Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 25797 |
| ensemblid | ENSG00000115828.17 |
| hgncid | 9753 |
| symbol | QPCT |
| name | glutaminyl-peptide cyclotransferase |
| refseq_nuc | NM_012413.4 |
| refseq_prot | NP_036545.1 |
| ensembl_nuc | ENST00000338415.8 |
| ensembl_prot | ENSP00000344829.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 37344630 |
| end | 37373322 |
| strand | + |
| ver | v1.2 |
| region | chr2:37344630-37373322 |
| region5000 | chr2:37339630-37378322 |
| regionname0 | QPCT_chr2_37344630_37373322 |
| regionname5000 | QPCT_chr2_37339630_37378322 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 361 | 318 | 89 | 64 | 111 | 12 | 40 | 86 | QPCT_chr2_37339630_37378322 | QPCT | MAGGR others(356): Show |
chr2 | 37339630 | 37378322 |
| a0002 | 0/0 | 361 | 71 | 0 | 9 | 62 | 0 | 0 | 48 | QPCT_chr2_37339630_37378322 | QPCT | MAGGR others(356): Show |
chr2 | 37339630 | 37378322 |
| a0003 | 0/0 | 361 | 32 | 0 | 4 | 25 | 2 | 1 | 22 | QPCT_chr2_37339630_37378322 | QPCT | MAGGR others(356): Show |
chr2 | 37339630 | 37378322 |
| a0004 | 0/0 | 361 | 19 | 5 | 3 | 10 | 0 | 1 | 8 | QPCT_chr2_37339630_37378322 | QPCT | MAGGR others(356): Show |
chr2 | 37339630 | 37378322 |
| a0005 | 0/0 | 361 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | MAGGR others(356): Show |
chr2 | 37339630 | 37378322 |
| a0006 | 0/0 | 361 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | MAGGR others(356): Show |
chr2 | 37339630 | 37378322 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1083 | 262 | 42 | 60 | 110 | 10 | 38 | QPCT_chr2_37339630_37378322 | QPCT | ATGGC others(1078): Show |
chr2 | 37339630 | 37378322 | ||
| a0001c0003 | 0/0 | 1083 | 55 | 47 | 4 | 0 | 2 | 2 | QPCT_chr2_37339630_37378322 | QPCT | ATGGC others(1078): Show |
chr2 | 37339630 | 37378322 | ||
| a0001c0006 | 0/0 | 1083 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | ATGGC others(1078): Show |
chr2 | 37339630 | 37378322 | ||
| a0002c0002 | 0/0 | 1083 | 71 | 0 | 9 | 62 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | ATGGC others(1078): Show |
chr2 | 37339630 | 37378322 | ||
| a0003c0004 | 0/0 | 1083 | 32 | 0 | 4 | 25 | 2 | 1 | QPCT_chr2_37339630_37378322 | QPCT | ATGGC others(1078): Show |
chr2 | 37339630 | 37378322 | ||
| a0004c0005 | 0/0 | 1083 | 19 | 5 | 3 | 10 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | ATGGC others(1078): Show |
chr2 | 37339630 | 37378322 | ||
| a0005c0007 | 0/0 | 1083 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | ATGGC others(1078): Show |
chr2 | 37339630 | 37378322 | ||
| a0006c0008 | 0/0 | 1083 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | ATGGC others(1078): Show |
chr2 | 37339630 | 37378322 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1683 | 240 | 35 | 57 | 105 | 10 | 32 | QPCT_chr2_37339630_37378322 | QPCT | AGTCG others(1678): Show |
chr2 | 37339630 | 37378322 |
| a0001c0001t0002 | 0/0 | 1683 | 12 | 5 | 1 | 5 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | AGTCG others(1678): Show |
chr2 | 37339630 | 37378322 |
| a0001c0001t0003 | 0/0 | 1681 | 2 | 2 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | AGTCG others(1676): Show |
chr2 | 37339630 | 37378322 |
| a0001c0001t0004 | 1/0 | 1683 | 6 | 0 | 1 | 0 | 0 | 4 | QPCT_chr2_37339630_37378322 | QPCT | AGTCG others(1678): Show |
chr2 | 37339630 | 37378322 |
| a0001c0001t0005 | 0/0 | 1683 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | AGTCG others(1678): Show |
chr2 | 37339630 | 37378322 |
| a0001c0001t0007 | 0/0 | 1683 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | AGTCG others(1678): Show |
chr2 | 37339630 | 37378322 |
| a0001c0003t0001 | 0/0 | 1683 | 41 | 36 | 3 | 0 | 0 | 2 | QPCT_chr2_37339630_37378322 | QPCT | AGTCG others(1678): Show |
chr2 | 37339630 | 37378322 |
| a0001c0003t0002 | 0/0 | 1683 | 5 | 4 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | AGTCG others(1678): Show |
chr2 | 37339630 | 37378322 |
| a0001c0003t0003 | 0/0 | 1681 | 6 | 6 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | AGTCG others(1676): Show |
chr2 | 37339630 | 37378322 |
| a0001c0003t0005 | 0/0 | 1683 | 3 | 1 | 0 | 0 | 2 | 0 | QPCT_chr2_37339630_37378322 | QPCT | AGTCG others(1678): Show |
chr2 | 37339630 | 37378322 |
| a0001c0006t0001 | 0/0 | 1683 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | AGTCG others(1678): Show |
chr2 | 37339630 | 37378322 |
| a0002c0002t0002 | 0/0 | 1683 | 70 | 0 | 9 | 61 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | AGTCG others(1678): Show |
chr2 | 37339630 | 37378322 |
| a0002c0002t0008 | 0/0 | 1683 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | AGTCG others(1678): Show |
chr2 | 37339630 | 37378322 |
| a0003c0004t0002 | 0/0 | 1683 | 31 | 0 | 4 | 25 | 2 | 0 | QPCT_chr2_37339630_37378322 | QPCT | AGTCG others(1678): Show |
chr2 | 37339630 | 37378322 |
| a0003c0004t0005 | 0/0 | 1683 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | AGTCG others(1678): Show |
chr2 | 37339630 | 37378322 |
| a0004c0005t0001 | 0/0 | 1683 | 17 | 4 | 3 | 9 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | AGTCG others(1678): Show |
chr2 | 37339630 | 37378322 |
| a0004c0005t0002 | 0/0 | 1683 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | AGTCG others(1678): Show |
chr2 | 37339630 | 37378322 |
| a0004c0005t0003 | 0/0 | 1681 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | AGTCG others(1676): Show |
chr2 | 37339630 | 37378322 |
| a0005c0007t0001 | 0/0 | 1683 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | AGTCG others(1678): Show |
chr2 | 37339630 | 37378322 |
| a0006c0008t0006 | 0/0 | 1683 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | AGTCG others(1678): Show |
chr2 | 37339630 | 37378322 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 6 | 1 | 1 | 1 | 1 | 2 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0004 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0007 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0045 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0048 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0002g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0002g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0002g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0002g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0004g0006 | 0/0 | 4 | 0 | 1 | 0 | 0 | 3 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0004g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0004g0334 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0005g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0001t0007g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0003t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0003t0001g0028 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0003t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0003t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0003t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0003t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0003t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0003t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0003t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0003t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0003t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0003t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0003t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0003t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0003t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0003t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0003t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0003t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0003t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0003t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0003t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0003t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0003t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0003t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0003t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0003t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0003t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0003t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0003t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0003t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0003t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0003t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0003t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0003t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0003t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0003t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0003t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0003t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0003t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0003t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0003t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0003t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0003t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0003t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0003t0003g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0003t0003g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0003t0003g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0003t0003g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0003t0005g0017 | 0/0 | 3 | 1 | 0 | 0 | 2 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0001c0006t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0002c0002t0002g0002 | 0/0 | 6 | 0 | 5 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0002c0002t0002g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0002c0002t0002g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0002c0002t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0002c0002t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0002c0002t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0002c0002t0002g0039 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0002c0002t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0002c0002t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0002c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0002c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0002c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0002c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0002c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0002c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0002c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0002c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0002c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0002c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0002c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0002c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0002c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0002c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0002c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0002c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0002c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0002c0002t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0002c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0002c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0002c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0002c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0002c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0002c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0002c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0002c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0002c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0002c0002t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0002c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0002c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0002c0002t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0002c0002t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0002c0002t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0002c0002t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0002c0002t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0002c0002t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0002c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0002c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0002c0002t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0002c0002t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0002c0002t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0002c0002t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0002c0002t0002g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0002c0002t0008g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0003c0004t0002g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0003c0004t0002g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0003c0004t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0003c0004t0002g0046 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0003c0004t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0003c0004t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0003c0004t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0003c0004t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0003c0004t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0003c0004t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0003c0004t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0003c0004t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0003c0004t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0003c0004t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0003c0004t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0003c0004t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0003c0004t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0003c0004t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0003c0004t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0003c0004t0002g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0003c0004t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0003c0004t0002g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0003c0004t0002g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0003c0004t0005g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0004c0005t0001g0035 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0004c0005t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0004c0005t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0004c0005t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0004c0005t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0004c0005t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0004c0005t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0004c0005t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0004c0005t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0004c0005t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0004c0005t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0004c0005t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0004c0005t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0004c0005t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0004c0005t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0004c0005t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0004c0005t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0005c0007t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| a0006c0008t0006g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0044 | EUR | GBR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0080 | EUR | GBR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0320 | EUR | GBR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | GBR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG00280 | hp1 | a0001 | c0003 | t0005 | g0017 | EUR | FIN | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | FIN | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | CHS | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG00438 | hp2 | a0004 | c0005 | t0001 | g0252 | EAS | CHS | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | CHS | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG00544 | hp2 | a0002 | c0002 | t0002 | g0288 | EAS | CHS | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG00558 | hp1 | a0003 | c0004 | t0002 | g0023 | EAS | CHS | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | CHS | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG00597 | hp1 | a0003 | c0004 | t0002 | g0111 | EAS | CHS | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | CHS | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG00621 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | CHS | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0308 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG00639 | hp2 | a0004 | c0005 | t0001 | g0257 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG00673 | hp1 | a0002 | c0002 | t0002 | g0246 | EAS | CHS | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | CHS | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG00738 | hp1 | a0003 | c0004 | t0002 | g0345 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG00738 | hp2 | a0001 | c0003 | t0001 | g0153 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG00741 | hp2 | a0001 | c0001 | t0005 | g0327 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01069 | hp2 | a0003 | c0004 | t0002 | g0346 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0347 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0314 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01106 | hp1 | a0004 | c0005 | t0001 | g0138 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0324 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0330 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0316 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01192 | hp2 | a0004 | c0005 | t0001 | g0035 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01243 | hp1 | a0001 | c0003 | t0001 | g0154 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0325 | AMR | CLM | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01255 | hp2 | a0003 | c0004 | t0002 | g0050 | AMR | CLM | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01257 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | CLM | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0341 | AMR | CLM | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0305 | AMR | CLM | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0303 | AMR | CLM | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01361 | hp1 | a0001 | c0001 | t0004 | g0006 | AMR | CLM | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01361 | hp2 | a0001 | c0003 | t0002 | g0224 | AMR | CLM | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01433 | hp1 | a0002 | c0002 | t0002 | g0258 | AMR | CLM | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0312 | AMR | CLM | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | CLM | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01515 | hp1 | a0003 | c0004 | t0002 | g0046 | EUR | IBS | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0222 | EUR | IBS | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01517 | hp1 | a0003 | c0004 | t0002 | g0046 | EUR | IBS | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0078 | EUR | IBS | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0300 | AFR | ACB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01884 | hp2 | a0001 | c0003 | t0001 | g0149 | AFR | ACB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01891 | hp1 | a0001 | c0003 | t0001 | g0162 | AFR | ACB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01891 | hp2 | a0001 | c0003 | t0001 | g0141 | AFR | ACB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01928 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01934 | hp1 | a0003 | c0004 | t0002 | g0317 | AMR | PEL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01934 | hp2 | a0002 | c0002 | t0002 | g0039 | AMR | PEL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0344 | AMR | PEL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01975 | hp2 | a0002 | c0002 | t0002 | g0272 | AMR | PEL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01981 | hp2 | a0001 | c0003 | t0001 | g0028 | AMR | PEL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01993 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02004 | hp1 | a0002 | c0002 | t0002 | g0291 | AMR | PEL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02015 | hp2 | a0002 | c0002 | t0002 | g0280 | EAS | KHV | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | KHV | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0297 | EAS | KHV | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0336 | AFR | ACB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | ACB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02056 | hp2 | a0002 | c0002 | t0002 | g0286 | EAS | KHV | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | KHV | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02071 | hp2 | a0003 | c0004 | t0002 | g0011 | EAS | KHV | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02074 | hp2 | a0004 | c0005 | t0002 | g0250 | EAS | KHV | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02080 | hp2 | a0002 | c0002 | t0008 | g0290 | EAS | KHV | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0343 | EAS | KHV | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02083 | hp2 | a0002 | c0002 | t0002 | g0010 | EAS | KHV | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02129 | hp1 | a0002 | c0002 | t0002 | g0277 | EAS | KHV | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0296 | EAS | KHV | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02132 | hp1 | a0002 | c0002 | t0002 | g0260 | EAS | KHV | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02132 | hp2 | a0002 | c0002 | t0002 | g0038 | EAS | KHV | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0311 | EAS | KHV | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02145 | hp1 | a0001 | c0003 | t0001 | g0128 | AFR | ACB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02145 | hp2 | a0001 | c0003 | t0001 | g0163 | AFR | ACB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02155 | hp1 | a0002 | c0002 | t0002 | g0281 | EAS | CDX | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02155 | hp2 | a0002 | c0002 | t0002 | g0268 | EAS | CDX | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | CDX | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CDX | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | ACB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0304 | AFR | ACB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | ACB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0318 | AMR | PEL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02280 | hp1 | a0001 | c0003 | t0003 | g0223 | AFR | ACB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0332 | AFR | ACB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02293 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02300 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02451 | hp1 | a0001 | c0003 | t0001 | g0029 | AFR | ACB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02451 | hp2 | a0001 | c0003 | t0003 | g0350 | AFR | ACB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0333 | AFR | GWD | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02602 | hp1 | a0001 | c0003 | t0001 | g0028 | SAS | PJL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0043 | AFR | GWD | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02615 | hp2 | a0001 | c0003 | t0001 | g0158 | AFR | GWD | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02630 | hp1 | a0001 | c0003 | t0001 | g0161 | AFR | GWD | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02630 | hp2 | a0001 | c0003 | t0001 | g0351 | AFR | GWD | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02647 | hp1 | a0001 | c0003 | t0001 | g0167 | AFR | GWD | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02698 | hp1 | a0001 | c0001 | t0004 | g0006 | SAS | PJL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02698 | hp2 | a0003 | c0004 | t0005 | g0259 | SAS | PJL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02717 | hp1 | a0004 | c0005 | t0003 | g0139 | AFR | GWD | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0184 | AFR | GWD | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02723 | hp1 | a0001 | c0003 | t0001 | g0144 | AFR | GWD | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02735 | hp1 | a0001 | c0001 | t0004 | g0006 | SAS | PJL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0340 | SAS | PJL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02809 | hp1 | a0001 | c0003 | t0001 | g0152 | AFR | GWD | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02809 | hp2 | a0001 | c0003 | t0001 | g0146 | AFR | GWD | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02818 | hp2 | a0001 | c0003 | t0001 | g0132 | AFR | GWD | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02895 | hp2 | a0001 | c0003 | t0001 | g0155 | AFR | GWD | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0337 | AFR | GWD | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0339 | AFR | GWD | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | GWD | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02922 | hp1 | a0001 | c0003 | t0001 | g0018 | AFR | ESN | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0301 | AFR | ESN | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0338 | AFR | ESN | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02976 | hp1 | a0001 | c0003 | t0001 | g0236 | AFR | ESN | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02976 | hp2 | a0001 | c0003 | t0003 | g0354 | AFR | ESN | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG03017 | hp1 | a0001 | c0001 | t0004 | g0313 | SAS | PJL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG03098 | hp2 | a0001 | c0003 | t0003 | g0129 | AFR | MSL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG03130 | hp1 | a0001 | c0003 | t0001 | g0157 | AFR | ESN | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG03130 | hp2 | a0001 | c0003 | t0001 | g0353 | AFR | ESN | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0235 | AFR | ESN | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG03139 | hp2 | a0001 | c0003 | t0001 | g0143 | AFR | ESN | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG03195 | hp1 | a0001 | c0003 | t0001 | g0029 | AFR | ESN | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG03195 | hp2 | a0001 | c0003 | t0003 | g0355 | AFR | ESN | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG03209 | hp1 | a0001 | c0003 | t0002 | g0225 | AFR | MSL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG03209 | hp2 | a0001 | c0003 | t0001 | g0018 | AFR | MSL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG03225 | hp1 | a0001 | c0003 | t0001 | g0159 | AFR | MSL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | MSL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG03239 | hp1 | a0001 | c0001 | t0007 | g0013 | SAS | PJL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0326 | SAS | PJL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG03453 | hp1 | a0004 | c0005 | t0001 | g0131 | AFR | MSL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG03453 | hp2 | a0001 | c0003 | t0001 | g0151 | AFR | MSL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0043 | AFR | MSL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG03486 | hp2 | a0001 | c0003 | t0001 | g0145 | AFR | MSL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG03492 | hp2 | a0001 | c0001 | t0004 | g0006 | SAS | PJL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG03540 | hp1 | a0001 | c0003 | t0001 | g0150 | AFR | GWD | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG03540 | hp2 | a0004 | c0005 | t0001 | g0140 | AFR | GWD | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG03579 | hp1 | a0001 | c0003 | t0002 | g0227 | AFR | MSL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG03579 | hp2 | a0001 | c0003 | t0001 | g0018 | AFR | MSL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0302 | SAS | PJL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | STU | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | STU | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0307 | SAS | PJL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | BEB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | BEB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | BEB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | BEB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG03942 | hp1 | a0001 | c0003 | t0001 | g0142 | SAS | BEB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | BEB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | BEB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | BEB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG04199 | hp1 | a0004 | c0005 | t0001 | g0273 | SAS | STU | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0292 | SAS | STU | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | STU | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | STU | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | STU | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18522 | hp1 | a0001 | c0003 | t0001 | g0228 | AFR | YRI | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18522 | hp2 | a0001 | c0003 | t0001 | g0165 | AFR | YRI | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18612 | hp2 | a0002 | c0002 | t0002 | g0241 | EAS | CHB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18747 | hp1 | a0002 | c0002 | t0002 | g0269 | EAS | CHB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | CHB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0309 | AFR | YRI | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0319 | AFR | YRI | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18940 | hp1 | a0002 | c0002 | t0002 | g0244 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18941 | hp1 | a0003 | c0004 | t0002 | g0003 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18941 | hp2 | a0002 | c0002 | t0002 | g0037 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18942 | hp1 | a0005 | c0007 | t0001 | g0009 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18944 | hp1 | a0002 | c0002 | t0002 | g0256 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18944 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18945 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18946 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18946 | hp2 | a0003 | c0004 | t0002 | g0055 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18947 | hp1 | a0002 | c0002 | t0002 | g0270 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18948 | hp1 | a0002 | c0002 | t0002 | g0255 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18949 | hp2 | a0002 | c0002 | t0002 | g0041 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18951 | hp1 | a0003 | c0004 | t0002 | g0011 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18952 | hp1 | a0002 | c0002 | t0002 | g0040 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18956 | hp1 | a0002 | c0002 | t0002 | g0247 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18959 | hp1 | a0003 | c0004 | t0002 | g0306 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18960 | hp2 | a0003 | c0004 | t0002 | g0051 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18961 | hp2 | a0002 | c0002 | t0002 | g0266 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18962 | hp1 | a0002 | c0002 | t0002 | g0271 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18962 | hp2 | a0002 | c0002 | t0002 | g0041 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18963 | hp2 | a0002 | c0002 | t0002 | g0279 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18964 | hp2 | a0002 | c0002 | t0002 | g0037 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18965 | hp2 | a0002 | c0002 | t0002 | g0283 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18968 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18969 | hp1 | a0003 | c0004 | t0002 | g0053 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18972 | hp1 | a0002 | c0002 | t0002 | g0034 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18972 | hp2 | a0003 | c0004 | t0002 | g0105 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18973 | hp2 | a0002 | c0002 | t0002 | g0240 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18975 | hp2 | a0002 | c0002 | t0002 | g0263 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18977 | hp2 | a0003 | c0004 | t0002 | g0249 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18979 | hp1 | a0004 | c0005 | t0001 | g0278 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18980 | hp1 | a0003 | c0004 | t0002 | g0003 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18980 | hp2 | a0002 | c0002 | t0002 | g0265 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18981 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18984 | hp1 | a0004 | c0005 | t0001 | g0289 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18986 | hp1 | a0004 | c0005 | t0001 | g0036 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18986 | hp2 | a0003 | c0004 | t0002 | g0063 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18987 | hp2 | a0003 | c0004 | t0002 | g0106 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18988 | hp2 | a0004 | c0005 | t0001 | g0285 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18989 | hp2 | a0002 | c0002 | t0002 | g0276 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18991 | hp1 | a0002 | c0002 | t0002 | g0239 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18994 | hp1 | a0002 | c0002 | t0002 | g0264 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18995 | hp1 | a0003 | c0004 | t0002 | g0003 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18995 | hp2 | a0002 | c0002 | t0002 | g0287 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19000 | hp1 | a0002 | c0002 | t0002 | g0237 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19002 | hp1 | a0002 | c0002 | t0002 | g0245 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19002 | hp2 | a0003 | c0004 | t0002 | g0023 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19003 | hp1 | a0003 | c0004 | t0002 | g0321 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19004 | hp2 | a0002 | c0002 | t0002 | g0242 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19005 | hp2 | a0004 | c0005 | t0001 | g0035 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19007 | hp1 | a0001 | c0006 | t0001 | g0193 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19011 | hp2 | a0002 | c0002 | t0002 | g0275 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19030 | hp1 | a0001 | c0003 | t0001 | g0156 | AFR | LWK | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19030 | hp2 | a0001 | c0003 | t0001 | g0164 | AFR | LWK | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | LWK | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | LWK | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19055 | hp1 | a0002 | c0002 | t0002 | g0248 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19056 | hp2 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19058 | hp1 | a0002 | c0002 | t0002 | g0253 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19060 | hp2 | a0003 | c0004 | t0002 | g0011 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19062 | hp1 | a0003 | c0004 | t0002 | g0057 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19062 | hp2 | a0002 | c0002 | t0002 | g0251 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19063 | hp1 | a0002 | c0002 | t0002 | g0038 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19063 | hp2 | a0006 | c0008 | t0006 | g0328 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19064 | hp2 | a0002 | c0002 | t0002 | g0267 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19065 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19066 | hp2 | a0002 | c0002 | t0002 | g0261 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19067 | hp1 | a0003 | c0004 | t0002 | g0107 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19067 | hp2 | a0002 | c0002 | t0002 | g0238 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19070 | hp2 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19074 | hp1 | a0003 | c0004 | t0002 | g0299 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19074 | hp2 | a0004 | c0005 | t0001 | g0274 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19077 | hp1 | a0003 | c0004 | t0002 | g0103 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19078 | hp1 | a0002 | c0002 | t0002 | g0254 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19079 | hp2 | a0004 | c0005 | t0001 | g0036 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19082 | hp2 | a0002 | c0002 | t0002 | g0040 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19083 | hp2 | a0002 | c0002 | t0002 | g0039 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19085 | hp1 | a0004 | c0005 | t0001 | g0284 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19086 | hp2 | a0002 | c0002 | t0002 | g0034 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19087 | hp1 | a0002 | c0002 | t0002 | g0243 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19087 | hp2 | a0003 | c0004 | t0002 | g0003 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19088 | hp1 | a0003 | c0004 | t0002 | g0230 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19088 | hp2 | a0003 | c0004 | t0002 | g0003 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19090 | hp2 | a0002 | c0002 | t0002 | g0282 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19091 | hp2 | a0002 | c0002 | t0002 | g0262 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19240 | hp1 | a0001 | c0003 | t0002 | g0166 | AFR | YRI | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA19240 | hp2 | a0001 | c0003 | t0003 | g0352 | AFR | YRI | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA20129 | hp1 | a0001 | c0003 | t0001 | g0147 | AFR | ASW | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0098 | AFR | ASW | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0331 | EUR | TSI | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0211 | EUR | TSI | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA20805 | hp2 | a0001 | c0003 | t0005 | g0017 | EUR | TSI | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0200 | SAS | GIH | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0342 | AMR | CLM | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02109 | hp1 | a0001 | c0003 | t0001 | g0349 | AFR | ACB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02486 | hp2 | a0001 | c0003 | t0001 | g0148 | AFR | ACB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02559 | hp1 | a0001 | c0003 | t0001 | g0348 | AFR | ACB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG02559 | hp2 | a0004 | c0005 | t0001 | g0137 | AFR | ACB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG03471 | hp1 | a0001 | c0003 | t0001 | g0160 | AFR | MSL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG03471 | hp2 | a0001 | c0003 | t0002 | g0226 | AFR | MSL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG06807 | hp1 | a0004 | c0005 | t0001 | g0130 | AFR | USA | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | USA | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | USA | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | USA | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA21309 | hp1 | a0001 | c0003 | t0005 | g0017 | AFR | LWK | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0335 | AFR | LWK | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0048 | REF | REF | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0334 | REF | REF | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:37352828 | C | T | 2 | a0002 a0004 |
90 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(87): Show |
missense_variant | MODERATE | c.160C>T | p.Arg54Trp | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/7 | 262/1683 | 160/1086 | 54/361 | chr2 | 37352828 | |||
| chr2:37372702 | A | T | 1 | a0006 | 1 | NA19063.hp2 | missense_variant | MODERATE | c.961A>T | p.Ile321Leu | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 7/7 | 1063/1683 | 961/1086 | 321/361 | chr2 | 37372702 | |||
| chr2:37372720 | G | A | 1 | a0005 | 1 | NA18942.hp1 | missense_variant | MODERATE | c.979G>A | p.Glu327Lys | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 7/7 | 1081/1683 | 979/1086 | 327/361 | chr2 | 37372720 | |||
| chr2:37372820 | A | C | 2 | a0002 a0003 |
103 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(100): Show |
missense_variant | MODERATE | c.1079A>C | p.His360Pro | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 7/7 | 1181/1683 | 1079/1086 | 360/361 | chr2 | 37372820 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:37344740 | C | A | 1 | a0001c0006 | 1 | NA19007.hp1 | synonymous_variant | LOW | c.9C>A | p.Gly3Gly | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/7 | 111/1683 | 9/1086 | 3/361 | chr2 | 37344740 | |||
| chr2:37352794 | C | T | 3 | a0001c0003 a0002c0002 a0004c0005 |
145 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(142): Show |
synonymous_variant | LOW | c.126C>T | p.Tyr42Tyr | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/7 | 228/1683 | 126/1086 | 42/361 | chr2 | 37352794 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:37372836 | T | A | 1 | a0006c0008t0006 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9T>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 7/7 | 9 | chr2 | 37372836 | ||||||
| chr2:37372845 | G | T | 9 | a0001c0001t0002 a0001c0001t0003 a0001c0003t0002 others(6): Show |
129 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*18G>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 7/7 | 18 | chr2 | 37372845 | ||||||
| chr2:37372955 | T | C | 1 | a0002c0002t0008 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*128T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 7/7 | 128 | chr2 | 37372955 | ||||||
| chr2:37372989 | T | C | 1 | a0001c0001t0007 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*162T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 7/7 | 162 | chr2 | 37372989 | ||||||
| chr2:37373149 | C | A | 19 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(16): Show |
435 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(432): Show |
3_prime_UTR_variant | MODIFIER | c.*322C>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 7/7 | 322 | chr2 | 37373149 | ||||||
| chr2:37373239 | CAT | C | 3 | a0001c0001t0003 a0001c0003t0003 a0004c0005t0003 |
9 | HG02280.hp1 HG02451.hp2 HG02717.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*413_*414delAT | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 7/7 | 413 | chr2 | 37373239 | ||||||
| chr2:37373284 | A | G | 12 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(9): Show |
134 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(131): Show |
3_prime_UTR_variant | MODIFIER | c.*457A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 7/7 | 457 | chr2 | 37373284 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:37344900 | G | T | 8 | a0001c0003t0001g0348 a0001c0003t0001g0349 a0001c0003t0001g0351 others(5): Show |
8 | HG02109.hp1 HG02451.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.120+49G>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37344900 | |||||||
| chr2:37345194 | C | A | 1 | a0001c0001t0001g0047 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.120+343C>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37345194 | |||||||
| chr2:37345207 | G | C | 217 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(214): Show |
269 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.120+356G>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37345207 | |||||||
| chr2:37345216 | C | A | 2 | a0001c0001t0001g0234 a0001c0001t0003g0235 |
2 | HG02109.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.120+365C>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37345216 | |||||||
| chr2:37345231 | GGGGCCGC others(2): Show |
G | 7 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0229 others(4): Show |
11 | HG00544.hp1 HG00558.hp2 NA18947.hp2 others(8): Show |
intron_variant | MODIFIER | c.120+384_120+392del others(9): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37345231 | ||||||
| chr2:37345301 | TGCTGGGG others(1): Show |
T | 100 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(97): Show |
127 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.120+455_120+462del others(8): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37345301 | ||||||
| chr2:37345322 | C | G | 7 | a0001c0003t0001g0349 a0001c0003t0001g0351 a0001c0003t0001g0353 others(4): Show |
7 | HG02109.hp1 HG02451.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.120+471C>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37345322 | |||||||
| chr2:37345420 | C | A | 7 | a0001c0003t0001g0349 a0001c0003t0001g0351 a0001c0003t0001g0353 others(4): Show |
7 | HG02109.hp1 HG02451.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.120+569C>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37345420 | |||||||
| chr2:37345427 | C | T | 1 | a0001c0003t0001g0228 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.120+576C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37345427 | |||||||
| chr2:37345458 | C | T | 2 | a0001c0003t0002g0226 a0001c0003t0002g0227 |
2 | HG03471.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.120+607C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37345458 | |||||||
| chr2:37345530 | C | G | 7 | a0001c0003t0001g0349 a0001c0003t0001g0351 a0001c0003t0001g0353 others(4): Show |
7 | HG02109.hp1 HG02451.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.120+679C>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37345530 | |||||||
| chr2:37345544 | G | A | 291 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(288): Show |
363 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(360): Show |
intron_variant | MODIFIER | c.120+693G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37345544 | |||||||
| chr2:37345573 | C | T | 1 | a0001c0001t0001g0347 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.120+722C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37345573 | |||||||
