Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 29889 |
| ensemblid | ENSG00000134697.13 |
| hgncid | 29925 |
| symbol | GNL2 |
| name | G protein nucleolar 2 |
| refseq_nuc | NM_013285.3 |
| refseq_prot | NP_037417.1 |
| ensembl_nuc | ENST00000373062.8 |
| ensembl_prot | ENSP00000362153.3 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 37566816 |
| end | 37595937 |
| strand | - |
| ver | v1.2 |
| region | chr1:37566816-37595937 |
| region5000 | chr1:37561816-37600937 |
| regionname0 | GNL2_chr1_37566816_37595937 |
| regionname5000 | GNL2_chr1_37561816_37600937 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 731 | 369 | 79 | 66 | 159 | 17 | 46 | 120 | GNL2_chr1_37561816_37600937 | GNL2 | MVKPK others(726): Show |
chr1 | 37561816 | 37600937 |
| a0002 | 0/0 | 731 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | MVKPK others(726): Show |
chr1 | 37561816 | 37600937 |
| a0003 | 0/0 | 731 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | MVKPK others(726): Show |
chr1 | 37561816 | 37600937 |
| a0004 | 0/0 | 731 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | MVKPK others(726): Show |
chr1 | 37561816 | 37600937 |
| a0005 | 0/0 | 731 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | MVKPK others(726): Show |
chr1 | 37561816 | 37600937 |
| a0006 | 0/0 | 731 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | MVKPK others(726): Show |
chr1 | 37561816 | 37600937 |
| a0007 | 0/0 | 731 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | MVKPK others(726): Show |
chr1 | 37561816 | 37600937 |
| a0008 | 0/0 | 731 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | MVKPK others(726): Show |
chr1 | 37561816 | 37600937 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2193 | 369 | 79 | 66 | 159 | 17 | 46 | GNL2_chr1_37561816_37600937 | GNL2 | ATGGT others(2188): Show |
chr1 | 37561816 | 37600937 | ||
| a0002c0007 | 0/0 | 2193 | 1 | 0 | 0 | 1 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | ATGGT others(2188): Show |
chr1 | 37561816 | 37600937 | ||
| a0003c0002 | 0/0 | 2193 | 1 | 0 | 1 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | ATGGT others(2188): Show |
chr1 | 37561816 | 37600937 | ||
| a0004c0004 | 0/0 | 2193 | 1 | 0 | 1 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | ATGGT others(2188): Show |
chr1 | 37561816 | 37600937 | ||
| a0005c0003 | 0/0 | 2193 | 1 | 1 | 0 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | ATGGT others(2188): Show |
chr1 | 37561816 | 37600937 | ||
| a0006c0006 | 0/0 | 2193 | 1 | 1 | 0 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | ATGGT others(2188): Show |
chr1 | 37561816 | 37600937 | ||
| a0007c0005 | 0/0 | 2193 | 1 | 1 | 0 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | ATGGT others(2188): Show |
chr1 | 37561816 | 37600937 | ||
| a0008c0008 | 0/0 | 2193 | 1 | 0 | 0 | 0 | 1 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | ATGGT others(2188): Show |
chr1 | 37561816 | 37600937 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2350 | 365 | 78 | 64 | 158 | 17 | 46 | GNL2_chr1_37561816_37600937 | GNL2 | GCACA others(2345): Show |
chr1 | 37561816 | 37600937 |
| a0001c0001t0002 | 0/0 | 2350 | 2 | 0 | 2 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | GCACA others(2345): Show |
chr1 | 37561816 | 37600937 |
| a0001c0001t0003 | 0/0 | 2350 | 1 | 0 | 0 | 1 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | GCACA others(2345): Show |
chr1 | 37561816 | 37600937 |
| a0001c0001t0004 | 0/0 | 2350 | 1 | 1 | 0 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | GCACA others(2345): Show |
chr1 | 37561816 | 37600937 |
| a0002c0007t0001 | 0/0 | 2350 | 1 | 0 | 0 | 1 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | GCACA others(2345): Show |
chr1 | 37561816 | 37600937 |
| a0003c0002t0001 | 0/0 | 2350 | 1 | 0 | 1 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | GCACA others(2345): Show |
chr1 | 37561816 | 37600937 |
| a0004c0004t0001 | 0/0 | 2350 | 1 | 0 | 1 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | GCACA others(2345): Show |
chr1 | 37561816 | 37600937 |
| a0005c0003t0001 | 0/0 | 2350 | 1 | 1 | 0 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | GCACA others(2345): Show |
chr1 | 37561816 | 37600937 |
| a0006c0006t0001 | 0/0 | 2350 | 1 | 1 | 0 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | GCACA others(2345): Show |
chr1 | 37561816 | 37600937 |
| a0007c0005t0001 | 0/0 | 2350 | 1 | 1 | 0 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | GCACA others(2345): Show |
chr1 | 37561816 | 37600937 |
| a0008c0008t0001 | 0/0 | 2350 | 1 | 0 | 0 | 0 | 1 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | GCACA others(2345): Show |
chr1 | 37561816 | 37600937 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 49 | 3 | 9 | 33 | 2 | 2 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0002 | 0/0 | 43 | 5 | 4 | 31 | 0 | 3 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0003 | 1/0 | 22 | 10 | 4 | 4 | 0 | 3 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0004 | 0/0 | 9 | 9 | 0 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0005 | 0/0 | 9 | 0 | 4 | 3 | 0 | 2 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0006 | 0/0 | 8 | 0 | 1 | 4 | 1 | 2 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0007 | 0/0 | 7 | 0 | 4 | 0 | 1 | 2 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0008 | 0/0 | 7 | 0 | 0 | 5 | 0 | 2 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0009 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0010 | 0/0 | 5 | 0 | 3 | 1 | 0 | 1 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 1 | 0 | 3 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0016 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0099 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0002g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0001c0001t0004g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0002c0007t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0003c0002t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0004c0004t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0005c0003t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0006c0006t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0007c0005t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| a0008c0008t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0061 | EUR | GBR | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0034 | EUR | GBR | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0140 | EUR | GBR | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | FIN | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | FIN | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0053 | EUR | FIN | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG00423 | hp1 | a0002 | c0007 | t0001 | g0147 | EAS | CHS | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | CHS | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG00642 | hp2 | a0003 | c0002 | t0001 | g0073 | AMR | PUR | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0041 | AMR | PUR | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0041 | AMR | PUR | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG01358 | hp2 | a0004 | c0004 | t0001 | g0097 | AMR | CLM | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0027 | EUR | IBS | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0098 | EUR | IBS | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0024 | EUR | IBS | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0024 | EUR | IBS | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0027 | EUR | IBS | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | ACB | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0077 | AFR | ACB | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ESN | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ESN | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ESN | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ESN | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | MSL | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG03098 | hp2 | a0005 | c0003 | t0001 | g0072 | AFR | MSL | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG03130 | hp1 | a0006 | c0006 | t0001 | g0044 | AFR | ESN | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ESN | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | MSL | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | MSL | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | STU | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | STU | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | BEB | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | BEB | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | BEB | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | BEB | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | STU | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | STU | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | BEB | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | BEB | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | STU | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | STU | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | STU | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | STU | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | YRI | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | CHB | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | YRI | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | LWK | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | LWK | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | LWK | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | YRI | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ASW | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ASW | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0119 | EUR | TSI | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | TSI | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA20805 | hp1 | a0008 | c0008 | t0001 | g0167 | EUR | TSI | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0115 | EUR | TSI | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | GIH | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | MSL | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG06807 | hp1 | a0007 | c0005 | t0001 | g0058 | AFR | USA | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | USA | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | USA | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | USA | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0099 | REF | REF | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0003 | REF | REF | GNL2_chr1_37561816_37600937 | GNL2 | chr1 | 37561816 | 37600937 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:37567006 | C | T | 1 | a0005 | 1 | HG03098.hp2 | missense_variant&splice_region_variant | MODERATE | c.2045G>A | p.Arg682Gln | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 16/16 | 2160/2350 | 2045/2196 | 682/731 | chr1 | 37567006 | |||
