Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 114794 |
|---|---|
| ensemblid | ENSG00000166897.16 |
| hgncid | 29396 |
| symbol | ELFN2 |
| name | extracellular leucine rich repeat and fibronectin type III domain containing 2 |
| refseq_nuc | NM_052906.5 |
| refseq_prot | NP_443138.2 |
| ensembl_nuc | ENST00000402918.7 |
| ensembl_prot | ENSP00000385277.1 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 37367960 |
| end | 37427479 |
| strand | - |
| ver | v1.2 |
| region | chr22:37367960-37427479 |
| region5000 | chr22:37362960-37432479 |
| regionname0 | ELFN2_chr22_37367960_37427479 |
| regionname5000 | ELFN2_chr22_37362960_37432479 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 820 | 326 | 92 | 56 | 123 | 15 | 38 | 78 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0002 | 0/0 | 820 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0003 | 0/0 | 820 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0004 | 0/0 | 820 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0005 | 0/0 | 820 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0006 | 0/0 | 820 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 2463 | 118 | 37 | 23 | 43 | 6 | 9 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| c0002 | 0/1 | 2463 | 104 | 21 | 18 | 47 | 3 | 14 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| c0003 | 1/0 | 2463 | 71 | 14 | 9 | 30 | 3 | 14 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| c0004 | 0/0 | 2463 | 6 | 0 | 3 | 0 | 3 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| c0005 | 0/0 | 2463 | 5 | 5 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| c0006 | 0/0 | 2463 | 5 | 3 | 1 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| c0007 | 0/0 | 2463 | 4 | 4 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| c0008 | 0/0 | 2463 | 4 | 4 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| c0009 | 0/0 | 2463 | 4 | 1 | 1 | 1 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| c0010 | 0/0 | 2463 | 3 | 3 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| c0011 | 0/0 | 2463 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| c0012 | 0/0 | 2463 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| c0013 | 0/0 | 2463 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| c0014 | 0/0 | 2463 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| c0015 | 0/0 | 2463 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| c0016 | 0/0 | 2463 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| c0017 | 0/0 | 2463 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| c0018 | 0/0 | 2463 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| c0019 | 0/0 | 2463 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| c0020 | 0/0 | 2463 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 5908 | 49 | 8 | 7 | 26 | 2 | 5 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0002 | 0/0 | 5910 | 35 | 0 | 4 | 29 | 1 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0003 | 0/0 | 5907 | 28 | 2 | 15 | 1 | 3 | 7 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0004 | 0/0 | 5910 | 27 | 3 | 3 | 12 | 3 | 6 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0005 | 0/0 | 5907 | 16 | 16 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0006 | 0/1 | 5910 | 14 | 0 | 6 | 4 | 0 | 3 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0007 | 0/0 | 5907 | 11 | 0 | 1 | 7 | 0 | 3 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0008 | 0/0 | 5907 | 9 | 2 | 1 | 6 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0009 | 0/0 | 5907 | 7 | 6 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0010 | 0/0 | 5911 | 6 | 0 | 3 | 0 | 3 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0011 | 0/0 | 5910 | 5 | 5 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0012 | 0/0 | 5908 | 5 | 0 | 1 | 0 | 1 | 3 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0013 | 0/0 | 5910 | 3 | 0 | 0 | 3 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0014 | 0/0 | 5907 | 3 | 0 | 0 | 3 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0015 | 0/0 | 5913 | 3 | 3 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0016 | 0/0 | 5909 | 3 | 3 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0017 | 0/0 | 5903 | 3 | 2 | 0 | 0 | 1 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0018 | 0/0 | 5910 | 3 | 1 | 2 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0019 | 0/0 | 5910 | 3 | 0 | 0 | 3 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0020 | 0/0 | 5908 | 3 | 0 | 0 | 3 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0021 | 0/0 | 5907 | 3 | 3 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0022 | 0/0 | 5903 | 3 | 3 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0023 | 0/0 | 5910 | 2 | 0 | 0 | 2 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0024 | 0/0 | 5916 | 2 | 0 | 0 | 2 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0025 | 0/0 | 5912 | 2 | 1 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0026 | 0/0 | 5913 | 2 | 0 | 0 | 2 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0027 | 0/0 | 5909 | 2 | 2 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0028 | 0/0 | 5910 | 2 | 0 | 0 | 2 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0029 | 0/0 | 5910 | 2 | 0 | 0 | 2 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0030 | 0/0 | 5906 | 2 | 2 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0031 | 0/0 | 5910 | 2 | 0 | 2 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0032 | 0/0 | 5910 | 2 | 0 | 0 | 2 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0033 | 0/0 | 5910 | 2 | 0 | 0 | 1 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0034 | 0/0 | 5908 | 2 | 0 | 0 | 0 | 0 | 2 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0035 | 0/0 | 5908 | 2 | 1 | 0 | 0 | 1 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0036 | 0/0 | 5907 | 2 | 2 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0037 | 0/0 | 5907 | 2 | 0 | 2 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0038 | 0/0 | 5911 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0039 | 0/0 | 5907 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0040 | 0/0 | 5907 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0041 | 0/0 | 5918 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0042 | 0/0 | 5915 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0043 | 0/0 | 5915 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0044 | 0/0 | 5916 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0045 | 0/0 | 5912 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0046 | 0/0 | 5913 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0047 | 0/0 | 5913 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0048 | 0/0 | 5913 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0049 | 0/0 | 5911 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0050 | 0/0 | 5909 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0051 | 0/0 | 5910 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0052 | 0/0 | 5910 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0053 | 0/0 | 5907 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0054 | 0/0 | 5908 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0055 | 0/0 | 5907 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0056 | 0/0 | 5907 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0057 | 0/0 | 5907 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0058 | 0/0 | 5907 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0059 | 0/0 | 5903 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0060 | 0/0 | 5903 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0061 | 0/0 | 5903 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0062 | 0/0 | 5904 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0063 | 0/0 | 5900 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0064 | 0/0 | 5901 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0065 | 0/0 | 5901 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0066 | 0/0 | 5916 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0067 | 0/0 | 5916 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0068 | 0/0 | 5916 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0069 | 0/0 | 5916 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0070 | 0/0 | 5914 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0071 | 0/0 | 5911 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0072 | 0/0 | 5911 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0073 | 0/0 | 5911 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0074 | 0/0 | 5909 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0075 | 0/0 | 5910 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0076 | 0/0 | 5910 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0077 | 0/0 | 5910 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0078 | 0/0 | 5910 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0079 | 0/0 | 5910 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0080 | 0/0 | 5910 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0081 | 0/0 | 5908 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0082 | 0/0 | 5907 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0083 | 0/0 | 5907 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0084 | 0/0 | 5908 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0085 | 0/0 | 5908 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0086 | 0/0 | 5908 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0087 | 0/0 | 5908 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0088 | 0/0 | 5906 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0089 | 0/0 | 5907 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0090 | 0/0 | 5907 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0091 | 0/0 | 5907 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0092 | 0/0 | 5907 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0093 | 0/0 | 5907 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0094 | 0/0 | 5907 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0095 | 0/0 | 5907 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0096 | 0/0 | 5907 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0097 | 0/0 | 5906 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0098 | 0/0 | 5910 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| t0099 | 0/0 | 5907 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0144 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0301 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2463 | 118 | 37 | 23 | 43 | 6 | 9 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0002 | 0/1 | 2463 | 104 | 21 | 18 | 47 | 3 | 14 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0003 | 1/0 | 2463 | 71 | 14 | 9 | 30 | 3 | 14 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0004 | 0/0 | 2463 | 6 | 0 | 3 | 0 | 3 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0005 | 0/0 | 2463 | 5 | 5 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0006 | 0/0 | 2463 | 5 | 3 | 1 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0008 | 0/0 | 2463 | 4 | 4 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0009 | 0/0 | 2463 | 4 | 1 | 1 | 1 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0010 | 0/0 | 2463 | 3 | 3 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0011 | 0/0 | 2463 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0013 | 0/0 | 2463 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0015 | 0/0 | 2463 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0018 | 0/0 | 2463 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0019 | 0/0 | 2463 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0020 | 0/0 | 2463 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0002c0007 | 0/0 | 2463 | 4 | 4 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0003c0017 | 0/0 | 2463 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0004c0012 | 0/0 | 2463 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0005c0014 | 0/0 | 2463 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0006c0016 | 0/0 | 2463 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/0 | 8372 | 30 | 0 | 3 | 25 | 1 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0001t0003 | 0/0 | 8369 | 28 | 2 | 15 | 1 | 3 | 7 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0001t0005 | 0/0 | 8369 | 16 | 16 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0001t0009 | 0/0 | 8369 | 7 | 6 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0001t0017 | 0/0 | 8365 | 3 | 2 | 0 | 0 | 1 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0001t0019 | 0/0 | 8372 | 3 | 0 | 0 | 3 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0001t0023 | 0/0 | 8372 | 2 | 0 | 0 | 2 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0001t0024 | 0/0 | 8378 | 2 | 0 | 0 | 2 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0001t0025 | 0/0 | 8374 | 2 | 1 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0001t0026 | 0/0 | 8375 | 2 | 0 | 0 | 2 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0001t0027 | 0/0 | 8371 | 2 | 2 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0001t0028 | 0/0 | 8372 | 2 | 0 | 0 | 2 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0001t0029 | 0/0 | 8372 | 2 | 0 | 0 | 2 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0001t0030 | 0/0 | 8368 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0001t0050 | 0/0 | 8371 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0001t0051 | 0/0 | 8372 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0001t0052 | 0/0 | 8372 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0001t0053 | 0/0 | 8369 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0001t0057 | 0/0 | 8369 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0001t0058 | 0/0 | 8369 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0001t0060 | 0/0 | 8365 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0001t0061 | 0/0 | 8365 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0001t0062 | 0/0 | 8366 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0001t0063 | 0/0 | 8362 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0001t0064 | 0/0 | 8363 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0001t0065 | 0/0 | 8363 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0001t0096 | 0/0 | 8369 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0001t0097 | 0/0 | 8368 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0001t0098 | 0/0 | 8372 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0001t0099 | 0/0 | 8369 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0002t0004 | 0/0 | 8372 | 26 | 3 | 3 | 11 | 3 | 6 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0002t0006 | 0/1 | 8372 | 13 | 0 | 5 | 4 | 0 | 3 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0002t0007 | 0/0 | 8369 | 11 | 0 | 1 | 7 | 0 | 3 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0002t0008 | 0/0 | 8369 | 9 | 2 | 1 | 6 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0002t0013 | 0/0 | 8372 | 3 | 0 | 0 | 3 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0002t0014 | 0/0 | 8369 | 3 | 0 | 0 | 3 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0002t0018 | 0/0 | 8372 | 3 | 1 | 2 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0002t0021 | 0/0 | 8369 | 3 | 3 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0002t0022 | 0/0 | 8365 | 3 | 3 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0002t0031 | 0/0 | 8372 | 2 | 0 | 2 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0002t0032 | 0/0 | 8372 | 2 | 0 | 0 | 2 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0002t0033 | 0/0 | 8372 | 2 | 0 | 0 | 1 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0002t0036 | 0/0 | 8369 | 2 | 2 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0002t0037 | 0/0 | 8369 | 2 | 0 | 2 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0002t0039 | 0/0 | 8369 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0002t0040 | 0/0 | 8369 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0002t0066 | 0/0 | 8378 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0002t0067 | 0/0 | 8378 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0002t0068 | 0/0 | 8378 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0002t0069 | 0/0 | 8378 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0002t0071 | 0/0 | 8373 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0002t0074 | 0/0 | 8371 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0002t0075 | 0/0 | 8372 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0002t0076 | 0/0 | 8372 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0002t0077 | 0/0 | 8372 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0002t0078 | 0/0 | 8372 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0002t0079 | 0/0 | 8372 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0002t0082 | 0/0 | 8369 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0002t0084 | 0/0 | 8370 