Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 84946 |
| ensemblid | ENSG00000135521.9 |
| hgncid | 21173 |
| symbol | LTV1 |
| name | LTV1 ribosome biogenesis factor |
| refseq_nuc | NM_032860.5 |
| refseq_prot | NP_116249.2 |
| ensembl_nuc | ENST00000367576.6 |
| ensembl_prot | ENSP00000356548.5 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 143843338 |
| end | 143863812 |
| strand | + |
| ver | v1.2 |
| region | chr6:143843338-143863812 |
| region5000 | chr6:143838338-143868812 |
| regionname0 | LTV1_chr6_143843338_143863812 |
| regionname5000 | LTV1_chr6_143838338_143868812 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 475 | 405 | 87 | 68 | 198 | 6 | 46 | 152 | LTV1_chr6_143838338_143868812 | LTV1 | MPHRK others(470): Show |
chr6 | 143838338 | 143868812 |
| a0002 | 0/0 | 475 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | MPHRK others(470): Show |
chr6 | 143838338 | 143868812 |
| a0003 | 0/0 | 475 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | MPHRK others(470): Show |
chr6 | 143838338 | 143868812 |
| a0004 | 0/0 | 475 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | MPHRK others(470): Show |
chr6 | 143838338 | 143868812 |
| a0005 | 0/0 | 475 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LTV1_chr6_143838338_143868812 | LTV1 | MPHRK others(470): Show |
chr6 | 143838338 | 143868812 |
| a0006 | 0/0 | 283 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LTV1_chr6_143838338_143868812 | LTV1 | MPHRK others(278): Show |
chr6 | 143838338 | 143868812 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1425 | 357 | 54 | 61 | 193 | 6 | 43 | LTV1_chr6_143838338_143868812 | LTV1 | ATGCC others(1420): Show |
chr6 | 143838338 | 143868812 | ||
| a0001c0002 | 0/0 | 1425 | 22 | 19 | 3 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | ATGCC others(1420): Show |
chr6 | 143838338 | 143868812 | ||
| a0001c0003 | 0/0 | 1425 | 16 | 9 | 4 | 0 | 0 | 3 | LTV1_chr6_143838338_143868812 | LTV1 | ATGCC others(1420): Show |
chr6 | 143838338 | 143868812 | ||
| a0001c0004 | 0/0 | 1425 | 4 | 0 | 0 | 4 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | ATGCC others(1420): Show |
chr6 | 143838338 | 143868812 | ||
| a0001c0005 | 0/0 | 1425 | 3 | 3 | 0 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | ATGCC others(1420): Show |
chr6 | 143838338 | 143868812 | ||
| a0001c0007 | 0/0 | 1425 | 2 | 2 | 0 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | ATGCC others(1420): Show |
chr6 | 143838338 | 143868812 | ||
| a0001c0009 | 0/0 | 1425 | 1 | 0 | 0 | 1 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | ATGCC others(1420): Show |
chr6 | 143838338 | 143868812 | ||
| a0002c0006 | 0/0 | 1425 | 2 | 2 | 0 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | ATGCC others(1420): Show |
chr6 | 143838338 | 143868812 | ||
| a0003c0008 | 0/0 | 1425 | 2 | 2 | 0 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | ATGCC others(1420): Show |
chr6 | 143838338 | 143868812 | ||
| a0004c0011 | 0/0 | 1425 | 1 | 1 | 0 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | ATGCC others(1420): Show |
chr6 | 143838338 | 143868812 | ||
| a0005c0010 | 0/0 | 1425 | 1 | 0 | 0 | 1 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | ATGCC others(1420): Show |
chr6 | 143838338 | 143868812 | ||
| a0006c0012 | 0/0 | 1425 | 1 | 0 | 0 | 1 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | ATGCC others(1420): Show |
chr6 | 143838338 | 143868812 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1853 | 356 | 54 | 61 | 192 | 6 | 43 | LTV1_chr6_143838338_143868812 | LTV1 | GTGAC others(1848): Show |
chr6 | 143838338 | 143868812 |
| a0001c0001t0005 | 0/0 | 1853 | 1 | 0 | 0 | 1 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | GTGAC others(1848): Show |
chr6 | 143838338 | 143868812 |
| a0001c0002t0001 | 0/0 | 1853 | 13 | 10 | 3 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | GTGAC others(1848): Show |
chr6 | 143838338 | 143868812 |
| a0001c0002t0002 | 0/0 | 1853 | 8 | 8 | 0 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | GTGAC others(1848): Show |
chr6 | 143838338 | 143868812 |
| a0001c0002t0006 | 0/0 | 1853 | 1 | 1 | 0 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | GTGAC others(1848): Show |
chr6 | 143838338 | 143868812 |
| a0001c0003t0001 | 0/0 | 1853 | 16 | 9 | 4 | 0 | 0 | 3 | LTV1_chr6_143838338_143868812 | LTV1 | GTGAC others(1848): Show |
chr6 | 143838338 | 143868812 |
| a0001c0004t0001 | 0/0 | 1853 | 4 | 0 | 0 | 4 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | GTGAC others(1848): Show |
chr6 | 143838338 | 143868812 |
| a0001c0005t0001 | 0/0 | 1853 | 3 | 3 | 0 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | GTGAC others(1848): Show |
chr6 | 143838338 | 143868812 |
| a0001c0007t0001 | 0/0 | 1853 | 2 | 2 | 0 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | GTGAC others(1848): Show |
chr6 | 143838338 | 143868812 |
| a0001c0009t0001 | 0/0 | 1853 | 1 | 0 | 0 | 1 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | GTGAC others(1848): Show |
chr6 | 143838338 | 143868812 |
| a0002c0006t0003 | 0/0 | 1853 | 2 | 2 | 0 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | GCGAC others(1848): Show |
chr6 | 143838338 | 143868812 |
| a0003c0008t0004 | 0/0 | 1853 | 2 | 2 | 0 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | GTGAC others(1848): Show |
chr6 | 143838338 | 143868812 |
| a0004c0011t0001 | 0/0 | 1853 | 1 | 1 | 0 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | GTGAC others(1848): Show |
chr6 | 143838338 | 143868812 |
| a0005c0010t0001 | 0/0 | 1853 | 1 | 0 | 0 | 1 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | GTGAC others(1848): Show |
chr6 | 143838338 | 143868812 |
| a0006c0012t0001 | 0/0 | 1853 | 1 | 0 | 0 | 1 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | GTGAC others(1848): Show |
chr6 | 143838338 | 143868812 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 94 | 7 | 26 | 43 | 1 | 17 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0002 | 0/0 | 46 | 0 | 5 | 34 | 1 | 6 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0003 | 0/0 | 26 | 0 | 2 | 24 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0004 | 0/0 | 23 | 0 | 0 | 16 | 1 | 6 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0005 | 0/0 | 15 | 1 | 8 | 5 | 0 | 1 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0007 | 0/0 | 9 | 9 | 0 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0008 | 0/0 | 8 | 0 | 0 | 7 | 0 | 1 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0009 | 0/0 | 8 | 0 | 4 | 0 | 2 | 2 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0010 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0014 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0016 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0001t0005g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0002t0001g0006 | 0/0 | 11 | 10 | 1 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0002t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0002t0002g0012 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0002t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0002t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0002t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0002t0006g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0003t0001g0018 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0003t0001g0019 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0003t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0003t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0003t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0003t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0003t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0003t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0003t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0003t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0003t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0004t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0005t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0005t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0007t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0007t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0001c0009t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0002c0006t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0002c0006t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0003c0008t0004g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0003c0008t0004g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0004c0011t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0005c0010t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| a0006c0012t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0118 | EUR | GBR | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | GBR | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG00438 | hp2 | a0001 | c0004 | t0001 | g0001 | EAS | CHS | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | CHS | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG00733 | hp2 | a0001 | c0003 | t0001 | g0018 | AMR | PUR | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG01070 | hp1 | a0001 | c0003 | t0001 | g0018 | AMR | PUR | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0030 | AMR | PUR | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0030 | AMR | PUR | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG01256 | hp2 | a0001 | c0003 | t0001 | g0019 | AMR | CLM | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG01258 | hp2 | a0001 | c0003 | t0001 | g0019 | AMR | CLM | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG01884 | hp1 | a0002 | c0006 | t0003 | g0042 | AFR | ACB | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PEL | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02040 | hp2 | a0001 | c0004 | t0001 | g0001 | EAS | KHV | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02055 | hp2 | a0004 | c0011 | t0001 | g0110 | AFR | ACB | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02056 | hp1 | a0001 | c0004 | t0001 | g0001 | EAS | KHV | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02074 | hp2 | a0001 | c0004 | t0001 | g0001 | EAS | KHV | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02145 | hp1 | a0001 | c0003 | t0001 | g0045 | AFR | ACB | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | CDX | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | CDX | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CDX | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02257 | hp2 | a0001 | c0003 | t0001 | g0019 | AFR | ACB | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02258 | hp1 | a0001 | c0007 | t0001 | g0040 | AFR | ACB | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02523 | hp2 | a0001 | c0001 | t0005 | g0097 | EAS | KHV | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02572 | hp1 | a0001 | c0002 | t0002 | g0012 | AFR | GWD | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02572 | hp2 | a0001 | c0003 | t0001 | g0049 | AFR | GWD | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02602 | hp1 | a0001 | c0003 | t0001 | g0046 | SAS | PJL | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02615 | hp2 | a0001 | c0002 | t0002 | g0107 | AFR | GWD | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0006 | AFR | GWD | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02630 | hp2 | a0001 | c0002 | t0006 | g0086 | AFR | GWD | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02647 | hp1 | a0001 | c0003 | t0001 | g0052 | AFR | GWD | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02717 | hp2 | a0001 | c0002 | t0002 | g0012 | AFR | GWD | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0006 | AFR | GWD | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02809 | hp1 | a0001 | c0003 | t0001 | g0044 | AFR | GWD | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02809 | hp2 | a0001 | c0002 | t0002 | g0012 | AFR | GWD | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02818 | hp2 | a0001 | c0007 | t0001 | g0119 | AFR | GWD | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02886 | hp1 | a0001 | c0002 | t0002 | g0012 | AFR | GWD | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0006 | AFR | GWD | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0006 | AFR | GWD | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02965 | hp2 | a0003 | c0008 | t0004 | g0106 | AFR | ESN | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02976 | hp1 | a0001 | c0003 | t0001 | g0043 | AFR | ESN | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0006 | AFR | GWD | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG03098 | hp1 | a0001 | c0005 | t0001 | g0024 | AFR | MSL | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG03139 | hp1 | a0001 | c0003 | t0001 | g0048 | AFR | ESN | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ESN | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG03195 | hp1 | a0001 | c0005 | t0001 | g0024 | AFR | ESN | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG03195 | hp2 | a0001 | c0003 | t0001 | g0047 | AFR | ESN | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | MSL | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG03225 | hp2 | a0001 | c0005 | t0001 | g0053 | AFR | MSL | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0006 | AFR | MSL | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | MSL | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG03516 | hp1 | a0001 | c0002 | t0002 | g0037 | AFR | ESN | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG03516 | hp2 | a0002 | c0006 | t0003 | g0041 | AFR | ESN | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0012 | AFR | GWD | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG03579 | hp1 | a0003 | c0008 | t0004 | g0037 | AFR | MSL | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0006 | AFR | MSL | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG03654 | hp2 | a0001 | c0003 | t0001 | g0051 | SAS | PJL | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | BEB | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | BEB | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG03942 | hp2 | a0001 | c0003 | t0001 | g0018 | SAS | BEB | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | STU | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | BEB | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | STU | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | STU | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0006 | AFR | YRI | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | YRI | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | CHB | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | YRI | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18944 | hp2 | a0001 | c0009 | t0001 | g0011 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18953 | hp1 | a0005 | c0010 | t0001 | g0026 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18971 | hp2 | a0006 | c0012 | t0001 | g0013 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | LWK | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0006 | AFR | YRI | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | YRI | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ASW | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | TSI | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | CLM | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0006 | AFR | ACB | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG03471 | hp2 | a0001 | c0003 | t0001 | g0050 | AFR | MSL | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG06807 | hp1 | a0001 | c0002 | t0002 | g0117 | AFR | USA | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | USA | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | USA | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | LWK | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | LWK | LTV1_chr6_143838338_143868812 | LTV1 | chr6 | 143838338 | 143868812 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:143857814 | A | G | 1 | a0003 | 2 | HG02965.hp2 HG03579.hp1 |
missense_variant | MODERATE | c.602A>G | p.Asn201Ser | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 6/11 | 742/1853 | 602/1428 | 201/475 | chr6 | 143857814 | |||
| chr6:143857904 | T | G | 1 | a0002 | 2 | HG01884.hp1 HG03516.hp2 |
missense_variant | MODERATE | c.692T>G | p.Phe231Cys | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 6/11 | 832/1853 | 692/1428 | 231/475 | chr6 | 143857904 | |||
| chr6:143860480 | G | T | 1 | a0006 | 1 | NA18971.hp2 | stop_gained | HIGH | c.850G>T | p.Glu284* | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 7/11 | 990/1853 | 850/1428 | 284/475 | chr6 | 143860480 | |||
| chr6:143862109 | T | C | 1 | a0005 | 1 | NA18953.hp1 | missense_variant | MODERATE | c.929T>C | p.Val310Ala | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 8/11 | 1069/1853 | 929/1428 | 310/475 | chr6 | 143862109 | |||
| chr6:143862214 | A | G | 1 | a0004 | 1 | HG02055.hp2 | missense_variant | MODERATE | c.1034A>G | p.Lys345Arg | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 8/11 | 1174/1853 | 1034/1428 | 345/475 | chr6 | 143862214 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:143858007 | G | A | 1 | a0001c0004 | 4 | HG00438.hp2 HG02040.hp2 HG02056.hp1 others(1): Show |
splice_region_variant&synonymous_variant | LOW | c.795G>A | p.Lys265Lys | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 6/11 | 935/1853 | 795/1428 | 265/475 | chr6 | 143858007 | |||
| chr6:143860482 | A | G | 1 | a0001c0003 | 16 | HG00733.hp2 HG01070.hp1 HG01256.hp2 others(13): Show |
synonymous_variant | LOW | c.852A>G | p.Glu284Glu | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 7/11 | 992/1853 | 852/1428 | 284/475 | chr6 | 143860482 | |||
| chr6:143860512 | A | G | 1 | a0001c0005 | 3 | HG03098.hp1 HG03195.hp1 HG03225.hp2 |
synonymous_variant | LOW | c.882A>G | p.Leu294Leu | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 7/11 | 1022/1853 | 882/1428 | 294/475 | chr6 | 143860512 | |||
| chr6:143860545 | G | A | 1 | a0001c0009 | 1 | NA18944.hp2 | synonymous_variant | LOW | c.915G>A | p.Lys305Lys | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 7/11 | 1055/1853 | 915/1428 | 305/475 | chr6 | 143860545 | |||
| chr6:143862132 | T | C | 3 | a0001c0007 a0002c0006 a0004c0011 |
5 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(2): Show |
synonymous_variant | LOW | c.952T>C | p.Leu318Leu | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 8/11 | 1092/1853 | 952/1428 | 318/475 | chr6 | 143862132 | |||
