Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9404 |
| ensemblid | ENSG00000110031.13 |
| hgncid | 14061 |
| symbol | LPXN |
| name | leupaxin |
| refseq_nuc | NM_004811.3 |
| refseq_prot | NP_004802.1 |
| ensembl_nuc | ENST00000395074.7 |
| ensembl_prot | ENSP00000378512.2 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 58526871 |
| end | 58575856 |
| strand | - |
| ver | v1.2 |
| region | chr11:58526871-58575856 |
| region5000 | chr11:58521871-58580856 |
| regionname0 | LPXN_chr11_58526871_58575856 |
| regionname5000 | LPXN_chr11_58521871_58580856 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 386 | 304 | 73 | 57 | 136 | 10 | 28 | 104 | LPXN_chr11_58521871_58580856 | LPXN | MEELD others(381): Show |
chr11 | 58521871 | 58580856 |
| a0002 | 0/0 | 386 | 11 | 9 | 2 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | MEELD others(381): Show |
chr11 | 58521871 | 58580856 |
| a0003 | 0/0 | 386 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | MEELD others(381): Show |
chr11 | 58521871 | 58580856 |
| a0004 | 0/0 | 386 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | MEELD others(381): Show |
chr11 | 58521871 | 58580856 |
| a0005 | 0/0 | 386 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | MEELD others(381): Show |
chr11 | 58521871 | 58580856 |
| a0006 | 0/0 | 386 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN | MEELD others(381): Show |
chr11 | 58521871 | 58580856 |
| a0007 | 0/0 | 19 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN | MEELD others(14): Show |
chr11 | 58521871 | 58580856 |
| a0008 | 0/0 | 357 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN | MEELD others(352): Show |
chr11 | 58521871 | 58580856 |
| a0009 | 0/0 | 173 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN | MEELD others(168): Show |
chr11 | 58521871 | 58580856 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1158 | 172 | 52 | 30 | 71 | 4 | 15 | LPXN_chr11_58521871_58580856 | LPXN | ATGGA others(1153): Show |
chr11 | 58521871 | 58580856 | ||
| a0001c0002 | 0/0 | 1158 | 127 | 21 | 27 | 61 | 5 | 13 | LPXN_chr11_58521871_58580856 | LPXN | ATGGA others(1153): Show |
chr11 | 58521871 | 58580856 | ||
| a0001c0004 | 0/0 | 1158 | 5 | 0 | 0 | 4 | 1 | 0 | LPXN_chr11_58521871_58580856 | LPXN | ATGGA others(1153): Show |
chr11 | 58521871 | 58580856 | ||
| a0002c0003 | 0/0 | 1158 | 11 | 9 | 2 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | ATGGA others(1153): Show |
chr11 | 58521871 | 58580856 | ||
| a0003c0005 | 0/0 | 1158 | 5 | 4 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | ATGGA others(1153): Show |
chr11 | 58521871 | 58580856 | ||
| a0004c0008 | 0/0 | 1158 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | ATGGA others(1153): Show |
chr11 | 58521871 | 58580856 | ||
| a0005c0010 | 0/0 | 1158 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | ATGGA others(1153): Show |
chr11 | 58521871 | 58580856 | ||
| a0006c0009 | 0/0 | 1158 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | ATGGA others(1153): Show |
chr11 | 58521871 | 58580856 | ||
| a0007c0006 | 0/0 | 1159 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | ATGGA others(1154): Show |
chr11 | 58521871 | 58580856 | ||
| a0008c0007 | 0/0 | 1154 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | ATGGA others(1149): Show |
chr11 | 58521871 | 58580856 | ||
| a0009c0011 | 0/0 | 1159 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | ATGGA others(1154): Show |
chr11 | 58521871 | 58580856 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1828 | 168 | 48 | 30 | 71 | 4 | 15 | LPXN_chr11_58521871_58580856 | LPXN | AGTTC others(1823): Show |
chr11 | 58521871 | 58580856 |
| a0001c0001t0002 | 0/0 | 1828 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | AGTTC others(1823): Show |
chr11 | 58521871 | 58580856 |
| a0001c0001t0003 | 0/0 | 1828 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | AGTTC others(1823): Show |
chr11 | 58521871 | 58580856 |
| a0001c0001t0004 | 0/0 | 1828 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | AGTTC others(1823): Show |
chr11 | 58521871 | 58580856 |
| a0001c0001t0006 | 0/0 | 1828 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | AGTTC others(1823): Show |
chr11 | 58521871 | 58580856 |
| a0001c0002t0001 | 0/0 | 1828 | 125 | 21 | 26 | 60 | 5 | 13 | LPXN_chr11_58521871_58580856 | LPXN | AGTTC others(1823): Show |
chr11 | 58521871 | 58580856 |
| a0001c0002t0005 | 0/0 | 1828 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | AGTTC others(1823): Show |
chr11 | 58521871 | 58580856 |
| a0001c0002t0007 | 0/0 | 1828 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | AGTTC others(1823): Show |
chr11 | 58521871 | 58580856 |
| a0001c0004t0001 | 0/0 | 1828 | 5 | 0 | 0 | 4 | 1 | 0 | LPXN_chr11_58521871_58580856 | LPXN | AGTTC others(1823): Show |
chr11 | 58521871 | 58580856 |
| a0002c0003t0001 | 0/0 | 1828 | 11 | 9 | 2 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | AGTTC others(1823): Show |
chr11 | 58521871 | 58580856 |
| a0003c0005t0001 | 0/0 | 1828 | 5 | 4 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | AGTTC others(1823): Show |
chr11 | 58521871 | 58580856 |
| a0004c0008t0001 | 0/0 | 1828 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | AGTTC others(1823): Show |
chr11 | 58521871 | 58580856 |
| a0005c0010t0001 | 0/0 | 1828 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | AGTTC others(1823): Show |
chr11 | 58521871 | 58580856 |
| a0006c0009t0001 | 0/0 | 1828 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | AGTTC others(1823): Show |
chr11 | 58521871 | 58580856 |
| a0007c0006t0001 | 0/0 | 1829 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | AGTTC others(1824): Show |
chr11 | 58521871 | 58580856 |
| a0008c0007t0001 | 0/0 | 1824 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | AGTTC others(1819): Show |
chr11 | 58521871 | 58580856 |
| a0009c0011t0001 | 0/0 | 1829 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | AGTTC others(1824): Show |
chr11 | 58521871 | 58580856 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 17 | 0 | 4 | 13 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0005 | 0/0 | 5 | 1 | 2 | 0 | 2 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0008 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0004g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0001t0006g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0002 | 0/0 | 14 | 0 | 5 | 8 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0003 | 0/0 | 8 | 0 | 3 | 5 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0006 | 0/0 | 5 | 1 | 3 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0034 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0005g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0002t0007g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0004t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0004t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0004t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0004t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0001c0004t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0002c0003t0001g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0002c0003t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0002c0003t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0002c0003t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0002c0003t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0002c0003t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0002c0003t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0002c0003t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0002c0003t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0003c0005t0001g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0003c0005t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0003c0005t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0003c0005t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0004c0008t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0005c0010t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0006c0009t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0007c0006t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0008c0007t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| a0009c0011t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0171 | EUR | GBR | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0228 | EUR | GBR | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG00280 | hp1 | a0001 | c0004 | t0001 | g0104 | EUR | FIN | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0160 | EUR | FIN | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0195 | EAS | CHS | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | CHS | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | CHS | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0194 | EAS | CHS | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0183 | EAS | CHS | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | CHS | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0146 | EAS | CHS | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0179 | AMR | PUR | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0034 | AMR | PUR | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0029 | AMR | PUR | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0204 | AMR | PUR | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG01106 | hp2 | a0001 | c0002 | t0007 | g0236 | AMR | PUR | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0198 | AMR | PUR | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0207 | AMR | PUR | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0035 | AMR | PUR | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG01243 | hp1 | a0002 | c0003 | t0001 | g0098 | AMR | PUR | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0208 | AMR | CLM | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0142 | AMR | CLM | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | CLM | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG01261 | hp2 | a0002 | c0003 | t0001 | g0094 | AMR | CLM | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0201 | AMR | CLM | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | CLM | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG01496 | hp1 | a0003 | c0005 | t0001 | g0020 | AMR | CLM | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0197 | EUR | IBS | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0233 | EUR | IBS | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0209 | EUR | IBS | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0199 | EUR | IBS | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0184 | AFR | ACB | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PEL | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0035 | AMR | PEL | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PEL | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0186 | AMR | PEL | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0151 | EAS | KHV | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | KHV | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0181 | AFR | ACB | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0141 | EAS | KHV | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0116 | EAS | KHV | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0153 | EAS | KHV | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0014 | AFR | ACB | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02145 | hp2 | a0004 | c0008 | t0001 | g0139 | AFR | ACB | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02148 | hp1 | a0001 | c0002 | t0001 | g0036 | AMR | PEL | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0163 | AMR | PEL | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0172 | EAS | CDX | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | CDX | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0196 | AFR | ACB | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02257 | hp2 | a0002 | c0003 | t0001 | g0093 | AFR | ACB | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0036 | AMR | PEL | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PEL | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0154 | AFR | ACB | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0031 | SAS | PJL | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02615 | hp1 | a0002 | c0003 | t0001 | g0095 | AFR | GWD | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0042 | AFR | GWD | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0191 | AFR | GWD | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0169 | AFR | GWD | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0084 | AFR | GWD | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0189 | AFR | GWD | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0030 | AFR | GWD | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0203 | SAS | PJL | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02809 | hp1 | a0002 | c0003 | t0001 | g0011 | AFR | GWD | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02818 | hp2 | a0002 | c0003 | t0001 | g0011 | AFR | GWD | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0190 | AFR | GWD | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0192 | AFR | GWD | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02897 | hp2 | a0002 | c0003 | t0001 | g0092 | AFR | GWD | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0014 | AFR | ESN | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02965 | hp1 | a0002 | c0003 | t0001 | g0091 | AFR | ESN | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ESN | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | ESN | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0034 | SAS | PJL | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG03041 | hp1 | a0001 | c0001 | t0006 | g0115 | AFR | GWD | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | MSL | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0030 | AFR | MSL | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0033 | AFR | ESN | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ESN | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ESN | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ESN | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0033 | AFR | ESN | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | MSL | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | MSL | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0210 | SAS | PJL | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0006 | SAS | PJL | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG03453 | hp1 | a0003 | c0005 | t0001 | g0113 | AFR | MSL | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | MSL | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG03486 | hp1 | a0003 | c0005 | t0001 | g0020 | AFR | MSL | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0205 | SAS | PJL | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0200 | SAS | PJL | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ESN | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG03516 | hp2 | a0005 | c0010 | t0001 | g0040 | AFR | ESN | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG03540 | hp1 | a0003 | c0005 | t0001 | g0111 | AFR | GWD | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG03579 | hp2 | a0002 | c0003 | t0001 | g0096 | AFR | MSL | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0188 | SAS | PJL | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0031 | SAS | PJL | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0177 | SAS | BEB | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0152 | SAS | BEB | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | BEB | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | BEB | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | BEB | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | BEB | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | STU | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | STU | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0159 | SAS | STU | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | STU | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0193 | AFR | YRI | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0121 | AFR | YRI | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | CHB | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0170 | EAS | CHB | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18939 | hp1 | a0006 | c0009 | t0001 | g0178 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0150 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0149 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18946 | hp2 | a0001 | c0002 | t0001 | g0155 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18952 | hp1 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18956 | hp2 | a0007 | c0006 | t0001 | g0212 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0143 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0176 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0158 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18965 | hp2 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0175 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0164 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18985 | hp1 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0147 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18987 | hp1 | a0001 | c0002 | t0001 | g0162 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18988 | hp2 | a0001 | c0002 | t0001 | g0173 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18991 | hp1 | a0001 | c0002 | t0001 | g0185 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18993 | hp2 | a0001 | c0002 | t0001 | g0161 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18997 | hp1 | a0008 | c0007 | t0001 | g0202 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0144 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0174 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA19005 | hp1 | a0001 | c0004 | t0001 | g0107 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA19005 | hp2 | a0001 | c0002 | t0005 | g0180 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0148 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | LWK | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0156 | AFR | LWK | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA19043 | hp1 | a0003 | c0005 | t0001 | g0112 | AFR | LWK | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | LWK | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0157 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA19056 | hp2 | a0001 | c0004 | t0001 | g0114 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA19058 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA19059 | hp2 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA19063 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA19065 | hp1 | a0001 | c0004 | t0001 | g0105 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0182 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA19072 | hp2 | a0001 | c0002 | t0001 | g0167 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA19077 | hp2 | a0001 | c0002 | t0001 | g0206 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA19078 | hp1 | a0009 | c0011 | t0001 | g0166 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA19078 | hp2 | a0001 | c0004 | t0001 | g0106 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0165 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA19089 | hp1 | a0001 | c0002 | t0001 | g0145 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0187 | AFR | YRI | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | ASW | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0006 | AFR | ASW | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0014 | AFR | ACB | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02486 | hp1 | a0002 | c0003 | t0001 | g0097 | AFR | ACB | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | MSL | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | MSL | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | USA | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| HG06807 | hp2 | a0002 | c0003 | t0001 | g0011 | AFR | USA | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0080 | AFR | USA | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | USA | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | LWK | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | LWK | LPXN_chr11_58521871_58580856 | LPXN | chr11 | 58521871 | 58580856 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:58527595 | ACAAC | A | 1 | a0008 | 1 | NA18997.hp1 | frameshift_variant | HIGH | c.1016_1019delGTTG | p.Arg339fs | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 9/9 | 1103/1828 | 1016/1161 | 339/386 | chr11 | 58527595 | |||
| chr11:58527600 | G | A | 1 | a0004 | 1 | HG02145.hp2 | missense_variant | MODERATE | c.1015C>T | p.Arg339Cys | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 9/9 | 1099/1828 | 1015/1161 | 339/386 | chr11 | 58527600 | |||
| chr11:58527642 | G | A | 1 | a0005 | 1 | HG03516.hp2 | missense_variant | MODERATE | c.973C>T | p.Arg325Trp | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 9/9 | 1057/1828 | 973/1161 | 325/386 | chr11 | 58527642 | |||
| chr11:58551078 | G | A | 1 | a0006 | 1 | NA18939.hp1 | missense_variant | MODERATE | c.473C>T | p.Pro158Leu | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 5/9 | 557/1828 | 473/1161 | 158/386 | chr11 | 58551078 | |||
| chr11:58551109 | G | T | 1 | a0002 | 11 | HG01243.hp1 HG01261.hp2 HG02257.hp2 others(8): Show |
missense_variant | MODERATE | c.442C>A | p.Pro148Thr | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 5/9 | 526/1828 | 442/1161 | 148/386 | chr11 | 58551109 | |||
| chr11:58551192 | T | TC | 1 | a0009 | 1 | NA19078.hp1 | frameshift_variant | HIGH | c.358dupG | p.Asp120fs | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 5/9 | 442/1828 | 358/1161 | 120/386 | chr11 | 58551192 | |||
| chr11:58570647 | G | A | 1 | a0003 | 5 | HG01496.hp1 HG03453.hp1 HG03486.hp1 others(2): Show |
missense_variant | MODERATE | c.80C>T | p.Pro27Leu | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/9 | 164/1828 | 80/1161 | 27/386 | chr11 | 58570647 | |||
| chr11:58570690 | G | GT | 1 | a0007 | 1 | NA18956.hp2 | frameshift_variant | HIGH | c.36dupA | p.Arg13fs | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/9 | 120/1828 | 36/1161 | 12/386 | chr11 | 58570690 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:58550126 | T | C | 1 | a0001c0004 | 5 | HG00280.hp1 NA19005.hp1 NA19056.hp2 others(2): Show |
synonymous_variant | LOW | c.507A>G | p.Gln169Gln | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 6/9 | 591/1828 | 507/1161 | 169/386 | chr11 | 58550126 | |||
| chr11:58551146 | C | G | 6 | a0001c0002 a0004c0008 a0006c0009 others(3): Show |
132 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(129): Show |
synonymous_variant | LOW | c.405G>C | p.Leu135Leu | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 5/9 | 489/1828 | 405/1161 | 135/386 | chr11 | 58551146 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:58526960 | T | A | 1 | a0001c0001t0003 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*494A>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 9/9 | 494 | chr11 | 58526960 | ||||||
| chr11:58527107 | T | C | 1 | a0001c0001t0004 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*347A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 9/9 | 347 | chr11 | 58527107 | ||||||
| chr11:58527118 | A | G | 1 | a0001c0001t0002 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*336T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 9/9 | 336 | chr11 | 58527118 | ||||||
| chr11:58527202 | G | A | 1 | a0001c0002t0005 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*252C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 9/9 | 252 | chr11 | 58527202 | ||||||
| chr11:58527274 | T | G | 1 | a0001c0001t0006 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*180A>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 9/9 | 180 | chr11 | 58527274 | ||||||
| chr11:58575851 | G | C | 1 | a0001c0002t0007 | 1 | HG01106.hp2 | 5_prime_UTR_variant | MODIFIER | c.-79C>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/9 | 79 | chr11 | 58575851 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:58527798 | C | T | 1 | a0001c0001t0001g0224 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.892-75G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 8/8 | chr11 | 58527798 | |||||||
| chr11:58527806 | T | A | 1 | a0001c0002t0001g0163 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.892-83A>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 8/8 | chr11 | 58527806 | |||||||
| chr11:58527819 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.892-96G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 8/8 | chr11 | 58527819 | |||||||
| chr11:58527831 | A | G | 1 | a0001c0002t0001g0162 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.892-108T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 8/8 | chr11 | 58527831 | |||||||
| chr11:58527874 | C | T | 10 | a0001c0001t0001g0010 a0001c0001t0001g0081 a0001c0001t0001g0082 others(7): Show |
12 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.892-151G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 8/8 | chr11 | 58527874 | |||||||
| chr11:58527962 | T | G | 1 | a0001c0002t0007g0236 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.891+81A>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 8/8 | chr11 | 58527962 | |||||||
| chr11:58528216 | A | G | 1 | a0005c0010t0001g0040 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.743-25T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58528216 | |||||||
| chr11:58528275 | TCA | T | 93 | a0001c0001t0001g0075 a0001c0002t0001g0002 a0001c0002t0001g0003 others(90): Show |
133 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.743-86_743-85delTG | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58528275 | |||||||
| chr11:58528427 | G | A | 29 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(26): Show |
48 | HG00099.hp2 HG00423.hp2 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.743-236C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58528427 | |||||||
| chr11:58528551 | C | T | 1 | a0001c0002t0001g0143 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.743-360G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58528551 | |||||||
| chr11:58528603 | T | G | 1 | a0001c0001t0001g0049 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.743-412A>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58528603 | |||||||
| chr11:58528625 | T | C | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG02976.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.743-434A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58528625 | |||||||
| chr11:58528644 | T | G | 1 | a0001c0002t0001g0175 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.743-453A>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58528644 | |||||||
| chr11:58528748 | A | C | 1 | a0001c0002t0001g0182 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.743-557T>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58528748 | |||||||
| chr11:58528786 | T | C | 1 | a0003c0005t0001g0112 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.743-595A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58528786 | |||||||
| chr11:58528805 | C | CATATATT others(3): Show |
2 | a0001c0002t0001g0152 a0001c0002t0001g0177 |
2 | HG03831.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.743-624_743-615dup others(10): Show |
LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58528805 | |||||||
| chr11:58528987 | T | A | 1 | a0001c0001t0001g0078 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.743-796A>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58528987 | |||||||
| chr11:58529126 | A | T | 1 | a0001c0001t0001g0123 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.743-935T>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58529126 | |||||||
| chr11:58529129 | A | T | 1 | a0001c0001t0001g0123 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.743-938T>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58529129 | |||||||
| chr11:58529333 | G | A | 67 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(64): Show |
90 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.743-1142C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58529333 | |||||||
| chr11:58529384 | G | A | 2 | a0001c0001t0001g0076 a0001c0001t0001g0090 |
2 | HG03041.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.743-1193C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58529384 | |||||||
| chr11:58529437 | C | T | 1 | a0002c0003t0001g0094 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.743-1246G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58529437 | |||||||
| chr11:58529458 | A | G | 1 | a0003c0005t0001g0113 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.743-1267T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58529458 | |||||||
| chr11:58529564 | C | T | 1 | a0001c0001t0002g0121 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.743-1373G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58529564 | |||||||
| chr11:58529607 | CA | C | 68 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(65): Show |
91 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.743-1417delT | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58529607 | |||||||
| chr11:58529634 | T | A | 1 | a0002c0003t0001g0096 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.743-1443A>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58529634 | |||||||
| chr11:58530069 | C | T | 29 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(26): Show |
48 | HG00099.hp2 HG00423.hp2 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.743-1878G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58530069 | |||||||
| chr11:58530253 | C | T | 1 | a0001c0004t0001g0104 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.743-2062G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58530253 | |||||||
| chr11:58530295 | C | T | 2 | a0001c0001t0001g0077 a0001c0001t0001g0078 |
2 | HG01884.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.743-2104G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58530295 | |||||||
| chr11:58530512 | G | C | 5 | a0001c0004t0001g0104 a0001c0004t0001g0105 a0001c0004t0001g0106 others(2): Show |
5 | HG00280.hp1 NA19005.hp1 NA19056.hp2 others(2): Show |
intron_variant | MODIFIER | c.743-2321C>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58530512 | |||||||
| chr11:58530596 | C | T | 6 | a0001c0001t0001g0041 a0003c0005t0001g0020 a0003c0005t0001g0111 others(3): Show |
