Item | Value |
---|---|
geneid | 55203 |
ensemblid | ENSG00000153012.12 |
hgncid | 18710 |
symbol | LGI2 |
name | leucine rich repeat LGI family member 2 |
refseq_nuc | NM_018176.4 |
refseq_prot | NP_060646.2 |
ensembl_nuc | ENST00000382114.9 |
ensembl_prot | ENSP00000371548.4 |
mane_status | MANE Select |
chr | chr4 |
start | 24998847 |
end | 25030946 |
strand | - |
ver | v1.2 |
region | chr4:24998847-25030946 |
region5000 | chr4:24993847-25035946 |
regionname0 | LGI2_chr4_24998847_25030946 |
regionname5000 | LGI2_chr4_24993847_25035946 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 545 | 359 | 82 | 56 | 174 | 9 | 36 | 135 | LGI2_chr4_24993847_25035946 | LGI2 | MALRR others(540): Show |
chr4 | 24993847 | 25035946 |
a0002 | 0/0 | 545 | 90 | 16 | 17 | 42 | 5 | 10 | 33 | LGI2_chr4_24993847_25035946 | LGI2 | MALRR others(540): Show |
chr4 | 24993847 | 25035946 |
a0003 | 0/0 | 545 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | MALRR others(540): Show |
chr4 | 24993847 | 25035946 |
a0004 | 0/0 | 545 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | MALRR others(540): Show |
chr4 | 24993847 | 25035946 |
a0005 | 0/0 | 545 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | MALRR others(540): Show |
chr4 | 24993847 | 25035946 |
a0006 | 0/0 | 545 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | MALRR others(540): Show |
chr4 | 24993847 | 25035946 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1635 | 307 | 76 | 39 | 161 | 5 | 26 | LGI2_chr4_24993847_25035946 | LGI2 | ATGGC others(1630): Show |
chr4 | 24993847 | 25035946 | ||
a0001c0003 | 1/1 | 1635 | 38 | 6 | 13 | 5 | 4 | 8 | LGI2_chr4_24993847_25035946 | LGI2 | ATGGC others(1630): Show |
chr4 | 24993847 | 25035946 | ||
a0001c0005 | 0/0 | 1635 | 7 | 0 | 0 | 7 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | ATGGC others(1630): Show |
chr4 | 24993847 | 25035946 | ||
a0001c0006 | 0/0 | 1635 | 3 | 0 | 2 | 0 | 0 | 1 | LGI2_chr4_24993847_25035946 | LGI2 | ATGGC others(1630): Show |
chr4 | 24993847 | 25035946 | ||
a0001c0008 | 0/0 | 1635 | 2 | 0 | 2 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | ATGGC others(1630): Show |
chr4 | 24993847 | 25035946 | ||
a0001c0013 | 0/0 | 1635 | 1 | 0 | 0 | 0 | 0 | 1 | LGI2_chr4_24993847_25035946 | LGI2 | ATGGC others(1630): Show |
chr4 | 24993847 | 25035946 | ||
a0001c0014 | 0/0 | 1635 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | ATGGC others(1630): Show |
chr4 | 24993847 | 25035946 | ||
a0002c0002 | 0/0 | 1635 | 72 | 15 | 9 | 37 | 3 | 8 | LGI2_chr4_24993847_25035946 | LGI2 | ATGGC others(1630): Show |
chr4 | 24993847 | 25035946 | ||
a0002c0004 | 0/0 | 1635 | 15 | 1 | 8 | 3 | 2 | 1 | LGI2_chr4_24993847_25035946 | LGI2 | ATGGC others(1630): Show |
chr4 | 24993847 | 25035946 | ||
a0002c0009 | 0/0 | 1635 | 1 | 0 | 0 | 0 | 0 | 1 | LGI2_chr4_24993847_25035946 | LGI2 | ATGGC others(1630): Show |
chr4 | 24993847 | 25035946 | ||
a0002c0010 | 0/0 | 1635 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | ATGGC others(1630): Show |
chr4 | 24993847 | 25035946 | ||
a0002c0011 | 0/0 | 1635 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | ATGGC others(1630): Show |
chr4 | 24993847 | 25035946 | ||
a0003c0007 | 0/0 | 1635 | 2 | 0 | 1 | 0 | 0 | 1 | LGI2_chr4_24993847_25035946 | LGI2 | ATGGC others(1630): Show |
chr4 | 24993847 | 25035946 | ||
a0004c0015 | 0/0 | 1635 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | ATGGC others(1630): Show |
chr4 | 24993847 | 25035946 | ||
a0005c0012 | 0/0 | 1635 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | ATGGC others(1630): Show |
chr4 | 24993847 | 25035946 | ||
a0006c0016 | 0/0 | 1635 | 1 | 0 | 0 | 0 | 0 | 1 | LGI2_chr4_24993847_25035946 | LGI2 | ATGGC others(1630): Show |
chr4 | 24993847 | 25035946 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6494 | 51 | 1 | 8 | 33 | 0 | 9 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6489): Show |
chr4 | 24993847 | 25035946 |
a0001c0001t0002 | 0/0 | 6493 | 56 | 1 | 10 | 41 | 1 | 3 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6488): Show |
chr4 | 24993847 | 25035946 |
a0001c0001t0003 | 0/0 | 6495 | 11 | 8 | 0 | 0 | 0 | 3 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6490): Show |
chr4 | 24993847 | 25035946 |
a0001c0001t0004 | 0/0 | 6493 | 39 | 14 | 1 | 18 | 1 | 5 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6488): Show |
chr4 | 24993847 | 25035946 |
a0001c0001t0005 | 0/0 | 6497 | 43 | 21 | 4 | 16 | 0 | 2 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6492): Show |
chr4 | 24993847 | 25035946 |
a0001c0001t0006 | 0/0 | 6494 | 24 | 0 | 11 | 9 | 2 | 2 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6489): Show |
chr4 | 24993847 | 25035946 |
a0001c0001t0007 | 0/0 | 6494 | 31 | 0 | 2 | 29 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6489): Show |
chr4 | 24993847 | 25035946 |
a0001c0001t0008 | 0/0 | 6494 | 9 | 8 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6489): Show |
chr4 | 24993847 | 25035946 |
a0001c0001t0009 | 0/0 | 6494 | 10 | 10 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6489): Show |
chr4 | 24993847 | 25035946 |
a0001c0001t0010 | 0/0 | 6493 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6488): Show |
chr4 | 24993847 | 25035946 |
a0001c0001t0011 | 0/0 | 6493 | 3 | 0 | 0 | 3 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6488): Show |
chr4 | 24993847 | 25035946 |
a0001c0001t0013 | 0/0 | 6495 | 4 | 0 | 0 | 4 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6490): Show |
chr4 | 24993847 | 25035946 |
a0001c0001t0014 | 0/0 | 6494 | 3 | 3 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6489): Show |
chr4 | 24993847 | 25035946 |
a0001c0001t0015 | 0/0 | 6494 | 3 | 3 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6489): Show |
chr4 | 24993847 | 25035946 |
a0001c0001t0016 | 0/0 | 6494 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6489): Show |
chr4 | 24993847 | 25035946 |
a0001c0001t0018 | 0/0 | 6494 | 2 | 2 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6489): Show |
chr4 | 24993847 | 25035946 |
a0001c0001t0019 | 0/0 | 6495 | 2 | 0 | 0 | 2 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6490): Show |
chr4 | 24993847 | 25035946 |
a0001c0001t0020 | 0/0 | 6497 | 2 | 0 | 0 | 0 | 0 | 2 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6492): Show |
chr4 | 24993847 | 25035946 |
a0001c0001t0021 | 0/0 | 6494 | 2 | 0 | 0 | 2 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6489): Show |
chr4 | 24993847 | 25035946 |
a0001c0001t0022 | 0/0 | 6497 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6492): Show |
chr4 | 24993847 | 25035946 |
a0001c0001t0023 | 0/0 | 6493 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6488): Show |
chr4 | 24993847 | 25035946 |
a0001c0001t0024 | 0/0 | 6492 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6487): Show |
chr4 | 24993847 | 25035946 |
a0001c0001t0025 | 0/0 | 6493 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6488): Show |
chr4 | 24993847 | 25035946 |
a0001c0001t0027 | 0/0 | 6493 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6488): Show |
chr4 | 24993847 | 25035946 |
a0001c0001t0028 | 0/0 | 6493 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6488): Show |
chr4 | 24993847 | 25035946 |
a0001c0001t0029 | 0/0 | 6494 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6489): Show |
chr4 | 24993847 | 25035946 |
a0001c0001t0034 | 0/0 | 6495 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6490): Show |
chr4 | 24993847 | 25035946 |
a0001c0001t0035 | 0/0 | 6494 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6489): Show |
chr4 | 24993847 | 25035946 |
a0001c0001t0037 | 0/0 | 6494 | 1 | 0 | 0 | 0 | 1 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6489): Show |
chr4 | 24993847 | 25035946 |
a0001c0003t0003 | 1/1 | 6495 | 32 | 6 | 12 | 1 | 3 | 8 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6490): Show |
chr4 | 24993847 | 25035946 |
a0001c0003t0012 | 0/0 | 6495 | 3 | 0 | 0 | 3 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6490): Show |
chr4 | 24993847 | 25035946 |
a0001c0003t0031 | 0/0 | 6495 | 1 | 0 | 0 | 0 | 1 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6490): Show |
chr4 | 24993847 | 25035946 |
a0001c0003t0032 | 0/0 | 6495 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6490): Show |
chr4 | 24993847 | 25035946 |
a0001c0003t0036 | 0/0 | 6495 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6490): Show |
chr4 | 24993847 | 25035946 |
a0001c0005t0006 | 0/0 | 6494 | 7 | 0 | 0 | 7 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6489): Show |
chr4 | 24993847 | 25035946 |
a0001c0006t0004 | 0/0 | 6493 | 3 | 0 | 2 | 0 | 0 | 1 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6488): Show |
chr4 | 24993847 | 25035946 |
a0001c0008t0001 | 0/0 | 6494 | 2 | 0 | 2 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6489): Show |
chr4 | 24993847 | 25035946 |
a0001c0013t0004 | 0/0 | 6493 | 1 | 0 | 0 | 0 | 0 | 1 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6488): Show |
chr4 | 24993847 | 25035946 |
a0001c0014t0004 | 0/0 | 6493 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6488): Show |
chr4 | 24993847 | 25035946 |
a0002c0002t0001 | 0/0 | 6494 | 15 | 0 | 0 | 11 | 2 | 2 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6489): Show |
chr4 | 24993847 | 25035946 |
a0002c0002t0002 | 0/0 | 6493 | 12 | 2 | 0 | 10 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6488): Show |
chr4 | 24993847 | 25035946 |
a0002c0002t0003 | 0/0 | 6495 | 5 | 1 | 0 | 4 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6490): Show |
chr4 | 24993847 | 25035946 |
a0002c0002t0004 | 0/0 | 6493 | 13 | 4 | 2 | 5 | 0 | 2 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6488): Show |
chr4 | 24993847 | 25035946 |
a0002c0002t0005 | 0/0 | 6497 | 7 | 2 | 0 | 3 | 0 | 2 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6492): Show |
chr4 | 24993847 | 25035946 |
a0002c0002t0006 | 0/0 | 6494 | 4 | 1 | 1 | 1 | 0 | 1 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6489): Show |
chr4 | 24993847 | 25035946 |
a0002c0002t0008 | 0/0 | 6494 | 2 | 1 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6489): Show |
chr4 | 24993847 | 25035946 |
a0002c0002t0010 | 0/0 | 6493 | 4 | 0 | 4 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6488): Show |
chr4 | 24993847 | 25035946 |
a0002c0002t0011 | 0/0 | 6493 | 2 | 0 | 0 | 2 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6488): Show |
chr4 | 24993847 | 25035946 |
a0002c0002t0016 | 0/0 | 6494 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6489): Show |
chr4 | 24993847 | 25035946 |
a0002c0002t0017 | 0/0 | 6494 | 2 | 2 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6489): Show |
chr4 | 24993847 | 25035946 |
a0002c0002t0026 | 0/0 | 6493 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6488): Show |
chr4 | 24993847 | 25035946 |
a0002c0002t0030 | 0/0 | 6498 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6493): Show |
chr4 | 24993847 | 25035946 |
a0002c0002t0033 | 0/0 | 6494 | 1 | 0 | 0 | 0 | 1 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6489): Show |
chr4 | 24993847 | 25035946 |
a0002c0002t0038 | 0/0 | 6493 | 1 | 0 | 0 | 0 | 0 | 1 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6488): Show |
chr4 | 24993847 | 25035946 |
a0002c0002t0039 | 0/0 | 6493 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6488): Show |
chr4 | 24993847 | 25035946 |
a0002c0004t0003 | 0/0 | 6495 | 14 | 1 | 8 | 2 | 2 | 1 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6490): Show |
chr4 | 24993847 | 25035946 |
a0002c0004t0012 | 0/0 | 6495 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6490): Show |
chr4 | 24993847 | 25035946 |
a0002c0009t0004 | 0/0 | 6493 | 1 | 0 | 0 | 0 | 0 | 1 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6488): Show |
chr4 | 24993847 | 25035946 |
a0002c0010t0006 | 0/0 | 6494 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6489): Show |
chr4 | 24993847 | 25035946 |
a0002c0011t0003 | 0/0 | 6495 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6490): Show |
chr4 | 24993847 | 25035946 |
a0003c0007t0003 | 0/0 | 6495 | 2 | 0 | 1 | 0 | 0 | 1 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6490): Show |
chr4 | 24993847 | 25035946 |
a0004c0015t0003 | 0/0 | 6495 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6490): Show |
chr4 | 24993847 | 25035946 |
a0005c0012t0001 | 0/0 | 6494 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6489): Show |
chr4 | 24993847 | 25035946 |
a0006c0016t0006 | 0/0 | 6494 | 1 | 0 | 0 | 0 | 0 | 1 | LGI2_chr4_24993847_25035946 | LGI2 | AGGCG others(6489): Show |
chr4 | 24993847 | 25035946 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0001g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0001g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0001g0386 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0001g0390 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0001g0393 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0001g0396 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0001g0397 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0002g0002 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0002g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0002g0008 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0002g0030 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0002g0031 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0002g0038 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0002g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0002g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0002g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0002g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0002g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0002g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0002g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0002g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0002g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0002g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0002g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0002g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0002g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0002g0398 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0003g0007 | 0/0 | 3 | 2 | 0 | 0 | 0 | 1 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0003g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0003g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0003g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0003g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0004g0023 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0004g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0004g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0004g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0004g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0004g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0004g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0004g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0004g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0004g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0004g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0004g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0004g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0004g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0004g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0004g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0004g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0004g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0004g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0004g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0004g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0004g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0004g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0004g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0004g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0004g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0004g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0004g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0004g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0004g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0004g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0004g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0004g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0005g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0005g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0005g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0005g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0005g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0005g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0005g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0005g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0005g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0005g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0005g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0005g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0005g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0005g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0005g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0005g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0005g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0005g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0005g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0005g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0005g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0005g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0005g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0005g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0005g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0005g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0005g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0005g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0005g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0005g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0005g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0005g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0005g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0005g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0005g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0005g0394 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0006g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0006g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0006g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0006g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0006g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0006g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0006g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0006g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0006g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0006g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0006g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0006g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0006g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0006g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0006g0332 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0006g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0006g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0006g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0006g0387 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0006g0388 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0006g0389 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0007g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0007g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0007g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0007g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0007g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0007g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0007g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0007g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0007g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0007g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0007g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0007g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0007g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0007g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0007g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0007g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0007g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0007g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0007g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0007g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0007g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0007g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0007g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0007g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0007g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0007g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0008g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0008g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0008g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0008g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0008g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0008g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0008g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0008g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0008g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0009g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0009g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0009g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0009g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0009g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0009g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0009g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0010g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0011g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0011g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0011g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0013g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0013g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0013g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0013g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0014g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0014g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0014g0395 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0015g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0015g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0016g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0018g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0018g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0019g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0019g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0020g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0020g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0021g0391 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0021g0392 