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0002t0088 | 0/0 | 8368 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0002t0089 | 0/0 | 8369 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0002t0090 | 0/0 | 8369 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0002t0091 | 0/0 | 8369 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0002t0095 | 0/0 | 8369 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0003t0001 | 1/0 | 8370 | 45 | 6 | 7 | 25 | 1 | 5 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0003t0006 | 0/0 | 8372 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0003t0012 | 0/0 | 8370 | 4 | 0 | 0 | 0 | 1 | 3 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0003t0020 | 0/0 | 8370 | 3 | 0 | 0 | 3 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0003t0034 | 0/0 | 8370 | 2 | 0 | 0 | 0 | 0 | 2 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0003t0035 | 0/0 | 8370 | 2 | 1 | 0 | 0 | 1 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0003t0038 | 0/0 | 8373 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0003t0041 | 0/0 | 8380 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0003t0042 | 0/0 | 8377 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0003t0043 | 0/0 | 8377 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0003t0044 | 0/0 | 8378 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0003t0070 | 0/0 | 8376 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0003t0073 | 0/0 | 8373 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0003t0081 | 0/0 | 8370 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0003t0083 | 0/0 | 8369 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0003t0085 | 0/0 | 8370 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0003t0087 | 0/0 | 8370 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0003t0092 | 0/0 | 8369 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0003t0093 | 0/0 | 8369 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0003t0094 | 0/0 | 8369 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0004t0010 | 0/0 | 8373 | 6 | 0 | 3 | 0 | 3 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0005t0011 | 0/0 | 8372 | 5 | 5 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0006t0001 | 0/0 | 8370 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0006t0047 | 0/0 | 8375 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0006t0048 | 0/0 | 8375 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0006t0054 | 0/0 | 8370 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0006t0056 | 0/0 | 8369 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0008t0015 | 0/0 | 8375 | 3 | 3 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0008t0046 | 0/0 | 8375 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0009t0002 | 0/0 | 8372 | 2 | 0 | 1 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0009t0049 | 0/0 | 8373 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0009t0055 | 0/0 | 8369 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0010t0016 | 0/0 | 8371 | 3 | 3 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0011t0059 | 0/0 | 8365 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0013t0012 | 0/0 | 8370 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0015t0080 | 0/0 | 8372 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0018t0045 | 0/0 | 8374 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0019t0030 | 0/0 | 8368 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0001c0020t0002 | 0/0 | 8372 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0002c0007t0001 | 0/0 | 8370 | 2 | 2 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0002c0007t0072 | 0/0 | 8373 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0002c0007t0086 | 0/0 | 8370 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0003c0017t0002 | 0/0 | 8372 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0004c0012t0001 | 0/0 | 8370 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0005c0014t0004 | 0/0 | 8372 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| a0006c0016t0002 | 0/0 | 8372 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | copy fasta | chr22 | 37362960 | 37432479 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0003g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0003g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0003g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0003g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0003g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0003g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0003g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0005g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0005g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0005g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0005g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0005g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0005g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0005g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0005g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0005g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0005g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0005g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0005g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0005g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0005g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0005g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0005g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0009g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0009g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0009g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0009g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0009g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0009g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0009g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0017g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0017g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0017g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0019g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0019g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0019g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0023g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0023g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0024g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0024g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0025g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0025g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0026g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0026g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0027g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0027g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0028g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0028g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0029g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0029g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0030g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0050g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0051g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0052g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0053g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0057g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0058g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0060g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0061g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0062g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0063g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0064g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0065g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0096g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0097g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0098g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0099g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0004g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0004g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0004g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0004g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0004g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0004g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