7 | HG01496.hp1 HG02922.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.743-2405G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58530596 | |||||||
| chr11:58530996 | G | A | 1 | a0001c0001t0001g0123 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.743-2805C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58530996 | |||||||
| chr11:58531017 | G | A | 221 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(218): Show |
312 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(309): Show |
intron_variant | MODIFIER | c.743-2826C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58531017 | |||||||
| chr11:58531043 | T | A | 1 | a0001c0001t0001g0131 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.743-2852A>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58531043 | |||||||
| chr11:58531149 | C | T | 1 | a0001c0001t0001g0211 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.743-2958G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58531149 | |||||||
| chr11:58531215 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.743-3024A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58531215 | |||||||
| chr11:58531256 | G | A | 4 | a0001c0001t0001g0056 a0001c0001t0001g0214 a0001c0001t0001g0218 others(1): Show |
4 | HG01168.hp1 HG01169.hp1 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.743-3065C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58531256 | |||||||
| chr11:58531271 | G | A | 9 | a0002c0003t0001g0011 a0002c0003t0001g0091 a0002c0003t0001g0092 others(6): Show |
11 | HG01243.hp1 HG01261.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.743-3080C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58531271 | |||||||
| chr11:58531350 | G | C | 8 | a0001c0001t0001g0010 a0001c0001t0001g0081 a0001c0001t0001g0082 others(5): Show |
10 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.743-3159C>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58531350 | |||||||
| chr11:58531419 | A | T | 8 | a0001c0001t0001g0010 a0001c0001t0001g0081 a0001c0001t0001g0082 others(5): Show |
10 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.743-3228T>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58531419 | |||||||
| chr11:58531576 | G | A | 1 | a0001c0002t0001g0173 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.743-3385C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58531576 | |||||||
| chr11:58531613 | A | G | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG02976.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.743-3422T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58531613 | |||||||
| chr11:58531626 | AAC | A | 14 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0043 others(11): Show |
21 | HG01981.hp1 HG02056.hp2 NA18747.hp1 others(18): Show |
intron_variant | MODIFIER | c.743-3437_743-3436d others(4): Show |
LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58531626 | |||||||
| chr11:58531660 | T | A | 3 | a0001c0002t0001g0013 a0001c0002t0001g0028 a0001c0002t0001g0206 |
6 | HG00558.hp1 HG02040.hp2 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.743-3469A>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58531660 | |||||||
| chr11:58531732 | G | A | 3 | a0001c0002t0001g0013 a0001c0002t0001g0028 a0001c0002t0001g0206 |
6 | HG00558.hp1 HG02040.hp2 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.743-3541C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58531732 | |||||||
| chr11:58531893 | A | G | 6 | a0001c0002t0001g0034 a0001c0002t0001g0036 a0001c0002t0001g0201 others(3): Show |
8 | HG00741.hp2 HG01099.hp1 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.743-3702T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58531893 | |||||||
| chr11:58531999 | A | G | 232 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(229): Show |
324 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.743-3808T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58531999 | |||||||
| chr11:58532000 | C | G | 93 | a0001c0001t0001g0075 a0001c0002t0001g0002 a0001c0002t0001g0003 others(90): Show |
133 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.743-3809G>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58532000 | |||||||
| chr11:58532021 | T | G | 1 | a0001c0001t0001g0074 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.743-3830A>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58532021 | |||||||
| chr11:58532033 | G | A | 3 | a0002c0003t0001g0092 a0002c0003t0001g0093 a0002c0003t0001g0094 |
3 | HG01261.hp2 HG02257.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.743-3842C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58532033 | |||||||
| chr11:58532047 | C | T | 7 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0070 others(4): Show |
9 | HG00741.hp1 HG01167.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.743-3856G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58532047 | |||||||
| chr11:58532057 | C | T | 2 | a0001c0001t0001g0233 a0001c0001t0001g0235 |
2 | HG01175.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.743-3866G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58532057 | |||||||
| chr11:58532154 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.743-3963C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58532154 | |||||||
| chr11:58532173 | G | A | 2 | a0001c0001t0001g0041 a0005c0010t0001g0040 |
2 | HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.743-3982C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58532173 | |||||||
| chr11:58532188 | C | T | 8 | a0001c0001t0001g0010 a0001c0001t0001g0081 a0001c0001t0001g0082 others(5): Show |
10 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.743-3997G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58532188 | |||||||
| chr11:58532226 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.743-4035G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58532226 | |||||||
| chr11:58532284 | G | A | 111 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(108): Show |
159 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.743-4093C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58532284 | |||||||
| chr11:58532294 | G | A | 9 | a0002c0003t0001g0011 a0002c0003t0001g0091 a0002c0003t0001g0092 others(6): Show |
11 | HG01243.hp1 HG01261.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.743-4103C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58532294 | |||||||
| chr11:58532305 | C | T | 5 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0076 others(2): Show |
9 | HG02280.hp2 HG02896.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.743-4114G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58532305 | |||||||
| chr11:58532334 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.743-4143C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58532334 | |||||||
| chr11:58532357 | C | T | 2 | a0001c0002t0001g0168 a0001c0002t0001g0174 |
2 | NA18969.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.743-4166G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58532357 | |||||||
| chr11:58532361 | C | T | 7 | a0001c0001t0001g0041 a0001c0001t0001g0044 a0003c0005t0001g0020 others(4): Show |
8 | HG01496.hp1 HG02922.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.743-4170G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58532361 | |||||||
| chr11:58532362 | G | A | 1 | a0001c0001t0001g0015 | 2 | HG02683.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.743-4171C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58532362 | |||||||
| chr11:58532433 | T | C | 111 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(108): Show |
159 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.743-4242A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58532433 | |||||||
| chr11:58532476 | G | C | 1 | a0001c0001t0001g0047 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.743-4285C>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58532476 | |||||||
| chr11:58532689 | C | G | 6 | a0001c0001t0001g0041 a0003c0005t0001g0020 a0003c0005t0001g0111 others(3): Show |
7 | HG01496.hp1 HG02922.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.743-4498G>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58532689 | |||||||
| chr11:58532875 | T | C | 1 | a0001c0001t0001g0053 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.743-4684A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58532875 | |||||||
| chr11:58532881 | T | C | 93 | a0001c0001t0001g0075 a0001c0002t0001g0002 a0001c0002t0001g0003 others(90): Show |
133 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.743-4690A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58532881 | |||||||
| chr11:58532887 | T | C | 1 | a0001c0001t0006g0115 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.743-4696A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58532887 | |||||||
| chr11:58532890 | G | A | 93 | a0001c0001t0001g0075 a0001c0002t0001g0002 a0001c0002t0001g0003 others(90): Show |
133 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.743-4699C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58532890 | |||||||
| chr11:58532921 | C | T | 5 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0076 others(2): Show |
9 | HG02280.hp2 HG02896.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.743-4730G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58532921 | |||||||
| chr11:58532946 | G | A | 9 | a0002c0003t0001g0011 a0002c0003t0001g0091 a0002c0003t0001g0092 others(6): Show |
11 | HG01243.hp1 HG01261.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.743-4755C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58532946 | |||||||
| chr11:58533045 | G | A | 1 | a0001c0001t0001g0070 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.743-4854C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58533045 | |||||||
| chr11:58533125 | AT | A | 3 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0004g0084 |
3 | HG02622.hp2 HG02717.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.743-4935delA | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58533125 | |||||||
| chr11:58533143 | C | T | 2 | a0001c0001t0001g0088 a0001c0002t0001g0142 |
2 | HG01257.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.743-4952G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58533143 | |||||||
| chr11:58533204 | A | T | 1 | a0002c0003t0001g0092 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.743-5013T>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58533204 | |||||||
| chr11:58533216 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.743-5025G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58533216 | |||||||
| chr11:58533233 | C | T | 3 | a0001c0002t0001g0162 a0001c0002t0001g0176 a0001c0002t0001g0194 |
3 | HG00597.hp1 NA18962.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.743-5042G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58533233 | |||||||
| chr11:58533281 | T | C | 44 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(41): Show |
69 | HG00099.hp2 HG00423.hp2 HG00733.hp1 others(66): Show |
intron_variant | MODIFIER | c.743-5090A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58533281 | |||||||
| chr11:58533320 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.743-5129C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58533320 | |||||||
| chr11:58533381 | A | T | 1 | a0001c0001t0001g0228 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.743-5190T>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58533381 | |||||||
| chr11:58533417 | A | C | 1 | a0001c0001t0001g0122 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.743-5226T>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58533417 | |||||||
| chr11:58533494 | C | T | 1 | a0001c0002t0001g0176 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.743-5303G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58533494 | |||||||
| chr11:58533634 | C | T | 1 | a0001c0004t0001g0107 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.743-5443G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58533634 | |||||||
| chr11:58533767 | T | C | 4 | a0003c0005t0001g0020 a0003c0005t0001g0111 a0003c0005t0001g0112 others(1): Show |
5 | HG01496.hp1 HG03453.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.743-5576A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58533767 | |||||||
| chr11:58533942 | G | A | 7 | a0001c0002t0001g0146 a0001c0002t0001g0147 a0001c0002t0001g0148 others(4): Show |
7 | HG00609.hp1 HG00621.hp2 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.743-5751C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58533942 | |||||||
| chr11:58534072 | G | C | 1 | a0001c0001t0001g0228 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.743-5881C>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58534072 | |||||||
| chr11:58534193 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.743-6002G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58534193 | |||||||
| chr11:58534341 | A | G | 5 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0076 others(2): Show |
9 | HG02280.hp2 HG02896.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.743-6150T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58534341 | |||||||
| chr11:58534382 | G | A | 25 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(22): Show |
44 | HG00099.hp2 HG00423.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.743-6191C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58534382 | |||||||
| chr11:58534413 | C | T | 2 | a0001c0002t0001g0006 a0001c0002t0001g0196 |
6 | HG00642.hp2 HG01106.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.743-6222G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58534413 | |||||||
| chr11:58534463 | A | G | 3 | a0001c0002t0001g0162 a0001c0002t0001g0176 a0001c0002t0001g0194 |
3 | HG00597.hp1 NA18962.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.743-6272T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58534463 | |||||||
| chr11:58534503 | C | A | 29 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(26): Show |
48 | HG00099.hp2 HG00423.hp2 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.743-6312G>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58534503 | |||||||
| chr11:58534625 | G | C | 6 | a0001c0001t0001g0041 a0003c0005t0001g0020 a0003c0005t0001g0111 others(3): Show |
7 | HG01496.hp1 HG02922.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.743-6434C>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58534625 | |||||||
| chr11:58534729 | C | T | 7 | a0001c0002t0001g0146 a0001c0002t0001g0147 a0001c0002t0001g0148 others(4): Show |
7 | HG00609.hp1 HG00621.hp2 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.743-6538G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58534729 | |||||||
| chr11:58534778 | C | T | 111 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(108): Show |
159 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.743-6587G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58534778 | |||||||
| chr11:58534833 | G | A | 4 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0234 others(1): Show |
4 | HG01175.hp2 HG01192.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.743-6642C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58534833 | |||||||
| chr11:58535086 | G | A | 1 | a0005c0010t0001g0040 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.743-6895C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58535086 | |||||||