| chr2:37345580 | A | T | 1 | a0001c0003t0002g0225 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.120+729A>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37345580 | |||||||
| chr2:37345663 | G | T | 278 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(275): Show |
347 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(344): Show |
intron_variant | MODIFIER | c.120+812G>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37345663 | |||||||
| chr2:37345826 | A | C | 1 | a0001c0003t0001g0236 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.120+975A>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37345826 | |||||||
| chr2:37345835 | C | CA | 64 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(61): Show |
79 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.120+1004dupA | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37345835 | ||||||
| chr2:37345835 | CA | C | 20 | a0001c0001t0001g0234 a0001c0001t0001g0344 a0001c0001t0002g0343 others(17): Show |
21 | HG00738.hp1 HG01069.hp2 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.120+1004delA | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37345835 | ||||||
| chr2:37345908 | G | T | 2 | a0001c0001t0001g0234 a0001c0001t0003g0235 |
2 | HG02109.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.120+1057G>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37345908 | |||||||
| chr2:37345976 | T | C | 73 | a0001c0003t0001g0141 a0002c0002t0002g0002 a0002c0002t0002g0005 others(70): Show |
93 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(90): Show |
intron_variant | MODIFIER | c.120+1125T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37345976 | |||||||
| chr2:37346051 | T | C | 2 | a0001c0001t0001g0049 a0003c0004t0002g0050 |
2 | HG01255.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.120+1200T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37346051 | |||||||
| chr2:37346068 | C | T | 3 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 |
3 | HG02622.hp2 HG02818.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.120+1217C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37346068 | |||||||
| chr2:37346103 | G | A | 283 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(280): Show |
355 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.120+1252G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37346103 | |||||||
| chr2:37346116 | C | T | 14 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0049 others(11): Show |
18 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.120+1265C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37346116 | |||||||
| chr2:37346136 | C | CAT | 7 | a0001c0003t0001g0349 a0001c0003t0001g0351 a0001c0003t0001g0353 others(4): Show |
7 | HG02109.hp1 HG02451.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.120+1294_120+1295d others(4): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37346136 | ||||||
| chr2:37346199 | C | A | 1 | a0004c0005t0001g0137 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.120+1348C>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37346199 | |||||||
| chr2:37346205 | G | A | 3 | a0001c0003t0001g0128 a0001c0003t0001g0348 a0001c0003t0003g0129 |
3 | HG02145.hp1 HG02559.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.120+1354G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37346205 | |||||||
| chr2:37346299 | A | G | 3 | a0001c0001t0001g0340 a0001c0001t0001g0341 a0001c0001t0001g0342 |
3 | HG01123.hp1 HG01261.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.120+1448A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37346299 | |||||||
| chr2:37346379 | C | G | 1 | a0001c0001t0001g0123 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.120+1528C>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37346379 | |||||||
| chr2:37346380 | T | C | 1 | a0001c0003t0001g0142 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.120+1529T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37346380 | |||||||
| chr2:37346413 | G | A | 291 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(288): Show |
363 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(360): Show |
intron_variant | MODIFIER | c.120+1562G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37346413 | |||||||
| chr2:37346444 | T | C | 290 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(287): Show |
362 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(359): Show |
intron_variant | MODIFIER | c.120+1593T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37346444 | |||||||
| chr2:37346754 | T | C | 290 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(287): Show |
362 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(359): Show |
intron_variant | MODIFIER | c.120+1903T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37346754 | |||||||
| chr2:37346847 | C | G | 4 | a0001c0001t0001g0336 a0001c0001t0001g0338 a0001c0001t0002g0337 others(1): Show |
4 | HG02055.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.120+1996C>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37346847 | |||||||
| chr2:37346876 | C | G | 3 | a0003c0004t0002g0046 a0003c0004t0002g0345 a0003c0004t0002g0346 |
4 | HG00738.hp1 HG01069.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.120+2025C>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37346876 | |||||||
| chr2:37346983 | G | A | 4 | a0001c0001t0001g0294 a0003c0004t0002g0046 a0003c0004t0002g0345 others(1): Show |
5 | HG00738.hp1 HG01069.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.120+2132G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37346983 | |||||||
| chr2:37346991 | G | C | 283 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(280): Show |
355 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.120+2140G>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37346991 | |||||||
| chr2:37347084 | A | C | 172 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(169): Show |
218 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.120+2233A>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347084 | |||||||
| chr2:37347141 | G | GT | 35 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(32): Show |
48 | HG00438.hp2 HG00621.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.120+2294dupT | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347141 | ||||||
| chr2:37347141 | G | GTT | 10 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0079 others(7): Show |
14 | HG00597.hp2 HG02040.hp1 HG02165.hp1 others(11): Show |
intron_variant | MODIFIER | c.120+2293_120+2294d others(4): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347141 | ||||||
| chr2:37347144 | T | TA | 4 | a0001c0003t0001g0348 a0002c0002t0002g0237 a0002c0002t0002g0241 others(1): Show |
4 | HG02559.hp1 NA18612.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.120+2293_120+2294i others(3): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347144 | |||||||
| chr2:37347144 | T | TTTA | 16 | a0002c0002t0002g0005 a0002c0002t0002g0039 a0002c0002t0002g0239 others(13): Show |
21 | HG01934.hp2 HG01975.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.120+2294_120+2295i others(5): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347144 | ||||||
| chr2:37347144 | T | TTTATA | 9 | a0002c0002t0002g0040 a0002c0002t0002g0281 a0002c0002t0002g0282 others(6): Show |
10 | HG02004.hp1 HG02056.hp2 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.120+2294_120+2295i others(7): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347144 | ||||||
| chr2:37347144 | T | TTTATATA | 4 | a0002c0002t0002g0041 a0002c0002t0002g0288 a0002c0002t0008g0290 others(1): Show |
5 | HG00544.hp2 HG02080.hp2 NA18949.hp2 others(2): Show |
intron_variant | MODIFIER | c.120+2294_120+2295i others(9): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347144 | ||||||
| chr2:37347144 | T | TTTTTTAT others(32): Show |
1 | a0001c0001t0001g0020 | 3 | HG02965.hp1 HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.120+2294_120+2295i others(41): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347144 | ||||||
| chr2:37347144 | T | TTTTTTTT others(32): Show |
1 | a0001c0001t0001g0222 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.120+2294_120+2295i others(41): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347144 | ||||||
| chr2:37347144 | TTA | T | 54 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0042 others(51): Show |
64 | HG00099.hp1 HG00140.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.120+2312_120+2313d others(4): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347144 | ||||||
| chr2:37347146 | A | T | 159 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(156): Show |
197 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(194): Show |
intron_variant | MODIFIER | c.120+2295A>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347146 | |||||||
| chr2:37347148 | A | T | 9 | a0001c0001t0001g0033 a0001c0001t0001g0210 a0001c0001t0001g0211 others(6): Show |
10 | HG01070.hp1 HG01070.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.120+2297A>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347148 | |||||||
| chr2:37347151 | T | TAAC | 2 | a0001c0001t0001g0020 a0001c0001t0001g0222 |
4 | HG01515.hp2 HG02965.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.120+2301_120+2302i others(5): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347151 | ||||||
| chr2:37347151 | T | TATATATA others(40): Show |
1 | a0001c0001t0001g0168 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.120+2309_120+2310i others(49): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347151 | ||||||
| chr2:37347151 | T | TATATATA others(38): Show |
1 | a0001c0001t0001g0169 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.120+2309_120+2310i others(47): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347151 | ||||||
| chr2:37347151 | T | TATATATA others(38): Show |
1 | a0001c0001t0001g0209 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.120+2308_120+2309i others(47): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347151 | ||||||
| chr2:37347153 | T | TATATATA others(19): Show |
6 | a0001c0001t0001g0294 a0001c0001t0001g0332 a0001c0001t0001g0347 others(3): Show |
7 | HG00738.hp1 HG01069.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.120+2311_120+2312i others(28): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347153 | ||||||
| chr2:37347153 | T | TATATATA others(119): Show |
1 | a0001c0003t0003g0354 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.120+2313_120+2314i others(128): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347153 | ||||||
| chr2:37347153 | T | TATATATA others(143): Show |
1 | a0001c0003t0001g0162 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.120+2313_120+2314i others(152): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347153 | ||||||
| chr2:37347153 | T | TATATATA others(141): Show |
1 | a0001c0003t0001g0163 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.120+2313_120+2314i others(150): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347153 | ||||||
| chr2:37347153 | T | TATATATA others(113): Show |
1 | a0001c0003t0003g0355 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.120+2313_120+2314i others(122): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347153 | ||||||
| chr2:37347153 | T | TATATATA others(139): Show |
1 | a0001c0003t0001g0164 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.120+2313_120+2314i others(148): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347153 | ||||||
| chr2:37347155 | T | TATATATA others(38): Show |
1 | a0001c0003t0001g0142 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.120+2313_120+2314i others(47): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347155 | ||||||
| chr2:37347155 | T | TATATCAT others(65): Show |
2 | a0001c0003t0001g0018 a0001c0003t0001g0165 |
4 | HG02922.hp1 HG03209.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.120+2308_120+2309i others(74): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347155 | ||||||
| chr2:37347155 | T | TATATCAT others(67): Show |
1 | a0001c0003t0002g0226 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.120+2308_120+2309i others(76): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347155 | ||||||
| chr2:37347155 | T | TATATCAT others(67): Show |
3 | a0001c0003t0001g0167 a0001c0003t0002g0166 a0001c0003t0002g0227 |
3 | HG02647.hp1 HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.120+2308_120+2309i others(76): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347155 | ||||||
| chr2:37347163 | T | A | 4 | a0001c0001t0001g0045 a0001c0001t0001g0234 a0001c0001t0001g0335 others(1): Show |
5 | HG01106.hp2 HG02109.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.120+2312T>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347163 | |||||||
| chr2:37347163 | TA | T | 24 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0021 others(21): Show |
29 | HG00642.hp2 HG00735.hp1 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.120+2314delA | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347163 | ||||||
| chr2:37347163 | TAAC | T | 14 | a0001c0001t0001g0016 a0001c0001t0001g0021 a0001c0001t0001g0022 others(11): Show |
19 | HG00544.hp1 HG02258.hp1 HG02572.hp2 others(16): Show |
intron_variant | MODIFIER | c.120+2314_120+2316d others(5): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347163 | ||||||
| chr2:37347164 | A | AT | 197 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(194): Show |
241 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(238): Show |
intron_variant | MODIFIER | c.120+2313_120+2314i others(3): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347164 | |||||||
| chr2:37347164 | A | ATAT | 16 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0133 others(13): Show |
16 | HG00438.hp1 HG01070.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.120+2313_120+2314i others(5): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347164 | |||||||
| chr2:37347164 | A | ATATAT | 8 | a0001c0001t0001g0027 a0001c0001t0001g0121 a0001c0001t0001g0122 others(5): Show |
10 | HG01981.hp2 HG02074.hp1 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.120+2313_120+2314i others(7): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347164 | |||||||
| chr2:37347164 | A | ATATATAT | 3 | a0001c0001t0001g0089 a0001c0003t0001g0143 a0001c0003t0001g0228 |
3 | HG03139.hp2 NA18522.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.120+2313_120+2314i others(9): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347164 | |||||||
| chr2:37347164 | A | ATATATAT others(4): Show |
1 | a0001c0003t0001g0144 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.120+2313_120+2314i others(13): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347164 | |||||||
| chr2:37347164 | A | ATATATAT others(6): Show |
1 | a0001c0003t0005g0017 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.120+2313_120+2314i others(15): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347164 | |||||||
| chr2:37347164 | A | ATATATAT others(8): Show |
1 | a0001c0003t0005g0017 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.120+2313_120+2314i others(17): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347164 | |||||||
| chr2:37347164 | A | C | 4 | a0001c0001t0001g0045 a0001c0001t0001g0234 a0001c0001t0001g0335 others(1): Show |
4 | HG01106.hp2 HG02109.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.120+2313A>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347164 | |||||||
| chr2:37347164 | A | T | 1 | a0001c0001t0001g0045 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.120+2313A>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347164 | |||||||
| chr2:37347165 | A | T | 13 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0079 others(10): Show |
17 | HG00099.hp2 HG00597.hp2 HG02040.hp1 others(14): Show |
intron_variant | MODIFIER | c.120+2314A>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347165 | |||||||
| chr2:37347166 | C | A | 1 | a0001c0006t0001g0193 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.120+2315C>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347166 | |||||||
| chr2:37347166 | C | T | 251 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(248): Show |
310 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(307): Show |
intron_variant | MODIFIER | c.120+2315C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347166 | |||||||
| chr2:37347166 | CAT | C | 5 | a0001c0003t0001g0018 a0001c0003t0001g0167 a0001c0003t0002g0166 others(2): Show |
7 | HG02647.hp1 HG02922.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.120+2327_120+2328d others(4): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347166 | ||||||
| chr2:37347167 | A | T | 1 | a0001c0006t0001g0193 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.120+2316A>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347167 | |||||||
| chr2:37347168 | T | C | 1 | a0001c0006t0001g0193 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.120+2317T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347168 | |||||||
| chr2:37347168 | T | TATATATA others(91): Show |
1 | a0001c0003t0001g0128 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.120+2328_120+2329i others(100): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347168 | ||||||
| chr2:37347168 | T | TATATATA others(67): Show |
1 | a0001c0003t0003g0129 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.120+2328_120+2329i others(76): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347168 | ||||||
| chr2:37347168 | T | TATATATA others(63): Show |
1 | a0001c0003t0001g0348 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.120+2325_120+2326i others(72): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347168 | ||||||
| chr2:37347168 | T | TATATATC others(72): Show |
1 | a0001c0001t0001g0090 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.120+2323_120+2324i others(81): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347168 | ||||||
| chr2:37347168 | T | TATATCTC others(61): Show |
1 | a0001c0003t0002g0225 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.120+2321_120+2322i others(70): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347168 | ||||||
| chr2:37347168 | T | TC | 4 | a0001c0001t0001g0089 a0001c0001t0001g0099 a0001c0001t0001g0100 others(1): Show |
4 | NA18966.hp1 NA18966.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.120+2317_120+2318i others(3): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347168 | |||||||
| chr2:37347168 | TATATATA others(6): Show |
T | 1 | a0001c0001t0001g0044 | 2 | HG00099.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.120+2353_120+2365d others(15): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347168 | ||||||
| chr2:37347170 | T | C | 1 | a0001c0001t0001g0333 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.120+2319T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347170 | |||||||
| chr2:37347170 | T | TATATAAC | 5 | a0001c0001t0001g0020 a0001c0001t0001g0168 a0001c0001t0001g0169 others(2): Show |
7 | HG01515.hp2 HG02965.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.120+2324_120+2325i others(9): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | ||||||
| chr2:37347170 | T | TATATATA others(37): Show |
1 | a0001c0001t0001g0080 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.120+2326_120+2327i others(46): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | ||||||
| chr2:37347170 | T | TATATATA others(28): Show |
10 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0079 others(7): Show |
14 | HG00597.hp2 HG02040.hp1 HG02165.hp1 others(11): Show |
intron_variant | MODIFIER | c.120+2326_120+2327i others(37): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | ||||||
| chr2:37347170 | T | TATATATA others(30): Show |
1 | a0001c0001t0001g0221 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.120+2326_120+2327i others(39): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | ||||||
| chr2:37347170 | T | TATATATA others(30): Show |
1 | a0001c0003t0001g0236 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.120+2355_120+2391d others(39): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | ||||||
| chr2:37347170 | T | TATATATA others(46): Show |
1 | a0001c0003t0001g0150 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.120+2328_120+2329i others(55): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | ||||||
| chr2:37347170 | T | TATATATA others(57): Show |
1 | a0001c0003t0001g0349 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.120+2328_120+2329i others(66): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | ||||||
| chr2:37347170 | T | TATATATA others(53): Show |
2 | a0001c0003t0001g0151 a0001c0003t0001g0152 |
2 | HG02809.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.120+2328_120+2329i others(62): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | ||||||
| chr2:37347170 | T | TATATATA others(49): Show |
1 | a0001c0003t0001g0153 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.120+2328_120+2329i others(58): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | ||||||
| chr2:37347170 | T | TATATATA others(51): Show |
6 | a0001c0003t0001g0154 a0001c0003t0001g0155 a0001c0003t0001g0156 others(3): Show |
6 | HG01243.hp1 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.120+2328_120+2329i others(60): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | ||||||
| chr2:37347170 | T | TATATATA others(55): Show |
1 | a0001c0001t0001g0196 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.120+2328_120+2329i others(64): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | ||||||
| chr2:37347170 | T | TATATATA others(47): Show |
1 | a0001c0003t0001g0158 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.120+2328_120+2329i others(56): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | ||||||
| chr2:37347170 | T | TATATATA others(101): Show |
1 | a0001c0003t0003g0223 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.120+2328_120+2329i others(110): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | ||||||
| chr2:37347170 | T | TATATATA others(49): Show |
3 | a0001c0003t0001g0159 a0001c0003t0001g0160 a0001c0003t0003g0352 |
3 | HG03225.hp1 HG03471.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.120+2328_120+2329i others(58): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | ||||||
| chr2:37347170 | T | TATATATA others(103): Show |
1 | a0001c0003t0002g0224 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.120+2328_120+2329i others(112): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | ||||||
| chr2:37347170 | T | TATATATA others(36): Show |
1 | a0001c0003t0001g0161 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.120+2328_120+2329i others(45): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | ||||||
| chr2:37347170 | T | TATATATA others(51): Show |
3 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 |
3 | HG03490.hp2 HG03492.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.120+2328_120+2329i others(60): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | ||||||
| chr2:37347170 | T | TATATATA others(45): Show |