| chr1:37569235 | G | A | 1 | a0004 | 1 | HG01358.hp2 | missense_variant | MODERATE | c.1484C>T | p.Thr495Ile | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 13/16 | 1599/2350 | 1484/2196 | 495/731 | chr1 | 37569235 | |||
| chr1:37582237 | G | A | 1 | a0007 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.895C>T | p.Arg299Trp | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/16 | 1010/2350 | 895/2196 | 299/731 | chr1 | 37582237 | |||
| chr1:37582830 | T | C | 1 | a0006 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.743A>G | p.Lys248Arg | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 7/16 | 858/2350 | 743/2196 | 248/731 | chr1 | 37582830 | |||
| chr1:37582903 | G | T | 1 | a0003 | 1 | HG00642.hp2 | missense_variant | MODERATE | c.670C>A | p.Leu224Ile | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 7/16 | 785/2350 | 670/2196 | 224/731 | chr1 | 37582903 | |||
| chr1:37583875 | G | C | 1 | a0002 | 1 | HG00423.hp1 | missense_variant | MODERATE | c.628C>G | p.Leu210Val | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 6/16 | 743/2350 | 628/2196 | 210/731 | chr1 | 37583875 | |||
| chr1:37593786 | T | G | 1 | a0008 | 1 | NA20805.hp1 | missense_variant | MODERATE | c.125A>C | p.Asn42Thr | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 2/16 | 240/2350 | 125/2196 | 42/731 | chr1 | 37593786 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:37566819 | C | T | 1 | a0001c0001t0004 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*36G>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 16/16 | 36 | chr1 | 37566819 | ||||||
| chr1:37595899 | C | T | 1 | a0001c0001t0003 | 1 | NA19010.hp1 | 5_prime_UTR_variant | MODIFIER | c.-77G>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 1/16 | 77 | chr1 | 37595899 | ||||||
| chr1:37595904 | G | A | 1 | a0001c0001t0002 | 2 | HG01074.hp2 HG01099.hp1 |
5_prime_UTR_variant | MODIFIER | c.-82C>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 1/16 | 82 | chr1 | 37595904 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:37567076 | G | A | 1 | a0001c0001t0001g0106 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2044-69C>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 15/15 | chr1 | 37567076 | |||||||
| chr1:37567161 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2044-154G>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 15/15 | chr1 | 37567161 | |||||||
| chr1:37567446 | T | G | 74 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(71): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.2043+227A>C | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 15/15 | chr1 | 37567446 | |||||||
| chr1:37567465 | C | T | 2 | a0001c0001t0001g0093 a0001c0001t0001g0095 |
2 | NA18747.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.2043+208G>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 15/15 | chr1 | 37567465 | |||||||
| chr1:37567616 | G | C | 3 | a0001c0001t0001g0012 a0001c0001t0001g0040 a0001c0001t0001g0103 |
7 | HG00280.hp1 HG00323.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.2043+57C>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 15/15 | chr1 | 37567616 | |||||||
| chr1:37567989 | T | C | 1 | a0001c0001t0004g0077 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1952-225A>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 14/15 | chr1 | 37567989 | |||||||
| chr1:37568164 | T | C | 1 | a0001c0001t0001g0146 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1951+111A>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 14/15 | chr1 | 37568164 | |||||||
| chr1:37568398 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1869-41G>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 13/15 | chr1 | 37568398 | |||||||
| chr1:37568427 | C | T | 1 | a0003c0002t0001g0073 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1869-70G>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 13/15 | chr1 | 37568427 | |||||||
| chr1:37568468 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1869-111A>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 13/15 | chr1 | 37568468 | |||||||
| chr1:37568558 | T | C | 1 | a0001c0001t0001g0168 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1869-201A>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 13/15 | chr1 | 37568558 | |||||||
| chr1:37568577 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1869-220G>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 13/15 | chr1 | 37568577 | |||||||
| chr1:37568706 | G | A | 72 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(69): Show |
155 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.1868+145C>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 13/15 | chr1 | 37568706 | |||||||
| chr1:37568839 | T | C | 1 | a0003c0002t0001g0073 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1868+12A>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 13/15 | chr1 | 37568839 | |||||||
| chr1:37569335 | G | C | 1 | a0001c0001t0001g0049 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1417-33C>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 12/15 | chr1 | 37569335 | |||||||
| chr1:37569340 | A | G | 1 | a0003c0002t0001g0073 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1417-38T>C | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 12/15 | chr1 | 37569340 | |||||||
| chr1:37569685 | G | T | 103 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(100): Show |
209 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.1417-383C>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 12/15 | chr1 | 37569685 | |||||||
| chr1:37569879 | C | G | 2 | a0001c0001t0001g0100 a0006c0006t0001g0044 |
2 | HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1417-577G>C | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 12/15 | chr1 | 37569879 | |||||||
| chr1:37570105 | T | C | 2 | a0001c0001t0001g0100 a0006c0006t0001g0044 |
2 | HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1417-803A>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 12/15 | chr1 | 37570105 | |||||||
| chr1:37570151 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1417-849C>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 12/15 | chr1 | 37570151 | |||||||
| chr1:37570360 | T | A | 1 | a0003c0002t0001g0073 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1417-1058A>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 12/15 | chr1 | 37570360 | |||||||
| chr1:37570410 | G | A | 1 | a0004c0004t0001g0097 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1417-1108C>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 12/15 | chr1 | 37570410 | |||||||
| chr1:37570448 | T | C | 6 | a0001c0001t0001g0014 a0001c0001t0001g0168 a0001c0001t0001g0169 others(3): Show |
9 | HG02145.hp1 HG02258.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1417-1146A>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 12/15 | chr1 | 37570448 | |||||||
| chr1:37570479 | G | A | 1 | a0003c0002t0001g0073 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1417-1177C>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 12/15 | chr1 | 37570479 | |||||||
| chr1:37570490 | A | G | 72 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(69): Show |
155 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.1417-1188T>C | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 12/15 | chr1 | 37570490 | |||||||
| chr1:37570519 | G | A | 72 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(69): Show |
155 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.1417-1217C>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 12/15 | chr1 | 37570519 | |||||||
| chr1:37570529 | C | CA | 5 | a0001c0001t0001g0012 a0001c0001t0001g0026 a0001c0001t0001g0040 others(2): Show |
10 | HG00280.hp1 HG00323.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1417-1228dupT | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 12/15 | chr1 | 37570529 | |||||||
| chr1:37570671 | A | C | 4 | a0001c0001t0001g0012 a0001c0001t0001g0040 a0001c0001t0001g0103 others(1): Show |
8 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(5): Show |
intron_variant | MODIFIER | c.1417-1369T>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 12/15 | chr1 | 37570671 | |||||||
