Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 3948 |
| ensemblid | ENSG00000166796.12 |
| hgncid | 6544 |
| symbol | LDHC |
| name | lactate dehydrogenase C |
| refseq_nuc | NM_017448.5 |
| refseq_prot | NP_059144.1 |
| ensembl_nuc | ENST00000541669.6 |
| ensembl_prot | ENSP00000437783.1 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 18412318 |
| end | 18452063 |
| strand | + |
| ver | v1.2 |
| region | chr11:18412318-18452063 |
| region5000 | chr11:18407318-18457063 |
| regionname0 | LDHC_chr11_18412318_18452063 |
| regionname5000 | LDHC_chr11_18407318_18457063 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 332 | 331 | 79 | 58 | 154 | 8 | 30 | 121 | LDHC_chr11_18407318_18457063 | LDHC | MSTVK others(327): Show |
chr11 | 18407318 | 18457063 |
| a0002 | 0/0 | 332 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | MSTVK others(327): Show |
chr11 | 18407318 | 18457063 |
| a0003 | 0/0 | 332 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | MSTVK others(327): Show |
chr11 | 18407318 | 18457063 |
| a0004 | 0/0 | 332 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | MSTVK others(327): Show |
chr11 | 18407318 | 18457063 |
| a0005 | 0/0 | 332 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | MSTVK others(327): Show |
chr11 | 18407318 | 18457063 |
| a0006 | 0/0 | 332 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | MSTVK others(327): Show |
chr11 | 18407318 | 18457063 |
| a0007 | 0/0 | 332 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LDHC_chr11_18407318_18457063 | LDHC | MSTVK others(327): Show |
chr11 | 18407318 | 18457063 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 996 | 327 | 78 | 58 | 152 | 8 | 30 | LDHC_chr11_18407318_18457063 | LDHC | ATGTC others(991): Show |
chr11 | 18407318 | 18457063 | ||
| a0001c0003 | 0/0 | 996 | 2 | 0 | 0 | 2 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | ATGTC others(991): Show |
chr11 | 18407318 | 18457063 | ||
| a0001c0007 | 0/0 | 996 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | ATGTC others(991): Show |
chr11 | 18407318 | 18457063 | ||
| a0001c0008 | 0/1 | 996 | 1 | 0 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | ATGTC others(991): Show |
chr11 | 18407318 | 18457063 | ||
| a0002c0002 | 0/0 | 996 | 9 | 9 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | ATGTC others(991): Show |
chr11 | 18407318 | 18457063 | ||
| a0003c0006 | 0/0 | 996 | 2 | 0 | 2 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | ATGTC others(991): Show |
chr11 | 18407318 | 18457063 | ||
| a0004c0005 | 0/0 | 996 | 2 | 2 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | ATGTC others(991): Show |
chr11 | 18407318 | 18457063 | ||
| a0005c0004 | 0/0 | 996 | 2 | 2 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | ATGTC others(991): Show |
chr11 | 18407318 | 18457063 | ||
| a0006c0010 | 0/0 | 996 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | ATGTC others(991): Show |
chr11 | 18407318 | 18457063 | ||
| a0007c0009 | 0/0 | 996 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | ATGTC others(991): Show |
chr11 | 18407318 | 18457063 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2035 | 232 | 47 | 39 | 119 | 5 | 22 | LDHC_chr11_18407318_18457063 | LDHC | GAGTC others(2030): Show |
chr11 | 18407318 | 18457063 |
| a0001c0001t0002 | 0/0 | 2038 | 49 | 26 | 8 | 8 | 2 | 5 | LDHC_chr11_18407318_18457063 | LDHC | GAGTC others(2033): Show |
chr11 | 18407318 | 18457063 |
| a0001c0001t0003 | 0/0 | 2035 | 26 | 3 | 9 | 10 | 1 | 3 | LDHC_chr11_18407318_18457063 | LDHC | GAGTC others(2030): Show |
chr11 | 18407318 | 18457063 |
| a0001c0001t0004 | 0/0 | 2035 | 12 | 0 | 1 | 11 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | GAGTC others(2030): Show |
chr11 | 18407318 | 18457063 |
| a0001c0001t0005 | 0/0 | 2035 | 4 | 0 | 0 | 4 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | GAGTC others(2030): Show |
chr11 | 18407318 | 18457063 |
| a0001c0001t0008 | 0/0 | 2035 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | GAGTC others(2030): Show |
chr11 | 18407318 | 18457063 |
| a0001c0001t0009 | 1/0 | 2035 | 1 | 0 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | GAGTC others(2030): Show |
chr11 | 18407318 | 18457063 |
| a0001c0001t0010 | 0/0 | 2035 | 1 | 0 | 1 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | GAGTC others(2030): Show |
chr11 | 18407318 | 18457063 |
| a0001c0001t0011 | 0/0 | 2035 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | GAGTC others(2030): Show |
chr11 | 18407318 | 18457063 |
| a0001c0003t0001 | 0/0 | 2035 | 2 | 0 | 0 | 2 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | GAGTC others(2030): Show |
chr11 | 18407318 | 18457063 |
| a0001c0007t0001 | 0/0 | 2035 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | GAGTC others(2030): Show |
chr11 | 18407318 | 18457063 |
| a0001c0008t0002 | 0/1 | 2038 | 1 | 0 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | GAGTC others(2033): Show |
chr11 | 18407318 | 18457063 |
| a0002c0002t0002 | 0/0 | 2038 | 9 | 9 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | GAGTC others(2033): Show |
chr11 | 18407318 | 18457063 |
| a0003c0006t0003 | 0/0 | 2035 | 2 | 0 | 2 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | GAGTC others(2030): Show |
chr11 | 18407318 | 18457063 |
| a0004c0005t0007 | 0/0 | 2038 | 2 | 2 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | GAGTC others(2033): Show |
chr11 | 18407318 | 18457063 |
| a0005c0004t0006 | 0/0 | 2038 | 2 | 2 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | GAGTC others(2033): Show |
chr11 | 18407318 | 18457063 |
| a0006c0010t0001 | 0/0 | 2035 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | GAGTC others(2030): Show |
chr11 | 18407318 | 18457063 |
| a0007c0009t0001 | 0/0 | 2035 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | GAGTC others(2030): Show |
chr11 | 18407318 | 18457063 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0003 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0002g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0002g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0002g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0003g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0003g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0003g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0003g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0003g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0003g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0003g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0003g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0003g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0003g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0003g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0003g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0003g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0003g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0003g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0003g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0003g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0004g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0004g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0004g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0004g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0004g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0004g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0004g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0004g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0004g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0004g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0004g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0005g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0005g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0005g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0005g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0008g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0009g0087 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0010g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0001t0011g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0003t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0003t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0007t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0001c0008t0002g0017 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0002c0002t0002g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0002c0002t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0002c0002t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0002c0002t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0002c0002t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0002c0002t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0002c0002t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0003c0006t0003g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0003c0006t0003g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0004c0005t0007g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0004c0005t0007g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0005c0004t0006g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0005c0004t0006g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0006c0010t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| a0007c0009t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0215 | EUR | FIN | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0038 | EUR | FIN | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0126 | EUR | FIN | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0240 | EUR | FIN | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG00423 | hp1 | a0006 | c0010 | t0001 | g0065 | EAS | CHS | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG00438 | hp1 | a0001 | c0001 | t0004 | g0297 | EAS | CHS | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | CHS | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | CHS | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | CHS | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG00597 | hp2 | a0001 | c0001 | t0004 | g0313 | EAS | CHS | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | CHS | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG00621 | hp1 | a0001 | c0001 | t0004 | g0304 | EAS | CHS | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | CHS | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0264 | AMR | PUR | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG00738 | hp2 | a0001 | c0001 | t0010 | g0164 | AMR | PUR | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0312 | AMR | PUR | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0238 | AMR | PUR | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0306 | AMR | PUR | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0317 | AMR | PUR | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0302 | AMR | PUR | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0239 | AMR | PUR | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0300 | AMR | PUR | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0301 | AMR | PUR | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0284 | AMR | PUR | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0309 | AMR | CLM | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | CLM | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0310 | AMR | CLM | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0305 | AMR | CLM | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG01358 | hp1 | a0003 | c0006 | t0003 | g0319 | AMR | CLM | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0246 | AMR | CLM | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0245 | AMR | CLM | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0170 | EUR | IBS | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0085 | EUR | IBS | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0316 | AFR | ACB | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | ACB | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG01928 | hp2 | a0001 | c0001 | t0004 | g0315 | AMR | PEL | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0269 | AMR | PEL | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PEL | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PEL | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PEL | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | KHV | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | KHV | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02083 | hp1 | a0001 | c0001 | t0004 | g0318 | EAS | KHV | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02135 | hp2 | a0001 | c0001 | t0004 | g0320 | EAS | KHV | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02145 | hp1 | a0004 | c0005 | t0007 | g0015 | AFR | ACB | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | CDX | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0261 | AFR | ACB | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0281 | AFR | ACB | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0267 | AFR | ACB | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | ACB | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02280 | hp1 | a0001 | c0007 | t0001 | g0285 | AFR | ACB | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | ACB | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PEL | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02293 | hp2 | a0003 | c0006 | t0003 | g0311 | AMR | PEL | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | ACB | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02572 | hp1 | a0001 | c0001 | t0008 | g0116 | AFR | GWD | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0265 | AFR | GWD | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0263 | AFR | GWD | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0298 | AFR | GWD | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0271 | AFR | GWD | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0296 | SAS | PJL | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0286 | AFR | GWD | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0280 | AFR | GWD | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0292 | AFR | GWD | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0274 | SAS | PJL | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02809 | hp1 | a0004 | c0005 | t0007 | g0016 | AFR | GWD | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02818 | hp1 | a0002 | c0002 | t0002 | g0249 | AFR | GWD | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02818 | hp2 | a0001 | c0001 | t0011 | g0299 | AFR | GWD | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02895 | hp1 | a0002 | c0002 | t0002 | g0236 | AFR | GWD | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0262 | AFR | GWD | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | GWD | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02896 | hp2 | a0002 | c0002 | t0002 | g0250 | AFR | GWD | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | GWD | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0241 | AFR | GWD | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | ESN | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ESN | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | ESN | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02965 | hp2 | a0002 | c0002 | t0002 | g0237 | AFR | ESN | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ESN | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | ESN | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0308 | SAS | PJL | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG03041 | hp1 | a0005 | c0004 | t0006 | g0014 | AFR | GWD | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | GWD | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | MSL | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0293 | AFR | MSL | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | ESN | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | ESN | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ESN | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG03209 | hp1 | a0002 | c0002 | t0002 | g0251 | AFR | MSL | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0282 | AFR | MSL | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | MSL | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | MSL | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG03453 | hp2 | a0002 | c0002 | t0002 | g0252 | AFR | MSL | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG03486 | hp2 | a0005 | c0004 | t0006 | g0013 | AFR | MSL | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ESN | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | ESN | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG03540 | hp2 | a0002 | c0002 | t0002 | g0005 | AFR | GWD | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0290 | AFR | MSL | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | MSL | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0257 | SAS | PJL | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0253 | SAS | STU | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | STU | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0322 | SAS | PJL | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0323 | SAS | BEB | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0247 | SAS | BEB | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | BEB | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0255 | SAS | BEB | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | BEB | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | STU | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | STU | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | BEB | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0009 | SAS | BEB | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18522 | hp1 | a0002 | c0002 | t0002 | g0005 | AFR | YRI | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | YRI | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | CHB | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18612 | hp2 | a0001 | c0003 | t0001 | g0118 | EAS | CHB | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0266 | AFR | YRI | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0303 | AFR | YRI | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18945 | hp1 | a0001 | c0001 | t0005 | g0177 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18953 | hp2 | a0001 | c0001 | t0004 | g0321 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18956 | hp1 | a0001 | c0001 | t0005 | g0035 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18965 | hp2 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18985 | hp2 | a0001 | c0001 | t0005 | g0067 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18988 | hp2 | a0001 | c0003 | t0001 | g0117 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0314 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA19001 | hp1 | a0001 | c0001 | t0004 | g0327 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA19009 | hp1 | a0001 | c0001 | t0004 | g0324 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0260 | AFR | LWK | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | LWK | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA19055 | hp2 | a0001 | c0001 | t0003 | g0095 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA19065 | hp2 | a0001 | c0001 | t0004 | g0012 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA19075 | hp1 | a0001 | c0001 | t0004 | g0326 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA19077 | hp2 | a0001 | c0001 | t0004 | g0012 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0115 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA19086 | hp1 | a0007 | c0009 | t0001 | g0212 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA19086 | hp2 | a0001 | c0001 | t0005 | g0112 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0098 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA19240 | hp1 | a0002 | c0002 | t0002 | g0005 | AFR | YRI | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | YRI | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ASW | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | ASW | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0307 | EUR | TSI | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0254 | EUR | TSI | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | GIH | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | GIH | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0259 | AFR | ACB | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0258 | AFR | ACB | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | MSL | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0289 | AFR | MSL | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | USA | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | USA | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0097 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| homoSapiens | chm13v2 | a0001 | c0008 | t0002 | g0017 | REF | REF | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0009 | g0087 | REF | REF | LDHC_chr11_18407318_18457063 | LDHC | chr11 | 18407318 | 18457063 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:18412754 | A | C | 1 | a0002 | 9 | HG02818.hp1 HG02895.hp1 HG02896.hp2 others(6): Show |