0004g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0004g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0004g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0004g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0004g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0004g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0004g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0004g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0004g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0004g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0004g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0004g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0004g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0004g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0004g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0004g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0004g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0004g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0006g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0006g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0006g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0006g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0006g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0006g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0006g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0006g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0006g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0006g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0006g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0006g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0006g0301 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0007g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0007g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0007g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0007g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0007g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0007g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0007g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0007g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0007g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0007g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0007g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0008g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0008g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0008g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0008g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0008g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0008g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0008g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0008g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0008g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0013g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0013g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0013g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0014g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0014g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0014g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0018g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0018g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0021g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0021g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0021g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0022g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0022g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0022g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0031g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0031g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0032g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0032g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0033g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0033g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0036g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0036g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0037g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0037g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0039g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0040g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0066g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0067g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0068g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0069g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0071g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0074g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0075g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0076g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0077g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0078g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0079g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0082g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0084g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0088g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0089g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0090g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0091g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0095g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0144 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0006g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0012g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0012g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0012g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0012g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0020g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0020g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0020g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0034g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0034g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0035g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0035g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0038g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0041g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0042g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0043g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0044g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0070g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0073g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0081g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0083g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0085g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0087g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0092g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0093g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0094g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0004t0010g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0004t0010g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0004t0010g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0004t0010g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0004t0010g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0004t0010g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0005t0011g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0005t0011g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0005t0011g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0005t0011g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0005t0011g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0006t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0006t0047g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0006t0048g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0006t0054g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0006t0056g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0008t0015g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0008t0015g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0008t0015g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0008t0046g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0009t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0009t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0009t0049g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0009t0055g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0010t0016g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0010t0016g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0010t0016g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0011t0059g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0013t0012g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0015t0080g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0018t0045g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0019t0030g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0020t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0002c0007t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0002c0007t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0002c0007t0072g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0002c0007t0086g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0003c0017t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0004c0012t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0005c0014t0004g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0006c0016t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0035 | g0057 | EUR | GBR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG00099 | hp2 | a0001 | c0001 | t0058 | g0186 | EUR | GBR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG00140 | hp1 | a0001 | c0003 | t0012 | g0245 | EUR | GBR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG00140 | hp2 | a0001 | c0002 | t0004 | g0238 | EUR | GBR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0300 | EUR | FIN | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG00323 | hp2 | a0001 | c0003 | t0001 | g0313 | EUR | FIN | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG00408 | hp1 | a0001 | c0003 | t0020 | g0115 | EAS | CHS | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG00408 | hp2 | a0001 | c0002 | t0007 | g0129 | EAS | CHS | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | CHS | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG00423 | hp2 | a0001 | c0002 | t0007 | g0205 | EAS | CHS | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG00438 | hp1 | a0001 | c0003 | t0001 | g0103 | EAS | CHS | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG00438 | hp2 | a0003 | c0017 | t0002 | g0046 | EAS | CHS | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG00544 | hp1 | a0001 | c0003 | t0001 | g0015 | EAS | CHS | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG00544 | hp2 | a0001 | c0002 | t0004 | g0302 | EAS | CHS | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0282 | EAS | CHS | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG00558 | hp2 | a0001 | c0006 | t0001 | g0277 | EAS | CHS | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG00597 | hp1 | a0001 | c0003 | t0020 | g0033 | EAS | CHS | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG00597 | hp2 | a0001 | c0002 | t0004 | g0297 | EAS | CHS | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG00609 | hp1 | a0001 | c0003 | t0001 | g0040 | EAS | CHS | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG00609 | hp2 | a0001 | c0003 | t0001 | g0065 | EAS | CHS | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG00621 | hp1 | a0001 | c0002 | t0004 | g0014 | EAS | CHS | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG00621 | hp2 | a0001 | c0001 | t0029 | g0098 | EAS | CHS | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG00639 | hp1 | a0001 | c0002 | t0007 | g0309 | AMR | PUR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG00639 | hp2 | a0001 | c0001 | t0009 | g0210 | AMR | PUR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG00642 | hp1 | a0001 | c0003 | t0001 | g0026 | AMR | PUR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG00642 | hp2 | a0001 | c0002 | t0004 | g0191 | AMR | PUR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG00733 | hp1 | a0001 | c0004 | t0010 | g0304 | AMR | PUR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0242 | AMR | PUR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG00735 | hp1 | a0001 | c0002 | t0004 | g0092 | AMR | PUR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0126 | AMR | PUR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG00741 | hp1 | a0001 | c0003 | t0001 | g0125 | AMR | PUR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0122 | AMR | PUR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01081 | hp1 | a0001 | c0002 | t0071 | g0069 | AMR | PUR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01081 | hp2 | a0001 | c0002 | t0006 | g0264 | AMR | PUR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01099 | hp1 | a0001 | c0002 | t0069 | g0009 | AMR | PUR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01099 | hp2 | a0001 | c0004 | t0010 | g0236 | AMR | PUR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01106 | hp1 | a0001 | c0003 | t0001 | g0064 | AMR | PUR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0269 | AMR | PUR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01109 | hp1 | a0001 | c0001 | t0062 | g0158 | AMR | PUR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01109 | hp2 | a0001 | c0002 | t0008 | g0231 | AMR | PUR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01167 | hp1 | a0001 | c0003 | t0006 | g0121 | AMR | PUR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | PUR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01168 | hp1 | a0001 | c0003 | t0081 | g0182 | AMR | PUR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01168 | hp2 | a0001 | c0002 | t0006 | g0272 | AMR | PUR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01169 | hp1 | a0001 | c0002 | t0006 | g0253 | AMR | PUR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01175 | hp1 | a0001 | c0002 | t0004 | g0143 | AMR | PUR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0054 | AMR | PUR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01192 | hp1 | a0001 | c0003 | t0001 | g0061 | AMR | PUR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01192 | hp2 | a0001 | c0003 | t0001 | g0124 | AMR | PUR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01255 | hp1 | a0001 | c0013 | t0012 | g0068 | AMR | CLM | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0193 | AMR | CLM | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01256 | hp1 | a0001 | c0002 | t0006 | g0271 | AMR | CLM | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01256 | hp2 | a0001 | c0002 | t0037 | g0110 | AMR | CLM | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0086 | AMR | CLM | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01257 | hp2 | a0001 | c0002 | t0031 | g0174 | AMR | CLM | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01258 | hp1 | a0001 | c0002 | t0006 | g0270 | AMR | CLM | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01258 | hp2 | a0001 | c0002 | t0031 | g0175 | AMR | CLM | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01261 | hp1 | a0001 | c0002 | t0018 | g0001 | AMR | CLM | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01346 | hp1 | a0001 | c0003 | t0001 | g0055 | AMR | CLM | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01346 | hp2 | a0001 | c0002 | t0018 | g0001 | AMR | CLM | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0180 | AMR | CLM | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01358 | hp2 | a0001 | c0001 | t0099 | g0331 | AMR | CLM | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01361 | hp1 | a0001 | c0002 | t0037 | g0113 | AMR | CLM | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0060 | AMR | CLM | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01433 | hp1 | a0001 | c0003 | t0001 | g0118 | AMR | CLM | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01433 | hp2 | a0001 | c0001 | t0025 | g0239 | AMR | CLM | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01496 | hp1 | a0001 | c0006 | t0056 | g0220 | AMR | CLM | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0206 | AMR | CLM | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01515 | hp1 | a0004 | c0012 | t0001 | g0243 | EUR | IBS | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01515 | hp2 | a0001 | c0004 | t0010 | g0179 | EUR | IBS | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01516 | hp1 | a0001 | c0001 | t0017 | g0319 | EUR | IBS | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0244 | EUR | IBS | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01517 | hp1 | a0001 | c0004 | t0010 | g0246 | EUR | IBS | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0178 | EUR | IBS | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01884 | hp1 | a0001 | c0006 | t0054 | g0020 | AFR | ACB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01884 | hp2 | a0001 | c0001 | t0005 | g0070 | AFR | ACB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01891 | hp1 | a0001 | c0010 | t0016 | g0296 | AFR | ACB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01891 | hp2 | a0001 | c0005 | t0011 | g0196 | AFR | ACB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01928 | hp2 | a0001 | c0009 | t0002 | g0251 | AMR | PEL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0045 | AMR | PEL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0185 | AMR | PEL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0221 | AMR | PEL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0087 | AMR | PEL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02015 | hp1 | a0001 | c0001 | t0026 | g0293 | EAS | KHV | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02015 | hp2 | a0001 | c0003 | t0001 | g0024 | EAS | KHV | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02027 | hp1 | a0001 | c0002 | t0095 | g0096 | EAS | KHV | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02027 | hp2 | a0001 | c0002 | t0004 | g0085 | EAS | KHV | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | KHV | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | KHV | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02055 | hp1 | a0001 | c0002 | t0004 | g0157 | AFR | ACB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02055 | hp2 | a0001 | c0006 | t0047 | g0203 | AFR | ACB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02056 | hp1 | a0001 | c0002 | t0014 | g0031 | EAS | KHV | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02056 | hp2 | a0001 | c0001 | t0051 | g0025 | EAS | KHV | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0306 | EAS | KHV | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02071 | hp2 | a0001 | c0002 | t0013 | g0076 | EAS | KHV | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02074 | hp1 | a0001 | c0020 | t0002 | g0256 | EAS | KHV | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02074 | hp2 | a0001 | c0003 | t0001 | g0030 | EAS | KHV | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | KHV | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02080 | hp2 | a0001 | c0002 | t0004 | g0192 | EAS | KHV | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | KHV | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02083 | hp2 | a0001 | c0003 | t0001 | g0066 | EAS | KHV | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | KHV | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02129 | hp2 | a0001 | c0002 | t0004 | g0290 | EAS | KHV | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02132 | hp1 | a0001 | c0002 | t0013 | g0075 | EAS | KHV | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02132 | hp2 | a0001 | c0002 | t0004 | g0263 | EAS | KHV | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02145 | hp1 | a0001 | c0010 | t0016 | g0288 | AFR | ACB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02145 | hp2 | a0001 | c0003 | t0001 | g0177 | AFR | ACB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02148 | hp1 | a0001 | c0001 | t0057 | g0194 | AMR | PEL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02148 | hp2 | a0001 | c0004 | t0010 | g0073 | AMR | PEL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02155 | hp1 | a0001 | c0002 | t0004 | g0173 | EAS | CDX | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02155 | hp2 | a0001 | c0003 | t0001 | g0274 | EAS | CDX | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02165 | hp1 | a0001 | c0002 | t0007 | g0117 | EAS | CDX | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02165 | hp2 | a0001 | c0002 | t0032 | g0037 | EAS | CDX | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02257 | hp1 | a0001 | c0001 | t0005 | g0202 | AFR | ACB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02257 | hp2 | a0001 | c0003 | t0035 | g0058 | AFR | ACB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02258 | hp1 | a0001 | c0002 | t0088 | g0289 | AFR | ACB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02258 | hp2 | a0001 | c0001 | t0009 | g0311 | AFR | ACB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02280 | hp1 | a0001 | c0001 | t0063 | g0325 | AFR | ACB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02280 | hp2 | a0002 | c0007 | t0001 | g0214 | AFR | ACB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02451 | hp1 | a0001 | c0003 | t0001 | g0043 | AFR | ACB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02451 | hp2 | a0001 | c0005 | t0011 | g0212 | AFR | ACB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02523 | hp1 | a0001 | c0001 | t0029 | g0114 | EAS | KHV | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02523 | hp2 | a0001 | c0001 | t0026 | g0059 | EAS | KHV | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02572 | hp1 | a0001 | c0002 | t0021 | g0134 | AFR | GWD | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02572 | hp2 | a0001 | c0001 | t0030 | g0153 | AFR | GWD | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02602 | hp1 | a0001 | c0002 | t0004 | g0089 | SAS | PJL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02602 | hp2 | a0001 | c0001 | t0052 | g0116 | SAS | PJL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02615 | hp1 | a0001 | c0002 | t0004 | g0146 | AFR | GWD | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02615 | hp2 | a0001 | c0008 | t0015 | g0160 | AFR | GWD | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02622 | hp1 | a0001 | c0001 | t0050 | g0145 | AFR | GWD | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02622 | hp2 | a0001 | c0001 | t0009 | g0168 | AFR | GWD | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02630 | hp1 | a0001 | c0003 | t0070 | g0166 | AFR | GWD | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02630 | hp2 | a0001 | c0003 | t0001 | g0149 | AFR | GWD | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02647 | hp1 | a0001 | c0001 | t0027 | g0204 | AFR | GWD | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02647 | hp2 | a0001 | c0001 | t0005 | g0136 | AFR | GWD | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02717 | hp1 | a0001 | c0019 | t0030 | g0127 | AFR | GWD | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02717 | hp2 | a0001 | c0003 | t0083 | g0219 | AFR | GWD | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0135 | AFR | GWD | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02723 | hp2 | a0001 | c0002 | t0036 | g0165 | AFR | GWD | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0273 | SAS | PJL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0084 | SAS | PJL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02738 | hp1 | a0001 | c0002 | t0007 | g0188 | SAS | PJL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02738 | hp2 | a0001 | c0003 | t0001 | g0016 | SAS | PJL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02809 | hp1 | a0001 | c0008 | t0046 | g0162 | AFR | GWD | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02809 | hp2 | a0001 | c0018 | t0045 | g0172 | AFR | GWD | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02818 | hp1 | a0001 | c0001 | t0060 | g0226 | AFR | GWD | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02818 | hp2 | a0001 | c0002 | t0067 | g0233 | AFR | GWD | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02886 | hp1 | a0001 | c0001 | t0009 | g0227 | AFR | GWD | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02886 | hp2 | a0002 | c0007 | t0072 | g0323 | AFR | GWD | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02895 | hp1 | a0001 | c0002 | t0066 | g0232 | AFR | GWD | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02895 | hp2 | a0001 | c0001 | t0005 | g0018 | AFR | GWD | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02896 | hp1 | a0001 | c0002 | t0077 | g0159 | AFR | GWD | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02896 | hp2 | a0001 | c0003 | t0001 | g0200 | AFR | GWD | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02897 | hp1 | a0001 | c0001 | t0005 | g0019 | AFR | GWD | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02897 | hp2 | a0001 | c0003 | t0001 | g0201 | AFR | GWD | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0209 | AFR | ESN | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02922 | hp2 | a0001 | c0005 | t0011 | g0211 | AFR | ESN | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02965 | hp1 | a0001 | c0002 | t0068 | g0133 | AFR | ESN | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0150 | AFR | ESN | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02970 | hp1 | a0001 | c0001 | t0005 | g0154 | AFR | ESN | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02970 | hp2 | a0001 | c0002 | t0021 | g0197 | AFR | ESN | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02976 | hp1 | a0001 | c0001 | t0064 | g0310 | AFR | ESN | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02976 | hp2 | a0001 | c0001 | t0005 | g0152 | AFR | ESN | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03017 | hp1 | a0001 | c0002 | t0007 | g0187 | SAS | PJL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03017 | hp2 | a0001 | c0003 | t0001 | g0062 | SAS | PJL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03041 | hp1 | a0001 | c0010 | t0016 | g0295 | AFR | GWD | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03041 | hp2 | a0001 | c0001 | t0005 | g0225 | AFR | GWD | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03098 | hp1 | a0002 | c0007 | t0086 | g0316 | AFR | MSL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03098 | hp2 | a0001 | c0001 | t0009 | g0167 | AFR | MSL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03130 | hp1 | a0001 | c0001 | t0005 | g0155 | AFR | ESN | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03130 | hp2 | a0001 | c0003 | t0001 | g0327 | AFR | ESN | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03195 | hp1 | a0001 | c0011 | t0059 | g0218 | AFR | ESN | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03195 | hp2 | a0001 | c0001 | t0017 | g0128 | AFR | ESN | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03209 | hp1 | a0001 | c0002 | t0022 | g0156 | AFR | MSL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03209 | hp2 | a0001 | c0003 | t0041 | g0163 | AFR | MSL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03225 | hp1 | a0001 | c0001 | t0027 | g0216 | AFR | MSL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03225 | hp2 | a0002 | c0007 | t0001 | g0215 | AFR | MSL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03239 | hp1 | a0001 | c0002 | t0006 | g0266 | SAS | PJL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03239 | hp2 | a0001 | c0003 | t0092 | g0322 | SAS | PJL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03453 | hp1 | a0001 | c0008 | t0015 | g0170 | AFR | MSL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0164 | AFR | MSL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03486 | hp1 | a0001 | c0006 | t0048 | g0132 | AFR | MSL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0151 | AFR | MSL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03490 | hp1 | a0001 | c0002 | t0004 | g0139 | SAS | PJL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03490 | hp2 | a0001 | c0003 | t0034 | g0279 | SAS | PJL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0286 | SAS | PJL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03491 | hp2 | a0001 | c0003 | t0012 | g0294 | SAS | PJL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03492 | hp1 | a0001 | c0003 | t0034 | g0278 | SAS | PJL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0265 | SAS | PJL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03516 | hp1 | a0001 | c0005 | t0011 | g0213 | AFR | ESN | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03516 | hp2 | a0001 | c0001 | t0009 | g0171 | AFR | ESN | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03540 | hp1 | a0001 | c0001 | t0097 | g0324 | AFR | GWD | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03540 | hp2 | a0001 | c0002 | t0082 | g0320 | AFR | GWD | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03579 | hp1 | a0001 | c0001 | t0005 | g0148 | AFR | MSL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03579 | hp2 | a0001 | c0001 | t0061 | g0183 | AFR | MSL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03654 | hp1 | a0001 | c0002 | t0004 | g0010 | SAS | PJL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03654 | hp2 | a0001 | c0003 | t0001 | g0022 | SAS | PJL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0042 | SAS | STU | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03688 | hp2 | a0001 | c0003 | t0012 | g0067 | SAS | STU | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03704 | hp1 | a0001 | c0003 | t0001 | g0141 | SAS | PJL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03704 | hp2 | a0001 | c0002 | t0004 | g0249 | SAS | PJL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03710 | hp1 | a0001 | c0003 | t0094 | g0008 | SAS | PJL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03710 | hp2 | a0001 | c0002 | t0004 | g0027 | SAS | PJL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03831 | hp1 | a0001 | c0002 | t0007 | g0190 | SAS | BEB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03831 | hp2 | a0001 | c0003 | t0001 | g0138 | SAS | BEB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03834 | hp1 | a0001 | c0002 | t0006 | g0137 | SAS | BEB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03834 | hp2 | a0001 | c0002 | t0033 | g0023 | SAS | BEB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03927 | hp1 | a0001 | c0009 | t0055 | g0013 | SAS | BEB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03927 | hp2 | a0001 | c0003 | t0073 | g0012 | SAS | BEB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG04115 | hp1 | a0001 | c0002 | t0006 | g0247 | SAS | STU | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG04115 | hp2 | a0001 | c0003 | t0012 | g0308 | SAS | STU | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0041 | SAS | BEB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG04184 | hp2 | a0001 | c0003 | t0085 | g0189 | SAS | BEB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG04228 | hp1 | a0001 | c0002 | t0089 | g0131 | SAS | STU | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG04228 | hp2 | a0001 | c0002 | t0004 | g0142 | SAS | STU | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18522 | hp1 | a0001 | c0002 | t0036 | g0321 | AFR | YRI | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18522 | hp2 | a0001 | c0005 | t0011 | g0207 | AFR | YRI | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18612 | hp1 | a0001 | c0002 | t0033 | g0198 | EAS | CHB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18612 | hp2 | a0001 | c0001 | t0023 | g0077 | EAS | CHB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18747 | hp1 | a0001 | c0003 | t0001 | g0036 | EAS | CHB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | CHB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18906 | hp1 | a0001 | c0003 | t0042 | g0229 | AFR | YRI | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18906 | hp2 | a0001 | c0002 | t0074 | g0223 | AFR | YRI | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18939 | hp1 | a0001 | c0003 | t0001 | g0109 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18939 | hp2 | a0001 | c0003 | t0001 | g0028 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18941 | hp1 | a0001 | c0002 | t0007 | g0106 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18941 | hp2 | a0001 | c0003 | t0020 | g0039 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18943 | hp1 | a0001 | c0001 | t0053 | g0090 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18943 | hp2 | a0001 | c0002 | t0008 | g0093 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18944 | hp1 | a0001 | c0003 | t0001 | g0268 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18945 | hp1 | a0001 | c0002 | t0090 | g0235 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18948 | hp1 | a0001 | c0001 | t0096 | g0050 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18948 | hp2 | a0006 | c0016 | t0002 | g0261 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18949 | hp1 | a0001 | c0002 | t0008 | g0047 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18949 | hp2 | a0001 | c0002 | t0039 | g0006 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18950 | hp1 | a0001 | c0001 | t0019 | g0108 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18950 | hp2 | a0001 | c0002 | t0079 | g0237 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18952 | hp1 | a0001 | c0002 | t0004 | g0021 