Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 84894 |
| ensemblid | ENSG00000169783.13 |
| hgncid | 21205 |
| symbol | LINGO1 |
| name | leucine rich repeat and Ig domain containing 1 |
| refseq_nuc | NM_032808.7 |
| refseq_prot | NP_116197.4 |
| ensembl_nuc | ENST00000355300.7 |
| ensembl_prot | ENSP00000347451.6 |
| mane_status | MANE Select |
| chr | chr15 |
| start | 77613027 |
| end | 77632912 |
| strand | - |
| ver | v1.2 |
| region | chr15:77613027-77632912 |
| region5000 | chr15:77608027-77637912 |
| regionname0 | LINGO1_chr15_77613027_77632912 |
| regionname5000 | LINGO1_chr15_77608027_77637912 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 620 | 379 | 94 | 80 | 151 | 18 | 36 | 111 | LINGO1_chr15_77608027_77637912 | LINGO1 | MQVSK others(615): Show |
chr15 | 77608027 | 77637912 |
| a0002 | 0/0 | 620 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | MQVSK others(615): Show |
chr15 | 77608027 | 77637912 |
| a0003 | 0/0 | 620 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | MQVSK others(615): Show |
chr15 | 77608027 | 77637912 |
| a0004 | 0/0 | 349 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LINGO1_chr15_77608027_77637912 | LINGO1 | MQVSK others(344): Show |
chr15 | 77608027 | 77637912 |
| a0005 | 0/0 | 130 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LINGO1_chr15_77608027_77637912 | LINGO1 | MQVSK others(125): Show |
chr15 | 77608027 | 77637912 |
| a0006 | 0/0 | 254 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LINGO1_chr15_77608027_77637912 | LINGO1 | MQVSK others(249): Show |
chr15 | 77608027 | 77637912 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1860 | 154 | 50 | 28 | 62 | 4 | 10 | LINGO1_chr15_77608027_77637912 | LINGO1 | ATGCA others(1855): Show |
chr15 | 77608027 | 77637912 | ||
| a0001c0002 | 0/0 | 1860 | 112 | 12 | 25 | 54 | 5 | 16 | LINGO1_chr15_77608027_77637912 | LINGO1 | ATGCA others(1855): Show |
chr15 | 77608027 | 77637912 | ||
| a0001c0003 | 0/0 | 1860 | 89 | 24 | 26 | 22 | 8 | 9 | LINGO1_chr15_77608027_77637912 | LINGO1 | ATGCA others(1855): Show |
chr15 | 77608027 | 77637912 | ||
| a0001c0004 | 0/0 | 1860 | 6 | 5 | 0 | 0 | 1 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | ATGCA others(1855): Show |
chr15 | 77608027 | 77637912 | ||
| a0001c0005 | 0/0 | 1860 | 5 | 0 | 0 | 5 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | ATGCA others(1855): Show |
chr15 | 77608027 | 77637912 | ||
| a0001c0006 | 0/0 | 1860 | 4 | 0 | 0 | 3 | 0 | 1 | LINGO1_chr15_77608027_77637912 | LINGO1 | ATGCA others(1855): Show |
chr15 | 77608027 | 77637912 | ||
| a0001c0007 | 0/0 | 1860 | 4 | 0 | 0 | 4 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | ATGCA others(1855): Show |
chr15 | 77608027 | 77637912 | ||
| a0001c0008 | 0/0 | 1860 | 3 | 3 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | ATGCA others(1855): Show |
chr15 | 77608027 | 77637912 | ||
| a0001c0010 | 0/0 | 1860 | 1 | 0 | 0 | 1 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | ATGCA others(1855): Show |
chr15 | 77608027 | 77637912 | ||
| a0001c0014 | 0/0 | 1860 | 1 | 0 | 1 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | ATGCA others(1855): Show |
chr15 | 77608027 | 77637912 | ||
| a0002c0009 | 0/0 | 1860 | 1 | 0 | 1 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | ATGCA others(1855): Show |
chr15 | 77608027 | 77637912 | ||
| a0003c0011 | 0/0 | 1860 | 1 | 0 | 1 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | ATGCA others(1855): Show |
chr15 | 77608027 | 77637912 | ||
| a0004c0013 | 0/0 | 1874 | 1 | 0 | 0 | 1 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | ATGCA others(1869): Show |
chr15 | 77608027 | 77637912 | ||
| a0005c0015 | 0/0 | 1858 | 1 | 0 | 0 | 1 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | ATGCA others(1853): Show |
chr15 | 77608027 | 77637912 | ||
| a0006c0012 | 0/0 | 1859 | 1 | 0 | 0 | 1 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | ATGCA others(1854): Show |
chr15 | 77608027 | 77637912 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3477 | 119 | 36 | 21 | 51 | 4 | 7 | LINGO1_chr15_77608027_77637912 | LINGO1 | AGTGC others(3472): Show |
chr15 | 77608027 | 77637912 |
| a0001c0001t0002 | 0/0 | 3477 | 5 | 0 | 4 | 0 | 0 | 1 | LINGO1_chr15_77608027_77637912 | LINGO1 | AGTGC others(3472): Show |
chr15 | 77608027 | 77637912 |
| a0001c0001t0006 | 0/0 | 3477 | 6 | 1 | 0 | 4 | 0 | 1 | LINGO1_chr15_77608027_77637912 | LINGO1 | AGTGC others(3472): Show |
chr15 | 77608027 | 77637912 |
| a0001c0001t0007 | 0/0 | 3477 | 6 | 4 | 2 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | AGTGC others(3472): Show |
chr15 | 77608027 | 77637912 |
| a0001c0001t0008 | 0/0 | 3477 | 1 | 1 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | AGTGC others(3472): Show |
chr15 | 77608027 | 77637912 |
| a0001c0001t0010 | 0/0 | 3477 | 4 | 0 | 0 | 3 | 0 | 1 | LINGO1_chr15_77608027_77637912 | LINGO1 | AGTGC others(3472): Show |
chr15 | 77608027 | 77637912 |
| a0001c0001t0015 | 0/0 | 3477 | 2 | 2 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | AGTGC others(3472): Show |
chr15 | 77608027 | 77637912 |
| a0001c0001t0016 | 0/0 | 3477 | 2 | 2 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | AGTGC others(3472): Show |
chr15 | 77608027 | 77637912 |
| a0001c0001t0017 | 0/0 | 3477 | 1 | 0 | 1 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | AGTGC others(3472): Show |
chr15 | 77608027 | 77637912 |
| a0001c0001t0019 | 0/0 | 3477 | 1 | 1 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | AGTGC others(3472): Show |
chr15 | 77608027 | 77637912 |
| a0001c0001t0020 | 0/0 | 3477 | 1 | 1 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | AGTGC others(3472): Show |
chr15 | 77608027 | 77637912 |
| a0001c0001t0022 | 0/0 | 3477 | 1 | 0 | 0 | 1 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | AGTGC others(3472): Show |
chr15 | 77608027 | 77637912 |
| a0001c0001t0024 | 0/0 | 3477 | 1 | 0 | 0 | 1 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | AGTGC others(3472): Show |
chr15 | 77608027 | 77637912 |
| a0001c0001t0025 | 0/0 | 3477 | 1 | 1 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | AGTGC others(3472): Show |
chr15 | 77608027 | 77637912 |
| a0001c0001t0026 | 0/0 | 3477 | 1 | 0 | 0 | 1 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | AGTGC others(3472): Show |
chr15 | 77608027 | 77637912 |
| a0001c0001t0027 | 0/0 | 3477 | 1 | 1 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | AGTGC others(3472): Show |
chr15 | 77608027 | 77637912 |
| a0001c0001t0029 | 0/0 | 3477 | 1 | 0 | 0 | 1 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | AGTGC others(3472): Show |
chr15 | 77608027 | 77637912 |
| a0001c0002t0002 | 0/0 | 3477 | 1 | 0 | 0 | 1 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | AGTGC others(3472): Show |
chr15 | 77608027 | 77637912 |
| a0001c0002t0003 | 0/0 | 3477 | 56 | 7 | 21 | 16 | 5 | 7 | LINGO1_chr15_77608027_77637912 | LINGO1 | AGTGC others(3472): Show |
chr15 | 77608027 | 77637912 |
| a0001c0002t0004 | 0/0 | 3477 | 48 | 3 | 2 | 34 | 0 | 9 | LINGO1_chr15_77608027_77637912 | LINGO1 | AGTGC others(3472): Show |
chr15 | 77608027 | 77637912 |
| a0001c0002t0011 | 0/0 | 3477 | 3 | 2 | 1 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | AGTGC others(3472): Show |
chr15 | 77608027 | 77637912 |
| a0001c0002t0013 | 0/0 | 3477 | 3 | 0 | 0 | 3 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | AGTGC others(3472): Show |
chr15 | 77608027 | 77637912 |
| a0001c0002t0021 | 0/0 | 3477 | 1 | 0 | 1 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | AGTGC others(3472): Show |
chr15 | 77608027 | 77637912 |
| a0001c0003t0002 | 0/0 | 3477 | 60 | 6 | 20 | 18 | 7 | 9 | LINGO1_chr15_77608027_77637912 | LINGO1 | AGTGC others(3472): Show |
chr15 | 77608027 | 77637912 |
| a0001c0003t0003 | 0/0 | 3477 | 1 | 1 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | AGTGC others(3472): Show |
chr15 | 77608027 | 77637912 |
| a0001c0003t0005 | 0/0 | 3477 | 10 | 0 | 5 | 4 | 1 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | AGTGC others(3472): Show |
chr15 | 77608027 | 77637912 |
| a0001c0003t0006 | 0/0 | 3477 | 3 | 3 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | AGTGC others(3472): Show |
chr15 | 77608027 | 77637912 |
| a0001c0003t0009 | 0/0 | 3477 | 5 | 5 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | AGTGC others(3472): Show |
chr15 | 77608027 | 77637912 |
| a0001c0003t0012 | 0/0 | 3483 | 3 | 2 | 1 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | AGTGC others(3478): Show |
chr15 | 77608027 | 77637912 |
| a0001c0003t0014 | 0/0 | 3477 | 2 | 2 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | AGTGC others(3472): Show |
chr15 | 77608027 | 77637912 |
| a0001c0003t0017 | 0/0 | 3477 | 1 | 1 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | AGTGC others(3472): Show |
chr15 | 77608027 | 77637912 |
| a0001c0003t0018 | 0/0 | 3462 | 2 | 2 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | AGTGC others(3457): Show |
chr15 | 77608027 | 77637912 |
| a0001c0003t0023 | 0/0 | 3477 | 1 | 1 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | AGTGC others(3472): Show |
chr15 | 77608027 | 77637912 |
| a0001c0003t0030 | 0/0 | 3483 | 1 | 1 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | AGTGC others(3478): Show |
chr15 | 77608027 | 77637912 |
| a0001c0004t0007 | 0/0 | 3477 | 2 | 1 | 0 | 0 | 1 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | AGTGC others(3472): Show |
chr15 | 77608027 | 77637912 |
| a0001c0004t0008 | 0/0 | 3477 | 4 | 4 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | AGTGC others(3472): Show |
chr15 | 77608027 | 77637912 |
| a0001c0005t0001 | 0/0 | 3477 | 5 | 0 | 0 | 5 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | AGTGC others(3472): Show |
chr15 | 77608027 | 77637912 |
| a0001c0006t0003 | 0/0 | 3477 | 4 | 0 | 0 | 3 | 0 | 1 | LINGO1_chr15_77608027_77637912 | LINGO1 | AGTGC others(3472): Show |
chr15 | 77608027 | 77637912 |
| a0001c0007t0003 | 0/0 | 3477 | 4 | 0 | 0 | 4 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | AGTGC others(3472): Show |
chr15 | 77608027 | 77637912 |
| a0001c0008t0001 | 0/0 | 3477 | 3 | 3 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | AGTGC others(3472): Show |
chr15 | 77608027 | 77637912 |
| a0001c0010t0002 | 0/0 | 3477 | 1 | 0 | 0 | 1 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | AGTGC others(3472): Show |
chr15 | 77608027 | 77637912 |
| a0001c0014t0001 | 0/0 | 3477 | 1 | 0 | 1 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | AGTGC others(3472): Show |
chr15 | 77608027 | 77637912 |
| a0002c0009t0003 | 0/0 | 3477 | 1 | 0 | 1 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | AGTGC others(3472): Show |
chr15 | 77608027 | 77637912 |
| a0003c0011t0001 | 0/0 | 3477 | 1 | 0 | 1 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | AGTGC others(3472): Show |
chr15 | 77608027 | 77637912 |
| a0004c0013t0028 | 0/0 | 3491 | 1 | 0 | 0 | 1 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | AGTGC others(3486): Show |
chr15 | 77608027 | 77637912 |
| a0005c0015t0003 | 0/0 | 3475 | 1 | 0 | 0 | 1 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | AGTGC others(3470): Show |
chr15 | 77608027 | 77637912 |
| a0006c0012t0004 | 0/0 | 3476 | 1 | 0 | 0 | 1 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | AGTGC others(3471): Show |
chr15 | 77608027 | 77637912 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 27 | 4 | 5 | 17 | 1 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0001g0006 | 0/0 | 10 | 4 | 2 | 2 | 0 | 2 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0001g0007 | 0/0 | 9 | 0 | 2 | 7 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0001g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0001g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0001g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0001g0050 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0001g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0002g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0006g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0006g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0006g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0006g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0006g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0007g0018 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0007g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0007g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0008g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0010g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0010g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0010g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0015g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0015g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0016g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0016g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0017g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0019g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0020g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0022g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0024g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0025g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0026g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0027g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0001t0029g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0002t0003g0003 | 0/0 | 15 | 0 | 9 | 6 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0002t0003g0008 | 0/0 | 7 | 0 | 4 | 0 | 3 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0002t0003g0009 | 0/0 | 7 | 5 | 0 | 2 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0002t0003g0011 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0002t0003g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0002t0003g0045 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0002t0003g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0002t0003g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0002t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0002t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0002t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0002t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0002t0003g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0002t0003g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0002t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0002t0003g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0002t0003g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0002t0003g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0002t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0002t0003g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0002t0003g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0002t0003g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0002t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0002t0003g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0002t0004g0001 | 0/0 | 31 | 0 | 1 | 22 | 0 | 8 