| chr1:37570717 | G | C | 1 | a0001c0001t0001g0122 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1417-1415C>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 12/15 | chr1 | 37570717 | |||||||
| chr1:37570983 | C | T | 1 | a0001c0001t0004g0077 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1417-1681G>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 12/15 | chr1 | 37570983 | |||||||
| chr1:37571285 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1417-1983G>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 12/15 | chr1 | 37571285 | |||||||
| chr1:37571374 | C | A | 1 | a0001c0001t0001g0057 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1417-2072G>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 12/15 | chr1 | 37571374 | |||||||
| chr1:37571431 | A | G | 18 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0036 others(15): Show |
34 | HG00639.hp1 HG01167.hp2 HG01516.hp2 others(31): Show |
intron_variant | MODIFIER | c.1417-2129T>C | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 12/15 | chr1 | 37571431 | |||||||
| chr1:37571496 | T | G | 4 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0059 others(1): Show |
13 | HG02109.hp1 HG02615.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.1417-2194A>C | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 12/15 | chr1 | 37571496 | |||||||
| chr1:37571638 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1417-2336G>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 12/15 | chr1 | 37571638 | |||||||
| chr1:37571894 | G | A | 1 | a0001c0001t0001g0128 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1416+2449C>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 12/15 | chr1 | 37571894 | |||||||
| chr1:37571946 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1416+2397G>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 12/15 | chr1 | 37571946 | |||||||
| chr1:37571977 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1416+2366G>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 12/15 | chr1 | 37571977 | |||||||
| chr1:37572093 | T | A | 1 | a0001c0001t0001g0127 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1416+2250A>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 12/15 | chr1 | 37572093 | |||||||
| chr1:37572189 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1416+2154C>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 12/15 | chr1 | 37572189 | |||||||
| chr1:37572431 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1416+1912G>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 12/15 | chr1 | 37572431 | |||||||
| chr1:37572546 | A | T | 1 | a0001c0001t0001g0064 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1416+1797T>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 12/15 | chr1 | 37572546 | |||||||
| chr1:37572787 | G | A | 102 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(99): Show |
208 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.1416+1556C>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 12/15 | chr1 | 37572787 | |||||||
| chr1:37572935 | G | A | 2 | a0001c0001t0001g0100 a0006c0006t0001g0044 |
2 | HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1416+1408C>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 12/15 | chr1 | 37572935 | |||||||
| chr1:37572994 | G | A | 2 | a0001c0001t0001g0116 a0001c0001t0001g0132 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1416+1349C>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 12/15 | chr1 | 37572994 | |||||||
| chr1:37573322 | C | T | 7 | a0001c0001t0001g0014 a0001c0001t0001g0168 a0001c0001t0001g0169 others(4): Show |
10 | HG02145.hp1 HG02258.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1416+1021G>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 12/15 | chr1 | 37573322 | |||||||
| chr1:37573401 | C | A | 1 | a0001c0001t0001g0035 | 2 | NA18979.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.1416+942G>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 12/15 | chr1 | 37573401 | |||||||
| chr1:37573433 | T | C | 11 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0024 others(8): Show |
23 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.1416+910A>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 12/15 | chr1 | 37573433 | |||||||
| chr1:37573436 | C | T | 2 | a0001c0001t0001g0100 a0006c0006t0001g0044 |
2 | HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1416+907G>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 12/15 | chr1 | 37573436 | |||||||
| chr1:37573899 | T | A | 1 | a0001c0001t0001g0110 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1416+444A>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 12/15 | chr1 | 37573899 | |||||||
| chr1:37574023 | G | T | 1 | a0001c0001t0001g0127 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1416+320C>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 12/15 | chr1 | 37574023 | |||||||
| chr1:37574619 | T | C | 1 | a0001c0001t0001g0160 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1302+46A>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 11/15 | chr1 | 37574619 | |||||||
| chr1:37574655 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1302+10C>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 11/15 | chr1 | 37574655 | |||||||
| chr1:37574983 | G | C | 3 | a0001c0001t0001g0117 a0001c0001t0001g0133 a0001c0001t0001g0135 |
3 | HG00738.hp2 HG01070.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.1144-160C>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 10/15 | chr1 | 37574983 | |||||||
| chr1:37575010 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1144-187A>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 10/15 | chr1 | 37575010 | |||||||
| chr1:37575247 | C | A | 1 | a0001c0001t0004g0077 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1143+348G>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 10/15 | chr1 | 37575247 | |||||||
| chr1:37575380 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1143+215A>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 10/15 | chr1 | 37575380 | |||||||
| chr1:37575471 | A | T | 1 | a0001c0001t0001g0049 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1143+124T>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 10/15 | chr1 | 37575471 | |||||||
| chr1:37575881 | G | A | 2 | a0001c0001t0001g0037 a0008c0008t0001g0167 |
3 | HG00639.hp1 NA20805.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1039-182C>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 9/15 | chr1 | 37575881 | |||||||
| chr1:37576009 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1039-310G>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 9/15 | chr1 | 37576009 | |||||||
| chr1:37576100 | T | G | 143 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(140): Show |
309 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(306): Show |
intron_variant | MODIFIER | c.1038+328A>C | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 9/15 | chr1 | 37576100 | |||||||
| chr1:37576311 | A | G | 1 | a0001c0001t0001g0050 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1038+117T>C | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 9/15 | chr1 | 37576311 | |||||||
| chr1:37577004 | T | C | 1 | a0001c0001t0001g0094 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.910-448A>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37577004 | |||||||
| chr1:37577107 | C | CA | 5 | a0001c0001t0001g0022 a0001c0001t0001g0060 a0001c0001t0001g0068 others(2): Show |
6 | HG01255.hp1 HG02145.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.910-552dupT | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37577107 | |||||||
| chr1:37577193 | G | A | 1 | a0001c0001t0001g0079 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.910-637C>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37577193 | |||||||
| chr1:37577247 | C | G | 3 | a0001c0001t0001g0012 a0001c0001t0001g0040 a0001c0001t0001g0103 |
7 | HG00280.hp1 HG00323.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.910-691G>C | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37577247 | |||||||
| chr1:37577265 | C | T | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG00323.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.910-709G>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37577265 | |||||||
| chr1:37577325 | C | A | 38 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0015 others(35): Show |
96 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.910-769G>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37577325 | |||||||
| chr1:37577437 | G | A | 1 | a0001c0001t0001g0165 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.910-881C>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37577437 | |||||||
| chr1:37577526 | T | C | 1 | a0001c0001t0001g0056 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.910-970A>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37577526 | |||||||
| chr1:37577636 | T | C | 15 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0032 others(12): Show |
29 | HG00733.hp1 HG00738.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.910-1080A>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37577636 | |||||||
| chr1:37577651 | T | C | 1 | a0001c0001t0001g0043 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.910-1095A>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37577651 | |||||||
| chr1:37577656 | CAAT | C | 3 | a0001c0001t0001g0012 a0001c0001t0001g0040 a0001c0001t0001g0103 |
7 | HG00280.hp1 HG00323.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.910-1103_910-1101d others(5): Show |
GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37577656 | |||||||
