Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51557 |
| ensemblid | ENSG00000146166.17 |
| hgncid | 21016 |
| symbol | LGSN |
| name | lengsin, lens protein with glutamine synthetase domain |
| refseq_nuc | NM_016571.3 |
| refseq_prot | NP_057655.2 |
| ensembl_nuc | ENST00000370657.9 |
| ensembl_prot | ENSP00000359691.4 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 63275951 |
| end | 63319983 |
| strand | - |
| ver | v1.2 |
| region | chr6:63275951-63319983 |
| region5000 | chr6:63270951-63324983 |
| regionname0 | LGSN_chr6_63275951_63319983 |
| regionname5000 | LGSN_chr6_63270951_63324983 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 509 | 281 | 54 | 59 | 132 | 12 | 22 | 105 | LGSN_chr6_63270951_63324983 | LGSN | MNNEE others(504): Show |
chr6 | 63270951 | 63324983 |
| a0002 | 0/0 | 509 | 20 | 19 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | MNNEE others(504): Show |
chr6 | 63270951 | 63324983 |
| a0003 | 0/0 | 509 | 3 | 1 | 2 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | MNNEE others(504): Show |
chr6 | 63270951 | 63324983 |
| a0004 | 0/0 | 509 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | MNNEE others(504): Show |
chr6 | 63270951 | 63324983 |
| a0005 | 0/0 | 509 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | LGSN_chr6_63270951_63324983 | LGSN | MNNEE others(504): Show |
chr6 | 63270951 | 63324983 |
| a0006 | 0/0 | 509 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | MNNEE others(504): Show |
chr6 | 63270951 | 63324983 |
| a0007 | 0/0 | 509 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | MNNEE others(504): Show |
chr6 | 63270951 | 63324983 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1527 | 271 | 53 | 54 | 130 | 10 | 22 | LGSN_chr6_63270951_63324983 | LGSN | ATGAA others(1522): Show |
chr6 | 63270951 | 63324983 | ||
| a0001c0004 | 0/0 | 1527 | 7 | 0 | 5 | 0 | 2 | 0 | LGSN_chr6_63270951_63324983 | LGSN | ATGAA others(1522): Show |
chr6 | 63270951 | 63324983 | ||
| a0001c0010 | 0/0 | 1527 | 2 | 0 | 0 | 2 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | ATGAA others(1522): Show |
chr6 | 63270951 | 63324983 | ||
| a0001c0012 | 0/0 | 1527 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | ATGAA others(1522): Show |
chr6 | 63270951 | 63324983 | ||
| a0002c0002 | 0/0 | 1527 | 10 | 10 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | ATGAA others(1522): Show |
chr6 | 63270951 | 63324983 | ||
| a0002c0003 | 0/0 | 1527 | 8 | 8 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | ATGAA others(1522): Show |
chr6 | 63270951 | 63324983 | ||
| a0002c0007 | 0/0 | 1527 | 2 | 1 | 1 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | ATGAA others(1522): Show |
chr6 | 63270951 | 63324983 | ||
| a0003c0005 | 0/0 | 1527 | 3 | 1 | 2 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | ATGAA others(1522): Show |
chr6 | 63270951 | 63324983 | ||
| a0004c0006 | 0/0 | 1527 | 3 | 3 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | ATGAA others(1522): Show |
chr6 | 63270951 | 63324983 | ||
| a0005c0008 | 0/0 | 1527 | 2 | 0 | 0 | 2 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | ATGAA others(1522): Show |
chr6 | 63270951 | 63324983 | ||
| a0006c0009 | 0/0 | 1527 | 2 | 2 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | ATGAA others(1522): Show |
chr6 | 63270951 | 63324983 | ||
| a0007c0011 | 0/0 | 1527 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | ATGAA others(1522): Show |
chr6 | 63270951 | 63324983 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5640 | 76 | 12 | 14 | 39 | 5 | 6 | LGSN_chr6_63270951_63324983 | LGSN | GATAT others(5635): Show |
chr6 | 63270951 | 63324983 |
| a0001c0001t0002 | 0/0 | 5640 | 66 | 2 | 19 | 36 | 3 | 6 | LGSN_chr6_63270951_63324983 | LGSN | GATAT others(5635): Show |
chr6 | 63270951 | 63324983 |
| a0001c0001t0003 | 1/0 | 5640 | 56 | 22 | 10 | 17 | 2 | 4 | LGSN_chr6_63270951_63324983 | LGSN | GATAT others(5635): Show |
chr6 | 63270951 | 63324983 |
| a0001c0001t0004 | 0/0 | 5640 | 14 | 0 | 1 | 9 | 0 | 4 | LGSN_chr6_63270951_63324983 | LGSN | GATAT others(5635): Show |
chr6 | 63270951 | 63324983 |
| a0001c0001t0006 | 0/0 | 5640 | 8 | 0 | 0 | 8 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | GATAT others(5635): Show |
chr6 | 63270951 | 63324983 |
| a0001c0001t0007 | 0/0 | 5641 | 8 | 1 | 1 | 6 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | GATAT others(5636): Show |
chr6 | 63270951 | 63324983 |
| a0001c0001t0008 | 0/0 | 5641 | 5 | 1 | 0 | 4 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | GATAT others(5636): Show |
chr6 | 63270951 | 63324983 |
| a0001c0001t0009 | 0/0 | 5641 | 6 | 0 | 5 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | GATAT others(5636): Show |
chr6 | 63270951 | 63324983 |
| a0001c0001t0011 | 0/0 | 5641 | 3 | 0 | 0 | 3 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | GATAT others(5636): Show |
chr6 | 63270951 | 63324983 |
| a0001c0001t0012 | 0/0 | 5640 | 3 | 3 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | GATAT others(5635): Show |
chr6 | 63270951 | 63324983 |
| a0001c0001t0013 | 0/1 | 5641 | 3 | 2 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | GATAT others(5636): Show |
chr6 | 63270951 | 63324983 |
| a0001c0001t0014 | 0/0 | 5639 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | GATAT others(5634): Show |
chr6 | 63270951 | 63324983 |
| a0001c0001t0015 | 0/0 | 5640 | 2 | 2 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | GATAT others(5635): Show |
chr6 | 63270951 | 63324983 |
| a0001c0001t0016 | 0/0 | 5638 | 2 | 2 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | GATAT others(5633): Show |
chr6 | 63270951 | 63324983 |
| a0001c0001t0017 | 0/0 | 5640 | 2 | 0 | 0 | 2 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | GATAT others(5635): Show |
chr6 | 63270951 | 63324983 |
| a0001c0001t0021 | 0/0 | 5641 | 1 | 0 | 0 | 0 | 0 | 1 | LGSN_chr6_63270951_63324983 | LGSN | GATAT others(5636): Show |
chr6 | 63270951 | 63324983 |
| a0001c0001t0022 | 0/0 | 5640 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | GATAT others(5635): Show |
chr6 | 63270951 | 63324983 |
| a0001c0001t0023 | 0/0 | 5640 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | GATAT others(5635): Show |
chr6 | 63270951 | 63324983 |
| a0001c0001t0024 | 0/0 | 5641 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | GATAT others(5636): Show |
chr6 | 63270951 | 63324983 |
| a0001c0001t0025 | 0/0 | 5641 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | GATAT others(5636): Show |
chr6 | 63270951 | 63324983 |
| a0001c0001t0029 | 0/0 | 5637 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | GATAT others(5632): Show |
chr6 | 63270951 | 63324983 |
| a0001c0001t0030 | 0/0 | 5640 | 1 | 0 | 1 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | GATAT others(5635): Show |
chr6 | 63270951 | 63324983 |
| a0001c0001t0031 | 0/0 | 5640 | 1 | 0 | 1 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | GATAT others(5635): Show |
chr6 | 63270951 | 63324983 |
| a0001c0001t0032 | 0/0 | 5640 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | GATAT others(5635): Show |
chr6 | 63270951 | 63324983 |
| a0001c0001t0033 | 0/0 | 5640 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | GATAT others(5635): Show |
chr6 | 63270951 | 63324983 |
| a0001c0001t0034 | 0/0 | 5640 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | GATAT others(5635): Show |
chr6 | 63270951 | 63324983 |
| a0001c0001t0035 | 0/0 | 5640 | 1 | 0 | 1 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | GATAT others(5635): Show |
chr6 | 63270951 | 63324983 |
| a0001c0001t0036 | 0/0 | 5640 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | GATAT others(5635): Show |
chr6 | 63270951 | 63324983 |
| a0001c0001t0037 | 0/0 | 5640 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | GATAT others(5635): Show |
chr6 | 63270951 | 63324983 |
| a0001c0001t0038 | 0/0 | 5640 | 1 | 0 | 1 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | GATAT others(5635): Show |
chr6 | 63270951 | 63324983 |
| a0001c0001t0042 | 0/0 | 5640 | 1 | 0 | 0 | 0 | 0 | 1 | LGSN_chr6_63270951_63324983 | LGSN | GATAT others(5635): Show |
chr6 | 63270951 | 63324983 |
| a0001c0004t0003 | 0/0 | 5640 | 6 | 0 | 4 | 0 | 2 | 0 | LGSN_chr6_63270951_63324983 | LGSN | GATAT others(5635): Show |
chr6 | 63270951 | 63324983 |
| a0001c0004t0008 | 0/0 | 5641 | 1 | 0 | 1 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | GATAT others(5636): Show |
chr6 | 63270951 | 63324983 |
| a0001c0010t0003 | 0/0 | 5640 | 2 | 0 | 0 | 2 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | GATAT others(5635): Show |
chr6 | 63270951 | 63324983 |
| a0001c0012t0001 | 0/0 | 5640 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | GATAT others(5635): Show |
chr6 | 63270951 | 63324983 |
| a0002c0002t0010 | 0/0 | 5633 | 6 | 6 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | GATAT others(5628): Show |
chr6 | 63270951 | 63324983 |
| a0002c0002t0018 | 0/0 | 5633 | 2 | 2 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | GATAT others(5628): Show |
chr6 | 63270951 | 63324983 |
| a0002c0002t0040 | 0/0 | 5640 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | GATAT others(5635): Show |
chr6 | 63270951 | 63324983 |
| a0002c0002t0041 | 0/0 | 5638 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | GATAT others(5633): Show |
chr6 | 63270951 | 63324983 |
| a0002c0003t0005 | 0/0 | 5639 | 8 | 8 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | GATAT others(5634): Show |
chr6 | 63270951 | 63324983 |
| a0002c0007t0019 | 0/0 | 5633 | 2 | 1 | 1 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | GATAT others(5628): Show |
chr6 | 63270951 | 63324983 |
| a0003c0005t0001 | 0/0 | 5640 | 2 | 0 | 2 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | GATAT others(5635): Show |
chr6 | 63270951 | 63324983 |
| a0003c0005t0004 | 0/0 | 5640 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | GATAT others(5635): Show |
chr6 | 63270951 | 63324983 |
| a0004c0006t0014 | 0/0 | 5639 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | GATAT others(5634): Show |
chr6 | 63270951 | 63324983 |
| a0004c0006t0027 | 0/0 | 5638 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | GATAT others(5633): Show |
chr6 | 63270951 | 63324983 |
| a0004c0006t0028 | 0/0 | 5639 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | GATAT others(5634): Show |
chr6 | 63270951 | 63324983 |
| a0005c0008t0001 | 0/0 | 5640 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | GATAT others(5635): Show |
chr6 | 63270951 | 63324983 |
| a0005c0008t0026 | 0/0 | 5642 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | GATAT others(5637): Show |
chr6 | 63270951 | 63324983 |
| a0006c0009t0020 | 0/0 | 5638 | 2 | 2 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | GATAT others(5633): Show |
chr6 | 63270951 | 63324983 |
| a0007c0011t0039 | 0/0 | 5633 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | GATAT others(5628): Show |
chr6 | 63270951 | 63324983 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0011 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0002g0004 | 0/0 | 5 | 0 | 2 | 2 | 0 | 1 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0002g0007 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0002g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0002g0010 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0002g0014 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0002g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0002g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0003g0002 | 0/0 | 6 | 0 | 1 | 2 | 1 | 2 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0003g0005 | 0/0 | 5 | 3 | 0 | 1 | 0 | 1 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0003g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0003g0024 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0003g0089 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0004g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0004g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0004g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0004g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0004g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0004g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0004g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0004g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0004g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0006g0001 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0006g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0006g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0007g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0007g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0007g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0007g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0007g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0007g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0007g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0008g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0008g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0008g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0008g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0008g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0009g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0009g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0009g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0009g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0009g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0009g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0011g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0011g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0011g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0012g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0013g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0013g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0013g0151 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0014g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0015g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0015g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0016g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0017g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0017g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0021g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0022g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0023g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0024g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0025g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0029g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0030g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0031g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0032g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0033g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0034g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0035g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0036g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0037g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0038g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0001t0042g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0004t0003g0008 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0004t0003g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0004t0003g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0004t0008g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0010t0003g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0001c0012t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0002c0002t0010g0006 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0002c0002t0010g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0002c0002t0018g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0002c0002t0018g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0002c0002t0040g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0002c0002t0041g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0002c0003t0005g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0002c0003t0005g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0002c0003t0005g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0002c0003t0005g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0002c0003t0005g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0002c0007t0019g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0002c0007t0019g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0003c0005t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0003c0005t0004g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0004c0006t0014g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0004c0006t0027g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0004c0006t0028g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0005c0008t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0005c0008t0026g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0006c0009t0020g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0006c0009t0020g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| a0007c0011t0039g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0004 | t0003 | g0008 | EUR | GBR | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0002 | EUR | GBR | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0147 | EUR | GBR | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0210 | EUR | GBR | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0148 | EUR | FIN | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0149 | EUR | FIN | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0145 | EUR | FIN | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0212 | EUR | FIN | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG00544 | hp1 | a0001 | c0001 | t0007 | g0093 | EAS | CHS | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG00544 | hp2 | a0001 | c0001 | t0006 | g0001 | EAS | CHS | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | CHS | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG00558 | hp2 | a0001 | c0010 | t0003 | g0023 | EAS | CHS | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG00597 | hp1 | a0001 | c0001 | t0006 | g0001 | EAS | CHS | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0191 | EAS | CHS | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | CHS | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0099 | AMR | PUR | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG00639 | hp2 | a0001 | c0001 | t0035 | g0127 | AMR | PUR | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0211 | AMR | PUR | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG00733 | hp2 | a0001 | c0001 | t0009 | g0162 | AMR | PUR | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG00735 | hp2 | a0001 | c0001 | t0009 | g0163 | AMR | PUR | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG00738 | hp1 | a0001 | c0001 | t0007 | g0133 | AMR | PUR | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG00738 | hp2 | a0001 | c0004 | t0003 | g0008 | AMR | PUR | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0167 | AMR | PUR | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0034 | AMR | PUR | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG01069 | hp2 | a0002 | c0007 | t0019 | g0228 | AMR | PUR | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG01070 | hp1 | a0001 | c0004 | t0003 | g0109 | AMR | PUR | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0070 | AMR | PUR | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG01071 | hp1 | a0001 | c0004 | t0003 | g0008 | AMR | PUR | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0034 | AMR | PUR | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0081 | AMR | PUR | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG01106 | hp2 | a0001 | c0001 | t0004 | g0220 | AMR | PUR | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG01109 | hp1 | a0001 | c0001 | t0030 | g0108 | AMR | PUR | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG01109 | hp2 | a0003 | c0005 | t0001 | g0031 | AMR | PUR | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0171 | AMR | PUR | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG01175 | hp1 | a0001 | c0004 | t0008 | g0152 | AMR | PUR | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0206 | AMR | PUR | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0024 | AMR | PUR | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0207 | AMR | PUR | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG01243 | hp1 | a0001 | c0004 | t0003 | g0153 | AMR | PUR | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0072 | AMR | PUR | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0154 | AMR | CLM | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | CLM | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG01358 | hp2 | a0003 | c0005 | t0001 | g0031 | AMR | CLM | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | CLM | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0071 | EUR | IBS | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0024 | EUR | IBS | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG01884 | hp1 | a0002 | c0002 | t0010 | g0239 | AFR | ACB | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | ACB | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0135 | AFR | ACB | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0204 | AMR | PEL | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG01934 | hp1 | a0001 | c0001 | t0009 | g0159 | AMR | PEL | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG01952 | hp1 | a0001 | c0001 | t0009 | g0095 | AMR | PEL | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG01952 | hp2 | a0001 | c0001 | t0009 | g0216 | AMR | PEL | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0110 | AMR | PEL | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG01978 | hp2 | a0001 | c0001 | t0038 | g0134 | AMR | PEL | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02027 | hp1 | a0005 | c0008 | t0026 | g0209 | EAS | KHV | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02027 | hp2 | a0001 | c0001 | t0011 | g0066 | EAS | KHV | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | ACB | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0138 | EAS | KHV | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02056 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | KHV | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | KHV | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0113 | EAS | KHV | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0096 | EAS | KHV | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02132 | hp1 | a0001 | c0001 | t0023 | g0061 | EAS | KHV | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02135 | hp1 | a0001 | c0001 | t0008 | g0155 | EAS | KHV | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02135 | hp2 | a0001 | c0001 | t0008 | g0174 | EAS | KHV | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02145 | hp1 | a0002 | c0003 | t0005 | g0015 | AFR | ACB | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0203 | AFR | ACB | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PEL | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0086 | AMR | PEL | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | CDX | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | CDX | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02257 | hp1 | a0001 | c0001 | t0015 | g0189 | AFR | ACB | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0085 | AFR | ACB | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02258 | hp1 | a0002 | c0002 | t0010 | g0006 | AFR | ACB | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02258 | hp2 | a0002 | c0003 | t0005 | g0015 | AFR | ACB | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0205 | AMR | PEL | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02280 | hp1 | a0004 | c0006 | t0014 | g0234 | AFR | ACB | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02280 | hp2 | a0001 | c0001 | t0034 | g0126 | AFR | ACB | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02293 | hp1 | a0001 | c0001 | t0031 | g0222 | AMR | PEL | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0129 | AMR | PEL | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0107 | AFR | ACB | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0180 | AFR | ACB | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | KHV | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02572 | hp1 | a0003 | c0005 | t0004 | g0188 | AFR | GWD | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0157 | AFR | GWD | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02615 | hp2 | a0002 | c0003 | t0005 | g0242 | AFR | GWD | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0016 | AFR | GWD | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02630 | hp1 | a0001 | c0001 | t0016 | g0030 | AFR | GWD | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0091 | AFR | GWD | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02647 | hp1 | a0002 | c0007 | t0019 | g0227 | AFR | GWD | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02647 | hp2 | a0002 | c0003 | t0005 | g0015 | AFR | GWD | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0076 | SAS | PJL | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0017 | SAS | PJL | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02717 | hp1 | a0002 | c0002 | t0018 | g0235 | AFR | GWD | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | GWD | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02735 | hp2 | a0001 | c0001 | t0004 | g0217 | SAS | PJL | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0060 | SAS | PJL | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0016 | AFR | GWD | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02809 | hp2 | a0001 | c0001 | t0016 | g0030 | AFR | GWD | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02818 | hp1 | a0001 | c0001 | t0013 | g0097 | AFR | GWD | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02818 | hp2 | a0004 | c0006 | t0028 | g0231 | AFR | GWD | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0128 | AFR | GWD | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02886 | hp2 | a0002 | c0003 | t0005 | g0240 | AFR | GWD | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0083 | AFR | GWD | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02896 | hp1 | a0002 | c0003 | t0005 | g0035 | AFR | GWD | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02897 | hp1 | a0002 | c0003 | t0005 | g0035 | AFR | GWD | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0082 | AFR | GWD | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02922 | hp1 | a0002 | c0002 | t0010 | g0006 | AFR | ESN | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0124 | AFR | ESN | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0169 | AFR | ESN | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02965 | hp2 | a0002 | c0002 | t0010 | g0006 | AFR | ESN | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02970 | hp1 | a0002 | c0002 | t0010 | g0006 | AFR | ESN | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0087 | AFR | ESN | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02976 | hp1 | a0002 | c0002 | t0041 | g0238 | AFR | ESN | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0116 | AFR | ESN | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG03017 | hp1 | a0001 | c0001 | t0004 | g0225 | SAS | PJL | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0114 | AFR | GWD | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG03041 | hp2 | a0001 | c0001 | t0032 | g0229 | AFR | GWD | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG03098 | hp1 | a0001 | c0001 | t0007 | g0037 | AFR | MSL | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG03098 | hp2 | a0004 | c0006 | t0027 | g0233 | AFR | MSL | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG03139 | hp1 | a0002 | c0003 | t0005 | g0241 | AFR | ESN | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0168 | AFR | ESN | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG03195 | hp1 | a0001 | c0001 | t0015 | g0190 | AFR | ESN | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG03195 | hp2 | a0001 | c0001 | t0013 | g0098 | AFR | ESN | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | MSL | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG03209 | hp2 | a0001 | c0001 | t0012 | g0013 | AFR | MSL | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG03225 | hp1 | a0001 | c0001 | t0014 | g0232 | AFR | MSL | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | MSL | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG03239 | hp1 | a0001 | c0001 | t0004 | g0219 | SAS | PJL | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0005 | SAS | PJL | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG03492 | hp1 | a0001 | c0001 | t0042 | g0245 | SAS | PJL | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG03516 | hp1 | a0001 | c0001 | t0008 | g0125 | AFR | ESN | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG03516 | hp2 | a0006 | c0009 | t0020 | g0243 | AFR | ESN | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | MSL | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG03579 | hp2 | a0006 | c0009 | t0020 | g0244 | AFR | MSL | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG03669 | hp1 | a0001 | c0001 | t0004 | g0218 | SAS | PJL | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0136 | SAS | PJL | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0047 | SAS | STU | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | STU | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | BEB | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | BEB | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG04184 | hp1 | a0001 | c0001 | t0021 | g0100 | SAS | BEB | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0017 | SAS | BEB | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18522 | hp1 | a0001 | c0001 | t0012 | g0013 | AFR | YRI | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18522 | hp2 | a0002 | c0002 | t0010 | g0006 | AFR | YRI | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | CHB | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0140 | EAS | CHB | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18942 | hp2 | a0001 | c0001 | t0006 | g0001 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18947 | hp1 | a0001 | c0001 | t0007 | g0195 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18948 | hp1 | a0001 | c0001 | t0006 | g0058 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18949 | hp1 | a0001 | c0001 | t0007 | g0160 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18952 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18953 | hp1 | a0001 | c0001 | t0007 | g0202 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18962 | hp1 | a0005 | c0008 | t0001 | g0103 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18962 | hp2 | a0001 | c0001 | t0006 | g0059 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0182 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18966 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18966 | hp2 | a0001 | c0001 | t0037 | g0198 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18970 | hp2 | a0001 | c0001 | t0022 | g0064 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18974 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18980 | hp2 | a0001 | c0001 | t0011 | g0063 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18983 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18986 | hp1 | a0001 | c0001 | t0004 | g0223 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18988 | hp1 | a0001 | c0001 | t0007 | g0032 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18991 | hp1 | a0001 | c0001 | t0007 | g0032 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18995 | hp1 | a0001 | c0001 | t0025 | g0046 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18995 | hp2 | a0001 | c0001 | t0004 | g0224 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18999 | hp1 | a0001 | c0001 | t0008 | g0170 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA19002 | hp1 | a0001 | c0001 | t0017 | g0186 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA19007 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA19010 | hp1 | a0001 | c0001 | t0011 | g0054 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA19010 | hp2 | a0001 | c0001 | t0008 | g0112 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA19030 | hp1 | a0001 | c0001 | t0036 | g0130 | AFR | LWK | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | LWK | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA19057 | hp1 | a0001 | c0010 | t0003 | g0023 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA19057 | hp2 | a0001 | c0001 | t0024 | g0065 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA19059 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA19059 | hp2 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA19063 | hp1 | a0001 | c0001 | t0017 | g0184 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA19074 | hp2 | a0001 | c0001 | t0006 | g0001 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA19075 | hp1 | a0001 | c0001 | t0006 | g0001 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA19078 | hp1 | a0001 | c0001 | t0009 | g0175 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA19078 | hp2 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA19079 | hp1 | a0001 | c0001 | t0004 | g0221 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA19082 | hp1 | a0001 | c0001 | t0006 | g0001 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA19089 | hp1 | a0001 | c0001 | t0003 | g0178 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA19240 | hp1 | a0001 | c0001 | t0012 | g0013 | AFR | YRI | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA19240 | hp2 | a0001 | c0012 | t0001 | g0187 | AFR | YRI | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA20129 | hp1 | a0001 | c0001 | t0029 | g0043 | AFR | ASW | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0044 | AFR | ASW | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0123 | EUR | TSI | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA20752 | hp2 | a0001 | c0004 | t0003 | g0008 | EUR | TSI | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0215 | AMR | CLM | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02486 | hp2 | a0007 | c0011 | t0039 | g0237 | AFR | ACB | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02559 | hp1 | a0001 | c0001 | t0033 | g0230 | AFR | ACB | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | ACB | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG06807 | hp1 | a0002 | c0002 | t0018 | g0236 | AFR | USA | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| HG06807 | hp2 | a0002 | c0002 | t0040 | g0226 | AFR | USA | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | USA | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0208 | AFR | USA | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0013 | g0151 | REF | REF | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0089 | REF | REF | LGSN_chr6_63270951_63324983 | LGSN | chr6 | 63270951 | 63324983 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:63280196 | G | A | 1 | a0005 | 2 | HG02027.hp1 NA18962.hp1 |