missense_variant | MODERATE | c.37A>C | p.Ile13Leu | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 2/8 | 137/2035 | 37/999 | 13/332 | chr11 | 18412754 | |||
| chr11:18438594 | C | T | 1 | a0006 | 1 | HG00423.hp1 | missense_variant | MODERATE | c.659C>T | p.Thr220Met | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/8 | 759/2035 | 659/999 | 220/332 | chr11 | 18438594 | |||
| chr11:18446281 | G | C | 1 | a0007 | 1 | NA19086.hp1 | missense_variant | MODERATE | c.782G>C | p.Gly261Ala | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/8 | 882/2035 | 782/999 | 261/332 | chr11 | 18446281 | |||
| chr11:18450978 | A | G | 1 | a0003 | 2 | HG01358.hp1 HG02293.hp2 |
missense_variant | MODERATE | c.850A>G | p.Lys284Glu | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 8/8 | 950/2035 | 850/999 | 284/332 | chr11 | 18450978 | |||
| chr11:18450981 | G | C | 1 | a0005 | 2 | HG03041.hp1 HG03486.hp2 |
missense_variant | MODERATE | c.853G>C | p.Glu285Gln | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 8/8 | 953/2035 | 853/999 | 285/332 | chr11 | 18450981 | |||
| chr11:18451116 | C | A | 1 | a0004 | 2 | HG02145.hp1 HG02809.hp1 |
missense_variant | MODERATE | c.988C>A | p.Leu330Ile | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 8/8 | 1088/2035 | 988/999 | 330/332 | chr11 | 18451116 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:18415252 | T | C | 1 | a0001c0003 | 2 | NA18612.hp2 NA18988.hp2 |
synonymous_variant | LOW | c.195T>C | p.Leu65Leu | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/8 | 295/2035 | 195/999 | 65/332 | chr11 | 18415252 | |||
| chr11:18434792 | T | C | 1 | a0001c0007 | 1 | HG02280.hp1 | synonymous_variant | LOW | c.471T>C | p.Arg157Arg | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 5/8 | 571/2035 | 471/999 | 157/332 | chr11 | 18434792 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:18412342 | A | C | 6 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0011 others(3): Show |
37 | HG00741.hp2 HG01074.hp1 HG01106.hp2 others(34): Show |
5_prime_UTR_variant | MODIFIER | c.-76A>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 1/8 | 376 | chr11 | 18412342 | ||||||
| chr11:18412342 | A | T | 1 | a0001c0001t0004 | 12 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-76A>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 1/8 | 376 | chr11 | 18412342 | ||||||
| chr11:18412357 | C | T | 2 | a0004c0005t0007 a0005c0004t0006 |
4 | HG02145.hp1 HG02809.hp1 HG03041.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-61C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 1/8 | 361 | chr11 | 18412357 | ||||||
| chr11:18451305 | A | G | 1 | a0004c0005t0007 | 2 | HG02145.hp1 HG02809.hp1 |
3_prime_UTR_variant | MODIFIER | c.*178A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 8/8 | 178 | chr11 | 18451305 | ||||||
| chr11:18451388 | G | A | 1 | a0001c0001t0008 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*261G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 8/8 | 261 | chr11 | 18451388 | ||||||
| chr11:18451591 | A | C | 12 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(9): Show |
305 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(302): Show |
3_prime_UTR_variant | MODIFIER | c.*464A>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 8/8 | 464 | chr11 | 18451591 | ||||||
| chr11:18451892 | T | C | 15 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(12): Show |
345 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(342): Show |
3_prime_UTR_variant | MODIFIER | c.*765T>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 8/8 | 765 | chr11 | 18451892 | ||||||
| chr11:18451969 | C | CAAG | 4 | a0001c0001t0002 a0002c0002t0002 a0004c0005t0007 others(1): Show |
62 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*850_*852dupAGA | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 8/8 | 853 | INFO_REALIGN_3_PRIME | chr11 | 18451969 | |||||
| chr11:18451999 | T | A | 3 | a0001c0001t0002 a0002c0002t0002 a0005c0004t0006 |
60 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*872T>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 8/8 | 872 | chr11 | 18451999 | ||||||
| chr11:18452006 | A | T | 1 | a0001c0001t0010 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*879A>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 8/8 | 879 | chr11 | 18452006 | ||||||
| chr11:18452009 | C | T | 4 | a0001c0001t0002 a0002c0002t0002 a0004c0005t0007 others(1): Show |
62 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*882C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 8/8 | 882 | chr11 | 18452009 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:18412469 | G | C | 4 | a0004c0005t0007g0015 a0004c0005t0007g0016 a0005c0004t0006g0013 others(1): Show |
4 | HG02145.hp1 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10+61G>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 1/7 | chr11 | 18412469 | |||||||
| chr11:18412600 | C | A | 4 | a0004c0005t0007g0015 a0004c0005t0007g0016 a0005c0004t0006g0013 others(1): Show |
4 | HG02145.hp1 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9-109C>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 1/7 | chr11 | 18412600 | |||||||
| chr11:18412612 | T | TC | 32 | a0001c0001t0001g0325 a0001c0001t0003g0298 a0001c0001t0003g0300 others(29): Show |
33 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.-9-91dupC | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 18412612 | ||||||
| chr11:18412965 | T | TCCTC | 9 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(6): Show |
9 | HG00642.hp2 HG00735.hp2 HG01993.hp1 others(6): Show |
intron_variant | MODIFIER | c.126+142_126+145dup others(4): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr11 | 18412965 | ||||||
| chr11:18412977 | CCCTCCCT others(9): Show |
C | 30 | a0001c0001t0001g0003 a0001c0001t0001g0272 a0001c0001t0001g0273 others(27): Show |
38 | HG01243.hp1 HG01891.hp1 HG02257.hp2 others(35): Show |
intron_variant | MODIFIER | c.126+138_126+153del others(16): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr11 | 18412977 | ||||||
| chr11:18412985 | C | A | 38 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(35): Show |
41 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.126+142C>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 2/7 | chr11 | 18412985 | |||||||
| chr11:18412985 | CCCTT | C | 4 | a0001c0001t0001g0008 a0001c0001t0001g0209 a0004c0005t0007g0015 others(1): Show |
4 | HG02145.hp1 HG02809.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+163_126+166del others(4): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr11 | 18412985 | ||||||
| chr11:18412985 | CCCTTCCT others(1): Show |
C | 42 | a0001c0001t0003g0093 a0001c0001t0003g0094 a0001c0001t0003g0095 others(39): Show |
43 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.126+159_126+166del others(8): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr11 | 18412985 | ||||||
| chr11:18412985 | CCCTTCCT others(5): Show |
C | 1 | a0001c0001t0011g0299 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.126+155_126+166del others(12): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr11 | 18412985 | ||||||
| chr11:18412989 | T | C | 168 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(165): Show |
174 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.126+146T>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 2/7 | chr11 | 18412989 | |||||||
| chr11:18413031 | C | CT | 42 | a0001c0001t0001g0234 a0001c0001t0002g0009 a0001c0001t0002g0235 others(39): Show |
46 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.126+197dupT | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr11 | 18413031 | ||||||
| chr11:18413169 | C | T | 197 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(194): Show |
212 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.126+326C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 2/7 | chr11 | 18413169 | |||||||
| chr11:18413171 | T | G | 5 | a0001c0001t0001g0119 a0001c0001t0001g0234 a0001c0001t0008g0116 others(2): Show |
5 | HG01243.hp2 HG01884.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.126+328T>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 2/7 | chr11 | 18413171 | |||||||
| chr11:18413328 | C | T | 2 | a0005c0004t0006g0013 a0005c0004t0006g0014 |
2 | HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.126+485C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 2/7 | chr11 | 18413328 | |||||||
| chr11:18413426 | T | C | 2 | a0005c0004t0006g0013 a0005c0004t0006g0014 |
2 | HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.126+583T>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 2/7 | chr11 | 18413426 | |||||||
| chr11:18413459 | C | CT | 21 | a0001c0001t0001g0006 a0001c0001t0001g0022 a0001c0001t0001g0101 others(18): Show |
22 | HG00621.hp2 HG01255.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.126+638dupT | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr11 | 18413459 | ||||||
| chr11:18413459 | CT | C | 171 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(168): Show |
186 | HG00280.hp1 HG00423.hp2 HG00544.hp2 others(183): Show |
intron_variant | MODIFIER | c.126+638delT | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr11 | 18413459 | ||||||
| chr11:18413459 | CTT | C | 18 | a0001c0001t0001g0027 a0001c0001t0001g0120 a0001c0001t0001g0121 others(15): Show |
18 | HG00323.hp1 HG00323.hp2 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.126+637_126+638del others(2): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr11 | 18413459 | ||||||
| chr11:18413547 | T | C | 2 | a0005c0004t0006g0013 a0005c0004t0006g0014 |
2 | HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.126+704T>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 2/7 | chr11 | 18413547 | |||||||
| chr11:18413694 | C | G | 38 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(35): Show |
41 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.126+851C>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 2/7 | chr11 | 18413694 | |||||||
| chr11:18413722 | A | G | 3 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 |
3 | HG03098.hp2 HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.126+879A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 2/7 | chr11 | 18413722 | |||||||
| chr11:18413909 | G | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02572.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.126+1066G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 2/7 | chr11 | 18413909 | |||||||
| chr11:18413911 | A | T | 43 | a0001c0001t0003g0093 a0001c0001t0003g0094 a0001c0001t0003g0095 others(40): Show |
44 | HG00597.hp2 HG00621.hp1 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.126+1068A>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 2/7 | chr11 | 18413911 | |||||||
| chr11:18413927 | C | T | 2 | a0001c0003t0001g0117 a0001c0003t0001g0118 |
2 | NA18612.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.126+1084C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 2/7 | chr11 | 18413927 | |||||||
| chr11:18413961 | G | A | 2 | a0005c0004t0006g0013 a0005c0004t0006g0014 |
2 | HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.126+1118G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 2/7 | chr11 | 18413961 | |||||||
| chr11:18413974 | C | G | 30 | a0001c0001t0001g0003 a0001c0001t0001g0272 a0001c0001t0001g0273 others(27): Show |
38 | HG01243.hp1 HG01891.hp1 HG02257.hp2 others(35): Show |
intron_variant | MODIFIER | c.126+1131C>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 2/7 | chr11 | 18413974 | |||||||
| chr11:18414153 | C | T | 29 | a0001c0001t0001g0008 a0001c0001t0001g0123 a0001c0001t0001g0124 others(26): Show |
30 | HG00280.hp1 HG00323.hp1 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.127-1031C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 2/7 | chr11 | 18414153 | |||||||
| chr11:18414197 | T | C | 2 | a0005c0004t0006g0013 a0005c0004t0006g0014 |
2 | HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.127-987T>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 2/7 | chr11 | 18414197 | |||||||
| chr11:18414270 | C | T | 3 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 |
3 | HG01169.hp1 HG01261.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.127-914C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 2/7 | chr11 | 18414270 | |||||||
| chr11:18414481 | C | T | 3 | a0001c0001t0001g0228 a0005c0004t0006g0013 a0005c0004t0006g0014 |
3 | HG01993.hp2 HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.127-703C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 2/7 | chr11 | 18414481 | |||||||
| chr11:18414553 | C | T | 2 | a0004c0005t0007g0015 a0004c0005t0007g0016 |
2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.127-631C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 2/7 | chr11 | 18414553 | |||||||
| chr11:18414657 | G | T | 29 | a0001c0001t0001g0008 a0001c0001t0001g0123 a0001c0001t0001g0124 others(26): Show |
30 | HG00280.hp1 HG00323.hp1 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.127-527G>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 2/7 | chr11 | 18414657 | |||||||
| chr11:18414685 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.127-499G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 2/7 | chr11 | 18414685 | |||||||
| chr11:18414713 | A | T | 3 | a0001c0001t0002g0242 a0001c0001t0002g0268 a0001c0001t0002g0269 |
3 | HG01981.hp1 HG02074.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.127-471A>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 2/7 | chr11 | 18414713 | |||||||
| chr11:18414748 | A | T | 42 | a0001c0001t0003g0093 a0001c0001t0003g0094 a0001c0001t0003g0095 others(39): Show |
43 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.127-436A>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 2/7 | chr11 | 18414748 | |||||||
| chr11:18414775 | C | T | 3 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0092 |
3 | HG02109.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.127-409C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 2/7 | chr11 | 18414775 | |||||||
| chr11:18414805 | C | T | 10 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(7): Show |
10 | HG02083.hp2 NA18961.hp2 NA18971.hp1 others(7): Show |
intron_variant | MODIFIER | c.127-379C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 2/7 | chr11 | 18414805 | |||||||
| chr11:18414898 | C | T | 2 | a0004c0005t0007g0015 a0004c0005t0007g0016 |
2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.127-286C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 2/7 | chr11 | 18414898 | |||||||
| chr11:18414901 | T | C | 42 | a0001c0001t0003g0093 a0001c0001t0003g0094 a0001c0001t0003g0095 others(39): Show |
43 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.127-283T>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 2/7 | chr11 | 18414901 | |||||||
| chr11:18414926 | CA | C | 44 | a0001c0001t0003g0093 a0001c0001t0003g0094 a0001c0001t0003g0095 others(41): Show |
45 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.127-249delA | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr11 | 18414926 | ||||||
| chr11:18415075 | C | T | 2 | a0001c0001t0001g0203 a0001c0001t0001g0204 |
2 | HG01261.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.127-109C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 2/7 | chr11 | 18415075 | |||||||
| chr11:18415457 | A | G | 42 | a0001c0001t0003g0093 a0001c0001t0003g0094 a0001c0001t0003g0095 others(39): Show |
43 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.244+156A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18415457 | |||||||
| chr11:18415495 | G | A | 1 | a0001c0001t0008g0116 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.244+194G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18415495 | |||||||
| chr11:18415548 | C | T | 1 | a0001c0001t0008g0116 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.244+247C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18415548 | |||||||
| chr11:18415786 | G | A | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | HG02109.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.244+485G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18415786 | |||||||
| chr11:18415817 | T | C | 44 | a0001c0001t0003g0093 a0001c0001t0003g0094 a0001c0001t0003g0095 others(41): Show |
45 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.244+516T>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18415817 | |||||||
| chr11:18415940 | T | C | 44 | a0001c0001t0003g0093 a0001c0001t0003g0094 a0001c0001t0003g0095 others(41): Show |
45 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.244+639T>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18415940 | |||||||
| chr11:18416085 | T | C | 2 | a0005c0004t0006g0013 a0005c0004t0006g0014 |
2 | HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.244+784T>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18416085 | |||||||
| chr11:18416140 | A | G | 1 | a0001c0001t0001g0089 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.244+839A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18416140 | |||||||
| chr11:18416195 | C | A | 1 | a0001c0001t0003g0298 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.244+894C>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18416195 | |||||||
| chr11:18416308 | C | G | 1 | a0001c0001t0001g0192 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.244+1007C>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18416308 | |||||||
| chr11:18416345 | T | C | 2 | a0005c0004t0006g0013 a0005c0004t0006g0014 |
2 | HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.244+1044T>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18416345 | |||||||
| chr11:18416397 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.244+1096A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18416397 | |||||||
| chr11:18416443 | G | A | 2 | a0005c0004t0006g0013 a0005c0004t0006g0014 |
2 | HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.244+1142G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18416443 | |||||||
| chr11:18416647 | A | G | 1 | a0001c0001t0002g0292 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.244+1346A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18416647 | |||||||
| chr11:18416694 | C | T | 1 | a0005c0004t0006g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.244+1393C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18416694 | |||||||
| chr11:18416731 | C | G | 5 | a0001c0001t0001g0272 a0001c0001t0001g0291 a0001c0001t0001g0293 others(2): Show |
5 | HG02965.hp1 HG03041.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.244+1430C>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18416731 | |||||||
| chr11:18416783 | C | T | 23 | a0001c0001t0001g0003 a0001c0001t0001g0272 a0001c0001t0001g0279 others(20): Show |
31 | HG01243.hp1 HG01891.hp1 HG02257.hp2 others(28): Show |
intron_variant | MODIFIER | c.244+1482C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18416783 | |||||||
| chr11:18416957 | C | T | 39 | a0001c0001t0003g0093 a0001c0001t0003g0094 a0001c0001t0003g0095 others(36): Show |
40 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.244+1656C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18416957 | |||||||
| chr11:18417050 | A | G | 2 | a0005c0004t0006g0013 a0005c0004t0006g0014 |
2 | HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.244+1749A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18417050 | |||||||
| chr11:18417138 | C | T | 11 | a0001c0001t0002g0241 a0001c0001t0002g0258 a0001c0001t0002g0259 others(8): Show |
11 | HG00735.hp1 HG02257.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.244+1837C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18417138 | |||||||
| chr11:18417223 | G | A | 44 | a0001c0001t0003g0093 a0001c0001t0003g0094 a0001c0001t0003g0095 others(41): Show |
45 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.244+1922G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18417223 | |||||||
| chr11:18417257 | C | T | 5 | a0001c0001t0002g0263 a0001c0001t0002g0264 a0001c0001t0002g0265 others(2): Show |
5 | HG00735.hp1 HG02258.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.244+1956C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18417257 | |||||||
| chr11:18417266 | G | T | 1 | a0001c0001t0001g0114 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.244+1965G>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18417266 | |||||||
| chr11:18417307 | A | G | 2 | a0005c0004t0006g0013 a0005c0004t0006g0014 |
2 | HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.244+2006A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18417307 | |||||||
| chr11:18417353 | A | G | 1 | a0001c0001t0001g0191 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.244+2052A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18417353 | |||||||
| chr11:18417454 | C | G | 40 | a0001c0001t0003g0093 a0001c0001t0003g0094 a0001c0001t0003g0095 others(37): Show |