| chr11:58535270 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.743-7079G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58535270 | |||||||
| chr11:58535305 | T | A | 93 | a0001c0001t0001g0075 a0001c0002t0001g0002 a0001c0002t0001g0003 others(90): Show |
133 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.743-7114A>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58535305 | |||||||
| chr11:58535324 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.743-7133G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58535324 | |||||||
| chr11:58535359 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.743-7168C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58535359 | |||||||
| chr11:58535665 | G | A | 93 | a0001c0001t0001g0075 a0001c0002t0001g0002 a0001c0002t0001g0003 others(90): Show |
133 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.743-7474C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58535665 | |||||||
| chr11:58535667 | T | C | 2 | a0003c0005t0001g0111 a0003c0005t0001g0112 |
2 | HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.743-7476A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58535667 | |||||||
| chr11:58535751 | G | T | 1 | a0001c0002t0001g0171 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.743-7560C>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58535751 | |||||||
| chr11:58535782 | A | G | 227 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(224): Show |
319 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(316): Show |
intron_variant | MODIFIER | c.743-7591T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58535782 | |||||||
| chr11:58535925 | T | A | 1 | a0001c0001t0001g0041 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.743-7734A>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58535925 | |||||||
| chr11:58535988 | CACTGTTC others(11): Show |
C | 1 | a0001c0002t0001g0206 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.743-7815_743-7798d others(20): Show |
LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58535988 | |||||||
| chr11:58536117 | T | A | 1 | a0001c0001t0001g0037 | 2 | HG01346.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.743-7926A>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58536117 | |||||||
| chr11:58536439 | G | C | 2 | a0001c0001t0001g0119 a0001c0001t0001g0120 |
2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.743-8248C>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58536439 | |||||||
| chr11:58536484 | C | T | 3 | a0001c0002t0001g0143 a0001c0002t0001g0150 a0001c0002t0001g0152 |
3 | HG03831.hp2 NA18942.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.743-8293G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58536484 | |||||||
| chr11:58536553 | T | C | 5 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0076 others(2): Show |
9 | HG02280.hp2 HG02896.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.743-8362A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58536553 | |||||||
| chr11:58536882 | A | G | 1 | a0001c0001t0001g0067 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.743-8691T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58536882 | |||||||
| chr11:58536918 | C | T | 1 | a0001c0002t0001g0186 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.743-8727G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58536918 | |||||||
| chr11:58536987 | C | T | 3 | a0001c0001t0001g0022 a0001c0001t0001g0118 a0001c0001t0001g0133 |
4 | NA18943.hp2 NA18961.hp2 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.743-8796G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58536987 | |||||||
| chr11:58537092 | AG | A | 111 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(108): Show |
159 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.743-8902delC | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58537092 | |||||||
| chr11:58537307 | T | C | 1 | a0001c0002t0007g0236 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.743-9116A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58537307 | |||||||
| chr11:58537337 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.743-9146T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58537337 | |||||||
| chr11:58537422 | A | G | 8 | a0001c0001t0001g0010 a0001c0001t0001g0081 a0001c0001t0001g0082 others(5): Show |
10 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.743-9231T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58537422 | |||||||
| chr11:58537442 | A | G | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG02976.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.743-9251T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58537442 | |||||||
| chr11:58537887 | G | C | 1 | a0001c0001t0001g0103 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.743-9696C>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58537887 | |||||||
| chr11:58537942 | T | G | 1 | a0001c0001t0001g0211 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.743-9751A>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58537942 | |||||||
| chr11:58537945 | C | A | 1 | a0001c0001t0001g0211 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.743-9754G>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58537945 | |||||||
| chr11:58538041 | C | A | 1 | a0001c0002t0007g0236 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.743-9850G>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58538041 | |||||||
| chr11:58538077 | C | A | 1 | a0001c0001t0001g0075 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.743-9886G>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58538077 | |||||||
| chr11:58538333 | C | A | 4 | a0003c0005t0001g0020 a0003c0005t0001g0111 a0003c0005t0001g0112 others(1): Show |
5 | HG01496.hp1 HG03453.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.743-10142G>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58538333 | |||||||
| chr11:58538524 | T | C | 1 | a0001c0001t0002g0121 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.743-10333A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58538524 | |||||||
| chr11:58538783 | CA | C | 19 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0018 others(16): Show |
25 | HG01175.hp2 HG01192.hp2 HG01515.hp2 others(22): Show |
intron_variant | MODIFIER | c.743-10593delT | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58538783 | |||||||
| chr11:58539002 | A | AAAC | 225 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(222): Show |
317 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(314): Show |
intron_variant | MODIFIER | c.742+10781_742+1078 others(7): Show |
LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58539002 | |||||||
| chr11:58539002 | A | C | 1 | a0001c0001t0001g0061 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.742+10784T>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58539002 | |||||||
| chr11:58539105 | G | A | 2 | a0001c0002t0001g0036 a0001c0002t0001g0204 |
3 | HG01099.hp1 HG02148.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.742+10681C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58539105 | |||||||
| chr11:58539399 | G | C | 126 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(123): Show |
177 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.742+10387C>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58539399 | |||||||
| chr11:58539529 | A | C | 1 | a0001c0002t0001g0170 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.742+10257T>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58539529 | |||||||
| chr11:58539570 | T | C | 2 | a0001c0004t0001g0106 a0001c0004t0001g0114 |
2 | NA19056.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.742+10216A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58539570 | |||||||
| chr11:58539793 | T | A | 3 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0117 |
5 | HG00438.hp1 HG02071.hp2 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.742+9993A>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58539793 | |||||||
| chr11:58539928 | A | T | 9 | a0002c0003t0001g0011 a0002c0003t0001g0091 a0002c0003t0001g0092 others(6): Show |
11 | HG01243.hp1 HG01261.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.742+9858T>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58539928 | |||||||
| chr11:58540051 | C | G | 2 | a0001c0001t0001g0041 a0005c0010t0001g0040 |
2 | HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.742+9735G>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58540051 | |||||||
| chr11:58540097 | A | G | 9 | a0002c0003t0001g0011 a0002c0003t0001g0091 a0002c0003t0001g0092 others(6): Show |
11 | HG01243.hp1 HG01261.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.742+9689T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58540097 | |||||||
| chr11:58540161 | A | C | 7 | a0001c0002t0001g0014 a0001c0002t0001g0033 a0001c0002t0001g0189 others(4): Show |
10 | HG02109.hp1 HG02145.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.742+9625T>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58540161 | |||||||
| chr11:58540186 | T | A | 8 | a0001c0001t0001g0010 a0001c0001t0001g0081 a0001c0001t0001g0082 others(5): Show |
10 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.742+9600A>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58540186 | |||||||
| chr11:58540490 | A | G | 9 | a0002c0003t0001g0011 a0002c0003t0001g0091 a0002c0003t0001g0092 others(6): Show |
11 | HG01243.hp1 HG01261.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.742+9296T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58540490 | |||||||
| chr11:58540495 | G | A | 9 | a0002c0003t0001g0011 a0002c0003t0001g0091 a0002c0003t0001g0092 others(6): Show |
11 | HG01243.hp1 HG01261.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.742+9291C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58540495 | |||||||
| chr11:58540537 | C | T | 9 | a0002c0003t0001g0011 a0002c0003t0001g0091 a0002c0003t0001g0092 others(6): Show |
11 | HG01243.hp1 HG01261.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.742+9249G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58540537 | |||||||
| chr11:58540672 | T | C | 1 | a0001c0001t0001g0135 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.742+9114A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58540672 | |||||||
| chr11:58540819 | G | A | 2 | a0001c0001t0001g0216 a0001c0001t0001g0223 |
2 | NA18988.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.742+8967C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58540819 | |||||||
| chr11:58540868 | T | C | 221 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(218): Show |
312 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(309): Show |
intron_variant | MODIFIER | c.742+8918A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58540868 | |||||||
| chr11:58540869 | G | A | 1 | a0005c0010t0001g0040 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.742+8917C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58540869 | |||||||
| chr11:58541048 | T | C | 1 | a0001c0001t0001g0231 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.742+8738A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58541048 | |||||||
| chr11:58541085 | C | A | 1 | a0001c0001t0001g0129 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.742+8701G>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58541085 | |||||||
| chr11:58541255 | T | C | 1 | a0001c0004t0001g0107 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.742+8531A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58541255 | |||||||
| chr11:58541363 | T | C | 93 | a0001c0001t0001g0075 a0001c0002t0001g0002 a0001c0002t0001g0003 others(90): Show |
133 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.742+8423A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58541363 | |||||||
| chr11:58541375 | C | G | 1 | a0001c0001t0001g0057 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.742+8411G>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58541375 | |||||||
| chr11:58541484 | A | T | 9 | a0002c0003t0001g0011 a0002c0003t0001g0091 a0002c0003t0001g0092 others(6): Show |
11 | HG01243.hp1 HG01261.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.742+8302T>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58541484 | |||||||
| chr11:58541550 | G | C | 1 | a0001c0001t0001g0048 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.742+8236C>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58541550 | |||||||
| chr11:58541565 | A | T | 1 | a0001c0002t0001g0189 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.742+8221T>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58541565 | |||||||
| chr11:58541709 | C | T | 221 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(218): Show |
312 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(309): Show |
intron_variant | MODIFIER | c.742+8077G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58541709 | |||||||
| chr11:58541741 | G | A | 3 | a0001c0002t0001g0162 a0001c0002t0001g0176 a0001c0002t0001g0194 |
3 | HG00597.hp1 NA18962.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.742+8045C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58541741 | |||||||
| chr11:58541753 | T | C | 126 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(123): Show |
177 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.742+8033A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58541753 | |||||||
| chr11:58541845 | A | G | 1 | a0001c0002t0001g0169 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.742+7941T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58541845 | |||||||
| chr11:58541870 | G | A | 126 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(123): Show |
177 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.742+7916C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58541870 | |||||||
| chr11:58541879 | T | C | 1 | a0002c0003t0001g0098 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.742+7907A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58541879 | |||||||
| chr11:58541972 | T | C | 93 | a0001c0001t0001g0075 a0001c0002t0001g0002 a0001c0002t0001g0003 others(90): Show |
133 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.742+7814A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58541972 | |||||||
| chr11:58542018 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.742+7768G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58542018 | |||||||
| chr11:58542031 | G | A | 9 | a0002c0003t0001g0011 a0002c0003t0001g0091 a0002c0003t0001g0092 others(6): Show |
11 | HG01243.hp1 HG01261.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.742+7755C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58542031 | |||||||
| chr11:58542150 | C | G | 1 | a0001c0004t0001g0104 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.742+7636G>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58542150 | |||||||
| chr11:58542159 | G | C | 1 | a0001c0002t0001g0177 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.742+7627C>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58542159 | |||||||
| chr11:58542235 | T | C | 93 | a0001c0001t0001g0075 a0001c0002t0001g0002 a0001c0002t0001g0003 others(90): Show |
133 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.742+7551A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58542235 | |||||||