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0022g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0023g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0024g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0025g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0027g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0028g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0029g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0034g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0035g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0001t0037g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0003t0003g0006 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0003t0003g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0003t0003g0174 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0003t0003g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0003t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0003t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0003t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0003t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0003t0003g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0003t0003g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0003t0003g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0003t0003g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0003t0003g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0003t0003g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0003t0003g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0003t0003g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0003t0003g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0003t0003g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0003t0003g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0003t0003g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0003t0003g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0003t0003g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0003t0003g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0003t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0003t0003g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0003t0003g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0003t0003g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0003t0003g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0003t0003g0368 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0003t0012g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0003t0012g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0003t0031g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0003t0032g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0003t0036g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0005t0006g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0005t0006g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0005t0006g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0005t0006g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0005t0006g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0005t0006g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0006t0004g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0006t0004g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0006t0004g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0008t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0013t0004g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0001c0014t0004g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0002g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0004g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0004g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0004g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0004g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0004g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0004g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0004g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0004g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0004g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0004g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0005g0012 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0005g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0005g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0005g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0005g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0005g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0006g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0006g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0006g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0006g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0008g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0008g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0010g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0010g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0010g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0011g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0011g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0016g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0017g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0026g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0030g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0033g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0038g0400 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0002t0039g0401 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0004t0003g0001 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0004t0003g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0004t0003g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0004t0003g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0004t0003g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0004t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0004t0003g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0004t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0004t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0004t0003g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0004t0012g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0009t0004g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0010t0006g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0002c0011t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0003c0007t0003g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0003c0007t0003g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0004c0015t0003g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0005c0012t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
a0006c0016t0006g0399 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0003 | t0003 | g0220 | EUR | GBR | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG00099 | hp2 | a0001 | c0001 | t0006 | g0332 | EUR | GBR | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG00140 | hp1 | a0001 | c0003 | t0003 | g0219 | EUR | GBR | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG00140 | hp2 | a0002 | c0002 | t0001 | g0062 | EUR | GBR | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG00280 | hp1 | a0001 | c0001 | t0004 | g0280 | EUR | FIN | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG00280 | hp2 | a0001 | c0003 | t0003 | g0247 | EUR | FIN | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG00408 | hp1 | a0001 | c0001 | t0004 | g0028 | EAS | CHS | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0341 | EAS | CHS | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG00423 | hp1 | a0002 | c0002 | t0002 | g0102 | EAS | CHS | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG00423 | hp2 | a0001 | c0001 | t0006 | g0389 | EAS | CHS | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG00438 | hp1 | a0001 | c0001 | t0004 | g0027 | EAS | CHS | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0386 | EAS | CHS | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG00544 | hp1 | a0001 | c0001 | t0005 | g0149 | EAS | CHS | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG00558 | hp1 | a0002 | c0002 | t0001 | g0073 | EAS | CHS | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG00558 | hp2 | a0002 | c0002 | t0001 | g0097 | EAS | CHS | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG00597 | hp1 | a0001 | c0001 | t0006 | g0303 | EAS | CHS | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG00597 | hp2 | a0001 | c0001 | t0007 | g0385 | EAS | CHS | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG00609 | hp1 | a0001 | c0001 | t0011 | g0129 | EAS | CHS | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG00609 | hp2 | a0002 | c0002 | t0003 | g0091 | EAS | CHS | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG00621 | hp1 | a0001 | c0001 | t0011 | g0125 | EAS | CHS | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | CHS | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG00639 | hp1 | a0002 | c0002 | t0039 | g0401 | AMR | PUR | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG00639 | hp2 | a0001 | c0001 | t0005 | g0178 | AMR | PUR | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG00642 | hp1 | a0001 | c0003 | t0003 | g0317 | AMR | PUR | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG00642 | hp2 | a0001 | c0001 | t0006 | g0282 | AMR | PUR | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | CHS | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG00673 | hp2 | a0001 | c0001 | t0006 | g0387 | EAS | CHS | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG00733 | hp1 | a0001 | c0003 | t0003 | g0273 | AMR | PUR | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG00733 | hp2 | a0002 | c0002 | t0006 | g0041 | AMR | PUR | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG00735 | hp1 | a0001 | c0001 | t0006 | g0279 | AMR | PUR | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG00735 | hp2 | a0004 | c0015 | t0003 | g0261 | AMR | PUR | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG00738 | hp1 | a0001 | c0001 | t0006 | g0281 | AMR | PUR | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG00738 | hp2 | a0001 | c0006 | t0004 | g0374 | AMR | PUR | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG00741 | hp1 | a0002 | c0002 | t0008 | g0087 | AMR | PUR | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0031 | AMR | PUR | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG01069 | hp1 | a0002 | c0004 | t0003 | g0001 | AMR | PUR | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG01070 | hp1 | a0001 | c0008 | t0001 | g0017 | AMR | PUR | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG01070 | hp2 | a0001 | c0003 | t0003 | g0216 | AMR | PUR | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG01071 | hp1 | a0001 | c0008 | t0001 | g0017 | AMR | PUR | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG01071 | hp2 | a0002 | c0004 | t0003 | g0001 | AMR | PUR | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0286 | AMR | PUR | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG01074 | hp2 | a0001 | c0006 | t0004 | g0269 | AMR | PUR | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG01081 | hp1 | a0001 | c0003 | t0003 | g0215 | AMR | PUR | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG01081 | hp2 | a0001 | c0001 | t0006 | g0312 | AMR | PUR | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG01099 | hp1 | a0002 | c0004 | t0003 | g0082 | AMR | PUR | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG01099 | hp2 | a0001 | c0003 | t0003 | g0268 | AMR | PUR | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG01106 | hp1 | a0001 | c0003 | t0003 | g0181 | AMR | PUR | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG01109 | hp1 | a0001 | c0001 | t0004 | g0023 | AMR | PUR | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG01109 | hp2 | a0001 | c0001 | t0008 | g0248 | AMR | PUR | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG01167 | hp2 | a0002 | c0004 | t0003 | g0014 | AMR | PUR | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG01168 | hp1 | a0001 | c0003 | t0003 | g0197 | AMR | PUR | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG01169 | hp1 | a0002 | c0004 | t0003 | g0014 | AMR | PUR | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG01175 | hp2 | a0003 | c0007 | t0003 | g0050 | AMR | PUR | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG01192 | hp1 | a0001 | c0003 | t0003 | g0025 | AMR | PUR | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG01192 | hp2 | a0001 | c0001 | t0006 | g0176 | AMR | PUR | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG01243 | hp2 | a0001 | c0001 | t0005 | g0277 | AMR | PUR | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG01255 | hp1 | a0001 | c0003 | t0036 | g0223 | AMR | CLM | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG01255 | hp2 | a0002 | c0002 | t0004 | g0046 | AMR | CLM | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG01257 | hp1 | a0001 | c0001 | t0007 | g0326 | AMR | CLM | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG01257 | hp2 | a0002 | c0004 | t0003 | g0115 | AMR | CLM | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG01258 | hp1 | a0001 | c0001 | t0007 | g0330 | AMR | CLM | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG01258 | hp2 | a0001 | c0001 | t0006 | g0177 | AMR | CLM | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG01261 | hp1 | a0005 | c0012 | t0001 | g0153 | AMR | CLM | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG01261 | hp2 | a0001 | c0003 | t0003 | g0180 | AMR | CLM | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0328 | AMR | CLM | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG01358 | hp2 | a0002 | c0002 | t0004 | g0108 | AMR | CLM | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG01361 | hp1 | a0001 | c0001 | t0006 | g0258 | AMR | CLM | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG01361 | hp2 | a0002 | c0004 | t0003 | g0001 | AMR | CLM | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG01496 | hp1 | a0001 | c0003 | t0003 | g0218 | AMR | CLM | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG01496 | hp2 | a0001 | c0001 | t0006 | g0217 | AMR | CLM | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG01516 | hp1 | a0002 | c0002 | t0001 | g0081 | EUR | IBS | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG01516 | hp2 | a0002 | c0004 | t0003 | g0063 | EUR | IBS | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0030 | EUR | IBS | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG01517 | hp2 | a0002 | c0004 | t0003 | g0065 | EUR | IBS | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG01884 | hp1 | a0002 | c0002 | t0004 | g0107 | AFR | ACB | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG01884 | hp2 | a0001 | c0003 | t0003 | g0229 | AFR | ACB | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG01891 | hp1 | a0001 | c0001 | t0003 | g0206 | AFR | ACB | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG01891 | hp2 | a0001 | c0001 | t0005 | g0187 | AFR | ACB | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG01928 | hp1 | a0001 | c0003 | t0003 | g0331 | AMR | PEL | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG01928 | hp2 | a0002 | c0002 | t0010 | g0047 | AMR | PEL | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG01943 | hp1 | a0002 | c0002 | t0010 | g0013 | AMR | PEL | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0038 | AMR | PEL | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0398 | AMR | PEL | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG01952 | hp2 | a0001 | c0001 | t0006 | g0337 | AMR | PEL | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG01978 | hp1 | a0001 | c0001 | t0027 | g0325 | AMR | PEL | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0297 | AMR | PEL | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG01993 | hp2 | a0001 | c0001 | t0010 | g0265 | AMR | PEL | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0396 | AMR | PEL | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0339 | EAS | KHV | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02015 | hp2 | a0001 | c0001 | t0007 | g0324 | EAS | KHV | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02027 | hp1 | a0001 | c0001 | t0007 | g0148 | EAS | KHV | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02027 | hp2 | a0001 | c0001 | t0004 | g0118 | EAS | KHV | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02040 | hp1 | a0001 | c0001 | t0005 | g0214 | EAS | KHV | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02040 | hp2 | a0002 | c0002 | t0001 | g0071 | EAS | KHV | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02055 | hp1 | a0001 | c0001 | t0008 | g0250 | AFR | ACB | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02055 | hp2 | a0001 | c0003 | t0003 | g0182 | AFR | ACB | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02056 | hp1 | a0001 | c0014 | t0004 | g0209 | EAS | KHV | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02056 | hp2 | a0002 | c0011 | t0003 | g0094 | EAS | KHV | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02071 | hp2 | a0001 | c0001 | t0006 | g0145 | EAS | KHV | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02080 | hp1 | a0001 | c0001 | t0004 | g0124 | EAS | KHV | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02080 | hp2 | a0001 | c0001 | t0007 | g0305 | EAS | KHV | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02083 | hp1 | a0001 | c0001 | t0006 | g0009 | EAS | KHV | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02083 | hp2 | a0001 | c0001 | t0007 | g0321 | EAS | KHV | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0340 | EAS | KHV | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02132 | hp1 | a0001 | c0001 | t0007 | g0033 | EAS | KHV | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02132 | hp2 | a0002 | c0002 | t0001 | g0061 | EAS | KHV | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0363 | EAS | KHV | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02135 | hp2 | a0001 | c0001 | t0004 | g0127 | EAS | KHV | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02145 | hp1 | a0001 | c0001 | t0005 | g0186 | AFR | ACB | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02145 | hp2 | a0001 | c0001 | t0008 | g0188 | AFR | ACB | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02148 | hp1 | a0001 | c0001 | t0005 | g0304 | AMR | PEL | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02148 | hp2 | a0001 | c0003 | t0003 | g0006 | AMR | PEL | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | CDX | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | CDX | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0272 | EAS | CDX | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | CDX | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02257 | hp1 | a0001 | c0001 | t0005 | g0004 | AFR | ACB | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02257 | hp2 | a0001 | c0001 | t0015 | g0245 | AFR | ACB | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02258 | hp1 | a0001 | c0001 | t0009 | g0244 | AFR | ACB | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02258 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | ACB | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02273 | hp1 | a0002 | c0002 | t0010 | g0013 | AMR | PEL | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02280 | hp1 | a0001 | c0001 | t0014 | g0200 | AFR | ACB | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | ACB | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02293 | hp1 | a0001 | c0001 | t0006 | g0388 | AMR | PEL | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02293 | hp2 | a0002 | c0004 | t0003 | g0001 | AMR | PEL | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02300 | hp1 | a0002 | c0002 | t0010 | g0045 | AMR | PEL | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02300 | hp2 | a0001 | c0001 | t0006 | g0302 | AMR | PEL | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02451 | hp1 | a0001 | c0001 | t0014 | g0395 | AFR | ACB | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02451 | hp2 | a0001 | c0001 | t0014 | g0203 | AFR | ACB | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02523 | hp1 | a0002 | c0002 | t0002 | g0070 | EAS | KHV | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0376 | EAS | KHV | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02572 | hp1 | a0002 | c0002 | t0002 | g0016 | AFR | GWD | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02572 | hp2 | a0001 | c0001 | t0004 | g0371 | AFR | GWD | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02615 | hp1 | a0001 | c0003 | t0003 | g0319 | AFR | GWD | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02615 | hp2 | a0001 | c0001 | t0005 | g0024 | AFR | GWD | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02622 | hp1 | a0001 | c0001 | t0005 | g0208 | AFR | GWD | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02622 | hp2 | a0001 | c0001 | t0004 | g0123 | AFR | GWD | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02630 | hp1 | a0001 | c0001 | t0008 | g0193 | AFR | GWD | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02630 | hp2 | a0001 | c0001 | t0004 | g0166 | AFR | GWD | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02647 | hp1 | a0001 | c0001 | t0008 | g0189 | AFR | GWD | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02647 | hp2 | a0001 | c0001 | t0034 | g0378 | AFR | GWD | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02683 | hp1 | a0002 | c0002 | t0001 | g0083 | SAS | PJL | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02683 | hp2 | a0002 | c0002 | t0005 | g0012 | SAS | PJL | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02698 | hp1 | a0001 | c0001 | t0020 | g0198 | SAS | PJL | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02698 | hp2 | a0002 | c0002 | t0004 | g0057 | SAS | PJL | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02717 | hp1 | a0001 | c0001 | t0015 | g0026 | AFR | GWD | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02717 | hp2 | a0001 | c0001 | t0009 | g0005 | AFR | GWD | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02723 | hp1 | a0001 | c0003 | t0003 | g0025 | AFR | GWD | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0359 | AFR | GWD | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02735 | hp1 | a0001 | c0003 | t0003 | g0006 | SAS | PJL | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02735 | hp2 | a0001 | c0001 | t0004 | g0173 | SAS | PJL | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02738 | hp1 | a0001 | c0003 | t0003 | g0311 | SAS | PJL | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02738 | hp2 | a0001 | c0001 | t0004 | g0310 | SAS | PJL | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02809 | hp1 | a0001 | c0001 | t0004 | g0289 | AFR | GWD | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02809 | hp2 | a0001 | c0001 | t0005 | g0024 | AFR | GWD | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02818 | hp1 | a0001 | c0001 | t0005 | g0162 | AFR | GWD | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02818 | hp2 | a0001 | c0001 | t0004 | g0355 | AFR | GWD | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02886 | hp1 | a0002 | c0002 | t0003 | g0088 | AFR | GWD | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02886 | hp2 | a0002 | c0002 | t0004 | g0043 | AFR | GWD | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02895 | hp1 | a0002 | c0002 | t0004 | g0085 | AFR | GWD | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02895 | hp2 | a0001 | c0001 | t0009 | g0021 | AFR | GWD | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02896 | hp1 | a0001 | c0001 | t0018 | g0171 | AFR | GWD | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02896 | hp2 | a0001 | c0001 | t0004 | g0370 | AFR | GWD | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02897 | hp1 | a0001 | c0001 | t0009 | g0168 | AFR | GWD | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02897 | hp2 | a0001 | c0001 | t0018 | g0170 | AFR | GWD | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02965 | hp1 | a0001 | c0001 | t0004 | g0132 | AFR | ESN | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02965 | hp2 | a0001 | c0001 | t0004 | g0151 | AFR | ESN | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02970 | hp1 | a0001 | c0001 | t0023 | g0179 | AFR | ESN | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02970 | hp2 | a0001 | c0001 | t0005 | g0004 | AFR | ESN | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02976 | hp1 | a0001 | c0001 | t0005 | g0184 | AFR | ESN | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02976 | hp2 | a0001 | c0001 | t0005 | g0183 | AFR | ESN | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG03017 | hp1 | a0001 | c0001 | t0004 | g0349 | SAS | PJL | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG03017 | hp2 | a0002 | c0002 | t0001 | g0080 | SAS | PJL | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG03041 | hp1 | a0002 | c0002 | t0017 | g0015 | AFR | GWD | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG03041 | hp2 | a0001 | c0001 | t0015 | g0026 | AFR | GWD | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG03098 | hp1 | a0001 | c0001 | t0005 | g0169 | AFR | MSL | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG03098 | hp2 | a0001 | c0001 | t0004 | g0165 | AFR | MSL | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG03130 | hp1 | a0002 | c0002 | t0005 | g0044 | AFR | ESN | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG03130 | hp2 | a0001 | c0001 | t0005 | g0228 | AFR | ESN | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG03139 | hp1 | a0001 | c0001 | t0009 | g0005 | AFR | ESN | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG03139 | hp2 | a0001 | c0001 | t0005 | g0022 | AFR | ESN | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG03195 | hp1 | a0001 | c0001 | t0003 | g0204 | AFR | ESN | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG03195 | hp2 | a0001 | c0001 | t0005 | g0004 | AFR | ESN | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG03209 | hp1 | a0001 | c0001 | t0004 | g0353 | AFR | MSL | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG03209 | hp2 | a0001 | c0001 | t0009 | g0021 | AFR | MSL | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG03225 | hp1 | a0001 | c0001 | t0004 | g0210 | AFR | MSL | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG03225 | hp2 | a0001 | c0001 | t0009 | g0005 | AFR | MSL | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG03239 | hp1 | a0002 | c0004 | t0003 | g0058 | SAS | PJL | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0278 | SAS | PJL | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG03453 | hp1 | a0002 | c0002 | t0002 | g0016 | AFR | MSL | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG03453 | hp2 | a0001 | c0001 | t0005 | g0190 | AFR | MSL | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG03486 | hp1 | a0001 | c0001 | t0029 | g0252 | AFR | MSL | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG03486 | hp2 | a0001 | c0001 | t0005 | g0022 | AFR | MSL | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG03490 | hp1 | a0002 | c0002 | t0005 | g0113 | SAS | PJL | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0320 | SAS | PJL | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG03491 | hp2 | a0001 | c0001 | t0006 | g0032 | SAS | PJL | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG03492 | hp2 | a0001 | c0001 | t0006 | g0032 | SAS | PJL | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG03516 | hp1 | a0001 | c0001 | t0016 | g0318 | AFR | ESN | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG03516 | hp2 | a0001 | c0001 | t0005 | g0130 | AFR | ESN | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG03540 | hp1 | a0001 | c0001 | t0009 | g0211 | AFR | GWD | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG03540 | hp2 | a0001 | c0001 | t0003 | g0207 | AFR | GWD | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG03579 | hp1 | a0002 | c0004 | t0003 | g0103 | AFR | MSL | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG03579 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | MSL | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG03654 | hp1 | a0001 | c0001 | t0004 | g0175 | SAS | PJL | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG03654 | hp2 | a0001 | c0003 | t0003 | g0006 | SAS | PJL | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0313 | SAS | PJL | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0284 | SAS | PJL | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG03688 | hp1 | a0001 | c0013 | t0004 | g0225 | SAS | STU | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0308 | SAS | STU | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG03704 | hp1 | a0002 | c0002 | t0006 | g0059 | SAS | PJL | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG03704 | hp2 | a0001 | c0001 | t0005 | g0243 | SAS | PJL | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG03710 | hp1 | a0002 | c0002 | t0038 | g0400 | SAS | PJL | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0274 | SAS | PJL | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG03831 | hp1 | a0002 | c0002 | t0004 | g0060 | SAS | BEB | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG03831 | hp2 | a0001 | c0003 | t0003 | g0270 | SAS | BEB | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG03834 | hp1 | a0003 | c0007 | t0003 | g0049 | SAS | BEB | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | BEB | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG03927 | hp1 | a0001 | c0001 | t0003 | g0007 | SAS | BEB | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG03927 | hp2 | a0002 | c0009 | t0004 | g0055 | SAS | BEB | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | BEB | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG03942 | hp2 | a0001 | c0003 | t0003 | g0224 | SAS | BEB | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG04115 | hp1 | a0001 | c0001 | t0005 | g0307 | SAS | STU | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG04115 | hp2 | a0001 | c0003 | t0003 | g0195 | SAS | STU | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0154 | SAS | BEB | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG04184 | hp2 | a0001 | c0001 | t0020 | g0199 | SAS | BEB | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG04199 | hp1 | a0001 | c0003 | t0003 | g0254 | SAS | STU | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0397 | SAS | STU | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG04204 | hp1 | a0001 | c0001 | t0004 | g0023 | SAS | STU | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG04204 | hp2 | a0006 | c0016 | t0006 | g0399 | SAS | STU | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG04228 | hp1 | a0001 | c0006 | t0004 | g0276 | SAS | STU | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG04228 | hp2 | a0001 | c0003 | t0003 | g0246 | SAS | STU | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18522 | hp1 | a0001 | c0003 | t0003 | g0191 | AFR | YRI | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0205 | AFR | YRI | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18612 | hp1 | a0001 | c0001 | t0006 | g0009 | EAS | CHB | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | CHB | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18747 | hp1 | a0002 | c0002 | t0002 | g0056 | EAS | CHB | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18747 | hp2 | a0001 | c0003 | t0032 | g0267 | EAS | CHB | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18906 | hp1 | a0002 | c0002 | t0016 | g0109 | AFR | YRI | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18906 | hp2 | a0001 | c0001 | t0009 | g0161 | AFR | YRI | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18939 | hp1 | a0002 | c0002 | t0002 | g0067 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18939 | hp2 | a0001 | c0003 | t0012 | g0018 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0352 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18940 | hp2 | a0002 | c0002 | t0002 | g0105 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18942 | hp1 | a0001 | c0001 | t0007 | g0213 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0382 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18944 | hp1 | a0001 | c0001 | t0021 | g0391 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18945 | hp1 | a0001 | c0005 | t0006 | g0264 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18945 | hp2 | a0001 | c0001 | t0007 | g0336 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18946 | hp1 | a0002 | c0002 | t0005 | g0106 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18947 | hp1 | a0001 | c0001 | t0028 | g0253 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18947 | hp2 | a0001 | c0001 | t0004 | g0266 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0329 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18949 | hp2 | a0001 | c0003 | t0012 | g0018 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18951 | hp1 | a0001 | c0003 | t0012 | g0375 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18951 | hp2 | a0002 | c0002 | t0005 | g0012 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18952 | hp1 | a0002 | c0002 | t0001 | g0074 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18952 | hp2 | a0001 | c0001 | t0007 | g0366 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18953 | hp1 | a0001 | c0001 | t0004 | g0150 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18953 | hp2 | a0002 | c0002 | t0002 | g0111 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18954 | hp2 | a0001 | c0001 | t0025 | g0142 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18956 | hp1 | a0001 | c0001 | t0005 | g0036 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18957 | hp1 | a0001 | c0001 | t0007 | g0143 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0383 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18960 | hp2 | a0002 | c0002 | t0026 | g0076 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18961 | hp1 | a0002 | c0002 | t0003 | g0092 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18962 | hp1 | a0002 | c0002 | t0005 | g0084 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18963 | hp1 | a0002 | c0002 | t0002 | g0075 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18963 | hp2 | a0001 | c0005 | t0006 | g0259 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18964 | hp1 | a0001 | c0001 | t0013 | g0358 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18965 | hp2 | a0001 | c0001 | t0005 | g0010 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18966 | hp1 | a0001 | c0001 | t0004 | g0027 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18967 | hp1 | a0001 | c0005 | t0006 | g0039 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18967 | hp2 | a0002 | c0002 | t0004 | g0079 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18968 | hp1 | a0002 | c0002 | t0001 | g0052 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18968 | hp2 | a0001 | c0001 | t0004 | g0260 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18970 | hp1 | a0001 | c0001 | t0005 | g0306 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18970 | hp2 | a0001 | c0001 | t0007 | g0144 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18971 | hp1 | a0001 | c0001 | t0006 | g0350 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18972 | hp1 | a0001 | c0001 | t0007 | g0333 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18972 | hp2 | a0002 | c0002 | t0001 | g0114 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18973 | hp2 | a0001 | c0001 | t0004 | g0028 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18975 | hp1 | a0002 | c0002 | t0001 | g0072 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0381 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18978 | hp1 | a0001 | c0005 | t0006 | g0296 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0360 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18979 | hp1 | a0001 | c0001 | t0019 | g0158 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18979 | hp2 | a0001 | c0001 | t0007 | g0011 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18980 | hp1 | a0001 | c0001 | t0005 | g0010 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18980 | hp2 | a0001 | c0001 | t0007 | g0019 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0380 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18981 | hp2 | a0001 | c0003 | t0003 | g0275 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18982 | hp1 | a0001 | c0001 | t0005 | g0010 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18982 | hp2 | a0002 | c0002 | t0004 | g0116 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18983 | hp1 | a0001 | c0005 | t0006 | g0039 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18983 | hp2 | a0001 | c0001 | t0004 | g0122 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18984 | hp1 | a0001 | c0001 | t0007 | g0344 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0323 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18985 | hp1 | a0001 | c0001 | t0007 | g0019 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18986 | hp1 | a0002 | c0002 | t0004 | g0054 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18986 | hp2 | a0001 | c0001 | t0006 | g0009 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18989 | hp1 | a0001 | c0001 | t0013 | g0367 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0373 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18991 | hp2 | a0001 | c0001 | t0005 | g0394 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18993 | hp1 | a0001 | c0001 | t0004 | g0241 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18993 | hp2 | a0002 | c0002 | t0001 | g0051 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18994 | hp1 | a0001 | c0001 | t0004 | g0314 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18994 | hp2 | a0001 | c0001 | t0005 | g0036 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18995 | hp1 | a0002 | c0002 | t0001 | g0069 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18995 | hp2 | a0001 | c0001 | t0006 | g0338 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18997 | hp1 | a0002 | c0002 | t0002 | g0110 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18997 | hp2 | a0001 | c0001 | t0007 | g0141 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18998 | hp2 | a0001 | c0001 | t0007 | g0011 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18999 | hp1 | a0001 | c0001 | t0005 | g0364 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19000 | hp1 | a0001 | c0001 | t0005 | g0347 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19000 | hp2 | a0001 | c0001 | t0007 | g0020 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19001 | hp2 | a0002 | c0002 | t0011 | g0100 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0351 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19003 | hp2 | a0002 | c0002 | t0006 | g0096 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0384 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19004 | hp2 | a0001 | c0001 | t0007 | g0334 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0361 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0377 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0393 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19006 | hp2 | a0001 | c0001 | t0007 | g0020 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19007 | hp1 | a0001 | c0001 | t0007 | g0033 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19007 | hp2 | a0001 | c0001 | t0022 | g0040 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19009 | hp2 | a0001 | c0001 | t0021 | g0392 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19010 | hp1 | a0001 | c0001 | t0005 | g0147 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19011 | hp1 | a0001 | c0001 | t0019 | g0159 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0379 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19012 | hp1 | a0002 | c0002 | t0004 | g0099 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19030 | hp1 | a0002 | c0002 | t0004 | g0048 | AFR | LWK | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19030 | hp2 | a0001 | c0001 | t0005 | g0163 | AFR | LWK | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19043 | hp1 | a0002 | c0002 | t0005 | g0078 | AFR | LWK | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19043 | hp2 | a0002 | c0002 | t0008 | g0086 | AFR | LWK | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19055 | hp1 | a0002 | c0002 | t0003 | g0089 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19055 | hp2 | a0001 | c0001 | t0007 | g0345 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19057 | hp1 | a0001 | c0001 | t0013 | g0155 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19057 | hp2 | a0002 | c0002 | t0002 | g0104 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19060 | hp1 | a0002 | c0004 | t0003 | g0077 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19060 | hp2 | a0001 | c0001 | t0004 | g0271 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19062 | hp1 | a0001 | c0005 | t0006 | g0262 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19062 | hp2 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0362 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19064 | hp1 | a0001 | c0001 | t0007 | g0233 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19065 | hp1 | a0001 | c0001 | t0007 | g0365 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19065 | hp2 | a0002 | c0010 | t0006 | g0112 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19066 | hp1 | a0002 | c0002 | t0003 | g0093 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19066 | hp2 | a0001 | c0001 | t0005 | g0121 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19067 | hp1 | a0002 | c0004 | t0012 | g0064 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19068 | hp1 | a0002 | c0004 | t0003 | g0090 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19074 | hp2 | a0001 | c0001 | t0007 | g0327 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19077 | hp2 | a0001 | c0001 | t0007 | g0335 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19080 | hp1 | a0002 | c0002 | t0011 | g0101 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19082 | hp1 | a0001 | c0001 | t0013 | g0157 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19082 | hp2 | a0001 | c0001 | t0004 | g0316 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19083 | hp1 | a0001 | c0005 | t0006 | g0263 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19083 | hp2 | a0001 | c0001 | t0004 | g0315 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19084 | hp1 | a0001 | c0001 | t0024 | g0357 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19084 | hp2 | a0001 | c0001 | t0007 | g0011 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19086 | hp1 | a0001 | c0001 | t0004 | g0135 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19086 | hp2 | a0002 | c0002 | t0002 | g0095 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19087 | hp1 | a0001 | c0001 | t0005 | g0348 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19089 | hp1 | a0001 | c0001 | t0005 | g0346 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19089 | hp2 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19090 | hp1 | a0001 | c0001 | t0007 | g0295 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19090 | hp2 | a0001 | c0001 | t0004 | g0285 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19091 | hp1 | a0001 | c0001 | t0011 | g0128 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19091 | hp2 | a0002 | c0002 | t0004 | g0098 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19240 | hp1 | a0001 | c0003 | t0003 | g0192 | AFR | YRI | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA19240 | hp2 | a0001 | c0001 | t0004 | g0372 | AFR | YRI | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0356 | AFR | ASW | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA20129 | hp2 | a0001 | c0001 | t0008 | g0291 | AFR | ASW | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA20752 | hp1 | a0001 | c0003 | t0031 | g0221 | EUR | TSI | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA20752 | hp2 | a0001 | c0001 | t0006 | g0139 | EUR | TSI | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA20805 | hp1 | a0002 | c0002 | t0033 | g0068 | EUR | TSI | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA20805 | hp2 | a0001 | c0001 | t0037 | g0283 | EUR | TSI | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0030 | SAS | GIH | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0390 | SAS | GIH | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG01123 | hp1 | a0001 | c0001 | t0005 | g0342 | AMR | CLM | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02109 | hp1 | a0001 | c0001 | t0003 | g0290 | AFR | ACB | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02109 | hp2 | a0002 | c0002 | t0006 | g0066 | AFR | ACB | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02486 | hp1 | a0001 | c0001 | t0005 | g0164 | AFR | ACB | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02486 | hp2 | a0001 | c0001 | t0004 | g0152 | AFR | ACB | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02559 | hp1 | a0001 | c0001 | t0008 | g0249 | AFR | ACB | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG02559 | hp2 | a0001 | c0001 | t0008 | g0251 | AFR | ACB | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG03471 | hp1 | a0001 | c0001 | t0008 | g0172 | AFR | MSL | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG03471 | hp2 | a0001 | c0001 | t0005 | g0185 | AFR | MSL | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG06807 | hp1 | a0002 | c0002 | t0030 | g0042 | AFR | USA | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
HG06807 | hp2 | a0001 | c0001 | t0009 | g0235 | AFR | USA | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18955 | hp1 | a0001 | c0001 | t0005 | g0343 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA20300 | hp1 | a0001 | c0001 | t0004 | g0354 | AFR | USA | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA20300 | hp2 | a0001 | c0001 | t0005 | g0167 | AFR | USA | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA21309 | hp1 | a0002 | c0002 | t0017 | g0015 | AFR | LWK | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
NA21309 | hp2 | a0001 | c0001 | t0035 | g0369 | AFR | LWK | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
homoSapiens | chm13v2 | a0001 | c0003 | t0003 | g0368 | REF | REF | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
homoSapiens | grch38p0 | a0001 | c0003 | t0003 | g0174 | REF | REF | LGI2_chr4_24993847_25035946 | LGI2 | chr4 | 24993847 | 25035946 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:25003734 | T | C | 2 | a0003 a0004 |
3 | HG00735.hp2 HG01175.hp2 HG03834.hp1 |
missense_variant | MODERATE | c.1355A>G | p.Gln452Arg | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 1608/6495 | 1355/1638 | 452/545 | chr4 | 25003734 | |||
chr4:25026907 | C | T | 1 | a0005 | 1 | HG01261.hp1 | missense_variant | MODERATE | c.302G>A | p.Arg101Gln | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 3/8 | 555/6495 | 302/1638 | 101/545 | chr4 | 25026907 | |||
chr4:25030500 | G | C | 1 | a0006 | 1 | HG04204.hp2 | missense_variant | MODERATE | c.194C>G | p.Ser65Cys | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 1/8 | 447/6495 | 194/1638 | 65/545 | chr4 | 25030500 | |||