1 | a0001c0003t0001g0353 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.120+2328_120+2329i others(54): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | ||||||
| chr2:37347170 | T | TATATATA others(56): Show |
1 | a0001c0001t0001g0101 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.120+2328_120+2329i others(65): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | ||||||
| chr2:37347170 | T | TATATATA others(47): Show |
1 | a0001c0001t0002g0200 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.120+2328_120+2329i others(56): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | ||||||
| chr2:37347170 | T | TATATATA others(91): Show |
3 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0003c0004t0002g0023 |
4 | HG00558.hp1 HG02257.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.120+2328_120+2329i others(100): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | ||||||
| chr2:37347170 | T | TATATATA others(45): Show |
1 | a0001c0001t0001g0203 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.120+2328_120+2329i others(54): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | ||||||
| chr2:37347170 | T | TATATATA others(52): Show |
3 | a0001c0001t0001g0081 a0001c0001t0001g0102 a0003c0004t0002g0055 |
3 | HG01346.hp2 NA18946.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.120+2328_120+2329i others(61): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | ||||||
| chr2:37347170 | T | TATATATA others(48): Show |
1 | a0001c0001t0001g0123 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.120+2327_120+2328i others(57): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | ||||||
| chr2:37347170 | T | TATATATA others(50): Show |
12 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0056 others(9): Show |
16 | HG01175.hp2 HG01256.hp1 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.120+2327_120+2328i others(59): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | ||||||
| chr2:37347170 | T | TATATATA others(87): Show |
1 | a0003c0004t0002g0057 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.120+2327_120+2328i others(96): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | ||||||
| chr2:37347170 | T | TATATATA others(41): Show |
3 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 |
3 | HG01099.hp2 HG02647.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.120+2327_120+2328i others(50): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | ||||||
| chr2:37347170 | T | TATATATC others(46): Show |
2 | a0003c0004t0002g0011 a0003c0004t0002g0063 |
4 | HG02071.hp2 NA18951.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.120+2325_120+2326i others(55): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | ||||||
| chr2:37347170 | T | TATATATC others(48): Show |
42 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(39): Show |
54 | HG00140.hp2 HG00280.hp2 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.120+2325_120+2326i others(57): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | ||||||
| chr2:37347170 | T | TATATATC others(85): Show |
1 | a0001c0001t0001g0064 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.120+2325_120+2326i others(94): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | ||||||
| chr2:37347170 | T | TATATATC others(39): Show |
2 | a0001c0001t0001g0047 a0001c0001t0001g0207 |
2 | HG01496.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.120+2325_120+2326i others(48): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | ||||||
| chr2:37347170 | T | TATATCAT others(46): Show |
8 | a0001c0001t0001g0026 a0001c0001t0001g0049 a0001c0001t0001g0078 others(5): Show |
9 | HG01255.hp2 HG01517.hp2 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.120+2323_120+2324i others(55): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | ||||||
| chr2:37347170 | T | TATATCAT others(83): Show |
2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG02818.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.120+2323_120+2324i others(92): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | ||||||
| chr2:37347170 | T | TATATCAT others(37): Show |
1 | a0001c0001t0001g0208 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.120+2323_120+2324i others(46): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | ||||||
| chr2:37347170 | T | TATCATAT others(20): Show |
1 | a0001c0003t0001g0029 | 2 | HG02451.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.120+2321_120+2322i others(29): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | ||||||
| chr2:37347170 | T | TC | 3 | a0001c0001t0001g0027 a0001c0001t0001g0121 a0001c0001t0001g0122 |
4 | HG02074.hp1 NA18948.hp2 NA18949.hp1 others(1): Show |
intron_variant | MODIFIER | c.120+2319_120+2320i others(3): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347170 | |||||||
| chr2:37347178 | T | A | 1 | a0001c0003t0001g0142 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.120+2327T>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347178 | |||||||
| chr2:37347178 | TA | T | 5 | a0001c0003t0001g0147 a0002c0002t0002g0260 a0002c0002t0002g0268 others(2): Show |
5 | HG02132.hp1 HG02155.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.120+2329delA | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347178 | ||||||
| chr2:37347179 | A | AT | 7 | a0001c0003t0001g0132 a0001c0003t0001g0141 a0001c0003t0001g0148 others(4): Show |
7 | HG01884.hp2 HG01891.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.120+2328_120+2329i others(3): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347179 | |||||||
| chr2:37347179 | A | C | 1 | a0001c0003t0001g0142 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.120+2328A>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347179 | |||||||
| chr2:37347179 | A | T | 61 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0010 others(58): Show |
81 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.120+2328A>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347179 | |||||||
| chr2:37347180 | A | T | 61 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(58): Show |
80 | HG00438.hp1 HG00544.hp1 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.120+2329A>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347180 | |||||||
| chr2:37347181 | C | T | 77 | a0001c0003t0001g0132 a0001c0003t0001g0141 a0001c0003t0001g0142 others(74): Show |
97 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(94): Show |
intron_variant | MODIFIER | c.120+2330C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347181 | |||||||
| chr2:37347183 | T | C | 1 | a0001c0003t0001g0165 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.120+2332T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347183 | |||||||
| chr2:37347183 | T | TATATATA others(79): Show |
1 | a0002c0002t0002g0243 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.120+2339_120+2340i others(88): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347183 | ||||||
| chr2:37347183 | T | TATATATA others(61): Show |
1 | a0001c0003t0001g0144 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.120+2339_120+2340i others(70): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347183 | ||||||
| chr2:37347183 | T | TATATATA others(85): Show |
1 | a0001c0003t0001g0143 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+2339_120+2340i others(94): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347183 | ||||||
| chr2:37347183 | T | TATATATA others(61): Show |
1 | a0001c0001t0001g0089 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.120+2339_120+2340i others(70): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347183 | ||||||
| chr2:37347183 | T | TATATATA others(63): Show |
3 | a0001c0001t0001g0027 a0001c0001t0001g0121 a0001c0001t0001g0122 |
4 | HG02074.hp1 NA18948.hp2 NA18949.hp1 others(1): Show |
intron_variant | MODIFIER | c.120+2339_120+2340i others(72): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347183 | ||||||
| chr2:37347183 | T | TATATATA others(4): Show |
1 | a0001c0001t0001g0054 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.120+2342_120+2352d others(13): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347183 | ||||||
| chr2:37347183 | T | TATATATA others(76): Show |
7 | a0001c0001t0001g0016 a0001c0001t0001g0021 a0001c0001t0001g0022 others(4): Show |
13 | HG00544.hp1 NA18947.hp2 NA18965.hp1 others(10): Show |
intron_variant | MODIFIER | c.120+2352_120+2353i others(85): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347183 | ||||||
| chr2:37347183 | T | TATATATA others(67): Show |
1 | a0001c0001t0001g0188 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.120+2354_120+2355i others(76): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347183 | ||||||
| chr2:37347183 | T | TATATATA others(91): Show |
1 | a0001c0001t0001g0133 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.120+2354_120+2355i others(100): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347183 | ||||||
| chr2:37347183 | T | TATATATA others(54): Show |
2 | a0001c0001t0001g0099 a0001c0001t0001g0100 |
2 | NA18966.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.120+2341_120+2342i others(63): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347183 | ||||||
| chr2:37347183 | T | TATATATA others(96): Show |
1 | a0002c0002t0002g0267 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.120+2341_120+2342i others(105): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347183 | ||||||
| chr2:37347183 | T | TATATCAT others(94): Show |
1 | a0001c0003t0001g0149 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.120+2336_120+2337i others(103): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347183 | ||||||
| chr2:37347183 | T | TATTATAT others(72): Show |
1 | a0004c0005t0001g0137 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.120+2334_120+2335i others(81): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347183 | ||||||
| chr2:37347191 | T | A | 1 | a0001c0001t0001g0090 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.120+2340T>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347191 | |||||||
| chr2:37347192 | A | AT | 2 | a0001c0003t0001g0028 a0001c0003t0005g0017 |
5 | HG00280.hp1 HG01981.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.120+2341_120+2342i others(3): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347192 | |||||||
| chr2:37347192 | A | C | 1 | a0001c0001t0001g0090 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.120+2341A>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347192 | |||||||
| chr2:37347192 | A | T | 1 | a0002c0002t0002g0268 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.120+2341A>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347192 | |||||||
| chr2:37347193 | A | T | 11 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0003t0001g0132 others(8): Show |
11 | HG01891.hp2 HG02486.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.120+2342A>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347193 | |||||||
| chr2:37347194 | C | A | 5 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0003t0001g0028 others(2): Show |
8 | HG00280.hp1 HG01981.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.120+2343C>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347194 | |||||||
| chr2:37347194 | C | T | 7 | a0001c0001t0001g0090 a0001c0003t0001g0141 a0002c0002t0002g0268 others(4): Show |
7 | HG01891.hp2 HG02155.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.120+2343C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347194 | |||||||
| chr2:37347194 | CAT | C | 3 | a0001c0003t0001g0145 a0001c0003t0001g0228 a0004c0005t0001g0137 |
3 | HG02559.hp2 HG03486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.120+2353_120+2354d others(4): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347194 | ||||||
| chr2:37347196 | T | C | 3 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0006t0001g0193 |
3 | NA18966.hp1 NA19007.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.120+2345T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347196 | |||||||
| chr2:37347196 | T | TATATAAC others(99): Show |
3 | a0002c0002t0002g0237 a0002c0002t0002g0241 a0002c0002t0002g0242 |
3 | NA18612.hp2 NA19000.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.120+2350_120+2351i others(108): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347196 | ||||||
| chr2:37347196 | T | TATATATA others(88): Show |
1 | a0002c0002t0002g0244 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.120+2352_120+2353i others(97): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347196 | ||||||
| chr2:37347196 | T | TATATATA others(99): Show |
1 | a0002c0002t0002g0245 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.120+2352_120+2353i others(108): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347196 | ||||||
| chr2:37347196 | T | TATATATA others(134): Show |
1 | a0002c0002t0002g0269 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.120+2352_120+2353i others(143): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347196 | ||||||
| chr2:37347196 | T | TATATATA others(101): Show |
1 | a0002c0002t0002g0239 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.120+2352_120+2353i others(110): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347196 | ||||||
| chr2:37347196 | T | TATATATA others(90): Show |
1 | a0002c0002t0002g0275 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.120+2352_120+2353i others(99): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347196 | ||||||
| chr2:37347196 | T | TATATATA others(101): Show |
16 | a0002c0002t0002g0034 a0002c0002t0002g0240 a0002c0002t0002g0251 others(13): Show |
19 | HG00438.hp2 HG01192.hp2 HG01975.hp2 others(16): Show |
intron_variant | MODIFIER | c.120+2352_120+2353i others(110): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347196 | ||||||
| chr2:37347196 | T | TATATATA others(112): Show |
2 | a0002c0002t0002g0247 a0002c0002t0002g0248 |
2 | NA18956.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.120+2352_120+2353i others(121): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347196 | ||||||
| chr2:37347196 | T | TATATATA others(90): Show |
1 | a0002c0002t0002g0262 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.120+2352_120+2353i others(99): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347196 | ||||||
| chr2:37347196 | T | TATATATA others(101): Show |
1 | a0002c0002t0002g0266 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.120+2352_120+2353i others(110): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347196 | ||||||
| chr2:37347196 | T | TATATATA others(37): Show |
1 | a0004c0005t0001g0138 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.120+2352_120+2353i others(46): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347196 | ||||||
| chr2:37347196 | T | TATATATA others(87): Show |
1 | a0003c0004t0002g0051 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.120+2352_120+2353i others(96): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347196 | ||||||
| chr2:37347196 | T | TATATATA others(87): Show |
3 | a0001c0001t0001g0052 a0001c0001t0001g0091 a0003c0004t0002g0053 |
3 | NA18960.hp1 NA18969.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.120+2352_120+2353i others(96): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347196 | ||||||
| chr2:37347196 | T | TATATATA others(85): Show |
1 | a0004c0005t0003g0139 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.120+2352_120+2353i others(94): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347196 | ||||||
| chr2:37347196 | T | TATATATA others(6): Show |
1 | a0001c0001t0001g0172 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.120+2354_120+2355i others(15): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347196 | ||||||
| chr2:37347202 | T | TAACATAT others(117): Show |
1 | a0002c0002t0002g0246 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.120+2352_120+2353i others(126): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347202 | ||||||
| chr2:37347202 | T | TAACATAT others(108): Show |
1 | a0002c0002t0002g0281 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.120+2352_120+2353i others(117): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347202 | ||||||
| chr2:37347202 | T | TAACATAT others(106): Show |
10 | a0002c0002t0002g0002 a0002c0002t0002g0041 a0002c0002t0002g0238 others(7): Show |
16 | HG00621.hp2 HG00639.hp2 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.120+2352_120+2353i others(115): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347202 | ||||||
| chr2:37347202 | T | TAACATAT others(84): Show |
1 | a0002c0002t0002g0261 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.120+2352_120+2353i others(93): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347202 | ||||||
| chr2:37347202 | T | TAACATAT others(95): Show |
16 | a0002c0002t0002g0010 a0002c0002t0002g0037 a0002c0002t0002g0039 others(13): Show |
22 | HG00544.hp2 HG01934.hp2 HG02083.hp2 others(19): Show |
intron_variant | MODIFIER | c.120+2352_120+2353i others(104): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347202 | ||||||
| chr2:37347202 | T | TAACATAT others(106): Show |
1 | a0002c0002t0002g0005 | 5 | NA18944.hp2 NA18945.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.120+2352_120+2353i others(115): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347202 | ||||||
| chr2:37347202 | T | TAACATAT others(106): Show |
2 | a0002c0002t0002g0286 a0002c0002t0008g0290 |
2 | HG02056.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.120+2352_120+2353i others(115): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347202 | ||||||
| chr2:37347202 | T | TAACATAT others(95): Show |
1 | a0002c0002t0002g0038 | 2 | HG02132.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.120+2352_120+2353i others(104): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347202 | ||||||
| chr2:37347202 | T | TAACATAT others(106): Show |
1 | a0002c0002t0002g0280 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.120+2352_120+2353i others(115): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347202 | ||||||
| chr2:37347204 | T | A | 7 | a0001c0001t0001g0064 a0001c0001t0001g0125 a0001c0001t0001g0126 others(4): Show |
8 | HG00558.hp1 HG00673.hp2 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.120+2353T>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347204 | |||||||
| chr2:37347205 | A | AT | 36 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0010 others(33): Show |
53 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.120+2354_120+2355i others(3): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347205 | |||||||
| chr2:37347205 | A | ATAACATA others(78): Show |
2 | a0001c0001t0001g0210 a0001c0001t0001g0211 |
2 | HG01070.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.120+2354_120+2355i others(87): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347205 | |||||||
| chr2:37347205 | A | ATAACATA others(78): Show |
1 | a0001c0001t0001g0173 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.120+2354_120+2355i others(87): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347205 | |||||||
| chr2:37347205 | A | ATAACATA others(80): Show |
27 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0030 others(24): Show |
40 | HG00642.hp2 HG00741.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.120+2354_120+2355i others(89): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347205 | |||||||
| chr2:37347205 | A | ATAACATA others(79): Show |
1 | a0001c0001t0001g0189 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.120+2354_120+2355i others(88): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347205 | |||||||
| chr2:37347205 | A | ATAACATA others(82): Show |
1 | a0001c0001t0002g0190 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.120+2354_120+2355i others(91): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347205 | |||||||
| chr2:37347205 | A | ATAACATA others(82): Show |
1 | a0001c0001t0001g0191 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.120+2354_120+2355i others(91): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347205 | |||||||
| chr2:37347205 | A | ATATAACA others(80): Show |
1 | a0001c0001t0001g0192 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.120+2354_120+2355i others(89): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347205 | |||||||
| chr2:37347205 | A | ATATATAA others(3): Show |
3 | a0001c0003t0001g0162 a0001c0003t0001g0163 a0001c0003t0001g0164 |
3 | HG01891.hp1 HG02145.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.120+2354_120+2355i others(12): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347205 | |||||||
| chr2:37347205 | A | C | 6 | a0001c0001t0001g0064 a0001c0001t0001g0125 a0001c0001t0001g0126 others(3): Show |
7 | HG00558.hp1 HG00673.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.120+2354A>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347205 | |||||||
| chr2:37347205 | A | T | 1 | a0001c0003t0002g0224 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.120+2354A>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347205 | |||||||
| chr2:37347207 | C | CAT | 7 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0003t0001g0128 others(4): Show |
7 | HG02145.hp1 HG02257.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.120+2364_120+2365d others(4): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347207 | ||||||
| chr2:37347207 | C | CATAT | 39 | a0001c0003t0001g0018 a0001c0003t0001g0142 a0001c0003t0001g0143 others(36): Show |
44 | HG00438.hp2 HG01192.hp2 HG01975.hp2 others(41): Show |
intron_variant | MODIFIER | c.120+2362_120+2365d others(6): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347207 | ||||||
| chr2:37347207 | C | CATATATA others(109): Show |
1 | a0002c0002t0002g0268 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.120+2376_120+2377i others(118): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347207 | ||||||
| chr2:37347207 | C | CATATATA others(153): Show |
1 | a0002c0002t0002g0287 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.120+2376_120+2377i others(162): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347207 | ||||||
| chr2:37347207 | C | CATATATA others(80): Show |
2 | a0001c0003t0001g0147 a0001c0003t0001g0148 |
2 | HG02486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.120+2376_120+2377i others(89): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347207 | ||||||
| chr2:37347207 | C | CATATATA others(69): Show |
1 | a0001c0003t0001g0132 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.120+2376_120+2377i others(78): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347207 | ||||||
| chr2:37347207 | C | T | 80 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0030 others(77): Show |
111 | HG00544.hp2 HG00558.hp1 HG00621.hp2 others(108): Show |
intron_variant | MODIFIER | c.120+2356C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347207 | |||||||
| chr2:37347220 | T | C | 1 | a0001c0003t0002g0225 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.120+2369T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347220 | |||||||
| chr2:37347220 | T | TATATATA others(89): Show |
1 | a0001c0001t0001g0171 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.120+2376_120+2377i others(98): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347220 | ||||||