41 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.244+2153C>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18417454 | |||||||
| chr11:18417602 | G | A | 2 | a0005c0004t0006g0013 a0005c0004t0006g0014 |
2 | HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.244+2301G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18417602 | |||||||
| chr11:18417665 | A | G | 240 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(237): Show |
256 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(253): Show |
intron_variant | MODIFIER | c.244+2364A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18417665 | |||||||
| chr11:18417935 | G | C | 3 | a0001c0001t0002g0292 a0005c0004t0006g0013 a0005c0004t0006g0014 |
3 | HG02723.hp2 HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.244+2634G>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18417935 | |||||||
| chr11:18417960 | A | G | 1 | a0001c0001t0001g0190 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.244+2659A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18417960 | |||||||
| chr11:18418020 | A | G | 38 | a0001c0001t0003g0093 a0001c0001t0003g0094 a0001c0001t0003g0095 others(35): Show |
39 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.244+2719A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18418020 | |||||||
| chr11:18418191 | G | A | 40 | a0001c0001t0003g0093 a0001c0001t0003g0094 a0001c0001t0003g0095 others(37): Show |
41 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.244+2890G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18418191 | |||||||
| chr11:18418239 | C | T | 2 | a0001c0001t0002g0241 a0001c0001t0002g0262 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.244+2938C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18418239 | |||||||
| chr11:18418244 | T | A | 4 | a0004c0005t0007g0015 a0004c0005t0007g0016 a0005c0004t0006g0013 others(1): Show |
4 | HG02145.hp1 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.244+2943T>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18418244 | |||||||
| chr11:18418291 | T | C | 3 | a0001c0001t0003g0300 a0001c0001t0003g0301 a0001c0001t0003g0302 |
3 | HG01109.hp2 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.244+2990T>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18418291 | |||||||
| chr11:18418362 | G | A | 1 | a0001c0001t0008g0116 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.244+3061G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18418362 | |||||||
| chr11:18418380 | A | C | 38 | a0001c0001t0003g0093 a0001c0001t0003g0094 a0001c0001t0003g0095 others(35): Show |
39 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.244+3079A>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18418380 | |||||||
| chr11:18418424 | C | CTATTT | 4 | a0004c0005t0007g0015 a0004c0005t0007g0016 a0005c0004t0006g0013 others(1): Show |
4 | HG02145.hp1 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.244+3140_244+3144d others(7): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 18418424 | ||||||
| chr11:18418481 | G | A | 2 | a0005c0004t0006g0013 a0005c0004t0006g0014 |
2 | HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.244+3180G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18418481 | |||||||
| chr11:18418539 | C | T | 2 | a0005c0004t0006g0013 a0005c0004t0006g0014 |
2 | HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.244+3238C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18418539 | |||||||
| chr11:18418570 | C | T | 1 | a0001c0001t0008g0116 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.244+3269C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18418570 | |||||||
| chr11:18418594 | T | G | 1 | a0001c0001t0001g0193 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.244+3293T>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18418594 | |||||||
| chr11:18418627 | A | G | 2 | a0004c0005t0007g0015 a0004c0005t0007g0016 |
2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.244+3326A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18418627 | |||||||
| chr11:18418664 | C | T | 1 | a0001c0001t0001g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.244+3363C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18418664 | |||||||
| chr11:18418758 | T | C | 42 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(39): Show |
45 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.244+3457T>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18418758 | |||||||
| chr11:18419028 | A | T | 1 | a0001c0001t0002g0257 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.244+3727A>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18419028 | |||||||
| chr11:18419088 | G | A | 42 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(39): Show |
45 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.244+3787G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18419088 | |||||||
| chr11:18419161 | C | T | 2 | a0001c0001t0001g0294 a0001c0001t0001g0295 |
2 | HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.244+3860C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18419161 | |||||||
| chr11:18419236 | T | C | 40 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(37): Show |
43 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.244+3935T>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18419236 | |||||||
| chr11:18419297 | A | C | 1 | a0001c0001t0001g0193 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.244+3996A>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18419297 | |||||||
| chr11:18419298 | T | A | 1 | a0001c0001t0001g0193 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.244+3997T>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18419298 | |||||||
| chr11:18419299 | C | T | 1 | a0001c0001t0001g0193 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.244+3998C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18419299 | |||||||
| chr11:18419418 | A | G | 1 | a0001c0001t0003g0322 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.244+4117A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18419418 | |||||||
| chr11:18419458 | C | T | 4 | a0001c0001t0002g0011 a0001c0001t0002g0271 a0001c0001t0002g0289 others(1): Show |
5 | HG02647.hp2 HG02922.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.244+4157C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18419458 | |||||||
| chr11:18419751 | G | A | 40 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(37): Show |
43 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.244+4450G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18419751 | |||||||
| chr11:18419891 | A | G | 2 | a0004c0005t0007g0015 a0004c0005t0007g0016 |
2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.244+4590A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18419891 | |||||||
| chr11:18420071 | C | T | 2 | a0004c0005t0007g0015 a0004c0005t0007g0016 |
2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.244+4770C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18420071 | |||||||
| chr11:18420092 | T | TAAA | 30 | a0001c0001t0001g0003 a0001c0001t0001g0272 a0001c0001t0001g0273 others(27): Show |
38 | HG01243.hp1 HG01891.hp1 HG02257.hp2 others(35): Show |
intron_variant | MODIFIER | c.244+4792_244+4793i others(5): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 18420092 | ||||||
| chr11:18420094 | G | A | 254 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(251): Show |
266 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(263): Show |
intron_variant | MODIFIER | c.244+4793G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18420094 | |||||||
| chr11:18420094 | G | C | 30 | a0001c0001t0001g0003 a0001c0001t0001g0272 a0001c0001t0001g0273 others(27): Show |
38 | HG01243.hp1 HG01891.hp1 HG02257.hp2 others(35): Show |
intron_variant | MODIFIER | c.244+4793G>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18420094 | |||||||
| chr11:18420103 | C | A | 1 | a0001c0001t0001g0092 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.244+4802C>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18420103 | |||||||
| chr11:18420135 | ATAGAT | A | 40 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(37): Show |
43 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.244+4839_244+4843d others(7): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 18420135 | ||||||
| chr11:18420420 | C | G | 40 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(37): Show |
43 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.244+5119C>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18420420 | |||||||
| chr11:18420641 | T | TA | 35 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0241 others(32): Show |
38 | HG00733.hp1 HG00735.hp1 HG01358.hp2 others(35): Show |
intron_variant | MODIFIER | c.244+5364dupA | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 18420641 | ||||||
| chr11:18420641 | TA | T | 213 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(210): Show |
230 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(227): Show |
intron_variant | MODIFIER | c.244+5364delA | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 18420641 | ||||||
| chr11:18420641 | TAA | T | 19 | a0001c0001t0001g0026 a0001c0001t0001g0085 a0001c0001t0001g0086 others(16): Show |
19 | HG00639.hp1 HG00639.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.244+5363_244+5364d others(4): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 18420641 | ||||||
| chr11:18420835 | C | A | 121 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(118): Show |
125 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.244+5534C>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18420835 | |||||||
| chr11:18420849 | T | C | 285 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(282): Show |
305 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(302): Show |
intron_variant | MODIFIER | c.244+5548T>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18420849 | |||||||
| chr11:18420861 | A | G | 85 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0018 others(82): Show |
90 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.244+5560A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18420861 | |||||||
| chr11:18420919 | G | A | 40 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(37): Show |
43 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.244+5618G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18420919 | |||||||
| chr11:18420982 | G | T | 2 | a0004c0005t0007g0015 a0004c0005t0007g0016 |
2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.244+5681G>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18420982 | |||||||
| chr11:18421076 | A | T | 40 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(37): Show |
43 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.244+5775A>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18421076 | |||||||
| chr11:18421149 | G | T | 1 | a0001c0001t0004g0320 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.244+5848G>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18421149 | |||||||
| chr11:18421358 | A | C | 1 | a0001c0001t0001g0232 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.244+6057A>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18421358 | |||||||
| chr11:18421383 | T | C | 42 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(39): Show |
45 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.244+6082T>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18421383 | |||||||
| chr11:18421479 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.244+6178C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18421479 | |||||||
| chr11:18421533 | C | T | 5 | a0001c0001t0002g0263 a0001c0001t0002g0264 a0001c0001t0002g0265 others(2): Show |
5 | HG00735.hp1 HG02258.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.244+6232C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18421533 | |||||||
| chr11:18421540 | A | T | 2 | a0004c0005t0007g0015 a0004c0005t0007g0016 |
2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.244+6239A>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18421540 | |||||||
| chr11:18421544 | A | G | 2 | a0004c0005t0007g0015 a0004c0005t0007g0016 |
2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.244+6243A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18421544 | |||||||
| chr11:18421546 | G | A | 38 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(35): Show |
41 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.244+6245G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18421546 | |||||||
| chr11:18421633 | A | G | 40 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(37): Show |
43 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.244+6332A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18421633 | |||||||
| chr11:18421753 | C | G | 40 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(37): Show |
43 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.244+6452C>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18421753 | |||||||
| chr11:18421922 | AAGACTAG others(1194): Show |
A | 2 | a0004c0005t0007g0015 a0004c0005t0007g0016 |
2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.244+6626_245-6610d others(2): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 18421922 | ||||||
| chr11:18422121 | A | C | 283 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(280): Show |
303 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(300): Show |
intron_variant | MODIFIER | c.244+6820A>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18422121 | |||||||
| chr11:18422142 | T | C | 40 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(37): Show |
43 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.244+6841T>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18422142 | |||||||
| chr11:18422188 | A | G | 3 | a0001c0001t0001g0176 a0001c0001t0001g0178 a0001c0001t0001g0179 |
3 | NA18956.hp2 NA18984.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.244+6887A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18422188 | |||||||
| chr11:18422229 | A | G | 40 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(37): Show |
43 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.244+6928A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18422229 | |||||||
| chr11:18422268 | AATC | A | 212 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(209): Show |
221 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.244+6969_244+6971d others(5): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 18422268 | ||||||
| chr11:18422272 | A | T | 212 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(209): Show |
221 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.244+6971A>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18422272 | |||||||
| chr11:18422352 | T | C | 277 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(274): Show |
294 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.244+7051T>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18422352 | |||||||
| chr11:18422392 | C | T | 2 | a0001c0001t0004g0315 a0001c0001t0004g0321 |
2 | HG01928.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.244+7091C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18422392 | |||||||
| chr11:18422522 | C | G | 2 | a0001c0001t0001g0294 a0001c0001t0001g0295 |
2 | HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.245-7215C>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18422522 | |||||||
| chr11:18422553 | C | CA | 33 | a0001c0001t0001g0026 a0001c0001t0001g0072 a0001c0001t0001g0073 others(30): Show |
34 | HG00323.hp2 HG00733.hp1 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.245-7169dupA | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 18422553 | ||||||
| chr11:18422553 | C | CAA | 18 | a0001c0001t0002g0241 a0001c0001t0002g0258 a0001c0001t0002g0259 others(15): Show |
20 | HG00735.hp1 HG02074.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.245-7170_245-7169d others(4): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 18422553 | ||||||
| chr11:18422686 | C | T | 1 | a0001c0001t0001g0050 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.245-7051C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18422686 | |||||||
| chr11:18422733 | A | G | 2 | a0005c0004t0006g0013 a0005c0004t0006g0014 |
2 | HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.245-7004A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18422733 | |||||||
| chr11:18422760 | A | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02572.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.245-6977A>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18422760 | |||||||
| chr11:18422761 | T | C | 1 | a0001c0001t0001g0167 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.245-6976T>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18422761 | |||||||
| chr11:18422996 | A | AAACAACA others(2): Show |
40 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(37): Show |
43 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.245-6733_245-6732i others(11): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 18422996 | ||||||
| chr11:18423015 | GA | G | 120 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
124 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.245-6720delA | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 18423015 | ||||||
| chr11:18423183 | A | G | 40 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(37): Show |
43 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.245-6554A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18423183 | |||||||
| chr11:18423190 | A | G | 40 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(37): Show |
43 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.245-6547A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18423190 | |||||||
| chr11:18423397 | G | T | 11 | a0001c0001t0002g0241 a0001c0001t0002g0258 a0001c0001t0002g0259 others(8): Show |
11 | HG00735.hp1 HG02257.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.245-6340G>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18423397 | |||||||
| chr11:18423424 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.245-6313T>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18423424 | |||||||
| chr11:18423442 | G | A | 40 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(37): Show |
43 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.245-6295G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18423442 | |||||||
| chr11:18423688 | G | A | 3 | a0001c0001t0002g0235 a0001c0001t0002g0243 a0001c0001t0002g0244 |
3 | NA18946.hp1 NA19070.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.245-6049G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18423688 | |||||||
| chr11:18423790 | A | T | 2 | a0005c0004t0006g0013 a0005c0004t0006g0014 |
2 | HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.245-5947A>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18423790 | |||||||
| chr11:18423856 | C | T | 1 | a0001c0001t0001g0180 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.245-5881C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18423856 | |||||||
| chr11:18423915 | T | A | 1 | a0001c0001t0001g0293 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.245-5822T>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18423915 | |||||||
| chr11:18424015 | TAGTA | T | 164 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(161): Show |
171 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.245-5718_245-5715d others(6): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 18424015 | ||||||
| chr11:18424112 | C | G | 40 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(37): Show |
43 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.245-5625C>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18424112 | |||||||
| chr11:18424158 | C | T | 38 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(35): Show |
41 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.245-5579C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18424158 | |||||||
| chr11:18424253 | G | A | 38 | a0001c0001t0003g0093 a0001c0001t0003g0094 a0001c0001t0003g0095 others(35): Show |
39 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.245-5484G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18424253 | |||||||
| chr11:18424254 | C | T | 3 | a0001c0001t0002g0253 a0001c0001t0002g0254 a0001c0001t0002g0255 |
3 | HG03688.hp1 HG03942.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.245-5483C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18424254 | |||||||
| chr11:18424282 | T | C | 1 | a0002c0002t0002g0236 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.245-5455T>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18424282 | |||||||
| chr11:18424336 | C | T | 2 | a0004c0005t0007g0015 a0004c0005t0007g0016 |
2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.245-5401C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18424336 | |||||||
| chr11:18424363 | T | C | 1 | a0001c0001t0002g0238 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.245-5374T>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18424363 | |||||||