| chr1:37577898 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.910-1342G>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37577898 | |||||||
| chr1:37577958 | T | C | 3 | a0001c0001t0001g0010 a0001c0001t0001g0027 a0001c0001t0001g0032 |
9 | HG01074.hp1 HG01515.hp1 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.910-1402A>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37577958 | |||||||
| chr1:37577969 | A | T | 2 | a0001c0001t0001g0100 a0006c0006t0001g0044 |
2 | HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.910-1413T>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37577969 | |||||||
| chr1:37578039 | A | G | 3 | a0001c0001t0001g0012 a0001c0001t0001g0040 a0001c0001t0001g0103 |
7 | HG00280.hp1 HG00323.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.910-1483T>C | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37578039 | |||||||
| chr1:37578135 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.910-1579G>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37578135 | |||||||
| chr1:37578242 | C | G | 3 | a0001c0001t0001g0017 a0001c0001t0001g0063 a0001c0001t0001g0064 |
5 | HG01891.hp1 HG02055.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.910-1686G>C | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37578242 | |||||||
| chr1:37578270 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.910-1714G>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37578270 | |||||||
| chr1:37578438 | C | CA | 6 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0036 others(3): Show |
12 | HG00280.hp1 HG00323.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.910-1883dupT | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37578438 | |||||||
| chr1:37578438 | CA | C | 4 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0023 others(1): Show |
9 | HG02257.hp2 HG02698.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.910-1883delT | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37578438 | |||||||
| chr1:37578604 | C | CT | 2 | a0001c0001t0001g0025 a0001c0001t0003g0042 |
3 | NA18992.hp1 NA19002.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.910-2049dupA | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37578604 | |||||||
| chr1:37578706 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.910-2150G>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37578706 | |||||||
| chr1:37578842 | G | C | 1 | a0001c0001t0001g0134 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.910-2286C>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37578842 | |||||||
| chr1:37578917 | T | C | 1 | a0001c0001t0001g0135 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.910-2361A>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37578917 | |||||||
| chr1:37579095 | C | G | 1 | a0001c0001t0001g0108 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.910-2539G>C | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37579095 | |||||||
| chr1:37579116 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.910-2560C>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37579116 | |||||||
| chr1:37579163 | A | G | 1 | a0001c0001t0001g0123 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.910-2607T>C | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37579163 | |||||||
| chr1:37579213 | T | C | 73 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(70): Show |
158 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.910-2657A>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37579213 | |||||||
| chr1:37579285 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.910-2729G>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37579285 | |||||||
| chr1:37579301 | A | G | 38 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0015 others(35): Show |
96 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.910-2745T>C | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37579301 | |||||||
| chr1:37579340 | A | G | 3 | a0001c0001t0001g0012 a0001c0001t0001g0040 a0001c0001t0001g0103 |
7 | HG00280.hp1 HG00323.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.910-2784T>C | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37579340 | |||||||
| chr1:37579356 | T | A | 1 | a0001c0001t0001g0122 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.910-2800A>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37579356 | |||||||
| chr1:37579377 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.910-2821C>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37579377 | |||||||
| chr1:37579420 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.909+2803C>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37579420 | |||||||
| chr1:37579524 | G | C | 93 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(90): Show |
194 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.909+2699C>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37579524 | |||||||
| chr1:37579673 | G | A | 38 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0015 others(35): Show |
96 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.909+2550C>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37579673 | |||||||
| chr1:37579713 | T | C | 2 | a0001c0001t0001g0105 a0001c0001t0001g0136 |
2 | NA18972.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.909+2510A>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37579713 | |||||||
| chr1:37579827 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.909+2396G>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37579827 | |||||||
| chr1:37579887 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.909+2336G>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37579887 | |||||||
| chr1:37579895 | CA | C | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(129): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.909+2327delT | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37579895 | |||||||
| chr1:37579895 | CAA | C | 7 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0084 others(4): Show |
7 | HG01069.hp2 HG01496.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.909+2326_909+2327d others(4): Show |
GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37579895 | |||||||
| chr1:37580112 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.909+2111T>C | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37580112 | |||||||
| chr1:37580154 | C | T | 1 | a0001c0001t0001g0158 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.909+2069G>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37580154 | |||||||
| chr1:37580334 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.909+1889C>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37580334 | |||||||
| chr1:37580426 | G | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0040 a0001c0001t0001g0103 |
7 | HG00280.hp1 HG00323.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.909+1797C>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37580426 | |||||||
| chr1:37580458 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.909+1765G>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37580458 | |||||||
| chr1:37580525 | G | T | 7 | a0001c0001t0001g0014 a0001c0001t0001g0168 a0001c0001t0001g0169 others(4): Show |
10 | HG02145.hp1 HG02258.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.909+1698C>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37580525 | |||||||
| chr1:37580553 | A | G | 3 | a0001c0001t0001g0012 a0001c0001t0001g0040 a0001c0001t0001g0103 |
7 | HG00280.hp1 HG00323.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.909+1670T>C | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37580553 | |||||||
| chr1:37580640 | C | T | 6 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0082 others(3): Show |
6 | HG00609.hp1 HG03831.hp1 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.909+1583G>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37580640 | |||||||
| chr1:37580845 | T | C | 4 | a0001c0001t0001g0012 a0001c0001t0001g0040 a0001c0001t0001g0103 others(1): Show |
8 | HG00280.hp1 HG00323.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.909+1378A>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37580845 | |||||||
| chr1:37580848 | C | G | 2 | a0001c0001t0001g0022 a0001c0001t0001g0060 |
3 | HG02145.hp2 HG02559.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.909+1375G>C | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37580848 | |||||||
| chr1:37580996 | AAAC | A | 4 | a0001c0001t0001g0096 a0001c0001t0001g0159 a0001c0001t0002g0041 others(1): Show |
5 | HG01074.hp2 HG01099.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.909+1224_909+1226d others(5): Show |
GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37580996 | |||||||
| chr1:37581048 | T | C | 1 | a0001c0001t0001g0016 | 3 | HG01109.hp1 HG02809.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.909+1175A>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37581048 | |||||||
| chr1:37581061 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.909+1162T>C | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37581061 | |||||||
| chr1:37581142 | T | C | 1 | a0001c0001t0001g0051 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.909+1081A>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37581142 | |||||||
| chr1:37581319 | G | T | 143 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(140): Show |
307 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(304): Show |
intron_variant | MODIFIER | c.909+904C>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37581319 | |||||||