| chr2:37347224 | T | TATAACAT others(133): Show |
4 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(1): Show |
4 | HG02258.hp1 HG02572.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.120+2376_120+2377i others(142): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347224 | ||||||
| chr2:37347226 | T | TAACATAT others(165): Show |
1 | a0001c0001t0001g0094 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.120+2376_120+2377i others(174): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347226 | ||||||
| chr2:37347229 | A | AT | 6 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(3): Show |
6 | HG02258.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.120+2378_120+2379i others(3): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347229 | |||||||
| chr2:37347231 | C | CAT | 13 | a0001c0001t0001g0234 a0001c0001t0003g0235 a0001c0003t0001g0132 others(10): Show |
13 | HG01069.hp2 HG01884.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.120+2394_120+2395d others(4): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | ||||||
| chr2:37347231 | C | CATAT | 14 | a0001c0001t0001g0064 a0001c0001t0001g0099 a0001c0001t0001g0100 others(11): Show |
15 | HG00558.hp1 HG00673.hp2 HG01952.hp2 others(12): Show |
intron_variant | MODIFIER | c.120+2392_120+2395d others(6): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | ||||||
| chr2:37347231 | C | CATATAT | 36 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0030 others(33): Show |
49 | HG00438.hp1 HG00642.hp2 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.120+2390_120+2395d others(8): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | ||||||
| chr2:37347231 | C | CATATATA others(1): Show |
17 | a0001c0001t0001g0016 a0001c0001t0001g0021 a0001c0001t0001g0022 others(14): Show |
24 | HG00544.hp1 HG00735.hp1 HG02074.hp1 others(21): Show |
intron_variant | MODIFIER | c.120+2388_120+2395d others(10): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | ||||||
| chr2:37347231 | C | CATATATA others(38): Show |
1 | a0001c0001t0001g0056 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.120+2389_120+2390i others(47): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | ||||||
| chr2:37347231 | C | CATATATA others(54): Show |
4 | a0001c0003t0001g0141 a0004c0005t0001g0130 a0004c0005t0001g0131 others(1): Show |
4 | HG01891.hp2 HG03453.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.120+2389_120+2390i others(63): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | ||||||
| chr2:37347231 | C | CATATATA others(108): Show |
1 | a0001c0001t0001g0054 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.120+2389_120+2390i others(117): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | ||||||
| chr2:37347231 | C | CATATATA others(25): Show |
1 | a0001c0001t0001g0026 | 2 | HG02165.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.120+2389_120+2390i others(34): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | ||||||
| chr2:37347231 | C | CATATATA others(34): Show |
1 | a0001c0001t0001g0203 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.120+2389_120+2390i others(43): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | ||||||
| chr2:37347231 | C | CATATATA others(27): Show |
3 | a0001c0001t0001g0118 a0001c0001t0001g0231 a0001c0001t0001g0232 |
3 | HG00558.hp2 NA18997.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.120+2389_120+2390i others(36): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | ||||||
| chr2:37347231 | C | CATATATA others(36): Show |
36 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0015 others(33): Show |
47 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(44): Show |
intron_variant | MODIFIER | c.120+2389_120+2390i others(45): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | ||||||
| chr2:37347231 | C | CATATATA others(38): Show |
26 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0025 others(23): Show |
34 | HG00735.hp2 HG01074.hp1 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.120+2389_120+2390i others(47): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | ||||||
| chr2:37347231 | C | CATATATA others(40): Show |
11 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0062 others(8): Show |
14 | HG01081.hp2 HG01099.hp2 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.120+2389_120+2390i others(49): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | ||||||
| chr2:37347231 | C | CATATATA others(42): Show |
2 | a0001c0001t0001g0206 a0003c0004t0002g0111 |
2 | HG00597.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.120+2389_120+2390i others(51): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | ||||||
| chr2:37347231 | C | CATATATA others(44): Show |
1 | a0001c0001t0001g0104 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.120+2389_120+2390i others(53): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | ||||||
| chr2:37347231 | C | CATATATA others(55): Show |
1 | a0001c0001t0001g0127 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.120+2389_120+2390i others(64): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | ||||||
| chr2:37347231 | C | CATATATA others(65): Show |
1 | a0001c0001t0001g0088 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.120+2389_120+2390i others(74): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | ||||||
| chr2:37347231 | C | CATATATA others(47): Show |
3 | a0001c0003t0001g0151 a0001c0003t0001g0158 a0001c0003t0001g0159 |
3 | HG02615.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.120+2389_120+2390i others(56): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | ||||||
| chr2:37347231 | C | CATATATA others(31): Show |
1 | a0001c0001t0001g0112 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.120+2389_120+2390i others(40): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | ||||||
| chr2:37347231 | C | CATATATA others(33): Show |
3 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 |
3 | HG00642.hp1 HG03834.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.120+2389_120+2390i others(42): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | ||||||
| chr2:37347231 | C | CATATATA others(31): Show |
1 | a0001c0001t0001g0116 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.120+2389_120+2390i others(40): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | ||||||
| chr2:37347231 | C | CATATATA others(35): Show |
1 | a0001c0001t0001g0117 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.120+2389_120+2390i others(44): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | ||||||
| chr2:37347231 | C | CATATATA others(3): Show |
1 | a0001c0003t0001g0348 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.120+2386_120+2395d others(12): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | ||||||
| chr2:37347231 | C | CATATATA others(106): Show |
1 | a0001c0001t0001g0172 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.120+2391_120+2392i others(115): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | ||||||
| chr2:37347231 | C | CATATATA others(71): Show |
1 | a0001c0006t0001g0193 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.120+2391_120+2392i others(80): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | ||||||
| chr2:37347231 | C | CATATATA others(73): Show |
1 | a0001c0001t0001g0194 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.120+2391_120+2392i others(82): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | ||||||
| chr2:37347231 | C | CATATATA others(60): Show |
3 | a0001c0003t0001g0145 a0001c0003t0001g0146 a0001c0003t0001g0228 |
3 | HG02809.hp2 HG03486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.120+2391_120+2392i others(69): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | ||||||
| chr2:37347231 | C | CATATATA others(21): Show |
1 | a0001c0003t0003g0350 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.120+2391_120+2392i others(30): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | ||||||
| chr2:37347231 | C | CATATATA others(75): Show |
1 | a0001c0001t0001g0195 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.120+2391_120+2392i others(84): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | ||||||
| chr2:37347231 | C | CATATATA others(23): Show |
11 | a0001c0003t0001g0029 a0001c0003t0001g0150 a0001c0003t0001g0152 others(8): Show |
12 | HG00738.hp2 HG01243.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.120+2393_120+2394i others(32): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | ||||||
| chr2:37347231 | C | CATATATA others(25): Show |
1 | a0001c0003t0001g0349 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.120+2393_120+2394i others(34): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | ||||||
| chr2:37347231 | C | CATATATA others(25): Show |
2 | a0001c0003t0001g0156 a0001c0003t0001g0157 |
2 | HG03130.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.120+2408_120+2409i others(34): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | ||||||
| chr2:37347231 | C | T | 7 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(4): Show |
7 | HG01106.hp1 HG02258.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.120+2380C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347231 | |||||||
| chr2:37347235 | T | TATATAAC others(13): Show |
5 | a0001c0001t0001g0019 a0001c0001t0001g0079 a0001c0001t0001g0136 others(2): Show |
7 | NA18953.hp2 NA18973.hp1 NA18979.hp2 others(4): Show |
intron_variant | MODIFIER | c.120+2389_120+2390i others(22): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347235 | ||||||
| chr2:37347442 | T | A | 1 | a0001c0001t0001g0218 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.120+2591T>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347442 | |||||||
| chr2:37347683 | C | T | 1 | a0001c0001t0001g0294 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.120+2832C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347683 | |||||||
| chr2:37347822 | T | G | 65 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0010 others(62): Show |
85 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(82): Show |
intron_variant | MODIFIER | c.120+2971T>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347822 | |||||||
| chr2:37347883 | C | G | 283 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(280): Show |
355 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.120+3032C>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347883 | |||||||
| chr2:37347897 | C | A | 1 | a0001c0001t0001g0295 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.120+3046C>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347897 | |||||||
| chr2:37347954 | A | G | 73 | a0001c0003t0001g0141 a0001c0003t0001g0157 a0002c0002t0002g0002 others(70): Show |
93 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(90): Show |
intron_variant | MODIFIER | c.120+3103A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347954 | |||||||
| chr2:37348038 | A | ATCTC | 77 | a0001c0003t0001g0028 a0001c0003t0001g0141 a0001c0003t0001g0157 others(74): Show |
102 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.120+3197_120+3200d others(6): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37348038 | ||||||
| chr2:37348038 | A | ATCTCTC | 212 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(209): Show |
259 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.120+3195_120+3200d others(8): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37348038 | ||||||
| chr2:37348054 | G | A | 1 | a0002c0002t0002g0037 | 2 | NA18941.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.120+3203G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37348054 | |||||||
| chr2:37348063 | C | CGT | 21 | a0001c0001t0001g0042 a0001c0001t0001g0295 a0001c0001t0001g0298 others(18): Show |
23 | HG00639.hp1 HG01261.hp2 HG01358.hp2 others(20): Show |
intron_variant | MODIFIER | c.120+3237_120+3238d others(4): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37348063 | ||||||
| chr2:37348063 | C | CGTGT | 4 | a0001c0001t0002g0296 a0001c0001t0002g0297 a0001c0001t0002g0343 others(1): Show |
4 | HG02040.hp2 HG02083.hp1 HG02129.hp2 others(1): Show |
intron_variant | MODIFIER | c.120+3235_120+3238d others(6): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37348063 | ||||||
| chr2:37348063 | C | T | 2 | a0001c0001t0001g0044 a0001c0001t0001g0331 |
3 | HG00099.hp1 HG03834.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.120+3212C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37348063 | |||||||
| chr2:37348063 | CGT | C | 241 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(238): Show |
308 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(305): Show |
intron_variant | MODIFIER | c.120+3237_120+3238d others(4): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37348063 | ||||||
| chr2:37348064 | G | A | 3 | a0001c0003t0001g0128 a0001c0003t0001g0348 a0001c0003t0003g0129 |
3 | HG02145.hp1 HG02559.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.120+3213G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37348064 | |||||||
| chr2:37348064 | G | T | 30 | a0001c0003t0001g0029 a0001c0003t0001g0132 a0001c0003t0001g0144 others(27): Show |
31 | HG00738.hp2 HG01243.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.120+3213G>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37348064 | |||||||
| chr2:37348065 | T | C | 1 | a0001c0001t0001g0089 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.120+3214T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37348065 | |||||||
| chr2:37348067 | T | C | 2 | a0001c0003t0001g0157 a0004c0005t0001g0137 |
2 | HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.120+3216T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37348067 | |||||||
| chr2:37348121 | C | T | 5 | a0001c0003t0001g0141 a0004c0005t0001g0130 a0004c0005t0001g0131 others(2): Show |
5 | HG01106.hp1 HG01891.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.120+3270C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37348121 | |||||||
| chr2:37348131 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.120+3280T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37348131 | |||||||
| chr2:37348144 | C | T | 279 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(276): Show |
351 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(348): Show |
intron_variant | MODIFIER | c.120+3293C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37348144 | |||||||
| chr2:37348238 | C | G | 90 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(87): Show |
117 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.120+3387C>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37348238 | |||||||
| chr2:37348300 | C | T | 1 | a0002c0002t0002g0256 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.120+3449C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37348300 | |||||||
| chr2:37348359 | A | G | 1 | a0001c0003t0001g0155 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.120+3508A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37348359 | |||||||
| chr2:37348434 | C | G | 69 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(66): Show |
88 | HG00438.hp1 HG00597.hp2 HG00642.hp2 others(85): Show |
intron_variant | MODIFIER | c.120+3583C>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37348434 | |||||||
| chr2:37348437 | C | G | 7 | a0001c0003t0001g0349 a0001c0003t0001g0351 a0001c0003t0001g0353 others(4): Show |
7 | HG02109.hp1 HG02451.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.120+3586C>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37348437 | |||||||
| chr2:37348478 | G | T | 1 | a0001c0001t0002g0343 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.120+3627G>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37348478 | |||||||
| chr2:37348512 | C | T | 8 | a0001c0003t0001g0143 a0001c0003t0001g0149 a0001c0003t0001g0151 others(5): Show |
8 | HG01884.hp2 HG01891.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.120+3661C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37348512 | |||||||
| chr2:37348604 | C | A | 5 | a0001c0001t0001g0020 a0001c0001t0001g0171 a0001c0001t0001g0172 others(2): Show |
7 | HG01099.hp2 HG01243.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.120+3753C>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37348604 | |||||||
| chr2:37348813 | G | A | 3 | a0001c0001t0001g0025 a0001c0001t0001g0101 a0001c0001t0001g0102 |
4 | NA18971.hp1 NA19004.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.120+3962G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37348813 | |||||||
| chr2:37348820 | T | C | 4 | a0001c0001t0001g0042 a0001c0001t0001g0295 a0001c0001t0001g0298 others(1): Show |
5 | HG02572.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.120+3969T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37348820 | |||||||
| chr2:37348867 | T | C | 3 | a0001c0003t0001g0128 a0001c0003t0001g0348 a0001c0003t0003g0129 |
3 | HG02145.hp1 HG02559.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.121-3922T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37348867 | |||||||
| chr2:37348993 | A | G | 55 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(52): Show |
70 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.121-3796A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37348993 | |||||||
| chr2:37349060 | C | T | 1 | a0004c0005t0003g0139 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.121-3729C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37349060 | |||||||
| chr2:37349134 | C | A | 2 | a0001c0003t0001g0028 a0001c0003t0005g0017 |
5 | HG00280.hp1 HG01981.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.121-3655C>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37349134 | |||||||
| chr2:37349259 | A | G | 1 | a0001c0003t0001g0142 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.121-3530A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37349259 | |||||||
| chr2:37349308 | A | G | 1 | a0001c0001t0001g0087 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.121-3481A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37349308 | |||||||
| chr2:37349410 | A | G | 292 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(289): Show |
364 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(361): Show |
intron_variant | MODIFIER | c.121-3379A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37349410 | |||||||
| chr2:37349495 | C | T | 282 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(279): Show |
352 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(349): Show |
intron_variant | MODIFIER | c.121-3294C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37349495 | |||||||
| chr2:37349606 | C | G | 1 | a0001c0003t0001g0236 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.121-3183C>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37349606 | |||||||
| chr2:37349709 | A | G | 280 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(277): Show |
347 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(344): Show |
intron_variant | MODIFIER | c.121-3080A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37349709 | |||||||
| chr2:37349772 | G | C | 66 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0010 others(63): Show |
86 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(83): Show |
intron_variant | MODIFIER | c.121-3017G>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37349772 | |||||||
| chr2:37349830 | G | GA | 281 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(278): Show |
351 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(348): Show |
intron_variant | MODIFIER | c.121-2954dupA | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37349830 | ||||||
| chr2:37349847 | C | G | 9 | a0001c0003t0001g0018 a0001c0003t0001g0165 a0001c0003t0001g0349 others(6): Show |
11 | HG02109.hp1 HG02451.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.121-2942C>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37349847 | |||||||
| chr2:37349880 | A | G | 9 | a0001c0003t0001g0018 a0001c0003t0001g0165 a0001c0003t0001g0349 others(6): Show |
11 | HG02109.hp1 HG02451.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.121-2909A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37349880 | |||||||
| chr2:37350242 | G | T | 10 | a0001c0003t0001g0018 a0001c0003t0001g0165 a0001c0003t0001g0236 others(7): Show |
12 | HG02109.hp1 HG02451.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.121-2547G>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37350242 | |||||||
| chr2:37350257 | G | C | 1 | a0001c0003t0001g0142 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.121-2532G>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37350257 | |||||||
| chr2:37350266 | C | A | 23 | a0001c0003t0001g0029 a0001c0003t0001g0132 a0001c0003t0001g0143 others(20): Show |
24 | HG00738.hp2 HG01243.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.121-2523C>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37350266 | |||||||
| chr2:37350352 | G | C | 1 | a0001c0001t0001g0294 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.121-2437G>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37350352 | |||||||
| chr2:37350635 | T | G | 3 | a0001c0003t0001g0128 a0001c0003t0001g0348 a0001c0003t0003g0129 |
3 | HG02145.hp1 HG02559.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.121-2154T>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37350635 | |||||||
| chr2:37350776 | A | G | 2 | a0001c0003t0001g0028 a0001c0003t0005g0017 |
5 | HG00280.hp1 HG01981.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.121-2013A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37350776 | |||||||
| chr2:37350907 | A | T | 1 | a0001c0003t0002g0224 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.121-1882A>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37350907 | |||||||
| chr2:37350973 | TGCTGAGT others(6): Show |
T | 1 | a0001c0001t0001g0074 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.121-1801_121-1789d others(15): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37350973 | ||||||
| chr2:37350992 | G | C | 1 | a0003c0004t0002g0299 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.121-1797G>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37350992 | |||||||
| chr2:37351002 | T | C | 1 | a0001c0001t0001g0222 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.121-1787T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37351002 | |||||||
| chr2:37351065 | G | A | 274 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(271): Show |
344 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.121-1724G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37351065 | |||||||
| chr2:37351079 | T | G | 2 | a0001c0001t0001g0234 a0001c0001t0003g0235 |
2 | HG02109.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.121-1710T>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37351079 | |||||||
| chr2:37351160 | G | C | 290 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(287): Show |
362 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(359): Show |
intron_variant | MODIFIER | c.121-1629G>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37351160 | |||||||
| chr2:37351179 | G | A | 1 | a0004c0005t0001g0137 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.121-1610G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37351179 | |||||||