| chr11:58542237 | A | ATGAG | 126 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(123): Show |
177 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.742+7548_742+7549i others(6): Show |
LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58542237 | |||||||
| chr11:58542350 | C | T | 1 | a0001c0002t0001g0203 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.742+7436G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58542350 | |||||||
| chr11:58542441 | C | T | 127 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(124): Show |
178 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(175): Show |
intron_variant | MODIFIER | c.742+7345G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58542441 | |||||||
| chr11:58542543 | A | G | 1 | a0001c0001t0002g0121 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.742+7243T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58542543 | |||||||
| chr11:58543017 | C | G | 2 | a0001c0002t0001g0006 a0001c0002t0001g0196 |
6 | HG00642.hp2 HG01106.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.742+6769G>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58543017 | |||||||
| chr11:58543114 | C | T | 67 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(64): Show |
90 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.742+6672G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58543114 | |||||||
| chr11:58543132 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.742+6654C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58543132 | |||||||
| chr11:58543404 | C | T | 7 | a0001c0002t0001g0014 a0001c0002t0001g0033 a0001c0002t0001g0189 others(4): Show |
10 | HG02109.hp1 HG02145.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.742+6382G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58543404 | |||||||
| chr11:58543576 | C | T | 1 | a0005c0010t0001g0040 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.742+6210G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58543576 | |||||||
| chr11:58543689 | C | T | 4 | a0003c0005t0001g0020 a0003c0005t0001g0111 a0003c0005t0001g0112 others(1): Show |
5 | HG01496.hp1 HG03453.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.742+6097G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58543689 | |||||||
| chr11:58543689 | CT | C | 8 | a0001c0001t0001g0010 a0001c0001t0001g0081 a0001c0001t0001g0082 others(5): Show |
10 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.742+6096delA | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58543689 | |||||||
| chr11:58543720 | C | A | 1 | a0002c0003t0001g0094 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.742+6066G>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58543720 | |||||||
| chr11:58543752 | A | C | 1 | a0001c0001t0001g0049 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.742+6034T>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58543752 | |||||||
| chr11:58543832 | T | A | 2 | a0001c0001t0001g0232 a0001c0001t0001g0234 |
2 | HG01192.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.742+5954A>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58543832 | |||||||
| chr11:58543873 | T | C | 1 | a0001c0004t0001g0107 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.742+5913A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58543873 | |||||||
| chr11:58543895 | G | T | 1 | a0001c0002t0001g0151 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.742+5891C>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58543895 | |||||||
| chr11:58543933 | A | C | 220 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(217): Show |
311 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.742+5853T>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58543933 | |||||||
| chr11:58544105 | C | T | 1 | a0001c0001t0006g0115 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.742+5681G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58544105 | |||||||
| chr11:58544442 | G | A | 1 | a0001c0001t0001g0215 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.742+5344C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58544442 | |||||||
| chr11:58544544 | G | C | 1 | a0001c0001t0001g0049 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.742+5242C>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58544544 | |||||||
| chr11:58544645 | A | C | 5 | a0002c0003t0001g0011 a0002c0003t0001g0092 a0002c0003t0001g0093 others(2): Show |
7 | HG01261.hp2 HG02257.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.742+5141T>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58544645 | |||||||
| chr11:58544726 | A | C | 6 | a0001c0001t0001g0041 a0003c0005t0001g0020 a0003c0005t0001g0111 others(3): Show |
7 | HG01496.hp1 HG02922.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.742+5060T>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58544726 | |||||||
| chr11:58544845 | G | A | 1 | a0001c0001t0002g0121 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.742+4941C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58544845 | |||||||
| chr11:58544893 | G | A | 1 | a0001c0002t0001g0194 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.742+4893C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58544893 | |||||||
| chr11:58544921 | G | A | 220 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(217): Show |
311 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.742+4865C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58544921 | |||||||
| chr11:58545102 | C | A | 1 | a0001c0001t0001g0131 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.742+4684G>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58545102 | |||||||
| chr11:58545383 | A | G | 1 | a0002c0003t0001g0097 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.742+4403T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58545383 | |||||||
| chr11:58545407 | C | A | 111 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(108): Show |
159 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.742+4379G>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58545407 | |||||||
| chr11:58545605 | T | C | 4 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0065 others(1): Show |
4 | HG01934.hp1 HG01943.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.742+4181A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58545605 | |||||||
| chr11:58545606 | A | G | 1 | a0001c0002t0001g0196 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.742+4180T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58545606 | |||||||
| chr11:58545712 | A | G | 1 | a0001c0001t0001g0007 | 4 | NA18939.hp2 NA18968.hp1 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.742+4074T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58545712 | |||||||
| chr11:58545838 | C | A | 1 | a0001c0002t0001g0163 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.742+3948G>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58545838 | |||||||
| chr11:58545949 | T | C | 1 | a0001c0001t0001g0063 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.742+3837A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58545949 | |||||||
| chr11:58546234 | C | T | 9 | a0002c0003t0001g0011 a0002c0003t0001g0091 a0002c0003t0001g0092 others(6): Show |
11 | HG01243.hp1 HG01261.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.742+3552G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58546234 | |||||||
| chr11:58546375 | CT | C | 4 | a0001c0002t0001g0142 a0001c0002t0001g0160 a0001c0002t0001g0188 others(1): Show |
4 | HG00280.hp2 HG01257.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.742+3410delA | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58546375 | |||||||
| chr11:58546395 | A | T | 9 | a0002c0003t0001g0011 a0002c0003t0001g0091 a0002c0003t0001g0092 others(6): Show |
11 | HG01243.hp1 HG01261.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.742+3391T>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58546395 | |||||||
| chr11:58546953 | G | T | 1 | a0002c0003t0001g0098 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.742+2833C>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58546953 | |||||||
| chr11:58546970 | C | G | 1 | a0001c0001t0001g0109 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.742+2816G>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58546970 | |||||||
| chr11:58547067 | G | A | 67 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(64): Show |
90 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.742+2719C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58547067 | |||||||
| chr11:58547360 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.742+2426G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58547360 | |||||||
| chr11:58547361 | T | C | 126 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(123): Show |
177 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.742+2425A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58547361 | |||||||
| chr11:58548233 | T | A | 93 | a0001c0001t0001g0075 a0001c0002t0001g0002 a0001c0002t0001g0003 others(90): Show |
133 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.742+1553A>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58548233 | |||||||
| chr11:58548260 | T | C | 2 | a0001c0001t0001g0224 a0001c0001t0001g0225 |
2 | HG02300.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.742+1526A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58548260 | |||||||
| chr11:58548342 | A | G | 1 | a0001c0001t0001g0102 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.742+1444T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58548342 | |||||||
| chr11:58548346 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.742+1440T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58548346 | |||||||
| chr11:58548454 | A | G | 7 | a0001c0002t0001g0014 a0001c0002t0001g0033 a0001c0002t0001g0189 others(4): Show |
10 | HG02109.hp1 HG02145.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.742+1332T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58548454 | |||||||
| chr11:58548623 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.742+1163G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58548623 | |||||||
| chr11:58548734 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.742+1052G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58548734 | |||||||
| chr11:58548869 | G | A | 1 | a0001c0001t0001g0130 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.742+917C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58548869 | |||||||
| chr11:58548902 | C | T | 1 | a0001c0002t0001g0151 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.742+884G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58548902 | |||||||
| chr11:58548909 | AC | A | 4 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0234 others(1): Show |
4 | HG01175.hp2 HG01192.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.742+876delG | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58548909 | |||||||
| chr11:58548930 | T | C | 1 | a0001c0004t0001g0105 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.742+856A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58548930 | |||||||
| chr11:58548961 | A | C | 1 | a0002c0003t0001g0091 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.742+825T>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58548961 | |||||||
| chr11:58548992 | G | A | 6 | a0001c0001t0001g0041 a0003c0005t0001g0020 a0003c0005t0001g0111 others(3): Show |
7 | HG01496.hp1 HG02922.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.742+794C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58548992 | |||||||
| chr11:58549001 | ATAACATT others(10): Show |
A | 1 | a0009c0011t0001g0166 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.742+768_742+784del others(17): Show |
LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58549001 | |||||||
| chr11:58549094 | T | C | 93 | a0001c0001t0001g0075 a0001c0002t0001g0002 a0001c0002t0001g0003 others(90): Show |
133 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.742+692A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58549094 | |||||||
| chr11:58549361 | G | A | 6 | a0001c0001t0001g0041 a0003c0005t0001g0020 a0003c0005t0001g0111 others(3): Show |
7 | HG01496.hp1 HG02922.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.742+425C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58549361 | |||||||
| chr11:58549429 | C | A | 1 | a0001c0001t0001g0066 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.742+357G>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58549429 | |||||||
| chr11:58549470 | T | G | 1 | a0001c0001t0001g0211 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.742+316A>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58549470 | |||||||
| chr11:58549643 | G | C | 1 | a0001c0001t0001g0085 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.742+143C>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58549643 | |||||||
| chr11:58549681 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.742+105A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 7/8 | chr11 | 58549681 | |||||||
| chr11:58550175 | G | A | 1 | a0001c0001t0001g0015 | 2 | HG02683.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.487-29C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 5/8 | chr11 | 58550175 | |||||||
| chr11:58550583 | T | C | 92 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(89): Show |
134 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.487-437A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 5/8 | chr11 | 58550583 | |||||||
| chr11:58550600 | G | A | 1 | a0001c0001t0001g0130 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.487-454C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 5/8 | chr11 | 58550600 | |||||||
| chr11:58550973 | A | G | 1 | a0001c0001t0001g0136 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.486+92T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 5/8 | chr11 | 58550973 | |||||||
| chr11:58550992 | G | A | 5 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0076 others(2): Show |
9 | HG02280.hp2 HG02896.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.486+73C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 5/8 | chr11 | 58550992 | |||||||
| chr11:58551033 | G | GGCTGTAG others(9): Show |
1 | a0009c0011t0001g0166 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.486+16_486+31dupAT others(14): Show |
LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 5/8 | chr11 | 58551033 | |||||||
| chr11:58551538 | A | T | 6 | a0001c0001t0001g0041 a0003c0005t0001g0020 a0003c0005t0001g0111 others(3): Show |
7 | HG01496.hp1 HG02922.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.319-306T>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 4/8 | chr11 | 58551538 | |||||||
| chr11:58551572 | G | A | 3 | a0001c0001t0001g0053 a0001c0001t0001g0059 a0001c0001t0001g0074 |
3 | HG02683.hp1 HG02735.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.319-340C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 4/8 | chr11 | 58551572 | |||||||
| chr11:58551685 | T | C | 1 | a0001c0002t0001g0150 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.319-453A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 4/8 | chr11 | 58551685 | |||||||
| chr11:58551768 | C | G | 1 | a0001c0001t0001g0126 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.319-536G>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 4/8 | chr11 | 58551768 | |||||||