| chr1:37581461 | C | G | 3 | a0001c0001t0001g0012 a0001c0001t0001g0040 a0001c0001t0001g0103 |
7 | HG00280.hp1 HG00323.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.909+762G>C | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37581461 | |||||||
| chr1:37581558 | T | C | 1 | a0001c0001t0001g0051 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.909+665A>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37581558 | |||||||
| chr1:37581625 | T | G | 3 | a0001c0001t0001g0012 a0001c0001t0001g0040 a0001c0001t0001g0103 |
7 | HG00280.hp1 HG00323.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.909+598A>C | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37581625 | |||||||
| chr1:37581667 | A | ATCT | 3 | a0001c0001t0001g0012 a0001c0001t0001g0040 a0001c0001t0001g0103 |
7 | HG00280.hp1 HG00323.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.909+553_909+555dup others(3): Show |
GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37581667 | |||||||
| chr1:37581741 | G | A | 18 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0036 others(15): Show |
34 | HG00639.hp1 HG01167.hp2 HG01516.hp2 others(31): Show |
intron_variant | MODIFIER | c.909+482C>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37581741 | |||||||
| chr1:37581784 | T | C | 3 | a0001c0001t0001g0012 a0001c0001t0001g0040 a0001c0001t0001g0103 |
7 | HG00280.hp1 HG00323.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.909+439A>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37581784 | |||||||
| chr1:37581790 | C | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0040 a0001c0001t0001g0103 |
7 | HG00280.hp1 HG00323.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.909+433G>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37581790 | |||||||
| chr1:37581853 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.909+370G>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37581853 | |||||||
| chr1:37581964 | C | T | 5 | a0001c0001t0001g0014 a0001c0001t0001g0168 a0001c0001t0001g0169 others(2): Show |
8 | HG02258.hp1 HG02486.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.909+259G>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37581964 | |||||||
| chr1:37581995 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.909+228G>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37581995 | |||||||
| chr1:37582117 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.909+106G>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37582117 | |||||||
| chr1:37582129 | A | C | 2 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
2 | HG00544.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.909+94T>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37582129 | |||||||
| chr1:37582207 | G | C | 3 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0104 |
7 | HG02055.hp2 HG02257.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.909+16C>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 8/15 | chr1 | 37582207 | |||||||
| chr1:37582383 | T | C | 1 | a0006c0006t0001g0044 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.796-47A>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 7/15 | chr1 | 37582383 | |||||||
| chr1:37582386 | C | T | 5 | a0001c0001t0001g0014 a0001c0001t0001g0168 a0001c0001t0001g0169 others(2): Show |
8 | HG02258.hp1 HG02486.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.796-50G>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 7/15 | chr1 | 37582386 | |||||||
| chr1:37582433 | T | C | 1 | a0003c0002t0001g0073 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.796-97A>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 7/15 | chr1 | 37582433 | |||||||
| chr1:37582690 | G | T | 1 | a0001c0001t0001g0081 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.795+88C>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 7/15 | chr1 | 37582690 | |||||||
| chr1:37582988 | G | T | 1 | a0001c0001t0001g0119 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.637-52C>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 6/15 | chr1 | 37582988 | |||||||
| chr1:37583004 | G | T | 1 | a0001c0001t0004g0077 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.637-68C>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 6/15 | chr1 | 37583004 | |||||||
| chr1:37583066 | C | T | 1 | a0001c0001t0004g0077 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.637-130G>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 6/15 | chr1 | 37583066 | |||||||
| chr1:37583072 | G | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0040 a0001c0001t0001g0103 |
7 | HG00280.hp1 HG00323.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.637-136C>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 6/15 | chr1 | 37583072 | |||||||
| chr1:37583133 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.637-197G>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 6/15 | chr1 | 37583133 | |||||||
| chr1:37583265 | T | C | 18 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0036 others(15): Show |
34 | HG00639.hp1 HG01167.hp2 HG01516.hp2 others(31): Show |
intron_variant | MODIFIER | c.637-329A>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 6/15 | chr1 | 37583265 | |||||||
| chr1:37583318 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.637-382G>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 6/15 | chr1 | 37583318 | |||||||
| chr1:37583667 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.636+200A>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 6/15 | chr1 | 37583667 | |||||||
| chr1:37583711 | C | T | 7 | a0001c0001t0001g0009 a0001c0001t0001g0036 a0001c0001t0001g0038 others(4): Show |
15 | NA18945.hp2 NA18946.hp1 NA18955.hp2 others(12): Show |
intron_variant | MODIFIER | c.636+156G>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 6/15 | chr1 | 37583711 | |||||||
| chr1:37583772 | C | T | 73 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(70): Show |
158 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.636+95G>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 6/15 | chr1 | 37583772 | |||||||
| chr1:37583806 | C | A | 1 | a0001c0001t0001g0049 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.636+61G>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 6/15 | chr1 | 37583806 | |||||||
| chr1:37583831 | G | C | 1 | a0001c0001t0001g0033 | 2 | NA18963.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.636+36C>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 6/15 | chr1 | 37583831 | |||||||
| chr1:37583837 | A | G | 1 | a0001c0001t0001g0118 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.636+30T>C | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 6/15 | chr1 | 37583837 | |||||||
| chr1:37583950 | C | T | 1 | a0001c0001t0001g0080 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.570-17G>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 5/15 | chr1 | 37583950 | |||||||
| chr1:37583951 | C | G | 143 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(140): Show |
309 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(306): Show |
intron_variant | MODIFIER | c.570-18G>C | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 5/15 | chr1 | 37583951 | |||||||
| chr1:37583965 | G | A | 18 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0036 others(15): Show |
34 | HG00639.hp1 HG01167.hp2 HG01516.hp2 others(31): Show |
intron_variant | MODIFIER | c.570-32C>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 5/15 | chr1 | 37583965 | |||||||
| chr1:37584062 | A | G | 1 | a0001c0001t0001g0047 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.570-129T>C | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 5/15 | chr1 | 37584062 | |||||||
| chr1:37584247 | G | A | 1 | a0001c0001t0001g0095 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.570-314C>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 5/15 | chr1 | 37584247 | |||||||
| chr1:37584307 | G | A | 73 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(70): Show |
158 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.570-374C>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 5/15 | chr1 | 37584307 | |||||||
| chr1:37584418 | G | T | 3 | a0001c0001t0001g0012 a0001c0001t0001g0040 a0001c0001t0001g0103 |
7 | HG00280.hp1 HG00323.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.570-485C>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 5/15 | chr1 | 37584418 | |||||||
| chr1:37584425 | T | C | 1 | a0001c0001t0001g0051 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.570-492A>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 5/15 | chr1 | 37584425 | |||||||
| chr1:37584461 | T | TA | 68 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(65): Show |
147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.570-529dupT | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 5/15 | chr1 | 37584461 | |||||||
| chr1:37584471 | AAAAAAAG | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0040 a0001c0001t0001g0103 |
7 | HG00280.hp1 HG00323.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.570-545_570-539del others(7): Show |
GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 5/15 | chr1 | 37584471 | |||||||
| chr1:37584477 | AG | A | 39 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(36): Show |
92 | HG00438.hp1 HG00544.hp1 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.570-545delC | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 5/15 | chr1 | 37584477 | |||||||
| chr1:37584478 | G | A | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(96): Show |
198 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.570-545C>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 5/15 | chr1 | 37584478 | |||||||
