr7:94648896 | T | A | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.109+7094A>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94648896 | |||||||
| chr7:94649094 | G | A | 6 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(3): Show |
6 | HG00738.hp2 HG02486.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.109+6896C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94649094 | |||||||
| chr7:94649176 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.109+6814G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94649176 | |||||||
| chr7:94649456 | A | T | 1 | a0001c0001t0001g0140 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.109+6534T>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94649456 | |||||||
| chr7:94649477 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.109+6513G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94649477 | |||||||
| chr7:94649484 | G | A | 1 | a0001c0001t0001g0311 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.109+6506C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94649484 | |||||||
| chr7:94649534 | A | T | 1 | a0001c0001t0001g0053 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.109+6456T>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94649534 | |||||||
| chr7:94649630 | T | A | 1 | a0001c0001t0001g0213 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.109+6360A>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94649630 | |||||||
| chr7:94649659 | G | A | 57 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(54): Show |
66 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.109+6331C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94649659 | |||||||
| chr7:94649834 | T | C | 81 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(78): Show |
98 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.109+6156A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94649834 | |||||||
| chr7:94650032 | C | A | 57 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(54): Show |
66 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.109+5958G>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94650032 | |||||||
| chr7:94650269 | C | T | 57 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(54): Show |
66 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.109+5721G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94650269 | |||||||
| chr7:94650463 | ATCT | A | 21 | a0001c0001t0001g0013 a0001c0001t0001g0134 a0001c0001t0001g0135 others(18): Show |
23 | HG00323.hp2 HG00735.hp2 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.109+5524_109+5526d others(5): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94650463 | |||||||
| chr7:94650589 | C | CA | 4 | a0001c0001t0001g0029 a0001c0001t0001g0105 a0001c0001t0001g0106 others(1): Show |
5 | HG00639.hp2 HG02055.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.109+5400dupT | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94650589 | |||||||
| chr7:94650599 | G | GA | 57 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(54): Show |
66 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.109+5390dupT | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94650599 | |||||||
| chr7:94650768 | G | A | 1 | a0001c0001t0001g0273 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.109+5222C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94650768 | |||||||
| chr7:94651048 | A | G | 1 | a0001c0001t0001g0284 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.109+4942T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94651048 | |||||||
| chr7:94651124 | A | T | 320 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(317): Show |
387 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(384): Show |
intron_variant | MODIFIER | c.109+4866T>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94651124 | |||||||
| chr7:94651334 | C | T | 2 | a0001c0001t0001g0172 a0001c0001t0001g0173 |
2 | HG03017.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.109+4656G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94651334 | |||||||
| chr7:94651455 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.109+4535G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94651455 | |||||||
| chr7:94651881 | T | C | 2 | a0001c0001t0001g0274 a0001c0001t0001g0275 |
2 | NA18980.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.109+4109A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94651881 | |||||||
| chr7:94651916 | A | G | 3 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0001g0237 |
3 | NA18953.hp1 NA18965.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.109+4074T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94651916 | |||||||
| chr7:94651930 | CT | C | 3 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0280 |
3 | HG01106.hp1 HG01123.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.109+4059delA | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94651930 | |||||||
| chr7:94651932 | TTA | T | 54 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(51): Show |
63 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.109+4056_109+4057d others(4): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94651932 | |||||||
| chr7:94651935 | T | A | 54 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(51): Show |
63 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.109+4055A>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94651935 | |||||||
| chr7:94651936 | T | A | 3 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0280 |
3 | HG01106.hp1 HG01123.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.109+4054A>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94651936 | |||||||
| chr7:94651937 | A | T | 3 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0280 |
3 | HG01106.hp1 HG01123.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.109+4053T>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94651937 | |||||||
| chr7:94651937 | AT | A | 10 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0089 others(7): Show |
16 | HG00673.hp2 HG01123.hp2 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.109+4052delA | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94651937 | |||||||
| chr7:94651939 | T | A | 2 | a0001c0001t0001g0276 a0001c0001t0001g0277 |
2 | HG02886.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.109+4051A>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94651939 | |||||||
| chr7:94651946 | T | G | 92 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(89): Show |
107 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(104): Show |
intron_variant | MODIFIER | c.109+4044A>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94651946 | |||||||
| chr7:94651947 | T | G | 1 | a0001c0001t0001g0097 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.109+4043A>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94651947 | |||||||
| chr7:94651953 | TCTCGTAC others(5): Show |
T | 1 | a0001c0001t0001g0171 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.109+4025_109+4036d others(14): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94651953 | |||||||
| chr7:94652023 | G | A | 64 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(61): Show |