| chr11:58551895 | A | G | 221 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(218): Show |
312 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(309): Show |
intron_variant | MODIFIER | c.319-663T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 4/8 | chr11 | 58551895 | |||||||
| chr11:58551911 | G | A | 2 | a0001c0002t0001g0035 a0001c0002t0001g0198 |
3 | HG01167.hp2 HG01169.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.319-679C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 4/8 | chr11 | 58551911 | |||||||
| chr11:58552164 | G | A | 1 | a0001c0002t0001g0179 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.319-932C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 4/8 | chr11 | 58552164 | |||||||
| chr11:58552272 | C | G | 1 | a0001c0001t0001g0037 | 2 | HG01346.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.319-1040G>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 4/8 | chr11 | 58552272 | |||||||
| chr11:58552318 | GA | G | 13 | a0001c0001t0001g0041 a0001c0001t0001g0126 a0001c0001t0001g0135 others(10): Show |
15 | HG01496.hp1 HG01978.hp2 HG02602.hp2 others(12): Show |
intron_variant | MODIFIER | c.319-1087delT | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 4/8 | chr11 | 58552318 | |||||||
| chr11:58552396 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.319-1164C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 4/8 | chr11 | 58552396 | |||||||
| chr11:58552541 | T | C | 1 | a0001c0002t0005g0180 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.319-1309A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 4/8 | chr11 | 58552541 | |||||||
| chr11:58552727 | T | C | 221 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(218): Show |
312 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(309): Show |
intron_variant | MODIFIER | c.319-1495A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 4/8 | chr11 | 58552727 | |||||||
| chr11:58552871 | C | T | 1 | a0001c0001t0001g0037 | 2 | HG01346.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.319-1639G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 4/8 | chr11 | 58552871 | |||||||
| chr11:58552883 | C | T | 1 | a0001c0002t0001g0033 | 2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.319-1651G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 4/8 | chr11 | 58552883 | |||||||
| chr11:58552886 | G | A | 4 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0234 others(1): Show |
4 | HG01175.hp2 HG01192.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.319-1654C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 4/8 | chr11 | 58552886 | |||||||
| chr11:58553319 | G | A | 1 | a0001c0002t0001g0181 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.318+1522C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 4/8 | chr11 | 58553319 | |||||||
| chr11:58553335 | C | CA | 97 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(94): Show |
139 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.318+1505dupT | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 4/8 | chr11 | 58553335 | |||||||
| chr11:58553335 | CA | C | 11 | a0001c0001t0001g0076 a0001c0001t0001g0102 a0001c0001t0001g0108 others(8): Show |
11 | HG01167.hp2 HG01258.hp2 HG01515.hp1 others(8): Show |
intron_variant | MODIFIER | c.318+1505delT | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 4/8 | chr11 | 58553335 | |||||||
| chr11:58553361 | G | T | 2 | a0001c0001t0001g0219 a0001c0001t0001g0220 |
2 | NA18975.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.318+1480C>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 4/8 | chr11 | 58553361 | |||||||
| chr11:58553405 | T | C | 1 | a0001c0001t0001g0131 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.318+1436A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 4/8 | chr11 | 58553405 | |||||||
| chr11:58553690 | T | C | 2 | a0001c0001t0001g0010 a0001c0001t0001g0085 |
4 | HG02280.hp1 HG02451.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.318+1151A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 4/8 | chr11 | 58553690 | |||||||
| chr11:58553976 | T | A | 14 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0043 others(11): Show |
21 | HG01981.hp1 HG02056.hp2 NA18747.hp1 others(18): Show |
intron_variant | MODIFIER | c.318+865A>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 4/8 | chr11 | 58553976 | |||||||
| chr11:58554033 | C | T | 1 | a0001c0001t0006g0115 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.318+808G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 4/8 | chr11 | 58554033 | |||||||
| chr11:58554078 | G | A | 1 | a0001c0002t0001g0181 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.318+763C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 4/8 | chr11 | 58554078 | |||||||
| chr11:58554228 | G | A | 3 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0231 |
7 | HG02280.hp2 HG02896.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.318+613C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 4/8 | chr11 | 58554228 | |||||||
| chr11:58554230 | T | C | 44 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(41): Show |
69 | HG00099.hp2 HG00423.hp2 HG00733.hp1 others(66): Show |
intron_variant | MODIFIER | c.318+611A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 4/8 | chr11 | 58554230 | |||||||
| chr11:58554317 | A | T | 1 | a0001c0001t0001g0039 | 2 | NA18983.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.318+524T>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 4/8 | chr11 | 58554317 | |||||||
| chr11:58554797 | G | A | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG02976.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.318+44C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 4/8 | chr11 | 58554797 | |||||||
| chr11:58555058 | A | G | 1 | a0002c0003t0001g0098 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.219-118T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58555058 | |||||||
| chr11:58555313 | G | C | 1 | a0001c0001t0001g0132 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.219-373C>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58555313 | |||||||
| chr11:58555594 | T | C | 1 | a0001c0001t0001g0133 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.219-654A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58555594 | |||||||
| chr11:58555739 | A | AAC | 27 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(24): Show |
46 | HG00099.hp2 HG00423.hp2 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.219-801_219-800dup others(2): Show |
LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58555739 | |||||||
| chr11:58555739 | A | AACAC | 4 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0234 others(1): Show |
4 | HG01175.hp2 HG01192.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.219-803_219-800dup others(4): Show |
LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58555739 | |||||||
| chr11:58555768 | G | GCA | 15 | a0001c0001t0001g0009 a0001c0001t0001g0214 a0001c0001t0001g0218 others(12): Show |
20 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.219-830_219-829dup others(2): Show |
LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58555768 | |||||||
| chr11:58555768 | GCA | G | 101 | a0001c0001t0001g0010 a0001c0001t0001g0075 a0001c0001t0001g0081 others(98): Show |
143 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.219-830_219-829del others(2): Show |
LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58555768 | |||||||
| chr11:58555768 | GCACA | G | 67 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(64): Show |
90 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.219-832_219-829del others(4): Show |
LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58555768 | |||||||
| chr11:58555883 | A | C | 1 | a0001c0001t0001g0053 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.219-943T>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58555883 | |||||||
| chr11:58555976 | A | G | 4 | a0001c0002t0001g0164 a0001c0002t0001g0165 a0001c0002t0001g0195 others(1): Show |
4 | HG00438.hp2 NA18975.hp1 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.219-1036T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58555976 | |||||||
| chr11:58555994 | T | C | 29 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0012 others(26): Show |
42 | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.219-1054A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58555994 | |||||||
| chr11:58556100 | C | T | 9 | a0002c0003t0001g0011 a0002c0003t0001g0091 a0002c0003t0001g0092 others(6): Show |
11 | HG01243.hp1 HG01261.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.219-1160G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58556100 | |||||||
| chr11:58556158 | A | T | 1 | a0001c0001t0001g0211 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.219-1218T>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58556158 | |||||||
| chr11:58556205 | C | T | 1 | a0001c0001t0001g0051 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.219-1265G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58556205 | |||||||
| chr11:58556261 | A | G | 2 | a0001c0001t0001g0041 a0005c0010t0001g0040 |
2 | HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.219-1321T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58556261 | |||||||
| chr11:58556372 | T | A | 1 | a0001c0001t0001g0052 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.219-1432A>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58556372 | |||||||
| chr11:58556627 | T | C | 1 | a0003c0005t0001g0112 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.219-1687A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58556627 | |||||||
| chr11:58556798 | A | G | 92 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(89): Show |
134 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.219-1858T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58556798 | |||||||
| chr11:58556888 | G | C | 1 | a0001c0002t0001g0182 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.219-1948C>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58556888 | |||||||
| chr11:58557090 | T | G | 1 | a0001c0001t0001g0072 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.219-2150A>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58557090 | |||||||
| chr11:58557289 | G | A | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG02976.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.219-2349C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58557289 | |||||||
| chr11:58557404 | T | A | 2 | a0001c0002t0001g0031 a0001c0002t0001g0159 |
3 | HG02602.hp1 HG03704.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.219-2464A>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58557404 | |||||||
| chr11:58557412 | G | C | 9 | a0002c0003t0001g0011 a0002c0003t0001g0091 a0002c0003t0001g0092 others(6): Show |
11 | HG01243.hp1 HG01261.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.219-2472C>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58557412 | |||||||
| chr11:58557545 | A | G | 1 | a0001c0001t0001g0015 | 2 | HG02683.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.219-2605T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58557545 | |||||||
| chr11:58557600 | T | C | 1 | a0001c0002t0001g0028 | 2 | NA18985.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.219-2660A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58557600 | |||||||
| chr11:58557760 | T | G | 1 | a0001c0001t0001g0228 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.219-2820A>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58557760 | |||||||
| chr11:58557773 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.219-2833G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58557773 | |||||||
| chr11:58558018 | C | A | 221 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(218): Show |
312 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(309): Show |
intron_variant | MODIFIER | c.219-3078G>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58558018 | |||||||
| chr11:58558031 | G | A | 6 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0063 others(3): Show |
10 | NA18950.hp1 NA18951.hp2 NA18984.hp2 others(7): Show |
intron_variant | MODIFIER | c.219-3091C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58558031 | |||||||
| chr11:58558165 | GA | G | 6 | a0001c0001t0001g0041 a0003c0005t0001g0020 a0003c0005t0001g0111 others(3): Show |
7 | HG01496.hp1 HG02922.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.219-3226delT | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58558165 | |||||||
| chr11:58558245 | T | C | 1 | a0002c0003t0001g0091 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.219-3305A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58558245 | |||||||
| chr11:58558324 | A | G | 221 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(218): Show |
312 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(309): Show |
intron_variant | MODIFIER | c.219-3384T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58558324 | |||||||
| chr11:58558355 | T | C | 2 | a0001c0002t0001g0036 a0001c0002t0001g0204 |
3 | HG01099.hp1 HG02148.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.219-3415A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58558355 | |||||||
| chr11:58558405 | C | T | 1 | a0001c0002t0001g0191 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.219-3465G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58558405 | |||||||
| chr11:58558417 | G | A | 1 | a0003c0005t0001g0020 | 2 | HG01496.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.219-3477C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58558417 | |||||||
| chr11:58558540 | C | CA | 22 | a0001c0001t0001g0019 a0001c0001t0001g0075 a0001c0001t0001g0099 others(19): Show |
23 | HG00280.hp1 HG00609.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.219-3601dupT | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58558540 | |||||||
| chr11:58558540 | CA | C | 86 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(83): Show |
123 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.219-3601delT | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58558540 | |||||||
| chr11:58558540 | CAA | C | 11 | a0001c0001t0001g0076 a0001c0001t0001g0081 a0001c0001t0001g0135 others(8): Show |
13 | HG01243.hp1 HG01261.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.219-3602_219-3601d others(4): Show |
LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58558540 | |||||||
| chr11:58558796 | T | C | 1 | a0001c0002t0001g0184 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.219-3856A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58558796 | |||||||
| chr11:58558801 | A | G | 6 | a0001c0001t0001g0041 a0003c0005t0001g0020 a0003c0005t0001g0111 others(3): Show |
7 | HG01496.hp1 HG02922.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.219-3861T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58558801 | |||||||
| chr11:58558824 | T | C | 4 | a0001c0002t0001g0032 a0001c0002t0001g0185 a0001c0002t0001g0186 others(1): Show |
5 | HG01978.hp2 NA18950.hp2 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.219-3884A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58558824 | |||||||
| chr11:58559157 | A | C | 1 | a0001c0001t0001g0124 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.219-4217T>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58559157 | |||||||