chr4:25030513 | C | T | 2 | a0002 a0003 |
92 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(89): Show |
missense_variant | MODERATE | c.181G>A | p.Gly61Ser | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 1/8 | 434/6495 | 181/1638 | 61/545 | chr4 | 25030513 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:25003571 | G | A | 12 | a0001c0001 a0001c0005 a0001c0006 others(9): Show |
398 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(395): Show |
synonymous_variant | LOW | c.1518C>T | p.Tyr506Tyr | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 1771/6495 | 1518/1638 | 506/545 | chr4 | 25003571 | |||
chr4:25003832 | G | A | 1 | a0001c0006 | 3 | HG00738.hp2 HG01074.hp2 HG04228.hp1 |
synonymous_variant | LOW | c.1257C>T | p.Asp419Asp | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 1510/6495 | 1257/1638 | 419/545 | chr4 | 25003832 | |||
chr4:25003934 | C | T | 1 | a0001c0014 | 1 | HG02056.hp1 | synonymous_variant | LOW | c.1155G>A | p.Ser385Ser | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 1408/6495 | 1155/1638 | 385/545 | chr4 | 25003934 | |||
chr4:25003952 | A | G | 2 | a0001c0013 a0002c0009 |
2 | HG03688.hp1 HG03927.hp2 |
synonymous_variant | LOW | c.1137T>C | p.Val379Val | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 1390/6495 | 1137/1638 | 379/545 | chr4 | 25003952 | |||
chr4:25003985 | G | A | 2 | a0001c0005 a0002c0010 |
8 | NA18945.hp1 NA18963.hp2 NA18967.hp1 others(5): Show |
synonymous_variant | LOW | c.1104C>T | p.His368His | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 1357/6495 | 1104/1638 | 368/545 | chr4 | 25003985 | |||
chr4:25004174 | G | A | 1 | a0002c0011 | 1 | HG02056.hp2 | synonymous_variant | LOW | c.915C>T | p.Tyr305Tyr | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 1168/6495 | 915/1638 | 305/545 | chr4 | 25004174 | |||
chr4:25024885 | A | G | 1 | a0001c0008 | 2 | HG01070.hp1 HG01071.hp1 |
synonymous_variant | LOW | c.348T>C | p.Ile116Ile | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/8 | 601/6495 | 348/1638 | 116/545 | chr4 | 25024885 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:24998933 | G | A | 8 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0021 others(5): Show |
71 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*4518C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 4518 | chr4 | 24998933 | ||||||
chr4:24998945 | T | C | 2 | a0001c0001t0011 a0002c0002t0011 |
5 | HG00609.hp1 HG00621.hp1 NA19001.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4506A>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 4506 | chr4 | 24998945 | ||||||
chr4:24999030 | G | A | 1 | a0001c0003t0031 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4421C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 4421 | chr4 | 24999030 | ||||||
chr4:24999184 | A | G | 1 | a0001c0001t0021 | 2 | NA18944.hp1 NA19009.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4267T>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 4267 | chr4 | 24999184 | ||||||
chr4:24999210 | G | A | 4 | a0001c0001t0005 a0001c0001t0020 a0001c0001t0022 others(1): Show |
53 | HG00544.hp1 HG00639.hp2 HG01123.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*4241C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 4241 | chr4 | 24999210 | ||||||
chr4:24999299 | T | C | 7 | a0001c0001t0008 a0001c0001t0016 a0001c0001t0029 others(4): Show |
17 | HG00741.hp1 HG01109.hp2 HG02055.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*4152A>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 4152 | chr4 | 24999299 | ||||||
chr4:24999462 | T | C | 1 | a0001c0001t0029 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3989A>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 3989 | chr4 | 24999462 | ||||||
chr4:24999499 | C | A | 6 | a0001c0001t0002 a0001c0001t0024 a0001c0001t0025 others(3): Show |
72 | HG00423.hp1 HG00621.hp2 HG00741.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*3952G>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 3952 | chr4 | 24999499 | ||||||
chr4:24999529 | G | A | 49 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(46): Show |
374 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(371): Show |
3_prime_UTR_variant | MODIFIER | c.*3922C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 3922 | chr4 | 24999529 | ||||||
chr4:24999554 | C | T | 1 | a0001c0001t0035 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3897G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 3897 | chr4 | 24999554 | ||||||
chr4:24999717 | G | A | 4 | a0001c0001t0008 a0001c0001t0029 a0002c0002t0008 others(1): Show |
14 | HG00741.hp1 HG01109.hp2 HG02055.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*3734C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 3734 | chr4 | 24999717 | ||||||
chr4:24999784 | G | A | 2 | a0001c0003t0012 a0002c0004t0012 |
4 | NA18939.hp2 NA18949.hp2 NA18951.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3667C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 3667 | chr4 | 24999784 | ||||||
chr4:24999817 | T | C | 39 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(36): Show |
305 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(302): Show |
3_prime_UTR_variant | MODIFIER | c.*3634A>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 3634 | chr4 | 24999817 | ||||||
chr4:24999954 | C | T | 39 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(36): Show |
305 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(302): Show |
3_prime_UTR_variant | MODIFIER | c.*3497G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 3497 | chr4 | 24999954 | ||||||
chr4:24999956 | C | T | 39 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(36): Show |
305 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(302): Show |
3_prime_UTR_variant | MODIFIER | c.*3495G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 3495 | chr4 | 24999956 | ||||||
chr4:24999992 | G | A | 1 | a0001c0001t0018 | 2 | HG02896.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3459C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 3459 | chr4 | 24999992 | ||||||
chr4:25000010 | T | A | 39 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(36): Show |
305 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(302): Show |
3_prime_UTR_variant | MODIFIER | c.*3441A>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 3441 | chr4 | 25000010 | ||||||
chr4:25000063 | A | C | 39 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(36): Show |
305 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(302): Show |
3_prime_UTR_variant | MODIFIER | c.*3388T>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 3388 | chr4 | 25000063 | ||||||
chr4:25000092 | A | G | 1 | a0001c0001t0015 | 3 | HG02257.hp2 HG02717.hp1 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3359T>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 3359 | chr4 | 25000092 | ||||||
chr4:25000220 | C | G | 45 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(42): Show |
321 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(318): Show |
3_prime_UTR_variant | MODIFIER | c.*3231G>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 3231 | chr4 | 25000220 | ||||||
chr4:25000257 | G | C | 1 | a0001c0003t0032 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3194C>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 3194 | chr4 | 25000257 | ||||||
chr4:25000281 | G | A | 1 | a0002c0002t0017 | 2 | HG03041.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3170C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 3170 | chr4 | 25000281 | ||||||
chr4:25000304 | A | C | 45 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(42): Show |
321 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(318): Show |
3_prime_UTR_variant | MODIFIER | c.*3147T>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 3147 | chr4 | 25000304 | ||||||
chr4:25000435 | GGTGA | G | 6 | a0001c0001t0008 a0001c0001t0016 a0001c0001t0029 others(3): Show |
16 | HG00741.hp1 HG01109.hp2 HG02055.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*3012_*3015delTCAC | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 3012 | chr4 | 25000435 | ||||||
chr4:25000440 | G | A | 39 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(36): Show |
305 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(302): Show |
3_prime_UTR_variant | MODIFIER | c.*3011C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 3011 | chr4 | 25000440 | ||||||
chr4:25000487 | G | A | 1 | a0001c0001t0037 | 1 | NA20805.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2964C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 2964 | chr4 | 25000487 | ||||||
chr4:25000497 | T | G | 43 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(40): Show |
358 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(355): Show |
3_prime_UTR_variant | MODIFIER | c.*2954A>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 2954 | chr4 | 25000497 | ||||||
chr4:25000535 | G | T | 39 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(36): Show |
305 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(302): Show |
3_prime_UTR_variant | MODIFIER | c.*2916C>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 2916 | chr4 | 25000535 | ||||||
chr4:25000575 | C | T | 39 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(36): Show |
305 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(302): Show |
3_prime_UTR_variant | MODIFIER | c.*2876G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 2876 | chr4 | 25000575 | ||||||
chr4:25000577 | T | C | 1 | a0001c0001t0007 | 31 | HG00597.hp2 HG01257.hp1 HG01258.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*2874A>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 2874 | chr4 | 25000577 | ||||||
chr4:25000580 | A | G | 1 | a0001c0001t0027 | 1 | HG01978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2871T>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 2871 | chr4 | 25000580 | ||||||
chr4:25000628 | C | T | 38 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(35): Show |
304 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(301): Show |
3_prime_UTR_variant | MODIFIER | c.*2823G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 2823 | chr4 | 25000628 | ||||||
chr4:25000662 | A | G | 39 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(36): Show |
305 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(302): Show |
3_prime_UTR_variant | MODIFIER | c.*2789T>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 2789 | chr4 | 25000662 | ||||||
chr4:25000696 | C | A | 39 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(36): Show |
305 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(302): Show |
3_prime_UTR_variant | MODIFIER | c.*2755G>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 2755 | chr4 | 25000696 | ||||||
chr4:25000759 | C | T | 1 | a0002c0002t0026 | 1 | NA18960.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2692G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 2692 | chr4 | 25000759 | ||||||
chr4:25000769 | C | T | 1 | a0001c0001t0025 | 1 | NA18954.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2682G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 2682 | chr4 | 25000769 | ||||||
chr4:25000833 | T | C | 4 | a0001c0001t0005 a0001c0001t0020 a0001c0001t0022 others(1): Show |
53 | HG00544.hp1 HG00639.hp2 HG01123.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*2618A>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 2618 | chr4 | 25000833 | ||||||
chr4:25000896 | T | A | 1 | a0002c0002t0033 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2555A>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 2555 | chr4 | 25000896 | ||||||
chr4:25000986 | A | T | 39 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(36): Show |
305 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(302): Show |
3_prime_UTR_variant | MODIFIER | c.*2465T>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 2465 | chr4 | 25000986 | ||||||
chr4:25000990 | C | T | 39 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(36): Show |
305 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(302): Show |
3_prime_UTR_variant | MODIFIER | c.*2461G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 2461 | chr4 | 25000990 | ||||||
chr4:25001189 | T | C | 2 | a0001c0001t0013 a0001c0001t0019 |
6 | NA18964.hp1 NA18979.hp1 NA18989.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2262A>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 2262 | chr4 | 25001189 | ||||||
chr4:25001308 | C | A | 1 | a0001c0001t0020 | 2 | HG02698.hp1 HG04184.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2143G>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 2143 | chr4 | 25001308 | ||||||
chr4:25001428 | A | G | 39 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(36): Show |
305 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(302): Show |
3_prime_UTR_variant | MODIFIER | c.*2023T>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 2023 | chr4 | 25001428 | ||||||
chr4:25001495 | C | T | 5 | a0001c0001t0001 a0001c0008t0001 a0002c0002t0001 others(2): Show |
70 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*1956G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 1956 | chr4 | 25001495 | ||||||
chr4:25001498 | T | C | 39 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(36): Show |
305 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(302): Show |
3_prime_UTR_variant | MODIFIER | c.*1953A>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 1953 | chr4 | 25001498 | ||||||
chr4:25001553 | CA | C | 21 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0010 others(18): Show |
145 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(142): Show |
3_prime_UTR_variant | MODIFIER | c.*1897delT | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 1897 | chr4 | 25001553 | ||||||
chr4:25001560 | G | GA | 38 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(35): Show |
304 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(301): Show |
3_prime_UTR_variant | MODIFIER | c.*1890dupT | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 1890 | chr4 | 25001560 | ||||||
chr4:25001714 | AG | A | 38 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(35): Show |
304 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(301): Show |
3_prime_UTR_variant | MODIFIER | c.*1736delC | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 1736 | chr4 | 25001714 | ||||||
chr4:25001820 | GA | G | 38 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(35): Show |
304 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(301): Show |
3_prime_UTR_variant | MODIFIER | c.*1630delT | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 1630 | chr4 | 25001820 | ||||||
chr4:25001881 | G | A | 49 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(46): Show |
374 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(371): Show |
3_prime_UTR_variant | MODIFIER | c.*1570C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 1570 | chr4 | 25001881 | ||||||
chr4:25001944 | T | C | 1 | a0001c0001t0019 | 2 | NA18979.hp1 NA19011.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1507A>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 1507 | chr4 | 25001944 | ||||||
chr4:25002154 | G | C | 1 | a0001c0001t0034 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1297C>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 1297 | chr4 | 25002154 | ||||||
chr4:25002243 | G | GGGC | 11 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0016 others(8): Show |
70 | HG00544.hp1 HG00639.hp2 HG00741.hp1 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*1207_*1208insGCC | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 1207 | chr4 | 25002243 | ||||||
chr4:25002245 | C | G | 11 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0016 others(8): Show |
70 | HG00544.hp1 HG00639.hp2 HG00741.hp1 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*1206G>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 1206 | chr4 | 25002245 | ||||||
chr4:25002380 | G | A | 2 | a0001c0001t0013 a0001c0001t0019 |
6 | NA18964.hp1 NA18979.hp1 NA18989.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1071C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 1071 | chr4 | 25002380 | ||||||
chr4:25002382 | G | A | 5 | a0001c0001t0005 a0001c0001t0015 a0001c0001t0020 others(2): Show |
56 | HG00544.hp1 HG00639.hp2 HG01123.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*1069C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 1069 | chr4 | 25002382 | ||||||
chr4:25002416 | C | T | 3 | a0001c0001t0010 a0002c0002t0010 a0002c0002t0039 |
6 | HG00639.hp1 HG01928.hp2 HG01943.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1035G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 1035 | chr4 | 25002416 | ||||||
chr4:25002472 | C | T | 1 | a0001c0001t0023 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*979G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 979 | chr4 | 25002472 | ||||||
chr4:25002522 | C | A | 1 | a0001c0001t0014 | 3 | HG02280.hp1 HG02451.hp1 HG02451.hp2 |
3_prime_UTR_variant | MODIFIER | c.*929G>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 929 | chr4 | 25002522 | ||||||
chr4:25002553 | G | A | 1 | a0001c0001t0035 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*898C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 898 | chr4 | 25002553 | ||||||
chr4:25002661 | T | C | 4 | a0001c0001t0005 a0001c0001t0020 a0001c0001t0022 others(1): Show |
53 | HG00544.hp1 HG00639.hp2 HG01123.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*790A>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 790 | chr4 | 25002661 | ||||||
chr4:25002766 | A | G | 4 | a0001c0001t0005 a0001c0001t0020 a0001c0001t0022 others(1): Show |
53 | HG00544.hp1 HG00639.hp2 HG01123.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*685T>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 685 | chr4 | 25002766 | ||||||
chr4:25002900 | C | A | 1 | a0001c0001t0028 | 1 | NA18947.hp1 | 3_prime_UTR_variant | MODIFIER | c.*551G>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 551 | chr4 | 25002900 | ||||||
chr4:25003090 | GT | G | 4 | a0001c0001t0005 a0001c0001t0020 a0001c0001t0022 others(1): Show |
53 | HG00544.hp1 HG00639.hp2 HG01123.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*360delA | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 360 | chr4 | 25003090 | ||||||
chr4:25003135 | G | T | 4 | a0001c0001t0005 a0001c0001t0020 a0001c0001t0022 others(1): Show |
53 | HG00544.hp1 HG00639.hp2 HG01123.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*316C>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 316 | chr4 | 25003135 | ||||||
chr4:25003156 | C | A | 4 | a0001c0001t0005 a0001c0001t0020 a0001c0001t0022 others(1): Show |
53 | HG00544.hp1 HG00639.hp2 HG01123.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*295G>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 295 | chr4 | 25003156 | ||||||
chr4:25003260 | T | C | 1 | a0001c0003t0036 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*191A>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 191 | chr4 | 25003260 | ||||||
chr4:25003349 | T | C | 8 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0021 others(5): Show |
71 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*102A>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 102 | chr4 | 25003349 | ||||||
chr4:25003401 | C | T | 21 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0010 others(18): Show |
147 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(144): Show |
3_prime_UTR_variant | MODIFIER | c.*50G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 8/8 | 50 | chr4 | 25003401 | ||||||
chr4:25030735 | C | T | 1 | a0001c0001t0022 | 1 | NA19007.hp2 | 5_prime_UTR_variant | MODIFIER | c.-42G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 1/8 | 42 | chr4 | 25030735 | ||||||
chr4:25030888 | C | A | 1 | a0002c0002t0038 | 1 | HG03710.hp1 | 5_prime_UTR_variant | MODIFIER | c.-195G>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 1/8 | 195 | chr4 | 25030888 | ||||||
chr4:25030890 | C | A | 1 | a0002c0002t0039 | 1 | HG00639.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-197G>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 1/8 | chr4 | 25030890 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:25004372 | C | T | 45 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0022 others(42): Show |
53 | HG00544.hp1 HG00639.hp2 HG01123.hp1 others(50): Show |
intron_variant | MODIFIER | c.821-104G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25004372 | |||||||
chr4:25004657 | T | G | 3 | a0001c0001t0005g0163 a0001c0001t0005g0164 a0001c0001t0005g0169 |
3 | HG02486.hp1 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.821-389A>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25004657 | |||||||
chr4:25004671 | A | G | 5 | a0001c0001t0009g0005 a0001c0001t0009g0021 a0001c0001t0009g0161 others(2): Show |
8 | HG02717.hp2 HG02895.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.821-403T>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25004671 | |||||||
chr4:25004713 | G | T | 140 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(137): Show |
157 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.821-445C>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25004713 | |||||||
chr4:25004714 | C | T | 140 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(137): Show |
157 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.821-446G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25004714 | |||||||
chr4:25004808 | C | T | 8 | a0001c0001t0004g0349 a0001c0001t0013g0155 a0001c0001t0013g0157 others(5): Show |
8 | HG03017.hp1 HG03579.hp1 NA18964.hp1 others(5): Show |
intron_variant | MODIFIER | c.821-540G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25004808 | |||||||
chr4:25004924 | G | A | 1 | a0001c0001t0001g0341 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.821-656C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25004924 | |||||||
chr4:25004958 | C | A | 1 | a0001c0001t0005g0208 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.821-690G>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25004958 | |||||||
chr4:25005045 | C | T | 2 | a0001c0001t0005g0364 a0001c0001t0005g0394 |
2 | NA18991.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.821-777G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25005045 | |||||||
chr4:25005057 | G | A | 1 | a0001c0001t0005g0228 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.821-789C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25005057 | |||||||
chr4:25005111 | A | C | 1 | a0002c0002t0002g0016 | 2 | HG02572.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.821-843T>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25005111 | |||||||
chr4:25005171 | A | G | 2 | a0001c0001t0001g0393 a0002c0002t0001g0053 |
2 | NA19006.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.821-903T>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25005171 | |||||||
chr4:25005304 | A | C | 2 | a0001c0001t0009g0235 a0001c0001t0009g0244 |
2 | HG02258.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.821-1036T>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25005304 | |||||||
chr4:25005345 | G | A | 1 | a0001c0001t0001g0286 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.821-1077C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25005345 | |||||||
chr4:25005357 | G | A | 1 | a0001c0001t0001g0288 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.821-1089C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25005357 | |||||||