| chr1:37584611 | C | A | 1 | a0001c0001t0001g0033 | 2 | NA18963.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.570-678G>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 5/15 | chr1 | 37584611 | |||||||
| chr1:37584740 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.570-807A>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 5/15 | chr1 | 37584740 | |||||||
| chr1:37584851 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.570-918C>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 5/15 | chr1 | 37584851 | |||||||
| chr1:37584863 | T | C | 103 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(100): Show |
211 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.570-930A>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 5/15 | chr1 | 37584863 | |||||||
| chr1:37584942 | C | T | 7 | a0001c0001t0001g0011 a0001c0001t0001g0045 a0001c0001t0001g0048 others(4): Show |
10 | HG00323.hp2 HG02735.hp2 HG03239.hp1 others(7): Show |
intron_variant | MODIFIER | c.570-1009G>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 5/15 | chr1 | 37584942 | |||||||
| chr1:37584943 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.570-1010C>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 5/15 | chr1 | 37584943 | |||||||
| chr1:37585059 | CT | C | 37 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0012 others(34): Show |
99 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.570-1127delA | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 5/15 | chr1 | 37585059 | |||||||
| chr1:37585077 | T | C | 3 | a0001c0001t0001g0017 a0001c0001t0001g0064 a0001c0001t0001g0065 |
5 | HG01891.hp1 HG02451.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.570-1144A>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 5/15 | chr1 | 37585077 | |||||||
| chr1:37585162 | G | A | 5 | a0001c0001t0001g0014 a0001c0001t0001g0168 a0001c0001t0001g0169 others(2): Show |
8 | HG02258.hp1 HG02486.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.570-1229C>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 5/15 | chr1 | 37585162 | |||||||
| chr1:37585208 | G | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0040 a0001c0001t0001g0103 |
7 | HG00280.hp1 HG00323.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.570-1275C>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 5/15 | chr1 | 37585208 | |||||||
| chr1:37585251 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.570-1318C>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 5/15 | chr1 | 37585251 | |||||||
| chr1:37585305 | C | T | 3 | a0001c0001t0001g0030 a0001c0001t0001g0113 a0001c0001t0001g0152 |
4 | NA18949.hp2 NA18957.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.570-1372G>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 5/15 | chr1 | 37585305 | |||||||
| chr1:37585411 | G | T | 1 | a0001c0001t0001g0079 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.570-1478C>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 5/15 | chr1 | 37585411 | |||||||
| chr1:37585560 | T | C | 1 | a0001c0001t0004g0077 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.570-1627A>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 5/15 | chr1 | 37585560 | |||||||
| chr1:37585658 | A | G | 1 | a0003c0002t0001g0073 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.569+1653T>C | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 5/15 | chr1 | 37585658 | |||||||
| chr1:37585984 | G | A | 39 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0015 others(36): Show |
97 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.569+1327C>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 5/15 | chr1 | 37585984 | |||||||
| chr1:37586156 | T | C | 1 | a0001c0001t0001g0142 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.569+1155A>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 5/15 | chr1 | 37586156 | |||||||
| chr1:37586390 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.569+921C>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 5/15 | chr1 | 37586390 | |||||||
| chr1:37586410 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.569+901C>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 5/15 | chr1 | 37586410 | |||||||
| chr1:37586460 | A | G | 142 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(139): Show |
308 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(305): Show |
intron_variant | MODIFIER | c.569+851T>C | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 5/15 | chr1 | 37586460 | |||||||
| chr1:37586603 | A | T | 1 | a0001c0001t0001g0049 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.569+708T>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 5/15 | chr1 | 37586603 | |||||||
| chr1:37586711 | A | G | 1 | a0001c0001t0001g0078 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.569+600T>C | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 5/15 | chr1 | 37586711 | |||||||
| chr1:37586844 | C | T | 103 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(100): Show |
211 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.569+467G>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 5/15 | chr1 | 37586844 | |||||||
| chr1:37587109 | T | G | 3 | a0001c0001t0001g0012 a0001c0001t0001g0040 a0001c0001t0001g0103 |
7 | HG00280.hp1 HG00323.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.569+202A>C | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 5/15 | chr1 | 37587109 | |||||||
| chr1:37587132 | A | G | 1 | a0003c0002t0001g0073 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.569+179T>C | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 5/15 | chr1 | 37587132 | |||||||
| chr1:37587198 | C | T | 3 | a0001c0001t0001g0012 a0001c0001t0001g0040 a0001c0001t0001g0103 |
7 | HG00280.hp1 HG00323.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.569+113G>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 5/15 | chr1 | 37587198 | |||||||
| chr1:37587199 | G | A | 4 | a0001c0001t0001g0017 a0001c0001t0001g0063 a0001c0001t0001g0064 others(1): Show |
6 | HG01891.hp1 HG02055.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.569+112C>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 5/15 | chr1 | 37587199 | |||||||
| chr1:37587222 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.569+89C>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 5/15 | chr1 | 37587222 | |||||||
| chr1:37587266 | C | CA | 76 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(73): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.569+44dupT | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 5/15 | chr1 | 37587266 | |||||||
| chr1:37587609 | A | G | 1 | a0001c0001t0001g0112 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.385-114T>C | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 4/15 | chr1 | 37587609 | |||||||
| chr1:37587636 | A | C | 2 | a0001c0001t0001g0111 a0001c0001t0001g0149 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.385-141T>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 4/15 | chr1 | 37587636 | |||||||
| chr1:37587756 | G | T | 1 | a0001c0001t0001g0024 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.385-261C>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 4/15 | chr1 | 37587756 | |||||||
| chr1:37587857 | C | T | 3 | a0001c0001t0001g0012 a0001c0001t0001g0040 a0001c0001t0001g0103 |
7 | HG00280.hp1 HG00323.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.385-362G>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 4/15 | chr1 | 37587857 | |||||||
| chr1:37587897 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.385-402C>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 4/15 | chr1 | 37587897 | |||||||
| chr1:37587990 | A | C | 1 | a0001c0001t0001g0049 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.385-495T>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 4/15 | chr1 | 37587990 | |||||||
| chr1:37588089 | A | G | 7 | a0001c0001t0001g0014 a0001c0001t0001g0168 a0001c0001t0001g0169 others(4): Show |
10 | HG02145.hp1 HG02258.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.385-594T>C | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 4/15 | chr1 | 37588089 | |||||||
| chr1:37588310 | A | G | 7 | a0001c0001t0001g0011 a0001c0001t0001g0045 a0001c0001t0001g0048 others(4): Show |
10 | HG00323.hp2 HG02735.hp2 HG03239.hp1 others(7): Show |
intron_variant | MODIFIER | c.385-815T>C | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 4/15 | chr1 | 37588310 | |||||||
| chr1:37588327 | C | T | 7 | a0001c0001t0001g0014 a0001c0001t0001g0168 a0001c0001t0001g0169 others(4): Show |
10 | HG02145.hp1 HG02258.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.385-832G>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 4/15 | chr1 | 37588327 | |||||||
| chr1:37588423 | T | C | 5 | a0001c0001t0001g0014 a0001c0001t0001g0168 a0001c0001t0001g0169 others(2): Show |
8 | HG02258.hp1 HG02486.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.385-928A>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 4/15 | chr1 | 37588423 | |||||||
| chr1:37588539 | G | A | 3 | a0001c0001t0001g0096 a0001c0001t0002g0041 a0004c0004t0001g0097 |
4 | HG01074.hp2 HG01099.hp1 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.385-1044C>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 4/15 | chr1 | 37588539 | |||||||
| chr1:37588671 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.385-1176T>C | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 4/15 | chr1 | 37588671 | |||||||
| chr1:37588759 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.385-1264T>C | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 4/15 | chr1 | 37588759 | |||||||