| chr11:58559245 | T | C | 1 | a0001c0002t0001g0200 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.219-4305A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58559245 | |||||||
| chr11:58559322 | G | C | 126 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(123): Show |
177 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.219-4382C>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58559322 | |||||||
| chr11:58559374 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.219-4434T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58559374 | |||||||
| chr11:58559522 | T | G | 4 | a0001c0002t0001g0190 a0001c0002t0001g0191 a0001c0002t0001g0192 others(1): Show |
4 | HG02647.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.219-4582A>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58559522 | |||||||
| chr11:58559704 | C | T | 21 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(18): Show |
40 | HG00099.hp2 HG00423.hp2 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.218+4451G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58559704 | |||||||
| chr11:58559767 | T | C | 1 | a0001c0001t0006g0115 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.218+4388A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58559767 | |||||||
| chr11:58559789 | T | C | 1 | a0001c0001t0001g0038 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.218+4366A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58559789 | |||||||
| chr11:58559925 | C | A | 93 | a0001c0001t0001g0075 a0001c0002t0001g0002 a0001c0002t0001g0003 others(90): Show |
133 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.218+4230G>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58559925 | |||||||
| chr11:58559954 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.218+4201G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58559954 | |||||||
| chr11:58560231 | A | G | 1 | a0001c0001t0001g0052 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.218+3924T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58560231 | |||||||
| chr11:58560492 | T | C | 4 | a0001c0002t0001g0190 a0001c0002t0001g0191 a0001c0002t0001g0192 others(1): Show |
4 | HG02647.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.218+3663A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58560492 | |||||||
| chr11:58560499 | G | T | 2 | a0003c0005t0001g0111 a0003c0005t0001g0112 |
2 | HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.218+3656C>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58560499 | |||||||
| chr11:58560997 | A | G | 8 | a0001c0001t0001g0010 a0001c0001t0001g0081 a0001c0001t0001g0082 others(5): Show |
10 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.218+3158T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58560997 | |||||||
| chr11:58561106 | C | T | 2 | a0001c0002t0001g0006 a0001c0002t0001g0196 |
6 | HG00642.hp2 HG01106.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.218+3049G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58561106 | |||||||
| chr11:58561119 | G | A | 111 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(108): Show |
159 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.218+3036C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58561119 | |||||||
| chr11:58561134 | TTCTC | T | 7 | a0001c0001t0001g0041 a0001c0002t0001g0146 a0003c0005t0001g0020 others(4): Show |
8 | HG00621.hp2 HG01496.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.218+3017_218+3020d others(6): Show |
LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58561134 | |||||||
| chr11:58561256 | G | A | 93 | a0001c0001t0001g0075 a0001c0002t0001g0002 a0001c0002t0001g0003 others(90): Show |
133 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.218+2899C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58561256 | |||||||
| chr11:58561379 | A | C | 1 | a0001c0001t0001g0069 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.218+2776T>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58561379 | |||||||
| chr11:58561479 | A | G | 220 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(217): Show |
311 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.218+2676T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58561479 | |||||||
| chr11:58561825 | T | C | 1 | a0001c0002t0001g0186 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.218+2330A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58561825 | |||||||
| chr11:58562496 | A | G | 3 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0231 |
7 | HG02280.hp2 HG02896.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.218+1659T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58562496 | |||||||
| chr11:58562811 | GT | G | 220 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(217): Show |
311 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.218+1343delA | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58562811 | |||||||
| chr11:58562813 | G | C | 1 | a0001c0001t0001g0110 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.218+1342C>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58562813 | |||||||
| chr11:58562814 | G | C | 3 | a0001c0002t0001g0160 a0001c0002t0001g0188 a0001c0002t0001g0209 |
3 | HG00280.hp2 HG01516.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.218+1341C>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58562814 | |||||||
| chr11:58562894 | A | G | 1 | a0001c0001t0001g0051 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.218+1261T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58562894 | |||||||
| chr11:58563201 | T | G | 1 | a0001c0001t0001g0117 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.218+954A>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58563201 | |||||||
| chr11:58563222 | T | C | 5 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0076 others(2): Show |
9 | HG02280.hp2 HG02896.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.218+933A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58563222 | |||||||
| chr11:58563836 | A | G | 29 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(26): Show |
48 | HG00099.hp2 HG00423.hp2 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.218+319T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58563836 | |||||||
| chr11:58563865 | C | T | 1 | a0001c0001t0002g0121 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.218+290G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58563865 | |||||||
| chr11:58563917 | G | T | 1 | a0001c0001t0001g0232 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.218+238C>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58563917 | |||||||
| chr11:58563976 | A | G | 1 | a0001c0001t0001g0023 | 2 | HG02071.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.218+179T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 3/8 | chr11 | 58563976 | |||||||
| chr11:58564249 | A | T | 1 | a0001c0002t0001g0030 | 2 | HG02723.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.172-48T>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58564249 | |||||||
| chr11:58564284 | A | G | 6 | a0001c0001t0001g0041 a0003c0005t0001g0020 a0003c0005t0001g0111 others(3): Show |
7 | HG01496.hp1 HG02922.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.172-83T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58564284 | |||||||
| chr11:58564367 | A | G | 1 | a0001c0001t0001g0217 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.172-166T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58564367 | |||||||
| chr11:58564369 | C | G | 3 | a0001c0002t0001g0160 a0001c0002t0001g0188 a0001c0002t0001g0209 |
3 | HG00280.hp2 HG01516.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.172-168G>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58564369 | |||||||
| chr11:58564395 | C | T | 14 | a0001c0001t0001g0019 a0001c0001t0001g0099 a0001c0001t0001g0100 others(11): Show |
15 | HG00280.hp1 HG01884.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.172-194G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58564395 | |||||||
| chr11:58564451 | C | G | 143 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(140): Show |
195 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(192): Show |
intron_variant | MODIFIER | c.172-250G>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58564451 | |||||||
| chr11:58564930 | G | A | 1 | a0001c0004t0001g0107 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.172-729C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58564930 | |||||||
| chr11:58564975 | C | T | 1 | a0001c0002t0001g0159 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.172-774G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58564975 | |||||||
| chr11:58564988 | G | A | 9 | a0002c0003t0001g0011 a0002c0003t0001g0091 a0002c0003t0001g0092 others(6): Show |
11 | HG01243.hp1 HG01261.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.172-787C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58564988 | |||||||
| chr11:58565073 | G | A | 1 | a0001c0002t0001g0187 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.172-872C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58565073 | |||||||
| chr11:58565138 | T | A | 1 | a0001c0002t0001g0201 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.172-937A>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58565138 | |||||||
| chr11:58565179 | G | A | 6 | a0001c0001t0001g0041 a0003c0005t0001g0020 a0003c0005t0001g0111 others(3): Show |
7 | HG01496.hp1 HG02922.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.172-978C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58565179 | |||||||
| chr11:58565260 | G | A | 19 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0018 others(16): Show |
25 | HG01175.hp2 HG01192.hp2 HG01515.hp2 others(22): Show |
intron_variant | MODIFIER | c.172-1059C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58565260 | |||||||
| chr11:58565308 | C | T | 1 | a0001c0002t0001g0158 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.172-1107G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58565308 | |||||||
| chr11:58565329 | C | G | 1 | a0001c0002t0001g0156 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.172-1128G>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58565329 | |||||||
| chr11:58565362 | T | C | 1 | a0001c0001t0002g0121 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.172-1161A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58565362 | |||||||
| chr11:58565533 | CA | C | 72 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(69): Show |
96 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.172-1333delT | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58565533 | |||||||
| chr11:58565741 | G | C | 1 | a0001c0001t0001g0039 | 2 | NA18983.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.172-1540C>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58565741 | |||||||
| chr11:58565747 | C | G | 1 | a0001c0002t0001g0157 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.172-1546G>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58565747 | |||||||
| chr11:58565891 | G | C | 1 | a0001c0002t0001g0188 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.172-1690C>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58565891 | |||||||
| chr11:58565979 | C | G | 37 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0015 others(34): Show |
47 | HG00544.hp1 HG00621.hp1 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.172-1778G>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58565979 | |||||||
| chr11:58565985 | G | T | 1 | a0002c0003t0001g0091 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.172-1784C>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58565985 | |||||||
| chr11:58566132 | CAT | C | 67 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(64): Show |
90 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.172-1933_172-1932d others(4): Show |
LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58566132 | |||||||
| chr11:58566430 | A | G | 2 | a0001c0001t0001g0041 a0005c0010t0001g0040 |
2 | HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.172-2229T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58566430 | |||||||
| chr11:58566431 | C | T | 2 | a0001c0001t0001g0041 a0005c0010t0001g0040 |
2 | HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.172-2230G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58566431 | |||||||
| chr11:58566579 | T | C | 5 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0076 others(2): Show |
9 | HG02280.hp2 HG02896.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.172-2378A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58566579 | |||||||
| chr11:58566615 | A | G | 111 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(108): Show |
159 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.172-2414T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58566615 | |||||||
| chr11:58566620 | T | C | 8 | a0001c0001t0001g0010 a0001c0001t0001g0081 a0001c0001t0001g0082 others(5): Show |
10 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.172-2419A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58566620 | |||||||
| chr11:58566630 | A | G | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG02976.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.172-2429T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58566630 | |||||||
| chr11:58566670 | G | A | 7 | a0001c0002t0001g0014 a0001c0002t0001g0033 a0001c0002t0001g0189 others(4): Show |
10 | HG02109.hp1 HG02145.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.172-2469C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58566670 | |||||||
| chr11:58566720 | A | G | 92 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(89): Show |
134 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.172-2519T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58566720 | |||||||
| chr11:58566782 | G | A | 1 | a0001c0001t0001g0215 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.172-2581C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58566782 | |||||||
| chr11:58566981 | G | T | 1 | a0001c0002t0001g0156 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.172-2780C>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58566981 | |||||||
| chr11:58567000 | C | CTG | 3 | a0001c0001t0001g0017 a0001c0001t0001g0216 a0001c0002t0001g0155 |
4 | HG00741.hp1 HG01167.hp1 NA18946.hp2 others(1): Show |
intron_variant | MODIFIER | c.172-2801_172-2800d others(4): Show |
LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58567000 | |||||||
| chr11:58567000 | CTG | C | 37 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0018 others(34): Show |
46 | HG00597.hp1 HG01175.hp2 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.172-2801_172-2800d others(4): Show |
LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58567000 | |||||||
| chr11:58567024 | A | G | 1 | a0001c0002t0001g0154 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.172-2823T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58567024 | |||||||
| chr11:58567095 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.172-2894C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58567095 | |||||||
| chr11:58567174 | A | G | 1 | a0001c0001t0001g0215 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.172-2973T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58567174 | |||||||