| chr6:143862239 | T | C | 2 | a0001c0002 a0003c0008 |
24 | HG01099.hp1 HG01123.hp1 HG01192.hp2 others(21): Show |
synonymous_variant | LOW | c.1059T>C | p.Ile353Ile | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 8/11 | 1199/1853 | 1059/1428 | 353/475 | chr6 | 143862239 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:143843339 | T | C | 1 | a0002c0006t0003 | 2 | HG01884.hp1 HG03516.hp2 |
5_prime_UTR_variant | MODIFIER | c.-139T>C | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 1/11 | 139 | chr6 | 143843339 | ||||||
| chr6:143843374 | G | A | 1 | a0001c0001t0005 | 1 | HG02523.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-104G>A | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 1/11 | chr6 | 143843374 | |||||||
| chr6:143843449 | G | T | 1 | a0001c0002t0006 | 1 | HG02630.hp2 | 5_prime_UTR_variant | MODIFIER | c.-29G>T | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 1/11 | 29 | chr6 | 143843449 | ||||||
| chr6:143863562 | G | A | 1 | a0003c0008t0004 | 2 | HG02965.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*35G>A | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 11/11 | 35 | chr6 | 143863562 | ||||||
| chr6:143863807 | C | T | 2 | a0001c0002t0002 a0003c0008t0004 |
10 | HG02572.hp1 HG02615.hp2 HG02717.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*280C>T | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 11/11 | 280 | chr6 | 143863807 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:143843534 | A | G | 1 | a0001c0001t0001g0022 | 3 | HG02886.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3+54A>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 1/10 | chr6 | 143843534 | |||||||
| chr6:143843634 | G | C | 3 | a0001c0007t0001g0040 a0002c0006t0003g0041 a0002c0006t0003g0042 |
3 | HG01884.hp1 HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3+154G>C | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 1/10 | chr6 | 143843634 | |||||||
| chr6:143843659 | C | G | 1 | a0001c0001t0001g0122 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3+179C>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 1/10 | chr6 | 143843659 | |||||||
| chr6:143843758 | A | G | 5 | a0001c0001t0001g0016 a0001c0001t0001g0022 a0001c0001t0001g0039 others(2): Show |
11 | HG01081.hp1 HG02055.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.3+278A>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 1/10 | chr6 | 143843758 | |||||||
| chr6:143843912 | C | G | 2 | a0002c0006t0003g0041 a0002c0006t0003g0042 |
2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3+432C>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 1/10 | chr6 | 143843912 | |||||||
| chr6:143844108 | C | A | 3 | a0001c0001t0001g0022 a0001c0001t0001g0039 a0001c0001t0001g0120 |
6 | HG02055.hp1 HG02559.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.4-378C>A | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 1/10 | chr6 | 143844108 | |||||||
| chr6:143844156 | A | C | 4 | a0001c0007t0001g0040 a0001c0007t0001g0119 a0002c0006t0003g0041 others(1): Show |
4 | HG01884.hp1 HG02258.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.4-330A>C | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 1/10 | chr6 | 143844156 | |||||||
| chr6:143844663 | T | G | 1 | a0001c0001t0001g0017 | 3 | NA18983.hp2 NA19084.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.135+46T>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 2/10 | chr6 | 143844663 | |||||||
| chr6:143844672 | CT | C | 63 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(60): Show |
198 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.135+68delT | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr6 | 143844672 | ||||||
| chr6:143844685 | T | A | 1 | a0001c0001t0001g0023 | 2 | HG02451.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.135+68T>A | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 2/10 | chr6 | 143844685 | |||||||
| chr6:143844779 | A | C | 1 | a0001c0001t0001g0118 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.135+162A>C | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 2/10 | chr6 | 143844779 | |||||||
| chr6:143844805 | A | G | 1 | a0001c0002t0002g0117 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.135+188A>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 2/10 | chr6 | 143844805 | |||||||
| chr6:143844838 | T | G | 1 | a0001c0001t0001g0077 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.135+221T>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 2/10 | chr6 | 143844838 | |||||||
| chr6:143844966 | C | T | 4 | a0001c0007t0001g0040 a0001c0007t0001g0119 a0002c0006t0003g0041 others(1): Show |
4 | HG01884.hp1 HG02258.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+349C>T | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 2/10 | chr6 | 143844966 | |||||||
| chr6:143844969 | G | T | 4 | a0001c0007t0001g0040 a0001c0007t0001g0119 a0002c0006t0003g0041 others(1): Show |
4 | HG01884.hp1 HG02258.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+352G>T | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 2/10 | chr6 | 143844969 | |||||||
| chr6:143845020 | C | T | 1 | a0001c0001t0001g0016 | 4 | HG01081.hp1 HG02258.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+403C>T | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 2/10 | chr6 | 143845020 | |||||||
| chr6:143845022 | G | T | 2 | a0001c0001t0001g0021 a0001c0001t0001g0076 |
4 | HG02109.hp2 HG02818.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+405G>T | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 2/10 | chr6 | 143845022 | |||||||
| chr6:143845079 | G | C | 15 | a0001c0001t0001g0023 a0001c0003t0001g0018 a0001c0003t0001g0019 others(12): Show |
21 | HG00733.hp2 HG01070.hp1 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.135+462G>C | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 2/10 | chr6 | 143845079 | |||||||
| chr6:143845115 | C | G | 4 | a0001c0007t0001g0040 a0001c0007t0001g0119 a0002c0006t0003g0041 others(1): Show |
4 | HG01884.hp1 HG02258.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+498C>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 2/10 | chr6 | 143845115 | |||||||
| chr6:143845136 | A | G | 3 | a0001c0001t0001g0023 a0001c0005t0001g0024 a0001c0005t0001g0053 |
5 | HG02451.hp2 HG02615.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.135+519A>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 2/10 | chr6 | 143845136 | |||||||
| chr6:143845345 | GA | G | 12 | a0001c0003t0001g0018 a0001c0003t0001g0019 a0001c0003t0001g0043 others(9): Show |
16 | HG00733.hp2 HG01070.hp1 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.136-705delA | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 2/10 | chr6 | 143845345 | |||||||
| chr6:143845372 | A | G | 1 | a0001c0001t0001g0116 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.136-679A>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 2/10 | chr6 | 143845372 | |||||||
| chr6:143845398 | G | A | 4 | a0001c0001t0001g0005 a0001c0001t0001g0054 a0001c0001t0001g0055 others(1): Show |
18 | HG01106.hp1 HG01358.hp1 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.136-653G>A | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 2/10 | chr6 | 143845398 | |||||||
| chr6:143845578 | A | G | 1 | a0001c0001t0001g0115 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.136-473A>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 2/10 | chr6 | 143845578 | |||||||
| chr6:143845636 | C | T | 1 | a0001c0001t0001g0114 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.136-415C>T | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 2/10 | chr6 | 143845636 | |||||||
| chr6:143845677 | C | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0078 a0001c0001t0001g0079 |
11 | HG02145.hp2 HG02647.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.136-374C>A | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 2/10 | chr6 | 143845677 | |||||||
| chr6:143845684 | G | A | 58 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(55): Show |
193 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.136-367G>A | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 2/10 | chr6 | 143845684 | |||||||
| chr6:143845767 | A | G | 3 | a0001c0001t0001g0038 a0001c0001t0001g0112 a0001c0001t0001g0113 |
4 | HG00738.hp1 HG02698.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-284A>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 2/10 | chr6 | 143845767 | |||||||
| chr6:143845880 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.136-171G>A | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 2/10 | chr6 | 143845880 | |||||||
| chr6:143845988 | G | A | 2 | a0001c0001t0001g0010 a0001c0001t0001g0057 |
7 | HG02165.hp2 NA18959.hp1 NA18979.hp2 others(4): Show |
intron_variant | MODIFIER | c.136-63G>A | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 2/10 | chr6 | 143845988 | |||||||
| chr6:143846300 | A | G | 1 | a0001c0001t0001g0073 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.309+76A>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 3/10 | chr6 | 143846300 | |||||||
| chr6:143846340 | G | A | 53 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(50): Show |