| chr1:37588819 | A | G | 5 | a0001c0001t0001g0014 a0001c0001t0001g0168 a0001c0001t0001g0169 others(2): Show |
8 | HG02258.hp1 HG02486.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.385-1324T>C | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 4/15 | chr1 | 37588819 | |||||||
| chr1:37588827 | T | C | 2 | a0001c0001t0001g0048 a0001c0001t0001g0062 |
2 | NA18987.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.385-1332A>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 4/15 | chr1 | 37588827 | |||||||
| chr1:37589081 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.385-1586C>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 4/15 | chr1 | 37589081 | |||||||
| chr1:37589128 | T | C | 4 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0028 others(1): Show |
8 | HG00733.hp2 HG01168.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.384+1578A>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 4/15 | chr1 | 37589128 | |||||||
| chr1:37589465 | C | T | 2 | a0001c0001t0001g0109 a0001c0001t0001g0110 |
2 | HG01346.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.384+1241G>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 4/15 | chr1 | 37589465 | |||||||
| chr1:37589621 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.384+1085G>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 4/15 | chr1 | 37589621 | |||||||
| chr1:37589622 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.384+1084C>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 4/15 | chr1 | 37589622 | |||||||
| chr1:37589756 | T | A | 1 | a0001c0001t0001g0048 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.384+950A>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 4/15 | chr1 | 37589756 | |||||||
| chr1:37589884 | C | T | 3 | a0001c0001t0001g0017 a0001c0001t0001g0063 a0001c0001t0001g0064 |
5 | HG01891.hp1 HG02055.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.384+822G>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 4/15 | chr1 | 37589884 | |||||||
| chr1:37590009 | T | G | 2 | a0001c0001t0001g0100 a0006c0006t0001g0044 |
2 | HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.384+697A>C | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 4/15 | chr1 | 37590009 | |||||||
| chr1:37590095 | G | C | 4 | a0001c0001t0001g0017 a0001c0001t0001g0063 a0001c0001t0001g0064 others(1): Show |
6 | HG01891.hp1 HG02055.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.384+611C>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 4/15 | chr1 | 37590095 | |||||||
| chr1:37590188 | T | C | 1 | a0002c0007t0001g0147 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.384+518A>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 4/15 | chr1 | 37590188 | |||||||
| chr1:37590194 | C | A | 1 | a0001c0001t0001g0156 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.384+512G>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 4/15 | chr1 | 37590194 | |||||||
| chr1:37590371 | T | C | 1 | a0001c0001t0001g0101 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.384+335A>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 4/15 | chr1 | 37590371 | |||||||
| chr1:37590403 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.384+303C>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 4/15 | chr1 | 37590403 | |||||||
| chr1:37590415 | C | G | 1 | a0001c0001t0001g0156 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.384+291G>C | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 4/15 | chr1 | 37590415 | |||||||
| chr1:37590470 | G | T | 1 | a0001c0001t0001g0108 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.384+236C>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 4/15 | chr1 | 37590470 | |||||||
| chr1:37590983 | A | C | 3 | a0001c0001t0001g0029 a0001c0001t0001g0106 a0001c0001t0001g0107 |
4 | HG04184.hp2 NA18990.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.245-138T>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 3/15 | chr1 | 37590983 | |||||||
| chr1:37590994 | A | G | 18 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0036 others(15): Show |
34 | HG00639.hp1 HG01167.hp2 HG01516.hp2 others(31): Show |
intron_variant | MODIFIER | c.245-149T>C | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 3/15 | chr1 | 37590994 | |||||||
| chr1:37591215 | T | G | 73 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(70): Show |
158 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.245-370A>C | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 3/15 | chr1 | 37591215 | |||||||
| chr1:37591407 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.245-562A>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 3/15 | chr1 | 37591407 | |||||||
| chr1:37591445 | G | A | 2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | HG01993.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.245-600C>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 3/15 | chr1 | 37591445 | |||||||
| chr1:37591504 | C | CT | 29 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0014 others(26): Show |
49 | HG00639.hp1 HG01167.hp2 HG01516.hp2 others(46): Show |
intron_variant | MODIFIER | c.245-660dupA | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 3/15 | chr1 | 37591504 | |||||||
| chr1:37591504 | CT | C | 6 | a0001c0001t0001g0048 a0001c0001t0001g0067 a0001c0001t0001g0102 others(3): Show |
6 | HG01070.hp2 HG01123.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.245-660delA | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 3/15 | chr1 | 37591504 | |||||||
| chr1:37591515 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.245-670A>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 3/15 | chr1 | 37591515 | |||||||
| chr1:37591628 | C | T | 72 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(69): Show |
155 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.245-783G>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 3/15 | chr1 | 37591628 | |||||||
| chr1:37592056 | T | C | 1 | a0001c0001t0001g0069 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.244+656A>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 3/15 | chr1 | 37592056 | |||||||
| chr1:37592147 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.244+565A>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 3/15 | chr1 | 37592147 | |||||||
| chr1:37592161 | G | A | 1 | a0001c0001t0001g0028 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.244+551C>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 3/15 | chr1 | 37592161 | |||||||
| chr1:37592185 | G | A | 1 | a0001c0001t0001g0034 | 2 | HG00099.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.244+527C>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 3/15 | chr1 | 37592185 | |||||||
| chr1:37592265 | A | G | 143 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(140): Show |
307 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(304): Show |
intron_variant | MODIFIER | c.244+447T>C | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 3/15 | chr1 | 37592265 | |||||||
| chr1:37592280 | C | T | 6 | a0001c0001t0001g0013 a0001c0001t0001g0035 a0001c0001t0001g0152 others(3): Show |
10 | HG00544.hp2 NA18946.hp2 NA18979.hp1 others(7): Show |
intron_variant | MODIFIER | c.244+432G>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 3/15 | chr1 | 37592280 | |||||||
| chr1:37592281 | C | A | 6 | a0001c0001t0001g0013 a0001c0001t0001g0035 a0001c0001t0001g0152 others(3): Show |
10 | HG00544.hp2 NA18946.hp2 NA18979.hp1 others(7): Show |
intron_variant | MODIFIER | c.244+431G>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 3/15 | chr1 | 37592281 | |||||||
| chr1:37592335 | G | GAACTTCG others(26): Show |
1 | a0001c0001t0001g0045 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.244+344_244+376dup others(33): Show |
GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 3/15 | chr1 | 37592335 | |||||||
| chr1:37592341 | C | T | 2 | a0001c0001t0001g0019 a0001c0001t0001g0104 |
4 | HG02055.hp2 HG03041.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.244+371G>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 3/15 | chr1 | 37592341 | |||||||
| chr1:37592342 | G | A | 3 | a0001c0001t0001g0014 a0001c0001t0001g0170 a0001c0001t0001g0171 |
6 | HG02486.hp1 HG02647.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.244+370C>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 3/15 | chr1 | 37592342 | |||||||
| chr1:37592353 | C | T | 72 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(69): Show |
155 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.244+359G>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 3/15 | chr1 | 37592353 | |||||||
| chr1:37592572 | T | C | 1 | a0006c0006t0001g0044 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.244+140A>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 3/15 | chr1 | 37592572 | |||||||
| chr1:37592829 | A | G | 1 | a0003c0002t0001g0073 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.150-23T>C | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 2/15 | chr1 | 37592829 | |||||||
| chr1:37592996 | T | C | 3 | a0001c0001t0001g0012 a0001c0001t0001g0040 a0001c0001t0001g0103 |
7 | HG00280.hp1 HG00323.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.150-190A>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 2/15 | chr1 | 37592996 | |||||||
| chr1:37593047 | C | T | 5 | a0001c0001t0001g0014 a0001c0001t0001g0168 a0001c0001t0001g0169 others(2): Show |
8 | HG02258.hp1 HG02486.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.150-241G>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 2/15 | chr1 | 37593047 | |||||||