| chr11:18424372 | ACT | A | 4 | a0001c0001t0001g0176 a0001c0001t0001g0178 a0001c0001t0001g0179 others(1): Show |
4 | NA18945.hp1 NA18956.hp2 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.245-5362_245-5361d others(4): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 18424372 | ||||||
| chr11:18424381 | C | CA | 41 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(38): Show |
44 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.245-5347dupA | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 18424381 | ||||||
| chr11:18424433 | C | T | 1 | a0001c0001t0001g0027 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.245-5304C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18424433 | |||||||
| chr11:18424693 | A | G | 1 | a0001c0001t0001g0175 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.245-5044A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18424693 | |||||||
| chr11:18424743 | G | C | 42 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(39): Show |
45 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.245-4994G>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18424743 | |||||||
| chr11:18424828 | C | T | 31 | a0001c0001t0001g0003 a0001c0001t0001g0233 a0001c0001t0001g0272 others(28): Show |
39 | HG01243.hp1 HG01891.hp1 HG02257.hp2 others(36): Show |
intron_variant | MODIFIER | c.245-4909C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18424828 | |||||||
| chr11:18424841 | C | T | 1 | a0001c0001t0002g0286 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.245-4896C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18424841 | |||||||
| chr11:18424922 | C | T | 40 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(37): Show |
43 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.245-4815C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18424922 | |||||||
| chr11:18424940 | G | A | 2 | a0004c0005t0007g0015 a0004c0005t0007g0016 |
2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.245-4797G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18424940 | |||||||
| chr11:18424941 | G | C | 1 | a0001c0001t0001g0296 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.245-4796G>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18424941 | |||||||
| chr11:18424958 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.245-4779A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18424958 | |||||||
| chr11:18424962 | C | T | 40 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(37): Show |
43 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.245-4775C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18424962 | |||||||
| chr11:18424984 | G | C | 2 | a0004c0005t0007g0015 a0004c0005t0007g0016 |
2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.245-4753G>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18424984 | |||||||
| chr11:18425116 | C | T | 40 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(37): Show |
43 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.245-4621C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18425116 | |||||||
| chr11:18425150 | G | A | 7 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0001g0275 others(4): Show |
7 | HG02451.hp2 HG02683.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.245-4587G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18425150 | |||||||
| chr11:18425178 | AT | A | 43 | a0001c0001t0001g0230 a0001c0001t0002g0009 a0001c0001t0002g0235 others(40): Show |
46 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.245-4548delT | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 18425178 | ||||||
| chr11:18425231 | C | T | 1 | a0001c0001t0011g0299 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.245-4506C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18425231 | |||||||
| chr11:18425279 | G | A | 3 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 |
3 | HG02486.hp1 HG02886.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.245-4458G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18425279 | |||||||
| chr11:18425470 | T | C | 75 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0018 others(72): Show |
80 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.245-4267T>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18425470 | |||||||
| chr11:18425556 | T | G | 40 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(37): Show |
43 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.245-4181T>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18425556 | |||||||
| chr11:18425676 | A | G | 27 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(24): Show |
30 | HG00323.hp2 HG00733.hp1 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.245-4061A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18425676 | |||||||
| chr11:18425740 | C | T | 2 | a0005c0004t0006g0013 a0005c0004t0006g0014 |
2 | HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.245-3997C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18425740 | |||||||
| chr11:18425753 | C | T | 121 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(118): Show |
125 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.245-3984C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18425753 | |||||||
| chr11:18425766 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.245-3971C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18425766 | |||||||
| chr11:18425813 | G | A | 121 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(118): Show |
125 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.245-3924G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18425813 | |||||||
| chr11:18425873 | G | A | 2 | a0004c0005t0007g0015 a0004c0005t0007g0016 |
2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.245-3864G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18425873 | |||||||
| chr11:18425942 | G | GA | 43 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(40): Show |
46 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.245-3786dupA | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 18425942 | ||||||
| chr11:18425974 | A | G | 40 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(37): Show |
43 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.245-3763A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18425974 | |||||||
| chr11:18426027 | CA | C | 81 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0018 others(78): Show |
86 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.245-3708delA | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 18426027 | ||||||
| chr11:18426029 | A | G | 7 | a0002c0002t0002g0005 a0002c0002t0002g0236 a0002c0002t0002g0237 others(4): Show |
9 | HG02818.hp1 HG02895.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.245-3708A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18426029 | |||||||
| chr11:18426029 | A | T | 2 | a0001c0001t0001g0083 a0001c0001t0001g0090 |
2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.245-3708A>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18426029 | |||||||
| chr11:18426029 | AT | A | 125 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(122): Show |
129 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.245-3693delT | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 18426029 | ||||||
| chr11:18426064 | G | A | 68 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0018 others(65): Show |
73 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.245-3673G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18426064 | |||||||
| chr11:18426129 | A | C | 42 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(39): Show |
45 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.245-3608A>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18426129 | |||||||
| chr11:18426235 | G | C | 2 | a0004c0005t0007g0015 a0004c0005t0007g0016 |
2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.245-3502G>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18426235 | |||||||
| chr11:18426264 | C | T | 1 | a0001c0001t0001g0101 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.245-3473C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18426264 | |||||||
| chr11:18426356 | G | A | 31 | a0001c0001t0001g0003 a0001c0001t0001g0233 a0001c0001t0001g0272 others(28): Show |
39 | HG01243.hp1 HG01891.hp1 HG02257.hp2 others(36): Show |
intron_variant | MODIFIER | c.245-3381G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18426356 | |||||||
| chr11:18426418 | T | A | 5 | a0001c0001t0004g0012 a0001c0001t0004g0297 a0001c0001t0004g0304 others(2): Show |
6 | HG00438.hp1 HG00621.hp1 NA19001.hp1 others(3): Show |
intron_variant | MODIFIER | c.245-3319T>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18426418 | |||||||
| chr11:18426441 | C | T | 2 | a0004c0005t0007g0015 a0004c0005t0007g0016 |
2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.245-3296C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18426441 | |||||||
| chr11:18426496 | C | T | 40 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(37): Show |
43 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.245-3241C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18426496 | |||||||
| chr11:18426516 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.245-3221G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18426516 | |||||||
| chr11:18426526 | C | CA | 126 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
132 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.245-3193dupA | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 18426526 | ||||||
| chr11:18426526 | C | CAA | 116 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(113): Show |
129 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.245-3194_245-3193d others(4): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 18426526 | ||||||
| chr11:18426526 | C | CAAA | 8 | a0001c0001t0001g0027 a0001c0001t0001g0039 a0001c0001t0001g0091 others(5): Show |
8 | HG00673.hp1 HG01884.hp2 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.245-3195_245-3193d others(5): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 18426526 | ||||||
| chr11:18426892 | A | G | 1 | a0001c0001t0001g0222 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.245-2845A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18426892 | |||||||
| chr11:18427084 | G | A | 3 | a0001c0001t0002g0253 a0001c0001t0002g0254 a0001c0001t0002g0255 |
3 | HG03688.hp1 HG03942.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.245-2653G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18427084 | |||||||
| chr11:18427212 | C | T | 2 | a0001c0001t0001g0071 a0001c0001t0001g0092 |
2 | NA18979.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.245-2525C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18427212 | |||||||
| chr11:18427287 | G | A | 1 | a0001c0001t0011g0299 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.245-2450G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18427287 | |||||||
| chr11:18427388 | A | C | 1 | a0001c0001t0003g0303 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.245-2349A>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18427388 | |||||||
| chr11:18427394 | A | C | 31 | a0001c0001t0001g0003 a0001c0001t0001g0233 a0001c0001t0001g0272 others(28): Show |
39 | HG01243.hp1 HG01891.hp1 HG02257.hp2 others(36): Show |
intron_variant | MODIFIER | c.245-2343A>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18427394 | |||||||
| chr11:18427419 | G | T | 40 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(37): Show |
43 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.245-2318G>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18427419 | |||||||
| chr11:18427508 | C | A | 1 | a0001c0001t0001g0040 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.245-2229C>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18427508 | |||||||
| chr11:18427677 | AT | A | 230 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(227): Show |
247 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(244): Show |
intron_variant | MODIFIER | c.245-2042delT | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 18427677 | ||||||
| chr11:18427677 | ATT | A | 43 | a0001c0001t0001g0041 a0001c0001t0001g0287 a0001c0001t0001g0291 others(40): Show |
46 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.245-2043_245-2042d others(4): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 18427677 | ||||||
| chr11:18427714 | G | T | 84 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0018 others(81): Show |
89 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.245-2023G>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18427714 | |||||||
| chr11:18427889 | C | T | 1 | a0003c0006t0003g0319 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.245-1848C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18427889 | |||||||
| chr11:18428166 | C | CT | 20 | a0001c0001t0001g0078 a0001c0001t0001g0088 a0001c0001t0001g0171 others(17): Show |
20 | HG00423.hp2 HG01070.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.245-1548dupT | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 18428166 | ||||||
| chr11:18428166 | C | CTT | 14 | a0001c0001t0001g0194 a0001c0001t0002g0241 a0001c0001t0002g0246 others(11): Show |
14 | HG00735.hp1 HG01358.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.245-1549_245-1548d others(4): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 18428166 | ||||||
| chr11:18428166 | C | CTTT | 21 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(18): Show |
24 | HG00323.hp2 HG00733.hp1 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.245-1550_245-1548d others(5): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 18428166 | ||||||
| chr11:18428166 | CT | C | 80 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0019 others(77): Show |
85 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.245-1548delT | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 18428166 | ||||||
| chr11:18428166 | CTT | C | 7 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0041 others(4): Show |
7 | HG02145.hp1 HG02523.hp1 HG03704.hp1 others(4): Show |
intron_variant | MODIFIER | c.245-1549_245-1548d others(4): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 18428166 | ||||||
| chr11:18428206 | C | CTGT | 7 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0001g0275 others(4): Show |
7 | HG02451.hp2 HG02683.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.245-1530_245-1528d others(5): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 18428206 | ||||||
| chr11:18428311 | A | AC | 42 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(39): Show |
45 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.245-1426_245-1425i others(3): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18428311 | |||||||
| chr11:18428494 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.245-1243G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18428494 | |||||||
| chr11:18428496 | G | T | 1 | a0001c0001t0003g0316 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.245-1241G>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18428496 | |||||||
| chr11:18428501 | G | T | 3 | a0001c0001t0001g0132 a0001c0001t0001g0186 a0001c0001t0001g0230 |
3 | NA18975.hp1 NA19001.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.245-1236G>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18428501 | |||||||
| chr11:18428554 | C | A | 2 | a0004c0005t0007g0015 a0004c0005t0007g0016 |
2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.245-1183C>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18428554 | |||||||
| chr11:18428673 | A | G | 42 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(39): Show |
45 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.245-1064A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18428673 | |||||||
| chr11:18428674 | A | G | 2 | a0001c0001t0001g0119 a0001c0001t0001g0234 |
2 | HG01243.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.245-1063A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18428674 | |||||||
| chr11:18428704 | G | A | 2 | a0005c0004t0006g0013 a0005c0004t0006g0014 |
2 | HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.245-1033G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18428704 | |||||||
| chr11:18428802 | G | A | 1 | a0001c0001t0001g0045 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.245-935G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18428802 | |||||||
| chr11:18428805 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.245-932G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18428805 | |||||||
| chr11:18428876 | GA | G | 258 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(255): Show |
275 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(272): Show |
intron_variant | MODIFIER | c.245-845delA | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 18428876 | ||||||
| chr11:18428876 | GAA | G | 26 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(23): Show |
27 | HG00323.hp1 HG00438.hp1 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.245-846_245-845del others(2): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 18428876 | ||||||
| chr11:18428897 | A | T | 42 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(39): Show |
45 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.245-840A>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18428897 | |||||||
| chr11:18429029 | A | G | 2 | a0001c0003t0001g0117 a0001c0003t0001g0118 |
2 | NA18612.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.245-708A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18429029 | |||||||
| chr11:18429102 | C | CTT | 42 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(39): Show |
45 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.245-634_245-633ins others(2): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 18429102 | ||||||
| chr11:18429116 | C | CT | 125 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(122): Show |
138 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.245-598dupT | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 18429116 | ||||||
| chr11:18429116 | C | CTT | 52 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0023 others(49): Show |
53 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.245-599_245-598dup others(2): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 18429116 | ||||||
| chr11:18429116 | C | CTTT | 9 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0202 others(6): Show |
9 | HG00741.hp1 HG01169.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.245-600_245-598dup others(3): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 18429116 | ||||||
| chr11:18429116 | CTT | C | 37 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(34): Show |
40 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.245-599_245-598del others(2): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 18429116 | ||||||
| chr11:18429346 | C | T | 38 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(35): Show |
41 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.245-391C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18429346 | |||||||
| chr11:18429353 | C | T | 1 | a0001c0001t0002g0255 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.245-384C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18429353 | |||||||
| chr11:18429403 | G | A | 1 | a0001c0001t0003g0303 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.245-334G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18429403 | |||||||
| chr11:18429539 | A | G | 2 | a0004c0005t0007g0015 a0004c0005t0007g0016 |
2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.245-198A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18429539 | |||||||
| chr11:18429549 | A | C | 18 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0239 others(15): Show |
19 | HG00323.hp2 HG00733.hp1 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.245-188A>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 3/7 | chr11 | 18429549 | |||||||
| chr11:18429922 | C | G | 2 | a0001c0001t0003g0099 a0001c0001t0003g0115 |
2 | NA18968.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.418+12C>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18429922 | |||||||
| chr11:18430074 | C | T | 11 | a0001c0001t0001g0030 a0001c0001t0001g0036 a0001c0001t0001g0037 others(8): Show |
11 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(8): Show |
intron_variant | MODIFIER | c.418+164C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18430074 | |||||||
| chr11:18430088 | T | TA | 85 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0018 others(82): Show |
90 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.418+179dupA | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 18430088 | ||||||
| chr11:18430132 | T | C | 2 | a0001c0001t0001g0027 a0001c0001t0001g0273 |
2 | HG03225.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.418+222T>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18430132 | |||||||