174 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.309+116G>A | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 3/10 | chr6 | 143846340 | |||||||
| chr6:143846376 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.309+152A>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 3/10 | chr6 | 143846376 | |||||||
| chr6:143846469 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.309+245A>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 3/10 | chr6 | 143846469 | |||||||
| chr6:143846479 | TAGAC | T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0078 a0001c0001t0001g0079 |
11 | HG02145.hp2 HG02647.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.309+258_309+261del others(4): Show |
LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr6 | 143846479 | ||||||
| chr6:143846497 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.309+273A>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 3/10 | chr6 | 143846497 | |||||||
| chr6:143846694 | C | T | 1 | a0001c0001t0001g0021 | 3 | HG02109.hp2 HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.309+470C>T | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 3/10 | chr6 | 143846694 | |||||||
| chr6:143846701 | A | G | 5 | a0001c0007t0001g0040 a0001c0007t0001g0119 a0002c0006t0003g0041 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.309+477A>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 3/10 | chr6 | 143846701 | |||||||
| chr6:143846731 | C | T | 2 | a0001c0001t0001g0015 a0001c0001t0001g0109 |
5 | HG02280.hp2 HG02622.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.309+507C>T | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 3/10 | chr6 | 143846731 | |||||||
| chr6:143846792 | G | C | 1 | a0001c0001t0001g0082 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.309+568G>C | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 3/10 | chr6 | 143846792 | |||||||
| chr6:143846906 | G | T | 1 | a0001c0001t0001g0108 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.309+682G>T | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 3/10 | chr6 | 143846906 | |||||||
| chr6:143846936 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.309+712G>A | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 3/10 | chr6 | 143846936 | |||||||
| chr6:143847454 | C | T | 1 | a0001c0001t0001g0029 | 2 | NA18940.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.309+1230C>T | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 3/10 | chr6 | 143847454 | |||||||
| chr6:143847522 | C | T | 5 | a0001c0007t0001g0040 a0001c0007t0001g0119 a0002c0006t0003g0041 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.309+1298C>T | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 3/10 | chr6 | 143847522 | |||||||
| chr6:143847561 | G | A | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG02109.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.309+1337G>A | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 3/10 | chr6 | 143847561 | |||||||
| chr6:143847653 | G | C | 2 | a0001c0007t0001g0040 a0001c0007t0001g0119 |
2 | HG02258.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.309+1429G>C | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 3/10 | chr6 | 143847653 | |||||||
| chr6:143847698 | TAAAAGCA others(3): Show |
T | 1 | a0001c0001t0001g0070 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.309+1476_309+1485d others(12): Show |
LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr6 | 143847698 | ||||||
| chr6:143847940 | A | G | 64 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(61): Show |
203 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.309+1716A>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 3/10 | chr6 | 143847940 | |||||||
| chr6:143847957 | T | C | 7 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0054 others(4): Show |
23 | HG01106.hp1 HG01358.hp1 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.309+1733T>C | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 3/10 | chr6 | 143847957 | |||||||
| chr6:143848159 | A | C | 3 | a0001c0001t0001g0023 a0001c0005t0001g0024 a0001c0005t0001g0053 |
5 | HG02451.hp2 HG02615.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.309+1935A>C | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 3/10 | chr6 | 143848159 | |||||||
| chr6:143848159 | A | G | 5 | a0001c0007t0001g0040 a0001c0007t0001g0119 a0002c0006t0003g0041 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.309+1935A>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 3/10 | chr6 | 143848159 | |||||||
| chr6:143848218 | A | G | 1 | a0001c0001t0001g0021 | 3 | HG02109.hp2 HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.310-1913A>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 3/10 | chr6 | 143848218 | |||||||
| chr6:143848317 | T | C | 1 | a0001c0001t0001g0021 | 3 | HG02109.hp2 HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.310-1814T>C | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 3/10 | chr6 | 143848317 | |||||||
| chr6:143848321 | C | T | 11 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0022 others(8): Show |
40 | HG00140.hp1 HG00673.hp2 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.310-1810C>T | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 3/10 | chr6 | 143848321 | |||||||
| chr6:143848360 | G | A | 1 | a0004c0011t0001g0110 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.310-1771G>A | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 3/10 | chr6 | 143848360 | |||||||
| chr6:143848378 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.310-1753T>C | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 3/10 | chr6 | 143848378 | |||||||
| chr6:143848463 | A | C | 1 | a0001c0001t0001g0028 | 2 | HG00621.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.310-1668A>C | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 3/10 | chr6 | 143848463 | |||||||
| chr6:143848532 | A | G | 1 | a0001c0001t0001g0021 | 3 | HG02109.hp2 HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.310-1599A>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 3/10 | chr6 | 143848532 | |||||||
| chr6:143848572 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.310-1559G>A | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 3/10 | chr6 | 143848572 | |||||||
| chr6:143848615 | T | G | 1 | a0001c0001t0001g0061 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.310-1516T>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 3/10 | chr6 | 143848615 | |||||||
| chr6:143848722 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.310-1409G>A | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 3/10 | chr6 | 143848722 | |||||||
| chr6:143848870 | C | G | 4 | a0001c0007t0001g0040 a0001c0007t0001g0119 a0002c0006t0003g0041 others(1): Show |
4 | HG01884.hp1 HG02258.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.310-1261C>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 3/10 | chr6 | 143848870 | |||||||
| chr6:143848903 | C | T | 1 | a0004c0011t0001g0110 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.310-1228C>T | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 3/10 | chr6 | 143848903 | |||||||
| chr6:143848933 | A | G | 2 | a0002c0006t0003g0041 a0002c0006t0003g0042 |
2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.310-1198A>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 3/10 | chr6 | 143848933 | |||||||
| chr6:143848967 | A | G | 2 | a0001c0001t0001g0036 a0001c0001t0001g0105 |
3 | NA18963.hp2 NA18984.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.310-1164A>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 3/10 | chr6 | 143848967 | |||||||
| chr6:143849142 | A | G | 1 | a0001c0001t0001g0104 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.310-989A>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 3/10 | chr6 | 143849142 | |||||||
| chr6:143849366 | T | A | 61 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(58): Show |
196 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.310-765T>A | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 3/10 | chr6 | 143849366 | |||||||
| chr6:143849638 | G | A | 7 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0066 others(4): Show |
30 | HG00140.hp1 HG00673.hp2 HG01256.hp1 others(27): Show |
intron_variant | MODIFIER | c.310-493G>A | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 3/10 | chr6 | 143849638 | |||||||
| chr6:143849647 | C | T | 2 | a0002c0006t0003g0041 a0002c0006t0003g0042 |
2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.310-484C>T | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 3/10 | chr6 | 143849647 | |||||||
| chr6:143849965 | CATGGTCC others(21): Show |
C | 4 | a0001c0001t0001g0013 a0001c0001t0001g0077 a0001c0001t0001g0084 others(1): Show |
6 | HG00673.hp1 NA18966.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.310-164_310-137del others(28): Show |
LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr6 | 143849965 | ||||||
| chr6:143849980 | C | A | 1 | a0001c0001t0001g0021 | 3 | HG02109.hp2 HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.310-151C>A | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 3/10 | chr6 | 143849980 | |||||||
| chr6:143850070 | G | A | 3 | a0001c0001t0001g0025 a0001c0007t0001g0040 a0001c0007t0001g0119 |