| chr2:37351221 | C | A | 2 | a0001c0003t0001g0028 a0001c0003t0005g0017 |
5 | HG00280.hp1 HG01981.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.121-1568C>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37351221 | |||||||
| chr2:37351437 | A | C | 1 | a0004c0005t0003g0139 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.121-1352A>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37351437 | |||||||
| chr2:37351455 | T | C | 1 | a0001c0001t0001g0310 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.121-1334T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37351455 | |||||||
| chr2:37351629 | C | T | 5 | a0001c0003t0001g0141 a0004c0005t0001g0130 a0004c0005t0001g0131 others(2): Show |
5 | HG01106.hp1 HG01891.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.121-1160C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37351629 | |||||||
| chr2:37351758 | T | C | 2 | a0001c0003t0001g0156 a0001c0003t0001g0236 |
2 | HG02976.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.121-1031T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37351758 | |||||||
| chr2:37351769 | C | G | 1 | a0003c0004t0002g0299 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.121-1020C>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37351769 | |||||||
| chr2:37351927 | G | C | 2 | a0001c0001t0001g0178 a0001c0001t0001g0197 |
2 | NA18964.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.121-862G>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37351927 | |||||||
| chr2:37351930 | T | C | 2 | a0001c0003t0001g0028 a0001c0003t0005g0017 |
5 | HG00280.hp1 HG01981.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.121-859T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37351930 | |||||||
| chr2:37352016 | G | C | 74 | a0001c0003t0001g0141 a0001c0003t0001g0157 a0002c0002t0002g0002 others(71): Show |
94 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(91): Show |
intron_variant | MODIFIER | c.121-773G>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37352016 | |||||||
| chr2:37352029 | C | CA | 4 | a0001c0001t0001g0179 a0001c0003t0001g0028 a0001c0003t0005g0017 others(1): Show |
7 | HG00280.hp1 HG01981.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.121-746dupA | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37352029 | ||||||
| chr2:37352029 | C | CAA | 72 | a0001c0003t0001g0141 a0001c0003t0001g0157 a0002c0002t0002g0002 others(69): Show |
92 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(89): Show |
intron_variant | MODIFIER | c.121-747_121-746dup others(2): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37352029 | ||||||
| chr2:37352039 | A | T | 9 | a0001c0003t0001g0018 a0001c0003t0001g0165 a0001c0003t0001g0349 others(6): Show |
11 | HG02109.hp1 HG02451.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.121-750A>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37352039 | |||||||
| chr2:37352043 | A | G | 1 | a0001c0001t0001g0052 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.121-746A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37352043 | |||||||
| chr2:37352049 | T | C | 74 | a0001c0003t0001g0141 a0001c0003t0001g0157 a0002c0002t0002g0002 others(71): Show |
94 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(91): Show |
intron_variant | MODIFIER | c.121-740T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37352049 | |||||||
| chr2:37352324 | T | A | 2 | a0001c0003t0001g0028 a0001c0003t0005g0017 |
5 | HG00280.hp1 HG01981.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.121-465T>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37352324 | |||||||
| chr2:37352368 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.121-421G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37352368 | |||||||
| chr2:37352440 | C | T | 3 | a0001c0001t0001g0015 a0001c0001t0001g0080 a0001c0001t0001g0083 |
5 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(2): Show |
intron_variant | MODIFIER | c.121-349C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37352440 | |||||||
| chr2:37352466 | G | T | 1 | a0001c0001t0001g0330 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.121-323G>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37352466 | |||||||
| chr2:37353019 | G | T | 1 | a0001c0003t0001g0236 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.267+84G>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37353019 | |||||||
| chr2:37353202 | A | T | 1 | a0001c0001t0001g0329 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.267+267A>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37353202 | |||||||
| chr2:37353323 | G | A | 2 | a0001c0001t0001g0174 a0004c0005t0001g0137 |
2 | HG02559.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.267+388G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37353323 | |||||||
| chr2:37353348 | G | C | 1 | a0001c0001t0001g0096 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.267+413G>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37353348 | |||||||
| chr2:37353430 | A | T | 1 | a0001c0001t0001g0216 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.267+495A>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37353430 | |||||||
| chr2:37353509 | T | A | 1 | a0001c0003t0003g0354 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.267+574T>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37353509 | |||||||
| chr2:37353540 | T | C | 2 | a0001c0001t0001g0201 a0001c0001t0001g0202 |
2 | HG02257.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.267+605T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37353540 | |||||||
| chr2:37353584 | A | G | 47 | a0001c0001t0001g0294 a0001c0001t0003g0235 a0001c0003t0001g0018 others(44): Show |
50 | HG00738.hp2 HG01243.hp1 HG01361.hp2 others(47): Show |
intron_variant | MODIFIER | c.267+649A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37353584 | |||||||
| chr2:37353603 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.267+668T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37353603 | |||||||
| chr2:37353667 | C | A | 1 | a0001c0001t0002g0311 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.267+732C>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37353667 | |||||||
| chr2:37353697 | A | G | 12 | a0001c0001t0003g0235 a0001c0003t0001g0018 a0001c0003t0001g0141 others(9): Show |
14 | HG01891.hp2 HG02109.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.267+762A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37353697 | |||||||
| chr2:37353717 | T | G | 51 | a0001c0001t0001g0294 a0001c0001t0003g0235 a0001c0003t0001g0018 others(48): Show |
54 | HG00738.hp2 HG01106.hp1 HG01243.hp1 others(51): Show |
intron_variant | MODIFIER | c.267+782T>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37353717 | |||||||
| chr2:37353820 | A | C | 1 | a0001c0001t0001g0032 | 2 | HG02735.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.267+885A>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37353820 | |||||||
| chr2:37353966 | A | G | 1 | a0001c0001t0001g0309 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.267+1031A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37353966 | |||||||
| chr2:37354007 | G | A | 2 | a0001c0003t0001g0128 a0001c0003t0003g0129 |
2 | HG02145.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.267+1072G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37354007 | |||||||
| chr2:37354111 | G | A | 64 | a0001c0003t0001g0156 a0002c0002t0002g0002 a0002c0002t0002g0005 others(61): Show |
84 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(81): Show |
intron_variant | MODIFIER | c.267+1176G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37354111 | |||||||
| chr2:37354224 | A | G | 65 | a0001c0001t0001g0031 a0001c0001t0001g0033 a0001c0001t0001g0176 others(62): Show |
71 | HG00735.hp1 HG00738.hp1 HG00738.hp2 others(68): Show |
intron_variant | MODIFIER | c.267+1289A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37354224 | |||||||
| chr2:37354504 | T | C | 4 | a0001c0001t0001g0079 a0003c0004t0002g0011 a0003c0004t0002g0055 others(1): Show |
6 | HG02071.hp2 NA18946.hp2 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.267+1569T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37354504 | |||||||
| chr2:37354614 | A | C | 1 | a0001c0001t0001g0220 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.267+1679A>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37354614 | |||||||
| chr2:37354619 | A | G | 2 | a0001c0003t0001g0157 a0004c0005t0001g0137 |
2 | HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.267+1684A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37354619 | |||||||
| chr2:37354642 | T | A | 2 | a0001c0001t0001g0047 a0001c0001t0001g0180 |
2 | HG03710.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.267+1707T>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37354642 | |||||||
| chr2:37354856 | G | T | 1 | a0001c0001t0001g0178 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.267+1921G>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37354856 | |||||||
| chr2:37354868 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.267+1933C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37354868 | |||||||
| chr2:37354973 | C | G | 49 | a0001c0001t0003g0235 a0001c0003t0001g0018 a0001c0003t0001g0029 others(46): Show |
52 | HG00738.hp2 HG01106.hp1 HG01243.hp1 others(49): Show |
intron_variant | MODIFIER | c.267+2038C>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37354973 | |||||||
| chr2:37355253 | G | T | 1 | a0001c0001t0001g0085 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.267+2318G>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37355253 | |||||||
| chr2:37355325 | A | G | 7 | a0001c0003t0001g0167 a0001c0003t0001g0348 a0001c0003t0002g0166 others(4): Show |
7 | HG01361.hp2 HG02280.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.267+2390A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37355325 | |||||||
| chr2:37355434 | A | G | 1 | a0001c0001t0002g0343 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.267+2499A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37355434 | |||||||
| chr2:37355530 | T | G | 1 | a0002c0002t0002g0260 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.267+2595T>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37355530 | |||||||
| chr2:37355543 | A | G | 2 | a0001c0001t0001g0049 a0003c0004t0002g0050 |
2 | HG01255.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.267+2608A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37355543 | |||||||
| chr2:37355545 | T | C | 1 | a0001c0001t0001g0083 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.267+2610T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37355545 | |||||||
| chr2:37355684 | G | A | 1 | a0001c0001t0001g0312 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.267+2749G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37355684 | |||||||
| chr2:37355773 | A | T | 49 | a0001c0003t0001g0018 a0001c0003t0001g0029 a0001c0003t0001g0132 others(46): Show |
52 | HG00738.hp2 HG01106.hp1 HG01243.hp1 others(49): Show |
intron_variant | MODIFIER | c.267+2838A>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37355773 | |||||||
| chr2:37355792 | G | A | 2 | a0001c0001t0001g0133 a0001c0001t0001g0188 |
2 | HG00438.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.267+2857G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37355792 | |||||||
| chr2:37355836 | A | T | 1 | a0001c0001t0001g0331 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.267+2901A>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37355836 | |||||||
| chr2:37355945 | C | T | 1 | a0002c0002t0002g0258 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.267+3010C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37355945 | |||||||
| chr2:37356093 | A | G | 1 | a0002c0002t0002g0256 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.267+3158A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37356093 | |||||||
| chr2:37356423 | C | A | 1 | a0002c0002t0002g0280 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.268-3157C>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37356423 | |||||||
| chr2:37356424 | G | T | 1 | a0002c0002t0002g0280 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.268-3156G>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37356424 | |||||||
| chr2:37356478 | C | T | 52 | a0001c0001t0001g0294 a0001c0003t0001g0018 a0001c0003t0001g0029 others(49): Show |
55 | HG00738.hp2 HG01106.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.268-3102C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37356478 | |||||||
| chr2:37356531 | T | C | 1 | a0001c0001t0001g0330 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.268-3049T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37356531 | |||||||
| chr2:37356547 | G | A | 1 | a0001c0003t0001g0348 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.268-3033G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37356547 | |||||||
| chr2:37356654 | C | G | 52 | a0001c0001t0001g0294 a0001c0003t0001g0018 a0001c0003t0001g0029 others(49): Show |
55 | HG00738.hp2 HG01106.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.268-2926C>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37356654 | |||||||
| chr2:37356831 | C | A | 1 | a0001c0001t0001g0180 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.268-2749C>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37356831 | |||||||
| chr2:37356843 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.268-2737C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37356843 | |||||||
| chr2:37356902 | A | C | 1 | a0002c0002t0002g0260 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.268-2678A>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37356902 | |||||||
| chr2:37356909 | G | T | 1 | a0001c0001t0001g0089 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.268-2671G>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37356909 | |||||||
| chr2:37357005 | C | CA | 61 | a0001c0001t0001g0013 a0001c0001t0001g0021 a0001c0001t0001g0065 others(58): Show |
67 | HG00738.hp2 HG01081.hp2 HG01106.hp1 others(64): Show |
intron_variant | MODIFIER | c.268-2558dupA | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 37357005 | ||||||
| chr2:37357282 | CT | C | 52 | a0001c0001t0001g0294 a0001c0003t0001g0018 a0001c0003t0001g0029 others(49): Show |
55 | HG00738.hp2 HG01106.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.268-2285delT | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 37357282 | ||||||
| chr2:37357315 | A | AT | 53 | a0001c0001t0001g0065 a0001c0001t0001g0294 a0001c0003t0001g0018 others(50): Show |
56 | HG00738.hp2 HG01106.hp1 HG01243.hp1 others(53): Show |
intron_variant | MODIFIER | c.268-2251dupT | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 37357315 | ||||||
| chr2:37357329 | T | A | 1 | a0001c0003t0001g0128 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.268-2251T>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37357329 | |||||||
| chr2:37357562 | A | G | 67 | a0001c0003t0001g0156 a0002c0002t0002g0002 a0002c0002t0002g0005 others(64): Show |
87 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.268-2018A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37357562 | |||||||
| chr2:37357724 | G | A | 1 | a0002c0002t0002g0246 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.268-1856G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37357724 | |||||||
| chr2:37357866 | C | A | 2 | a0001c0003t0001g0028 a0001c0003t0005g0017 |
5 | HG00280.hp1 HG01981.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.268-1714C>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37357866 | |||||||
| chr2:37357878 | A | T | 37 | a0001c0003t0001g0029 a0001c0003t0001g0132 a0001c0003t0001g0142 others(34): Show |
38 | HG00738.hp2 HG01106.hp1 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.268-1702A>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37357878 | |||||||
| chr2:37357883 | GA | G | 52 | a0001c0001t0001g0294 a0001c0003t0001g0018 a0001c0003t0001g0029 others(49): Show |
55 | HG00738.hp2 HG01106.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.268-1687delA | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 37357883 | ||||||
| chr2:37357907 | A | G | 3 | a0001c0001t0002g0043 a0001c0001t0002g0184 a0001c0001t0002g0308 |
4 | HG00639.hp1 HG02615.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.268-1673A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37357907 | |||||||
| chr2:37358026 | G | T | 1 | a0001c0001t0001g0070 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.268-1554G>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37358026 | |||||||
| chr2:37358108 | G | GA | 7 | a0001c0001t0001g0065 a0001c0001t0001g0179 a0001c0001t0001g0340 others(4): Show |
7 | HG02027.hp1 HG02717.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.268-1456dupA | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 37358108 | ||||||
| chr2:37358108 | GA | G | 8 | a0001c0001t0001g0089 a0001c0001t0001g0325 a0002c0002t0002g0040 others(5): Show |
9 | HG01255.hp1 HG01975.hp2 NA18948.hp1 others(6): Show |
intron_variant | MODIFIER | c.268-1456delA | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 37358108 | ||||||
| chr2:37358121 | A | AAAAG | 11 | a0001c0003t0001g0018 a0001c0003t0001g0141 a0001c0003t0001g0145 others(8): Show |
13 | HG01891.hp2 HG02109.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.268-1455_268-1452d others(6): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 37358121 | ||||||
| chr2:37358121 | A | AAAG | 35 | a0001c0001t0001g0294 a0001c0003t0001g0029 a0001c0003t0001g0128 others(32): Show |
36 | HG00738.hp2 HG01243.hp1 HG01361.hp2 others(33): Show |
intron_variant | MODIFIER | c.268-1457_268-1456i others(5): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 37358121 | ||||||
| chr2:37358121 | A | AAG | 6 | a0001c0003t0001g0157 a0004c0005t0001g0130 a0004c0005t0001g0131 others(3): Show |
6 | HG01106.hp1 HG02559.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.268-1458_268-1457i others(4): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 37358121 | ||||||
| chr2:37358121 | A | G | 2 | a0001c0001t0001g0326 a0001c0001t0005g0327 |
2 | HG00741.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.268-1459A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37358121 | |||||||
| chr2:37358126 | A | G | 1 | a0001c0003t0001g0142 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.268-1454A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37358126 | |||||||
| chr2:37358211 | G | C | 6 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0336 others(3): Show |
6 | HG01884.hp1 HG02055.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.268-1369G>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37358211 | |||||||
| chr2:37358264 | A | G | 2 | a0001c0003t0002g0224 a0001c0003t0003g0223 |
2 | HG01361.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.268-1316A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37358264 | |||||||
| chr2:37358267 | A | G | 3 | a0001c0001t0001g0294 a0001c0003t0001g0128 a0001c0003t0003g0129 |
3 | HG02055.hp2 HG02145.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.268-1313A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37358267 | |||||||
| chr2:37358274 | A | G | 1 | a0001c0001t0001g0074 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.268-1306A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37358274 | |||||||
| chr2:37358277 | A | C | 2 | a0001c0003t0001g0142 a0001c0003t0002g0225 |
2 | HG03209.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.268-1303A>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37358277 | |||||||
| chr2:37358340 | G | T | 1 | a0001c0001t0001g0176 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.268-1240G>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37358340 | |||||||
| chr2:37358438 | C | CAACAAAA others(3): Show |
2 | a0001c0003t0001g0018 a0001c0003t0001g0165 |
4 | HG02922.hp1 HG03209.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.268-1125_268-1116d others(12): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 37358438 | ||||||
| chr2:37358438 | C | CAACAAAA others(8): Show |
43 | a0001c0003t0001g0029 a0001c0003t0001g0132 a0001c0003t0001g0141 others(40): Show |
44 | HG00738.hp2 HG01106.hp1 HG01243.hp1 others(41): Show |
intron_variant | MODIFIER | c.268-1130_268-1116d others(17): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 37358438 | ||||||
| chr2:37358438 | C | CAACAAAA others(13): Show |
3 | a0001c0003t0001g0142 a0001c0003t0002g0166 a0004c0005t0001g0137 |
3 | HG02559.hp2 HG03942.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.268-1135_268-1116d others(22): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 37358438 | ||||||
| chr2:37358442 | A | T | 2 | a0001c0001t0001g0133 a0001c0001t0001g0188 |
2 | HG00438.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.268-1138A>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37358442 | |||||||
| chr2:37358461 | C | CAAAACAA others(4): Show |
1 | a0001c0003t0001g0236 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.268-1116_268-1115i others(13): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 37358461 | ||||||
| chr2:37358565 | C | T | 1 | a0001c0001t0001g0045 | 2 | HG01106.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.268-1015C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37358565 | |||||||
| chr2:37358633 | G | C | 50 | a0001c0001t0003g0235 a0001c0003t0001g0018 a0001c0003t0001g0029 others(47): Show |
53 | HG00738.hp2 HG01106.hp1 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.268-947G>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37358633 | |||||||
| chr2:37358814 | C | G | 1 | a0001c0001t0002g0311 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.268-766C>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37358814 | |||||||
| chr2:37358843 | T | C | 50 | a0001c0001t0003g0235 a0001c0003t0001g0018 a0001c0003t0001g0029 others(47): Show |
53 | HG00738.hp2 HG01106.hp1 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.268-737T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37358843 | |||||||
| chr2:37358853 | C | G | 2 | a0001c0001t0001g0013 a0001c0001t0007g0013 |
3 | HG01081.hp2 HG01943.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.268-727C>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37358853 | |||||||
| chr2:37358866 | G | A | 2 | a0001c0003t0001g0142 a0001c0003t0002g0225 |
2 | HG03209.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.268-714G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37358866 | |||||||
| chr2:37358922 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.268-658C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37358922 | |||||||
| chr2:37358929 | A | G | 2 | a0001c0003t0001g0157 a0004c0005t0001g0137 |
2 | HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.268-651A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37358929 | |||||||
| chr2:37358934 | T | C | 2 | a0001c0003t0001g0028 a0001c0003t0005g0017 |
5 | HG00280.hp1 HG01981.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.268-646T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37358934 | |||||||