chr4:25005519 | A | G | 7 | a0001c0001t0008g0188 a0001c0001t0008g0248 a0001c0001t0008g0249 others(4): Show |
7 | HG01109.hp2 HG02055.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.821-1251T>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25005519 | |||||||
chr4:25005538 | C | T | 121 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0030 others(118): Show |
136 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.821-1270G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25005538 | |||||||
chr4:25005539 | A | G | 1 | a0001c0001t0002g0298 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.821-1271T>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25005539 | |||||||
chr4:25005575 | GA | G | 155 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(152): Show |
175 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.821-1308delT | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25005575 | |||||||
chr4:25005593 | C | T | 35 | a0001c0001t0004g0023 a0001c0001t0004g0027 a0001c0001t0004g0028 others(32): Show |
38 | HG00408.hp1 HG00438.hp1 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.821-1325G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25005593 | |||||||
chr4:25005909 | G | A | 5 | a0001c0001t0005g0228 a0001c0001t0014g0200 a0001c0001t0014g0395 others(2): Show |
5 | HG02280.hp1 HG02451.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.821-1641C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25005909 | |||||||
chr4:25005987 | C | T | 1 | a0002c0002t0017g0015 | 2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.821-1719G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25005987 | |||||||
chr4:25006026 | C | A | 154 | a0001c0001t0001g0274 a0001c0001t0002g0002 a0001c0001t0002g0003 others(151): Show |
183 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(180): Show |
intron_variant | MODIFIER | c.821-1758G>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25006026 | |||||||
chr4:25006206 | C | T | 1 | a0001c0001t0004g0210 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.821-1938G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25006206 | |||||||
chr4:25006265 | GC | G | 160 | a0001c0001t0001g0274 a0001c0001t0002g0002 a0001c0001t0002g0003 others(157): Show |
191 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(188): Show |
intron_variant | MODIFIER | c.821-1998delG | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25006265 | |||||||
chr4:25006276 | C | T | 8 | a0001c0001t0008g0172 a0001c0001t0008g0189 a0001c0001t0008g0193 others(5): Show |
8 | HG00741.hp1 HG02630.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.821-2008G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25006276 | |||||||
chr4:25006339 | C | G | 1 | a0001c0001t0004g0370 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.821-2071G>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25006339 | |||||||
chr4:25006342 | G | C | 112 | a0001c0001t0001g0274 a0001c0001t0002g0002 a0001c0001t0002g0003 others(109): Show |
132 | HG00423.hp1 HG00438.hp1 HG00609.hp2 others(129): Show |
intron_variant | MODIFIER | c.821-2074C>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25006342 | |||||||
chr4:25006346 | A | C | 112 | a0001c0001t0001g0274 a0001c0001t0002g0002 a0001c0001t0002g0003 others(109): Show |
132 | HG00423.hp1 HG00438.hp1 HG00609.hp2 others(129): Show |
intron_variant | MODIFIER | c.821-2078T>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25006346 | |||||||
chr4:25006352 | T | C | 33 | a0001c0001t0003g0154 a0001c0001t0004g0023 a0001c0001t0004g0118 others(30): Show |
34 | HG00609.hp1 HG00621.hp1 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.821-2084A>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25006352 | |||||||
chr4:25006417 | C | T | 1 | a0002c0002t0017g0015 | 2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.821-2149G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25006417 | |||||||
chr4:25006460 | C | T | 1 | a0002c0002t0017g0015 | 2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.821-2192G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25006460 | |||||||
chr4:25006483 | T | G | 50 | a0001c0001t0003g0207 a0001c0001t0005g0004 a0001c0001t0005g0010 others(47): Show |
61 | HG00544.hp1 HG00639.hp2 HG01123.hp1 others(58): Show |
intron_variant | MODIFIER | c.821-2215A>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25006483 | |||||||
chr4:25006620 | T | C | 1 | a0001c0001t0004g0271 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.821-2352A>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25006620 | |||||||
chr4:25006630 | T | C | 5 | a0001c0001t0009g0005 a0001c0001t0009g0021 a0001c0001t0009g0161 others(2): Show |
8 | HG02717.hp2 HG02895.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.821-2362A>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25006630 | |||||||
chr4:25006709 | G | A | 2 | a0001c0001t0002g0030 a0006c0016t0006g0399 |
3 | HG01517.hp1 HG04204.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.821-2441C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25006709 | |||||||
chr4:25006780 | C | T | 49 | a0001c0001t0003g0207 a0001c0001t0005g0004 a0001c0001t0005g0010 others(46): Show |
59 | HG00544.hp1 HG00639.hp2 HG01123.hp1 others(56): Show |
intron_variant | MODIFIER | c.821-2512G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25006780 | |||||||
chr4:25006814 | T | A | 1 | a0002c0002t0017g0015 | 2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.821-2546A>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25006814 | |||||||
chr4:25006901 | C | T | 111 | a0001c0001t0001g0274 a0001c0001t0002g0002 a0001c0001t0002g0003 others(108): Show |
131 | HG00423.hp1 HG00438.hp1 HG00609.hp2 others(128): Show |
intron_variant | MODIFIER | c.821-2633G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25006901 | |||||||
chr4:25006984 | G | A | 161 | a0001c0001t0001g0274 a0001c0001t0002g0002 a0001c0001t0002g0003 others(158): Show |
192 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(189): Show |
intron_variant | MODIFIER | c.821-2716C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25006984 | |||||||
chr4:25007010 | TA | T | 51 | a0001c0001t0002g0323 a0001c0001t0002g0360 a0001c0001t0003g0207 others(48): Show |
61 | HG00544.hp1 HG00639.hp2 HG01123.hp1 others(58): Show |
intron_variant | MODIFIER | c.821-2743delT | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25007010 | |||||||
chr4:25007011 | A | T | 109 | a0001c0001t0001g0274 a0001c0001t0002g0002 a0001c0001t0002g0003 others(106): Show |
129 | HG00423.hp1 HG00438.hp1 HG00609.hp2 others(126): Show |
intron_variant | MODIFIER | c.821-2743T>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25007011 | |||||||
chr4:25007027 | C | T | 1 | a0001c0003t0003g0311 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.821-2759G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25007027 | |||||||
chr4:25007028 | G | A | 10 | a0001c0001t0001g0196 a0001c0001t0005g0022 a0001c0001t0005g0167 others(7): Show |
11 | HG01891.hp2 HG02145.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.821-2760C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25007028 | |||||||
chr4:25007042 | T | C | 110 | a0001c0001t0001g0274 a0001c0001t0002g0002 a0001c0001t0002g0003 others(107): Show |
130 | HG00423.hp1 HG00438.hp1 HG00609.hp2 others(127): Show |
intron_variant | MODIFIER | c.821-2774A>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25007042 | |||||||
chr4:25007133 | C | G | 49 | a0001c0001t0003g0207 a0001c0001t0005g0004 a0001c0001t0005g0010 others(46): Show |
59 | HG00544.hp1 HG00639.hp2 HG01123.hp1 others(56): Show |
intron_variant | MODIFIER | c.821-2865G>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25007133 | |||||||
chr4:25007229 | C | A | 1 | a0001c0003t0003g0181 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.821-2961G>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25007229 | |||||||
chr4:25007229 | C | T | 49 | a0001c0001t0003g0207 a0001c0001t0005g0004 a0001c0001t0005g0010 others(46): Show |
59 | HG00544.hp1 HG00639.hp2 HG01123.hp1 others(56): Show |
intron_variant | MODIFIER | c.821-2961G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25007229 | |||||||
chr4:25007255 | A | AC | 111 | a0001c0001t0001g0274 a0001c0001t0002g0002 a0001c0001t0002g0003 others(108): Show |
131 | HG00423.hp1 HG00438.hp1 HG00609.hp2 others(128): Show |
intron_variant | MODIFIER | c.821-2988dupG | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25007255 | |||||||
chr4:25007257 | G | A | 49 | a0001c0001t0003g0207 a0001c0001t0005g0004 a0001c0001t0005g0010 others(46): Show |
59 | HG00544.hp1 HG00639.hp2 HG01123.hp1 others(56): Show |
intron_variant | MODIFIER | c.821-2989C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25007257 | |||||||
chr4:25007283 | C | G | 1 | a0002c0002t0017g0015 | 2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.821-3015G>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25007283 | |||||||
chr4:25007286 | G | T | 49 | a0001c0001t0003g0207 a0001c0001t0005g0004 a0001c0001t0005g0010 others(46): Show |
59 | HG00544.hp1 HG00639.hp2 HG01123.hp1 others(56): Show |
intron_variant | MODIFIER | c.821-3018C>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25007286 | |||||||
chr4:25007310 | T | C | 49 | a0001c0001t0003g0207 a0001c0001t0005g0004 a0001c0001t0005g0010 others(46): Show |
59 | HG00544.hp1 HG00639.hp2 HG01123.hp1 others(56): Show |
intron_variant | MODIFIER | c.821-3042A>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25007310 | |||||||
chr4:25007414 | C | T | 1 | a0001c0001t0004g0266 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.821-3146G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25007414 | |||||||
chr4:25007436 | T | C | 1 | a0001c0001t0008g0248 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.821-3168A>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25007436 | |||||||
chr4:25007466 | G | C | 1 | a0002c0002t0002g0016 | 2 | HG02572.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.821-3198C>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25007466 | |||||||
chr4:25007494 | G | A | 49 | a0001c0001t0003g0207 a0001c0001t0005g0004 a0001c0001t0005g0010 others(46): Show |
59 | HG00544.hp1 HG00639.hp2 HG01123.hp1 others(56): Show |
intron_variant | MODIFIER | c.821-3226C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25007494 | |||||||
chr4:25007543 | A | C | 1 | a0002c0004t0012g0064 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.821-3275T>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25007543 | |||||||
chr4:25007578 | A | AGT | 20 | a0001c0001t0001g0226 a0001c0001t0004g0127 a0001c0001t0004g0175 others(17): Show |
20 | HG00099.hp2 HG00140.hp1 HG00673.hp2 others(17): Show |
intron_variant | MODIFIER | c.821-3312_821-3311d others(4): Show |
LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25007578 | |||||||
chr4:25007578 | A | AGTGT | 15 | a0001c0001t0001g0339 a0001c0001t0001g0386 a0001c0001t0004g0132 others(12): Show |
15 | HG00423.hp2 HG00438.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.821-3314_821-3311d others(6): Show |
LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25007578 | |||||||
chr4:25007578 | A | AGTGTGT | 4 | a0001c0001t0006g0337 a0001c0001t0010g0265 a0002c0002t0010g0013 others(1): Show |
5 | HG00639.hp1 HG01943.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.821-3316_821-3311d others(8): Show |
LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25007578 | |||||||
chr4:25007578 | A | AGTGTGTG others(1): Show |
4 | a0001c0001t0004g0260 a0001c0005t0006g0264 a0002c0002t0004g0116 others(1): Show |
4 | HG01928.hp2 NA18945.hp1 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.821-3318_821-3311d others(10): Show |
LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25007578 | |||||||
chr4:25007578 | A | AGTGTGTG others(3): Show |
3 | a0001c0005t0006g0259 a0001c0005t0006g0263 a0002c0002t0010g0045 |
3 | HG02300.hp1 NA18963.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.821-3320_821-3311d others(12): Show |
LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25007578 | |||||||
chr4:25007578 | A | AGTGTGTG others(5): Show |
1 | a0001c0005t0006g0262 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.821-3322_821-3311d others(14): Show |
LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25007578 | |||||||
chr4:25007578 | AGT | A | 30 | a0001c0001t0001g0120 a0001c0001t0001g0133 a0001c0001t0001g0146 others(27): Show |
33 | HG01099.hp1 HG01167.hp1 HG01258.hp2 others(30): Show |
intron_variant | MODIFIER | c.821-3312_821-3311d others(4): Show |
LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25007578 | |||||||
chr4:25007578 | AGTGT | A | 70 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0117 others(67): Show |
77 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.821-3314_821-3311d others(6): Show |
LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25007578 | |||||||
chr4:25007578 | AGTGTGT | A | 29 | a0001c0001t0001g0029 a0001c0001t0001g0194 a0001c0001t0001g0202 others(26): Show |
33 | HG00741.hp1 HG01168.hp2 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.821-3316_821-3311d others(8): Show |
LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25007578 | |||||||
chr4:25007578 | AGTGTGTG others(1): Show |
A | 39 | a0001c0001t0001g0286 a0001c0001t0001g0393 a0001c0001t0005g0004 others(36): Show |
49 | HG00544.hp1 HG00639.hp2 HG01074.hp1 others(46): Show |
intron_variant | MODIFIER | c.821-3318_821-3311d others(10): Show |
LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25007578 | |||||||
chr4:25007578 | AGTGTGTG others(3): Show |
A | 2 | a0001c0001t0005g0307 a0001c0001t0006g0279 |
2 | HG00735.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.821-3320_821-3311d others(12): Show |
LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25007578 | |||||||
chr4:25007578 | AGTGTGTG others(5): Show |
A | 1 | a0001c0001t0005g0208 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.821-3322_821-3311d others(14): Show |
LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25007578 | |||||||
chr4:25007578 | AGTGTGTG others(7): Show |
A | 10 | a0001c0001t0002g0297 a0001c0001t0013g0155 a0001c0001t0013g0157 others(7): Show |
10 | HG00733.hp1 HG01099.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.821-3324_821-3311d others(16): Show |
LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25007578 | |||||||
chr4:25007578 | AGTGTGTG others(9): Show |
A | 101 | a0001c0001t0001g0274 a0001c0001t0002g0002 a0001c0001t0002g0003 others(98): Show |
121 | HG00423.hp1 HG00438.hp1 HG00609.hp2 others(118): Show |
intron_variant | MODIFIER | c.821-3326_821-3311d others(18): Show |
LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25007578 | |||||||
chr4:25007581 | G | C | 1 | a0001c0001t0005g0183 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.821-3313C>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25007581 | |||||||
chr4:25007583 | G | C | 5 | a0001c0001t0005g0022 a0001c0001t0005g0167 a0001c0001t0005g0185 others(2): Show |
6 | HG01891.hp2 HG02145.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.821-3315C>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25007583 | |||||||
chr4:25007585 | G | C | 8 | a0001c0001t0003g0207 a0001c0001t0005g0162 a0001c0001t0005g0184 others(5): Show |
8 | HG01243.hp2 HG02280.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.821-3317C>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25007585 | |||||||
chr4:25007587 | G | C | 33 | a0001c0001t0005g0004 a0001c0001t0005g0010 a0001c0001t0005g0024 others(30): Show |
42 | HG00544.hp1 HG00639.hp2 HG01123.hp1 others(39): Show |
intron_variant | MODIFIER | c.821-3319C>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25007587 | |||||||
chr4:25007589 | G | C | 1 | a0001c0001t0005g0307 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.821-3321C>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25007589 | |||||||
chr4:25007591 | G | C | 1 | a0001c0001t0005g0208 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.821-3323C>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25007591 | |||||||
chr4:25007770 | T | C | 1 | a0001c0001t0001g0035 | 2 | NA18955.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.821-3502A>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25007770 | |||||||
chr4:25007828 | A | G | 2 | a0001c0001t0021g0391 a0001c0001t0021g0392 |
2 | NA18944.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.821-3560T>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25007828 | |||||||
chr4:25007869 | T | C | 161 | a0001c0001t0001g0274 a0001c0001t0002g0002 a0001c0001t0002g0003 others(158): Show |
192 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(189): Show |
intron_variant | MODIFIER | c.821-3601A>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25007869 | |||||||
chr4:25008057 | A | T | 49 | a0001c0001t0003g0207 a0001c0001t0005g0004 a0001c0001t0005g0010 others(46): Show |
59 | HG00544.hp1 HG00639.hp2 HG01123.hp1 others(56): Show |
intron_variant | MODIFIER | c.821-3789T>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25008057 | |||||||
chr4:25008165 | T | C | 49 | a0001c0001t0003g0207 a0001c0001t0005g0004 a0001c0001t0005g0010 others(46): Show |
59 | HG00544.hp1 HG00639.hp2 HG01123.hp1 others(56): Show |
intron_variant | MODIFIER | c.821-3897A>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25008165 | |||||||
chr4:25008272 | G | T | 1 | a0002c0002t0006g0096 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.821-4004C>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25008272 | |||||||
chr4:25008468 | A | G | 319 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(316): Show |
362 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(359): Show |
intron_variant | MODIFIER | c.820+3867T>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25008468 | |||||||
chr4:25008501 | T | C | 163 | a0001c0001t0001g0274 a0001c0001t0002g0002 a0001c0001t0002g0003 others(160): Show |
194 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(191): Show |
intron_variant | MODIFIER | c.820+3834A>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25008501 | |||||||
chr4:25008532 | G | A | 1 | a0002c0004t0003g0082 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.820+3803C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25008532 | |||||||
chr4:25008549 | GTC | G | 6 | a0001c0001t0005g0163 a0001c0001t0005g0186 a0001c0001t0005g0208 others(3): Show |
6 | HG02145.hp1 HG02148.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.820+3784_820+3785d others(4): Show |
LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25008549 | |||||||
chr4:25008551 | CTCA | C | 43 | a0001c0001t0003g0207 a0001c0001t0005g0004 a0001c0001t0005g0010 others(40): Show |
53 | HG00544.hp1 HG00639.hp2 HG01123.hp1 others(50): Show |
intron_variant | MODIFIER | c.820+3781_820+3783d others(5): Show |
LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25008551 | |||||||
chr4:25008553 | C | CA | 10 | a0001c0001t0001g0232 a0001c0001t0001g0322 a0001c0001t0006g0258 others(7): Show |
11 | HG01099.hp1 HG01361.hp1 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.820+3781dupT | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25008553 | |||||||
chr4:25008553 | C | CAA | 9 | a0001c0001t0002g0293 a0001c0001t0002g0373 a0001c0001t0013g0155 others(6): Show |
9 | HG02451.hp2 NA18747.hp2 NA18964.hp1 others(6): Show |
intron_variant | MODIFIER | c.820+3780_820+3781d others(4): Show |
LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25008553 | |||||||
chr4:25008553 | C | CAAA | 81 | a0001c0001t0001g0274 a0001c0001t0002g0002 a0001c0001t0002g0003 others(78): Show |
101 | HG00423.hp1 HG00609.hp2 HG00733.hp1 others(98): Show |
intron_variant | MODIFIER | c.820+3779_820+3781d others(5): Show |
LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25008553 | |||||||
chr4:25008553 | C | CAAAA | 20 | a0001c0001t0002g0230 a0001c0001t0002g0299 a0001c0001t0002g0301 others(17): Show |
21 | HG00438.hp1 HG00621.hp2 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.820+3778_820+3781d others(6): Show |
LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25008553 | |||||||
chr4:25008553 | CA | C | 48 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(45): Show |
54 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.820+3781delT | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25008553 | |||||||
chr4:25008553 | CAA | C | 57 | a0001c0001t0001g0238 a0001c0001t0001g0284 a0001c0001t0001g0386 others(54): Show |
62 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.820+3780_820+3781d others(4): Show |
LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25008553 | |||||||
chr4:25008791 | G | A | 1 | a0001c0013t0004g0225 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.820+3544C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25008791 | |||||||
chr4:25008825 | A | G | 1 | a0001c0001t0010g0265 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.820+3510T>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25008825 | |||||||
chr4:25008883 | C | T | 1 | a0001c0001t0002g0003 | 4 | NA18944.hp2 NA18950.hp1 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.820+3452G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25008883 | |||||||
chr4:25008905 | C | A | 1 | a0002c0002t0017g0015 | 2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.820+3430G>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25008905 | |||||||
chr4:25008917 | G | T | 2 | a0001c0001t0014g0200 a0001c0001t0014g0395 |
2 | HG02280.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.820+3418C>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25008917 | |||||||
chr4:25008935 | C | T | 2 | a0001c0013t0004g0225 a0002c0009t0004g0055 |
2 | HG03688.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.820+3400G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25008935 | |||||||
chr4:25009003 | C | T | 4 | a0001c0001t0001g0236 a0001c0001t0001g0237 a0001c0001t0001g0238 others(1): Show |
4 | HG00673.hp1 NA18949.hp1 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.820+3332G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25009003 | |||||||
chr4:25009026 | G | A | 2 | a0001c0001t0014g0200 a0001c0001t0014g0395 |
2 | HG02280.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.820+3309C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25009026 | |||||||
chr4:25009122 | C | A | 1 | a0001c0003t0003g0229 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.820+3213G>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25009122 | |||||||
chr4:25009123 | A | G | 47 | a0001c0001t0003g0207 a0001c0001t0005g0004 a0001c0001t0005g0010 others(44): Show |
57 | HG00544.hp1 HG00639.hp2 HG01123.hp1 others(54): Show |
intron_variant | MODIFIER | c.820+3212T>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25009123 | |||||||
chr4:25009142 | T | C | 161 | a0001c0001t0001g0274 a0001c0001t0002g0002 a0001c0001t0002g0003 others(158): Show |
192 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(189): Show |
intron_variant | MODIFIER | c.820+3193A>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25009142 | |||||||
chr4:25009214 | G | C | 2 | a0001c0001t0011g0128 a0001c0001t0011g0129 |
2 | HG00609.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.820+3121C>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25009214 | |||||||
chr4:25009236 | G | C | 161 | a0001c0001t0001g0274 a0001c0001t0002g0002 a0001c0001t0002g0003 others(158): Show |
192 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(189): Show |