missense_variant | MODERATE | c.1355C>T | p.Pro452Leu | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 4/4 | 1395/5640 | 1355/1530 | 452/509 | chr6 | 63280196 | |||
| chr6:63280226 | T | C | 1 | a0003 | 3 | HG01109.hp2 HG01358.hp2 HG02572.hp1 |
missense_variant | MODERATE | c.1325A>G | p.Asp442Gly | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 4/4 | 1365/5640 | 1325/1530 | 442/509 | chr6 | 63280226 | |||
| chr6:63281142 | T | G | 3 | a0002 a0006 a0007 |
23 | HG01069.hp2 HG01884.hp1 HG02145.hp1 others(20): Show |
missense_variant | MODERATE | c.409A>C | p.Asn137His | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 4/4 | 449/5640 | 409/1530 | 137/509 | chr6 | 63281142 | |||
| chr6:63294933 | G | A | 1 | a0007 | 1 | HG02486.hp2 | missense_variant | MODERATE | c.143C>T | p.Thr48Met | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/4 | 183/5640 | 143/1530 | 48/509 | chr6 | 63294933 | |||
| chr6:63294939 | C | T | 2 | a0002 a0007 |
21 | HG01069.hp2 HG01884.hp1 HG02145.hp1 others(18): Show |
missense_variant | MODERATE | c.137G>A | p.Gly46Glu | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/4 | 177/5640 | 137/1530 | 46/509 | chr6 | 63294939 | |||
| chr6:63295000 | T | A | 1 | a0004 | 3 | HG02280.hp1 HG02818.hp2 HG03098.hp2 |
missense_variant | MODERATE | c.76A>T | p.Asn26Tyr | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/4 | 116/5640 | 76/1530 | 26/509 | chr6 | 63295000 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:63280189 | C | T | 1 | a0001c0004 | 7 | HG00099.hp1 HG00738.hp2 HG01070.hp1 others(4): Show |
synonymous_variant | LOW | c.1362G>A | p.Glu454Glu | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 4/4 | 1402/5640 | 1362/1530 | 454/509 | chr6 | 63280189 | |||
| chr6:63280510 | T | A | 1 | a0002c0003 | 8 | HG02145.hp1 HG02258.hp2 HG02615.hp2 others(5): Show |
synonymous_variant | LOW | c.1041A>T | p.Gly347Gly | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 4/4 | 1081/5640 | 1041/1530 | 347/509 | chr6 | 63280510 | |||
| chr6:63280573 | G | A | 1 | a0001c0012 | 1 | NA19240.hp2 | synonymous_variant | LOW | c.978C>T | p.Asn326Asn | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 4/4 | 1018/5640 | 978/1530 | 326/509 | chr6 | 63280573 | |||
| chr6:63280699 | G | A | 1 | a0002c0007 | 2 | HG01069.hp2 HG02647.hp1 |
synonymous_variant | LOW | c.852C>T | p.Thr284Thr | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 4/4 | 892/5640 | 852/1530 | 284/509 | chr6 | 63280699 | |||
| chr6:63294962 | T | A | 1 | a0001c0010 | 2 | HG00558.hp2 NA19057.hp1 |
synonymous_variant | LOW | c.114A>T | p.Pro38Pro | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/4 | 154/5640 | 114/1530 | 38/509 | chr6 | 63294962 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:63276396 | CTAA | C | 6 | a0001c0001t0014 a0001c0001t0016 a0001c0001t0029 others(3): Show |
7 | HG02280.hp1 HG02630.hp1 HG02809.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3622_*3624delTTA | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 4/4 | 3622 | chr6 | 63276396 | ||||||
| chr6:63276443 | A | G | 1 | a0001c0001t0023 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3578T>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 4/4 | 3578 | chr6 | 63276443 | ||||||
| chr6:63276447 | C | A | 1 | a0001c0001t0036 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3574G>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 4/4 | 3574 | chr6 | 63276447 | ||||||
| chr6:63276569 | G | A | 19 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0009 others(16): Show |
111 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*3452C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 4/4 | 3452 | chr6 | 63276569 | ||||||
| chr6:63276607 | C | T | 19 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0009 others(16): Show |
111 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*3414G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 4/4 | 3414 | chr6 | 63276607 | ||||||
| chr6:63276636 | A | T | 1 | a0001c0001t0030 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3385T>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 4/4 | 3385 | chr6 | 63276636 | ||||||
| chr6:63276830 | T | C | 20 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0009 others(17): Show |
113 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*3191A>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 4/4 | 3191 | chr6 | 63276830 | ||||||
| chr6:63276877 | G | A | 1 | a0001c0001t0031 | 1 | HG02293.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3144C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 4/4 | 3144 | chr6 | 63276877 | ||||||
| chr6:63276941 | C | T | 1 | a0001c0001t0035 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3080G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 4/4 | 3080 | chr6 | 63276941 | ||||||
| chr6:63277017 | C | CA | 20 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0009 others(17): Show |
113 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*3003dupT | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 4/4 | 3003 | chr6 | 63277017 | ||||||
| chr6:63277075 | C | T | 1 | a0001c0001t0022 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2946G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 4/4 | 2946 | chr6 | 63277075 | ||||||
| chr6:63277076 | G | A | 1 | a0001c0001t0037 | 1 | NA18966.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2945C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 4/4 | 2945 | chr6 | 63277076 | ||||||
| chr6:63277116 | T | C | 2 | a0001c0001t0006 a0001c0001t0025 |
9 | HG00544.hp2 HG00597.hp1 NA18942.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2905A>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 4/4 | 2905 | chr6 | 63277116 | ||||||
| chr6:63277570 | A | G | 9 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0009 others(6): Show |
97 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*2451T>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 4/4 | 2451 | chr6 | 63277570 | ||||||
| chr6:63277659 | AC | A | 19 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0009 others(16): Show |
111 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*2361delG | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 4/4 | 2361 | chr6 | 63277659 | ||||||
| chr6:63277682 | C | T | 6 | a0001c0001t0014 a0001c0001t0016 a0001c0001t0029 others(3): Show |
7 | HG02280.hp1 HG02630.hp1 HG02809.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2339G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 4/4 | 2339 | chr6 | 63277682 | ||||||
| chr6:63277776 | G | A | 1 | a0002c0002t0010 | 6 | HG01884.hp1 HG02258.hp1 HG02922.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2245C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 4/4 | 2245 | chr6 | 63277776 | ||||||
| chr6:63277989 | A | G | 13 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0009 others(10): Show |
104 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*2032T>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 4/4 | 2032 | chr6 | 63277989 | ||||||
| chr6:63278027 | C | G | 1 | a0001c0001t0032 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1994G>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 4/4 | 1994 | chr6 | 63278027 | ||||||
| chr6:63278077 | G | A | 1 | a0001c0001t0032 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1944C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 4/4 | 1944 | chr6 | 63278077 | ||||||
| chr6:63278077 | G | GA | 9 | a0001c0001t0009 a0001c0001t0014 a0001c0001t0016 others(6): Show |
15 | HG00733.hp2 HG00735.hp2 HG01934.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1943dupT | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 4/4 | 1943 | chr6 | 63278077 | ||||||
| chr6:63278077 | GAA | G | 4 | a0002c0002t0010 a0002c0002t0018 a0002c0007t0019 others(1): Show |
11 | HG01069.hp2 HG01884.hp1 HG02258.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1942_*1943delTT | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 4/4 | 1942 | chr6 | 63278077 | ||||||
| chr6:63278092 | T | A | 6 | a0001c0001t0014 a0001c0001t0016 a0001c0001t0032 others(3): Show |
7 | HG02280.hp1 HG02630.hp1 HG02809.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1929A>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 4/4 | 1929 | chr6 | 63278092 | ||||||
| chr6:63278207 | TATC | T | 4 | a0002c0002t0010 a0002c0002t0018 a0002c0007t0019 others(1): Show |
11 | HG01069.hp2 HG01884.hp1 HG02258.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1811_*1813delGAT | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 4/4 | 1811 | chr6 | 63278207 | ||||||
| chr6:63278282 | A | T | 1 | a0001c0001t0034 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1739T>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 4/4 | 1739 | chr6 | 63278282 | ||||||
| chr6:63278337 | T | A | 1 | a0001c0001t0033 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1684A>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 4/4 | 1684 | chr6 | 63278337 | ||||||
| chr6:63278457 | C | T | 37 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(34): Show |
231 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
3_prime_UTR_variant | MODIFIER | c.*1564G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 4/4 | 1564 | chr6 | 63278457 | ||||||
| chr6:63278614 | A | AT | 9 | a0001c0001t0007 a0001c0001t0008 a0001c0001t0011 others(6): Show |
22 | HG00544.hp1 HG00738.hp1 HG01175.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1406dupA | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 4/4 | 1406 | chr6 | 63278614 | ||||||
| chr6:63278614 | AT | A | 1 | a0002c0003t0005 | 8 | HG02145.hp1 HG02258.hp2 HG02615.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1406delA | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 4/4 | 1406 | chr6 | 63278614 | ||||||
| chr6:63278614 | ATT | A | 6 | a0002c0002t0010 a0002c0002t0018 a0002c0002t0041 others(3): Show |
14 | HG01069.hp2 HG01884.hp1 HG02258.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1405_*1406delAA | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 4/4 | 1405 | chr6 | 63278614 | ||||||
| chr6:63278885 | C | T | 2 | a0002c0002t0018 a0007c0011t0039 |
3 | HG02486.hp2 HG02717.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1136G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 4/4 | 1136 | chr6 | 63278885 | ||||||
| chr6:63278901 | T | C | 8 | a0002c0002t0010 a0002c0002t0018 a0002c0002t0040 others(5): Show |
23 | HG01069.hp2 HG01884.hp1 HG02145.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1120A>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 4/4 | 1120 | chr6 | 63278901 | ||||||
| chr6:63279002 | C | A | 8 | a0002c0002t0010 a0002c0002t0018 a0002c0002t0040 others(5): Show |
23 | HG01069.hp2 HG01884.hp1 HG02145.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1019G>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 4/4 | 1019 | chr6 | 63279002 | ||||||
| chr6:63279059 | G | C | 8 | a0002c0002t0010 a0002c0002t0018 a0002c0002t0040 others(5): Show |
23 | HG01069.hp2 HG01884.hp1 HG02145.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*962C>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 4/4 | 962 | chr6 | 63279059 | ||||||
| chr6:63279155 | G | A | 8 | a0002c0002t0010 a0002c0002t0018 a0002c0002t0040 others(5): Show |
23 | HG01069.hp2 HG01884.hp1 HG02145.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*866C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 4/4 | 866 | chr6 | 63279155 | ||||||
| chr6:63279277 | T | A | 1 | a0001c0001t0038 | 1 | HG01978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*744A>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 4/4 | 744 | chr6 | 63279277 | ||||||
| chr6:63279359 | C | T | 7 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0011 others(4): Show |
81 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*662G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 4/4 | 662 | chr6 | 63279359 | ||||||
| chr6:63279376 | G | A | 1 | a0002c0003t0005 | 8 | HG02145.hp1 HG02258.hp2 HG02615.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*645C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 4/4 | 645 | chr6 | 63279376 | ||||||
| chr6:63279589 | G | A | 8 | a0002c0002t0010 a0002c0002t0018 a0002c0002t0040 others(5): Show |
23 | HG01069.hp2 HG01884.hp1 HG02145.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*432C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 4/4 | 432 | chr6 | 63279589 | ||||||
| chr6:63279784 | C | G | 1 | a0002c0003t0005 | 8 | HG02145.hp1 HG02258.hp2 HG02615.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*237G>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 4/4 | 237 | chr6 | 63279784 | ||||||
| chr6:63279821 | G | T | 1 | a0001c0001t0021 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*200C>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 4/4 | 200 | chr6 | 63279821 | ||||||
| chr6:63319966 | G | A | 1 | a0001c0001t0042 | 1 | HG03492.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-23C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/4 | chr6 | 63319966 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:63281302 | A | AAAATATA others(30): Show |
1 | a0001c0001t0002g0019 | 2 | NA19059.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.331-83_331-82insAT others(35): Show |
LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63281302 | |||||||
| chr6:63281302 | A | AAAATATA others(32): Show |
2 | a0001c0001t0001g0119 a0001c0001t0001g0142 |
2 | HG02622.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.331-83_331-82insAT others(37): Show |
LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63281302 | |||||||
| chr6:63281302 | A | AAAATATA others(34): Show |
1 | a0001c0001t0002g0071 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.331-83_331-82insAT others(39): Show |
LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63281302 | |||||||
| chr6:63281302 | A | AAAATATA others(40): Show |
1 | a0001c0001t0001g0165 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.331-83_331-82insAT others(45): Show |
LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63281302 | |||||||
| chr6:63281304 | A | AAAATATA others(3): Show |
1 | a0001c0001t0001g0149 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.331-85_331-84insAT others(8): Show |
LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63281304 | |||||||
| chr6:63281304 | A | AAT | 4 | a0001c0001t0003g0124 a0001c0001t0003g0191 a0001c0001t0029g0043 others(1): Show |
4 | HG00597.hp2 HG02922.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.331-86_331-85dupAT | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63281304 | |||||||
| chr6:63281304 | A | AATAT | 9 | a0001c0001t0002g0045 a0001c0001t0002g0050 a0001c0001t0002g0051 others(6): Show |
9 | HG02257.hp2 HG02523.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.331-88_331-85dupAT others(2): Show |
LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63281304 | |||||||
| chr6:63281304 | A | AATATAT | 31 | a0001c0001t0001g0123 a0001c0001t0002g0004 a0001c0001t0002g0009 others(28): Show |
48 | HG00544.hp2 HG00597.hp1 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.331-90_331-85dupAT others(4): Show |
LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63281304 | |||||||
| chr6:63281304 | A | AATATATA others(1): Show |
62 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0022 others(59): Show |
77 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.331-92_331-85dupAT others(6): Show |
LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63281304 | |||||||
| chr6:63281304 | A | AATATATA others(3): Show |
20 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0036 others(17): Show |
27 | HG01884.hp2 HG02056.hp2 HG02132.hp2 others(24): Show |
intron_variant | MODIFIER | c.331-94_331-85dupAT others(8): Show |
LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63281304 | |||||||
| chr6:63281304 | A | AATATATA others(5): Show |
17 | a0001c0001t0001g0029 a0001c0001t0001g0040 a0001c0001t0001g0042 others(14): Show |
19 | HG00609.hp1 HG00735.hp2 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.331-96_331-85dupAT others(10): Show |
LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63281304 | |||||||
| chr6:63281304 | A | AATATATA others(9): Show |
6 | a0001c0001t0001g0131 a0001c0001t0001g0146 a0001c0001t0001g0164 others(3): Show |
6 | HG01106.hp2 HG01109.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.331-100_331-85dupA others(15): Show |
LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63281304 | |||||||
| chr6:63281304 | A | AATATATA others(13): Show |
1 | a0001c0001t0004g0217 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.331-104_331-85dupA others(19): Show |
LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63281304 | |||||||
| chr6:63281304 | A | AATATATA others(40): Show |
1 | a0001c0001t0015g0189 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.331-85_331-84insAT others(45): Show |
LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63281304 | |||||||
| chr6:63281304 | A | AATATATA others(34): Show |
1 | a0001c0001t0001g0118 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.331-85_331-84insAT others(39): Show |
LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63281304 | |||||||
| chr6:63281304 | A | AATATATA others(31): Show |