| chr2:37359044 | A | G | 4 | a0001c0001t0001g0307 a0001c0001t0001g0326 a0001c0001t0001g0331 others(1): Show |
4 | HG00741.hp2 HG03239.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.268-536A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37359044 | |||||||
| chr2:37359092 | G | T | 50 | a0001c0001t0003g0235 a0001c0003t0001g0018 a0001c0003t0001g0029 others(47): Show |
53 | HG00738.hp2 HG01106.hp1 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.268-488G>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37359092 | |||||||
| chr2:37359103 | C | T | 50 | a0001c0001t0003g0235 a0001c0003t0001g0018 a0001c0003t0001g0029 others(47): Show |
53 | HG00738.hp2 HG01106.hp1 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.268-477C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37359103 | |||||||
| chr2:37359104 | G | T | 2 | a0001c0003t0001g0028 a0001c0003t0005g0017 |
5 | HG00280.hp1 HG01981.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.268-476G>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37359104 | |||||||
| chr2:37359194 | T | TTCTTTTT others(300): Show |
1 | a0004c0005t0003g0139 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.268-380_268-379ins others(307): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 37359194 | ||||||
| chr2:37359283 | G | A | 2 | a0001c0001t0001g0052 a0001c0001t0001g0061 |
2 | NA18951.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.268-297G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37359283 | |||||||
| chr2:37359352 | A | G | 2 | a0001c0003t0001g0128 a0001c0003t0003g0129 |
2 | HG02145.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.268-228A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37359352 | |||||||
| chr2:37359359 | G | T | 49 | a0001c0003t0001g0018 a0001c0003t0001g0029 a0001c0003t0001g0132 others(46): Show |
52 | HG00738.hp2 HG01106.hp1 HG01243.hp1 others(49): Show |
intron_variant | MODIFIER | c.268-221G>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37359359 | |||||||
| chr2:37359537 | C | T | 45 | a0001c0001t0003g0235 a0001c0003t0001g0018 a0001c0003t0001g0029 others(42): Show |
48 | HG00738.hp2 HG01243.hp1 HG01361.hp2 others(45): Show |
intron_variant | MODIFIER | c.268-43C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37359537 | |||||||
| chr2:37359538 | A | G | 178 | a0001c0001t0001g0031 a0001c0001t0001g0033 a0001c0001t0001g0042 others(175): Show |
211 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.268-42A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37359538 | |||||||
| chr2:37359897 | C | A | 67 | a0001c0003t0001g0156 a0002c0002t0002g0002 a0002c0002t0002g0005 others(64): Show |
87 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.546+39C>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37359897 | |||||||
| chr2:37359922 | C | T | 34 | a0001c0001t0003g0235 a0001c0003t0001g0018 a0001c0003t0001g0029 others(31): Show |
37 | HG00738.hp2 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.546+64C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37359922 | |||||||
| chr2:37359989 | C | T | 67 | a0001c0003t0001g0156 a0002c0002t0002g0002 a0002c0002t0002g0005 others(64): Show |
87 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.546+131C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37359989 | |||||||
| chr2:37359997 | G | GT | 17 | a0001c0003t0001g0143 a0001c0003t0001g0144 a0001c0003t0001g0146 others(14): Show |
17 | HG00738.hp2 HG01243.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.546+140dupT | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 37359997 | ||||||
| chr2:37360089 | T | C | 1 | a0001c0003t0002g0225 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.546+231T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37360089 | |||||||
| chr2:37360253 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.546+395C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37360253 | |||||||
| chr2:37360376 | C | T | 1 | a0001c0001t0001g0030 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.546+518C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37360376 | |||||||
| chr2:37360504 | A | G | 1 | a0001c0003t0002g0225 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.546+646A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37360504 | |||||||
| chr2:37360524 | T | C | 1 | a0001c0001t0002g0343 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.546+666T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37360524 | |||||||
| chr2:37360746 | G | A | 2 | a0001c0003t0001g0149 a0001c0003t0001g0159 |
2 | HG01884.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.546+888G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37360746 | |||||||
| chr2:37360759 | T | C | 1 | a0001c0003t0001g0349 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.546+901T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37360759 | |||||||
| chr2:37360864 | G | C | 1 | a0001c0003t0001g0236 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.546+1006G>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37360864 | |||||||
| chr2:37360887 | T | C | 1 | a0001c0001t0001g0314 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.546+1029T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37360887 | |||||||
| chr2:37360904 | A | G | 1 | a0001c0001t0001g0324 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.546+1046A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37360904 | |||||||
| chr2:37360923 | A | T | 6 | a0001c0003t0001g0142 a0001c0003t0001g0167 a0001c0003t0001g0348 others(3): Show |
6 | HG02559.hp1 HG02647.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.546+1065A>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37360923 | |||||||
| chr2:37361063 | G | GATTAAAA others(6): Show |
1 | a0001c0001t0001g0181 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.546+1208_546+1209i others(15): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 37361063 | ||||||
| chr2:37361067 | G | T | 1 | a0001c0001t0001g0181 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.546+1209G>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37361067 | |||||||
| chr2:37361068 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.546+1210G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37361068 | |||||||
| chr2:37361069 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.546+1211G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37361069 | |||||||
| chr2:37361070 | G | T | 1 | a0001c0001t0001g0181 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.546+1212G>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37361070 | |||||||
| chr2:37361075 | C | A | 1 | a0001c0001t0001g0181 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.546+1217C>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37361075 | |||||||
| chr2:37361145 | G | A | 1 | a0003c0004t0002g0057 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.546+1287G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37361145 | |||||||
| chr2:37361333 | C | T | 1 | a0001c0001t0001g0183 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.546+1475C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37361333 | |||||||
| chr2:37361353 | C | G | 1 | a0001c0001t0001g0077 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.546+1495C>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37361353 | |||||||
| chr2:37361466 | G | C | 17 | a0001c0003t0001g0143 a0001c0003t0001g0144 a0001c0003t0001g0146 others(14): Show |
17 | HG00738.hp2 HG01243.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.546+1608G>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37361466 | |||||||
| chr2:37361550 | G | A | 4 | a0001c0003t0001g0167 a0001c0003t0002g0166 a0001c0003t0002g0226 others(1): Show |
4 | HG02647.hp1 HG03471.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.546+1692G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37361550 | |||||||
| chr2:37361906 | G | A | 28 | a0001c0003t0001g0142 a0001c0003t0001g0143 a0001c0003t0001g0144 others(25): Show |
28 | HG00738.hp2 HG01243.hp1 HG01361.hp2 others(25): Show |
intron_variant | MODIFIER | c.546+2048G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37361906 | |||||||
| chr2:37361962 | C | A | 4 | a0001c0003t0001g0157 a0001c0003t0002g0224 a0001c0003t0003g0223 others(1): Show |
4 | HG01361.hp2 HG02280.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.546+2104C>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37361962 | |||||||
| chr2:37362075 | G | A | 2 | a0001c0003t0002g0226 a0001c0003t0002g0227 |
2 | HG03471.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.546+2217G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37362075 | |||||||
| chr2:37362133 | T | A | 1 | a0001c0003t0001g0156 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.546+2275T>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37362133 | |||||||
| chr2:37362186 | T | C | 2 | a0001c0001t0001g0207 a0001c0001t0001g0208 |
2 | HG01496.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.546+2328T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37362186 | |||||||
| chr2:37362221 | T | C | 1 | a0001c0001t0001g0032 | 2 | HG02735.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.546+2363T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37362221 | |||||||
| chr2:37362236 | C | T | 23 | a0001c0003t0001g0029 a0001c0003t0001g0132 a0001c0003t0001g0143 others(20): Show |
24 | HG00738.hp2 HG01243.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.546+2378C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37362236 | |||||||
| chr2:37362345 | C | T | 3 | a0001c0001t0001g0340 a0001c0001t0001g0341 a0001c0001t0001g0342 |
3 | HG01123.hp1 HG01261.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.546+2487C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37362345 | |||||||
| chr2:37362668 | A | G | 52 | a0001c0001t0001g0294 a0001c0003t0001g0018 a0001c0003t0001g0029 others(49): Show |
55 | HG00738.hp2 HG01106.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.546+2810A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37362668 | |||||||
| chr2:37362705 | A | T | 1 | a0003c0004t0002g0345 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.546+2847A>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37362705 | |||||||
| chr2:37362806 | G | C | 1 | a0001c0003t0003g0350 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.546+2948G>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37362806 | |||||||
| chr2:37362902 | G | A | 4 | a0001c0001t0001g0042 a0001c0001t0001g0295 a0001c0001t0001g0298 others(1): Show |
5 | HG02572.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.546+3044G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37362902 | |||||||
| chr2:37362941 | A | AT | 53 | a0001c0001t0001g0294 a0001c0001t0003g0235 a0001c0003t0001g0018 others(50): Show |
56 | HG00738.hp2 HG01106.hp1 HG01243.hp1 others(53): Show |
intron_variant | MODIFIER | c.546+3088dupT | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 37362941 | ||||||
| chr2:37363141 | G | A | 161 | a0001c0001t0001g0042 a0001c0001t0001g0044 a0001c0001t0001g0045 others(158): Show |
191 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.546+3283G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37363141 | |||||||
| chr2:37363303 | A | G | 1 | a0001c0003t0001g0157 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.546+3445A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37363303 | |||||||
| chr2:37363459 | C | CA | 34 | a0001c0001t0001g0075 a0001c0001t0001g0089 a0001c0001t0001g0120 others(31): Show |
35 | HG01109.hp1 HG01109.hp2 HG01175.hp1 others(32): Show |
intron_variant | MODIFIER | c.546+3623dupA | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 37363459 | ||||||
| chr2:37363459 | C | CAA | 80 | a0001c0003t0001g0143 a0001c0003t0001g0144 a0001c0003t0001g0146 others(77): Show |
100 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(97): Show |
intron_variant | MODIFIER | c.546+3622_546+3623d others(4): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 37363459 | ||||||
| chr2:37363459 | C | CAAA | 16 | a0001c0003t0001g0018 a0001c0003t0001g0141 a0001c0003t0001g0145 others(13): Show |
18 | HG00438.hp2 HG00738.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.546+3621_546+3623d others(5): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 37363459 | ||||||
| chr2:37363614 | G | A | 36 | a0001c0001t0001g0294 a0001c0003t0001g0029 a0001c0003t0001g0128 others(33): Show |
37 | HG00738.hp2 HG01243.hp1 HG01361.hp2 others(34): Show |
intron_variant | MODIFIER | c.547-3618G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37363614 | |||||||
| chr2:37363631 | TTAAA | T | 3 | a0001c0001t0001g0234 a0001c0003t0001g0028 a0001c0003t0005g0017 |
6 | HG00280.hp1 HG01981.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.547-3590_547-3587d others(6): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 37363631 | ||||||
| chr2:37363659 | T | TA | 11 | a0001c0001t0001g0047 a0001c0001t0001g0065 a0001c0001t0001g0075 others(8): Show |
11 | HG01952.hp2 HG02055.hp1 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.547-3552dupA | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 37363659 | ||||||
| chr2:37363659 | TA | T | 10 | a0001c0001t0001g0069 a0001c0001t0001g0084 a0001c0001t0001g0122 others(7): Show |
10 | HG01168.hp1 HG01169.hp1 HG02897.hp2 others(7): Show |
intron_variant | MODIFIER | c.547-3552delA | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 37363659 | ||||||
| chr2:37363659 | TAAA | T | 6 | a0001c0003t0001g0142 a0001c0003t0001g0157 a0001c0003t0002g0224 others(3): Show |
6 | HG01361.hp2 HG02280.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.547-3554_547-3552d others(5): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 37363659 | ||||||
| chr2:37363659 | TAAAA | T | 107 | a0001c0001t0003g0235 a0001c0003t0001g0018 a0001c0003t0001g0029 others(104): Show |
129 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(126): Show |
intron_variant | MODIFIER | c.547-3555_547-3552d others(6): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 37363659 | ||||||
| chr2:37363659 | TAAAAA | T | 6 | a0001c0001t0001g0294 a0001c0003t0001g0128 a0001c0003t0001g0132 others(3): Show |
7 | HG02055.hp2 HG02145.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.547-3556_547-3552d others(7): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 37363659 | ||||||
| chr2:37363775 | G | C | 2 | a0001c0001t0001g0234 a0001c0001t0003g0235 |
2 | HG02109.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.547-3457G>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37363775 | |||||||
| chr2:37363851 | C | G | 2 | a0001c0003t0002g0224 a0001c0003t0003g0223 |
2 | HG01361.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.547-3381C>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37363851 | |||||||
| chr2:37363894 | T | C | 14 | a0001c0001t0001g0031 a0001c0001t0001g0033 a0001c0001t0001g0081 others(11): Show |
17 | HG00735.hp1 HG00735.hp2 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.547-3338T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37363894 | |||||||
| chr2:37363938 | A | G | 12 | a0001c0001t0003g0235 a0001c0003t0001g0018 a0001c0003t0001g0141 others(9): Show |
14 | HG01891.hp2 HG02109.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.547-3294A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37363938 | |||||||
| chr2:37364017 | T | C | 1 | a0001c0001t0001g0234 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.547-3215T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37364017 | |||||||
| chr2:37364129 | A | G | 1 | a0001c0001t0001g0301 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.547-3103A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37364129 | |||||||
| chr2:37364309 | T | A | 1 | a0001c0003t0003g0223 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.547-2923T>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37364309 | |||||||
| chr2:37364359 | C | T | 1 | a0001c0001t0002g0343 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.547-2873C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37364359 | |||||||
| chr2:37364372 | A | G | 1 | a0001c0001t0001g0068 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.547-2860A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37364372 | |||||||
| chr2:37364387 | C | T | 1 | a0001c0001t0001g0330 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.547-2845C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37364387 | |||||||
| chr2:37364388 | G | A | 1 | a0001c0001t0002g0043 | 2 | HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.547-2844G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37364388 | |||||||
| chr2:37364595 | C | A | 50 | a0001c0001t0003g0235 a0001c0003t0001g0018 a0001c0003t0001g0029 others(47): Show |
53 | HG00738.hp2 HG01106.hp1 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.547-2637C>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37364595 | |||||||
| chr2:37364622 | T | C | 1 | a0001c0003t0001g0236 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.547-2610T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37364622 | |||||||
| chr2:37364665 | T | C | 1 | a0001c0001t0001g0319 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.547-2567T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37364665 | |||||||
| chr2:37364863 | T | C | 42 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0021 others(39): Show |
54 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.547-2369T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37364863 | |||||||
| chr2:37364981 | A | G | 2 | a0001c0003t0001g0141 a0001c0003t0001g0349 |
2 | HG01891.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.547-2251A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37364981 | |||||||
| chr2:37365001 | A | ATAT | 66 | a0001c0003t0001g0156 a0002c0002t0002g0002 a0002c0002t0002g0005 others(63): Show |
86 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(83): Show |
intron_variant | MODIFIER | c.547-2211_547-2209d others(5): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 37365001 | ||||||
| chr2:37365001 | ATAT | A | 50 | a0001c0001t0003g0235 a0001c0003t0001g0018 a0001c0003t0001g0029 others(47): Show |
53 | HG00738.hp2 HG01106.hp1 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.547-2211_547-2209d others(5): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 37365001 | ||||||
| chr2:37365077 | G | GCA | 4 | a0001c0001t0001g0004 a0001c0001t0001g0135 a0001c0001t0001g0318 others(1): Show |
8 | HG00642.hp2 HG01928.hp1 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.547-2136_547-2135d others(4): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 37365077 | ||||||
| chr2:37365077 | GCA | G | 4 | a0004c0005t0001g0130 a0004c0005t0001g0131 a0004c0005t0001g0138 others(1): Show |
4 | HG01106.hp1 HG03453.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.547-2136_547-2135d others(4): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 37365077 | ||||||
| chr2:37365192 | C | T | 37 | a0001c0003t0001g0029 a0001c0003t0001g0132 a0001c0003t0001g0142 others(34): Show |
38 | HG00738.hp2 HG01106.hp1 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.547-2040C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37365192 | |||||||
| chr2:37365330 | T | A | 1 | a0002c0002t0002g0277 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.547-1902T>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37365330 | |||||||
| chr2:37365485 | C | T | 242 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(239): Show |
296 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.547-1747C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37365485 | |||||||
| chr2:37365491 | T | C | 1 | a0001c0003t0001g0150 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.547-1741T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37365491 | |||||||
| chr2:37365613 | GGAATTAT others(6): Show |
G | 5 | a0001c0001t0001g0044 a0001c0001t0001g0307 a0001c0001t0001g0326 others(2): Show |
6 | HG00099.hp1 HG00741.hp2 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.547-1616_547-1604d others(15): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 37365613 | ||||||
| chr2:37365639 | T | C | 5 | a0002c0002t0002g0034 a0002c0002t0002g0255 a0002c0002t0002g0266 others(2): Show |
6 | NA18747.hp1 NA18948.hp1 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.547-1593T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37365639 | |||||||
| chr2:37365693 | A | C | 1 | a0003c0004t0005g0259 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.547-1539A>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37365693 | |||||||
| chr2:37365696 | G | A | 1 | a0002c0002t0002g0276 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.547-1536G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37365696 | |||||||
| chr2:37365848 | A | G | 2 | a0001c0003t0001g0128 a0001c0003t0003g0129 |
2 | HG02145.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.547-1384A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37365848 | |||||||
| chr2:37365875 | A | T | 1 | a0001c0003t0002g0225 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.547-1357A>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37365875 | |||||||
| chr2:37365901 | G | A | 9 | a0001c0001t0001g0045 a0001c0001t0001g0310 a0001c0001t0001g0320 others(6): Show |
10 | HG00140.hp1 HG01106.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.547-1331G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37365901 | |||||||
| chr2:37365995 | G | A | 1 | a0001c0001t0001g0204 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.547-1237G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37365995 | |||||||
| chr2:37366100 | T | C | 37 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0114 others(34): Show |
40 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.547-1132T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37366100 | |||||||
| chr2:37366122 | G | A | 1 | a0001c0001t0001g0304 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.547-1110G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37366122 | |||||||
| chr2:37366155 | A | C | 2 | a0001c0001t0001g0300 a0001c0001t0001g0301 |
2 | HG01884.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.547-1077A>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37366155 | |||||||
| chr2:37366163 | AG | A | 59 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(56): Show |
80 | HG00438.hp1 HG00621.hp1 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.547-1065delG | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 37366163 | ||||||
| chr2:37366212 | A | C | 1 | a0001c0001t0004g0313 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.547-1020A>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37366212 | |||||||
| chr2:37366240 | C | T | 1 | a0001c0001t0001g0033 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.547-992C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37366240 | |||||||
| chr2:37366261 | T | G | 2 | a0001c0001t0001g0201 a0001c0001t0001g0202 |
2 | HG02257.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.547-971T>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37366261 | |||||||