intron_variant | MODIFIER | c.820+3099C>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25009236 | |||||||
chr4:25009237 | C | T | 1 | a0002c0002t0017g0015 | 2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.820+3098G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25009237 | |||||||
chr4:25009257 | C | T | 53 | a0001c0001t0001g0386 a0001c0001t0003g0154 a0001c0001t0004g0023 others(50): Show |
54 | HG00438.hp2 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.820+3078G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25009257 | |||||||
chr4:25009337 | G | C | 11 | a0001c0001t0008g0172 a0001c0001t0008g0189 a0001c0001t0008g0193 others(8): Show |
11 | HG00741.hp1 HG02630.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.820+2998C>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25009337 | |||||||
chr4:25009362 | C | T | 1 | a0001c0001t0004g0310 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.820+2973G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25009362 | |||||||
chr4:25009372 | C | T | 1 | a0001c0001t0014g0203 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.820+2963G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25009372 | |||||||
chr4:25009379 | T | C | 112 | a0001c0001t0001g0274 a0001c0001t0002g0002 a0001c0001t0002g0003 others(109): Show |
133 | HG00423.hp1 HG00438.hp1 HG00609.hp2 others(130): Show |
intron_variant | MODIFIER | c.820+2956A>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25009379 | |||||||
chr4:25009401 | G | A | 2 | a0001c0003t0003g0191 a0001c0003t0003g0192 |
2 | NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.820+2934C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25009401 | |||||||
chr4:25009461 | A | G | 2 | a0001c0001t0005g0004 a0001c0001t0005g0130 |
4 | HG02257.hp1 HG02970.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.820+2874T>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25009461 | |||||||
chr4:25009470 | C | G | 1 | a0002c0002t0017g0015 | 2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.820+2865G>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25009470 | |||||||
chr4:25009566 | A | G | 1 | a0002c0002t0017g0015 | 2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.820+2769T>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25009566 | |||||||
chr4:25009591 | C | T | 1 | a0002c0004t0003g0090 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.820+2744G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25009591 | |||||||
chr4:25009698 | C | T | 1 | a0001c0003t0003g0229 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.820+2637G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25009698 | |||||||
chr4:25009713 | G | A | 1 | a0001c0003t0003g0254 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.820+2622C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25009713 | |||||||
chr4:25009879 | C | A | 49 | a0001c0001t0003g0207 a0001c0001t0005g0004 a0001c0001t0005g0010 others(46): Show |
59 | HG00544.hp1 HG00639.hp2 HG01123.hp1 others(56): Show |
intron_variant | MODIFIER | c.820+2456G>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25009879 | |||||||
chr4:25009925 | C | T | 2 | a0001c0001t0014g0200 a0001c0001t0014g0395 |
2 | HG02280.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.820+2410G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25009925 | |||||||
chr4:25009926 | G | A | 6 | a0001c0001t0013g0155 a0001c0001t0013g0157 a0001c0001t0013g0358 others(3): Show |
6 | NA18964.hp1 NA18979.hp1 NA18989.hp1 others(3): Show |
intron_variant | MODIFIER | c.820+2409C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25009926 | |||||||
chr4:25009995 | G | A | 49 | a0001c0001t0003g0207 a0001c0001t0005g0004 a0001c0001t0005g0010 others(46): Show |
59 | HG00544.hp1 HG00639.hp2 HG01123.hp1 others(56): Show |
intron_variant | MODIFIER | c.820+2340C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25009995 | |||||||
chr4:25010001 | G | A | 1 | a0001c0001t0006g0176 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.820+2334C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25010001 | |||||||
chr4:25010143 | G | A | 1 | a0001c0001t0006g0303 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.820+2192C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25010143 | |||||||
chr4:25010267 | G | A | 47 | a0001c0001t0003g0207 a0001c0001t0005g0004 a0001c0001t0005g0010 others(44): Show |
57 | HG00544.hp1 HG00639.hp2 HG01123.hp1 others(54): Show |
intron_variant | MODIFIER | c.820+2068C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25010267 | |||||||
chr4:25010504 | A | G | 115 | a0001c0001t0001g0274 a0001c0001t0001g0320 a0001c0001t0001g0390 others(112): Show |
136 | HG00423.hp1 HG00438.hp1 HG00609.hp2 others(133): Show |
intron_variant | MODIFIER | c.820+1831T>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25010504 | |||||||
chr4:25010529 | T | C | 5 | a0001c0001t0009g0005 a0001c0001t0009g0021 a0001c0001t0009g0161 others(2): Show |
8 | HG02717.hp2 HG02895.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.820+1806A>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25010529 | |||||||
chr4:25010735 | T | C | 2 | a0001c0001t0002g0373 a0002c0002t0002g0070 |
2 | HG02523.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.820+1600A>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25010735 | |||||||
chr4:25010996 | C | T | 2 | a0001c0001t0015g0026 a0001c0001t0015g0245 |
3 | HG02257.hp2 HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.820+1339G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25010996 | |||||||
chr4:25011026 | G | C | 3 | a0001c0003t0003g0246 a0001c0003t0003g0247 a0001c0006t0004g0374 |
3 | HG00280.hp2 HG00738.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.820+1309C>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25011026 | |||||||
chr4:25011081 | C | CA | 123 | a0001c0001t0001g0274 a0001c0001t0001g0320 a0001c0001t0001g0352 others(120): Show |
144 | HG00423.hp1 HG00438.hp1 HG00609.hp2 others(141): Show |
intron_variant | MODIFIER | c.820+1253dupT | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25011081 | |||||||
chr4:25011081 | CA | C | 10 | a0001c0001t0001g0234 a0001c0001t0005g0022 a0001c0001t0005g0167 others(7): Show |
11 | HG01169.hp2 HG01891.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.820+1253delT | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25011081 | |||||||
chr4:25011106 | C | A | 185 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(182): Show |
214 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.820+1229G>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25011106 | |||||||
chr4:25011253 | C | T | 2 | a0002c0002t0011g0100 a0002c0002t0011g0101 |
2 | NA19001.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.820+1082G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25011253 | |||||||
chr4:25011311 | G | T | 1 | a0002c0002t0001g0080 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.820+1024C>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25011311 | |||||||
chr4:25011334 | G | A | 1 | a0001c0001t0006g0303 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.820+1001C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25011334 | |||||||
chr4:25011369 | C | A | 1 | a0003c0007t0003g0050 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.820+966G>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25011369 | |||||||
chr4:25011382 | C | T | 1 | a0002c0002t0004g0048 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.820+953G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25011382 | |||||||
chr4:25011422 | G | A | 2 | a0001c0001t0004g0210 a0001c0001t0004g0355 |
2 | HG02818.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.820+913C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25011422 | |||||||
chr4:25011583 | C | T | 3 | a0001c0001t0003g0204 a0001c0001t0003g0205 a0001c0001t0003g0206 |
3 | HG01891.hp1 HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.820+752G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25011583 | |||||||
chr4:25011591 | C | T | 1 | a0001c0003t0003g0273 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.820+744G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25011591 | |||||||
chr4:25011694 | C | T | 1 | a0001c0001t0004g0175 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.820+641G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25011694 | |||||||
chr4:25011954 | G | A | 173 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(170): Show |
198 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.820+381C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25011954 | |||||||
chr4:25012007 | G | A | 1 | a0001c0001t0004g0316 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.820+328C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25012007 | |||||||
chr4:25012082 | C | G | 7 | a0001c0001t0008g0188 a0001c0001t0008g0248 a0001c0001t0008g0249 others(4): Show |
7 | HG01109.hp2 HG02055.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.820+253G>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25012082 | |||||||
chr4:25012276 | C | T | 1 | a0001c0001t0005g0147 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.820+59G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25012276 | |||||||
chr4:25012278 | C | T | 2 | a0001c0001t0008g0188 a0001c0001t0008g0251 |
2 | HG02145.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.820+57G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25012278 | |||||||
chr4:25012280 | G | C | 2 | a0001c0001t0007g0344 a0001c0001t0007g0345 |
2 | NA18984.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.820+55C>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 7/7 | chr4 | 25012280 | |||||||
chr4:25012505 | G | A | 15 | a0001c0001t0008g0188 a0001c0001t0008g0248 a0001c0001t0008g0249 others(12): Show |
15 | HG00558.hp1 HG01109.hp2 HG02055.hp1 others(12): Show |
splice_region_variant&intron_variant | LOW | c.656-6C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25012505 | |||||||
chr4:25012569 | G | T | 71 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(68): Show |
78 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.656-70C>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25012569 | |||||||
chr4:25012887 | G | A | 2 | a0001c0001t0001g0202 a0001c0001t0004g0210 |
2 | HG01243.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.656-388C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25012887 | |||||||
chr4:25012948 | G | T | 21 | a0001c0001t0001g0126 a0001c0001t0001g0227 a0001c0001t0001g0231 others(18): Show |
22 | HG00280.hp1 HG00558.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.656-449C>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25012948 | |||||||
chr4:25013019 | C | A | 1 | a0001c0001t0014g0200 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.656-520G>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25013019 | |||||||
chr4:25013171 | G | A | 368 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(365): Show |
420 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(417): Show |
intron_variant | MODIFIER | c.656-672C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25013171 | |||||||
chr4:25013268 | T | C | 6 | a0001c0001t0013g0155 a0001c0001t0013g0157 a0001c0001t0013g0358 others(3): Show |
6 | NA18964.hp1 NA18979.hp1 NA18989.hp1 others(3): Show |
intron_variant | MODIFIER | c.656-769A>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25013268 | |||||||
chr4:25013273 | G | T | 2 | a0001c0001t0001g0231 a0001c0001t0001g0232 |
2 | NA18946.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.656-774C>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25013273 | |||||||
chr4:25013275 | C | T | 68 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(65): Show |
75 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.656-776G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25013275 | |||||||
chr4:25013462 | C | A | 1 | a0002c0002t0010g0047 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.656-963G>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25013462 | |||||||
chr4:25013480 | G | A | 6 | a0001c0001t0008g0188 a0001c0001t0008g0248 a0001c0001t0008g0249 others(3): Show |
6 | HG01109.hp2 HG02055.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.656-981C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25013480 | |||||||
chr4:25013500 | G | A | 9 | a0001c0001t0005g0022 a0001c0001t0005g0167 a0001c0001t0005g0183 others(6): Show |
10 | HG01891.hp2 HG02145.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.656-1001C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25013500 | |||||||
chr4:25013583 | T | G | 1 | a0001c0001t0006g0303 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.656-1084A>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25013583 | |||||||
chr4:25013701 | T | C | 1 | a0001c0001t0003g0308 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.656-1202A>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25013701 | |||||||
chr4:25013706 | A | T | 1 | a0001c0001t0003g0308 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.656-1207T>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25013706 | |||||||
chr4:25013894 | A | G | 366 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(363): Show |
418 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(415): Show |
intron_variant | MODIFIER | c.656-1395T>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25013894 | |||||||
chr4:25013905 | C | T | 1 | a0002c0002t0004g0057 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.656-1406G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25013905 | |||||||
chr4:25013965 | C | T | 1 | a0001c0003t0003g0182 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.656-1466G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25013965 | |||||||
chr4:25014100 | C | T | 4 | a0001c0001t0001g0202 a0001c0001t0004g0210 a0001c0001t0015g0026 others(1): Show |
5 | HG01243.hp1 HG02257.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.656-1601G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25014100 | |||||||
chr4:25014145 | C | T | 1 | a0001c0003t0003g0275 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.656-1646G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25014145 | |||||||
chr4:25014343 | G | A | 1 | a0002c0002t0004g0107 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.656-1844C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25014343 | |||||||
chr4:25014448 | G | C | 366 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(363): Show |
418 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(415): Show |
intron_variant | MODIFIER | c.656-1949C>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25014448 | |||||||
chr4:25014484 | C | CA | 388 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(385): Show |
441 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(438): Show |
intron_variant | MODIFIER | c.656-1986dupT | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25014484 | |||||||
chr4:25014830 | CA | C | 26 | a0001c0001t0002g0031 a0001c0001t0002g0300 a0001c0001t0002g0384 others(23): Show |
28 | HG00280.hp2 HG00423.hp2 HG00597.hp1 others(25): Show |
intron_variant | MODIFIER | c.656-2332delT | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25014830 | |||||||
chr4:25014830 | CAA | C | 92 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(89): Show |
114 | HG00099.hp2 HG00423.hp1 HG00597.hp2 others(111): Show |
intron_variant | MODIFIER | c.656-2333_656-2332d others(4): Show |
LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25014830 | |||||||
chr4:25014830 | CAAA | C | 63 | a0001c0001t0001g0274 a0001c0001t0001g0320 a0001c0001t0001g0322 others(60): Show |
72 | HG00438.hp1 HG00609.hp2 HG00642.hp1 others(69): Show |
intron_variant | MODIFIER | c.656-2334_656-2332d others(5): Show |
LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25014830 | |||||||
chr4:25014830 | CAAAA | C | 73 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(70): Show |
81 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.656-2335_656-2332d others(6): Show |
LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25014830 | |||||||
chr4:25014830 | CAAAAA | C | 6 | a0001c0001t0001g0351 a0001c0001t0005g0024 a0001c0001t0005g0162 others(3): Show |
7 | HG02615.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.656-2336_656-2332d others(7): Show |
LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25014830 | |||||||
chr4:25014830 | CAAAAAAA | C | 7 | a0001c0001t0003g0207 a0001c0001t0005g0004 a0001c0001t0005g0130 others(4): Show |
9 | HG01243.hp2 HG02257.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.656-2338_656-2332d others(9): Show |
LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25014830 | |||||||
chr4:25014845 | AAAAAAAA others(3): Show |
A | 1 | a0001c0001t0023g0179 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.656-2356_656-2347d others(12): Show |
LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25014845 | |||||||
chr4:25014846 | AAAAAAAA others(4): Show |
A | 2 | a0001c0001t0004g0349 a0002c0002t0005g0078 |
2 | HG03017.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.656-2358_656-2348d others(13): Show |
LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25014846 | |||||||
chr4:25014847 | AAAAAAAA others(3): Show |
A | 49 | a0001c0001t0001g0117 a0001c0001t0001g0386 a0001c0001t0003g0154 others(46): Show |
50 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.656-2358_656-2349d others(12): Show |
LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25014847 | |||||||
chr4:25014850 | AAAAAGAG | A | 6 | a0001c0001t0003g0204 a0001c0001t0003g0205 a0001c0001t0003g0206 others(3): Show |
6 | HG01891.hp1 HG03195.hp1 NA18522.hp2 others(3): Show |
intron_variant | MODIFIER | c.656-2358_656-2352d others(9): Show |
LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25014850 | |||||||
chr4:25014850 | AAAAAGAG others(2): Show |
A | 34 | a0001c0001t0005g0010 a0001c0001t0005g0022 a0001c0001t0005g0036 others(31): Show |
41 | HG00544.hp1 HG00639.hp2 HG01123.hp1 others(38): Show |
intron_variant | MODIFIER | c.656-2360_656-2352d others(11): Show |
LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25014850 | |||||||
chr4:25014853 | A | G | 6 | a0001c0001t0005g0024 a0001c0001t0005g0162 a0001c0001t0005g0184 others(3): Show |
8 | HG02257.hp2 HG02615.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.656-2354T>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25014853 | |||||||
chr4:25015008 | A | G | 1 | a0002c0002t0030g0042 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.656-2509T>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25015008 | |||||||
chr4:25015209 | G | A | 61 | a0001c0001t0002g0008 a0001c0001t0002g0328 a0001c0001t0002g0329 others(58): Show |
73 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.656-2710C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25015209 | |||||||
chr4:25015365 | G | A | 2 | a0001c0001t0007g0344 a0001c0001t0007g0345 |
2 | NA18984.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.655+2624C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25015365 | |||||||
chr4:25015448 | C | G | 1 | a0002c0002t0003g0091 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.655+2541G>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25015448 | |||||||
chr4:25015544 | A | G | 175 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(172): Show |
203 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.655+2445T>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25015544 | |||||||
chr4:25015601 | C | T | 2 | a0001c0001t0005g0304 a0001c0001t0005g0342 |
2 | HG01123.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.655+2388G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25015601 | |||||||
chr4:25015949 | C | T | 1 | a0002c0002t0003g0093 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.655+2040G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25015949 | |||||||
chr4:25015996 | A | G | 1 | a0001c0001t0004g0310 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.655+1993T>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25015996 | |||||||
chr4:25016099 | A | T | 1 | a0001c0001t0014g0200 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.655+1890T>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25016099 | |||||||
chr4:25016113 | C | A | 75 | a0001c0001t0001g0202 a0001c0001t0002g0008 a0001c0001t0002g0328 others(72): Show |
85 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.655+1876G>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25016113 | |||||||
chr4:25016229 | G | A | 1 | a0001c0001t0007g0335 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.655+1760C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25016229 | |||||||
chr4:25016401 | G | C | 1 | a0001c0001t0008g0291 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.655+1588C>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25016401 | |||||||
chr4:25016434 | G | A | 2 | a0001c0001t0004g0165 a0001c0001t0004g0166 |
2 | HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.655+1555C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25016434 | |||||||
chr4:25016521 | C | T | 1 | a0001c0003t0003g0311 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.655+1468G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25016521 | |||||||
chr4:25016613 | C | A | 1 | a0002c0002t0004g0085 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.655+1376G>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25016613 | |||||||
chr4:25016647 | A | G | 37 | a0001c0001t0005g0010 a0001c0001t0005g0022 a0001c0001t0005g0036 others(34): Show |
44 | HG00544.hp1 HG01123.hp1 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.655+1342T>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25016647 | |||||||
chr4:25016700 | C | T | 2 | a0001c0001t0001g0117 a0001c0001t0004g0127 |
2 | HG00544.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.655+1289G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25016700 | |||||||
chr4:25016995 | C | G | 1 | a0001c0001t0001g0126 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.655+994G>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25016995 | |||||||
chr4:25017003 | C | T | 257 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(254): Show |
292 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(289): Show |
intron_variant | MODIFIER | c.655+986G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25017003 | |||||||
chr4:25017127 | G | A | 361 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(358): Show |
412 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(409): Show |
intron_variant | MODIFIER | c.655+862C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25017127 | |||||||
chr4:25017292 | C | T | 1 | a0001c0001t0029g0252 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.655+697G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25017292 | |||||||
chr4:25017398 | C | T | 1 | a0001c0001t0004g0241 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.655+591G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25017398 | |||||||
chr4:25017457 | G | A | 1 | a0001c0001t0014g0203 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.655+532C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25017457 | |||||||
chr4:25017533 | C | T | 1 | a0006c0016t0006g0399 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.655+456G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25017533 | |||||||
chr4:25017541 | C | CAA | 19 | a0001c0001t0004g0123 a0001c0001t0004g0132 a0001c0001t0004g0150 others(16): Show |