4 | HG02135.hp1 HG02258.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.310-61G>A | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 3/10 | chr6 | 143850070 | |||||||
| chr6:143850100 | A | C | 1 | a0001c0001t0001g0103 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.310-31A>C | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 3/10 | chr6 | 143850100 | |||||||
| chr6:143850105 | A | T | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 |
3 | HG02109.hp1 HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.310-26A>T | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 3/10 | chr6 | 143850105 | |||||||
| chr6:143850110 | T | C | 4 | a0001c0007t0001g0040 a0001c0007t0001g0119 a0002c0006t0003g0041 others(1): Show |
4 | HG01884.hp1 HG02258.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.310-21T>C | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 3/10 | chr6 | 143850110 | |||||||
| chr6:143850230 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.397+12T>C | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143850230 | |||||||
| chr6:143850264 | C | A | 12 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0022 others(9): Show |
41 | HG00140.hp1 HG00673.hp2 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.397+46C>A | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143850264 | |||||||
| chr6:143850483 | T | G | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 |
3 | HG02109.hp1 HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.397+265T>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143850483 | |||||||
| chr6:143850553 | C | A | 1 | a0001c0001t0001g0085 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.397+335C>A | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143850553 | |||||||
| chr6:143850569 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.397+351C>T | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143850569 | |||||||
| chr6:143850720 | A | G | 1 | a0001c0001t0001g0069 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.397+502A>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143850720 | |||||||
| chr6:143850764 | A | C | 1 | a0002c0006t0003g0042 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.397+546A>C | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143850764 | |||||||
| chr6:143850894 | A | C | 4 | a0001c0001t0001g0005 a0001c0001t0001g0054 a0001c0001t0001g0055 others(1): Show |
18 | HG01106.hp1 HG01358.hp1 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.397+676A>C | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143850894 | |||||||
| chr6:143850917 | T | A | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 |
3 | HG02109.hp1 HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.397+699T>A | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143850917 | |||||||
| chr6:143850945 | A | C | 65 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(62): Show |
208 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.397+727A>C | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143850945 | |||||||
| chr6:143851037 | T | G | 3 | a0001c0001t0001g0007 a0001c0001t0001g0078 a0001c0001t0001g0079 |
11 | HG02145.hp2 HG02647.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.397+819T>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143851037 | |||||||
| chr6:143851043 | C | A | 1 | a0001c0001t0001g0054 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.397+825C>A | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143851043 | |||||||
| chr6:143851194 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.397+976T>C | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143851194 | |||||||
| chr6:143851327 | T | G | 3 | a0001c0002t0001g0006 a0001c0002t0001g0030 a0001c0002t0006g0086 |
14 | HG01099.hp1 HG01123.hp1 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.397+1109T>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143851327 | |||||||
| chr6:143851379 | G | A | 10 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0017 others(7): Show |
21 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(18): Show |
intron_variant | MODIFIER | c.397+1161G>A | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143851379 | |||||||
| chr6:143851379 | G | T | 4 | a0001c0007t0001g0040 a0001c0007t0001g0119 a0002c0006t0003g0041 others(1): Show |
4 | HG01884.hp1 HG02258.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.397+1161G>T | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143851379 | |||||||
| chr6:143851423 | C | CATTT | 66 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(63): Show |
209 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.397+1205_397+1206i others(6): Show |
LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143851423 | |||||||
| chr6:143851586 | T | A | 5 | a0001c0007t0001g0040 a0001c0007t0001g0119 a0002c0006t0003g0041 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.397+1368T>A | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143851586 | |||||||
| chr6:143851630 | G | T | 1 | a0001c0001t0001g0105 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.397+1412G>T | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143851630 | |||||||
| chr6:143851794 | A | C | 1 | a0001c0001t0001g0102 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.397+1576A>C | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143851794 | |||||||
| chr6:143851816 | A | G | 3 | a0001c0001t0001g0038 a0001c0001t0001g0112 a0001c0001t0001g0113 |
4 | HG00738.hp1 HG02698.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.397+1598A>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143851816 | |||||||
| chr6:143852075 | T | C | 1 | a0001c0001t0001g0081 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.397+1857T>C | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143852075 | |||||||
| chr6:143852078 | G | A | 3 | a0001c0001t0001g0023 a0001c0005t0001g0024 a0001c0005t0001g0053 |
5 | HG02451.hp2 HG02615.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.397+1860G>A | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143852078 | |||||||
| chr6:143852101 | G | T | 12 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0022 others(9): Show |
41 | HG00140.hp1 HG00673.hp2 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.397+1883G>T | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143852101 | |||||||
| chr6:143852143 | C | T | 1 | a0001c0001t0001g0101 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.397+1925C>T | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143852143 | |||||||
| chr6:143852180 | A | G | 1 | a0001c0001t0001g0082 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.397+1962A>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143852180 | |||||||
| chr6:143852215 | C | A | 38 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(35): Show |
130 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(127): Show |
intron_variant | MODIFIER | c.397+1997C>A | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143852215 | |||||||
| chr6:143852247 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.397+2029C>T | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143852247 | |||||||
| chr6:143852267 | T | C | 3 | a0001c0001t0001g0023 a0001c0005t0001g0024 a0001c0005t0001g0053 |
5 | HG02451.hp2 HG02615.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.397+2049T>C | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143852267 | |||||||
| chr6:143852331 | T | G | 12 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0022 others(9): Show |
41 | HG00140.hp1 HG00673.hp2 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.397+2113T>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143852331 | |||||||
| chr6:143852411 | A | G | 1 | a0001c0001t0001g0079 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.397+2193A>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143852411 | |||||||
| chr6:143852512 | G | A | 3 | a0001c0001t0001g0023 a0001c0005t0001g0024 a0001c0005t0001g0053 |
5 | HG02451.hp2 HG02615.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.397+2294G>A | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143852512 | |||||||
| chr6:143852518 | T | C | 5 | a0001c0007t0001g0040 a0001c0007t0001g0119 a0002c0006t0003g0041 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.397+2300T>C | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143852518 | |||||||
| chr6:143852696 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.397+2478T>C | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143852696 | |||||||
| chr6:143852763 | G | T | 3 | a0001c0001t0001g0038 a0001c0001t0001g0112 a0001c0001t0001g0113 |
4 | HG00738.hp1 HG02698.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.397+2545G>T | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143852763 | |||||||
| chr6:143852785 | A | G | 1 | a0001c0001t0001g0035 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.397+2567A>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143852785 | |||||||
| chr6:143852823 | G | A | 4 | a0001c0007t0001g0040 a0001c0007t0001g0119 a0002c0006t0003g0041 others(1): Show |
4 | HG01884.hp1 HG02258.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.397+2605G>A | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143852823 | |||||||