| chr1:37593092 | T | C | 91 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(88): Show |
192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.150-286A>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 2/15 | chr1 | 37593092 | |||||||
| chr1:37593382 | C | A | 1 | a0001c0001t0001g0166 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.149+380G>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 2/15 | chr1 | 37593382 | |||||||
| chr1:37593392 | A | G | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(141): Show |
310 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(307): Show |
intron_variant | MODIFIER | c.149+370T>C | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 2/15 | chr1 | 37593392 | |||||||
| chr1:37593494 | A | T | 1 | a0001c0001t0001g0049 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.149+268T>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 2/15 | chr1 | 37593494 | |||||||
| chr1:37593659 | A | T | 1 | a0005c0003t0001g0072 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.149+103T>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 2/15 | chr1 | 37593659 | |||||||
| chr1:37594278 | C | A | 1 | a0001c0001t0001g0070 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.65-432G>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 1/15 | chr1 | 37594278 | |||||||
| chr1:37594430 | C | A | 5 | a0001c0001t0001g0014 a0001c0001t0001g0168 a0001c0001t0001g0169 others(2): Show |
8 | HG02258.hp1 HG02486.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.65-584G>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 1/15 | chr1 | 37594430 | |||||||
| chr1:37594455 | G | A | 1 | a0001c0001t0001g0039 | 2 | HG01358.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.65-609C>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 1/15 | chr1 | 37594455 | |||||||
| chr1:37594530 | T | C | 1 | a0001c0001t0001g0172 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.65-684A>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 1/15 | chr1 | 37594530 | |||||||
| chr1:37594716 | A | T | 1 | a0001c0001t0001g0048 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.65-870T>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 1/15 | chr1 | 37594716 | |||||||
| chr1:37594910 | T | C | 1 | a0001c0001t0001g0173 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.64+849A>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 1/15 | chr1 | 37594910 | |||||||
| chr1:37594957 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.64+802G>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 1/15 | chr1 | 37594957 | |||||||
| chr1:37595121 | C | A | 1 | a0001c0001t0001g0045 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.64+638G>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 1/15 | chr1 | 37595121 | |||||||
| chr1:37595122 | T | A | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(138): Show |
305 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(302): Show |
intron_variant | MODIFIER | c.64+637A>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 1/15 | chr1 | 37595122 | |||||||
| chr1:37595132 | ATTGTCAA others(14): Show |
A | 1 | a0001c0001t0001g0045 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.64+606_64+626delAT others(19): Show |
GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 1/15 | chr1 | 37595132 | |||||||
| chr1:37595157 | T | G | 1 | a0001c0001t0001g0045 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.64+602A>C | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 1/15 | chr1 | 37595157 | |||||||
| chr1:37595166 | A | T | 1 | a0001c0001t0001g0045 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.64+593T>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 1/15 | chr1 | 37595166 | |||||||
| chr1:37595181 | A | T | 1 | a0001c0001t0001g0045 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.64+578T>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 1/15 | chr1 | 37595181 | |||||||
| chr1:37595182 | C | A | 1 | a0001c0001t0001g0045 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.64+577G>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 1/15 | chr1 | 37595182 | |||||||
| chr1:37595191 | A | G | 1 | a0001c0001t0001g0045 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.64+568T>C | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 1/15 | chr1 | 37595191 | |||||||
| chr1:37595192 | A | T | 1 | a0001c0001t0001g0045 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.64+567T>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 1/15 | chr1 | 37595192 | |||||||
| chr1:37595197 | C | A | 1 | a0001c0001t0001g0045 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.64+562G>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 1/15 | chr1 | 37595197 | |||||||
| chr1:37595199 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.64+560G>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 1/15 | chr1 | 37595199 | |||||||
| chr1:37595201 | C | A | 1 | a0001c0001t0001g0045 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.64+558G>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 1/15 | chr1 | 37595201 | |||||||
| chr1:37595213 | C | G | 1 | a0001c0001t0001g0045 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.64+546G>C | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 1/15 | chr1 | 37595213 | |||||||
| chr1:37595215 | T | TAGTAAAT others(15): Show |
1 | a0001c0001t0001g0045 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.64+543_64+544insTT others(20): Show |
GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 1/15 | chr1 | 37595215 | |||||||
| chr1:37595230 | T | C | 1 | a0001c0001t0001g0040 | 2 | HG02683.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.64+529A>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 1/15 | chr1 | 37595230 | |||||||
| chr1:37595236 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.64+523G>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 1/15 | chr1 | 37595236 | |||||||
| chr1:37595240 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.64+519G>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 1/15 | chr1 | 37595240 | |||||||
| chr1:37595241 | C | A | 1 | a0001c0001t0001g0045 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.64+518G>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 1/15 | chr1 | 37595241 | |||||||
| chr1:37595241 | C | G | 1 | a0001c0001t0001g0047 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.64+518G>C | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 1/15 | chr1 | 37595241 | |||||||
| chr1:37595243 | A | G | 1 | a0001c0001t0001g0045 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.64+516T>C | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 1/15 | chr1 | 37595243 | |||||||
| chr1:37595259 | C | A | 1 | a0001c0001t0001g0045 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.64+500G>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 1/15 | chr1 | 37595259 | |||||||
| chr1:37595268 | C | G | 1 | a0001c0001t0001g0045 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.64+491G>C | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 1/15 | chr1 | 37595268 | |||||||
| chr1:37595276 | C | A | 1 | a0001c0001t0001g0045 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.64+483G>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 1/15 | chr1 | 37595276 | |||||||
| chr1:37595282 | T | G | 1 | a0001c0001t0001g0045 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.64+477A>C | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 1/15 | chr1 | 37595282 | |||||||
| chr1:37595289 | G | C | 1 | a0001c0001t0001g0015 | 3 | HG02976.hp1 HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.64+470C>G | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 1/15 | chr1 | 37595289 | |||||||
| chr1:37595290 | A | T | 1 | a0001c0001t0001g0015 | 3 | HG02976.hp1 HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.64+469T>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 1/15 | chr1 | 37595290 | |||||||
| chr1:37595297 | T | A | 1 | a0001c0001t0001g0045 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.64+462A>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 1/15 | chr1 | 37595297 | |||||||
| chr1:37595302 | GGTTCTCT others(21): Show |
G | 1 | a0001c0001t0001g0045 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.64+429_64+456delAT others(26): Show |
GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 1/15 | chr1 | 37595302 | |||||||
| chr1:37595332 | A | G | 1 | a0001c0001t0001g0045 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.64+427T>C | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 1/15 | chr1 | 37595332 | |||||||
| chr1:37595363 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+396G>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 1/15 | chr1 | 37595363 | |||||||
| chr1:37595364 | A | T | 1 | a0001c0001t0001g0045 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.64+395T>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 1/15 | chr1 | 37595364 | |||||||
| chr1:37595486 | C | T | 1 | a0006c0006t0001g0044 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.64+273G>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 1/15 | chr1 | 37595486 | |||||||
| chr1:37595563 | C | A | 1 | a0001c0001t0001g0174 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.64+196G>T | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 1/15 | chr1 | 37595563 | |||||||
| chr1:37595689 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.64+70G>A | GNL2 | ENSG00000134697.13 | transcript | ENST00000373062.8 | protein_coding | 1/15 | chr1 | 37595689 |