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0002t0004g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0002t0004g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0002t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0002t0004g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0002t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0002t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0002t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0002t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0002t0004g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0002t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0002t0004g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0002t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0002t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0002t0004g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0002t0004g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0002t0011g0019 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0002t0013g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0002t0013g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0002t0021g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0003t0002g0004 | 0/0 | 13 | 0 | 3 | 8 | 0 | 2 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0003t0002g0005 | 0/0 | 12 | 4 | 5 | 0 | 2 | 1 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0003t0002g0012 | 0/0 | 4 | 0 | 1 | 0 | 2 | 1 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0003t0002g0015 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0003t0002g0024 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0003t0002g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0003t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0003t0002g0037 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0003t0002g0038 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0003t0002g0039 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0003t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0003t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0003t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0003t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0003t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0003t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0003t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0003t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0003t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0003t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0003t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0003t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0003t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0003t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0003t0005g0010 | 0/0 | 6 | 0 | 3 | 3 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0003t0005g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0003t0005g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0003t0005g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0003t0006g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0003t0006g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0003t0006g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0003t0009g0027 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0003t0009g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0003t0009g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0003t0012g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0003t0012g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0003t0012g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0003t0014g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0003t0014g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0003t0017g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0003t0018g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0003t0018g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0003t0023g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0003t0030g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0004t0007g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0004t0007g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0004t0008g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0004t0008g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0005t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0005t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0006t0003g0022 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0006t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0007t0003g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0008t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0008t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0010t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0001c0014t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0002c0009t0003g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0003c0011t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0004c0013t0028g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0005c0015t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| a0006c0012t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0002 | g0160 | EUR | GBR | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG00099 | hp2 | a0001 | c0003 | t0002 | g0005 | EUR | GBR | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG00140 | hp1 | a0001 | c0002 | t0003 | g0008 | EUR | GBR | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG00140 | hp2 | a0001 | c0002 | t0003 | g0090 | EUR | GBR | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG00280 | hp1 | a0001 | c0003 | t0002 | g0162 | EUR | FIN | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG00280 | hp2 | a0001 | c0002 | t0003 | g0008 | EUR | FIN | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG00323 | hp2 | a0001 | c0003 | t0002 | g0150 | EUR | FIN | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG00408 | hp1 | a0001 | c0006 | t0003 | g0097 | EAS | CHS | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | CHS | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG00423 | hp2 | a0001 | c0002 | t0004 | g0001 | EAS | CHS | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG00438 | hp1 | a0001 | c0002 | t0003 | g0009 | EAS | CHS | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG00609 | hp2 | a0001 | c0002 | t0003 | g0023 | EAS | CHS | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG00621 | hp2 | a0001 | c0002 | t0013 | g0100 | EAS | CHS | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG00639 | hp1 | a0001 | c0003 | t0002 | g0005 | AMR | PUR | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG00639 | hp2 | a0001 | c0002 | t0021 | g0054 | AMR | PUR | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG00642 | hp1 | a0001 | c0002 | t0004 | g0063 | AMR | PUR | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG00642 | hp2 | a0001 | c0002 | t0003 | g0008 | AMR | PUR | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG00673 | hp1 | a0001 | c0002 | t0002 | g0135 | EAS | CHS | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG00673 | hp2 | a0001 | c0002 | t0004 | g0001 | EAS | CHS | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG00733 | hp1 | a0001 | c0002 | t0003 | g0003 | AMR | PUR | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0082 | AMR | PUR | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG00735 | hp2 | a0001 | c0002 | t0003 | g0003 | AMR | PUR | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG00738 | hp1 | a0001 | c0002 | t0003 | g0008 | AMR | PUR | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG00738 | hp2 | a0001 | c0003 | t0002 | g0024 | AMR | PUR | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG00741 | hp1 | a0001 | c0003 | t0002 | g0024 | AMR | PUR | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG00741 | hp2 | a0001 | c0003 | t0002 | g0037 | AMR | PUR | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01069 | hp1 | a0001 | c0003 | t0002 | g0005 | AMR | PUR | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01070 | hp1 | a0001 | c0003 | t0002 | g0039 | AMR | PUR | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01070 | hp2 | a0001 | c0002 | t0003 | g0011 | AMR | PUR | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01071 | hp1 | a0001 | c0003 | t0002 | g0005 | AMR | PUR | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01071 | hp2 | a0001 | c0002 | t0003 | g0011 | AMR | PUR | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01074 | hp1 | a0001 | c0014 | t0001 | g0129 | AMR | PUR | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01081 | hp2 | a0001 | c0003 | t0002 | g0005 | AMR | PUR | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01099 | hp1 | a0001 | c0003 | t0002 | g0012 | AMR | PUR | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01109 | hp1 | a0001 | c0001 | t0007 | g0018 | AMR | PUR | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01109 | hp2 | a0001 | c0003 | t0002 | g0091 | AMR | PUR | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01167 | hp2 | a0001 | c0002 | t0003 | g0008 | AMR | PUR | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01175 | hp1 | a0001 | c0003 | t0005 | g0036 | AMR | PUR | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01243 | hp1 | a0001 | c0003 | t0012 | g0187 | AMR | PUR | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01255 | hp1 | a0002 | c0009 | t0003 | g0127 | AMR | CLM | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01255 | hp2 | a0001 | c0002 | t0011 | g0019 | AMR | CLM | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01256 | hp1 | a0001 | c0002 | t0003 | g0011 | AMR | CLM | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01257 | hp2 | a0001 | c0003 | t0002 | g0004 | AMR | CLM | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01258 | hp1 | a0001 | c0002 | t0003 | g0011 | AMR | CLM | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01258 | hp2 | a0001 | c0003 | t0002 | g0004 | AMR | CLM | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01261 | hp2 | a0001 | c0003 | t0002 | g0015 | AMR | CLM | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01358 | hp1 | a0001 | c0002 | t0003 | g0008 | AMR | CLM | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01358 | hp2 | a0001 | c0001 | t0017 | g0116 | AMR | CLM | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01361 | hp1 | a0001 | c0003 | t0002 | g0015 | AMR | CLM | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01433 | hp1 | a0001 | c0003 | t0002 | g0004 | AMR | CLM | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01433 | hp2 | a0001 | c0003 | t0002 | g0024 | AMR | CLM | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01496 | hp1 | a0001 | c0001 | t0007 | g0031 | AMR | CLM | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01496 | hp2 | a0001 | c0003 | t0002 | g0015 | AMR | CLM | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01515 | hp1 | a0001 | c0003 | t0005 | g0125 | EUR | IBS | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0041 | EUR | IBS | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01516 | hp1 | a0001 | c0003 | t0002 | g0012 | EUR | IBS | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01516 | hp2 | a0001 | c0004 | t0007 | g0073 | EUR | IBS | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0041 | EUR | IBS | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01517 | hp2 | a0001 | c0003 | t0002 | g0012 | EUR | IBS | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01884 | hp2 | a0001 | c0003 | t0030 | g0194 | AFR | ACB | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01891 | hp1 | a0001 | c0001 | t0008 | g0179 | AFR | ACB | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01928 | hp1 | a0001 | c0002 | t0003 | g0003 | AMR | PEL | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01928 | hp2 | a0001 | c0003 | t0005 | g0010 | AMR | PEL | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01943 | hp1 | a0001 | c0002 | t0003 | g0172 | AMR | PEL | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01943 | hp2 | a0001 | c0003 | t0005 | g0010 | AMR | PEL | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01952 | hp1 | a0001 | c0002 | t0003 | g0079 | AMR | PEL | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01952 | hp2 | a0001 | c0002 | t0003 | g0003 | AMR | PEL | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01975 | hp1 | a0001 | c0002 | t0003 | g0003 | AMR | PEL | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01975 | hp2 | a0001 | c0002 | t0003 | g0152 | AMR | PEL | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01978 | hp1 | a0001 | c0003 | t0002 | g0148 | AMR | PEL | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01978 | hp2 | a0001 | c0002 | t0003 | g0164 | AMR | PEL | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01993 | hp1 | a0001 | c0002 | t0003 | g0003 | AMR | PEL | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02004 | hp1 | a0001 | c0003 | t0002 | g0142 | AMR | PEL | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02004 | hp2 | a0001 | c0002 | t0004 | g0001 | AMR | PEL | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02055 | hp1 | a0001 | c0003 | t0014 | g0075 | AFR | ACB | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02055 | hp2 | a0001 | c0001 | t0016 | g0183 | AFR | ACB | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02071 | hp1 | a0001 | c0003 | t0002 | g0025 | EAS | KHV | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02071 | hp2 | a0001 | c0002 | t0004 | g0001 | EAS | KHV | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02080 | hp1 | a0001 | c0003 | t0002 | g0004 | EAS | KHV | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02080 | hp2 | a0001 | c0003 | t0002 | g0149 | EAS | KHV | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02083 | hp1 | a0001 | c0003 | t0002 | g0004 | EAS | KHV | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02129 | hp1 | a0001 | c0002 | t0003 | g0009 | EAS | KHV | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02129 | hp2 | a0001 | c0001 | t0006 | g0155 | EAS | KHV | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02135 | hp1 | a0001 | c0001 | t0010 | g0066 | EAS | KHV | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02135 | hp2 | a0001 | c0003 | t0002 | g0086 | EAS | KHV | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | ACB | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02145 | hp2 | a0001 | c0002 | t0003 | g0009 | AFR | ACB | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02148 | hp2 | a0001 | c0002 | t0003 | g0003 | AMR | PEL | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CDX | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02155 | hp2 | a0001 | c0002 | t0003 | g0098 | EAS | CDX | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | CDX | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02258 | hp1 | a0001 | c0002 | t0004 | g0070 | AFR | ACB | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02258 | hp2 | a0001 | c0008 | t0001 | g0046 | AFR | ACB | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02273 | hp1 | a0001 | c0002 | t0003 | g0003 | AMR | PEL | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02273 | hp2 | a0003 | c0011 | t0001 | g0088 | AMR | PEL | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02280 | hp1 | a0001 | c0002 | t0003 | g0009 | AFR | ACB | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02300 | hp1 | a0001 | c0002 | t0003 | g0003 | AMR | PEL | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02300 | hp2 | a0001 | c0003 | t0005 | g0010 | AMR | PEL | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02451 | hp1 | a0001 | c0004 | t0008 | g0026 | AFR | ACB | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02451 | hp2 | a0001 | c0001 | t0015 | g0132 | AFR | ACB | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02523 | hp1 | a0001 | c0003 | t0002 | g0025 | EAS | KHV | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02602 | hp1 | a0001 | c0003 | t0002 | g0015 | SAS | PJL | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02602 | hp2 | a0001 | c0003 | t0002 | g0005 | SAS | PJL | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02615 | hp1 | a0001 | c0003 | t0009 | g0171 | AFR | GWD | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02622 | hp2 | a0001 | c0003 | t0002 | g0188 | AFR | GWD | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02630 | hp1 | a0001 | c0001 | t0007 | g0018 | AFR | GWD | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02647 | hp1 | a0001 | c0001 | t0007 | g0072 | AFR | GWD | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0080 | SAS | PJL | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02683 | hp2 | a0001 | c0002 | t0004 | g0001 | SAS | PJL | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02717 | hp1 | a0001 | c0001 | t0027 | g0184 | AFR | GWD | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02717 | hp2 | a0001 | c0003 | t0009 | g0027 | AFR | GWD | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02735 | hp1 | a0001 | c0002 | t0004 | g0001 | SAS | PJL | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02735 | hp2 | a0001 | c0002 | t0003 | g0134 | SAS | PJL | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02738 | hp1 | a0001 | c0002 | t0003 | g0045 | SAS | PJL | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02738 | hp2 | a0001 | c0003 | t0002 | g0012 | SAS | PJL | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02809 | hp1 | a0001 | c0001 | t0007 | g0031 | AFR | GWD | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02886 | hp1 | a0001 | c0003 | t0003 | g0186 | AFR | GWD | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02886 | hp2 | a0001 | c0003 | t0006 | g0176 | AFR | GWD | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02896 | hp1 | a0001 | c0003 | t0009 | g0027 | AFR | GWD | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02922 | hp1 | a0001 | c0008 | t0001 | g0078 | AFR | ESN | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02922 | hp2 | a0001 | c0001 | t0025 | g0126 | AFR | ESN | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02965 | hp1 | a0001 | c0003 | t0018 | g0192 | AFR | ESN | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | ESN | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02970 | hp1 | a0001 | c0001 | t0007 | g0018 | AFR | ESN | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02970 | hp2 | a0001 | c0003 | t0023 | g0077 | AFR | ESN | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02976 | hp2 | a0001 | c0002 | t0003 | g0009 | AFR | ESN | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG03017 | hp2 | a0001 | c0003 | t0002 | g0004 | SAS | PJL | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG03041 | hp1 | a0001 | c0004 | t0008 | g0026 | AFR | GWD | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG03041 | hp2 | a0001 | c0004 | t0008 | g0139 | AFR | GWD | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG03098 | hp1 | a0001 | c0003 | t0012 | g0159 | AFR | MSL | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG03098 | hp2 | a0001 | c0001 | t0020 | g0053 | AFR | MSL | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG03130 | hp1 | a0001 | c0003 | t0018 | g0191 | AFR | ESN | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ESN | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG03139 | hp1 | a0001 | c0002 | t0003 | g0009 | AFR | ESN | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG03139 | hp2 | a0001 | c0003 | t0006 | g0174 | AFR | ESN | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG03195 | hp1 | a0001 | c0003 | t0002 | g0005 | AFR | ESN | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG03195 | hp2 | a0001 | c0003 | t0014 | g0076 | AFR | ESN | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG03209 | hp1 | a0001 | c0001 | t0006 | g0168 | AFR | MSL | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG03225 | hp2 | a0001 | c0002 | t0003 | g0105 | AFR | MSL | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG03239 | hp1 | a0001 | c0003 | t0002 | g0039 | SAS | PJL | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG03239 | hp2 | a0001 | c0001 | t0010 | g0064 | SAS | PJL | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG03453 | hp1 | a0001 | c0003 | t0002 | g0005 | AFR | MSL | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | MSL | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG03486 | hp2 | a0001 | c0003 | t0002 | g0146 | AFR | MSL | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG03490 | hp1 | a0001 | c0002 | t0003 | g0118 | SAS | PJL | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG03490 | hp2 | a0001 | c0002 | t0004 | g0001 | SAS | PJL | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG03491 | hp1 | a0001 | c0002 | t0003 | g0045 | SAS | PJL | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG03492 | hp1 | a0001 | c0002 | t0004 | g0001 | SAS | PJL | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG03516 | hp1 | a0001 | c0002 | t0003 | g0009 | AFR | ESN | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG03516 | hp2 | a0001 | c0003 | t0017 | g0165 | AFR | ESN | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG03540 | hp1 | a0001 | c0003 | t0009 | g0027 | AFR | GWD | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | MSL | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG03579 | hp2 | a0001 | c0004 | t0008 | g0026 | AFR | MSL | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG03654 | hp1 | a0001 | c0003 | t0002 | g0037 | SAS | PJL | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG03654 | hp2 | a0001 | c0002 | t0004 | g0001 | SAS | PJL | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | STU | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG03688 | hp2 | a0001 | c0002 | t0004 | g0067 | SAS | STU | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG03704 | hp1 | a0001 | c0001 | t0006 | g0120 | SAS | PJL | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG03704 | hp2 | a0001 | c0002 | t0003 | g0145 | SAS | PJL | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG03710 | hp1 | a0001 | c0003 | t0002 | g0038 | SAS | PJL | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG03710 | hp2 | a0001 | c0002 | t0003 | g0143 | SAS | PJL | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG03834 | hp1 | a0001 | c0006 | t0003 | g0022 | SAS | BEB | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG03834 | hp2 | a0001 | c0002 | t0004 | g0001 | SAS | BEB | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | BEB | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG03927 | hp2 | a0001 | c0003 | t0002 | g0004 | SAS | BEB | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG04115 | hp1 | a0001 | c0002 | t0004 | g0001 | SAS | STU | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG04115 | hp2 | a0001 | c0003 | t0002 | g0140 | SAS | STU | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG04204 | hp1 | a0001 | c0002 | t0003 | g0122 | SAS | STU | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | STU | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | STU | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG04228 | hp2 | a0001 | c0002 | t0004 | g0001 | SAS | STU | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | YRI | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18612 | hp1 | a0001 | c0003 | t0002 | g0038 | EAS | CHB | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18612 | hp2 | a0001 | c0002 | t0004 | g0001 | EAS | CHB | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18747 | hp2 | a0001 | c0002 | t0004 | g0065 | EAS | CHB | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18906 | hp1 | a0001 | c0003 | t0006 | g0173 | AFR | YRI | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18906 | hp2 | a0001 | c0003 | t0012 | g0128 | AFR | YRI | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18939 | hp1 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18939 | hp2 | a0001 | c0001 | t0024 | g0107 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18940 | hp1 | a0001 | c0007 | t0003 | g0016 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18944 | hp1 | a0001 | c0002 | t0003 | g0106 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18947 | hp2 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18948 | hp1 | a0001 | c0002 | t0013 | g0034 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18948 | hp2 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18949 | hp1 | a0001 | c0003 | t0002 | g0004 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18950 | hp1 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18950 | hp2 | a0001 | c0003 | t0005 | g0010 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18951 | hp1 | a0001 | c0001 | t0010 | g0030 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18951 | hp2 | a0001 | c0003 | t0005 | g0010 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18953 | hp1 | a0001 | c0006 | t0003 | g0022 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18954 | hp1 | a0001 | c0002 | t0004 | g0068 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18954 | hp2 | a0001 | c0003 | t0002 | g0004 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18956 | hp1 | a0001 | c0001 | t0006 | g0131 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18956 | hp2 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18959 | hp1 | a0001 | c0006 | t0003 | g0022 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18959 | hp2 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18960 | hp2 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18964 | hp1 | a0001 | c0003 | t0002 | g0032 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18966 | hp1 | a0001 | c0001 | t0026 | g0109 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18966 | hp2 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18969 | hp2 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18970 | hp2 | a0001 | c0002 | t0004 | g0057 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18971 | hp1 | a0001 | c0005 | t0001 | g0013 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18971 | hp2 | a0001 | c0003 | t0002 | g0025 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18974 | hp2 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18975 | hp1 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18975 | hp2 | a0001 | c0005 | t0001 | g0013 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18979 | hp1 | a0004 | c0013 | t0028 | g0087 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18979 | hp2 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18980 | hp1 | a0001 | c0002 | t0003 | g0147 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18980 | hp2 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18983 | hp1 | a0001 | c0007 | t0003 | g0016 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18983 | hp2 | a0001 | c0002 | t0004 | g0056 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18984 | hp1 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18984 | hp2 | a0001 | c0003 | t0002 | g0004 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18985 | hp1 | a0001 | c0002 | t0004 | g0028 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18985 | hp2 | a0001 | c0002 | t0003 | g0023 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18991 | hp2 | a0001 | c0002 | t0004 | g0058 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18992 | hp1 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18992 | hp2 | a0005 | c0015 | t0003 | g0093 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18994 | hp1 | a0001 | c0003 | t0002 | g0190 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18994 | hp2 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18997 | hp1 | a0001 | c0002 | t0013 | g0034 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18997 | hp2 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18998 | hp1 | a0001 | c0003 | t0002 | g0004 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA19000 | hp2 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA19002 | hp1 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA19002 | hp2 | a0001 | c0010 | t0002 | g0092 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA19004 | hp1 | a0001 | c0002 | t0004 | g0029 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA19004 | hp2 | a0001 | c0002 | t0004 | g0061 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA19007 | hp1 | a0001 | c0001 | t0006 | g0035 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA19007 | hp2 | a0001 | c0005 | t0001 | g0104 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA19009 | hp1 | a0001 | c0002 | t0004 | g0060 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | LWK | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA19030 | hp2 | a0001 | c0008 | t0001 | g0046 | AFR | LWK | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | LWK | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | LWK | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA19054 | hp2 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA19055 | hp1 | a0001 | c0007 | t0003 | g0016 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA19055 | hp2 | a0001 | c0002 | t0003 | g0023 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA19056 | hp1 | a0001 | c0002 | t0003 | g0096 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA19056 | hp2 | a0001 | c0001 | t0029 | g0193 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA19057 | hp2 | a0001 | c0002 | t0004 | g0029 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA19060 | hp1 | a0001 | c0003 | t0005 | g0157 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA19060 | hp2 | a0001 | c0001 | t0010 | g0030 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA19064 | hp1 | a0001 | c0003 | t0002 | g0032 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA19065 | hp1 | a0001 | c0003 | t0002 | g0136 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA19066 | hp1 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA19070 | hp2 | a0001 | c0001 | t0006 | g0035 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA19074 | hp2 | a0001 | c0003 | t0002 | g0004 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA19076 | hp1 | a0001 | c0002 | t0004 | g0062 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA19079 | hp1 | a0001 | c0005 | t0001 | g0013 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA19079 | hp2 | a0001 | c0007 | t0003 | g0016 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA19081 | hp1 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA19081 | hp2 | a0001 | c0003 | t0005 | g0010 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA19083 | hp1 | a0001 | c0001 | t0022 | g0055 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA19083 | hp2 | a0006 | c0012 | t0004 | g0059 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA19084 | hp2 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA19086 | hp1 | a0001 | c0002 | t0003 | g0123 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA19086 | hp2 | a0001 | c0005 | t0001 | g0013 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA19087 | hp1 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA19091 | hp1 | a0001 | c0003 | t0002 | g0004 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA20129 | hp1 | a0001 | c0002 | t0011 | g0019 | AFR | ASW | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA20129 | hp2 | a0001 | c0001 | t0019 | g0052 | AFR | ASW | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA20752 | hp1 | a0001 | c0003 | t0002 | g0005 | EUR | TSI | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0099 | EUR | TSI | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA20805 | hp1 | a0001 | c0002 | t0003 | g0008 | EUR | TSI | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA20805 | hp2 | a0001 | c0002 | t0003 | g0163 | EUR | TSI | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01123 | hp1 | a0001 | c0003 | t0002 | g0005 | AMR | CLM | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG01123 | hp2 | a0001 | c0003 | t0005 | g0036 | AMR | CLM | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02109 | hp1 | a0001 | c0001 | t0015 | g0130 | AFR | ACB | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02109 | hp2 | a0001 | c0002 | t0011 | g0019 | AFR | ACB | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02486 | hp1 | a0001 | c0003 | t0002 | g0005 | AFR | ACB | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02486 | hp2 | a0001 | c0002 | t0004 | g0071 | AFR | ACB | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG02559 | hp2 | a0001 | c0003 | t0009 | g0095 | AFR | ACB | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG03471 | hp1 | a0001 | c0002 | t0004 | g0069 | AFR | MSL | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG03471 | hp2 | a0001 | c0001 | t0016 | g0182 | AFR | MSL | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG06807 | hp1 | a0001 | c0004 | t0007 | g0074 | AFR | USA | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| HG06807 | hp2 | a0001 | c0002 | t0003 | g0169 | AFR | USA | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA18955 | hp2 | a0001 | c0002 | t0004 | g0028 | EAS | JPT | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA20300 | hp1 | a0001 | c0003 | t0002 | g0005 | AFR | USA | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | USA | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | LWK | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | LWK | LINGO1_chr15_77608027_77637912 | LINGO1 | chr15 | 77608027 | 77637912 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:77614223 | T | TG | 1 | a0004 | 1 | NA18979.hp1 | frameshift_variant | HIGH | c.1683dupC | p.Thr562fs | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 2/2 | 2280/3477 | 1683/1863 | 561/620 | chr15 | 77614223 | |||
| chr15:77614273 | C | CG | 1 | a0004 | 1 | NA18979.hp1 | frameshift_variant | HIGH | c.1633dupC | p.Arg545fs | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 2/2 | 2230/3477 | 1633/1863 | 545/620 | chr15 | 77614273 | |||
| chr15:77614380 | G | GGT | 1 | a0004 | 1 | NA18979.hp1 | frameshift_variant | HIGH | c.1526_1527insAC | p.Ala510fs | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 2/2 | 2123/3477 | 1526/1863 | 509/620 | chr15 | 77614380 | |||
| chr15:77614384 | A | AT | 1 | a0004 | 1 | NA18979.hp1 | frameshift_variant | HIGH | c.1522dupA | p.Met508fs | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 2/2 | 2119/3477 | 1522/1863 | 508/620 | chr15 | 77614384 | |||
| chr15:77614508 | A | AG | 1 | a0004 | 1 | NA18979.hp1 | frameshift_variant | HIGH | c.1398dupC | p.Ser467fs | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 2/2 | 1995/3477 | 1398/1863 | 466/620 | chr15 | 77614508 | |||
| chr15:77614934 | C | CGGCCAGC others(1): Show |
1 | a0004 | 1 | NA18979.hp1 | frameshift_variant | HIGH | c.965_972dupAGCTGGCC | p.Val325fs | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 2/2 | 1569/3477 | 972/1863 | 324/620 | chr15 | 77614934 | |||
| chr15:77614947 | GC | G | 1 | a0005 | 1 | NA18992.hp2 | frameshift_variant | HIGH | c.959delG | p.Gly320fs | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 2/2 | 1556/3477 | 959/1863 | 320/620 | chr15 | 77614947 | |||
| chr15:77615237 | GC | G | 1 | a0006 | 1 | NA19083.hp2 | frameshift_variant | HIGH | c.669delG | p.His224fs | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 2/2 | 1266/3477 | 669/1863 | 223/620 | chr15 | 77615237 | |||
| chr15:77615387 | C | T | 1 | a0003 | 1 | HG02273.hp2 | missense_variant | MODERATE | c.520G>A | p.Val174Ile | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 2/2 | 1117/3477 | 520/1863 | 174/620 | chr15 | 77615387 | |||
| chr15:77615532 | AC | A | 1 | a0005 | 1 | NA18992.hp2 | frameshift_variant | HIGH | c.374delG | p.Gly125fs | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 2/2 | 971/3477 | 374/1863 | 125/620 | chr15 | 77615532 | |||
| chr15:77615866 | C | T | 1 | a0002 | 1 | HG01255.hp1 | missense_variant | MODERATE | c.41G>A | p.Ser14Asn | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 2/2 | 638/3477 | 41/1863 | 14/620 | chr15 | 77615866 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:77614194 | G | A | 1 | a0001c0007 | 4 | NA18940.hp1 NA18983.hp1 NA19055.hp1 others(1): Show |
synonymous_variant | LOW | c.1713C>T | p.Val571Val | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 2/2 | 2310/3477 | 1713/1863 | 571/620 | chr15 | 77614194 | |||
| chr15:77614332 | G | A | 1 | a0001c0004 | 6 | HG01516.hp2 HG02451.hp1 HG03041.hp1 others(3): Show |
synonymous_variant | LOW | c.1575C>T | p.Pro525Pro | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 2/2 | 2172/3477 | 1575/1863 | 525/620 | chr15 | 77614332 | |||
| chr15:77614350 | G | A | 1 | a0001c0008 | 3 | HG02258.hp2 HG02922.hp1 NA19030.hp2 |
synonymous_variant | LOW | c.1557C>T | p.Pro519Pro | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 2/2 | 2154/3477 | 1557/1863 | 519/620 | chr15 | 77614350 | |||
| chr15:77614797 | C | T | 1 | a0001c0014 | 1 | HG01074.hp1 | synonymous_variant | LOW | c.1110G>A | p.Pro370Pro | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 2/2 | 1707/3477 | 1110/1863 | 370/620 | chr15 | 77614797 | |||
| chr15:77614803 | G | A | 7 | a0001c0001 a0001c0004 a0001c0005 others(4): Show |
171 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(168): Show |
synonymous_variant | LOW | c.1104C>T | p.Ser368Ser | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 2/2 | 1701/3477 | 1104/1863 | 368/620 | chr15 | 77614803 | |||
| chr15:77615028 | G | A | 1 | a0001c0010 | 1 | NA19002.hp2 | synonymous_variant | LOW | c.879C>T | p.Asn293Asn | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 2/2 | 1476/3477 | 879/1863 | 293/620 | chr15 | 77615028 | |||
| chr15:77615193 | C | G | 12 | a0001c0001 a0001c0002 a0001c0004 others(9): Show |
291 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(288): Show |
synonymous_variant | LOW | c.714G>C | p.Leu238Leu | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 2/2 | 1311/3477 | 714/1863 | 238/620 | chr15 | 77615193 | |||
| chr15:77615433 | T | C | 13 | a0001c0001 a0001c0002 a0001c0004 others(10): Show |
295 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(292): Show |
synonymous_variant | LOW | c.474A>G | p.Leu158Leu | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 2/2 | 1071/3477 | 474/1863 | 158/620 | chr15 | 77615433 | |||
| chr15:77615442 | G | A | 11 | a0001c0001 a0001c0002 a0001c0004 others(8): Show |
286 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(283): Show |
synonymous_variant | LOW | c.465C>T | p.Ile155Ile | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 2/2 | 1062/3477 | 465/1863 | 155/620 | chr15 | 77615442 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:77613224 | T | G | 1 | a0001c0001t0016 | 2 | HG02055.hp2 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*820A>C | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 2/2 | 820 | chr15 | 77613224 | ||||||
| chr15:77613319 | A | G | 41 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(38): Show |
306 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(303): Show |
3_prime_UTR_variant | MODIFIER | c.*725T>C | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 2/2 | 725 | chr15 | 77613319 | ||||||
| chr15:77613344 | G | A | 23 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0010 others(20): Show |
163 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(160): Show |
3_prime_UTR_variant | MODIFIER | c.*700C>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 2/2 | 700 | chr15 | 77613344 | ||||||
| chr15:77613381 | C | T | 1 | a0001c0001t0025 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*663G>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 2/2 | 663 | chr15 | 77613381 | ||||||
| chr15:77613452 | C | T | 1 | a0001c0001t0025 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*592G>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 2/2 | 592 | chr15 | 77613452 | ||||||
| chr15:77613571 | A | AGAGGAG | 2 | a0001c0003t0012 a0001c0003t0030 |
4 | HG01243.hp1 HG01884.hp2 HG03098.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*467_*472dupCTCCTC | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 2/2 | 472 | chr15 | 77613571 | ||||||
| chr15:77613635 | C | T | 1 | a0001c0001t0015 | 2 | HG02109.hp1 HG02451.hp2 |
3_prime_UTR_variant | MODIFIER | c.*409G>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 2/2 | 409 | chr15 | 77613635 | ||||||
| chr15:77613654 | G | A | 1 | a0001c0001t0026 | 1 | NA18966.hp1 | 3_prime_UTR_variant | MODIFIER | c.*390C>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 2/2 | 390 | chr15 | 77613654 | ||||||
| chr15:77613835 | G | C | 1 | a0001c0001t0027 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*209C>G | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 2/2 | 209 | chr15 | 77613835 | ||||||
| chr15:77613862 | T | C | 15 | a0001c0001t0017 a0001c0001t0022 a0001c0002t0003 others(12): Show |
137 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*182A>G | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 2/2 | 182 | chr15 | 77613862 | ||||||
| chr15:77613883 | T | A | 1 | a0004c0013t0028 | 1 | NA18979.hp1 | 3_prime_UTR_variant | MODIFIER | c.*161A>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 2/2 | 161 | chr15 | 77613883 | ||||||
| chr15:77613889 | C | G | 21 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0008 others(18): Show |
161 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(158): Show |
3_prime_UTR_variant | MODIFIER | c.*155G>C | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 2/2 | 155 | chr15 | 77613889 | ||||||
| chr15:77613934 | C | T | 1 | a0001c0001t0024 | 1 | NA18939.hp2 | 3_prime_UTR_variant | MODIFIER | c.*110G>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 2/2 | 110 | chr15 | 77613934 | ||||||
| chr15:77614016 | C | T | 2 | a0001c0003t0012 a0001c0003t0030 |
4 | HG01243.hp1 HG01884.hp2 HG03098.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*28G>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 2/2 | 28 | chr15 | 77614016 | ||||||
| chr15:77632403 | CCCTCCTC others(8): Show |
C | 1 | a0001c0003t0018 | 2 | HG02965.hp1 HG03130.hp1 |
5_prime_UTR_variant | MODIFIER | c.-103_-89delAGGAAAC others(8): Show |
LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/2 | 89 | chr15 | 77632403 | ||||||
| chr15:77632652 | C | G | 5 | a0001c0001t0007 a0001c0002t0011 a0001c0003t0014 others(2): Show |
14 | HG01109.hp1 HG01255.hp2 HG01496.hp1 others(11): Show |
5_prime_UTR_variant | MODIFIER | c.-337G>C | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/2 | 337 | chr15 | 77632652 | ||||||
| chr15:77632654 | G | A | 1 | a0001c0001t0029 | 1 | NA19056.hp2 | 5_prime_UTR_variant | MODIFIER | c.-339C>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/2 | 339 | chr15 | 77632654 | ||||||
| chr15:77632746 | G | A | 5 | a0001c0001t0010 a0001c0001t0022 a0001c0002t0004 others(2): Show |
55 | HG00423.hp2 HG00642.hp1 HG00673.hp2 others(52): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-431C>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/2 | chr15 | 77632746 | |||||||
| chr15:77632895 | G | T | 7 | a0001c0001t0010 a0001c0001t0019 a0001c0001t0020 others(4): Show |
57 | HG00423.hp2 HG00639.hp2 HG00642.hp1 others(54): Show |
5_prime_UTR_variant | MODIFIER | c.-580C>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/2 | 580 | chr15 | 77632895 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:77615908 | C | T | 1 | a0001c0004t0007g0073 | 1 | HG01516.hp2 | splice_region_variant&intron_variant | LOW | c.7-8G>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77615908 | |||||||
| chr15:77615909 | G | A | 2 | a0001c0001t0001g0014 a0001c0001t0001g0141 |
5 | HG01261.hp1 HG01934.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.7-9C>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77615909 | |||||||
| chr15:77615935 | G | A | 6 | a0001c0003t0003g0186 a0001c0003t0006g0173 a0001c0003t0006g0174 others(3): Show |
8 | HG02559.hp2 HG02615.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.7-35C>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77615935 | |||||||
| chr15:77615962 | C | T | 5 | a0001c0003t0003g0186 a0001c0003t0006g0173 a0001c0003t0006g0174 others(2): Show |
7 | HG02615.hp1 HG02717.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.7-62G>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77615962 | |||||||
| chr15:77616018 | G | C | 1 | a0001c0001t0010g0064 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.7-118C>G | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77616018 | |||||||
| chr15:77616044 | C | T | 1 | a0001c0002t0013g0034 | 2 | NA18948.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.7-144G>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77616044 | |||||||
| chr15:77616183 | C | T | 1 | a0001c0003t0002g0190 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.7-283G>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77616183 | |||||||
| chr15:77616218 | C | T | 1 | a0001c0003t0014g0075 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.7-318G>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77616218 | |||||||
| chr15:77616291 | T | C | 168 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(165): Show |
316 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(313): Show |
intron_variant | MODIFIER | c.7-391A>G | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77616291 | |||||||
| chr15:77616359 | C | T | 1 | a0001c0001t0010g0064 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.7-459G>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77616359 | |||||||