| chr6:143852837 | A | G | 21 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(18): Show |
105 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(102): Show |
intron_variant | MODIFIER | c.397+2619A>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143852837 | |||||||
| chr6:143853307 | A | G | 1 | a0001c0001t0001g0060 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.397+3089A>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143853307 | |||||||
| chr6:143853546 | C | T | 6 | a0001c0001t0001g0100 a0001c0007t0001g0040 a0001c0007t0001g0119 others(3): Show |
6 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.397+3328C>T | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143853546 | |||||||
| chr6:143853657 | T | G | 1 | a0004c0011t0001g0110 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.397+3439T>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143853657 | |||||||
| chr6:143853675 | T | C | 4 | a0001c0001t0001g0005 a0001c0001t0001g0054 a0001c0001t0001g0055 others(1): Show |
18 | HG01106.hp1 HG01358.hp1 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.397+3457T>C | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143853675 | |||||||
| chr6:143853682 | G | T | 2 | a0001c0007t0001g0040 a0001c0007t0001g0119 |
2 | HG02258.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.397+3464G>T | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143853682 | |||||||
| chr6:143853763 | G | C | 1 | a0001c0001t0001g0084 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.398-3540G>C | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143853763 | |||||||
| chr6:143853988 | C | G | 4 | a0001c0001t0001g0005 a0001c0001t0001g0054 a0001c0001t0001g0055 others(1): Show |
18 | HG01106.hp1 HG01358.hp1 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.398-3315C>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143853988 | |||||||
| chr6:143854023 | G | A | 126 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(123): Show |
410 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(407): Show |
intron_variant | MODIFIER | c.398-3280G>A | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143854023 | |||||||
| chr6:143854112 | T | A | 12 | a0001c0003t0001g0018 a0001c0003t0001g0019 a0001c0003t0001g0043 others(9): Show |
16 | HG00733.hp2 HG01070.hp1 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.398-3191T>A | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143854112 | |||||||
| chr6:143854206 | A | G | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 |
3 | HG02109.hp1 HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.398-3097A>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143854206 | |||||||
| chr6:143854285 | C | T | 2 | a0001c0001t0001g0098 a0001c0001t0001g0099 |
2 | HG01106.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.398-3018C>T | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143854285 | |||||||
| chr6:143854374 | A | G | 7 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0027 others(4): Show |
36 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.398-2929A>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143854374 | |||||||
| chr6:143854435 | G | A | 1 | a0001c0001t0001g0087 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.398-2868G>A | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143854435 | |||||||
| chr6:143854476 | C | G | 12 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0022 others(9): Show |
41 | HG00140.hp1 HG00673.hp2 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.398-2827C>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143854476 | |||||||
| chr6:143854665 | C | T | 1 | a0001c0003t0001g0052 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.398-2638C>T | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143854665 | |||||||
| chr6:143854669 | G | T | 1 | a0001c0001t0001g0021 | 3 | HG02109.hp2 HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.398-2634G>T | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143854669 | |||||||
| chr6:143854707 | C | A | 61 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(58): Show |
196 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.398-2596C>A | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143854707 | |||||||
| chr6:143854773 | A | T | 5 | a0001c0007t0001g0040 a0001c0007t0001g0119 a0002c0006t0003g0041 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.398-2530A>T | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143854773 | |||||||
| chr6:143854944 | C | T | 3 | a0001c0001t0001g0023 a0001c0005t0001g0024 a0001c0005t0001g0053 |
5 | HG02451.hp2 HG02615.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.398-2359C>T | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143854944 | |||||||
| chr6:143855017 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.398-2286C>T | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143855017 | |||||||
| chr6:143855095 | G | T | 1 | a0001c0001t0001g0120 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.398-2208G>T | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143855095 | |||||||
| chr6:143855129 | C | G | 3 | a0001c0002t0001g0006 a0001c0002t0001g0030 a0001c0002t0006g0086 |
14 | HG01099.hp1 HG01123.hp1 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.398-2174C>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143855129 | |||||||
| chr6:143855336 | G | A | 1 | a0001c0001t0001g0055 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.398-1967G>A | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143855336 | |||||||
| chr6:143855379 | G | A | 4 | a0001c0001t0001g0005 a0001c0001t0001g0054 a0001c0001t0001g0055 others(1): Show |
18 | HG01106.hp1 HG01358.hp1 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.398-1924G>A | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143855379 | |||||||
| chr6:143855511 | A | G | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 |
3 | HG02109.hp1 HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.398-1792A>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143855511 | |||||||
| chr6:143855518 | T | G | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 |
3 | HG02109.hp1 HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.398-1785T>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143855518 | |||||||
| chr6:143855580 | C | G | 1 | a0001c0001t0001g0089 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.398-1723C>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143855580 | |||||||
| chr6:143855790 | T | C | 4 | a0001c0001t0001g0005 a0001c0001t0001g0054 a0001c0001t0001g0055 others(1): Show |
18 | HG01106.hp1 HG01358.hp1 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.398-1513T>C | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143855790 | |||||||
| chr6:143855792 | C | T | 2 | a0001c0003t0001g0019 a0001c0003t0001g0051 |
4 | HG01256.hp2 HG01258.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.398-1511C>T | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143855792 | |||||||
| chr6:143855947 | C | T | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 |
3 | HG02109.hp1 HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.398-1356C>T | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143855947 | |||||||
| chr6:143855954 | G | GTGTTCTC others(5): Show |
65 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(62): Show |
208 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.398-1348_398-1347i others(14): Show |
LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 143855954 | ||||||
| chr6:143855979 | T | C | 12 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0022 others(9): Show |
41 | HG00140.hp1 HG00673.hp2 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.398-1324T>C | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143855979 | |||||||
| chr6:143856009 | A | G | 7 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0066 others(4): Show |
30 | HG00140.hp1 HG00673.hp2 HG01256.hp1 others(27): Show |
intron_variant | MODIFIER | c.398-1294A>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143856009 | |||||||
| chr6:143856087 | G | T | 1 | a0001c0001t0001g0065 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.398-1216G>T | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143856087 | |||||||
| chr6:143856158 | G | A | 1 | a0001c0001t0001g0014 | 4 | HG01433.hp1 HG02559.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.398-1145G>A | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143856158 | |||||||
| chr6:143856328 | A | G | 1 | a0001c0002t0002g0107 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.398-975A>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143856328 | |||||||
| chr6:143856450 | G | A | 5 | a0001c0007t0001g0040 a0001c0007t0001g0119 a0002c0006t0003g0041 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.398-853G>A | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143856450 | |||||||
| chr6:143856456 | T | G | 4 | a0001c0007t0001g0040 a0001c0007t0001g0119 a0002c0006t0003g0041 others(1): Show |
4 | HG01884.hp1 HG02258.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.398-847T>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143856456 | |||||||