19 | HG00558.hp2 HG02451.hp2 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.655+446_655+447dup others(2): Show |
LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25017541 | |||||||
chr4:25017541 | C | CAAA | 20 | a0001c0001t0001g0117 a0001c0001t0001g0386 a0001c0001t0004g0127 others(17): Show |
20 | HG00438.hp2 HG00544.hp2 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.655+445_655+447dup others(3): Show |
LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25017541 | |||||||
chr4:25017541 | C | CAAAA | 15 | a0001c0001t0003g0154 a0001c0001t0004g0122 a0001c0001t0004g0124 others(12): Show |
15 | HG00609.hp1 HG01358.hp2 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.655+444_655+447dup others(4): Show |
LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25017541 | |||||||
chr4:25017541 | C | CAAAAA | 5 | a0001c0001t0004g0023 a0001c0001t0004g0118 a0001c0001t0004g0316 others(2): Show |
6 | HG00621.hp1 HG01109.hp1 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.655+443_655+447dup others(5): Show |
LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25017541 | |||||||
chr4:25017541 | C | CAAAAAAA others(3): Show |
2 | a0001c0001t0008g0188 a0001c0001t0008g0251 |
2 | HG02145.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.655+438_655+447dup others(10): Show |
LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25017541 | |||||||
chr4:25017541 | CA | C | 229 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(226): Show |
274 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(271): Show |
intron_variant | MODIFIER | c.655+447delT | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25017541 | |||||||
chr4:25017541 | CAA | C | 6 | a0001c0001t0004g0280 a0001c0001t0005g0346 a0001c0001t0007g0326 others(3): Show |
6 | HG00280.hp1 HG01257.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.655+446_655+447del others(2): Show |
LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25017541 | |||||||
chr4:25017633 | C | T | 159 | a0001c0001t0001g0117 a0001c0001t0001g0386 a0001c0001t0002g0003 others(156): Show |
179 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(176): Show |
intron_variant | MODIFIER | c.655+356G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25017633 | |||||||
chr4:25017641 | C | T | 208 | a0001c0001t0001g0117 a0001c0001t0001g0386 a0001c0001t0002g0003 others(205): Show |
235 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(232): Show |
intron_variant | MODIFIER | c.655+348G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25017641 | |||||||
chr4:25017773 | A | C | 12 | a0001c0001t0005g0022 a0001c0001t0005g0162 a0001c0001t0005g0167 others(9): Show |
13 | HG01891.hp2 HG02145.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.655+216T>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25017773 | |||||||
chr4:25017826 | C | T | 1 | a0001c0001t0001g0351 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.655+163G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25017826 | |||||||
chr4:25017850 | T | TAGAATGT others(296): Show |
4 | a0001c0001t0013g0155 a0001c0001t0013g0157 a0001c0001t0013g0358 others(1): Show |
4 | NA18964.hp1 NA18979.hp1 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.655+138_655+139ins others(303): Show |
LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25017850 | |||||||
chr4:25017850 | T | TAGAATGT others(297): Show |
1 | a0001c0001t0019g0159 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.655+138_655+139ins others(304): Show |
LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25017850 | |||||||
chr4:25017850 | T | TAGAATGT others(303): Show |
1 | a0001c0001t0013g0367 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.655+138_655+139ins others(310): Show |
LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25017850 | |||||||
chr4:25017854 | A | G | 2 | a0001c0001t0015g0026 a0001c0001t0015g0245 |
3 | HG02257.hp2 HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.655+135T>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25017854 | |||||||
chr4:25017978 | G | T | 1 | a0001c0001t0006g0281 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.655+11C>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 6/7 | chr4 | 25017978 | |||||||
chr4:25018230 | C | T | 7 | a0001c0001t0003g0308 a0002c0002t0003g0089 a0002c0002t0003g0091 others(4): Show |
7 | HG00609.hp2 HG02056.hp2 HG03688.hp2 others(4): Show |
intron_variant | MODIFIER | c.486-72G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 5/7 | chr4 | 25018230 | |||||||
chr4:25018324 | T | C | 1 | a0001c0001t0006g0177 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.486-166A>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 5/7 | chr4 | 25018324 | |||||||
chr4:25018405 | G | A | 1 | a0002c0002t0004g0107 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.486-247C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 5/7 | chr4 | 25018405 | |||||||
chr4:25018415 | C | G | 1 | a0001c0001t0014g0203 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.486-257G>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 5/7 | chr4 | 25018415 | |||||||
chr4:25018509 | G | A | 1 | a0001c0001t0006g0389 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.486-351C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 5/7 | chr4 | 25018509 | |||||||
chr4:25018545 | G | GAAACTTC others(5): Show |
1 | a0001c0001t0001g0287 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.486-399_486-388dup others(12): Show |
LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 5/7 | chr4 | 25018545 | |||||||
chr4:25018572 | G | A | 100 | a0001c0001t0001g0117 a0001c0001t0001g0386 a0001c0001t0003g0154 others(97): Show |
111 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.486-414C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 5/7 | chr4 | 25018572 | |||||||
chr4:25018609 | T | A | 227 | a0001c0001t0001g0117 a0001c0001t0001g0202 a0001c0001t0001g0386 others(224): Show |
255 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(252): Show |
intron_variant | MODIFIER | c.486-451A>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 5/7 | chr4 | 25018609 | |||||||
chr4:25018789 | G | A | 1 | a0001c0001t0029g0252 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.485+378C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 5/7 | chr4 | 25018789 | |||||||
chr4:25018821 | C | T | 7 | a0001c0001t0003g0308 a0002c0002t0003g0089 a0002c0002t0003g0091 others(4): Show |
7 | HG00609.hp2 HG02056.hp2 HG03688.hp2 others(4): Show |
intron_variant | MODIFIER | c.485+346G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 5/7 | chr4 | 25018821 | |||||||
chr4:25018847 | G | A | 1 | a0001c0001t0008g0189 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.485+320C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 5/7 | chr4 | 25018847 | |||||||
chr4:25018860 | T | TA | 8 | a0001c0001t0008g0172 a0001c0001t0008g0189 a0001c0001t0014g0200 others(5): Show |
8 | HG00741.hp1 HG02280.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.485+306dupT | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 5/7 | chr4 | 25018860 | |||||||
chr4:25018916 | A | C | 1 | a0001c0001t0001g0226 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.485+251T>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 5/7 | chr4 | 25018916 | |||||||
chr4:25019412 | T | G | 6 | a0001c0001t0006g0032 a0001c0001t0006g0281 a0001c0001t0006g0282 others(3): Show |
7 | HG00642.hp2 HG00733.hp2 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.414-174A>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25019412 | |||||||
chr4:25019420 | CT | C | 368 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(365): Show |
420 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(417): Show |
intron_variant | MODIFIER | c.414-183delA | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25019420 | |||||||
chr4:25019521 | G | A | 4 | a0001c0001t0007g0295 a0001c0005t0006g0039 a0001c0005t0006g0296 others(1): Show |
5 | NA18967.hp1 NA18978.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.414-283C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25019521 | |||||||
chr4:25020016 | AAAG | A | 5 | a0001c0001t0005g0024 a0001c0001t0005g0163 a0001c0001t0005g0164 others(2): Show |
6 | HG02486.hp1 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.414-781_414-779del others(3): Show |
LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25020016 | |||||||
chr4:25020111 | T | A | 227 | a0001c0001t0001g0117 a0001c0001t0001g0202 a0001c0001t0001g0386 others(224): Show |
255 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(252): Show |
intron_variant | MODIFIER | c.414-873A>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25020111 | |||||||
chr4:25020284 | G | A | 66 | a0001c0001t0001g0117 a0001c0001t0001g0386 a0001c0001t0003g0154 others(63): Show |
73 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.414-1046C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25020284 | |||||||
chr4:25020301 | A | G | 3 | a0001c0001t0002g0037 a0001c0001t0002g0360 a0001c0001t0002g0361 |
4 | NA18942.hp2 NA18961.hp2 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.414-1063T>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25020301 | |||||||
chr4:25020345 | C | T | 123 | a0001c0001t0001g0117 a0001c0001t0001g0386 a0001c0001t0003g0154 others(120): Show |
137 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(134): Show |
intron_variant | MODIFIER | c.414-1107G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25020345 | |||||||
chr4:25020541 | G | T | 91 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0037 others(88): Show |
104 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.414-1303C>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25020541 | |||||||
chr4:25020562 | C | T | 123 | a0001c0001t0001g0117 a0001c0001t0001g0386 a0001c0001t0003g0154 others(120): Show |
137 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(134): Show |
intron_variant | MODIFIER | c.414-1324G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25020562 | |||||||
chr4:25020563 | G | A | 67 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(64): Show |
74 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.414-1325C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25020563 | |||||||
chr4:25020653 | T | G | 13 | a0001c0001t0001g0202 a0001c0001t0004g0210 a0001c0001t0008g0248 others(10): Show |
14 | HG01109.hp2 HG01243.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.414-1415A>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25020653 | |||||||
chr4:25020661 | A | G | 13 | a0001c0001t0001g0202 a0001c0001t0004g0210 a0001c0001t0008g0248 others(10): Show |
14 | HG01109.hp2 HG01243.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.414-1423T>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25020661 | |||||||
chr4:25020677 | A | T | 2 | a0001c0001t0014g0200 a0001c0001t0014g0395 |
2 | HG02280.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.414-1439T>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25020677 | |||||||
chr4:25020786 | C | T | 227 | a0001c0001t0001g0117 a0001c0001t0001g0202 a0001c0001t0001g0386 others(224): Show |
255 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(252): Show |
intron_variant | MODIFIER | c.414-1548G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25020786 | |||||||
chr4:25020856 | G | T | 227 | a0001c0001t0001g0117 a0001c0001t0001g0202 a0001c0001t0001g0386 others(224): Show |
255 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(252): Show |
intron_variant | MODIFIER | c.414-1618C>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25020856 | |||||||
chr4:25020879 | G | T | 1 | a0001c0001t0008g0248 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.414-1641C>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25020879 | |||||||
chr4:25020921 | T | G | 10 | a0001c0001t0008g0172 a0001c0001t0008g0189 a0001c0001t0008g0193 others(7): Show |
10 | HG00741.hp1 HG02451.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.414-1683A>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25020921 | |||||||
chr4:25021107 | C | CA | 119 | a0001c0001t0001g0117 a0001c0001t0001g0386 a0001c0001t0003g0154 others(116): Show |
133 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.414-1870dupT | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25021107 | |||||||
chr4:25021107 | C | CAA | 20 | a0001c0001t0001g0202 a0001c0001t0004g0210 a0001c0001t0004g0314 others(17): Show |
21 | HG00741.hp1 HG01109.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.414-1871_414-1870d others(4): Show |
LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25021107 | |||||||
chr4:25021194 | T | C | 227 | a0001c0001t0001g0117 a0001c0001t0001g0202 a0001c0001t0001g0386 others(224): Show |
255 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(252): Show |
intron_variant | MODIFIER | c.414-1956A>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25021194 | |||||||
chr4:25021227 | T | C | 15 | a0001c0001t0003g0204 a0001c0001t0003g0205 a0001c0001t0003g0206 others(12): Show |
15 | HG00741.hp1 HG01891.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.414-1989A>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25021227 | |||||||
chr4:25021275 | CTATT | C | 3 | a0001c0001t0001g0284 a0002c0002t0001g0062 a0002c0002t0033g0068 |
3 | HG00140.hp2 HG03669.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.414-2041_414-2038d others(6): Show |
LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25021275 | |||||||
chr4:25021477 | A | C | 2 | a0001c0001t0014g0200 a0001c0001t0014g0395 |
2 | HG02280.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.414-2239T>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25021477 | |||||||
chr4:25021487 | C | G | 100 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(97): Show |
111 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.414-2249G>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25021487 | |||||||
chr4:25021697 | C | T | 1 | a0001c0001t0005g0178 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.414-2459G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25021697 | |||||||
chr4:25021698 | G | A | 1 | a0001c0001t0002g0373 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.414-2460C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25021698 | |||||||
chr4:25021748 | G | A | 13 | a0001c0001t0003g0205 a0001c0001t0003g0206 a0001c0001t0008g0172 others(10): Show |
13 | HG00741.hp1 HG01891.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.414-2510C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25021748 | |||||||
chr4:25021761 | C | T | 108 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(105): Show |
123 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.414-2523G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25021761 | |||||||
chr4:25021803 | C | A | 14 | a0001c0001t0003g0204 a0001c0001t0003g0205 a0001c0001t0003g0206 others(11): Show |
14 | HG00741.hp1 HG01891.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.414-2565G>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25021803 | |||||||
chr4:25021824 | A | G | 368 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(365): Show |
420 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(417): Show |
intron_variant | MODIFIER | c.414-2586T>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25021824 | |||||||
chr4:25021863 | T | A | 368 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(365): Show |
420 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(417): Show |
intron_variant | MODIFIER | c.414-2625A>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25021863 | |||||||
chr4:25021914 | G | A | 3 | a0001c0001t0003g0204 a0001c0001t0003g0205 a0001c0001t0003g0206 |
3 | HG01891.hp1 HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.414-2676C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25021914 | |||||||
chr4:25021930 | C | CA | 119 | a0001c0001t0001g0117 a0001c0001t0001g0227 a0001c0001t0001g0234 others(116): Show |
131 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.414-2693dupT | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25021930 | |||||||
chr4:25021930 | C | CAA | 23 | a0001c0001t0003g0205 a0001c0001t0003g0206 a0001c0001t0005g0190 others(20): Show |
25 | HG00423.hp2 HG00597.hp1 HG00673.hp2 others(22): Show |
intron_variant | MODIFIER | c.414-2694_414-2693d others(4): Show |
LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25021930 | |||||||
chr4:25021930 | CA | C | 31 | a0001c0001t0001g0351 a0001c0001t0002g0002 a0001c0001t0002g0030 others(28): Show |
38 | HG00423.hp1 HG01081.hp1 HG01123.hp2 others(35): Show |
intron_variant | MODIFIER | c.414-2693delT | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25021930 | |||||||
chr4:25021948 | A | AC | 23 | a0001c0001t0004g0241 a0001c0001t0005g0010 a0001c0001t0005g0036 others(20): Show |
29 | HG00544.hp1 HG01123.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.414-2711_414-2710i others(3): Show |
LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25021948 | |||||||
chr4:25021948 | A | C | 10 | a0001c0001t0005g0022 a0001c0001t0005g0167 a0001c0001t0005g0183 others(7): Show |
11 | HG01891.hp2 HG02145.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.414-2710T>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25021948 | |||||||
chr4:25022020 | C | A | 195 | a0001c0001t0001g0117 a0001c0001t0001g0202 a0001c0001t0001g0227 others(192): Show |
219 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(216): Show |
intron_variant | MODIFIER | c.414-2782G>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25022020 | |||||||
chr4:25022103 | A | G | 18 | a0001c0001t0002g0160 a0001c0001t0003g0207 a0001c0001t0005g0004 others(15): Show |
21 | HG01243.hp2 HG02257.hp1 HG02486.hp1 others(18): Show |
intron_variant | MODIFIER | c.413+2717T>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25022103 | |||||||
chr4:25022131 | C | G | 1 | a0002c0002t0005g0113 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.413+2689G>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25022131 | |||||||
chr4:25022131 | C | T | 1 | a0001c0001t0002g0380 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.413+2689G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25022131 | |||||||
chr4:25022253 | A | C | 96 | a0001c0001t0001g0226 a0001c0001t0001g0386 a0001c0001t0002g0003 others(93): Show |
108 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.413+2567T>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25022253 | |||||||
chr4:25022271 | C | T | 264 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0117 others(261): Show |
301 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.413+2549G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25022271 | |||||||
chr4:25022505 | C | T | 2 | a0001c0003t0003g0247 a0001c0006t0004g0374 |
2 | HG00280.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.413+2315G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25022505 | |||||||
chr4:25022506 | G | A | 1 | a0001c0001t0002g0309 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.413+2314C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25022506 | |||||||
chr4:25022903 | C | G | 1 | a0001c0001t0004g0118 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.413+1917G>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25022903 | |||||||
chr4:25023068 | T | TTGATGA | 101 | a0001c0001t0001g0029 a0001c0001t0001g0131 a0001c0001t0001g0133 others(98): Show |
114 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.413+1746_413+1751d others(8): Show |
LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25023068 | |||||||
chr4:25023068 | T | TTGATGAT others(5): Show |
66 | a0001c0001t0001g0194 a0001c0001t0001g0222 a0001c0001t0002g0257 others(63): Show |
77 | HG00140.hp2 HG00438.hp1 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.413+1740_413+1751d others(14): Show |
LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25023068 | |||||||
chr4:25023068 | T | TTGATGAT others(8): Show |
5 | a0001c0001t0001g0274 a0001c0001t0003g0207 a0001c0003t0003g0275 others(2): Show |
5 | HG01175.hp2 HG03540.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.413+1737_413+1751d others(17): Show |
LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25023068 | |||||||
chr4:25023068 | TTGATGA | T | 186 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0117 others(183): Show |
212 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(209): Show |
intron_variant | MODIFIER | c.413+1746_413+1751d others(8): Show |
LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25023068 | |||||||
chr4:25023068 | TTGATGAT others(5): Show |
T | 1 | a0002c0002t0017g0015 | 2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.413+1740_413+1751d others(14): Show |
LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25023068 | |||||||
chr4:25023087 | T | A | 1 | a0001c0001t0001g0196 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.413+1733A>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25023087 | |||||||
chr4:25023101 | A | G | 76 | a0001c0001t0001g0194 a0001c0001t0001g0202 a0001c0001t0001g0222 others(73): Show |
88 | HG00140.hp2 HG00438.hp1 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.413+1719T>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25023101 | |||||||
chr4:25023165 | T | C | 7 | a0001c0001t0002g0156 a0001c0001t0002g0160 a0001c0001t0013g0155 others(4): Show |
7 | NA18959.hp2 NA18964.hp1 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.413+1655A>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25023165 | |||||||
chr4:25023210 | A | G | 76 | a0001c0001t0001g0194 a0001c0001t0001g0202 a0001c0001t0001g0222 others(73): Show |
88 | HG00140.hp2 HG00438.hp1 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.413+1610T>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25023210 | |||||||
chr4:25023313 | T | C | 61 | a0001c0001t0001g0202 a0001c0001t0001g0222 a0001c0001t0001g0255 others(58): Show |
73 | HG00140.hp2 HG00438.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.413+1507A>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25023313 | |||||||
chr4:25023452 | T | C | 7 | a0001c0001t0005g0022 a0001c0001t0005g0183 a0001c0001t0005g0184 others(4): Show |
9 | HG01891.hp2 HG02145.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.413+1368A>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25023452 | |||||||
chr4:25023513 | G | A | 55 | a0001c0001t0001g0202 a0001c0001t0001g0222 a0001c0001t0001g0255 others(52): Show |
64 | HG00140.hp2 HG00438.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.413+1307C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25023513 | |||||||
chr4:25023528 | G | A | 69 | a0001c0001t0001g0194 a0001c0001t0001g0202 a0001c0001t0001g0222 others(66): Show |
79 | HG00140.hp2 HG00438.hp1 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.413+1292C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25023528 | |||||||
chr4:25023545 | A | G | 16 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0322 others(13): Show |
16 | HG00558.hp1 HG00621.hp2 HG02040.hp2 others(13): Show |
intron_variant | MODIFIER | c.413+1275T>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25023545 | |||||||
chr4:25023702 | T | C | 76 | a0001c0001t0001g0194 a0001c0001t0001g0202 a0001c0001t0001g0222 others(73): Show |
88 | HG00140.hp2 HG00438.hp1 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.413+1118A>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25023702 | |||||||
chr4:25023767 | C | T | 273 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(270): Show |
313 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(310): Show |