| chr15:77616382 | G | A | 3 | a0001c0001t0001g0017 a0001c0001t0001g0177 a0001c0001t0001g0178 |
6 | HG02572.hp1 HG02895.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.7-482C>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77616382 | |||||||
| chr15:77616463 | C | A | 3 | a0001c0003t0003g0186 a0001c0003t0009g0027 a0001c0003t0009g0171 |
5 | HG02615.hp1 HG02717.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.7-563G>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77616463 | |||||||
| chr15:77616463 | C | G | 2 | a0001c0008t0001g0046 a0001c0008t0001g0078 |
3 | HG02258.hp2 HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.7-563G>C | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77616463 | |||||||
| chr15:77616625 | C | G | 1 | a0001c0003t0002g0146 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.7-725G>C | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77616625 | |||||||
| chr15:77616739 | G | A | 3 | a0001c0003t0003g0186 a0001c0003t0009g0027 a0001c0003t0009g0171 |
5 | HG02615.hp1 HG02717.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.7-839C>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77616739 | |||||||
| chr15:77616850 | C | T | 3 | a0001c0003t0003g0186 a0001c0003t0009g0027 a0001c0003t0009g0171 |
5 | HG02615.hp1 HG02717.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.7-950G>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77616850 | |||||||
| chr15:77616864 | C | T | 3 | a0001c0003t0003g0186 a0001c0003t0009g0027 a0001c0003t0009g0171 |
5 | HG02615.hp1 HG02717.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.7-964G>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77616864 | |||||||
| chr15:77616910 | C | G | 2 | a0001c0001t0025g0126 a0001c0003t0006g0176 |
2 | HG02886.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.7-1010G>C | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77616910 | |||||||
| chr15:77617021 | T | C | 13 | a0001c0001t0007g0018 a0001c0001t0007g0031 a0001c0001t0007g0072 others(10): Show |
22 | HG01109.hp1 HG01255.hp2 HG01496.hp1 others(19): Show |
intron_variant | MODIFIER | c.7-1121A>G | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77617021 | |||||||
| chr15:77617128 | G | A | 2 | a0001c0004t0008g0026 a0001c0004t0008g0139 |
4 | HG02451.hp1 HG03041.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.7-1228C>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77617128 | |||||||
| chr15:77617191 | C | T | 1 | a0001c0003t0002g0038 | 2 | HG03710.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.7-1291G>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77617191 | |||||||
| chr15:77617275 | C | A | 1 | a0001c0001t0001g0180 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.7-1375G>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77617275 | |||||||
| chr15:77617369 | CA | C | 7 | a0001c0002t0003g0134 a0001c0002t0021g0054 a0001c0003t0002g0024 others(4): Show |
10 | HG00323.hp2 HG00639.hp2 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.7-1470delT | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77617369 | |||||||
| chr15:77617449 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.7-1549G>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77617449 | |||||||
| chr15:77617570 | A | C | 1 | a0001c0003t0002g0091 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.7-1670T>G | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77617570 | |||||||
| chr15:77617623 | T | C | 159 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(156): Show |
306 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(303): Show |
intron_variant | MODIFIER | c.7-1723A>G | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77617623 | |||||||
| chr15:77617753 | C | T | 162 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(159): Show |
311 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.7-1853G>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77617753 | |||||||
| chr15:77617757 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.7-1857G>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77617757 | |||||||
| chr15:77617860 | G | T | 136 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(133): Show |
271 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(268): Show |
intron_variant | MODIFIER | c.7-1960C>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77617860 | |||||||
| chr15:77617960 | C | T | 7 | a0001c0001t0001g0153 a0001c0001t0007g0018 a0001c0001t0007g0031 others(4): Show |
12 | HG01109.hp1 HG01255.hp2 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.7-2060G>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77617960 | |||||||
| chr15:77618061 | G | A | 1 | a0001c0003t0002g0188 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.7-2161C>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77618061 | |||||||
| chr15:77618146 | C | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0051 |
4 | HG01346.hp2 HG02559.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.7-2246G>C | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77618146 | |||||||
| chr15:77618225 | G | C | 3 | a0001c0002t0003g0169 a0001c0003t0006g0173 a0001c0003t0006g0174 |
3 | HG03139.hp2 HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.7-2325C>G | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77618225 | |||||||
| chr15:77618233 | G | A | 1 | a0001c0001t0015g0132 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.7-2333C>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77618233 | |||||||
| chr15:77618278 | A | G | 148 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(145): Show |
294 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(291): Show |
intron_variant | MODIFIER | c.7-2378T>C | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77618278 | |||||||
| chr15:77618331 | G | A | 1 | a0001c0002t0004g0065 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.7-2431C>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77618331 | |||||||
| chr15:77618519 | ACTGTTAT others(367): Show |
A | 192 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(189): Show |
384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.7-2993_7-2620del | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77618519 | |||||||
| chr15:77618526 | TTCTTTTT others(366): Show |
T | 1 | a0001c0001t0022g0055 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.7-2999_7-2627del | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77618526 | |||||||
| chr15:77618900 | T | C | 1 | a0001c0001t0022g0055 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.7-3000A>G | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77618900 | |||||||
| chr15:77619062 | G | A | 1 | a0001c0003t0002g0038 | 2 | HG03710.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.7-3162C>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77619062 | |||||||
| chr15:77619144 | G | GTATGTT | 145 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(142): Show |
289 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(286): Show |
intron_variant | MODIFIER | c.7-3245_7-3244insAA others(4): Show |
LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77619144 | |||||||
| chr15:77619166 | T | C | 1 | a0001c0003t0002g0162 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.7-3266A>G | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77619166 | |||||||
| chr15:77619188 | G | A | 1 | a0001c0003t0006g0176 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.7-3288C>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77619188 | |||||||
| chr15:77619286 | A | C | 6 | a0001c0001t0001g0185 a0001c0001t0027g0184 a0001c0003t0002g0146 others(3): Show |
6 | HG01243.hp1 HG02622.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.7-3386T>G | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77619286 | |||||||
| chr15:77619389 | C | T | 1 | a0001c0003t0009g0095 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.7-3489G>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77619389 | |||||||
| chr15:77619498 | A | G | 6 | a0001c0001t0001g0185 a0001c0001t0027g0184 a0001c0003t0002g0146 others(3): Show |
6 | HG01243.hp1 HG02622.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.7-3598T>C | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77619498 | |||||||
| chr15:77619586 | T | C | 6 | a0001c0001t0001g0185 a0001c0001t0027g0184 a0001c0003t0002g0146 others(3): Show |
6 | HG01243.hp1 HG02622.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.7-3686A>G | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77619586 | |||||||
| chr15:77619702 | T | TAAATA | 20 | a0001c0001t0001g0102 a0001c0001t0001g0108 a0001c0001t0001g0133 others(17): Show |
32 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(29): Show |
intron_variant | MODIFIER | c.7-3807_7-3803dupTA others(3): Show |
LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77619702 | |||||||
| chr15:77619702 | T | TAAATAAA others(3): Show |
3 | a0001c0001t0001g0050 a0001c0001t0016g0183 a0001c0003t0017g0165 |
4 | HG01346.hp2 HG02055.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.7-3812_7-3803dupTA others(8): Show |
LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77619702 | |||||||
| chr15:77619702 | TAAATA | T | 35 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0001t0001g0049 others(32): Show |
48 | HG01109.hp1 HG01255.hp2 HG01358.hp2 others(45): Show |
intron_variant | MODIFIER | c.7-3807_7-3803delTA others(3): Show |
LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77619702 | |||||||
| chr15:77619702 | TAAATAAA others(3): Show |
T | 28 | a0001c0001t0001g0185 a0001c0001t0006g0168 a0001c0001t0010g0030 others(25): Show |
78 | HG00423.hp2 HG00673.hp2 HG00733.hp1 others(75): Show |
intron_variant | MODIFIER | c.7-3812_7-3803delTA others(8): Show |
LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77619702 | |||||||
| chr15:77619702 | TAAATAAA others(8): Show |
T | 1 | a0001c0002t0004g0063 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.7-3817_7-3803delTA others(13): Show |
LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77619702 | |||||||
| chr15:77619702 | TAAATAAA others(13): Show |
T | 3 | a0001c0002t0004g0069 a0001c0002t0004g0070 a0001c0002t0004g0071 |
3 | HG02258.hp1 HG02486.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.7-3822_7-3803delTA others(18): Show |
LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77619702 | |||||||
| chr15:77619848 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.7-3948C>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77619848 | |||||||
| chr15:77619880 | G | A | 1 | a0001c0002t0003g0079 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.7-3980C>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77619880 | |||||||
| chr15:77619909 | C | A | 1 | a0001c0003t0017g0165 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.7-4009G>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77619909 | |||||||
| chr15:77619909 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.7-4009G>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77619909 | |||||||
| chr15:77619931 | G | A | 1 | a0001c0003t0002g0142 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.7-4031C>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77619931 | |||||||
| chr15:77619944 | A | C | 1 | a0001c0002t0004g0058 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.7-4044T>G | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77619944 | |||||||
| chr15:77620061 | G | A | 1 | a0001c0001t0008g0179 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.7-4161C>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77620061 | |||||||
| chr15:77620066 | C | A | 188 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(185): Show |
365 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(362): Show |
intron_variant | MODIFIER | c.7-4166G>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77620066 | |||||||
| chr15:77620087 | G | A | 2 | a0001c0003t0002g0015 a0001c0003t0002g0039 |
6 | HG01070.hp1 HG01261.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.7-4187C>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77620087 | |||||||
| chr15:77620188 | A | C | 1 | a0001c0001t0001g0048 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.7-4288T>G | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77620188 | |||||||
| chr15:77620192 | T | G | 68 | a0001c0001t0001g0017 a0001c0001t0001g0047 a0001c0001t0001g0048 others(65): Show |
133 | HG00423.hp2 HG00642.hp1 HG00673.hp2 others(130): Show |
intron_variant | MODIFIER | c.7-4292A>C | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77620192 | |||||||
| chr15:77620235 | T | TAAAAATT others(308): Show |
2 | a0001c0001t0001g0050 a0001c0001t0016g0182 |
3 | HG01346.hp2 HG02559.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.7-4336_7-4335insTT others(313): Show |
LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77620235 | |||||||
| chr15:77620235 | T | TAAAAATT others(309): Show |
1 | a0001c0001t0016g0183 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.7-4336_7-4335insTT others(314): Show |
LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77620235 | |||||||
| chr15:77620341 | C | A | 1 | a0001c0001t0001g0111 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.7-4441G>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77620341 | |||||||
| chr15:77620374 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.7-4474G>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77620374 | |||||||
| chr15:77620375 | A | G | 149 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(146): Show |
297 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(294): Show |
intron_variant | MODIFIER | c.7-4475T>C | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77620375 | |||||||
| chr15:77620383 | A | T | 63 | a0001c0001t0001g0017 a0001c0001t0001g0047 a0001c0001t0001g0048 others(60): Show |
127 | HG00423.hp2 HG00642.hp1 HG00673.hp2 others(124): Show |
intron_variant | MODIFIER | c.7-4483T>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77620383 | |||||||
| chr15:77620459 | C | T | 4 | a0001c0001t0001g0085 a0001c0001t0001g0161 a0001c0003t0002g0086 others(1): Show |
4 | HG00597.hp1 HG02135.hp2 NA18949.hp2 others(1): Show |
intron_variant | MODIFIER | c.7-4559G>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77620459 | |||||||
| chr15:77620482 | C | T | 1 | a0001c0003t0030g0194 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.7-4582G>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77620482 | |||||||
| chr15:77620594 | G | A | 1 | a0001c0003t0030g0194 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.7-4694C>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77620594 | |||||||
| chr15:77620600 | C | T | 67 | a0001c0001t0001g0017 a0001c0001t0001g0047 a0001c0001t0001g0048 others(64): Show |
132 | HG00423.hp2 HG00642.hp1 HG00673.hp2 others(129): Show |
intron_variant | MODIFIER | c.7-4700G>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77620600 | |||||||