| chr11:18430257 | A | G | 1 | a0005c0004t0006g0013 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.418+347A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18430257 | |||||||
| chr11:18430339 | T | G | 42 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(39): Show |
45 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.418+429T>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18430339 | |||||||
| chr11:18430369 | T | C | 40 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(37): Show |
43 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.418+459T>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18430369 | |||||||
| chr11:18430412 | T | C | 2 | a0005c0004t0006g0013 a0005c0004t0006g0014 |
2 | HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.418+502T>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18430412 | |||||||
| chr11:18430437 | CATTGATC others(17): Show |
C | 10 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(7): Show |
10 | HG02083.hp2 NA18961.hp2 NA18971.hp1 others(7): Show |
intron_variant | MODIFIER | c.418+551_418+574del others(24): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 18430437 | ||||||
| chr11:18430527 | A | C | 1 | a0001c0001t0001g0162 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.418+617A>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18430527 | |||||||
| chr11:18430571 | A | G | 40 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(37): Show |
43 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.418+661A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18430571 | |||||||
| chr11:18430599 | C | T | 20 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(17): Show |
21 | HG00323.hp2 HG00733.hp1 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.418+689C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18430599 | |||||||
| chr11:18430604 | T | C | 2 | a0004c0005t0007g0015 a0004c0005t0007g0016 |
2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.418+694T>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18430604 | |||||||
| chr11:18430685 | A | G | 1 | a0001c0001t0001g0109 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.418+775A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18430685 | |||||||
| chr11:18430738 | A | G | 1 | a0001c0001t0002g0261 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.418+828A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18430738 | |||||||
| chr11:18430809 | A | G | 40 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(37): Show |
43 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.418+899A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18430809 | |||||||
| chr11:18430832 | G | A | 3 | a0001c0001t0003g0305 a0001c0001t0003g0306 a0001c0001t0003g0307 |
3 | HG01074.hp1 HG01346.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.418+922G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18430832 | |||||||
| chr11:18430892 | T | C | 2 | a0004c0005t0007g0015 a0004c0005t0007g0016 |
2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.418+982T>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18430892 | |||||||
| chr11:18431008 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.418+1098A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18431008 | |||||||
| chr11:18431092 | C | T | 3 | a0001c0001t0003g0300 a0001c0001t0003g0301 a0001c0001t0003g0302 |
3 | HG01109.hp2 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.418+1182C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18431092 | |||||||
| chr11:18431185 | T | C | 40 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(37): Show |
43 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.418+1275T>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18431185 | |||||||
| chr11:18431208 | C | T | 40 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(37): Show |
43 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.418+1298C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18431208 | |||||||
| chr11:18431266 | G | C | 2 | a0005c0004t0006g0013 a0005c0004t0006g0014 |
2 | HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.418+1356G>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18431266 | |||||||
| chr11:18431290 | A | G | 40 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(37): Show |
43 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.418+1380A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18431290 | |||||||
| chr11:18431348 | G | A | 11 | a0001c0001t0002g0241 a0001c0001t0002g0258 a0001c0001t0002g0259 others(8): Show |
11 | HG00735.hp1 HG02257.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.418+1438G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18431348 | |||||||
| chr11:18431501 | C | A | 40 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(37): Show |
43 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.418+1591C>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18431501 | |||||||
| chr11:18431558 | T | G | 1 | a0001c0001t0001g0060 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.418+1648T>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18431558 | |||||||
| chr11:18431619 | C | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0018 others(82): Show |
90 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.418+1709C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18431619 | |||||||
| chr11:18431688 | G | A | 3 | a0001c0001t0001g0176 a0001c0001t0001g0178 a0001c0001t0001g0179 |
3 | NA18956.hp2 NA18984.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.418+1778G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18431688 | |||||||
| chr11:18431718 | T | A | 1 | a0001c0001t0001g0133 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.418+1808T>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18431718 | |||||||
| chr11:18432027 | G | A | 40 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(37): Show |
43 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.418+2117G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18432027 | |||||||
| chr11:18432085 | T | C | 2 | a0004c0005t0007g0015 a0004c0005t0007g0016 |
2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.418+2175T>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18432085 | |||||||
| chr11:18432127 | A | G | 40 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(37): Show |
43 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.418+2217A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18432127 | |||||||
| chr11:18432146 | G | A | 40 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(37): Show |
43 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.418+2236G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18432146 | |||||||
| chr11:18432179 | A | G | 42 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(39): Show |
45 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.418+2269A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18432179 | |||||||
| chr11:18432195 | A | T | 38 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(35): Show |
41 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.418+2285A>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18432195 | |||||||
| chr11:18432197 | T | G | 2 | a0005c0004t0006g0013 a0005c0004t0006g0014 |
2 | HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.418+2287T>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18432197 | |||||||
| chr11:18432343 | A | G | 2 | a0005c0004t0006g0013 a0005c0004t0006g0014 |
2 | HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.419-2397A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18432343 | |||||||
| chr11:18432466 | T | A | 2 | a0005c0004t0006g0013 a0005c0004t0006g0014 |
2 | HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.419-2274T>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18432466 | |||||||
| chr11:18432486 | C | A | 1 | a0001c0001t0002g0258 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.419-2254C>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18432486 | |||||||
| chr11:18432489 | G | A | 2 | a0005c0004t0006g0013 a0005c0004t0006g0014 |
2 | HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.419-2251G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18432489 | |||||||
| chr11:18432519 | G | A | 86 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0018 others(83): Show |
91 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.419-2221G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18432519 | |||||||
| chr11:18432568 | T | TC | 41 | a0001c0001t0001g0037 a0001c0001t0002g0009 a0001c0001t0002g0235 others(38): Show |
44 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.419-2168dupC | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 18432568 | ||||||
| chr11:18432770 | G | A | 40 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(37): Show |
43 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.419-1970G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18432770 | |||||||
| chr11:18432846 | G | T | 1 | a0001c0001t0003g0322 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.419-1894G>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18432846 | |||||||
| chr11:18432863 | A | C | 42 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(39): Show |
45 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.419-1877A>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18432863 | |||||||
| chr11:18433398 | T | TA | 23 | a0001c0001t0001g0031 a0001c0001t0001g0194 a0001c0001t0002g0009 others(20): Show |
24 | HG00323.hp2 HG00733.hp1 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.419-1328dupA | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 18433398 | ||||||
| chr11:18433398 | T | TAA | 17 | a0001c0001t0002g0241 a0001c0001t0002g0258 a0001c0001t0002g0259 others(14): Show |
19 | HG00735.hp1 HG02257.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.419-1329_419-1328d others(4): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 18433398 | ||||||
| chr11:18433553 | T | C | 1 | a0001c0001t0003g0308 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.419-1187T>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18433553 | |||||||
| chr11:18433633 | T | C | 40 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(37): Show |
43 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.419-1107T>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18433633 | |||||||
| chr11:18433648 | G | A | 1 | a0001c0001t0004g0304 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.419-1092G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18433648 | |||||||
| chr11:18433659 | G | T | 1 | a0001c0001t0002g0290 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.419-1081G>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18433659 | |||||||
| chr11:18433675 | T | C | 3 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0184 |
3 | HG02630.hp2 HG02976.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.419-1065T>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18433675 | |||||||
| chr11:18433737 | C | T | 40 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(37): Show |
43 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.419-1003C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18433737 | |||||||
| chr11:18433943 | T | C | 85 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0018 others(82): Show |
90 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.419-797T>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18433943 | |||||||
| chr11:18434088 | G | A | 324 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(321): Show |
345 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(342): Show |
intron_variant | MODIFIER | c.419-652G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18434088 | |||||||
| chr11:18434096 | G | T | 1 | a0001c0001t0001g0152 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.419-644G>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18434096 | |||||||
| chr11:18434097 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.419-643C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18434097 | |||||||
| chr11:18434168 | C | T | 2 | a0004c0005t0007g0015 a0004c0005t0007g0016 |
2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.419-572C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18434168 | |||||||
| chr11:18434217 | A | AT | 121 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(118): Show |
125 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.419-510dupT | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 18434217 | ||||||
| chr11:18434217 | AT | A | 38 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(35): Show |
41 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.419-510delT | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 18434217 | ||||||
| chr11:18434341 | A | C | 42 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(39): Show |
45 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.419-399A>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18434341 | |||||||
| chr11:18434349 | G | T | 1 | a0001c0001t0001g0107 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.419-391G>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18434349 | |||||||
| chr11:18434388 | C | A | 42 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(39): Show |
45 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.419-352C>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18434388 | |||||||
| chr11:18434406 | A | G | 42 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(39): Show |
45 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.419-334A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18434406 | |||||||
| chr11:18434586 | A | T | 40 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(37): Show |
43 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.419-154A>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18434586 | |||||||
| chr11:18434593 | G | A | 285 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(282): Show |
305 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(302): Show |
intron_variant | MODIFIER | c.419-147G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18434593 | |||||||
| chr11:18434602 | C | T | 2 | a0004c0005t0007g0015 a0004c0005t0007g0016 |
2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.419-138C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18434602 | |||||||
| chr11:18434634 | A | G | 285 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(282): Show |
305 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(302): Show |
intron_variant | MODIFIER | c.419-106A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18434634 | |||||||
| chr11:18434678 | GA | G | 8 | a0001c0001t0001g0031 a0001c0001t0001g0058 a0001c0001t0001g0059 others(5): Show |
8 | HG00639.hp1 HG00639.hp2 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.419-52delA | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 18434678 | ||||||
| chr11:18434688 | A | T | 167 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(164): Show |
172 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(169): Show |
intron_variant | MODIFIER | c.419-52A>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18434688 | |||||||
| chr11:18434689 | T | A | 5 | a0001c0001t0002g0263 a0001c0001t0002g0264 a0001c0001t0002g0265 others(2): Show |
5 | HG00735.hp1 HG02258.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.419-51T>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 4/7 | chr11 | 18434689 | |||||||
| chr11:18434964 | G | A | 42 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(39): Show |
45 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.592+51G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 5/7 | chr11 | 18434964 | |||||||
| chr11:18434989 | C | T | 40 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(37): Show |
43 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.592+76C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 5/7 | chr11 | 18434989 | |||||||
| chr11:18435183 | A | G | 2 | a0005c0004t0006g0013 a0005c0004t0006g0014 |
2 | HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.592+270A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 5/7 | chr11 | 18435183 | |||||||
| chr11:18435184 | T | C | 1 | a0001c0001t0001g0123 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.592+271T>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 5/7 | chr11 | 18435184 | |||||||
| chr11:18435190 | A | T | 42 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(39): Show |
45 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.592+277A>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 5/7 | chr11 | 18435190 | |||||||
| chr11:18435327 | T | C | 2 | a0001c0001t0002g0002 a0001c0001t0002g0286 |
5 | HG02451.hp1 HG02615.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.592+414T>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 5/7 | chr11 | 18435327 | |||||||
| chr11:18435342 | T | C | 42 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(39): Show |
45 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.592+429T>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 5/7 | chr11 | 18435342 | |||||||
| chr11:18435418 | G | A | 2 | a0004c0005t0007g0015 a0004c0005t0007g0016 |
2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.592+505G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 5/7 | chr11 | 18435418 | |||||||
| chr11:18435989 | T | A | 1 | a0001c0001t0002g0242 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.592+1076T>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 5/7 | chr11 | 18435989 | |||||||
| chr11:18436035 | T | G | 1 | a0001c0001t0001g0047 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.592+1122T>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 5/7 | chr11 | 18436035 | |||||||
| chr11:18436132 | C | A | 3 | a0001c0001t0001g0119 a0001c0001t0001g0234 a0001c0001t0008g0116 |
3 | HG01243.hp2 HG01884.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.592+1219C>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 5/7 | chr11 | 18436132 | |||||||
| chr11:18436140 | G | T | 30 | a0001c0001t0001g0003 a0001c0001t0001g0233 a0001c0001t0001g0272 others(27): Show |
38 | HG01243.hp1 HG01891.hp1 HG02257.hp2 others(35): Show |
intron_variant | MODIFIER | c.592+1227G>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 5/7 | chr11 | 18436140 | |||||||
| chr11:18436157 | T | C | 2 | a0005c0004t0006g0013 a0005c0004t0006g0014 |
2 | HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.592+1244T>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 5/7 | chr11 | 18436157 | |||||||
| chr11:18436455 | T | C | 2 | a0004c0005t0007g0015 a0004c0005t0007g0016 |
2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.592+1542T>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 5/7 | chr11 | 18436455 | |||||||
| chr11:18436481 | G | GAT | 5 | a0001c0001t0002g0258 a0001c0001t0002g0259 a0001c0001t0002g0261 others(2): Show |
5 | HG02257.hp1 HG02486.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.592+1568_592+1569i others(4): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 5/7 | chr11 | 18436481 | |||||||
| chr11:18436481 | G | GATT | 30 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(27): Show |
33 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.592+1568_592+1569i others(5): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 5/7 | chr11 | 18436481 | |||||||
| chr11:18436481 | G | GATTT | 3 | a0001c0001t0002g0245 a0001c0001t0002g0265 a0001c0001t0002g0269 |
3 | HG01433.hp2 HG01981.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.592+1568_592+1569i others(6): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 5/7 | chr11 | 18436481 | |||||||
| chr11:18436481 | G | GT | 141 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(138): Show |
146 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.592+1590dupT | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr11 | 18436481 | ||||||
| chr11:18436481 | G | GTT | 25 | a0001c0001t0001g0025 a0001c0001t0001g0131 a0001c0001t0001g0133 others(22): Show |
25 | HG00423.hp2 HG00544.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.592+1589_592+1590d others(4): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr11 | 18436481 | ||||||
| chr11:18436481 | GT | G | 29 | a0001c0001t0001g0003 a0001c0001t0001g0272 a0001c0001t0001g0274 others(26): Show |
37 | HG01243.hp1 HG01891.hp1 HG02257.hp2 others(34): Show |
intron_variant | MODIFIER | c.592+1590delT | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr11 | 18436481 | ||||||
| chr11:18436482 | T | A | 2 | a0004c0005t0007g0015 a0004c0005t0007g0016 |
2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.592+1569T>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 5/7 | chr11 | 18436482 | |||||||
| chr11:18436506 | G | A | 2 | a0001c0003t0001g0117 a0001c0003t0001g0118 |
2 | NA18612.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.592+1593G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 5/7 | chr11 | 18436506 | |||||||
| chr11:18436590 | G | A | 40 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(37): Show |