| chr11:58567197 | G | T | 6 | a0001c0001t0001g0041 a0003c0005t0001g0020 a0003c0005t0001g0111 others(3): Show |
7 | HG01496.hp1 HG02922.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.172-2996C>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58567197 | |||||||
| chr11:58567369 | A | C | 1 | a0001c0002t0001g0205 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.172-3168T>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58567369 | |||||||
| chr11:58567455 | C | T | 9 | a0001c0002t0001g0013 a0001c0002t0001g0027 a0001c0002t0001g0028 others(6): Show |
13 | HG00558.hp1 HG02015.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.171+3101G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58567455 | |||||||
| chr11:58567665 | C | G | 1 | a0001c0001t0001g0099 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.171+2891G>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58567665 | |||||||
| chr11:58568070 | A | G | 2 | a0001c0001t0001g0041 a0005c0010t0001g0040 |
2 | HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.171+2486T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58568070 | |||||||
| chr11:58568075 | A | G | 9 | a0002c0003t0001g0011 a0002c0003t0001g0091 a0002c0003t0001g0092 others(6): Show |
11 | HG01243.hp1 HG01261.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.171+2481T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58568075 | |||||||
| chr11:58568077 | C | T | 4 | a0001c0002t0001g0146 a0001c0002t0001g0147 a0001c0002t0001g0148 others(1): Show |
4 | HG00621.hp2 NA18942.hp2 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.171+2479G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58568077 | |||||||
| chr11:58568464 | A | G | 1 | a0002c0003t0001g0098 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.171+2092T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58568464 | |||||||
| chr11:58568506 | G | T | 2 | a0001c0001t0001g0043 a0001c0001t0001g0050 |
2 | NA18991.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.171+2050C>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58568506 | |||||||
| chr11:58568602 | C | CA | 5 | a0001c0001t0001g0019 a0001c0001t0001g0108 a0001c0001t0001g0109 others(2): Show |
6 | HG00438.hp2 HG02486.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.171+1953dupT | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58568602 | |||||||
| chr11:58568602 | CA | C | 90 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(87): Show |
120 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.171+1953delT | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58568602 | |||||||
| chr11:58568876 | A | G | 19 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0018 others(16): Show |
25 | HG01175.hp2 HG01192.hp2 HG01515.hp2 others(22): Show |
intron_variant | MODIFIER | c.171+1680T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58568876 | |||||||
| chr11:58568943 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.171+1613C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58568943 | |||||||
| chr11:58569071 | G | C | 143 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(140): Show |
195 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(192): Show |
intron_variant | MODIFIER | c.171+1485C>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58569071 | |||||||
| chr11:58569147 | G | A | 4 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0122 others(1): Show |
9 | HG01074.hp1 HG01243.hp2 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.171+1409C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58569147 | |||||||
| chr11:58569378 | T | G | 15 | a0001c0002t0001g0006 a0001c0002t0001g0034 a0001c0002t0001g0035 others(12): Show |
22 | HG00642.hp2 HG00741.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.171+1178A>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58569378 | |||||||
| chr11:58569493 | ATCC | A | 6 | a0001c0001t0001g0041 a0003c0005t0001g0020 a0003c0005t0001g0111 others(3): Show |
7 | HG01496.hp1 HG02922.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.171+1060_171+1062d others(5): Show |
LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58569493 | |||||||
| chr11:58569551 | G | A | 111 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(108): Show |
159 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.171+1005C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58569551 | |||||||
| chr11:58569675 | C | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0123 |
4 | HG00558.hp2 NA18946.hp1 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.171+881G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58569675 | |||||||
| chr11:58569816 | C | G | 1 | a0001c0001t0001g0117 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.171+740G>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58569816 | |||||||
| chr11:58569852 | G | A | 2 | a0001c0001t0001g0009 a0001c0001t0001g0231 |
5 | HG02896.hp2 HG03098.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.171+704C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58569852 | |||||||
| chr11:58569944 | A | C | 5 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(2): Show |
5 | HG00621.hp1 HG02523.hp1 NA18949.hp2 others(2): Show |
intron_variant | MODIFIER | c.171+612T>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58569944 | |||||||
| chr11:58570036 | G | A | 1 | a0008c0007t0001g0202 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.171+520C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58570036 | |||||||
| chr11:58570075 | G | A | 3 | a0001c0002t0001g0036 a0001c0002t0001g0203 a0001c0002t0001g0204 |
4 | HG01099.hp1 HG02148.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.171+481C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58570075 | |||||||
| chr11:58570082 | T | A | 8 | a0001c0001t0001g0010 a0001c0001t0001g0081 a0001c0001t0001g0082 others(5): Show |
10 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.171+474A>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58570082 | |||||||
| chr11:58570334 | A | T | 1 | a0001c0002t0001g0025 | 2 | NA18965.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.171+222T>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 2/8 | chr11 | 58570334 | |||||||
| chr11:58570740 | T | C | 1 | a0001c0002t0001g0205 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.14-27A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58570740 | |||||||
| chr11:58570820 | A | G | 1 | a0001c0001t0006g0115 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.14-107T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58570820 | |||||||
| chr11:58570829 | A | G | 1 | a0003c0005t0001g0020 | 2 | HG01496.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.14-116T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58570829 | |||||||
| chr11:58571041 | T | A | 1 | a0001c0002t0001g0206 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.14-328A>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58571041 | |||||||
| chr11:58571122 | C | T | 8 | a0001c0001t0001g0010 a0001c0001t0001g0081 a0001c0001t0001g0082 others(5): Show |
10 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.14-409G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58571122 | |||||||
| chr11:58571155 | T | C | 67 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(64): Show |
90 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.14-442A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58571155 | |||||||
| chr11:58571342 | A | AAAAT | 50 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(47): Show |
69 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.14-633_14-630dupAT others(2): Show |
LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58571342 | |||||||
| chr11:58571342 | A | AAAATAAA others(1): Show |
8 | a0001c0001t0001g0021 a0001c0001t0001g0043 a0001c0001t0001g0044 others(5): Show |
9 | HG01074.hp1 HG01255.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.14-637_14-630dupAT others(6): Show |
LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58571342 | |||||||
| chr11:58571342 | AAAAT | A | 106 | a0001c0001t0001g0010 a0001c0001t0001g0075 a0001c0001t0001g0081 others(103): Show |
149 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.14-633_14-630delAT others(2): Show |
LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58571342 | |||||||
| chr11:58571342 | AAAATAAA others(1): Show |
A | 26 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0100 others(23): Show |
29 | HG00280.hp1 HG01243.hp1 HG01261.hp2 others(26): Show |
intron_variant | MODIFIER | c.14-637_14-630delAT others(6): Show |
LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58571342 | |||||||
| chr11:58571562 | T | G | 1 | a0001c0001t0006g0115 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.14-849A>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58571562 | |||||||
| chr11:58571651 | T | C | 67 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(64): Show |
90 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.14-938A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58571651 | |||||||
| chr11:58571663 | C | CT | 13 | a0001c0001t0001g0019 a0001c0001t0001g0099 a0001c0001t0001g0100 others(10): Show |
14 | HG00280.hp1 HG01884.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.14-951dupA | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58571663 | |||||||
| chr11:58571812 | T | C | 1 | a0001c0002t0001g0207 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.14-1099A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58571812 | |||||||
| chr11:58571867 | G | A | 1 | a0001c0002t0001g0208 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.14-1154C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58571867 | |||||||
| chr11:58571943 | T | C | 1 | a0001c0002t0001g0209 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.14-1230A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58571943 | |||||||
| chr11:58572041 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.14-1328A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58572041 | |||||||
| chr11:58572094 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.14-1381C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58572094 | |||||||
| chr11:58572729 | A | C | 1 | a0001c0001t0001g0117 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.14-2016T>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58572729 | |||||||
| chr11:58573011 | C | T | 67 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(64): Show |
90 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.14-2298G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58573011 | |||||||
| chr11:58573021 | G | A | 1 | a0002c0003t0001g0098 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.14-2308C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58573021 | |||||||
| chr11:58573072 | C | T | 1 | a0001c0002t0001g0116 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.14-2359G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58573072 | |||||||
| chr11:58573186 | C | T | 9 | a0002c0003t0001g0011 a0002c0003t0001g0091 a0002c0003t0001g0092 others(6): Show |
11 | HG01243.hp1 HG01261.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.14-2473G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58573186 | |||||||
| chr11:58573190 | G | A | 1 | a0001c0002t0001g0210 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.14-2477C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58573190 | |||||||
| chr11:58573246 | CAA | C | 75 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(72): Show |
104 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.13+2512_13+2513del others(2): Show |
LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58573246 | |||||||
| chr11:58573262 | G | A | 1 | a0007c0006t0001g0212 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.13+2498C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58573262 | |||||||
| chr11:58573263 | A | G | 1 | a0007c0006t0001g0212 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.13+2497T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58573263 | |||||||
| chr11:58573279 | A | G | 1 | a0001c0001t0001g0213 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.13+2481T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58573279 | |||||||
| chr11:58573897 | T | C | 1 | a0001c0001t0001g0211 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.13+1863A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58573897 | |||||||
| chr11:58573923 | C | T | 1 | a0005c0010t0001g0040 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.13+1837G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58573923 | |||||||
| chr11:58574033 | CATTTCTC others(11): Show |
C | 44 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(41): Show |
69 | HG00099.hp2 HG00423.hp2 HG00733.hp1 others(66): Show |
intron_variant | MODIFIER | c.13+1709_13+1726del others(18): Show |
LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58574033 | |||||||
| chr11:58574547 | C | G | 1 | a0001c0001t0001g0075 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.13+1213G>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58574547 | |||||||
| chr11:58574608 | G | A | 1 | a0007c0006t0001g0212 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.13+1152C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58574608 | |||||||
| chr11:58574838 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.13+922G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58574838 | |||||||
| chr11:58574877 | T | C | 21 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(18): Show |
40 | HG00099.hp2 HG00423.hp2 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.13+883A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58574877 | |||||||
| chr11:58575156 | A | G | 37 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0015 others(34): Show |
47 | HG00544.hp1 HG00621.hp1 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.13+604T>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58575156 | |||||||
| chr11:58575241 | T | C | 1 | a0001c0001t0001g0230 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.13+519A>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58575241 | |||||||
| chr11:58575290 | C | A | 2 | a0001c0001t0001g0009 a0001c0001t0001g0231 |
5 | HG02896.hp2 HG03098.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.13+470G>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58575290 | |||||||
| chr11:58575336 | G | A | 4 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0234 others(1): Show |
4 | HG01175.hp2 HG01192.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.13+424C>T | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58575336 | |||||||
| chr11:58575413 | C | T | 1 | a0001c0002t0001g0042 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.13+347G>A | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58575413 | |||||||
| chr11:58575425 | A | C | 2 | a0001c0001t0001g0041 a0005c0010t0001g0040 |
2 | HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.13+335T>G | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58575425 | |||||||
| chr11:58575748 | C | G | 2 | a0001c0001t0001g0041 a0005c0010t0001g0040 |
2 | HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.13+12G>C | LPXN | ENSG00000110031.13 | transcript | ENST00000395074.7 | protein_coding | 1/8 | chr11 | 58575748 |