intron_variant | MODIFIER | c.413+1053G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25023767 | |||||||
chr4:25023815 | G | A | 2 | a0001c0003t0003g0247 a0001c0006t0004g0374 |
2 | HG00280.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.413+1005C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25023815 | |||||||
chr4:25024008 | A | G | 1 | a0001c0001t0002g0140 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.413+812T>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25024008 | |||||||
chr4:25024214 | C | T | 34 | a0001c0001t0001g0117 a0001c0001t0001g0120 a0001c0001t0001g0126 others(31): Show |
36 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.413+606G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25024214 | |||||||
chr4:25024218 | A | G | 1 | a0001c0001t0001g0320 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.413+602T>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25024218 | |||||||
chr4:25024280 | G | A | 7 | a0001c0001t0002g0156 a0001c0001t0002g0160 a0001c0001t0013g0155 others(4): Show |
7 | NA18959.hp2 NA18964.hp1 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.413+540C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25024280 | |||||||
chr4:25024331 | T | G | 17 | a0001c0001t0002g0002 a0001c0001t0002g0031 a0001c0001t0002g0038 others(14): Show |
22 | HG00423.hp1 HG00741.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.413+489A>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25024331 | |||||||
chr4:25024385 | G | A | 3 | a0001c0001t0003g0204 a0001c0001t0003g0205 a0001c0001t0003g0206 |
3 | HG01891.hp1 HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.413+435C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25024385 | |||||||
chr4:25024412 | G | T | 273 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(270): Show |
313 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(310): Show |
intron_variant | MODIFIER | c.413+408C>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25024412 | |||||||
chr4:25024432 | T | A | 1 | a0001c0001t0003g0205 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.413+388A>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25024432 | |||||||
chr4:25024509 | G | A | 8 | a0001c0001t0003g0204 a0001c0001t0003g0205 a0001c0001t0003g0206 others(5): Show |
8 | HG01109.hp2 HG01891.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.413+311C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25024509 | |||||||
chr4:25024520 | A | G | 15 | a0001c0001t0001g0194 a0001c0001t0004g0165 a0001c0001t0005g0024 others(12): Show |
16 | HG02280.hp2 HG02486.hp1 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.413+300T>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25024520 | |||||||
chr4:25024573 | G | A | 183 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0117 others(180): Show |
209 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(206): Show |
intron_variant | MODIFIER | c.413+247C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25024573 | |||||||
chr4:25024693 | A | G | 27 | a0001c0001t0002g0002 a0001c0001t0002g0030 a0001c0001t0002g0031 others(24): Show |
34 | HG00423.hp1 HG00741.hp2 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.413+127T>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25024693 | |||||||
chr4:25024789 | G | C | 27 | a0001c0001t0002g0002 a0001c0001t0002g0030 a0001c0001t0002g0031 others(24): Show |
34 | HG00423.hp1 HG00741.hp2 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.413+31C>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 4/7 | chr4 | 25024789 | |||||||
chr4:25024933 | T | C | 1 | a0002c0002t0004g0048 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.342-42A>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 3/7 | chr4 | 25024933 | |||||||
chr4:25025075 | C | T | 3 | a0001c0001t0005g0004 a0001c0001t0005g0130 a0001c0001t0005g0277 |
5 | HG01243.hp2 HG02257.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.342-184G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 3/7 | chr4 | 25025075 | |||||||
chr4:25025121 | C | T | 69 | a0001c0001t0001g0202 a0001c0001t0001g0222 a0001c0001t0001g0255 others(66): Show |
80 | HG00140.hp2 HG00438.hp1 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.342-230G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 3/7 | chr4 | 25025121 | |||||||
chr4:25025143 | C | CA | 94 | a0001c0001t0001g0029 a0001c0001t0001g0131 a0001c0001t0001g0133 others(91): Show |
108 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.342-253dupT | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 3/7 | chr4 | 25025143 | |||||||
chr4:25025159 | C | T | 69 | a0001c0001t0001g0202 a0001c0001t0001g0222 a0001c0001t0001g0255 others(66): Show |
80 | HG00140.hp2 HG00438.hp1 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.342-268G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 3/7 | chr4 | 25025159 | |||||||
chr4:25025163 | G | A | 1 | a0002c0004t0003g0058 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.342-272C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 3/7 | chr4 | 25025163 | |||||||
chr4:25025318 | T | C | 62 | a0001c0001t0001g0202 a0001c0001t0001g0222 a0001c0001t0001g0255 others(59): Show |
71 | HG00140.hp2 HG00438.hp1 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.342-427A>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 3/7 | chr4 | 25025318 | |||||||
chr4:25025398 | T | G | 2 | a0001c0001t0011g0128 a0001c0001t0011g0129 |
2 | HG00609.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.342-507A>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 3/7 | chr4 | 25025398 | |||||||
chr4:25025399 | C | T | 1 | a0002c0002t0004g0085 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.342-508G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 3/7 | chr4 | 25025399 | |||||||
chr4:25025415 | T | C | 8 | a0001c0001t0003g0204 a0001c0001t0003g0205 a0001c0001t0003g0206 others(5): Show |
8 | HG01109.hp2 HG01891.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.342-524A>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 3/7 | chr4 | 25025415 | |||||||
chr4:25025535 | C | T | 1 | a0001c0003t0003g0319 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.342-644G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 3/7 | chr4 | 25025535 | |||||||
chr4:25025602 | TTGA | T | 18 | a0001c0001t0001g0194 a0001c0001t0004g0165 a0001c0001t0005g0024 others(15): Show |
19 | HG02280.hp2 HG02486.hp1 HG02615.hp1 others(16): Show |
intron_variant | MODIFIER | c.342-714_342-712del others(3): Show |
LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 3/7 | chr4 | 25025602 | |||||||
chr4:25025617 | T | C | 1 | a0002c0002t0004g0057 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.342-726A>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 3/7 | chr4 | 25025617 | |||||||
chr4:25025619 | C | T | 69 | a0001c0001t0001g0202 a0001c0001t0001g0222 a0001c0001t0001g0255 others(66): Show |
78 | HG00140.hp2 HG00438.hp1 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.342-728G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 3/7 | chr4 | 25025619 | |||||||
chr4:25025650 | T | G | 3 | a0002c0002t0002g0016 a0002c0002t0004g0107 a0002c0004t0003g0103 |
4 | HG01884.hp1 HG02572.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.342-759A>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 3/7 | chr4 | 25025650 | |||||||
chr4:25025749 | C | T | 17 | a0001c0001t0001g0194 a0001c0001t0004g0165 a0001c0001t0005g0024 others(14): Show |
18 | HG02280.hp2 HG02486.hp1 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.342-858G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 3/7 | chr4 | 25025749 | |||||||
chr4:25025805 | G | T | 8 | a0001c0001t0003g0204 a0001c0001t0003g0205 a0001c0001t0003g0206 others(5): Show |
8 | HG01109.hp2 HG01891.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.342-914C>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 3/7 | chr4 | 25025805 | |||||||
chr4:25025837 | C | T | 2 | a0001c0001t0004g0166 a0001c0001t0029g0252 |
2 | HG02630.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.342-946G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 3/7 | chr4 | 25025837 | |||||||
chr4:25025890 | T | C | 2 | a0001c0001t0015g0026 a0001c0001t0015g0245 |
3 | HG02257.hp2 HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.341+978A>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 3/7 | chr4 | 25025890 | |||||||
chr4:25025908 | C | T | 1 | a0001c0006t0004g0276 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.341+960G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 3/7 | chr4 | 25025908 | |||||||
chr4:25025959 | C | T | 1 | a0001c0003t0003g0254 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.341+909G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 3/7 | chr4 | 25025959 | |||||||
chr4:25026011 | C | T | 8 | a0001c0001t0003g0204 a0001c0001t0003g0205 a0001c0001t0003g0206 others(5): Show |
8 | HG01109.hp2 HG01891.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.341+857G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 3/7 | chr4 | 25026011 | |||||||
chr4:25026018 | A | C | 2 | a0001c0001t0004g0151 a0001c0001t0004g0152 |
2 | HG02486.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.341+850T>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 3/7 | chr4 | 25026018 | |||||||
chr4:25026176 | C | T | 8 | a0001c0001t0003g0204 a0001c0001t0003g0205 a0001c0001t0003g0206 others(5): Show |
8 | HG01109.hp2 HG01891.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.341+692G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 3/7 | chr4 | 25026176 | |||||||
chr4:25026195 | C | A | 8 | a0001c0001t0003g0204 a0001c0001t0003g0205 a0001c0001t0003g0206 others(5): Show |
8 | HG01109.hp2 HG01891.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.341+673G>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 3/7 | chr4 | 25026195 | |||||||
chr4:25026244 | A | G | 2 | a0001c0001t0004g0166 a0001c0001t0029g0252 |
2 | HG02630.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.341+624T>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 3/7 | chr4 | 25026244 | |||||||
chr4:25026282 | G | A | 6 | a0001c0001t0005g0022 a0001c0001t0005g0183 a0001c0001t0005g0184 others(3): Show |
7 | HG01891.hp2 HG02145.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.341+586C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 3/7 | chr4 | 25026282 | |||||||
chr4:25026315 | G | A | 1 | a0001c0001t0011g0129 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.341+553C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 3/7 | chr4 | 25026315 | |||||||
chr4:25026344 | C | CA | 157 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0146 others(154): Show |
178 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.341+523dupT | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 3/7 | chr4 | 25026344 | |||||||
chr4:25026354 | A | G | 61 | a0001c0001t0001g0202 a0001c0001t0001g0222 a0001c0001t0001g0255 others(58): Show |
70 | HG00140.hp2 HG00438.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.341+514T>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 3/7 | chr4 | 25026354 | |||||||
chr4:25026516 | C | T | 2 | a0001c0001t0004g0166 a0001c0001t0029g0252 |
2 | HG02630.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.341+352G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 3/7 | chr4 | 25026516 | |||||||
chr4:25026536 | G | T | 359 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(356): Show |
411 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(408): Show |
intron_variant | MODIFIER | c.341+332C>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 3/7 | chr4 | 25026536 | |||||||
chr4:25026547 | C | T | 1 | a0001c0013t0004g0225 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.341+321G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 3/7 | chr4 | 25026547 | |||||||
chr4:25026850 | A | G | 44 | a0001c0001t0001g0117 a0001c0001t0001g0120 a0001c0001t0001g0126 others(41): Show |
50 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.341+18T>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 3/7 | chr4 | 25026850 | |||||||
chr4:25026970 | G | A | 1 | a0002c0002t0006g0041 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.270-31C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 2/7 | chr4 | 25026970 | |||||||
chr4:25027090 | T | C | 1 | a0001c0001t0006g0032 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.270-151A>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 2/7 | chr4 | 25027090 | |||||||
chr4:25027114 | G | A | 2 | a0001c0001t0004g0166 a0001c0001t0029g0252 |
2 | HG02630.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.270-175C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 2/7 | chr4 | 25027114 | |||||||
chr4:25027143 | T | A | 1 | a0001c0001t0003g0206 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.270-204A>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 2/7 | chr4 | 25027143 | |||||||
chr4:25027164 | C | G | 94 | a0001c0001t0001g0029 a0001c0001t0001g0131 a0001c0001t0001g0133 others(91): Show |
108 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.270-225G>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 2/7 | chr4 | 25027164 | |||||||
chr4:25027269 | T | C | 2 | a0001c0001t0015g0026 a0001c0001t0015g0245 |
3 | HG02257.hp2 HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.270-330A>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 2/7 | chr4 | 25027269 | |||||||
chr4:25027394 | T | TA | 8 | a0001c0001t0003g0204 a0001c0001t0003g0205 a0001c0001t0003g0206 others(5): Show |
8 | HG01109.hp2 HG01891.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.270-456dupT | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 2/7 | chr4 | 25027394 | |||||||
chr4:25027394 | T | TAAA | 10 | a0001c0001t0001g0234 a0001c0001t0004g0166 a0001c0001t0005g0167 others(7): Show |
13 | HG01169.hp2 HG02630.hp2 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.270-458_270-456dup others(3): Show |
LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 2/7 | chr4 | 25027394 | |||||||
chr4:25027394 | T | TAAAA | 34 | a0001c0001t0001g0120 a0001c0001t0001g0126 a0001c0001t0001g0236 others(31): Show |
37 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.270-459_270-456dup others(4): Show |
LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 2/7 | chr4 | 25027394 | |||||||
chr4:25027394 | TAA | T | 303 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(300): Show |
347 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.270-457_270-456del others(2): Show |
LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 2/7 | chr4 | 25027394 | |||||||
chr4:25027394 | TAAA | T | 8 | a0001c0001t0002g0376 a0001c0001t0005g0130 a0001c0001t0007g0233 others(5): Show |
8 | HG01175.hp2 HG02145.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.270-458_270-456del others(3): Show |
LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 2/7 | chr4 | 25027394 | |||||||
chr4:25027458 | A | G | 1 | a0001c0001t0015g0026 | 2 | HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.270-519T>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 2/7 | chr4 | 25027458 | |||||||
chr4:25027470 | A | G | 54 | a0001c0001t0001g0202 a0001c0001t0001g0222 a0001c0001t0001g0255 others(51): Show |
63 | HG00140.hp2 HG00438.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.270-531T>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 2/7 | chr4 | 25027470 | |||||||
chr4:25027941 | G | A | 6 | a0001c0001t0005g0167 a0001c0001t0009g0005 a0001c0001t0009g0021 others(3): Show |
9 | HG02717.hp2 HG02895.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.269+566C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 2/7 | chr4 | 25027941 | |||||||
chr4:25028047 | G | A | 2 | a0002c0002t0002g0016 a0002c0002t0004g0107 |
3 | HG01884.hp1 HG02572.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.269+460C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 2/7 | chr4 | 25028047 | |||||||
chr4:25028119 | C | A | 1 | a0001c0003t0003g0311 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.269+388G>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 2/7 | chr4 | 25028119 | |||||||
chr4:25028195 | G | A | 315 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(312): Show |
360 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(357): Show |
intron_variant | MODIFIER | c.269+312C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 2/7 | chr4 | 25028195 | |||||||
chr4:25028226 | A | G | 1 | a0002c0002t0030g0042 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.269+281T>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 2/7 | chr4 | 25028226 | |||||||
chr4:25028323 | T | C | 7 | a0001c0001t0002g0156 a0001c0001t0002g0160 a0001c0001t0013g0155 others(4): Show |
7 | NA18959.hp2 NA18964.hp1 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.269+184A>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 2/7 | chr4 | 25028323 | |||||||
chr4:25028334 | C | T | 38 | a0001c0001t0001g0117 a0001c0001t0001g0120 a0001c0001t0001g0126 others(35): Show |
41 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.269+173G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 2/7 | chr4 | 25028334 | |||||||
chr4:25028390 | G | A | 1 | a0001c0001t0006g0312 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.269+117C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 2/7 | chr4 | 25028390 | |||||||
chr4:25028447 | G | A | 1 | a0001c0001t0002g0313 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.269+60C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 2/7 | chr4 | 25028447 | |||||||
chr4:25028582 | C | T | 1 | a0002c0004t0003g0058 | 1 | HG03239.hp1 | splice_region_variant&intron_variant | LOW | c.198-4G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 1/7 | chr4 | 25028582 | |||||||
chr4:25028690 | G | C | 166 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0146 others(163): Show |
192 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.198-112C>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 1/7 | chr4 | 25028690 | |||||||
chr4:25028917 | C | T | 1 | a0001c0001t0007g0233 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.198-339G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 1/7 | chr4 | 25028917 | |||||||
chr4:25028932 | G | C | 1 | a0001c0001t0014g0203 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.198-354C>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 1/7 | chr4 | 25028932 | |||||||
chr4:25028950 | G | T | 2 | a0001c0001t0001g0202 a0001c0001t0004g0210 |
2 | HG01243.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.198-372C>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 1/7 | chr4 | 25028950 | |||||||
chr4:25029051 | G | A | 1 | a0001c0001t0002g0160 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.198-473C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 1/7 | chr4 | 25029051 | |||||||
chr4:25029056 | A | T | 86 | a0001c0001t0001g0202 a0001c0001t0001g0222 a0001c0001t0001g0226 others(83): Show |
93 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.198-478T>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 1/7 | chr4 | 25029056 | |||||||
chr4:25029197 | A | C | 7 | a0001c0001t0004g0166 a0001c0001t0005g0167 a0001c0001t0005g0169 others(4): Show |
10 | HG02630.hp2 HG02717.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.198-619T>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 1/7 | chr4 | 25029197 | |||||||
chr4:25029218 | G | C | 4 | a0001c0001t0014g0200 a0001c0001t0020g0198 a0001c0001t0020g0199 others(1): Show |
4 | HG01168.hp1 HG02280.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.198-640C>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 1/7 | chr4 | 25029218 | |||||||
chr4:25029381 | G | A | 1 | a0002c0002t0001g0114 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.198-803C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 1/7 | chr4 | 25029381 | |||||||
chr4:25029493 | C | T | 10 | a0001c0001t0002g0003 a0001c0001t0002g0037 a0001c0001t0002g0360 others(7): Show |
14 | HG02135.hp1 NA18942.hp2 NA18944.hp2 others(11): Show |
intron_variant | MODIFIER | c.198-915G>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 1/7 | chr4 | 25029493 | |||||||
chr4:25029496 | T | G | 1 | a0001c0001t0001g0201 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.198-918A>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 1/7 | chr4 | 25029496 | |||||||
chr4:25029586 | G | A | 1 | a0001c0001t0003g0359 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.197+911C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 1/7 | chr4 | 25029586 | |||||||
chr4:25029758 | G | T | 5 | a0001c0001t0004g0165 a0001c0001t0005g0162 a0001c0001t0005g0163 others(2): Show |
5 | HG02486.hp1 HG02818.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.197+739C>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 1/7 | chr4 | 25029758 | |||||||
chr4:25029886 | G | T | 48 | a0001c0001t0001g0117 a0001c0001t0001g0120 a0001c0001t0001g0126 others(45): Show |
54 | HG00544.hp1 HG00544.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.197+611C>A | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 1/7 | chr4 | 25029886 | |||||||
chr4:25029904 | G | A | 84 | a0001c0001t0002g0398 a0002c0002t0001g0051 a0002c0002t0001g0052 others(81): Show |
92 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.197+593C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 1/7 | chr4 | 25029904 | |||||||
chr4:25030057 | A | G | 1 | a0001c0014t0004g0209 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.197+440T>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 1/7 | chr4 | 25030057 | |||||||
chr4:25030091 | A | AAC | 173 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(170): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.197+404_197+405dup others(2): Show |
LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 1/7 | chr4 | 25030091 | |||||||
chr4:25030091 | A | AACAC | 7 | a0001c0001t0002g0156 a0001c0001t0002g0160 a0001c0001t0003g0154 others(4): Show |
7 | HG04184.hp1 NA18959.hp2 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.197+402_197+405dup others(4): Show |
LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 1/7 | chr4 | 25030091 | |||||||
chr4:25030091 | A | AACACAC | 7 | a0001c0001t0001g0202 a0001c0001t0003g0204 a0001c0001t0003g0205 others(4): Show |
7 | HG01243.hp1 HG01891.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.197+400_197+405dup others(6): Show |
LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 1/7 | chr4 | 25030091 | |||||||
chr4:25030130 | A | G | 1 | a0005c0012t0001g0153 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.197+367T>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 1/7 | chr4 | 25030130 | |||||||
chr4:25030204 | T | C | 263 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(260): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.197+293A>G | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 1/7 | chr4 | 25030204 | |||||||
chr4:25030243 | A | G | 41 | a0001c0001t0001g0117 a0001c0001t0001g0120 a0001c0001t0001g0126 others(38): Show |
47 | HG00544.hp1 HG00544.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.197+254T>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 1/7 | chr4 | 25030243 | |||||||
chr4:25030319 | A | G | 1 | a0006c0016t0006g0399 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.197+178T>C | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 1/7 | chr4 | 25030319 | |||||||
chr4:25030459 | G | A | 1 | a0002c0002t0004g0116 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.197+38C>T | LGI2 | ENSG00000153012.12 | transcript | ENST00000382114.9 | protein_coding | 1/7 | chr4 | 25030459 |