| chr15:77620662 | T | A | 1 | a0001c0001t0010g0066 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.7-4762A>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77620662 | |||||||
| chr15:77620801 | C | A | 3 | a0001c0001t0001g0099 a0001c0001t0001g0138 a0001c0002t0003g0137 |
3 | HG01891.hp2 NA20752.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.7-4901G>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77620801 | |||||||
| chr15:77620802 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.7-4902C>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77620802 | |||||||
| chr15:77620829 | C | G | 76 | a0001c0001t0001g0017 a0001c0001t0001g0047 a0001c0001t0001g0048 others(73): Show |
141 | HG00423.hp2 HG00642.hp1 HG00673.hp2 others(138): Show |
intron_variant | MODIFIER | c.7-4929G>C | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77620829 | |||||||
| chr15:77620829 | C | T | 1 | a0001c0002t0003g0123 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.7-4929G>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77620829 | |||||||
| chr15:77620874 | G | A | 3 | a0001c0001t0001g0153 a0001c0003t0014g0075 a0001c0003t0014g0076 |
3 | HG02055.hp1 HG02280.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.7-4974C>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77620874 | |||||||
| chr15:77620903 | G | A | 67 | a0001c0001t0001g0017 a0001c0001t0001g0047 a0001c0001t0001g0048 others(64): Show |
132 | HG00423.hp2 HG00642.hp1 HG00673.hp2 others(129): Show |
intron_variant | MODIFIER | c.7-5003C>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77620903 | |||||||
| chr15:77620976 | A | C | 67 | a0001c0001t0001g0017 a0001c0001t0001g0047 a0001c0001t0001g0048 others(64): Show |
132 | HG00423.hp2 HG00642.hp1 HG00673.hp2 others(129): Show |
intron_variant | MODIFIER | c.7-5076T>G | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77620976 | |||||||
| chr15:77621058 | C | CTTTTT | 62 | a0001c0001t0001g0017 a0001c0001t0001g0047 a0001c0001t0001g0048 others(59): Show |
127 | HG00423.hp2 HG00642.hp1 HG00673.hp2 others(124): Show |
intron_variant | MODIFIER | c.7-5163_7-5159dupAA others(3): Show |
LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77621058 | |||||||
| chr15:77621069 | C | T | 3 | a0001c0001t0001g0189 a0001c0001t0019g0052 a0001c0001t0020g0053 |
3 | HG02145.hp1 HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.7-5169G>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77621069 | |||||||
| chr15:77621162 | T | C | 1 | a0001c0002t0004g0058 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.7-5262A>G | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77621162 | |||||||
| chr15:77621165 | T | C | 1 | a0001c0002t0004g0058 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.7-5265A>G | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77621165 | |||||||
| chr15:77621166 | G | T | 1 | a0001c0002t0004g0058 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.7-5266C>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77621166 | |||||||
| chr15:77621179 | C | T | 1 | a0001c0002t0004g0058 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.7-5279G>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77621179 | |||||||
| chr15:77621180 | A | G | 1 | a0001c0002t0004g0058 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.7-5280T>C | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77621180 | |||||||
| chr15:77621181 | G | A | 1 | a0001c0002t0004g0058 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.7-5281C>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77621181 | |||||||
| chr15:77621182 | A | G | 1 | a0001c0002t0004g0058 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.7-5282T>C | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77621182 | |||||||
| chr15:77621189 | C | G | 1 | a0001c0002t0004g0058 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.7-5289G>C | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77621189 | |||||||
| chr15:77621195 | T | C | 1 | a0001c0002t0004g0058 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.7-5295A>G | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77621195 | |||||||
| chr15:77621199 | T | C | 1 | a0001c0002t0004g0058 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.7-5299A>G | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77621199 | |||||||
| chr15:77621200 | G | A | 1 | a0001c0002t0004g0058 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.7-5300C>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77621200 | |||||||
| chr15:77621201 | T | C | 1 | a0001c0002t0004g0058 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.7-5301A>G | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77621201 | |||||||
| chr15:77621203 | C | T | 1 | a0001c0002t0004g0058 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.7-5303G>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77621203 | |||||||
| chr15:77621204 | A | G | 1 | a0001c0002t0004g0058 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.7-5304T>C | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77621204 | |||||||
| chr15:77621215 | A | C | 1 | a0001c0002t0004g0058 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.7-5315T>G | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77621215 | |||||||
| chr15:77621216 | G | A | 1 | a0001c0002t0004g0058 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.7-5316C>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77621216 | |||||||
| chr15:77621227 | G | A | 1 | a0001c0002t0004g0058 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.7-5327C>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77621227 | |||||||
| chr15:77621236 | C | G | 1 | a0001c0002t0004g0058 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.7-5336G>C | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77621236 | |||||||
| chr15:77621244 | A | G | 1 | a0001c0002t0004g0058 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.7-5344T>C | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77621244 | |||||||
| chr15:77621247 | G | A | 1 | a0001c0002t0004g0058 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.7-5347C>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77621247 | |||||||
| chr15:77621434 | A | C | 1 | a0001c0001t0001g0101 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.7-5534T>G | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77621434 | |||||||
| chr15:77621494 | G | C | 1 | a0001c0003t0030g0194 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.7-5594C>G | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77621494 | |||||||
| chr15:77621541 | C | T | 3 | a0001c0001t0001g0181 a0001c0001t0017g0116 a0001c0002t0003g0090 |
3 | HG00140.hp2 HG01358.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.7-5641G>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77621541 | |||||||
| chr15:77621573 | A | AG | 4 | a0001c0001t0001g0175 a0001c0002t0004g0062 a0001c0003t0006g0173 others(1): Show |
4 | HG02647.hp2 HG03139.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.7-5674dupC | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77621573 | |||||||
| chr15:77621577 | G | A | 9 | a0001c0001t0001g0153 a0001c0001t0007g0018 a0001c0001t0007g0031 others(6): Show |
14 | HG01109.hp1 HG01255.hp2 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.7-5677C>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77621577 | |||||||
| chr15:77621578 | A | G | 63 | a0001c0001t0001g0017 a0001c0001t0001g0047 a0001c0001t0001g0048 others(60): Show |
127 | HG00423.hp2 HG00642.hp1 HG00673.hp2 others(124): Show |
intron_variant | MODIFIER | c.7-5678T>C | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77621578 | |||||||
| chr15:77621719 | C | T | 1 | a0001c0003t0017g0165 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.7-5819G>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77621719 | |||||||
| chr15:77621948 | C | T | 3 | a0001c0001t0001g0050 a0001c0001t0016g0182 a0001c0001t0016g0183 |
4 | HG01346.hp2 HG02055.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.7-6048G>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77621948 | |||||||
| chr15:77622073 | G | A | 3 | a0001c0001t0001g0047 a0001c0004t0008g0026 a0001c0004t0008g0139 |
6 | HG01167.hp1 HG01169.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.7-6173C>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77622073 | |||||||
| chr15:77622130 | G | T | 4 | a0001c0001t0001g0050 a0001c0001t0016g0182 a0001c0001t0016g0183 others(1): Show |
5 | HG01346.hp2 HG02055.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.7-6230C>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77622130 | |||||||
| chr15:77622234 | C | T | 4 | a0001c0001t0001g0050 a0001c0001t0016g0182 a0001c0001t0016g0183 others(1): Show |
5 | HG01346.hp2 HG02055.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.7-6334G>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77622234 | |||||||
| chr15:77622346 | G | C | 4 | a0001c0001t0001g0050 a0001c0001t0016g0182 a0001c0001t0016g0183 others(1): Show |
5 | HG01346.hp2 HG02055.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.7-6446C>G | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77622346 | |||||||
| chr15:77622474 | A | G | 1 | a0001c0002t0004g0029 | 2 | NA19004.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.7-6574T>C | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77622474 | |||||||
| chr15:77622563 | G | A | 1 | a0001c0004t0008g0139 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.7-6663C>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77622563 | |||||||
| chr15:77622647 | C | T | 1 | a0001c0003t0002g0140 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.7-6747G>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77622647 | |||||||
| chr15:77622761 | C | T | 61 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0001t0001g0049 others(58): Show |
124 | HG00423.hp2 HG00642.hp1 HG00673.hp2 others(121): Show |
intron_variant | MODIFIER | c.7-6861G>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77622761 | |||||||
| chr15:77622799 | T | C | 65 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0001t0001g0049 others(62): Show |
129 | HG00423.hp2 HG00642.hp1 HG00673.hp2 others(126): Show |
intron_variant | MODIFIER | c.7-6899A>G | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77622799 | |||||||
| chr15:77622885 | A | G | 174 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(171): Show |
337 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(334): Show |
intron_variant | MODIFIER | c.7-6985T>C | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77622885 | |||||||
| chr15:77622917 | G | A | 1 | a0001c0002t0004g0070 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.7-7017C>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77622917 | |||||||
| chr15:77622940 | T | G | 65 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0001t0001g0049 others(62): Show |
129 | HG00423.hp2 HG00642.hp1 HG00673.hp2 others(126): Show |
intron_variant | MODIFIER | c.7-7040A>C | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77622940 | |||||||
| chr15:77622943 | G | A | 2 | a0001c0003t0014g0075 a0001c0003t0014g0076 |
2 | HG02055.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.7-7043C>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77622943 | |||||||
| chr15:77622959 | T | C | 73 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0001t0001g0049 others(70): Show |
137 | HG00423.hp2 HG00642.hp1 HG00673.hp2 others(134): Show |
intron_variant | MODIFIER | c.7-7059A>G | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77622959 | |||||||
| chr15:77623063 | C | A | 1 | a0001c0002t0003g0163 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.7-7163G>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77623063 | |||||||
| chr15:77623066 | A | G | 66 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0001t0001g0049 others(63): Show |
130 | HG00423.hp2 HG00642.hp1 HG00673.hp2 others(127): Show |
intron_variant | MODIFIER | c.7-7166T>C | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77623066 | |||||||
| chr15:77623072 | A | C | 172 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(169): Show |
331 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(328): Show |
intron_variant | MODIFIER | c.7-7172T>G | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77623072 | |||||||
| chr15:77623103 | A | C | 74 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0001t0001g0049 others(71): Show |
138 | HG00423.hp2 HG00642.hp1 HG00673.hp2 others(135): Show |
intron_variant | MODIFIER | c.7-7203T>G | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77623103 | |||||||
| chr15:77623124 | G | A | 1 | a0001c0001t0001g0051 | 2 | HG02630.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.7-7224C>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77623124 | |||||||
| chr15:77623171 | T | C | 72 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0001t0001g0049 others(69): Show |
134 | HG00423.hp2 HG00642.hp1 HG00673.hp2 others(131): Show |
intron_variant | MODIFIER | c.7-7271A>G | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77623171 | |||||||
| chr15:77623240 | G | A | 1 | a0001c0002t0004g0060 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.7-7340C>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77623240 | |||||||
| chr15:77623244 | G | C | 2 | a0001c0003t0009g0027 a0001c0003t0009g0171 |
4 | HG02615.hp1 HG02717.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.7-7344C>G | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77623244 | |||||||
| chr15:77623374 | A | G | 65 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0001t0001g0049 others(62): Show |
129 | HG00423.hp2 HG00642.hp1 HG00673.hp2 others(126): Show |
intron_variant | MODIFIER | c.7-7474T>C | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77623374 | |||||||
| chr15:77623413 | T | G | 1 | a0001c0001t0001g0117 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.7-7513A>C | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77623413 | |||||||
| chr15:77623509 | T | C | 73 | a0001c0001t0001g0017 a0001c0001t0001g0040 a0001c0001t0001g0048 others(70): Show |
138 | HG00423.hp2 HG00642.hp1 HG00673.hp2 others(135): Show |
intron_variant | MODIFIER | c.7-7609A>G | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77623509 | |||||||
| chr15:77623521 | C | T | 1 | a0001c0003t0018g0191 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.7-7621G>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77623521 | |||||||
| chr15:77623641 | G | A | 1 | a0001c0001t0001g0180 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.7-7741C>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77623641 | |||||||
| chr15:77623663 | C | T | 1 | a0001c0001t0001g0177 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.7-7763G>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77623663 | |||||||
| chr15:77623722 | G | A | 1 | a0001c0002t0004g0058 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.7-7822C>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77623722 | |||||||
| chr15:77623723 | A | T | 1 | a0001c0002t0004g0058 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.7-7823T>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77623723 | |||||||