1 | a0001c0001t0004g0218 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.331-85_331-84insAT others(36): Show |
LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63281304 | |||||||
| chr6:63281304 | A | ATATATAT others(4): Show |
1 | a0001c0001t0001g0041 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.331-85_331-84insAT others(9): Show |
LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63281304 | |||||||
| chr6:63281304 | AAT | A | 6 | a0002c0002t0018g0235 a0002c0002t0018g0236 a0002c0003t0005g0241 others(3): Show |
6 | HG01069.hp2 HG02486.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.331-86_331-85delAT | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63281304 | |||||||
| chr6:63281305 | AT | A | 5 | a0002c0002t0040g0226 a0002c0003t0005g0015 a0002c0003t0005g0035 others(2): Show |
8 | HG02145.hp1 HG02258.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.331-86delA | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63281305 | |||||||
| chr6:63281305 | ATAT | A | 5 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0041g0238 others(2): Show |
9 | HG01884.hp1 HG02258.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.331-88_331-86delAT others(1): Show |
LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63281305 | |||||||
| chr6:63281306 | T | TATATATA others(22): Show |
1 | a0001c0001t0001g0164 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.331-115_331-87dupT others(28): Show |
LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63281306 | |||||||
| chr6:63281306 | T | TATATATA others(28): Show |
1 | a0001c0001t0011g0066 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.331-87_331-86insTT others(33): Show |
LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63281306 | |||||||
| chr6:63281306 | T | TATATATA others(55): Show |
1 | a0001c0001t0001g0150 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.331-87_331-86insTA others(60): Show |
LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63281306 | |||||||
| chr6:63281306 | T | TATATATA others(42): Show |
1 | a0001c0001t0001g0120 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.331-87_331-86insTT others(47): Show |
LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63281306 | |||||||
| chr6:63281308 | T | A | 11 | a0002c0002t0018g0235 a0002c0002t0018g0236 a0002c0002t0040g0226 others(8): Show |
14 | HG01069.hp2 HG02145.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.331-88A>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63281308 | |||||||
| chr6:63281310 | T | A | 16 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0018g0235 others(13): Show |
23 | HG01069.hp2 HG01884.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.331-90A>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63281310 | |||||||
| chr6:63281312 | T | A | 12 | a0002c0002t0018g0235 a0002c0002t0018g0236 a0002c0002t0040g0226 others(9): Show |
14 | HG01069.hp2 HG02145.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.331-92A>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63281312 | |||||||
| chr6:63281314 | T | A | 1 | a0002c0003t0005g0241 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.331-94A>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63281314 | |||||||
| chr6:63281316 | T | A | 1 | a0002c0003t0005g0241 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.331-96A>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63281316 | |||||||
| chr6:63281318 | T | TATATATA others(5): Show |
1 | a0003c0005t0001g0031 | 2 | HG01109.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.331-99_331-98insGT others(10): Show |
LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63281318 | |||||||
| chr6:63281330 | T | A | 20 | a0001c0001t0003g0107 a0002c0002t0010g0006 a0002c0002t0010g0239 others(17): Show |
27 | HG01069.hp2 HG01884.hp1 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.331-110A>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63281330 | |||||||
| chr6:63281330 | T | TATATATA others(19): Show |
1 | a0001c0001t0001g0038 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.331-111_331-110ins others(26): Show |
LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63281330 | |||||||
| chr6:63281454 | C | T | 5 | a0002c0003t0005g0015 a0002c0003t0005g0035 a0002c0003t0005g0240 others(2): Show |
8 | HG02145.hp1 HG02258.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.331-234G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63281454 | |||||||
| chr6:63281582 | C | T | 2 | a0001c0001t0032g0229 a0001c0001t0033g0230 |
2 | HG02559.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.331-362G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63281582 | |||||||
| chr6:63281653 | C | A | 5 | a0002c0003t0005g0015 a0002c0003t0005g0035 a0002c0003t0005g0240 others(2): Show |
8 | HG02145.hp1 HG02258.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.331-433G>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63281653 | |||||||
| chr6:63281855 | C | A | 5 | a0002c0003t0005g0015 a0002c0003t0005g0035 a0002c0003t0005g0240 others(2): Show |
8 | HG02145.hp1 HG02258.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.331-635G>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63281855 | |||||||
| chr6:63282022 | T | C | 1 | a0001c0001t0029g0043 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.331-802A>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63282022 | |||||||
| chr6:63282104 | G | A | 1 | a0001c0001t0029g0043 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.331-884C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63282104 | |||||||
| chr6:63282370 | T | C | 11 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0018g0235 others(8): Show |
18 | HG01884.hp1 HG02145.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.331-1150A>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63282370 | |||||||
| chr6:63282548 | A | T | 3 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 |
3 | HG00621.hp1 NA18942.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.331-1328T>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63282548 | |||||||
| chr6:63282669 | T | C | 16 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0018g0235 others(13): Show |
23 | HG01069.hp2 HG01884.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.331-1449A>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63282669 | |||||||
| chr6:63282670 | G | A | 4 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0040g0226 others(1): Show |
8 | HG01884.hp1 HG02258.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.331-1450C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63282670 | |||||||
| chr6:63282708 | C | T | 2 | a0006c0009t0020g0243 a0006c0009t0020g0244 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.331-1488G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63282708 | |||||||
| chr6:63282961 | A | C | 2 | a0001c0001t0001g0121 a0001c0001t0001g0172 |
2 | HG01074.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.331-1741T>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63282961 | |||||||
| chr6:63283073 | C | T | 7 | a0001c0001t0001g0029 a0001c0001t0001g0036 a0001c0001t0001g0038 others(4): Show |
9 | HG01884.hp2 HG02630.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.331-1853G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63283073 | |||||||
| chr6:63283140 | T | G | 54 | a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0009 others(51): Show |
78 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.331-1920A>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63283140 | |||||||
| chr6:63283184 | G | A | 1 | a0001c0001t0003g0128 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.331-1964C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63283184 | |||||||
| chr6:63283459 | T | C | 1 | a0001c0001t0037g0198 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.330+2128A>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63283459 | |||||||
| chr6:63283470 | C | T | 179 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0022 others(176): Show |
229 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.330+2117G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63283470 | |||||||
| chr6:63283487 | A | AT | 16 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0018g0235 others(13): Show |
23 | HG01069.hp2 HG01884.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.330+2099dupA | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63283487 | |||||||
| chr6:63283550 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.330+2037C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63283550 | |||||||
| chr6:63283592 | G | A | 1 | a0001c0001t0002g0021 | 2 | HG01257.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.330+1995C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63283592 | |||||||
| chr6:63283618 | C | CT | 62 | a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0009 others(59): Show |
86 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.330+1968dupA | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63283618 | |||||||
| chr6:63283618 | CT | C | 80 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0022 others(77): Show |
91 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.330+1968delA | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63283618 | |||||||
| chr6:63283649 | T | TACAC | 10 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0018g0235 others(7): Show |
14 | HG01884.hp1 HG02258.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.330+1934_330+1937d others(6): Show |
LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63283649 | |||||||
| chr6:63283649 | T | TACACAC | 6 | a0002c0003t0005g0015 a0002c0003t0005g0035 a0002c0003t0005g0240 others(3): Show |
9 | HG01069.hp2 HG02145.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.330+1932_330+1937d others(8): Show |
LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63283649 | |||||||
| chr6:63283942 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.330+1645G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63283942 | |||||||
| chr6:63284075 | A | C | 22 | a0001c0001t0014g0232 a0001c0001t0032g0229 a0001c0001t0033g0230 others(19): Show |
29 | HG01069.hp2 HG01884.hp1 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.330+1512T>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63284075 | |||||||
| chr6:63284155 | C | G | 7 | a0001c0001t0001g0029 a0001c0001t0001g0036 a0001c0001t0001g0038 others(4): Show |
9 | HG01884.hp2 HG02630.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.330+1432G>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63284155 | |||||||
| chr6:63284228 | T | C | 1 | a0001c0001t0002g0074 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.330+1359A>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63284228 | |||||||
| chr6:63284292 | T | TAAAC | 16 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0018g0235 others(13): Show |
23 | HG01069.hp2 HG01884.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.330+1291_330+1294d others(6): Show |
LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63284292 | |||||||
| chr6:63284568 | C | T | 179 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0022 others(176): Show |
229 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.330+1019G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63284568 | |||||||
| chr6:63284590 | C | G | 16 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0018g0235 others(13): Show |
23 | HG01069.hp2 HG01884.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.330+997G>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63284590 | |||||||
| chr6:63284684 | A | AT | 3 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0041g0238 |
7 | HG01884.hp1 HG02258.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.330+902dupA | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63284684 | |||||||
| chr6:63284774 | A | T | 1 | a0001c0001t0037g0198 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.330+813T>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63284774 | |||||||
| chr6:63284874 | A | C | 5 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(2): Show |
5 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(2): Show |
intron_variant | MODIFIER | c.330+713T>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63284874 | |||||||
| chr6:63284880 | G | C | 1 | a0001c0001t0009g0216 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.330+707C>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63284880 | |||||||
| chr6:63284945 | G | A | 3 | a0001c0001t0001g0120 a0001c0001t0001g0164 a0001c0001t0001g0165 |
3 | HG01361.hp1 HG02300.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.330+642C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63284945 | |||||||
| chr6:63285087 | T | G | 11 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0018g0235 others(8): Show |
18 | HG01884.hp1 HG02145.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.330+500A>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63285087 | |||||||
| chr6:63285123 | C | A | 2 | a0001c0001t0003g0167 a0001c0001t0003g0171 |
2 | HG00741.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.330+464G>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63285123 | |||||||
| chr6:63285290 | G | A | 4 | a0001c0001t0014g0232 a0004c0006t0014g0234 a0004c0006t0027g0233 others(1): Show |
4 | HG02280.hp1 HG02818.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.330+297C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63285290 | |||||||
| chr6:63285572 | C | CTG | 22 | a0001c0001t0014g0232 a0001c0001t0032g0229 a0001c0001t0033g0230 others(19): Show |
29 | HG01069.hp2 HG01884.hp1 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.330+13_330+14dupCA | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 3/3 | chr6 | 63285572 | |||||||
| chr6:63285792 | T | C | 2 | a0002c0007t0019g0227 a0002c0007t0019g0228 |
2 | HG01069.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.164-39A>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63285792 | |||||||
| chr6:63285921 | G | A | 2 | a0006c0009t0020g0243 a0006c0009t0020g0244 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.164-168C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63285921 | |||||||
| chr6:63286107 | C | A | 1 | a0002c0003t0005g0241 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.164-354G>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63286107 | |||||||
| chr6:63286290 | A | G | 16 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0018g0235 others(13): Show |
23 | HG01069.hp2 HG01884.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.164-537T>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63286290 | |||||||
| chr6:63286526 | C | T | 1 | a0001c0001t0003g0180 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.164-773G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63286526 | |||||||
| chr6:63286578 | T | C | 1 | a0001c0001t0036g0130 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.164-825A>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63286578 | |||||||
| chr6:63286596 | C | T | 1 | a0001c0001t0009g0162 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.164-843G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63286596 | |||||||
| chr6:63286988 | C | G | 16 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0018g0235 others(13): Show |
23 | HG01069.hp2 HG01884.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.164-1235G>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63286988 | |||||||
| chr6:63287087 | C | T | 3 | a0001c0001t0001g0120 a0001c0001t0001g0164 a0001c0001t0001g0165 |
3 | HG01361.hp1 HG02300.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.164-1334G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63287087 | |||||||
| chr6:63287161 | ACT | A | 16 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0018g0235 others(13): Show |
23 | HG01069.hp2 HG01884.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.164-1410_164-1409d others(4): Show |
LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63287161 | |||||||
| chr6:63287324 | A | G | 16 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0018g0235 others(13): Show |
23 | HG01069.hp2 HG01884.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.164-1571T>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63287324 | |||||||
| chr6:63287328 | A | G | 3 | a0004c0006t0014g0234 a0004c0006t0027g0233 a0004c0006t0028g0231 |
3 | HG02280.hp1 HG02818.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.164-1575T>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63287328 | |||||||
| chr6:63287413 | G | A | 99 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0022 others(96): Show |
118 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.164-1660C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63287413 | |||||||
| chr6:63287580 | C | T | 2 | a0006c0009t0020g0243 a0006c0009t0020g0244 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.164-1827G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63287580 | |||||||
| chr6:63287687 | A | G | 16 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0018g0235 others(13): Show |
23 | HG01069.hp2 HG01884.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.164-1934T>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63287687 | |||||||
| chr6:63287712 | T | C | 2 | a0001c0001t0003g0135 a0001c0001t0003g0157 |
2 | HG01891.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.164-1959A>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63287712 | |||||||