| chr2:37366285 | G | C | 4 | a0001c0001t0001g0086 a0001c0001t0005g0327 a0001c0003t0001g0028 others(1): Show |
7 | HG00280.hp1 HG00741.hp2 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.547-947G>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37366285 | |||||||
| chr2:37366335 | G | A | 1 | a0001c0003t0001g0156 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.547-897G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37366335 | |||||||
| chr2:37366375 | A | C | 1 | a0001c0001t0001g0114 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.547-857A>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37366375 | |||||||
| chr2:37366504 | T | C | 1 | a0001c0001t0001g0331 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.547-728T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37366504 | |||||||
| chr2:37366632 | T | C | 9 | a0001c0001t0001g0294 a0001c0001t0001g0309 a0001c0001t0003g0235 others(6): Show |
11 | HG00280.hp1 HG00741.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.547-600T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37366632 | |||||||
| chr2:37366682 | G | A | 2 | a0001c0001t0001g0084 a0001c0001t0001g0124 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.547-550G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37366682 | |||||||
| chr2:37366820 | C | A | 1 | a0001c0003t0002g0166 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.547-412C>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37366820 | |||||||
| chr2:37366875 | C | T | 17 | a0001c0001t0003g0098 a0001c0001t0003g0235 a0001c0003t0001g0018 others(14): Show |
19 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.547-357C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37366875 | |||||||
| chr2:37366911 | T | C | 1 | a0001c0003t0003g0223 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.547-321T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37366911 | |||||||
| chr2:37366974 | G | A | 1 | a0002c0002t0002g0265 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.547-258G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37366974 | |||||||
| chr2:37367013 | G | C | 1 | a0003c0004t0002g0051 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.547-219G>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37367013 | |||||||
| chr2:37367015 | G | T | 2 | a0001c0001t0005g0327 a0001c0003t0005g0017 |
4 | HG00280.hp1 HG00741.hp2 NA20805.hp2 others(1): Show |
intron_variant | MODIFIER | c.547-217G>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37367015 | |||||||
| chr2:37367082 | G | C | 1 | a0001c0001t0001g0319 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.547-150G>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37367082 | |||||||
| chr2:37367173 | A | G | 2 | a0001c0001t0005g0327 a0001c0003t0005g0017 |
4 | HG00280.hp1 HG00741.hp2 NA20805.hp2 others(1): Show |
intron_variant | MODIFIER | c.547-59A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37367173 | |||||||
| chr2:37367451 | G | A | 4 | a0001c0001t0002g0200 a0001c0001t0005g0327 a0001c0003t0001g0144 others(1): Show |
6 | HG00280.hp1 HG00741.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.723+43G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37367451 | |||||||
| chr2:37367500 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.723+92C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37367500 | |||||||
| chr2:37367551 | G | A | 6 | a0001c0001t0001g0234 a0001c0001t0001g0309 a0001c0003t0001g0161 others(3): Show |
6 | HG02109.hp2 HG02630.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.723+143G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37367551 | |||||||
| chr2:37367598 | T | A | 3 | a0001c0001t0002g0200 a0001c0001t0005g0327 a0001c0003t0005g0017 |
5 | HG00280.hp1 HG00741.hp2 NA20805.hp2 others(2): Show |
intron_variant | MODIFIER | c.723+190T>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37367598 | |||||||
| chr2:37367641 | G | T | 6 | a0001c0001t0001g0234 a0001c0001t0001g0309 a0001c0003t0001g0161 others(3): Show |
6 | HG02109.hp2 HG02630.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.723+233G>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37367641 | |||||||
| chr2:37367700 | C | T | 11 | a0001c0003t0001g0018 a0001c0003t0001g0141 a0001c0003t0001g0145 others(8): Show |
14 | HG00738.hp1 HG01069.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.723+292C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37367700 | |||||||
| chr2:37367701 | G | A | 1 | a0001c0001t0002g0184 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.723+293G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37367701 | |||||||
| chr2:37367738 | G | A | 6 | a0001c0001t0001g0234 a0001c0001t0001g0309 a0001c0003t0001g0161 others(3): Show |
6 | HG02109.hp2 HG02630.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.723+330G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37367738 | |||||||
| chr2:37367802 | G | A | 10 | a0001c0001t0001g0042 a0001c0001t0001g0125 a0001c0001t0001g0127 others(7): Show |
11 | HG01106.hp1 HG02572.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.723+394G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37367802 | |||||||
| chr2:37367827 | C | G | 6 | a0001c0001t0001g0234 a0001c0001t0001g0309 a0001c0003t0001g0161 others(3): Show |
6 | HG02109.hp2 HG02630.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.723+419C>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37367827 | |||||||
| chr2:37367845 | G | T | 1 | a0003c0004t0002g0051 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.723+437G>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37367845 | |||||||
| chr2:37367951 | T | C | 1 | a0001c0001t0001g0307 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.723+543T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37367951 | |||||||
| chr2:37368382 | A | G | 133 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(130): Show |
175 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.723+974A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37368382 | |||||||
| chr2:37368408 | C | A | 1 | a0001c0001t0001g0206 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.723+1000C>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37368408 | |||||||
| chr2:37368461 | C | T | 136 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(133): Show |
174 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(171): Show |
intron_variant | MODIFIER | c.723+1053C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37368461 | |||||||
| chr2:37368553 | A | C | 264 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(261): Show |
334 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(331): Show |
intron_variant | MODIFIER | c.724-1132A>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37368553 | |||||||
| chr2:37368618 | C | T | 6 | a0001c0003t0001g0147 a0001c0003t0001g0148 a0001c0003t0001g0152 others(3): Show |
6 | HG01243.hp1 HG02486.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.724-1067C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37368618 | |||||||
| chr2:37368641 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.724-1044A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37368641 | |||||||
| chr2:37368647 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.724-1038C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37368647 | |||||||
| chr2:37368718 | C | G | 7 | a0001c0001t0001g0234 a0001c0001t0001g0309 a0001c0001t0002g0200 others(4): Show |
7 | HG02109.hp2 HG02630.hp1 HG03471.hp2 others(4): Show |
intron_variant | MODIFIER | c.724-967C>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37368718 | |||||||
| chr2:37368731 | G | A | 6 | a0001c0003t0001g0029 a0001c0003t0001g0128 a0001c0003t0001g0132 others(3): Show |
7 | HG02145.hp1 HG02451.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.724-954G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37368731 | |||||||
| chr2:37368787 | G | A | 1 | a0001c0003t0002g0225 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.724-898G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37368787 | |||||||
| chr2:37368816 | A | G | 1 | a0001c0001t0001g0104 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.724-869A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37368816 | |||||||
| chr2:37368826 | G | C | 1 | a0001c0001t0001g0319 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.724-859G>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37368826 | |||||||
| chr2:37368934 | T | G | 7 | a0001c0001t0001g0234 a0001c0001t0001g0309 a0001c0001t0002g0200 others(4): Show |
7 | HG02109.hp2 HG02630.hp1 HG03471.hp2 others(4): Show |
intron_variant | MODIFIER | c.724-751T>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37368934 | |||||||
| chr2:37368946 | C | T | 275 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(272): Show |
346 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(343): Show |
intron_variant | MODIFIER | c.724-739C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37368946 | |||||||
| chr2:37368951 | A | G | 1 | a0001c0001t0001g0183 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.724-734A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37368951 | |||||||
| chr2:37368955 | T | A | 247 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(244): Show |
313 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(310): Show |
intron_variant | MODIFIER | c.724-730T>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37368955 | |||||||
| chr2:37368955 | T | G | 11 | a0001c0003t0001g0018 a0001c0003t0001g0141 a0001c0003t0001g0145 others(8): Show |
14 | HG00738.hp1 HG01069.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.724-730T>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37368955 | |||||||
| chr2:37369006 | G | A | 1 | a0001c0001t0001g0302 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.724-679G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37369006 | |||||||
| chr2:37369198 | A | C | 73 | a0001c0001t0001g0174 a0002c0002t0002g0002 a0002c0002t0002g0005 others(70): Show |
98 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.724-487A>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37369198 | |||||||
| chr2:37369235 | A | C | 81 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(78): Show |
105 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(102): Show |
intron_variant | MODIFIER | c.724-450A>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37369235 | |||||||
| chr2:37369256 | T | C | 1 | a0002c0002t0002g0266 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.724-429T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37369256 | |||||||
| chr2:37369291 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.724-394A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37369291 | |||||||
| chr2:37369352 | G | C | 2 | a0001c0003t0002g0226 a0001c0003t0002g0227 |
2 | HG03471.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.724-333G>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37369352 | |||||||
| chr2:37369432 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.724-253G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37369432 | |||||||
| chr2:37369574 | A | G | 2 | a0001c0003t0001g0157 a0004c0005t0001g0137 |
2 | HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.724-111A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37369574 | |||||||
| chr2:37369796 | T | C | 7 | a0001c0001t0001g0234 a0001c0001t0001g0309 a0001c0003t0001g0161 others(4): Show |
7 | HG02109.hp2 HG02630.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.823+12T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37369796 | |||||||
| chr2:37369958 | C | A | 6 | a0001c0003t0001g0147 a0001c0003t0001g0148 a0001c0003t0001g0152 others(3): Show |
6 | HG01243.hp1 HG02486.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.823+174C>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37369958 | |||||||
| chr2:37370242 | T | A | 1 | a0001c0001t0001g0116 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.823+458T>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37370242 | |||||||
| chr2:37370243 | T | C | 85 | a0001c0001t0001g0109 a0001c0001t0001g0174 a0001c0001t0002g0043 others(82): Show |
111 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.823+459T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37370243 | |||||||
| chr2:37370246 | CT | C | 6 | a0001c0003t0001g0147 a0001c0003t0001g0148 a0001c0003t0001g0152 others(3): Show |
6 | HG01243.hp1 HG02486.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.823+469delT | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 37370246 | ||||||
| chr2:37370347 | AAATACTA others(12): Show |
A | 1 | a0001c0003t0001g0156 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.823+564_823+582del others(19): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37370347 | |||||||
| chr2:37370369 | A | G | 1 | a0001c0001t0001g0329 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.823+585A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37370369 | |||||||
| chr2:37370545 | G | A | 1 | a0001c0001t0001g0231 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.823+761G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37370545 | |||||||
| chr2:37370546 | T | C | 11 | a0001c0001t0001g0042 a0001c0001t0001g0125 a0001c0001t0001g0126 others(8): Show |
12 | HG01106.hp1 HG02572.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.823+762T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37370546 | |||||||
| chr2:37370604 | C | G | 1 | a0001c0001t0001g0312 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.823+820C>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37370604 | |||||||
| chr2:37370712 | A | AGGTCAGG others(17): Show |
1 | a0006c0008t0006g0328 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.823+943_823+944ins others(24): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 37370712 | ||||||
| chr2:37370737 | C | T | 1 | a0001c0001t0002g0200 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.823+953C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37370737 | |||||||
| chr2:37370910 | G | T | 7 | a0001c0001t0001g0056 a0001c0001t0001g0074 a0001c0001t0001g0181 others(4): Show |
7 | HG01074.hp1 HG01109.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.823+1126G>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37370910 | |||||||
| chr2:37370947 | C | T | 105 | a0001c0001t0001g0174 a0001c0001t0001g0234 a0001c0001t0001g0309 others(102): Show |
131 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(128): Show |
intron_variant | MODIFIER | c.823+1163C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37370947 | |||||||
| chr2:37370975 | T | C | 1 | a0001c0001t0001g0310 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.823+1191T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37370975 | |||||||
| chr2:37371136 | A | G | 1 | a0001c0001t0001g0196 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.824-1220A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37371136 | |||||||
| chr2:37371258 | C | G | 1 | a0001c0003t0003g0129 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.824-1098C>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37371258 | |||||||
| chr2:37371258 | C | T | 1 | a0006c0008t0006g0328 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.824-1098C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37371258 | |||||||
| chr2:37371278 | T | C | 121 | a0001c0001t0001g0033 a0001c0001t0001g0044 a0001c0001t0001g0079 others(118): Show |
151 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.824-1078T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37371278 | |||||||
| chr2:37371328 | T | A | 1 | a0006c0008t0006g0328 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.824-1028T>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37371328 | |||||||
| chr2:37371359 | T | G | 7 | a0001c0001t0003g0098 a0001c0001t0003g0235 a0001c0003t0003g0350 others(4): Show |
7 | HG02451.hp2 HG02717.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.824-997T>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37371359 | |||||||
| chr2:37371369 | G | A | 100 | a0001c0001t0001g0234 a0001c0001t0002g0043 a0001c0001t0002g0184 others(97): Show |
127 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(124): Show |
intron_variant | MODIFIER | c.824-987G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37371369 | |||||||
| chr2:37371431 | C | CA | 177 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(174): Show |
216 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(213): Show |
intron_variant | MODIFIER | c.824-904dupA | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 37371431 | ||||||
| chr2:37371431 | C | CAA | 11 | a0001c0001t0001g0092 a0001c0001t0001g0118 a0001c0001t0001g0201 others(8): Show |
13 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.824-905_824-904dup others(2): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 37371431 | ||||||
| chr2:37371431 | C | CAAAAA | 6 | a0001c0001t0002g0297 a0002c0002t0002g0247 a0002c0002t0002g0248 others(3): Show |
6 | HG02040.hp2 NA18956.hp1 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.824-908_824-904dup others(5): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 37371431 | ||||||
| chr2:37371431 | C | CAAAAAA | 74 | a0001c0001t0002g0043 a0001c0001t0002g0184 a0001c0001t0002g0190 others(71): Show |
101 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.824-909_824-904dup others(6): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 37371431 | ||||||
| chr2:37371431 | C | CAAAAAAA | 10 | a0001c0001t0001g0234 a0001c0001t0002g0311 a0002c0002t0002g0237 others(7): Show |
10 | HG02015.hp2 HG02109.hp2 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.824-910_824-904dup others(7): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 37371431 | ||||||
| chr2:37371431 | CAAA | C | 9 | a0001c0001t0003g0098 a0001c0001t0003g0235 a0001c0003t0003g0129 others(6): Show |
9 | HG02280.hp1 HG02451.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.824-906_824-904del others(3): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 37371431 | ||||||
| chr2:37371453 | G | A | 1 | a0006c0008t0006g0328 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.824-903G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37371453 | |||||||
| chr2:37371454 | A | G | 1 | a0006c0008t0006g0328 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.824-902A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37371454 | |||||||
| chr2:37371507 | A | G | 4 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(1): Show |
4 | HG02258.hp1 HG02572.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.824-849A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37371507 | |||||||
| chr2:37371531 | G | T | 1 | a0001c0001t0001g0234 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.824-825G>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37371531 | |||||||
| chr2:37371566 | A | T | 1 | a0006c0008t0006g0328 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.824-790A>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37371566 | |||||||
| chr2:37371578 | T | C | 1 | a0001c0001t0001g0066 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.824-778T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37371578 | |||||||
| chr2:37371771 | C | T | 13 | a0001c0001t0001g0234 a0001c0001t0003g0098 a0001c0001t0003g0235 others(10): Show |
13 | HG02109.hp2 HG02280.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.824-585C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37371771 | |||||||
| chr2:37371855 | A | G | 104 | a0001c0001t0001g0234 a0001c0001t0002g0043 a0001c0001t0002g0184 others(101): Show |
131 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(128): Show |
intron_variant | MODIFIER | c.824-501A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37371855 | |||||||
| chr2:37371958 | T | C | 5 | a0001c0001t0002g0337 a0001c0001t0002g0339 a0001c0003t0002g0166 others(2): Show |
5 | HG02896.hp1 HG02897.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.824-398T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37371958 | |||||||
| chr2:37372052 | C | T | 1 | a0004c0005t0001g0130 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.824-304C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37372052 | |||||||
| chr2:37372084 | T | C | 103 | a0001c0001t0002g0043 a0001c0001t0002g0184 a0001c0001t0002g0190 others(100): Show |
130 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(127): Show |
intron_variant | MODIFIER | c.824-272T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37372084 | |||||||
| chr2:37372147 | G | T | 2 | a0001c0001t0001g0075 a0001c0001t0001g0076 |
2 | HG02004.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.824-209G>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37372147 | |||||||
| chr2:37372194 | C | G | 103 | a0001c0001t0002g0043 a0001c0001t0002g0184 a0001c0001t0002g0190 others(100): Show |
130 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(127): Show |
intron_variant | MODIFIER | c.824-162C>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37372194 | |||||||
| chr2:37372210 | T | C | 4 | a0001c0001t0001g0042 a0001c0001t0001g0295 a0001c0001t0001g0298 others(1): Show |
5 | HG02572.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.824-146T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37372210 | |||||||
| chr2:37372510 | G | A | 1 | a0001c0001t0001g0045 | 2 | HG01106.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.940+38G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 6/6 | chr2 | 37372510 | |||||||
| chr2:37372537 | G | A | 6 | a0001c0001t0001g0056 a0001c0001t0001g0074 a0001c0001t0001g0211 others(3): Show |
6 | HG01074.hp1 HG01109.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.940+65G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 6/6 | chr2 | 37372537 | |||||||
| chr2:37372545 | A | G | 94 | a0001c0001t0002g0043 a0001c0001t0002g0184 a0001c0001t0002g0190 others(91): Show |
121 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.940+73A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 6/6 | chr2 | 37372545 | |||||||
| chr2:37372568 | T | G | 5 | a0001c0001t0002g0337 a0001c0001t0002g0339 a0001c0003t0002g0166 others(2): Show |
5 | HG02896.hp1 HG02897.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.940+96T>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 6/6 | chr2 | 37372568 | |||||||
| chr2:37372569 | G | A | 5 | a0001c0001t0002g0337 a0001c0001t0002g0339 a0001c0003t0002g0166 others(2): Show |
5 | HG02896.hp1 HG02897.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.940+97G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 6/6 | chr2 | 37372569 | |||||||
| chr2:37372639 | C | T | 6 | a0001c0001t0003g0098 a0001c0001t0003g0235 a0001c0003t0003g0350 others(3): Show |
6 | HG02451.hp2 HG02976.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.941-43C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 6/6 | chr2 | 37372639 | |||||||
| chr2:37372652 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.941-30C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 6/6 | chr2 | 37372652 |