| chr15:77623763 | T | C | 65 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0001t0001g0049 others(62): Show |
129 | HG00423.hp2 HG00642.hp1 HG00673.hp2 others(126): Show |
intron_variant | MODIFIER | c.7-7863A>G | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77623763 | |||||||
| chr15:77623830 | C | CTG | 3 | a0001c0001t0001g0119 a0001c0001t0006g0120 a0001c0002t0003g0118 |
3 | HG03490.hp1 HG03704.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.7-7932_7-7931dupCA | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77623830 | |||||||
| chr15:77623853 | CTG | C | 60 | a0001c0001t0001g0040 a0001c0001t0001g0048 a0001c0001t0001g0049 others(57): Show |
121 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(118): Show |
intron_variant | MODIFIER | c.7-7955_7-7954delCA | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77623853 | |||||||
| chr15:77623853 | CTGTG | C | 6 | a0001c0001t0001g0017 a0001c0001t0001g0151 a0001c0001t0001g0177 others(3): Show |
9 | HG01884.hp2 HG01975.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.7-7957_7-7954delCA others(2): Show |
LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77623853 | |||||||
| chr15:77623857 | G | A | 1 | a0001c0002t0004g0068 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.7-7957C>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77623857 | |||||||
| chr15:77623902 | T | A | 63 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0001t0001g0049 others(60): Show |
127 | HG00423.hp2 HG00642.hp1 HG00673.hp2 others(124): Show |
intron_variant | MODIFIER | c.7-8002A>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77623902 | |||||||
| chr15:77623932 | A | ACT | 63 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0001t0001g0049 others(60): Show |
127 | HG00423.hp2 HG00642.hp1 HG00673.hp2 others(124): Show |
intron_variant | MODIFIER | c.7-8034_7-8033dupAG | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77623932 | |||||||
| chr15:77624005 | T | C | 64 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0001t0001g0049 others(61): Show |
128 | HG00423.hp2 HG00642.hp1 HG00673.hp2 others(125): Show |
intron_variant | MODIFIER | c.7-8105A>G | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77624005 | |||||||
| chr15:77624163 | C | CTG | 2 | a0001c0002t0013g0034 a0001c0002t0013g0100 |
3 | HG00621.hp2 NA18948.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.6+8145_6+8146dupCA | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77624163 | |||||||
| chr15:77624163 | CTG | C | 104 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0014 others(101): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.6+8145_6+8146delCA | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77624163 | |||||||
| chr15:77624163 | CTGTG | C | 3 | a0001c0001t0001g0040 a0001c0001t0001g0044 a0001c0001t0001g0154 |
5 | HG02074.hp2 HG03491.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.6+8143_6+8146delCA others(2): Show |
LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77624163 | |||||||
| chr15:77624163 | CTGTGTG | C | 3 | a0001c0002t0003g0011 a0001c0002t0003g0164 a0001c0003t0030g0194 |
6 | HG01070.hp2 HG01071.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.6+8141_6+8146delCA others(4): Show |
LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77624163 | |||||||
| chr15:77624163 | CTGTGTGT others(3): Show |
C | 62 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0001t0001g0049 others(59): Show |
126 | HG00423.hp2 HG00642.hp1 HG00673.hp2 others(123): Show |
intron_variant | MODIFIER | c.6+8137_6+8146delCA others(8): Show |
LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77624163 | |||||||
| chr15:77624199 | T | C | 1 | a0001c0001t0001g0181 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.6+8111A>G | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77624199 | |||||||
| chr15:77624288 | C | T | 63 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0001t0001g0049 others(60): Show |
127 | HG00423.hp2 HG00642.hp1 HG00673.hp2 others(124): Show |
intron_variant | MODIFIER | c.6+8022G>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77624288 | |||||||
| chr15:77624336 | A | G | 1 | a0001c0001t0007g0072 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.6+7974T>C | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77624336 | |||||||
| chr15:77624374 | T | C | 63 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0001t0001g0049 others(60): Show |
127 | HG00423.hp2 HG00642.hp1 HG00673.hp2 others(124): Show |
intron_variant | MODIFIER | c.6+7936A>G | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77624374 | |||||||
| chr15:77624392 | T | C | 6 | a0001c0001t0001g0051 a0001c0001t0001g0185 a0001c0001t0027g0184 others(3): Show |
7 | HG01243.hp1 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.6+7918A>G | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77624392 | |||||||
| chr15:77624403 | C | T | 1 | a0001c0003t0002g0012 | 4 | HG01099.hp1 HG01516.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.6+7907G>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77624403 | |||||||
| chr15:77624489 | T | C | 1 | a0001c0001t0001g0041 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.6+7821A>G | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77624489 | |||||||
| chr15:77624646 | C | G | 1 | a0001c0001t0001g0099 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.6+7664G>C | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77624646 | |||||||
| chr15:77624758 | G | C | 63 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0001t0001g0049 others(60): Show |
127 | HG00423.hp2 HG00642.hp1 HG00673.hp2 others(124): Show |
intron_variant | MODIFIER | c.6+7552C>G | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77624758 | |||||||
| chr15:77624761 | C | T | 1 | a0001c0003t0006g0176 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.6+7549G>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77624761 | |||||||
| chr15:77624763 | T | A | 1 | a0001c0003t0030g0194 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.6+7547A>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77624763 | |||||||
| chr15:77625012 | T | A | 1 | a0001c0002t0004g0058 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.6+7298A>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77625012 | |||||||
| chr15:77625076 | G | A | 63 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0001t0001g0049 others(60): Show |
127 | HG00423.hp2 HG00642.hp1 HG00673.hp2 others(124): Show |
intron_variant | MODIFIER | c.6+7234C>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77625076 | |||||||
| chr15:77625162 | G | A | 1 | a0001c0001t0001g0042 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.6+7148C>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77625162 | |||||||
| chr15:77625278 | T | A | 1 | a0001c0002t0004g0058 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.6+7032A>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77625278 | |||||||
| chr15:77625279 | G | A | 1 | a0001c0003t0006g0176 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.6+7031C>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77625279 | |||||||
| chr15:77625414 | G | A | 63 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0001t0001g0049 others(60): Show |
127 | HG00423.hp2 HG00642.hp1 HG00673.hp2 others(124): Show |
intron_variant | MODIFIER | c.6+6896C>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77625414 | |||||||
| chr15:77625445 | G | T | 2 | a0001c0002t0004g0056 a0001c0002t0004g0060 |
2 | NA18983.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.6+6865C>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77625445 | |||||||
| chr15:77625665 | C | T | 1 | a0001c0003t0030g0194 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.6+6645G>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77625665 | |||||||
| chr15:77625974 | C | T | 64 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0001t0001g0049 others(61): Show |
128 | HG00423.hp2 HG00642.hp1 HG00673.hp2 others(125): Show |
intron_variant | MODIFIER | c.6+6336G>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77625974 | |||||||
| chr15:77625983 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.6+6327C>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77625983 | |||||||
| chr15:77626013 | T | A | 2 | a0001c0010t0002g0092 a0005c0015t0003g0093 |
2 | NA18992.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.6+6297A>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77626013 | |||||||
| chr15:77626036 | C | T | 3 | a0001c0002t0004g0069 a0001c0002t0004g0070 a0001c0002t0004g0071 |
3 | HG02258.hp1 HG02486.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.6+6274G>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77626036 | |||||||
| chr15:77626137 | T | C | 64 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0001t0001g0049 others(61): Show |
128 | HG00423.hp2 HG00642.hp1 HG00673.hp2 others(125): Show |
intron_variant | MODIFIER | c.6+6173A>G | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77626137 | |||||||
| chr15:77626151 | A | C | 64 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0001t0001g0049 others(61): Show |
128 | HG00423.hp2 HG00642.hp1 HG00673.hp2 others(125): Show |
intron_variant | MODIFIER | c.6+6159T>G | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77626151 | |||||||
| chr15:77626194 | G | A | 64 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0001t0001g0049 others(61): Show |
128 | HG00423.hp2 HG00642.hp1 HG00673.hp2 others(125): Show |
intron_variant | MODIFIER | c.6+6116C>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77626194 | |||||||
| chr15:77626196 | G | A | 66 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0001t0001g0049 others(63): Show |
130 | HG00423.hp2 HG00642.hp1 HG00673.hp2 others(127): Show |
intron_variant | MODIFIER | c.6+6114C>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77626196 | |||||||
| chr15:77626248 | G | A | 1 | a0001c0002t0004g0071 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.6+6062C>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77626248 | |||||||
| chr15:77626268 | TGA | T | 64 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0001t0001g0049 others(61): Show |
128 | HG00423.hp2 HG00642.hp1 HG00673.hp2 others(125): Show |
intron_variant | MODIFIER | c.6+6040_6+6041delTC | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77626268 | |||||||
| chr15:77626322 | CT | C | 64 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0001t0001g0049 others(61): Show |
128 | HG00423.hp2 HG00642.hp1 HG00673.hp2 others(125): Show |
intron_variant | MODIFIER | c.6+5987delA | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77626322 | |||||||
| chr15:77626360 | T | A | 64 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0001t0001g0049 others(61): Show |
128 | HG00423.hp2 HG00642.hp1 HG00673.hp2 others(125): Show |
intron_variant | MODIFIER | c.6+5950A>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77626360 | |||||||
| chr15:77626391 | A | G | 1 | a0001c0002t0003g0098 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.6+5919T>C | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77626391 | |||||||
| chr15:77626422 | A | G | 1 | a0001c0006t0003g0097 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.6+5888T>C | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77626422 | |||||||
| chr15:77626573 | A | AC | 4 | a0001c0001t0001g0033 a0001c0002t0003g0096 a0001c0002t0004g0028 others(1): Show |
6 | HG00423.hp1 NA18955.hp2 NA18985.hp1 others(3): Show |
intron_variant | MODIFIER | c.6+5736dupG | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77626573 | |||||||
| chr15:77626763 | C | T | 1 | a0001c0003t0006g0176 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.6+5547G>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77626763 | |||||||
| chr15:77626769 | A | G | 6 | a0001c0001t0001g0051 a0001c0001t0001g0185 a0001c0001t0027g0184 others(3): Show |
7 | HG01243.hp1 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.6+5541T>C | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77626769 | |||||||
| chr15:77626781 | C | G | 63 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0001t0001g0049 others(60): Show |
127 | HG00423.hp2 HG00642.hp1 HG00673.hp2 others(124): Show |
intron_variant | MODIFIER | c.6+5529G>C | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77626781 | |||||||
| chr15:77626846 | T | G | 64 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0001t0001g0049 others(61): Show |
128 | HG00423.hp2 HG00642.hp1 HG00673.hp2 others(125): Show |
intron_variant | MODIFIER | c.6+5464A>C | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77626846 | |||||||
| chr15:77626878 | A | T | 1 | a0001c0002t0004g0058 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.6+5432T>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77626878 | |||||||
| chr15:77626973 | C | T | 3 | a0001c0001t0001g0094 a0001c0003t0006g0173 a0001c0003t0009g0095 |
3 | HG00621.hp1 HG02559.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.6+5337G>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77626973 | |||||||
| chr15:77626991 | T | C | 64 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0001t0001g0049 others(61): Show |
128 | HG00423.hp2 HG00642.hp1 HG00673.hp2 others(125): Show |
intron_variant | MODIFIER | c.6+5319A>G | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77626991 | |||||||
| chr15:77626995 | CAGA | C | 64 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0001t0001g0049 others(61): Show |
128 | HG00423.hp2 HG00642.hp1 HG00673.hp2 others(125): Show |
intron_variant | MODIFIER | c.6+5312_6+5314delTC others(1): Show |
LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77626995 | |||||||
| chr15:77627072 | GT | G | 3 | a0001c0001t0002g0021 a0001c0001t0002g0080 a0001c0001t0002g0082 |
5 | HG00733.hp2 HG01069.hp2 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.6+5237delA | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77627072 | |||||||
| chr15:77627095 | T | C | 70 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0001t0001g0049 others(67): Show |
135 | HG00423.hp2 HG00642.hp1 HG00673.hp2 others(132): Show |
intron_variant | MODIFIER | c.6+5215A>G | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77627095 | |||||||
| chr15:77627106 | A | G | 6 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0170 others(3): Show |
9 | HG02258.hp2 HG02615.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.6+5204T>C | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77627106 | |||||||
| chr15:77627159 | G | T | 2 | a0001c0010t0002g0092 a0005c0015t0003g0093 |
2 | NA18992.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.6+5151C>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77627159 | |||||||
| chr15:77627238 | C | T | 64 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0001t0001g0049 others(61): Show |
128 | HG00423.hp2 HG00642.hp1 HG00673.hp2 others(125): Show |
intron_variant | MODIFIER | c.6+5072G>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77627238 | |||||||