| chr6:63287926 | T | C | 1 | a0001c0001t0001g0115 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.164-2173A>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63287926 | |||||||
| chr6:63287951 | C | T | 2 | a0001c0001t0015g0189 a0001c0001t0015g0190 |
2 | HG02257.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.164-2198G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63287951 | |||||||
| chr6:63288148 | G | T | 1 | a0001c0001t0008g0174 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.164-2395C>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63288148 | |||||||
| chr6:63288168 | A | C | 1 | a0001c0001t0001g0213 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.164-2415T>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63288168 | |||||||
| chr6:63288226 | C | CAAAA | 3 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0041g0238 |
7 | HG01884.hp1 HG02258.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.164-2477_164-2474d others(6): Show |
LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63288226 | |||||||
| chr6:63288230 | A | AAAAT | 39 | a0001c0001t0001g0011 a0001c0001t0001g0048 a0001c0001t0001g0084 others(36): Show |
47 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.164-2481_164-2478d others(6): Show |
LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63288230 | |||||||
| chr6:63288230 | A | AAAATAAA others(1): Show |
15 | a0001c0001t0001g0025 a0001c0001t0001g0028 a0001c0001t0001g0033 others(12): Show |
18 | HG00280.hp2 HG01243.hp2 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.164-2485_164-2478d others(10): Show |
LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63288230 | |||||||
| chr6:63288230 | A | AAAATAAA others(5): Show |
1 | a0001c0001t0001g0200 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.164-2489_164-2478d others(14): Show |
LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63288230 | |||||||
| chr6:63288230 | AAAAT | A | 8 | a0001c0001t0002g0207 a0001c0001t0002g0210 a0001c0001t0002g0211 others(5): Show |
9 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(6): Show |
intron_variant | MODIFIER | c.164-2481_164-2478d others(6): Show |
LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63288230 | |||||||
| chr6:63288230 | AAAATAAA others(5): Show |
A | 2 | a0001c0001t0002g0077 a0001c0001t0002g0099 |
2 | HG00639.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.164-2489_164-2478d others(14): Show |
LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63288230 | |||||||
| chr6:63288234 | T | A | 2 | a0001c0001t0017g0184 a0001c0001t0017g0186 |
2 | NA19002.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.164-2481A>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63288234 | |||||||
| chr6:63288263 | AAATAAAT | A | 4 | a0001c0001t0003g0024 a0001c0001t0003g0154 a0001c0001t0003g0203 others(1): Show |
6 | HG00558.hp2 HG01192.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-2517_164-2511d others(9): Show |
LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63288263 | |||||||
| chr6:63288267 | AAAT | A | 27 | a0001c0001t0003g0002 a0001c0001t0003g0005 a0001c0001t0003g0080 others(24): Show |
35 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(32): Show |
intron_variant | MODIFIER | c.164-2517_164-2515d others(5): Show |
LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63288267 | |||||||
| chr6:63288326 | T | C | 2 | a0001c0001t0032g0229 a0001c0001t0033g0230 |
2 | HG02559.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.164-2573A>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63288326 | |||||||
| chr6:63288362 | C | G | 1 | a0002c0002t0040g0226 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.164-2609G>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63288362 | |||||||
| chr6:63289014 | A | T | 16 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0018g0235 others(13): Show |
23 | HG01069.hp2 HG01884.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.164-3261T>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63289014 | |||||||
| chr6:63289015 | A | T | 16 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0018g0235 others(13): Show |
23 | HG01069.hp2 HG01884.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.164-3262T>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63289015 | |||||||
| chr6:63289051 | T | C | 1 | a0001c0001t0001g0092 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.164-3298A>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63289051 | |||||||
| chr6:63289083 | C | A | 16 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0018g0235 others(13): Show |
23 | HG01069.hp2 HG01884.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.164-3330G>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63289083 | |||||||
| chr6:63289099 | T | C | 1 | a0001c0001t0003g0136 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.164-3346A>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63289099 | |||||||
| chr6:63289625 | T | A | 1 | a0001c0001t0013g0097 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.164-3872A>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63289625 | |||||||
| chr6:63289626 | TA | T | 85 | a0001c0001t0001g0029 a0001c0001t0001g0036 a0001c0001t0001g0038 others(82): Show |
117 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(114): Show |
intron_variant | MODIFIER | c.164-3874delT | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63289626 | |||||||
| chr6:63289834 | C | T | 1 | a0001c0001t0003g0113 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.164-4081G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63289834 | |||||||
| chr6:63289867 | C | T | 1 | a0001c0001t0002g0205 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.164-4114G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63289867 | |||||||
| chr6:63289886 | G | A | 2 | a0006c0009t0020g0243 a0006c0009t0020g0244 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.164-4133C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63289886 | |||||||
| chr6:63289888 | C | T | 1 | a0001c0001t0002g0070 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.164-4135G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63289888 | |||||||
| chr6:63290058 | GA | G | 14 | a0001c0001t0003g0111 a0001c0001t0003g0138 a0001c0001t0008g0170 others(11): Show |
21 | HG01884.hp1 HG02056.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.164-4306delT | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63290058 | |||||||
| chr6:63290129 | T | C | 3 | a0001c0001t0001g0027 a0001c0001t0001g0139 a0001c0001t0001g0185 |
4 | NA18999.hp2 NA19012.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.164-4376A>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63290129 | |||||||
| chr6:63290320 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.164-4567G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63290320 | |||||||
| chr6:63290407 | T | G | 3 | a0002c0002t0018g0235 a0002c0002t0018g0236 a0007c0011t0039g0237 |
3 | HG02486.hp2 HG02717.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.163+4506A>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63290407 | |||||||
| chr6:63290508 | A | G | 1 | a0001c0001t0001g0149 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.163+4405T>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63290508 | |||||||
| chr6:63290640 | G | T | 2 | a0002c0007t0019g0227 a0002c0007t0019g0228 |
2 | HG01069.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.163+4273C>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63290640 | |||||||
| chr6:63290972 | G | A | 12 | a0002c0002t0010g0239 a0002c0002t0018g0235 a0002c0002t0018g0236 others(9): Show |
15 | HG01069.hp2 HG01884.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.163+3941C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63290972 | |||||||
| chr6:63291082 | G | A | 3 | a0001c0001t0002g0070 a0001c0001t0002g0071 a0001c0001t0002g0072 |
3 | HG01070.hp2 HG01243.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.163+3831C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63291082 | |||||||
| chr6:63291124 | G | A | 1 | a0001c0001t0002g0071 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.163+3789C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63291124 | |||||||
| chr6:63291199 | A | T | 1 | a0001c0001t0001g0143 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.163+3714T>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63291199 | |||||||
| chr6:63291242 | C | T | 1 | a0003c0005t0004g0188 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.163+3671G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63291242 | |||||||
| chr6:63291271 | T | G | 103 | a0001c0001t0001g0029 a0001c0001t0001g0036 a0001c0001t0001g0038 others(100): Show |
142 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(139): Show |
intron_variant | MODIFIER | c.163+3642A>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63291271 | |||||||
| chr6:63291282 | G | A | 1 | a0001c0001t0003g0081 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.163+3631C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63291282 | |||||||
| chr6:63291299 | T | G | 3 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0161 |
3 | NA18957.hp2 NA18961.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.163+3614A>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63291299 | |||||||
| chr6:63291475 | G | A | 5 | a0002c0003t0005g0015 a0002c0003t0005g0035 a0002c0003t0005g0240 others(2): Show |
8 | HG02145.hp1 HG02258.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.163+3438C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63291475 | |||||||
| chr6:63292210 | A | G | 2 | a0006c0009t0020g0243 a0006c0009t0020g0244 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.163+2703T>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63292210 | |||||||
| chr6:63292334 | T | C | 5 | a0002c0003t0005g0015 a0002c0003t0005g0035 a0002c0003t0005g0240 others(2): Show |
8 | HG02145.hp1 HG02258.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.163+2579A>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63292334 | |||||||
| chr6:63292464 | G | C | 3 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0041g0238 |
7 | HG01884.hp1 HG02258.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.163+2449C>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63292464 | |||||||
| chr6:63292645 | T | G | 1 | a0001c0001t0002g0078 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.163+2268A>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63292645 | |||||||
| chr6:63292664 | C | T | 1 | a0001c0001t0042g0245 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.163+2249G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63292664 | |||||||
| chr6:63292868 | C | T | 1 | a0001c0001t0003g0154 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.163+2045G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63292868 | |||||||
| chr6:63292937 | C | T | 3 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0041g0238 |
7 | HG01884.hp1 HG02258.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.163+1976G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63292937 | |||||||
| chr6:63293027 | G | T | 1 | a0001c0001t0012g0013 | 3 | HG03209.hp2 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.163+1886C>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63293027 | |||||||
| chr6:63293156 | T | C | 242 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0022 others(239): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.163+1757A>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63293156 | |||||||
| chr6:63293265 | G | A | 1 | a0001c0001t0001g0027 | 2 | NA19012.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.163+1648C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63293265 | |||||||
| chr6:63293275 | G | A | 6 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0018g0235 others(3): Show |
10 | HG01884.hp1 HG02258.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.163+1638C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63293275 | |||||||
| chr6:63293326 | G | A | 11 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0018g0235 others(8): Show |
18 | HG01884.hp1 HG02145.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.163+1587C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63293326 | |||||||
| chr6:63293342 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.163+1571C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63293342 | |||||||
| chr6:63293460 | C | T | 2 | a0006c0009t0020g0243 a0006c0009t0020g0244 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.163+1453G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63293460 | |||||||
| chr6:63293486 | G | A | 2 | a0001c0001t0003g0080 a0001c0001t0008g0112 |
2 | NA19010.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.163+1427C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63293486 | |||||||
| chr6:63293554 | G | A | 56 | a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0009 others(53): Show |
80 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.163+1359C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63293554 | |||||||
| chr6:63293719 | G | A | 1 | a0001c0001t0014g0232 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.163+1194C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63293719 | |||||||
| chr6:63293763 | T | A | 1 | a0001c0001t0009g0162 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.163+1150A>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63293763 | |||||||
| chr6:63293793 | G | A | 1 | a0001c0001t0004g0224 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.163+1120C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63293793 | |||||||
| chr6:63293810 | G | T | 1 | a0002c0002t0040g0226 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.163+1103C>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63293810 | |||||||
| chr6:63294077 | G | A | 1 | a0001c0001t0014g0232 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.163+836C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63294077 | |||||||
| chr6:63294199 | G | T | 1 | a0001c0001t0003g0104 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.163+714C>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63294199 | |||||||
| chr6:63294207 | G | A | 2 | a0001c0001t0032g0229 a0001c0001t0033g0230 |
2 | HG02559.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.163+706C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63294207 | |||||||
| chr6:63294273 | T | G | 1 | a0001c0001t0002g0069 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.163+640A>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63294273 | |||||||
| chr6:63294554 | C | T | 1 | a0001c0001t0002g0068 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.163+359G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63294554 | |||||||
| chr6:63294744 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.163+169A>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63294744 | |||||||
| chr6:63294746 | C | T | 1 | a0001c0001t0029g0043 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.163+167G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63294746 | |||||||
| chr6:63294892 | G | T | 1 | a0001c0001t0042g0245 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.163+21C>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 2/3 | chr6 | 63294892 | |||||||
| chr6:63295054 | A | G | 1 | a0001c0001t0003g0179 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.31-9T>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63295054 | |||||||
| chr6:63295110 | G | A | 2 | a0001c0001t0032g0229 a0001c0001t0033g0230 |
2 | HG02559.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.31-65C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63295110 | |||||||
| chr6:63295428 | A | T | 1 | a0001c0001t0014g0232 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.31-383T>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63295428 | |||||||
| chr6:63295593 | G | A | 2 | a0006c0009t0020g0243 a0006c0009t0020g0244 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.31-548C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63295593 | |||||||
| chr6:63295769 | G | C | 2 | a0006c0009t0020g0243 a0006c0009t0020g0244 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.31-724C>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63295769 | |||||||
| chr6:63295794 | G | C | 1 | a0001c0001t0001g0197 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.31-749C>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63295794 | |||||||
| chr6:63295817 | C | T | 1 | a0001c0001t0001g0040 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.31-772G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63295817 | |||||||
| chr6:63295999 | C | T | 56 | a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0009 others(53): Show |
80 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.31-954G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63295999 | |||||||
| chr6:63296000 | G | T | 14 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0018g0235 others(11): Show |
21 | HG01069.hp2 HG01884.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.31-955C>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63296000 | |||||||
| chr6:63296292 | C | T | 1 | a0002c0002t0040g0226 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.31-1247G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63296292 | |||||||