43 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.592+1677G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 5/7 | chr11 | 18436590 | |||||||
| chr11:18436716 | C | T | 2 | a0005c0004t0006g0013 a0005c0004t0006g0014 |
2 | HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.592+1803C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 5/7 | chr11 | 18436716 | |||||||
| chr11:18436732 | C | T | 2 | a0005c0004t0006g0013 a0005c0004t0006g0014 |
2 | HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.593-1796C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 5/7 | chr11 | 18436732 | |||||||
| chr11:18436738 | A | C | 1 | a0001c0001t0001g0031 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.593-1790A>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 5/7 | chr11 | 18436738 | |||||||
| chr11:18436911 | TC | T | 40 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(37): Show |
43 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.593-1612delC | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr11 | 18436911 | ||||||
| chr11:18437161 | T | G | 1 | a0001c0001t0001g0031 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.593-1367T>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 5/7 | chr11 | 18437161 | |||||||
| chr11:18437306 | C | T | 5 | a0001c0001t0001g0272 a0001c0001t0001g0291 a0001c0001t0001g0293 others(2): Show |
5 | HG02965.hp1 HG03041.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.593-1222C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 5/7 | chr11 | 18437306 | |||||||
| chr11:18437333 | T | C | 1 | a0001c0001t0001g0034 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.593-1195T>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 5/7 | chr11 | 18437333 | |||||||
| chr11:18437475 | G | A | 2 | a0004c0005t0007g0015 a0004c0005t0007g0016 |
2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.593-1053G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 5/7 | chr11 | 18437475 | |||||||
| chr11:18437557 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.593-971C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 5/7 | chr11 | 18437557 | |||||||
| chr11:18437569 | A | G | 42 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(39): Show |
45 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.593-959A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 5/7 | chr11 | 18437569 | |||||||
| chr11:18437579 | C | T | 2 | a0001c0001t0001g0056 a0001c0001t0001g0085 |
2 | HG00738.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.593-949C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 5/7 | chr11 | 18437579 | |||||||
| chr11:18437657 | C | T | 2 | a0001c0001t0001g0047 a0001c0001t0001g0074 |
2 | NA18964.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.593-871C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 5/7 | chr11 | 18437657 | |||||||
| chr11:18437707 | G | A | 38 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(35): Show |
41 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.593-821G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 5/7 | chr11 | 18437707 | |||||||
| chr11:18437751 | CA | C | 273 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(270): Show |
291 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(288): Show |
intron_variant | MODIFIER | c.593-761delA | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr11 | 18437751 | ||||||
| chr11:18437751 | CAAA | C | 41 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0239 others(38): Show |
44 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.593-763_593-761del others(3): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr11 | 18437751 | ||||||
| chr11:18437833 | C | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0018 others(82): Show |
90 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.593-695C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 5/7 | chr11 | 18437833 | |||||||
| chr11:18437958 | G | A | 3 | a0001c0001t0001g0119 a0001c0001t0001g0234 a0001c0001t0008g0116 |
3 | HG01243.hp2 HG01884.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.593-570G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 5/7 | chr11 | 18437958 | |||||||
| chr11:18438022 | G | GCCACTAT others(29): Show |
1 | a0001c0001t0001g0031 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.593-505_593-470dup others(36): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr11 | 18438022 | ||||||
| chr11:18438050 | G | GA | 8 | a0001c0001t0001g0101 a0001c0001t0001g0129 a0001c0001t0001g0134 others(5): Show |
8 | HG02074.hp1 HG02738.hp1 HG03704.hp2 others(5): Show |
intron_variant | MODIFIER | c.593-468dupA | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr11 | 18438050 | ||||||
| chr11:18438092 | A | T | 1 | a0001c0001t0001g0075 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.593-436A>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 5/7 | chr11 | 18438092 | |||||||
| chr11:18438103 | G | A | 2 | a0004c0005t0007g0015 a0004c0005t0007g0016 |
2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.593-425G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 5/7 | chr11 | 18438103 | |||||||
| chr11:18438132 | G | A | 2 | a0001c0003t0001g0117 a0001c0003t0001g0118 |
2 | NA18612.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.593-396G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 5/7 | chr11 | 18438132 | |||||||
| chr11:18438132 | G | T | 2 | a0001c0001t0001g0121 a0001c0001t0001g0160 |
2 | NA18946.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.593-396G>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 5/7 | chr11 | 18438132 | |||||||
| chr11:18438168 | A | G | 42 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(39): Show |
45 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.593-360A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 5/7 | chr11 | 18438168 | |||||||
| chr11:18438175 | G | A | 30 | a0001c0001t0001g0003 a0001c0001t0001g0233 a0001c0001t0001g0272 others(27): Show |
38 | HG01243.hp1 HG01891.hp1 HG02257.hp2 others(35): Show |
intron_variant | MODIFIER | c.593-353G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 5/7 | chr11 | 18438175 | |||||||
| chr11:18438238 | C | T | 27 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(24): Show |
30 | HG00323.hp2 HG00733.hp1 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.593-290C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 5/7 | chr11 | 18438238 | |||||||
| chr11:18438259 | T | C | 40 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(37): Show |
43 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.593-269T>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 5/7 | chr11 | 18438259 | |||||||
| chr11:18438312 | A | G | 40 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(37): Show |
43 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.593-216A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 5/7 | chr11 | 18438312 | |||||||
| chr11:18438391 | A | C | 2 | a0004c0005t0007g0015 a0004c0005t0007g0016 |
2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.593-137A>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 5/7 | chr11 | 18438391 | |||||||
| chr11:18438753 | T | C | 40 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(37): Show |
43 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.710+108T>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18438753 | |||||||
| chr11:18438761 | C | T | 284 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(281): Show |
304 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(301): Show |
intron_variant | MODIFIER | c.710+116C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18438761 | |||||||
| chr11:18439129 | G | T | 2 | a0005c0004t0006g0013 a0005c0004t0006g0014 |
2 | HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.710+484G>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18439129 | |||||||
| chr11:18439383 | T | C | 11 | a0001c0001t0002g0241 a0001c0001t0002g0258 a0001c0001t0002g0259 others(8): Show |
11 | HG00735.hp1 HG02257.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.710+738T>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18439383 | |||||||
| chr11:18439421 | G | C | 2 | a0004c0005t0007g0015 a0004c0005t0007g0016 |
2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.710+776G>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18439421 | |||||||
| chr11:18439435 | C | T | 87 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0018 others(84): Show |
92 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.710+790C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18439435 | |||||||
| chr11:18439436 | G | A | 1 | a0001c0001t0002g0268 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.710+791G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18439436 | |||||||
| chr11:18439477 | C | A | 1 | a0001c0001t0002g0258 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.710+832C>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18439477 | |||||||
| chr11:18439507 | G | C | 243 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(240): Show |
260 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.710+862G>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18439507 | |||||||
| chr11:18439563 | C | CA | 39 | a0001c0001t0001g0199 a0001c0001t0001g0205 a0001c0001t0001g0219 others(36): Show |
42 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.710+939dupA | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr11 | 18439563 | ||||||
| chr11:18439563 | CA | C | 148 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(145): Show |
159 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.710+939delA | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr11 | 18439563 | ||||||
| chr11:18439563 | CAA | C | 6 | a0001c0001t0001g0036 a0001c0001t0001g0066 a0001c0001t0002g0002 others(3): Show |
9 | HG00558.hp1 HG02145.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.710+938_710+939del others(2): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr11 | 18439563 | ||||||
| chr11:18439625 | T | C | 2 | a0004c0005t0007g0015 a0004c0005t0007g0016 |
2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.710+980T>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18439625 | |||||||
| chr11:18439631 | T | G | 4 | a0001c0001t0001g0205 a0001c0001t0001g0215 a0001c0001t0001g0216 others(1): Show |
4 | HG00280.hp1 HG02148.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.710+986T>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18439631 | |||||||
| chr11:18439667 | A | C | 42 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(39): Show |
45 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.710+1022A>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18439667 | |||||||
| chr11:18439729 | C | G | 75 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0018 others(72): Show |
80 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.710+1084C>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18439729 | |||||||
| chr11:18439773 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.710+1128G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18439773 | |||||||
| chr11:18439811 | T | TA | 30 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0037 others(27): Show |
30 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.710+1191dupA | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr11 | 18439811 | ||||||
| chr11:18439811 | T | TAA | 97 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(94): Show |
101 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.710+1190_710+1191d others(4): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr11 | 18439811 | ||||||
| chr11:18439811 | T | TAAA | 25 | a0001c0001t0001g0025 a0001c0001t0001g0120 a0001c0001t0001g0134 others(22): Show |
25 | HG00423.hp2 HG00597.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.710+1189_710+1191d others(5): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr11 | 18439811 | ||||||
| chr11:18439822 | A | C | 6 | a0001c0001t0001g0003 a0001c0001t0001g0279 a0001c0001t0001g0283 others(3): Show |
9 | HG02258.hp2 HG02280.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.710+1177A>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18439822 | |||||||
| chr11:18439824 | A | C | 1 | a0001c0001t0003g0323 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.710+1179A>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18439824 | |||||||
| chr11:18439829 | A | AAAC | 24 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(21): Show |
27 | HG00323.hp2 HG00733.hp1 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.710+1186_710+1187i others(5): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr11 | 18439829 | ||||||
| chr11:18439830 | A | C | 2 | a0001c0001t0001g0119 a0001c0001t0001g0234 |
2 | HG01243.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.710+1185A>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18439830 | |||||||
| chr11:18439832 | A | C | 1 | a0001c0001t0001g0039 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.710+1187A>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18439832 | |||||||
| chr11:18439836 | A | AAAC | 8 | a0001c0001t0002g0241 a0001c0001t0002g0260 a0001c0001t0002g0262 others(5): Show |
8 | HG00735.hp1 HG02258.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.710+1191_710+1192i others(5): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18439836 | |||||||
| chr11:18439836 | A | C | 27 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(24): Show |
30 | HG00323.hp2 HG00733.hp1 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.710+1191A>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18439836 | |||||||
| chr11:18439837 | C | A | 3 | a0001c0001t0001g0152 a0004c0005t0007g0015 a0004c0005t0007g0016 |
3 | HG02145.hp1 HG02809.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.710+1192C>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18439837 | |||||||
| chr11:18439908 | C | G | 4 | a0001c0001t0002g0011 a0001c0001t0002g0271 a0001c0001t0002g0289 others(1): Show |
5 | HG02647.hp2 HG02922.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.710+1263C>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18439908 | |||||||
| chr11:18439942 | A | G | 3 | a0001c0001t0003g0305 a0001c0001t0003g0306 a0001c0001t0003g0307 |
3 | HG01074.hp1 HG01346.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.710+1297A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18439942 | |||||||
| chr11:18439958 | A | G | 38 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(35): Show |
41 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.710+1313A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18439958 | |||||||
| chr11:18439964 | C | T | 2 | a0004c0005t0007g0015 a0004c0005t0007g0016 |
2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.710+1319C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18439964 | |||||||
| chr11:18440015 | T | C | 5 | a0001c0001t0002g0241 a0001c0001t0002g0258 a0001c0001t0002g0259 others(2): Show |
5 | HG02257.hp1 HG02486.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.710+1370T>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18440015 | |||||||
| chr11:18440077 | T | C | 40 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(37): Show |
43 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.710+1432T>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18440077 | |||||||
| chr11:18440102 | C | T | 2 | a0005c0004t0006g0013 a0005c0004t0006g0014 |
2 | HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.710+1457C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18440102 | |||||||
| chr11:18440144 | C | CA | 11 | a0001c0001t0001g0023 a0001c0001t0001g0137 a0001c0001t0001g0149 others(8): Show |
11 | HG00741.hp1 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.710+1519dupA | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr11 | 18440144 | ||||||
| chr11:18440144 | C | CAA | 108 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0018 others(105): Show |
114 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.710+1518_710+1519d others(4): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr11 | 18440144 | ||||||
| chr11:18440144 | C | CAAA | 15 | a0001c0001t0001g0037 a0001c0001t0001g0079 a0001c0001t0001g0089 others(12): Show |
17 | HG02257.hp1 HG02818.hp1 HG02895.hp1 others(14): Show |
intron_variant | MODIFIER | c.710+1517_710+1519d others(5): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr11 | 18440144 | ||||||
| chr11:18440178 | G | A | 1 | a0001c0001t0001g0092 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.710+1533G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18440178 | |||||||
| chr11:18440231 | C | T | 42 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(39): Show |
45 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.710+1586C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18440231 | |||||||
| chr11:18440283 | C | A | 40 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(37): Show |
43 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.710+1638C>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18440283 | |||||||
| chr11:18440331 | A | G | 38 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(35): Show |
41 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.710+1686A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18440331 | |||||||
| chr11:18440554 | A | G | 42 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(39): Show |
45 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.710+1909A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18440554 | |||||||
| chr11:18440647 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.710+2002G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18440647 | |||||||
| chr11:18440715 | G | T | 1 | a0001c0001t0001g0288 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.710+2070G>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18440715 | |||||||
| chr11:18440776 | A | T | 4 | a0001c0001t0002g0011 a0001c0001t0002g0271 a0001c0001t0002g0289 others(1): Show |
5 | HG02647.hp2 HG02922.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.710+2131A>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18440776 | |||||||
| chr11:18440787 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.710+2142C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18440787 | |||||||
| chr11:18440791 | CATG | C | 242 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(239): Show |
259 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.710+2147_710+2149d others(5): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18440791 | |||||||
| chr11:18440830 | G | A | 40 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(37): Show |
43 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.710+2185G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18440830 | |||||||
| chr11:18440857 | C | A | 42 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(39): Show |
45 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.710+2212C>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18440857 | |||||||
| chr11:18440928 | A | G | 40 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(37): Show |
43 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.710+2283A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18440928 | |||||||
| chr11:18440939 | T | TA | 38 | a0001c0001t0001g0031 a0001c0001t0002g0009 a0001c0001t0002g0235 others(35): Show |
41 | HG00323.hp2 HG00733.hp1 HG01070.hp2 others(38): Show |
intron_variant | MODIFIER | c.710+2301dupA | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr11 | 18440939 | ||||||
| chr11:18440947 | T | A | 278 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(275): Show |
298 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.710+2302T>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18440947 | |||||||
| chr11:18440947 | T | TA | 3 | a0001c0001t0002g0264 a0001c0001t0002g0266 a0001c0001t0002g0267 |
3 | HG00735.hp1 HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.710+2305dupA | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr11 | 18440947 | ||||||
| chr11:18441018 | T | C | 1 | a0001c0001t0001g0172 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.710+2373T>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18441018 | |||||||
| chr11:18441137 | C | T | 40 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(37): Show |
43 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.710+2492C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18441137 | |||||||
| chr11:18441152 | A | G | 11 | a0001c0001t0001g0003 a0001c0001t0001g0272 a0001c0001t0001g0279 others(8): Show |
14 | HG02258.hp2 HG02280.hp1 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.710+2507A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18441152 | |||||||
| chr11:18441280 | C | G | 6 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(3): Show |
6 | HG01255.hp2 HG01496.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.710+2635C>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18441280 | |||||||