76 | HG00323.hp2 HG00609.hp1 HG00735.hp2 others(73): Show |
intron_variant | MODIFIER | c.109+3967C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94652023 | |||||||
| chr7:94652032 | A | T | 57 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(54): Show |
66 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.109+3958T>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94652032 | |||||||
| chr7:94652054 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.109+3936C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94652054 | |||||||
| chr7:94652435 | G | A | 1 | a0001c0001t0001g0218 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.109+3555C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94652435 | |||||||
| chr7:94652446 | T | C | 57 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(54): Show |
66 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.109+3544A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94652446 | |||||||
| chr7:94652670 | T | A | 1 | a0001c0001t0001g0132 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.109+3320A>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94652670 | |||||||
| chr7:94653037 | T | C | 1 | a0001c0001t0001g0231 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.109+2953A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94653037 | |||||||
| chr7:94653164 | G | A | 1 | a0001c0001t0001g0219 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.109+2826C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94653164 | |||||||
| chr7:94653224 | G | T | 6 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(3): Show |
6 | HG00738.hp2 HG02486.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.109+2766C>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94653224 | |||||||
| chr7:94653268 | A | G | 2 | a0001c0001t0001g0134 a0001c0001t0001g0135 |
2 | HG01099.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.109+2722T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94653268 | |||||||
| chr7:94653379 | TA | T | 4 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(1): Show |
4 | HG00738.hp2 HG02486.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.109+2610delT | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94653379 | |||||||
| chr7:94653645 | G | T | 1 | a0001c0001t0001g0051 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.109+2345C>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94653645 | |||||||
| chr7:94653709 | T | A | 1 | a0001c0001t0001g0220 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.109+2281A>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94653709 | |||||||
| chr7:94653762 | G | A | 5 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(2): Show |
5 | HG01261.hp2 HG01928.hp2 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.109+2228C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94653762 | |||||||
| chr7:94653792 | A | G | 57 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(54): Show |
66 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.109+2198T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94653792 | |||||||
| chr7:94654014 | T | C | 1 | a0001c0001t0001g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.109+1976A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94654014 | |||||||
| chr7:94654355 | T | C | 1 | a0001c0001t0001g0104 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.109+1635A>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94654355 | |||||||
| chr7:94654441 | G | A | 1 | a0001c0001t0001g0133 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.109+1549C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94654441 | |||||||
| chr7:94654480 | G | A | 5 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0100 others(2): Show |
9 | NA18948.hp1 NA18957.hp1 NA18962.hp1 others(6): Show |
intron_variant | MODIFIER | c.109+1510C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94654480 | |||||||
| chr7:94654560 | A | C | 1 | a0001c0001t0001g0050 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.109+1430T>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94654560 | |||||||
| chr7:94654633 | T | TTCTC | 66 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(63): Show |
75 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.109+1356_109+1357i others(6): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94654633 | |||||||
| chr7:94654657 | T | G | 1 | a0001c0001t0001g0104 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.109+1333A>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94654657 | |||||||
| chr7:94654836 | T | G | 7 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0280 others(4): Show |
7 | HG01106.hp1 HG01123.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.109+1154A>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94654836 | |||||||
| chr7:94654837 | T | G | 57 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(54): Show |
66 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.109+1153A>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94654837 | |||||||
| chr7:94655046 | A | G | 1 | a0001c0001t0001g0028 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.109+944T>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94655046 | |||||||
| chr7:94655141 | T | G | 41 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(38): Show |
45 | HG01243.hp2 HG01884.hp1 HG01891.hp2 others(42): Show |
intron_variant | MODIFIER | c.109+849A>C | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94655141 | |||||||
| chr7:94655216 | C | T | 1 | a0001c0001t0001g0133 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.109+774G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94655216 | |||||||
| chr7:94655290 | G | A | 1 | a0001c0001t0001g0104 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.109+700C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94655290 | |||||||
| chr7:94655582 | G | A | 1 | a0001c0001t0001g0318 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.109+408C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94655582 | |||||||
| chr7:94655619 | C | T | 35 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0029 others(32): Show |
42 | HG00597.hp2 HG00639.hp2 HG01257.hp2 others(39): Show |
intron_variant | MODIFIER | c.109+371G>A | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94655619 | |||||||
| chr7:94655671 | G | A | 1 | a0001c0001t0001g0319 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.109+319C>T | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94655671 | |||||||
| chr7:94655777 | G | GAAA | 248 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(245): Show |
290 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(287): Show |
intron_variant | MODIFIER | c.109+210_109+212dup others(3): Show |
SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94655777 | |||||||
| chr7:94655880 | G | C | 3 | a0001c0001t0001g0320 a0001c0001t0001g0321 a0001c0001t0001g0322 |
3 | HG02630.hp1 HG02809.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.109+110C>G | SGCE | ENSG00000127990.19 | transcript | ENST00000648936.2 | protein_coding | 1/10 | chr7 | 94655880 |