| chr6:63296390 | A | G | 14 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0018g0235 others(11): Show |
21 | HG01069.hp2 HG01884.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.31-1345T>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63296390 | |||||||
| chr6:63296655 | G | T | 1 | a0001c0001t0042g0245 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.31-1610C>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63296655 | |||||||
| chr6:63296955 | C | T | 3 | a0001c0001t0001g0022 a0001c0001t0001g0092 a0001c0001t0009g0175 |
4 | NA18948.hp2 NA19009.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-1910G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63296955 | |||||||
| chr6:63296975 | C | T | 2 | a0002c0007t0019g0227 a0002c0007t0019g0228 |
2 | HG01069.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.31-1930G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63296975 | |||||||
| chr6:63297060 | G | A | 2 | a0006c0009t0020g0243 a0006c0009t0020g0244 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.31-2015C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63297060 | |||||||
| chr6:63297083 | T | G | 1 | a0002c0002t0040g0226 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.31-2038A>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63297083 | |||||||
| chr6:63297229 | G | A | 16 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0018g0235 others(13): Show |
23 | HG01069.hp2 HG01884.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.31-2184C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63297229 | |||||||
| chr6:63297287 | G | A | 1 | a0001c0001t0001g0137 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.31-2242C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63297287 | |||||||
| chr6:63297354 | C | CA | 73 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0039 others(70): Show |
108 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.31-2310dupT | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63297354 | |||||||
| chr6:63297354 | CA | C | 11 | a0001c0001t0001g0166 a0001c0001t0003g0082 a0001c0001t0003g0114 others(8): Show |
15 | HG01167.hp1 HG01167.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.31-2310delT | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63297354 | |||||||
| chr6:63297369 | A | C | 2 | a0006c0009t0020g0243 a0006c0009t0020g0244 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.31-2324T>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63297369 | |||||||
| chr6:63297713 | C | G | 2 | a0002c0007t0019g0227 a0002c0007t0019g0228 |
2 | HG01069.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.31-2668G>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63297713 | |||||||
| chr6:63297832 | A | T | 1 | a0001c0001t0001g0115 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.31-2787T>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63297832 | |||||||
| chr6:63298047 | G | C | 4 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0039 others(1): Show |
4 | HG01884.hp2 HG03098.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-3002C>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63298047 | |||||||
| chr6:63298219 | C | G | 3 | a0004c0006t0014g0234 a0004c0006t0027g0233 a0004c0006t0028g0231 |
3 | HG02280.hp1 HG02818.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.31-3174G>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63298219 | |||||||
| chr6:63298223 | C | T | 5 | a0002c0003t0005g0015 a0002c0003t0005g0035 a0002c0003t0005g0240 others(2): Show |
8 | HG02145.hp1 HG02258.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.31-3178G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63298223 | |||||||
| chr6:63298240 | A | G | 2 | a0006c0009t0020g0243 a0006c0009t0020g0244 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.31-3195T>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63298240 | |||||||
| chr6:63298254 | T | C | 4 | a0001c0001t0002g0055 a0001c0001t0002g0056 a0001c0001t0002g0067 others(1): Show |
4 | HG02155.hp2 NA18940.hp2 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-3209A>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63298254 | |||||||
| chr6:63298465 | T | C | 1 | a0002c0002t0040g0226 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.31-3420A>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63298465 | |||||||
| chr6:63298589 | A | G | 1 | a0001c0001t0003g0114 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.31-3544T>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63298589 | |||||||
| chr6:63298788 | A | G | 1 | a0002c0002t0040g0226 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.31-3743T>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63298788 | |||||||
| chr6:63298985 | G | T | 1 | a0001c0001t0001g0105 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.31-3940C>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63298985 | |||||||
| chr6:63299090 | C | T | 1 | a0001c0001t0002g0074 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.31-4045G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63299090 | |||||||
| chr6:63299649 | A | C | 1 | a0001c0001t0001g0079 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.31-4604T>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63299649 | |||||||
| chr6:63299840 | T | C | 12 | a0001c0001t0001g0094 a0001c0001t0001g0141 a0001c0001t0001g0142 others(9): Show |
12 | HG00544.hp1 HG00733.hp2 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.31-4795A>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63299840 | |||||||
| chr6:63300054 | G | C | 3 | a0001c0001t0003g0096 a0001c0001t0003g0113 a0001c0001t0008g0155 |
3 | HG02080.hp2 HG02129.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.31-5009C>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63300054 | |||||||
| chr6:63300223 | C | T | 2 | a0002c0007t0019g0227 a0002c0007t0019g0228 |
2 | HG01069.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.31-5178G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63300223 | |||||||
| chr6:63300256 | C | A | 1 | a0001c0001t0003g0104 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.31-5211G>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63300256 | |||||||
| chr6:63300309 | G | A | 1 | a0001c0001t0003g0104 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.31-5264C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63300309 | |||||||
| chr6:63300311 | G | A | 54 | a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0009 others(51): Show |
78 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.31-5266C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63300311 | |||||||
| chr6:63300453 | C | G | 20 | a0001c0001t0014g0232 a0002c0002t0010g0006 a0002c0002t0010g0239 others(17): Show |
27 | HG01069.hp2 HG01884.hp1 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.31-5408G>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63300453 | |||||||
| chr6:63300458 | G | A | 5 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(2): Show |
5 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(2): Show |
intron_variant | MODIFIER | c.31-5413C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63300458 | |||||||
| chr6:63300533 | G | C | 1 | a0002c0002t0040g0226 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.31-5488C>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63300533 | |||||||
| chr6:63300559 | G | A | 11 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0018g0235 others(8): Show |
18 | HG01884.hp1 HG02145.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.31-5514C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63300559 | |||||||
| chr6:63300651 | G | A | 3 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0041g0238 |
7 | HG01884.hp1 HG02258.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.31-5606C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63300651 | |||||||
| chr6:63300664 | CA | C | 4 | a0001c0001t0006g0001 a0001c0001t0006g0058 a0001c0001t0006g0059 others(1): Show |
9 | HG00544.hp2 HG00597.hp1 NA18942.hp2 others(6): Show |
intron_variant | MODIFIER | c.31-5620delT | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63300664 | |||||||
| chr6:63300698 | G | GA | 3 | a0002c0002t0040g0226 a0002c0007t0019g0227 a0002c0007t0019g0228 |
3 | HG01069.hp2 HG02647.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.31-5654dupT | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63300698 | |||||||
| chr6:63300797 | T | G | 1 | a0002c0002t0040g0226 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.31-5752A>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63300797 | |||||||
| chr6:63301033 | G | A | 1 | a0001c0001t0002g0051 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.31-5988C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63301033 | |||||||
| chr6:63301206 | G | A | 1 | a0001c0001t0002g0068 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.31-6161C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63301206 | |||||||
| chr6:63301247 | C | T | 2 | a0006c0009t0020g0243 a0006c0009t0020g0244 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.31-6202G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63301247 | |||||||
| chr6:63301468 | G | A | 1 | a0001c0001t0002g0009 | 3 | NA18943.hp1 NA18950.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.31-6423C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63301468 | |||||||
| chr6:63301470 | A | G | 3 | a0001c0001t0004g0220 a0001c0001t0004g0221 a0001c0001t0031g0222 |
3 | HG01106.hp2 HG02293.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.31-6425T>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63301470 | |||||||
| chr6:63301852 | A | G | 1 | a0002c0002t0040g0226 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.31-6807T>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63301852 | |||||||
| chr6:63301913 | C | T | 1 | a0001c0001t0003g0110 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.31-6868G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63301913 | |||||||
| chr6:63301914 | G | A | 1 | a0001c0001t0002g0069 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.31-6869C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63301914 | |||||||
| chr6:63301994 | A | G | 5 | a0001c0001t0030g0108 a0001c0004t0003g0008 a0001c0004t0003g0109 others(2): Show |
8 | HG00099.hp1 HG00738.hp2 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.31-6949T>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63301994 | |||||||
| chr6:63302383 | A | C | 1 | a0001c0001t0029g0043 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.31-7338T>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63302383 | |||||||
| chr6:63302635 | A | C | 1 | a0002c0003t0005g0241 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.31-7590T>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63302635 | |||||||
| chr6:63302944 | T | G | 1 | a0001c0001t0002g0072 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.31-7899A>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63302944 | |||||||
| chr6:63303042 | C | T | 1 | a0001c0001t0002g0057 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.31-7997G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63303042 | |||||||
| chr6:63303135 | G | A | 2 | a0006c0009t0020g0243 a0006c0009t0020g0244 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.31-8090C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63303135 | |||||||
| chr6:63303262 | G | T | 6 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0018g0235 others(3): Show |
10 | HG01884.hp1 HG02258.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.31-8217C>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63303262 | |||||||
| chr6:63303402 | G | T | 1 | a0001c0010t0003g0023 | 2 | HG00558.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.31-8357C>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63303402 | |||||||
| chr6:63303460 | G | C | 1 | a0001c0001t0001g0028 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.31-8415C>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63303460 | |||||||
| chr6:63303491 | T | G | 1 | a0001c0001t0001g0201 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.31-8446A>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63303491 | |||||||
| chr6:63303932 | A | G | 1 | a0001c0001t0004g0219 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.31-8887T>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63303932 | |||||||
| chr6:63304046 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.31-9001C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63304046 | |||||||
| chr6:63304252 | C | A | 2 | a0001c0001t0032g0229 a0001c0001t0033g0230 |
2 | HG02559.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.31-9207G>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63304252 | |||||||
| chr6:63304315 | T | C | 2 | a0001c0001t0002g0196 a0001c0001t0007g0202 |
2 | NA18953.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.31-9270A>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63304315 | |||||||
| chr6:63304422 | G | C | 54 | a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0009 others(51): Show |
78 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.31-9377C>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63304422 | |||||||
| chr6:63304522 | T | G | 5 | a0002c0003t0005g0015 a0002c0003t0005g0035 a0002c0003t0005g0240 others(2): Show |
8 | HG02145.hp1 HG02258.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.31-9477A>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63304522 | |||||||
| chr6:63304823 | A | G | 2 | a0001c0001t0032g0229 a0001c0001t0033g0230 |
2 | HG02559.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.31-9778T>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63304823 | |||||||
| chr6:63304827 | G | A | 12 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0018g0235 others(9): Show |
19 | HG01884.hp1 HG02145.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.31-9782C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63304827 | |||||||
| chr6:63304907 | A | C | 51 | a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0009 others(48): Show |
75 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.31-9862T>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63304907 | |||||||
| chr6:63305099 | C | T | 6 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0018g0235 others(3): Show |
10 | HG01884.hp1 HG02258.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.31-10054G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63305099 | |||||||
| chr6:63305143 | G | GT | 7 | a0001c0001t0003g0088 a0001c0001t0009g0175 a0002c0003t0005g0015 others(4): Show |
10 | HG02145.hp1 HG02258.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.31-10099dupA | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63305143 | |||||||
| chr6:63305301 | C | T | 1 | a0001c0001t0004g0217 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.31-10256G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63305301 | |||||||
| chr6:63305310 | A | C | 2 | a0001c0001t0003g0082 a0001c0001t0003g0083 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.31-10265T>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63305310 | |||||||
| chr6:63305318 | C | T | 12 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0018g0235 others(9): Show |
19 | HG01884.hp1 HG02145.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.31-10273G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63305318 | |||||||
| chr6:63305340 | G | C | 1 | a0001c0001t0002g0053 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.31-10295C>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63305340 | |||||||
| chr6:63305622 | T | C | 11 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0018g0235 others(8): Show |
18 | HG01884.hp1 HG02145.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.31-10577A>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63305622 | |||||||
| chr6:63305649 | C | A | 2 | a0002c0007t0019g0227 a0002c0007t0019g0228 |
2 | HG01069.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.31-10604G>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63305649 | |||||||
| chr6:63305673 | G | T | 3 | a0004c0006t0014g0234 a0004c0006t0027g0233 a0004c0006t0028g0231 |
3 | HG02280.hp1 HG02818.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.31-10628C>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63305673 | |||||||
| chr6:63305689 | G | T | 1 | a0001c0001t0001g0200 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.31-10644C>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63305689 | |||||||
| chr6:63305710 | C | G | 2 | a0006c0009t0020g0243 a0006c0009t0020g0244 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.31-10665G>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63305710 | |||||||
| chr6:63305725 | G | T | 3 | a0001c0001t0002g0055 a0001c0001t0002g0056 a0001c0001t0011g0054 |
3 | NA18940.hp2 NA18974.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.31-10680C>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63305725 | |||||||
| chr6:63305733 | A | G | 3 | a0001c0001t0002g0020 a0001c0001t0002g0052 a0001c0001t0002g0053 |
4 | HG00558.hp1 HG00609.hp2 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-10688T>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63305733 | |||||||
| chr6:63305955 | T | G | 1 | a0002c0007t0019g0227 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.31-10910A>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63305955 | |||||||