| chr11:18441295 | G | C | 1 | a0001c0001t0001g0274 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.710+2650G>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18441295 | |||||||
| chr11:18441483 | A | G | 2 | a0004c0005t0007g0015 a0004c0005t0007g0016 |
2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.710+2838A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18441483 | |||||||
| chr11:18441583 | G | A | 2 | a0004c0005t0007g0015 a0004c0005t0007g0016 |
2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.710+2938G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18441583 | |||||||
| chr11:18441584 | C | A | 2 | a0004c0005t0007g0015 a0004c0005t0007g0016 |
2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.710+2939C>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18441584 | |||||||
| chr11:18441625 | C | T | 2 | a0004c0005t0007g0015 a0004c0005t0007g0016 |
2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.710+2980C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18441625 | |||||||
| chr11:18441681 | T | G | 40 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(37): Show |
43 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.710+3036T>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18441681 | |||||||
| chr11:18441766 | G | A | 1 | a0001c0001t0002g0269 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.710+3121G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18441766 | |||||||
| chr11:18441781 | G | A | 1 | a0001c0001t0001g0064 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.710+3136G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18441781 | |||||||
| chr11:18441784 | C | T | 1 | a0002c0002t0002g0252 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.710+3139C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18441784 | |||||||
| chr11:18441797 | A | T | 1 | a0001c0001t0003g0316 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.710+3152A>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18441797 | |||||||
| chr11:18441972 | T | C | 1 | a0001c0001t0001g0045 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.710+3327T>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18441972 | |||||||
| chr11:18442044 | C | G | 1 | a0001c0001t0001g0156 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.710+3399C>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18442044 | |||||||
| chr11:18442071 | G | T | 1 | a0001c0001t0001g0031 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.710+3426G>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18442071 | |||||||
| chr11:18442071 | GT | G | 40 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(37): Show |
43 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.710+3435delT | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr11 | 18442071 | ||||||
| chr11:18442124 | C | T | 40 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(37): Show |
43 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.710+3479C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18442124 | |||||||
| chr11:18442229 | CTA | C | 7 | a0002c0002t0002g0005 a0002c0002t0002g0236 a0002c0002t0002g0237 others(4): Show |
9 | HG02818.hp1 HG02895.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.710+3586_710+3587d others(4): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr11 | 18442229 | ||||||
| chr11:18442231 | A | G | 2 | a0004c0005t0007g0015 a0004c0005t0007g0016 |
2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.710+3586A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18442231 | |||||||
| chr11:18442489 | A | C | 2 | a0004c0005t0007g0015 a0004c0005t0007g0016 |
2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.711-3721A>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18442489 | |||||||
| chr11:18442573 | C | T | 42 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(39): Show |
45 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.711-3637C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18442573 | |||||||
| chr11:18442601 | G | A | 10 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(7): Show |
10 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(7): Show |
intron_variant | MODIFIER | c.711-3609G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18442601 | |||||||
| chr11:18442660 | C | CT | 121 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(118): Show |
125 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.711-3530dupT | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr11 | 18442660 | ||||||
| chr11:18442660 | CT | C | 12 | a0001c0001t0001g0072 a0001c0001t0001g0113 a0001c0001t0001g0279 others(9): Show |
12 | HG01167.hp1 HG01167.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.711-3530delT | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr11 | 18442660 | ||||||
| chr11:18442663 | T | C | 2 | a0005c0004t0006g0013 a0005c0004t0006g0014 |
2 | HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.711-3547T>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18442663 | |||||||
| chr11:18442809 | T | C | 285 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(282): Show |
305 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(302): Show |
intron_variant | MODIFIER | c.711-3401T>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18442809 | |||||||
| chr11:18442910 | G | C | 2 | a0004c0005t0007g0015 a0004c0005t0007g0016 |
2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.711-3300G>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18442910 | |||||||
| chr11:18442922 | T | C | 40 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(37): Show |
43 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.711-3288T>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18442922 | |||||||
| chr11:18442933 | C | T | 2 | a0001c0001t0001g0233 a0001c0001t0002g0282 |
2 | HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.711-3277C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18442933 | |||||||
| chr11:18442934 | G | A | 2 | a0005c0004t0006g0013 a0005c0004t0006g0014 |
2 | HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.711-3276G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18442934 | |||||||
| chr11:18442960 | G | T | 1 | a0001c0001t0001g0228 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.711-3250G>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18442960 | |||||||
| chr11:18443135 | G | T | 5 | a0001c0001t0002g0263 a0001c0001t0002g0264 a0001c0001t0002g0265 others(2): Show |
5 | HG00735.hp1 HG02258.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.711-3075G>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18443135 | |||||||
| chr11:18443330 | C | T | 1 | a0001c0001t0002g0258 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.711-2880C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18443330 | |||||||
| chr11:18443386 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.711-2824C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18443386 | |||||||
| chr11:18443447 | C | T | 283 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(280): Show |
303 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(300): Show |
intron_variant | MODIFIER | c.711-2763C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18443447 | |||||||
| chr11:18443452 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.711-2758C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18443452 | |||||||
| chr11:18443460 | C | CT | 87 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0018 others(84): Show |
92 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.711-2733dupT | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr11 | 18443460 | ||||||
| chr11:18443460 | CT | C | 39 | a0001c0001t0001g0003 a0001c0001t0001g0027 a0001c0001t0001g0185 others(36): Show |
47 | HG00639.hp1 HG00639.hp2 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.711-2733delT | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr11 | 18443460 | ||||||
| chr11:18443463 | T | TC | 38 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(35): Show |
41 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.711-2747_711-2746i others(3): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18443463 | |||||||
| chr11:18443845 | C | T | 30 | a0001c0001t0001g0003 a0001c0001t0001g0233 a0001c0001t0001g0272 others(27): Show |
38 | HG01243.hp1 HG01891.hp1 HG02257.hp2 others(35): Show |
intron_variant | MODIFIER | c.711-2365C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18443845 | |||||||
| chr11:18444001 | A | T | 1 | a0001c0001t0001g0127 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.711-2209A>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18444001 | |||||||
| chr11:18444201 | C | T | 1 | a0002c0002t0002g0236 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.711-2009C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18444201 | |||||||
| chr11:18444226 | G | A | 2 | a0005c0004t0006g0013 a0005c0004t0006g0014 |
2 | HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.711-1984G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18444226 | |||||||
| chr11:18444300 | C | G | 1 | a0001c0001t0001g0233 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.711-1910C>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18444300 | |||||||
| chr11:18444381 | A | G | 87 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0018 others(84): Show |
92 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.711-1829A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18444381 | |||||||
| chr11:18444422 | C | G | 87 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0018 others(84): Show |
92 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.711-1788C>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18444422 | |||||||
| chr11:18444461 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.711-1749C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18444461 | |||||||
| chr11:18444462 | G | A | 2 | a0004c0005t0007g0015 a0004c0005t0007g0016 |
2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.711-1748G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18444462 | |||||||
| chr11:18444604 | G | GTA | 13 | a0001c0001t0001g0120 a0001c0001t0001g0141 a0001c0001t0001g0157 others(10): Show |
13 | HG01106.hp2 HG01109.hp2 HG01993.hp2 others(10): Show |
intron_variant | MODIFIER | c.711-1562_711-1561d others(4): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr11 | 18444604 | ||||||
| chr11:18444604 | G | GTATA | 5 | a0001c0001t0001g0129 a0001c0001t0001g0134 a0001c0001t0001g0140 others(2): Show |
5 | NA18612.hp2 NA18977.hp1 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.711-1564_711-1561d others(6): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr11 | 18444604 | ||||||
| chr11:18444604 | G | GTATATA | 6 | a0001c0001t0001g0088 a0001c0001t0001g0161 a0001c0001t0001g0206 others(3): Show |
6 | HG00544.hp2 HG01099.hp2 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.711-1566_711-1561d others(8): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr11 | 18444604 | ||||||
| chr11:18444604 | G | GTATATAT others(1): Show |
9 | a0001c0001t0001g0008 a0001c0001t0001g0126 a0001c0001t0001g0127 others(6): Show |
10 | HG00323.hp1 HG00558.hp2 HG00673.hp2 others(7): Show |
intron_variant | MODIFIER | c.711-1568_711-1561d others(10): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr11 | 18444604 | ||||||
| chr11:18444604 | G | GTATATAT others(3): Show |
18 | a0001c0001t0001g0026 a0001c0001t0001g0125 a0001c0001t0001g0149 others(15): Show |
18 | HG00423.hp2 HG00639.hp1 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.711-1570_711-1561d others(12): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr11 | 18444604 | ||||||
| chr11:18444604 | G | GTATATAT others(5): Show |
7 | a0001c0001t0001g0155 a0001c0001t0001g0168 a0001c0001t0001g0188 others(4): Show |
7 | HG00741.hp1 HG01952.hp1 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.711-1572_711-1561d others(14): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr11 | 18444604 | ||||||
| chr11:18444604 | G | GTATATAT others(7): Show |
4 | a0001c0001t0001g0132 a0001c0001t0001g0163 a0001c0001t0001g0176 others(1): Show |
4 | NA18984.hp1 NA19000.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.711-1574_711-1561d others(16): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr11 | 18444604 | ||||||
| chr11:18444604 | G | GTATATAT others(9): Show |
3 | a0001c0001t0001g0178 a0001c0001t0001g0186 a0001c0001t0001g0225 |
3 | NA18955.hp2 NA18956.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.711-1576_711-1561d others(18): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr11 | 18444604 | ||||||
| chr11:18444604 | G | GTATATAT others(11): Show |
1 | a0001c0001t0001g0230 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.711-1578_711-1561d others(20): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr11 | 18444604 | ||||||
| chr11:18444604 | G | GTATATAT others(13): Show |
1 | a0001c0001t0001g0219 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.711-1580_711-1561d others(22): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr11 | 18444604 | ||||||
| chr11:18444604 | G | GTATATAT others(15): Show |
1 | a0001c0001t0001g0124 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.711-1582_711-1561d others(24): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr11 | 18444604 | ||||||
| chr11:18444604 | G | GTATATAT others(27): Show |
1 | a0001c0001t0001g0224 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.711-1594_711-1561d others(36): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr11 | 18444604 | ||||||
| chr11:18444604 | G | GTATGTAT others(5): Show |
1 | a0001c0001t0001g0121 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.711-1603_711-1602i others(14): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr11 | 18444604 | ||||||
| chr11:18444604 | GTA | G | 28 | a0001c0001t0001g0004 a0001c0001t0001g0119 a0001c0001t0001g0122 others(25): Show |
30 | HG00280.hp1 HG00609.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.711-1562_711-1561d others(4): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr11 | 18444604 | ||||||
| chr11:18444604 | GTATA | G | 11 | a0001c0001t0001g0023 a0001c0001t0001g0165 a0001c0001t0001g0167 others(8): Show |
11 | HG00438.hp1 HG00597.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.711-1564_711-1561d others(6): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr11 | 18444604 | ||||||
| chr11:18444604 | GTATATA | G | 16 | a0001c0001t0001g0024 a0001c0001t0001g0154 a0001c0001t0001g0184 others(13): Show |
18 | HG00597.hp2 HG00621.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.711-1566_711-1561d others(8): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr11 | 18444604 | ||||||
| chr11:18444604 | GTATATAT others(1): Show |
G | 4 | a0001c0001t0001g0179 a0001c0001t0002g0011 a0001c0001t0002g0280 others(1): Show |
5 | HG02717.hp2 HG02818.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.711-1568_711-1561d others(10): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr11 | 18444604 | ||||||
| chr11:18444604 | GTATATAT others(3): Show |
G | 6 | a0001c0001t0001g0027 a0001c0001t0002g0002 a0001c0001t0002g0271 others(3): Show |
9 | HG02451.hp1 HG02615.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.711-1570_711-1561d others(12): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr11 | 18444604 | ||||||
| chr11:18444604 | GTATATAT others(5): Show |
G | 12 | a0001c0001t0001g0003 a0001c0001t0001g0233 a0001c0001t0001g0272 others(9): Show |
15 | HG02258.hp2 HG02280.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.711-1572_711-1561d others(14): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr11 | 18444604 | ||||||
| chr11:18444604 | GTATATAT others(7): Show |
G | 8 | a0001c0001t0001g0218 a0001c0001t0001g0274 a0001c0001t0001g0275 others(5): Show |
8 | HG02083.hp1 HG02451.hp2 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.711-1574_711-1561d others(16): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr11 | 18444604 | ||||||
| chr11:18444604 | GTATATAT others(9): Show |
G | 1 | a0001c0001t0001g0135 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.711-1576_711-1561d others(18): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr11 | 18444604 | ||||||
| chr11:18444604 | GTATATAT others(11): Show |
G | 7 | a0001c0001t0002g0009 a0001c0001t0002g0240 a0001c0001t0003g0316 others(4): Show |
8 | HG00323.hp2 HG00733.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.711-1578_711-1561d others(20): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr11 | 18444604 | ||||||
| chr11:18444604 | GTATATAT others(13): Show |
G | 19 | a0001c0001t0001g0152 a0001c0001t0002g0235 a0001c0001t0002g0238 others(16): Show |
19 | HG01070.hp2 HG01167.hp1 HG01358.hp2 others(16): Show |
intron_variant | MODIFIER | c.711-1580_711-1561d others(22): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr11 | 18444604 | ||||||
| chr11:18444604 | GTATATAT others(15): Show |
G | 6 | a0001c0001t0001g0123 a0001c0001t0002g0241 a0001c0001t0002g0258 others(3): Show |
6 | HG02257.hp1 HG02486.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.711-1582_711-1561d others(24): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr11 | 18444604 | ||||||
| chr11:18444604 | GTATATAT others(17): Show |
G | 14 | a0001c0001t0002g0260 a0001c0001t0002g0263 a0001c0001t0002g0264 others(11): Show |
16 | HG00735.hp1 HG02258.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.711-1584_711-1561d others(26): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr11 | 18444604 | ||||||
| chr11:18444604 | GTATATAT others(19): Show |
G | 1 | a0001c0001t0001g0175 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.711-1586_711-1561d others(28): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr11 | 18444604 | ||||||
| chr11:18444604 | GTATATAT others(21): Show |
G | 85 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0018 others(82): Show |
90 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.711-1588_711-1561d others(30): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr11 | 18444604 | ||||||
| chr11:18444645 | T | C | 30 | a0001c0001t0001g0003 a0001c0001t0001g0233 a0001c0001t0001g0272 others(27): Show |
38 | HG01243.hp1 HG01891.hp1 HG02257.hp2 others(35): Show |
intron_variant | MODIFIER | c.711-1565T>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18444645 | |||||||
| chr11:18444700 | C | G | 1 | a0001c0001t0001g0160 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.711-1510C>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18444700 | |||||||
| chr11:18444700 | C | T | 119 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(116): Show |
123 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.711-1510C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18444700 | |||||||
| chr11:18445064 | T | C | 1 | a0005c0004t0006g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.711-1146T>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18445064 | |||||||
| chr11:18445153 | C | G | 38 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(35): Show |
41 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.711-1057C>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18445153 | |||||||
| chr11:18445317 | T | C | 2 | a0004c0005t0007g0015 a0004c0005t0007g0016 |
2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.711-893T>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18445317 | |||||||
| chr11:18445420 | A | C | 85 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0018 others(82): Show |
90 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.711-790A>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18445420 | |||||||
| chr11:18445435 | G | C | 5 | a0001c0001t0001g0031 a0001c0001t0001g0049 a0001c0001t0001g0058 others(2): Show |
5 | NA18948.hp2 NA18965.hp1 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.711-775G>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18445435 | |||||||
| chr11:18445659 | G | C | 7 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0128 others(4): Show |
7 | HG01891.hp2 HG02622.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.711-551G>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18445659 | |||||||
| chr11:18445736 | T | C | 42 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(39): Show |
45 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.711-474T>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18445736 | |||||||
| chr11:18445750 | C | T | 2 | a0004c0005t0007g0015 a0004c0005t0007g0016 |
2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.711-460C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18445750 | |||||||
| chr11:18445751 | G | A | 2 | a0005c0004t0006g0013 a0005c0004t0006g0014 |
2 | HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.711-459G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18445751 | |||||||
| chr11:18446039 | A | G | 1 | a0001c0001t0001g0155 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.711-171A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18446039 | |||||||