| chr6:143856527 | G | C | 1 | a0001c0001t0001g0102 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.398-776G>C | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143856527 | |||||||
| chr6:143856578 | A | G | 1 | a0001c0001t0001g0021 | 3 | HG02109.hp2 HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.398-725A>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143856578 | |||||||
| chr6:143856585 | G | T | 1 | a0001c0001t0001g0116 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.398-718G>T | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143856585 | |||||||
| chr6:143856647 | A | T | 1 | a0001c0001t0001g0021 | 3 | HG02109.hp2 HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.398-656A>T | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143856647 | |||||||
| chr6:143856655 | C | T | 1 | a0001c0001t0001g0088 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.398-648C>T | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143856655 | |||||||
| chr6:143856727 | G | A | 1 | a0001c0002t0006g0086 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.398-576G>A | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143856727 | |||||||
| chr6:143856727 | G | C | 66 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(63): Show |
209 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.398-576G>C | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143856727 | |||||||
| chr6:143856828 | G | A | 14 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0022 others(11): Show |
44 | HG00140.hp1 HG00673.hp2 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.398-475G>A | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143856828 | |||||||
| chr6:143856855 | A | G | 1 | a0001c0001t0005g0097 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.398-448A>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143856855 | |||||||
| chr6:143856975 | C | T | 7 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0066 others(4): Show |
30 | HG00140.hp1 HG00673.hp2 HG01256.hp1 others(27): Show |
intron_variant | MODIFIER | c.398-328C>T | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143856975 | |||||||
| chr6:143856993 | C | T | 5 | a0001c0001t0001g0033 a0001c0003t0001g0047 a0001c0003t0001g0048 others(2): Show |
6 | HG01981.hp2 HG02572.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.398-310C>T | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143856993 | |||||||
| chr6:143857197 | C | T | 1 | a0004c0011t0001g0110 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.398-106C>T | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143857197 | |||||||
| chr6:143857282 | T | C | 74 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(71): Show |
232 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.398-21T>C | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 4/10 | chr6 | 143857282 | |||||||
| chr6:143857520 | T | A | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 |
3 | HG02109.hp1 HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.539+76T>A | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 5/10 | chr6 | 143857520 | |||||||
| chr6:143858054 | T | A | 2 | a0002c0006t0003g0041 a0002c0006t0003g0042 |
2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.795+47T>A | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 6/10 | chr6 | 143858054 | |||||||
| chr6:143858199 | A | C | 1 | a0001c0001t0001g0079 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.795+192A>C | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 6/10 | chr6 | 143858199 | |||||||
| chr6:143858212 | G | A | 20 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(17): Show |
104 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(101): Show |
intron_variant | MODIFIER | c.795+205G>A | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 6/10 | chr6 | 143858212 | |||||||
| chr6:143858668 | A | G | 5 | a0001c0007t0001g0040 a0001c0007t0001g0119 a0002c0006t0003g0041 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.795+661A>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 6/10 | chr6 | 143858668 | |||||||
| chr6:143858690 | G | T | 4 | a0001c0001t0001g0005 a0001c0001t0001g0054 a0001c0001t0001g0055 others(1): Show |
18 | HG01106.hp1 HG01358.hp1 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.795+683G>T | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 6/10 | chr6 | 143858690 | |||||||
| chr6:143858728 | C | T | 15 | a0001c0001t0001g0023 a0001c0003t0001g0018 a0001c0003t0001g0019 others(12): Show |
21 | HG00733.hp2 HG01070.hp1 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.795+721C>T | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 6/10 | chr6 | 143858728 | |||||||
| chr6:143858856 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.795+849A>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 6/10 | chr6 | 143858856 | |||||||
| chr6:143859430 | A | C | 5 | a0001c0007t0001g0040 a0001c0007t0001g0119 a0002c0006t0003g0041 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.796-996A>C | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 6/10 | chr6 | 143859430 | |||||||
| chr6:143859581 | C | T | 2 | a0001c0001t0001g0098 a0001c0001t0005g0097 |
2 | HG02523.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.796-845C>T | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 6/10 | chr6 | 143859581 | |||||||
| chr6:143859626 | A | G | 1 | a0001c0001t0001g0069 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.796-800A>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 6/10 | chr6 | 143859626 | |||||||
| chr6:143859668 | C | A | 2 | a0001c0007t0001g0040 a0001c0007t0001g0119 |
2 | HG02258.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.796-758C>A | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 6/10 | chr6 | 143859668 | |||||||
| chr6:143859726 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.796-700A>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 6/10 | chr6 | 143859726 | |||||||
| chr6:143859840 | G | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0079 |
10 | HG02145.hp2 HG02647.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.796-586G>A | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 6/10 | chr6 | 143859840 | |||||||
| chr6:143859891 | C | G | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 |
3 | HG02109.hp1 HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.796-535C>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 6/10 | chr6 | 143859891 | |||||||
| chr6:143859939 | A | T | 1 | a0001c0001t0001g0096 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.796-487A>T | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 6/10 | chr6 | 143859939 | |||||||
| chr6:143860011 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.796-415G>A | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 6/10 | chr6 | 143860011 | |||||||
| chr6:143860065 | T | C | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 |
3 | HG02109.hp1 HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.796-361T>C | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 6/10 | chr6 | 143860065 | |||||||
| chr6:143860171 | G | C | 2 | a0001c0002t0002g0012 a0001c0002t0002g0107 |
6 | HG02572.hp1 HG02615.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.796-255G>C | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 6/10 | chr6 | 143860171 | |||||||
| chr6:143860179 | A | T | 2 | a0001c0002t0002g0012 a0001c0002t0002g0107 |
6 | HG02572.hp1 HG02615.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.796-247A>T | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 6/10 | chr6 | 143860179 | |||||||
| chr6:143860236 | A | C | 1 | a0001c0001t0001g0076 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.796-190A>C | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 6/10 | chr6 | 143860236 | |||||||
| chr6:143860372 | G | A | 1 | a0004c0011t0001g0110 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.796-54G>A | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 6/10 | chr6 | 143860372 | |||||||
| chr6:143860595 | T | A | 1 | a0001c0001t0001g0091 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.923+42T>A | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 7/10 | chr6 | 143860595 | |||||||
| chr6:143860664 | A | G | 1 | a0001c0001t0001g0064 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.923+111A>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 7/10 | chr6 | 143860664 | |||||||
| chr6:143860705 | A | G | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 |
3 | HG02109.hp1 HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.923+152A>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 7/10 | chr6 | 143860705 | |||||||
| chr6:143860721 | C | T | 1 | a0001c0005t0001g0053 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.923+168C>T | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 7/10 | chr6 | 143860721 | |||||||
| chr6:143860801 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.923+248G>A | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 7/10 | chr6 | 143860801 | |||||||
| chr6:143860815 | C | T | 74 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(71): Show |
232 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.923+262C>T | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 7/10 | chr6 | 143860815 | |||||||