| chr6:63306009 | G | A | 1 | a0001c0001t0001g0150 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.31-10964C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63306009 | |||||||
| chr6:63306025 | C | T | 6 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0045 others(3): Show |
8 | HG02523.hp1 NA18957.hp1 NA18970.hp1 others(5): Show |
intron_variant | MODIFIER | c.31-10980G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63306025 | |||||||
| chr6:63306072 | CA | C | 25 | a0001c0001t0001g0084 a0001c0001t0001g0102 a0001c0001t0001g0165 others(22): Show |
35 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.31-11028delT | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63306072 | |||||||
| chr6:63306141 | A | T | 11 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0018g0235 others(8): Show |
18 | HG01884.hp1 HG02145.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.31-11096T>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63306141 | |||||||
| chr6:63306254 | A | G | 4 | a0001c0001t0014g0232 a0004c0006t0014g0234 a0004c0006t0027g0233 others(1): Show |
4 | HG02280.hp1 HG02818.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-11209T>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63306254 | |||||||
| chr6:63306756 | G | C | 22 | a0001c0001t0014g0232 a0001c0001t0032g0229 a0001c0001t0033g0230 others(19): Show |
29 | HG01069.hp2 HG01884.hp1 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.31-11711C>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63306756 | |||||||
| chr6:63306782 | G | A | 5 | a0002c0003t0005g0015 a0002c0003t0005g0035 a0002c0003t0005g0240 others(2): Show |
8 | HG02145.hp1 HG02258.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.31-11737C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63306782 | |||||||
| chr6:63306822 | G | A | 2 | a0006c0009t0020g0243 a0006c0009t0020g0244 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.31-11777C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63306822 | |||||||
| chr6:63306919 | A | C | 1 | a0002c0002t0040g0226 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.31-11874T>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63306919 | |||||||
| chr6:63307209 | ATCC | A | 5 | a0002c0003t0005g0015 a0002c0003t0005g0035 a0002c0003t0005g0240 others(2): Show |
8 | HG02145.hp1 HG02258.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.31-12167_31-12165d others(5): Show |
LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63307209 | |||||||
| chr6:63307343 | C | G | 5 | a0002c0003t0005g0015 a0002c0003t0005g0035 a0002c0003t0005g0240 others(2): Show |
8 | HG02145.hp1 HG02258.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.31-12298G>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63307343 | |||||||
| chr6:63307615 | A | G | 2 | a0006c0009t0020g0243 a0006c0009t0020g0244 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.30+12299T>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63307615 | |||||||
| chr6:63307791 | C | T | 1 | a0002c0002t0040g0226 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.30+12123G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63307791 | |||||||
| chr6:63308084 | C | T | 11 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0018g0235 others(8): Show |
18 | HG01884.hp1 HG02145.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.30+11830G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63308084 | |||||||
| chr6:63308132 | T | C | 22 | a0001c0001t0014g0232 a0001c0001t0032g0229 a0001c0001t0033g0230 others(19): Show |
29 | HG01069.hp2 HG01884.hp1 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.30+11782A>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63308132 | |||||||
| chr6:63308233 | A | C | 14 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0018g0235 others(11): Show |
21 | HG01884.hp1 HG02145.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.30+11681T>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63308233 | |||||||
| chr6:63308551 | A | T | 12 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0018g0235 others(9): Show |
19 | HG01884.hp1 HG02145.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.30+11363T>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63308551 | |||||||
| chr6:63308614 | C | CA | 101 | a0001c0001t0001g0029 a0001c0001t0001g0036 a0001c0001t0001g0038 others(98): Show |
134 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(131): Show |
intron_variant | MODIFIER | c.30+11299dupT | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63308614 | |||||||
| chr6:63308614 | C | CAA | 14 | a0001c0001t0002g0073 a0002c0002t0010g0006 a0002c0002t0010g0239 others(11): Show |
21 | HG01884.hp1 HG02080.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.30+11298_30+11299d others(4): Show |
LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63308614 | |||||||
| chr6:63308767 | T | TAGAAATA others(343): Show |
1 | a0002c0002t0040g0226 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.30+11146_30+11147i others(352): Show |
LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63308767 | |||||||
| chr6:63309020 | C | T | 1 | a0001c0001t0003g0107 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.30+10894G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63309020 | |||||||
| chr6:63309239 | C | T | 1 | a0001c0001t0030g0108 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.30+10675G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63309239 | |||||||
| chr6:63309260 | C | T | 3 | a0001c0001t0001g0039 a0003c0005t0001g0031 a0003c0005t0004g0188 |
4 | HG01109.hp2 HG01358.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+10654G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63309260 | |||||||
| chr6:63309301 | G | C | 2 | a0006c0009t0020g0243 a0006c0009t0020g0244 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.30+10613C>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63309301 | |||||||
| chr6:63309451 | T | G | 14 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0018g0235 others(11): Show |
21 | HG01884.hp1 HG02145.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.30+10463A>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63309451 | |||||||
| chr6:63309468 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.30+10446A>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63309468 | |||||||
| chr6:63309703 | C | T | 16 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0018g0235 others(13): Show |
23 | HG01069.hp2 HG01884.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.30+10211G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63309703 | |||||||
| chr6:63309742 | T | A | 4 | a0001c0001t0014g0232 a0004c0006t0014g0234 a0004c0006t0027g0233 others(1): Show |
4 | HG02280.hp1 HG02818.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.30+10172A>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63309742 | |||||||
| chr6:63310007 | G | A | 2 | a0002c0007t0019g0227 a0002c0007t0019g0228 |
2 | HG01069.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.30+9907C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63310007 | |||||||
| chr6:63310230 | G | A | 2 | a0001c0001t0013g0097 a0001c0001t0013g0098 |
2 | HG02818.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.30+9684C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63310230 | |||||||
| chr6:63310243 | T | A | 1 | a0001c0001t0001g0101 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.30+9671A>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63310243 | |||||||
| chr6:63310396 | A | G | 2 | a0006c0009t0020g0243 a0006c0009t0020g0244 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.30+9518T>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63310396 | |||||||
| chr6:63310534 | G | T | 12 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0018g0235 others(9): Show |
19 | HG01884.hp1 HG02145.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.30+9380C>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63310534 | |||||||
| chr6:63310560 | T | C | 1 | a0001c0001t0001g0165 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.30+9354A>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63310560 | |||||||
| chr6:63310656 | G | A | 11 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0018g0235 others(8): Show |
18 | HG01884.hp1 HG02145.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.30+9258C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63310656 | |||||||
| chr6:63310903 | G | T | 1 | a0001c0001t0003g0107 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.30+9011C>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63310903 | |||||||
| chr6:63310922 | T | C | 22 | a0001c0001t0014g0232 a0001c0001t0032g0229 a0001c0001t0033g0230 others(19): Show |
29 | HG01069.hp2 HG01884.hp1 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.30+8992A>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63310922 | |||||||
| chr6:63311011 | T | C | 11 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0018g0235 others(8): Show |
18 | HG01884.hp1 HG02145.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.30+8903A>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63311011 | |||||||
| chr6:63311196 | G | A | 1 | a0001c0001t0002g0208 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.30+8718C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63311196 | |||||||
| chr6:63311397 | T | C | 22 | a0001c0001t0014g0232 a0001c0001t0032g0229 a0001c0001t0033g0230 others(19): Show |
29 | HG01069.hp2 HG01884.hp1 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.30+8517A>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63311397 | |||||||
| chr6:63311740 | G | A | 2 | a0002c0007t0019g0227 a0002c0007t0019g0228 |
2 | HG01069.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.30+8174C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63311740 | |||||||
| chr6:63311759 | C | T | 6 | a0001c0001t0001g0029 a0001c0001t0001g0036 a0001c0001t0001g0038 others(3): Show |
8 | HG01884.hp2 HG02630.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.30+8155G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63311759 | |||||||
| chr6:63311897 | T | C | 14 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0018g0235 others(11): Show |
21 | HG01884.hp1 HG02145.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.30+8017A>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63311897 | |||||||
| chr6:63311989 | G | A | 6 | a0001c0001t0001g0166 a0001c0001t0003g0016 a0001c0001t0003g0044 others(3): Show |
7 | HG00741.hp2 HG01167.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.30+7925C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63311989 | |||||||
| chr6:63312006 | G | A | 1 | a0001c0001t0008g0170 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.30+7908C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63312006 | |||||||
| chr6:63312040 | A | T | 3 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0041g0238 |
7 | HG01884.hp1 HG02258.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.30+7874T>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63312040 | |||||||
| chr6:63312224 | A | C | 2 | a0001c0001t0003g0082 a0001c0001t0003g0083 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.30+7690T>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63312224 | |||||||
| chr6:63312602 | G | T | 2 | a0002c0007t0019g0227 a0002c0007t0019g0228 |
2 | HG01069.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.30+7312C>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63312602 | |||||||
| chr6:63312775 | G | A | 6 | a0001c0001t0002g0010 a0001c0001t0002g0074 a0001c0001t0002g0075 others(3): Show |
8 | HG01993.hp2 HG02273.hp1 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.30+7139C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63312775 | |||||||
| chr6:63312776 | C | G | 1 | a0001c0001t0001g0101 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.30+7138G>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63312776 | |||||||
| chr6:63312845 | A | G | 2 | a0002c0007t0019g0227 a0002c0007t0019g0228 |
2 | HG01069.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.30+7069T>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63312845 | |||||||
| chr6:63313110 | C | A | 1 | a0002c0002t0040g0226 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.30+6804G>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63313110 | |||||||
| chr6:63313213 | T | C | 1 | a0001c0001t0012g0013 | 3 | HG03209.hp2 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.30+6701A>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63313213 | |||||||
| chr6:63313294 | T | A | 7 | a0001c0001t0001g0028 a0001c0001t0001g0172 a0001c0001t0001g0173 others(4): Show |
8 | HG01074.hp2 HG01106.hp1 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.30+6620A>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63313294 | |||||||
| chr6:63313394 | C | T | 2 | a0001c0001t0003g0081 a0001c0001t0042g0245 |
2 | HG01074.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.30+6520G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63313394 | |||||||
| chr6:63313445 | A | C | 2 | a0006c0009t0020g0243 a0006c0009t0020g0244 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.30+6469T>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63313445 | |||||||
| chr6:63313500 | A | C | 2 | a0006c0009t0020g0243 a0006c0009t0020g0244 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.30+6414T>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63313500 | |||||||
| chr6:63313614 | G | C | 14 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0018g0235 others(11): Show |
21 | HG01884.hp1 HG02145.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.30+6300C>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63313614 | |||||||
| chr6:63313696 | C | T | 1 | a0001c0001t0002g0204 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.30+6218G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63313696 | |||||||
| chr6:63313703 | G | A | 6 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0018g0235 others(3): Show |
10 | HG01884.hp1 HG02258.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.30+6211C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63313703 | |||||||
| chr6:63313837 | A | AAAAT | 7 | a0001c0001t0001g0022 a0001c0001t0001g0025 a0001c0001t0001g0092 others(4): Show |
8 | HG02132.hp2 HG04184.hp1 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.30+6073_30+6076dup others(4): Show |
LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63313837 | |||||||
| chr6:63313837 | AAAAT | A | 110 | a0001c0001t0001g0029 a0001c0001t0001g0036 a0001c0001t0001g0038 others(107): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.30+6073_30+6076del others(4): Show |
LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63313837 | |||||||
| chr6:63313863 | A | C | 12 | a0001c0001t0032g0229 a0002c0002t0010g0006 a0002c0002t0010g0239 others(9): Show |
19 | HG01884.hp1 HG02145.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.30+6051T>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63313863 | |||||||
| chr6:63313867 | A | C | 19 | a0001c0001t0001g0079 a0001c0001t0001g0105 a0001c0001t0001g0106 others(16): Show |
26 | HG01884.hp1 HG02145.hp1 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.30+6047T>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63313867 | |||||||
| chr6:63313871 | C | A | 3 | a0002c0007t0019g0228 a0006c0009t0020g0243 a0006c0009t0020g0244 |
3 | HG01069.hp2 HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.30+6043G>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63313871 | |||||||
| chr6:63313873 | TACATACA others(6): Show |
T | 1 | a0002c0002t0040g0226 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.30+6028_30+6040del others(13): Show |
LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63313873 | |||||||
| chr6:63313875 | C | A | 2 | a0002c0007t0019g0227 a0002c0007t0019g0228 |
2 | HG01069.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.30+6039G>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63313875 | |||||||
| chr6:63313886 | A | G | 5 | a0002c0003t0005g0015 a0002c0003t0005g0035 a0002c0003t0005g0240 others(2): Show |
8 | HG02145.hp1 HG02258.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.30+6028T>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63313886 | |||||||
| chr6:63313890 | A | G | 12 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0018g0235 others(9): Show |
19 | HG01884.hp1 HG02145.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.30+6024T>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63313890 | |||||||
| chr6:63313894 | G | A | 12 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0018g0235 others(9): Show |
19 | HG01884.hp1 HG02145.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.30+6020C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63313894 | |||||||
| chr6:63314057 | A | G | 5 | a0001c0001t0001g0102 a0001c0001t0001g0177 a0002c0002t0040g0226 others(2): Show |
5 | HG02027.hp1 HG06807.hp2 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.30+5857T>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63314057 | |||||||
| chr6:63314119 | G | A | 84 | a0001c0001t0001g0029 a0001c0001t0001g0036 a0001c0001t0001g0038 others(81): Show |
115 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(112): Show |
intron_variant | MODIFIER | c.30+5795C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63314119 | |||||||