| chr15:77627352 | A | T | 64 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0001t0001g0049 others(61): Show |
128 | HG00423.hp2 HG00642.hp1 HG00673.hp2 others(125): Show |
intron_variant | MODIFIER | c.6+4958T>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77627352 | |||||||
| chr15:77627466 | A | T | 1 | a0001c0002t0004g0058 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.6+4844T>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77627466 | |||||||
| chr15:77627498 | C | T | 7 | a0001c0002t0003g0008 a0001c0002t0003g0011 a0001c0002t0003g0045 others(4): Show |
17 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.6+4812G>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77627498 | |||||||
| chr15:77627508 | G | A | 2 | a0001c0001t0001g0156 a0001c0001t0006g0155 |
2 | HG02129.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.6+4802C>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77627508 | |||||||
| chr15:77627609 | G | C | 1 | a0001c0003t0005g0157 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.6+4701C>G | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77627609 | |||||||
| chr15:77627622 | G | A | 13 | a0001c0001t0001g0017 a0001c0001t0001g0050 a0001c0001t0001g0177 others(10): Show |
17 | HG01346.hp2 HG01891.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.6+4688C>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77627622 | |||||||
| chr15:77627811 | G | T | 64 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0001t0001g0049 others(61): Show |
128 | HG00423.hp2 HG00642.hp1 HG00673.hp2 others(125): Show |
intron_variant | MODIFIER | c.6+4499C>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77627811 | |||||||
| chr15:77628248 | T | C | 2 | a0001c0001t0001g0048 a0001c0001t0001g0049 |
4 | HG02572.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.6+4062A>G | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77628248 | |||||||
| chr15:77628301 | A | T | 6 | a0001c0001t0001g0051 a0001c0001t0001g0185 a0001c0001t0027g0184 others(3): Show |
7 | HG01243.hp1 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.6+4009T>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77628301 | |||||||
| chr15:77628343 | G | A | 3 | a0001c0002t0004g0069 a0001c0002t0004g0070 a0001c0002t0004g0071 |
3 | HG02258.hp1 HG02486.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.6+3967C>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77628343 | |||||||
| chr15:77628387 | A | T | 70 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0001t0001g0049 others(67): Show |
135 | HG00423.hp2 HG00642.hp1 HG00673.hp2 others(132): Show |
intron_variant | MODIFIER | c.6+3923T>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77628387 | |||||||
| chr15:77628393 | A | G | 70 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0001t0001g0049 others(67): Show |
135 | HG00423.hp2 HG00642.hp1 HG00673.hp2 others(132): Show |
intron_variant | MODIFIER | c.6+3917T>C | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77628393 | |||||||
| chr15:77628402 | A | G | 10 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0081 others(7): Show |
20 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.6+3908T>C | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77628402 | |||||||
| chr15:77628504 | T | A | 2 | a0001c0003t0006g0173 a0001c0003t0006g0174 |
2 | HG03139.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.6+3806A>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77628504 | |||||||
| chr15:77628504 | T | G | 62 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0001t0001g0049 others(59): Show |
126 | HG00423.hp2 HG00642.hp1 HG00673.hp2 others(123): Show |
intron_variant | MODIFIER | c.6+3806A>C | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77628504 | |||||||
| chr15:77628580 | T | C | 1 | a0001c0001t0001g0158 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.6+3730A>G | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77628580 | |||||||
| chr15:77628595 | C | T | 64 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0001t0001g0049 others(61): Show |
128 | HG00423.hp2 HG00642.hp1 HG00673.hp2 others(125): Show |
intron_variant | MODIFIER | c.6+3715G>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77628595 | |||||||
| chr15:77628667 | T | C | 3 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0083 |
5 | HG00558.hp1 HG02056.hp1 HG02074.hp2 others(2): Show |
intron_variant | MODIFIER | c.6+3643A>G | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77628667 | |||||||
| chr15:77628675 | C | T | 1 | a0001c0001t0008g0179 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.6+3635G>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77628675 | |||||||
| chr15:77628700 | G | A | 70 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0001t0001g0049 others(67): Show |
135 | HG00423.hp2 HG00642.hp1 HG00673.hp2 others(132): Show |
intron_variant | MODIFIER | c.6+3610C>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77628700 | |||||||
| chr15:77628727 | G | C | 63 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0001t0001g0049 others(60): Show |
127 | HG00423.hp2 HG00642.hp1 HG00673.hp2 others(124): Show |
intron_variant | MODIFIER | c.6+3583C>G | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77628727 | |||||||
| chr15:77628834 | C | T | 63 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0001t0001g0049 others(60): Show |
127 | HG00423.hp2 HG00642.hp1 HG00673.hp2 others(124): Show |
intron_variant | MODIFIER | c.6+3476G>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77628834 | |||||||
| chr15:77628836 | C | G | 2 | a0001c0003t0006g0173 a0001c0003t0006g0174 |
2 | HG03139.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.6+3474G>C | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77628836 | |||||||
| chr15:77628901 | C | T | 1 | a0001c0003t0017g0165 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.6+3409G>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77628901 | |||||||
| chr15:77628959 | C | G | 6 | a0001c0001t0001g0051 a0001c0001t0001g0185 a0001c0001t0027g0184 others(3): Show |
7 | HG01243.hp1 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.6+3351G>C | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77628959 | |||||||
| chr15:77629029 | A | G | 1 | a0001c0002t0003g0172 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.6+3281T>C | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77629029 | |||||||
| chr15:77629031 | G | C | 1 | a0001c0002t0003g0164 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.6+3279C>G | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77629031 | |||||||
| chr15:77629105 | C | G | 1 | a0001c0001t0001g0084 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.6+3205G>C | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77629105 | |||||||
| chr15:77629298 | G | GTTCA | 61 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0001t0001g0049 others(58): Show |
125 | HG00423.hp2 HG00642.hp1 HG00673.hp2 others(122): Show |
intron_variant | MODIFIER | c.6+3008_6+3011dupTG others(2): Show |
LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77629298 | |||||||
| chr15:77629368 | T | C | 1 | a0001c0003t0012g0159 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.6+2942A>G | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77629368 | |||||||
| chr15:77629387 | C | G | 1 | a0001c0001t0001g0083 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.6+2923G>C | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77629387 | |||||||
| chr15:77629438 | C | CT | 3 | a0001c0001t0002g0021 a0001c0001t0002g0080 a0001c0001t0002g0082 |
5 | HG00733.hp2 HG01069.hp2 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.6+2871dupA | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77629438 | |||||||
| chr15:77629725 | G | T | 3 | a0001c0001t0001g0017 a0001c0001t0001g0177 a0001c0001t0001g0178 |
6 | HG02572.hp1 HG02895.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.6+2585C>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77629725 | |||||||
| chr15:77629730 | G | C | 1 | a0001c0003t0002g0160 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.6+2580C>G | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77629730 | |||||||
| chr15:77629905 | A | G | 1 | a0001c0001t0027g0184 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.6+2405T>C | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77629905 | |||||||
| chr15:77629976 | G | A | 70 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0001t0001g0049 others(67): Show |
135 | HG00423.hp2 HG00642.hp1 HG00673.hp2 others(132): Show |
intron_variant | MODIFIER | c.6+2334C>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77629976 | |||||||
| chr15:77629998 | G | C | 3 | a0001c0001t0001g0170 a0001c0003t0009g0027 a0001c0003t0009g0171 |
5 | HG02615.hp1 HG02717.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.6+2312C>G | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77629998 | |||||||
| chr15:77630061 | T | C | 59 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0001t0001g0049 others(56): Show |
122 | HG00423.hp2 HG00642.hp1 HG00673.hp2 others(119): Show |
intron_variant | MODIFIER | c.6+2249A>G | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77630061 | |||||||
| chr15:77630062 | G | A | 3 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0003t0006g0176 |
5 | HG02572.hp2 HG02886.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.6+2248C>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77630062 | |||||||
| chr15:77630170 | A | G | 59 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0001t0001g0049 others(56): Show |
122 | HG00423.hp2 HG00642.hp1 HG00673.hp2 others(119): Show |
intron_variant | MODIFIER | c.6+2140T>C | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77630170 | |||||||
| chr15:77630178 | C | G | 2 | a0001c0001t0001g0185 a0001c0001t0027g0184 |
2 | HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.6+2132G>C | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77630178 | |||||||
| chr15:77630492 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.6+1818G>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77630492 | |||||||
| chr15:77630553 | GAC | G | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0175 others(3): Show |
8 | HG02572.hp2 HG02647.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.6+1755_6+1756delGT | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77630553 | |||||||
| chr15:77630697 | C | T | 1 | a0001c0001t0002g0080 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.6+1613G>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77630697 | |||||||
| chr15:77630730 | A | G | 72 | a0001c0001t0001g0017 a0001c0001t0001g0047 a0001c0001t0001g0048 others(69): Show |
138 | HG00423.hp2 HG00639.hp2 HG00642.hp1 others(135): Show |
intron_variant | MODIFIER | c.6+1580T>C | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77630730 | |||||||
| chr15:77630744 | G | A | 1 | a0001c0001t0001g0161 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.6+1566C>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77630744 | |||||||
| chr15:77630881 | G | T | 61 | a0001c0001t0001g0017 a0001c0001t0001g0047 a0001c0001t0001g0048 others(58): Show |
125 | HG00423.hp2 HG00639.hp2 HG00642.hp1 others(122): Show |
intron_variant | MODIFIER | c.6+1429C>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77630881 | |||||||
| chr15:77631068 | C | T | 25 | a0001c0001t0010g0030 a0001c0001t0010g0064 a0001c0001t0010g0066 others(22): Show |
75 | HG00423.hp2 HG00639.hp2 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.6+1242G>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77631068 | |||||||
| chr15:77631086 | C | T | 1 | a0001c0003t0002g0032 | 2 | NA18964.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.6+1224G>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77631086 | |||||||
| chr15:77631101 | G | A | 7 | a0001c0001t0001g0051 a0001c0001t0001g0185 a0001c0001t0001g0189 others(4): Show |
8 | HG01243.hp1 HG02145.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.6+1209C>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77631101 | |||||||
| chr15:77631117 | T | C | 1 | a0001c0001t0022g0055 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.6+1193A>G | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77631117 | |||||||
| chr15:77631192 | C | T | 1 | a0001c0002t0004g0057 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.6+1118G>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77631192 | |||||||
| chr15:77631219 | C | T | 12 | a0001c0001t0001g0047 a0001c0001t0001g0166 a0001c0001t0001g0167 others(9): Show |
16 | HG01167.hp1 HG01169.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.6+1091G>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77631219 | |||||||
| chr15:77631261 | G | A | 1 | a0001c0003t0002g0162 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.6+1049C>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77631261 | |||||||
| chr15:77631304 | G | A | 1 | a0001c0002t0011g0019 | 3 | HG01255.hp2 HG02109.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.6+1006C>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77631304 | |||||||
| chr15:77631323 | G | C | 72 | a0001c0001t0001g0017 a0001c0001t0001g0047 a0001c0001t0001g0048 others(69): Show |
138 | HG00423.hp2 HG00639.hp2 HG00642.hp1 others(135): Show |
intron_variant | MODIFIER | c.6+987C>G | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77631323 | |||||||
| chr15:77631512 | C | G | 1 | a0001c0002t0004g0056 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.6+798G>C | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77631512 | |||||||
| chr15:77631575 | T | C | 75 | a0001c0001t0001g0017 a0001c0001t0001g0047 a0001c0001t0001g0048 others(72): Show |
142 | HG00423.hp2 HG00639.hp2 HG00642.hp1 others(139): Show |
intron_variant | MODIFIER | c.6+735A>G | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77631575 | |||||||
| chr15:77631730 | C | T | 2 | a0001c0001t0002g0021 a0001c0001t0002g0080 |
4 | HG01069.hp2 HG01106.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.6+580G>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77631730 | |||||||
| chr15:77631792 | C | T | 1 | a0001c0002t0003g0079 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.6+518G>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77631792 | |||||||
| chr15:77631825 | T | A | 1 | a0001c0008t0001g0078 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.6+485A>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77631825 | |||||||
| chr15:77631918 | C | T | 1 | a0001c0001t0001g0020 | 3 | HG00597.hp2 NA19057.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.6+392G>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77631918 | |||||||
| chr15:77632200 | C | A | 1 | a0001c0003t0002g0190 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.6+110G>T | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77632200 | |||||||
| chr15:77632301 | C | T | 1 | a0001c0008t0001g0078 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.6+9G>A | LINGO1 | ENSG00000169783.13 | transcript | ENST00000355300.7 | protein_coding | 1/1 | chr15 | 77632301 |