| chr6:143860847 | C | T | 1 | a0001c0001t0001g0087 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.923+294C>T | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 7/10 | chr6 | 143860847 | |||||||
| chr6:143860868 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.923+315G>A | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 7/10 | chr6 | 143860868 | |||||||
| chr6:143860898 | A | AT | 9 | a0001c0001t0001g0026 a0001c0001t0001g0057 a0001c0001t0001g0095 others(6): Show |
9 | HG00639.hp1 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.923+360dupT | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr6 | 143860898 | ||||||
| chr6:143860898 | AT | A | 6 | a0001c0001t0001g0007 a0001c0001t0001g0063 a0001c0001t0001g0064 others(3): Show |
14 | HG02145.hp2 HG02647.hp2 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.923+360delT | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr6 | 143860898 | ||||||
| chr6:143860899 | T | A | 1 | a0001c0001t0001g0001 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.923+346T>A | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 7/10 | chr6 | 143860899 | |||||||
| chr6:143860982 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.923+429C>T | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 7/10 | chr6 | 143860982 | |||||||
| chr6:143861046 | A | G | 61 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(58): Show |
196 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.923+493A>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 7/10 | chr6 | 143861046 | |||||||
| chr6:143861049 | A | G | 5 | a0001c0007t0001g0040 a0001c0007t0001g0119 a0002c0006t0003g0041 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.923+496A>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 7/10 | chr6 | 143861049 | |||||||
| chr6:143861198 | A | G | 1 | a0001c0001t0001g0020 | 3 | HG02132.hp1 HG02155.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.923+645A>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 7/10 | chr6 | 143861198 | |||||||
| chr6:143861238 | A | G | 1 | a0001c0001t0001g0032 | 2 | HG02970.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.923+685A>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 7/10 | chr6 | 143861238 | |||||||
| chr6:143861274 | T | C | 1 | a0001c0003t0001g0043 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.923+721T>C | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 7/10 | chr6 | 143861274 | |||||||
| chr6:143861357 | C | T | 1 | a0001c0001t0001g0031 | 2 | NA18955.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.924-747C>T | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 7/10 | chr6 | 143861357 | |||||||
| chr6:143861424 | ACT | A | 5 | a0001c0007t0001g0040 a0001c0007t0001g0119 a0002c0006t0003g0041 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.924-677_924-676del others(2): Show |
LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr6 | 143861424 | ||||||
| chr6:143861433 | C | CA | 6 | a0001c0001t0001g0011 a0001c0007t0001g0040 a0001c0007t0001g0119 others(3): Show |
10 | HG01884.hp1 HG02258.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.924-658dupA | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr6 | 143861433 | ||||||
| chr6:143861525 | C | T | 1 | a0001c0001t0001g0055 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.924-579C>T | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 7/10 | chr6 | 143861525 | |||||||
| chr6:143861700 | C | G | 1 | a0001c0001t0001g0093 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.924-404C>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 7/10 | chr6 | 143861700 | |||||||
| chr6:143861811 | A | ATGAGTTA others(306): Show |
2 | a0001c0003t0001g0043 a0001c0003t0001g0044 |
2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.924-277_924-276ins others(313): Show |
LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr6 | 143861811 | ||||||
| chr6:143861811 | A | ATGAGTTA others(319): Show |
1 | a0001c0003t0001g0047 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.924-277_924-276ins others(326): Show |
LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr6 | 143861811 | ||||||
| chr6:143861811 | A | ATGAGTTA others(321): Show |
1 | a0001c0003t0001g0045 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.924-277_924-276ins others(328): Show |
LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr6 | 143861811 | ||||||
| chr6:143861811 | A | ATGAGTTA others(322): Show |
1 | a0001c0003t0001g0052 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.924-277_924-276ins others(329): Show |
LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr6 | 143861811 | ||||||
| chr6:143861811 | A | ATGAGTTA others(328): Show |
1 | a0001c0003t0001g0051 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.924-277_924-276ins others(335): Show |
LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr6 | 143861811 | ||||||
| chr6:143861811 | A | ATGAGTTA others(330): Show |
1 | a0001c0003t0001g0046 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.924-277_924-276ins others(337): Show |
LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr6 | 143861811 | ||||||
| chr6:143861811 | A | ATGAGTTA others(331): Show |
2 | a0001c0003t0001g0018 a0001c0003t0001g0019 |
6 | HG00733.hp2 HG01070.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.924-277_924-276ins others(338): Show |
LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr6 | 143861811 | ||||||
| chr6:143861811 | A | ATGAGTTA others(335): Show |
1 | a0001c0003t0001g0048 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.924-277_924-276ins others(342): Show |
LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr6 | 143861811 | ||||||
| chr6:143861811 | A | ATGAGTTA others(336): Show |
1 | a0001c0003t0001g0049 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.924-277_924-276ins others(343): Show |
LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr6 | 143861811 | ||||||
| chr6:143861811 | A | ATGAGTTA others(338): Show |
1 | a0001c0003t0001g0050 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.924-277_924-276ins others(345): Show |
LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr6 | 143861811 | ||||||
| chr6:143861819 | T | C | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 |
3 | HG02109.hp1 HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.924-285T>C | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 7/10 | chr6 | 143861819 | |||||||
| chr6:143861832 | T | A | 12 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0022 others(9): Show |
41 | HG00140.hp1 HG00673.hp2 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.924-272T>A | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 7/10 | chr6 | 143861832 | |||||||
| chr6:143861913 | A | G | 2 | a0001c0007t0001g0040 a0001c0007t0001g0119 |
2 | HG02258.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.924-191A>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 7/10 | chr6 | 143861913 | |||||||
| chr6:143862248 | G | A | 1 | a0001c0001t0001g0065 | 1 | NA19075.hp1 | splice_region_variant&intron_variant | LOW | c.1063+5G>A | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 8/10 | chr6 | 143862248 | |||||||
| chr6:143862355 | C | T | 2 | a0001c0001t0001g0009 a0001c0001t0001g0099 |
9 | HG00140.hp2 HG00642.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.1063+112C>T | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 8/10 | chr6 | 143862355 | |||||||
| chr6:143862357 | G | C | 1 | a0001c0001t0001g0092 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1063+114G>C | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 8/10 | chr6 | 143862357 | |||||||
| chr6:143862416 | G | C | 5 | a0001c0007t0001g0040 a0001c0007t0001g0119 a0002c0006t0003g0041 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1063+173G>C | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 8/10 | chr6 | 143862416 | |||||||
| chr6:143862482 | A | G | 1 | a0001c0001t0001g0087 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1063+239A>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 8/10 | chr6 | 143862482 | |||||||
| chr6:143862534 | C | T | 1 | a0001c0001t0001g0109 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1063+291C>T | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 8/10 | chr6 | 143862534 | |||||||
| chr6:143862694 | G | A | 1 | a0001c0002t0002g0107 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1064-150G>A | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 8/10 | chr6 | 143862694 | |||||||
| chr6:143862765 | A | C | 1 | a0001c0001t0001g0027 | 2 | HG01943.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1064-79A>C | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 8/10 | chr6 | 143862765 | |||||||
| chr6:143862997 | T | C | 12 | a0001c0003t0001g0018 a0001c0003t0001g0019 a0001c0003t0001g0043 others(9): Show |
16 | HG00733.hp2 HG01070.hp1 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.1117-89T>C | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 9/10 | chr6 | 143862997 | |||||||
| chr6:143863031 | C | G | 1 | a0001c0001t0001g0089 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1117-55C>G | LTV1 | ENSG00000135521.9 | transcript | ENST00000367576.6 | protein_coding | 9/10 | chr6 | 143863031 |