| chr11:18446081 | A | G | 1 | a0001c0001t0003g0322 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.711-129A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 6/7 | chr11 | 18446081 | |||||||
| chr11:18446351 | C | A | 30 | a0001c0001t0001g0003 a0001c0001t0001g0233 a0001c0001t0001g0272 others(27): Show |
38 | HG01243.hp1 HG01891.hp1 HG02257.hp2 others(35): Show |
intron_variant | MODIFIER | c.834+18C>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | chr11 | 18446351 | |||||||
| chr11:18446831 | G | A | 38 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(35): Show |
41 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.834+498G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | chr11 | 18446831 | |||||||
| chr11:18446882 | T | G | 2 | a0001c0003t0001g0117 a0001c0003t0001g0118 |
2 | NA18612.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.834+549T>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | chr11 | 18446882 | |||||||
| chr11:18446910 | AGTTT | A | 6 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 others(3): Show |
6 | HG02451.hp2 HG02683.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.834+593_834+596del others(4): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr11 | 18446910 | ||||||
| chr11:18446968 | G | T | 1 | a0001c0001t0001g0168 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.834+635G>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | chr11 | 18446968 | |||||||
| chr11:18447078 | G | T | 3 | a0001c0001t0002g0248 a0001c0001t0002g0256 a0001c0001t0002g0270 |
3 | NA18968.hp1 NA18977.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.834+745G>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | chr11 | 18447078 | |||||||
| chr11:18447134 | A | AT | 8 | a0001c0001t0001g0068 a0001c0001t0001g0126 a0001c0001t0001g0205 others(5): Show |
8 | HG00280.hp1 HG00323.hp1 HG02148.hp2 others(5): Show |
intron_variant | MODIFIER | c.834+818dupT | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr11 | 18447134 | ||||||
| chr11:18447134 | AT | A | 8 | a0001c0001t0001g0064 a0001c0001t0001g0170 a0001c0001t0001g0230 others(5): Show |
8 | HG01517.hp1 HG02145.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.834+818delT | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr11 | 18447134 | ||||||
| chr11:18447373 | A | G | 42 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(39): Show |
45 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.834+1040A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | chr11 | 18447373 | |||||||
| chr11:18447374 | A | C | 1 | a0001c0001t0001g0052 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.834+1041A>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | chr11 | 18447374 | |||||||
| chr11:18447383 | C | T | 38 | a0001c0001t0003g0093 a0001c0001t0003g0094 a0001c0001t0003g0095 others(35): Show |
39 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.834+1050C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | chr11 | 18447383 | |||||||
| chr11:18447434 | C | T | 17 | a0001c0001t0001g0003 a0001c0001t0001g0272 a0001c0001t0001g0274 others(14): Show |
20 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.834+1101C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | chr11 | 18447434 | |||||||
| chr11:18447449 | T | C | 38 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(35): Show |
41 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.834+1116T>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | chr11 | 18447449 | |||||||
| chr11:18447729 | G | C | 2 | a0005c0004t0006g0013 a0005c0004t0006g0014 |
2 | HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.834+1396G>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | chr11 | 18447729 | |||||||
| chr11:18447822 | G | A | 39 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(36): Show |
42 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.834+1489G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | chr11 | 18447822 | |||||||
| chr11:18447837 | G | C | 2 | a0001c0001t0001g0185 a0001c0001t0001g0214 |
2 | HG00639.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.834+1504G>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | chr11 | 18447837 | |||||||
| chr11:18448048 | C | CA | 11 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(8): Show |
11 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.834+1736dupA | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr11 | 18448048 | ||||||
| chr11:18448048 | CA | C | 78 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0119 others(75): Show |
87 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.834+1736delA | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr11 | 18448048 | ||||||
| chr11:18448048 | CAA | C | 6 | a0001c0001t0001g0027 a0001c0001t0001g0296 a0001c0001t0002g0244 others(3): Show |
6 | HG02074.hp2 HG02683.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.834+1735_834+1736d others(4): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr11 | 18448048 | ||||||
| chr11:18448048 | CAAA | C | 34 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(31): Show |
37 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.834+1734_834+1736d others(5): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr11 | 18448048 | ||||||
| chr11:18448112 | A | AC | 5 | a0001c0001t0002g0263 a0001c0001t0002g0264 a0001c0001t0002g0265 others(2): Show |
5 | HG00735.hp1 HG02258.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.834+1783dupC | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr11 | 18448112 | ||||||
| chr11:18448230 | T | C | 2 | a0001c0001t0001g0145 a0001c0001t0001g0170 |
2 | HG01106.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.834+1897T>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | chr11 | 18448230 | |||||||
| chr11:18448267 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.834+1934C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | chr11 | 18448267 | |||||||
| chr11:18448318 | C | G | 1 | a0001c0001t0001g0038 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.834+1985C>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | chr11 | 18448318 | |||||||
| chr11:18448344 | C | T | 1 | a0001c0001t0003g0322 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.834+2011C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | chr11 | 18448344 | |||||||
| chr11:18448387 | G | A | 30 | a0001c0001t0001g0003 a0001c0001t0001g0233 a0001c0001t0001g0272 others(27): Show |
38 | HG01243.hp1 HG01891.hp1 HG02257.hp2 others(35): Show |
intron_variant | MODIFIER | c.834+2054G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | chr11 | 18448387 | |||||||
| chr11:18448430 | C | A | 1 | a0001c0001t0001g0218 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.834+2097C>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | chr11 | 18448430 | |||||||
| chr11:18448440 | C | G | 1 | a0001c0001t0001g0077 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.834+2107C>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | chr11 | 18448440 | |||||||
| chr11:18448520 | C | T | 3 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 |
3 | HG02486.hp1 HG02886.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.834+2187C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | chr11 | 18448520 | |||||||
| chr11:18448535 | G | A | 124 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(121): Show |
128 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.834+2202G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | chr11 | 18448535 | |||||||
| chr11:18448573 | G | A | 4 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0278 others(1): Show |
4 | HG02683.hp1 HG02738.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.834+2240G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | chr11 | 18448573 | |||||||
| chr11:18448618 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.834+2285C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | chr11 | 18448618 | |||||||
| chr11:18448745 | A | AT | 126 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
131 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.835-2208dupT | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr11 | 18448745 | ||||||
| chr11:18448755 | TG | T | 4 | a0001c0001t0001g0064 a0004c0005t0007g0015 a0004c0005t0007g0016 others(1): Show |
4 | HG02145.hp1 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.835-2207delG | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | chr11 | 18448755 | |||||||
| chr11:18448756 | G | T | 320 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(317): Show |
341 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(338): Show |
intron_variant | MODIFIER | c.835-2207G>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | chr11 | 18448756 | |||||||
| chr11:18448758 | G | T | 285 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(282): Show |
305 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(302): Show |
intron_variant | MODIFIER | c.835-2205G>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | chr11 | 18448758 | |||||||
| chr11:18448820 | G | C | 1 | a0005c0004t0006g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.835-2143G>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | chr11 | 18448820 | |||||||
| chr11:18448940 | G | A | 38 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(35): Show |
41 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.835-2023G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | chr11 | 18448940 | |||||||
| chr11:18449065 | AGGAGGTA others(3): Show |
A | 1 | a0005c0004t0006g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.835-1894_835-1885d others(12): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr11 | 18449065 | ||||||
| chr11:18449073 | A | G | 1 | a0001c0001t0001g0274 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.835-1890A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | chr11 | 18449073 | |||||||
| chr11:18449142 | C | G | 39 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(36): Show |
42 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.835-1821C>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | chr11 | 18449142 | |||||||
| chr11:18449186 | A | G | 1 | a0005c0004t0006g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.835-1777A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | chr11 | 18449186 | |||||||
| chr11:18449253 | A | G | 38 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(35): Show |
41 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.835-1710A>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | chr11 | 18449253 | |||||||
| chr11:18449428 | T | TAAAA | 9 | a0001c0001t0003g0301 a0001c0001t0003g0302 a0001c0001t0003g0307 others(6): Show |
9 | HG00741.hp2 HG01109.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.835-1505_835-1502d others(6): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr11 | 18449428 | ||||||
| chr11:18449428 | T | TAAAAA | 10 | a0001c0001t0001g0027 a0001c0001t0001g0079 a0001c0001t0001g0080 others(7): Show |
10 | HG01074.hp1 HG01106.hp2 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.835-1506_835-1502d others(7): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr11 | 18449428 | ||||||
| chr11:18449428 | T | TAAAAAAA | 30 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0038 others(27): Show |
34 | HG00280.hp2 HG00738.hp1 HG01517.hp2 others(31): Show |
intron_variant | MODIFIER | c.835-1508_835-1502d others(9): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr11 | 18449428 | ||||||
| chr11:18449428 | T | TAAAAAAA others(1): Show |
29 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0022 others(26): Show |
30 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.835-1509_835-1502d others(10): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr11 | 18449428 | ||||||
| chr11:18449428 | T | TAAAAAAA others(2): Show |
8 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0031 others(5): Show |
8 | HG00642.hp2 HG00735.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.835-1510_835-1502d others(11): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr11 | 18449428 | ||||||
| chr11:18449428 | T | TAAAAAAA others(3): Show |
2 | a0001c0001t0001g0058 a0001c0001t0001g0084 |
2 | NA18948.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.835-1511_835-1502d others(12): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr11 | 18449428 | ||||||
| chr11:18449428 | T | TAAAAAAA others(4): Show |
2 | a0001c0001t0001g0092 a0001c0001t0001g0110 |
2 | HG02015.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.835-1512_835-1502d others(13): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr11 | 18449428 | ||||||
| chr11:18449428 | T | TAAAAAAA others(6): Show |
1 | a0006c0010t0001g0065 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.835-1514_835-1502d others(15): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr11 | 18449428 | ||||||
| chr11:18449428 | TA | T | 41 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0023 others(38): Show |
45 | HG00558.hp2 HG00673.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.835-1502delA | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr11 | 18449428 | ||||||
| chr11:18449428 | TAA | T | 78 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0026 others(75): Show |
81 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.835-1503_835-1502d others(4): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr11 | 18449428 | ||||||
| chr11:18449428 | TAAA | T | 7 | a0001c0001t0001g0018 a0001c0001t0001g0128 a0001c0001t0001g0143 others(4): Show |
7 | HG01257.hp1 HG02886.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.835-1504_835-1502d others(5): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr11 | 18449428 | ||||||
| chr11:18449428 | TAAAAA | T | 11 | a0001c0001t0002g0002 a0001c0001t0002g0010 a0001c0001t0002g0011 others(8): Show |
16 | HG01243.hp1 HG01891.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.835-1506_835-1502d others(7): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr11 | 18449428 | ||||||
| chr11:18449428 | TAAAAAAA others(2): Show |
T | 6 | a0001c0001t0002g0263 a0001c0001t0002g0264 a0001c0001t0002g0265 others(3): Show |
6 | HG00735.hp1 HG02145.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.835-1510_835-1502d others(11): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr11 | 18449428 | ||||||
| chr11:18449428 | TAAAAAAA others(3): Show |
T | 8 | a0001c0001t0001g0233 a0001c0001t0002g0241 a0001c0001t0002g0258 others(5): Show |
8 | HG02074.hp2 HG02257.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.835-1511_835-1502d others(12): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr11 | 18449428 | ||||||
| chr11:18449428 | TAAAAAAA others(4): Show |
T | 25 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(22): Show |
28 | HG00323.hp2 HG00733.hp1 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.835-1512_835-1502d others(13): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr11 | 18449428 | ||||||
| chr11:18449428 | TAAAAAAA others(5): Show |
T | 2 | a0001c0001t0002g0239 a0001c0001t0008g0116 |
2 | HG01167.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.835-1513_835-1502d others(14): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr11 | 18449428 | ||||||
| chr11:18449428 | TAAAAAAA others(6): Show |
T | 2 | a0001c0001t0001g0105 a0001c0001t0001g0109 |
2 | HG02523.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.835-1514_835-1502d others(15): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr11 | 18449428 | ||||||
| chr11:18449428 | TAAAAAAA others(12): Show |
T | 22 | a0001c0001t0003g0093 a0001c0001t0003g0094 a0001c0001t0003g0095 others(19): Show |
23 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.835-1520_835-1502d others(21): Show |
LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr11 | 18449428 | ||||||
| chr11:18449551 | G | A | 7 | a0002c0002t0002g0005 a0002c0002t0002g0236 a0002c0002t0002g0237 others(4): Show |
9 | HG02818.hp1 HG02895.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.835-1412G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | chr11 | 18449551 | |||||||
| chr11:18449569 | A | C | 2 | a0004c0005t0007g0015 a0004c0005t0007g0016 |
2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.835-1394A>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | chr11 | 18449569 | |||||||
| chr11:18449655 | G | T | 2 | a0004c0005t0007g0015 a0004c0005t0007g0016 |
2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.835-1308G>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | chr11 | 18449655 | |||||||
| chr11:18449761 | G | A | 2 | a0004c0005t0007g0015 a0004c0005t0007g0016 |
2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.835-1202G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | chr11 | 18449761 | |||||||
| chr11:18449781 | G | A | 12 | a0001c0001t0002g0002 a0001c0001t0002g0010 a0001c0001t0002g0011 others(9): Show |
17 | HG01243.hp1 HG01891.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.835-1182G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | chr11 | 18449781 | |||||||
| chr11:18449823 | T | C | 54 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(51): Show |
62 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.835-1140T>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | chr11 | 18449823 | |||||||
| chr11:18449824 | G | A | 38 | a0001c0001t0003g0093 a0001c0001t0003g0094 a0001c0001t0003g0095 others(35): Show |
39 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.835-1139G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | chr11 | 18449824 | |||||||
| chr11:18449896 | A | C | 1 | a0001c0001t0001g0161 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.835-1067A>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | chr11 | 18449896 | |||||||
| chr11:18449951 | T | C | 11 | a0001c0001t0001g0030 a0001c0001t0001g0036 a0001c0001t0001g0037 others(8): Show |
11 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(8): Show |
intron_variant | MODIFIER | c.835-1012T>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | chr11 | 18449951 | |||||||
| chr11:18449967 | G | A | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | HG02109.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.835-996G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | chr11 | 18449967 | |||||||
| chr11:18450042 | C | CT | 22 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0049 others(19): Show |
25 | HG02258.hp2 HG02280.hp1 HG02280.hp2 others(22): Show |
intron_variant | MODIFIER | c.835-908dupT | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr11 | 18450042 | ||||||
| chr11:18450042 | CT | C | 7 | a0001c0001t0001g0064 a0001c0001t0001g0119 a0001c0001t0001g0234 others(4): Show |
7 | HG01243.hp2 HG01884.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.835-908delT | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr11 | 18450042 | ||||||
| chr11:18450047 | T | A | 1 | a0001c0001t0001g0120 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.835-916T>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | chr11 | 18450047 | |||||||
| chr11:18450080 | T | A | 38 | a0001c0001t0002g0009 a0001c0001t0002g0235 a0001c0001t0002g0238 others(35): Show |
41 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.835-883T>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | chr11 | 18450080 | |||||||
| chr11:18450114 | C | T | 3 | a0001c0001t0001g0138 a0001c0001t0001g0162 a0001c0001t0001g0229 |
3 | HG01981.hp2 HG03491.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.835-849C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | chr11 | 18450114 | |||||||
| chr11:18450131 | G | C | 1 | a0001c0001t0001g0070 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.835-832G>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | chr11 | 18450131 | |||||||
| chr11:18450399 | C | G | 1 | a0001c0001t0001g0089 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.835-564C>G | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | chr11 | 18450399 | |||||||
| chr11:18450473 | G | T | 2 | a0004c0005t0007g0015 a0004c0005t0007g0016 |
2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.835-490G>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | chr11 | 18450473 | |||||||
| chr11:18450586 | G | A | 85 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0018 others(82): Show |
90 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.835-377G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | chr11 | 18450586 | |||||||
| chr11:18450787 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.835-176C>T | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | chr11 | 18450787 | |||||||
| chr11:18450852 | G | A | 1 | a0001c0001t0001g0283 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.835-111G>A | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | chr11 | 18450852 | |||||||
| chr11:18450889 | T | C | 4 | a0001c0001t0002g0241 a0001c0001t0002g0259 a0001c0001t0002g0261 others(1): Show |
4 | HG02257.hp1 HG02486.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.835-74T>C | LDHC | ENSG00000166796.12 | transcript | ENST00000541669.6 | protein_coding | 7/7 | chr11 | 18450889 |