| chr6:63314170 | A | C | 1 | a0001c0001t0001g0176 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.30+5744T>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63314170 | |||||||
| chr6:63314206 | G | A | 14 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0018g0235 others(11): Show |
21 | HG01884.hp1 HG02145.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.30+5708C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63314206 | |||||||
| chr6:63314434 | C | T | 22 | a0001c0001t0014g0232 a0001c0001t0032g0229 a0001c0001t0033g0230 others(19): Show |
29 | HG01069.hp2 HG01884.hp1 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.30+5480G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63314434 | |||||||
| chr6:63314449 | T | G | 14 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0018g0235 others(11): Show |
21 | HG01884.hp1 HG02145.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.30+5465A>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63314449 | |||||||
| chr6:63314450 | T | C | 14 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0018g0235 others(11): Show |
21 | HG01884.hp1 HG02145.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.30+5464A>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63314450 | |||||||
| chr6:63314511 | G | A | 2 | a0006c0009t0020g0243 a0006c0009t0020g0244 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.30+5403C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63314511 | |||||||
| chr6:63314556 | C | A | 6 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0018g0235 others(3): Show |
10 | HG01884.hp1 HG02258.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.30+5358G>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63314556 | |||||||
| chr6:63314596 | C | T | 2 | a0006c0009t0020g0243 a0006c0009t0020g0244 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.30+5318G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63314596 | |||||||
| chr6:63314717 | T | C | 2 | a0002c0007t0019g0227 a0002c0007t0019g0228 |
2 | HG01069.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.30+5197A>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63314717 | |||||||
| chr6:63314800 | G | C | 6 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0018g0235 others(3): Show |
10 | HG01884.hp1 HG02258.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.30+5114C>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63314800 | |||||||
| chr6:63314863 | G | T | 12 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0018g0235 others(9): Show |
19 | HG01884.hp1 HG02145.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.30+5051C>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63314863 | |||||||
| chr6:63314927 | C | T | 2 | a0001c0001t0001g0101 a0001c0001t0009g0175 |
2 | HG01496.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.30+4987G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63314927 | |||||||
| chr6:63315194 | C | T | 4 | a0001c0001t0002g0047 a0001c0001t0002g0210 a0001c0001t0002g0211 others(1): Show |
4 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+4720G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63315194 | |||||||
| chr6:63315231 | C | T | 12 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0018g0235 others(9): Show |
19 | HG01884.hp1 HG02145.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.30+4683G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63315231 | |||||||
| chr6:63315248 | T | C | 6 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0018g0235 others(3): Show |
10 | HG01884.hp1 HG02258.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.30+4666A>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63315248 | |||||||
| chr6:63315326 | A | G | 1 | a0001c0001t0008g0174 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.30+4588T>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63315326 | |||||||
| chr6:63315483 | A | C | 1 | a0001c0001t0021g0100 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.30+4431T>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63315483 | |||||||
| chr6:63315530 | G | A | 2 | a0006c0009t0020g0243 a0006c0009t0020g0244 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.30+4384C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63315530 | |||||||
| chr6:63315602 | T | TTCTC | 8 | a0002c0002t0018g0235 a0002c0002t0018g0236 a0002c0003t0005g0015 others(5): Show |
11 | HG02145.hp1 HG02258.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.30+4308_30+4311dup others(4): Show |
LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63315602 | |||||||
| chr6:63315602 | T | TTCTCTC | 3 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0041g0238 |
7 | HG01884.hp1 HG02258.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.30+4306_30+4311dup others(6): Show |
LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63315602 | |||||||
| chr6:63315602 | TTC | T | 48 | a0001c0001t0001g0048 a0001c0001t0002g0004 a0001c0001t0002g0007 others(45): Show |
72 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.30+4310_30+4311del others(2): Show |
LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63315602 | |||||||
| chr6:63315616 | C | CTG | 3 | a0001c0001t0002g0045 a0001c0001t0032g0229 a0001c0001t0033g0230 |
3 | HG02523.hp1 HG02559.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.30+4297_30+4298ins others(2): Show |
LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63315616 | |||||||
| chr6:63315618 | C | G | 6 | a0001c0001t0002g0045 a0001c0001t0025g0046 a0001c0001t0032g0229 others(3): Show |
6 | HG02523.hp1 HG02559.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.30+4296G>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63315618 | |||||||
| chr6:63315618 | CTG | C | 108 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0025 others(105): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.30+4294_30+4295del others(2): Show |
LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63315618 | |||||||
| chr6:63315618 | CTGTG | C | 32 | a0001c0001t0001g0029 a0001c0001t0001g0036 a0001c0001t0001g0038 others(29): Show |
40 | HG01106.hp2 HG01109.hp2 HG01358.hp2 others(37): Show |
intron_variant | MODIFIER | c.30+4292_30+4295del others(4): Show |
LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63315618 | |||||||
| chr6:63315618 | CTGTGTG | C | 10 | a0001c0001t0001g0194 a0001c0001t0001g0197 a0001c0001t0002g0192 others(7): Show |
11 | HG03516.hp2 HG03579.hp2 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.30+4290_30+4295del others(6): Show |
LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63315618 | |||||||
| chr6:63315620 | G | C | 8 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0041g0238 others(5): Show |
15 | HG01884.hp1 HG02145.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.30+4294C>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63315620 | |||||||
| chr6:63315622 | G | C | 9 | a0001c0001t0003g0191 a0002c0002t0010g0006 a0002c0002t0010g0239 others(6): Show |
16 | HG00597.hp2 HG01884.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.30+4292C>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63315622 | |||||||
| chr6:63315624 | G | C | 6 | a0001c0001t0004g0225 a0002c0003t0005g0015 a0002c0003t0005g0035 others(3): Show |
9 | HG02145.hp1 HG02258.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.30+4290C>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63315624 | |||||||
| chr6:63315626 | G | C | 2 | a0006c0009t0020g0243 a0006c0009t0020g0244 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.30+4288C>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63315626 | |||||||
| chr6:63315628 | G | C | 2 | a0006c0009t0020g0243 a0006c0009t0020g0244 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.30+4286C>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63315628 | |||||||
| chr6:63315630 | G | C | 2 | a0006c0009t0020g0243 a0006c0009t0020g0244 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.30+4284C>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63315630 | |||||||
| chr6:63315873 | T | TA | 10 | a0001c0001t0001g0033 a0001c0001t0001g0199 a0001c0001t0001g0200 others(7): Show |
13 | HG02129.hp2 HG02145.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.30+4040dupT | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63315873 | |||||||
| chr6:63315970 | C | T | 2 | a0006c0009t0020g0243 a0006c0009t0020g0244 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.30+3944G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63315970 | |||||||
| chr6:63316010 | A | G | 2 | a0006c0009t0020g0243 a0006c0009t0020g0244 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.30+3904T>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63316010 | |||||||
| chr6:63316123 | A | G | 2 | a0006c0009t0020g0243 a0006c0009t0020g0244 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.30+3791T>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63316123 | |||||||
| chr6:63316213 | A | G | 1 | a0001c0001t0029g0043 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.30+3701T>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63316213 | |||||||
| chr6:63316248 | C | T | 2 | a0006c0009t0020g0243 a0006c0009t0020g0244 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.30+3666G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63316248 | |||||||
| chr6:63316534 | C | A | 2 | a0006c0009t0020g0243 a0006c0009t0020g0244 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.30+3380G>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63316534 | |||||||
| chr6:63316579 | G | C | 1 | a0001c0001t0003g0203 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.30+3335C>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63316579 | |||||||
| chr6:63316842 | G | A | 7 | a0001c0001t0002g0014 a0001c0001t0002g0034 a0001c0001t0002g0204 others(4): Show |
10 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.30+3072C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63316842 | |||||||
| chr6:63316930 | G | A | 2 | a0006c0009t0020g0243 a0006c0009t0020g0244 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.30+2984C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63316930 | |||||||
| chr6:63317266 | C | G | 2 | a0002c0007t0019g0227 a0002c0007t0019g0228 |
2 | HG01069.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.30+2648G>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63317266 | |||||||
| chr6:63317474 | A | T | 2 | a0006c0009t0020g0243 a0006c0009t0020g0244 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.30+2440T>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63317474 | |||||||
| chr6:63317500 | C | T | 1 | a0001c0001t0003g0044 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.30+2414G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63317500 | |||||||
| chr6:63317739 | G | A | 1 | a0001c0001t0004g0225 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.30+2175C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63317739 | |||||||
| chr6:63317798 | C | G | 1 | a0001c0001t0029g0043 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.30+2116G>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63317798 | |||||||
| chr6:63317895 | G | A | 2 | a0006c0009t0020g0243 a0006c0009t0020g0244 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.30+2019C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63317895 | |||||||
| chr6:63317903 | T | A | 11 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0018g0235 others(8): Show |
18 | HG01884.hp1 HG02145.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.30+2011A>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63317903 | |||||||
| chr6:63317943 | C | T | 1 | a0001c0001t0003g0016 | 2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.30+1971G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63317943 | |||||||
| chr6:63318006 | T | C | 2 | a0006c0009t0020g0243 a0006c0009t0020g0244 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.30+1908A>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63318006 | |||||||
| chr6:63318037 | G | GTACTACT others(1): Show |
12 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0018g0235 others(9): Show |
19 | HG01884.hp1 HG02145.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.30+1876_30+1877ins others(8): Show |
LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63318037 | |||||||
| chr6:63318111 | T | C | 5 | a0001c0001t0014g0232 a0001c0001t0033g0230 a0004c0006t0014g0234 others(2): Show |
5 | HG02280.hp1 HG02559.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.30+1803A>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63318111 | |||||||
| chr6:63318142 | C | A | 2 | a0006c0009t0020g0243 a0006c0009t0020g0244 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.30+1772G>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63318142 | |||||||
| chr6:63318150 | G | A | 2 | a0006c0009t0020g0243 a0006c0009t0020g0244 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.30+1764C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63318150 | |||||||
| chr6:63318161 | C | T | 12 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0018g0235 others(9): Show |
19 | HG01884.hp1 HG02145.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.30+1753G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63318161 | |||||||
| chr6:63318180 | A | G | 1 | a0002c0002t0040g0226 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.30+1734T>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63318180 | |||||||
| chr6:63318269 | G | T | 3 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 |
3 | HG00621.hp1 NA18942.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.30+1645C>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63318269 | |||||||
| chr6:63318317 | A | G | 4 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0039 others(1): Show |
4 | HG01884.hp2 HG03098.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+1597T>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63318317 | |||||||
| chr6:63318355 | A | G | 2 | a0006c0009t0020g0243 a0006c0009t0020g0244 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.30+1559T>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63318355 | |||||||
| chr6:63318458 | A | C | 2 | a0006c0009t0020g0243 a0006c0009t0020g0244 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.30+1456T>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63318458 | |||||||
| chr6:63318487 | T | C | 14 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0018g0235 others(11): Show |
21 | HG01884.hp1 HG02145.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.30+1427A>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63318487 | |||||||
| chr6:63318496 | G | C | 1 | a0005c0008t0026g0209 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.30+1418C>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63318496 | |||||||
| chr6:63318551 | C | T | 2 | a0006c0009t0020g0243 a0006c0009t0020g0244 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.30+1363G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63318551 | |||||||
| chr6:63318568 | G | A | 2 | a0006c0009t0020g0243 a0006c0009t0020g0244 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.30+1346C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63318568 | |||||||
| chr6:63318640 | A | G | 2 | a0006c0009t0020g0243 a0006c0009t0020g0244 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.30+1274T>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63318640 | |||||||
| chr6:63319317 | C | T | 2 | a0006c0009t0020g0243 a0006c0009t0020g0244 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.30+597G>A | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63319317 | |||||||
| chr6:63319333 | G | A | 6 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0002g0210 others(3): Show |
6 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+581C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63319333 | |||||||
| chr6:63319473 | C | G | 12 | a0002c0002t0010g0006 a0002c0002t0010g0239 a0002c0002t0018g0235 others(9): Show |
19 | HG01884.hp1 HG02145.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.30+441G>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63319473 | |||||||
| chr6:63319620 | AT | A | 22 | a0001c0001t0004g0003 a0001c0001t0004g0217 a0001c0001t0004g0218 others(19): Show |
34 | HG01106.hp2 HG01884.hp1 HG01952.hp2 others(31): Show |
intron_variant | MODIFIER | c.30+293delA | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63319620 | |||||||
| chr6:63319621 | T | A | 2 | a0006c0009t0020g0243 a0006c0009t0020g0244 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.30+293A>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63319621 | |||||||
| chr6:63319628 | A | G | 2 | a0006c0009t0020g0243 a0006c0009t0020g0244 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.30+286T>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63319628 | |||||||
| chr6:63319718 | T | G | 2 | a0006c0009t0020g0243 a0006c0009t0020g0244 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.30+196A>C | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63319718 | |||||||
| chr6:63319724 | G | A | 2 | a0006c0009t0020g0243 a0006c0009t0020g0244 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.30+190C>T | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63319724 | |||||||
| chr6:63319744 | T | C | 22 | a0001c0001t0014g0232 a0001c0001t0032g0229 a0001c0001t0033g0230 others(19): Show |
29 | HG01069.hp2 HG01884.hp1 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.30+170A>G | LGSN | ENSG00000146166.17 | transcript | ENST00000370657.9 | protein_coding | 1/3 | chr6 | 63319744 |