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18952 | hp2 | a0001 | c0003 | t0087 | g0299 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18960 | hp1 | a0001 | c0001 | t0023 | g0120 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18960 | hp2 | a0001 | c0002 | t0014 | g0080 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18962 | hp1 | a0001 | c0003 | t0038 | g0074 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18962 | hp2 | a0001 | c0002 | t0006 | g0095 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18964 | hp1 | a0001 | c0001 | t0024 | g0260 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18964 | hp2 | a0001 | c0002 | t0008 | g0049 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18966 | hp1 | a0001 | c0002 | t0084 | g0048 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18967 | hp1 | a0001 | c0002 | t0078 | g0104 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18968 | hp1 | a0001 | c0002 | t0091 | g0051 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18969 | hp2 | a0001 | c0003 | t0001 | g0082 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18971 | hp1 | a0001 | c0003 | t0001 | g0063 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18971 | hp2 | a0001 | c0003 | t0001 | g0101 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18973 | hp2 | a0001 | c0002 | t0014 | g0078 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18975 | hp2 | a0001 | c0002 | t0006 | g0195 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18980 | hp1 | a0001 | c0003 | t0001 | g0099 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18981 | hp1 | a0001 | c0002 | t0007 | g0072 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18981 | hp2 | a0001 | c0002 | t0008 | g0081 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18982 | hp2 | a0001 | c0003 | t0001 | g0094 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18983 | hp1 | a0001 | c0001 | t0098 | g0330 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18983 | hp2 | a0001 | c0001 | t0019 | g0107 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18986 | hp1 | a0001 | c0009 | t0002 | g0112 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18986 | hp2 | a0001 | c0003 | t0001 | g0303 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18991 | hp1 | a0001 | c0002 | t0075 | g0088 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18991 | hp2 | a0001 | c0003 | t0001 | g0011 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18995 | hp1 | a0001 | c0003 | t0001 | g0100 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18995 | hp2 | a0001 | c0002 | t0008 | g0184 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18998 | hp1 | a0001 | c0002 | t0008 | g0056 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19000 | hp2 | a0001 | c0001 | t0028 | g0276 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19005 | hp1 | a0001 | c0003 | t0001 | g0053 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19005 | hp2 | a0001 | c0001 | t0019 | g0258 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19012 | hp1 | a0001 | c0001 | t0028 | g0312 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19030 | hp1 | a0001 | c0001 | t0017 | g0208 | AFR | LWK | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0292 | AFR | LWK | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0217 | AFR | LWK | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19043 | hp2 | a0001 | c0002 | t0018 | g0176 | AFR | LWK | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19056 | hp2 | a0001 | c0002 | t0006 | g0280 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19058 | hp1 | a0001 | c0002 | t0076 | g0035 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19058 | hp2 | a0001 | c0003 | t0001 | g0234 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19065 | hp1 | a0001 | c0001 | t0024 | g0259 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19065 | hp2 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19066 | hp1 | a0001 | c0002 | t0032 | g0305 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19066 | hp2 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19068 | hp1 | a0001 | c0002 | t0004 | g0038 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19068 | hp2 | a0001 | c0002 | t0007 | g0071 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19074 | hp1 | a0001 | c0003 | t0001 | g0083 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19080 | hp1 | a0001 | c0002 | t0040 | g0007 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19085 | hp2 | a0001 | c0002 | t0013 | g0079 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19088 | hp1 | a0001 | c0002 | t0006 | g0181 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19088 | hp2 | a0001 | c0002 | t0004 | g0034 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19089 | hp1 | a0005 | c0014 | t0004 | g0032 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19089 | hp2 | a0001 | c0002 | t0007 | g0091 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19240 | hp1 | a0001 | c0001 | t0065 | g0169 | AFR | YRI | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19240 | hp2 | a0001 | c0001 | t0009 | g0017 | AFR | YRI | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA20129 | hp1 | a0001 | c0003 | t0044 | g0329 | AFR | ASW | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA20129 | hp2 | a0001 | c0003 | t0043 | g0230 | AFR | ASW | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0287 | EUR | TSI | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA20752 | hp2 | a0001 | c0002 | t0004 | g0199 | EUR | TSI | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA20805 | hp1 | a0001 | c0004 | t0010 | g0307 | EUR | TSI | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA20805 | hp2 | a0001 | c0002 | t0004 | g0254 | EUR | TSI | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0140 | SAS | GIH | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0224 | SAS | GIH | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02109 | hp1 | a0001 | c0008 | t0015 | g0161 | AFR | ACB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02109 | hp2 | a0001 | c0002 | t0004 | g0328 | AFR | ACB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02486 | hp1 | a0001 | c0002 | t0022 | g0317 | AFR | ACB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02486 | hp2 | a0001 | c0015 | t0080 | g0222 | AFR | ACB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02559 | hp1 | a0001 | c0002 | t0008 | g0314 | AFR | ACB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02559 | hp2 | a0001 | c0001 | t0025 | g0326 | AFR | ACB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03471 | hp1 | a0001 | c0002 | t0008 | g0228 | AFR | MSL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0044 | AFR | MSL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA20300 | hp1 | a0001 | c0009 | t0049 | g0291 | AFR | USA | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA20300 | hp2 | a0001 | c0002 | t0021 | g0147 | AFR | USA | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA21309 | hp1 | a0001 | c0003 | t0093 | g0318 | AFR | LWK | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA21309 | hp2 | a0001 | c0002 | t0022 | g0315 | AFR | LWK | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0006 | g0301 | REF | REF | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| homoSapiens_grch38 | hp1 | a0001 | c0003 | t0001 | g0144 | REF | REF | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:37373356
|
G | A | 1 | a0004 | 1 | HG01515.hp1 | missense_variant | MODERATE | c.2179C>T | p.Arg727Cys | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 2974/8370 | 2179/2463 | 727/820 | chr22 | 37373356 | ||
| chr22:37373455
|
T | C | 1 | a0005 | 1 | NA19089.hp1 | missense_variant | MODERATE | c.2080A>G | p.Ile694Val | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 2875/8370 | 2080/2463 | 694/820 | chr22 | 37373455 | ||
| chr22:37373646
|
C | T | 1 | a0003 | 1 | HG00438.hp2 | missense_variant | MODERATE | c.1889G>A | p.Ser630Asn | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 2684/8370 | 1889/2463 | 630/820 | chr22 | 37373646 | ||
| chr22:37373983
|
C | T | 1 | a0006 | 1 | NA18948.hp2 | missense_variant | MODERATE | c.1552G>A | p.Glu518Lys | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 2347/8370 | 1552/2463 | 518/820 | chr22 | 37373983 | ||
| chr22:37374750
|
G | T | 1 | a0002 | 4 | HG02280.hp2 HG02886.hp2 HG03098.hp1 others(1): Show |
missense_variant | MODERATE | c.785C>A | p.Ser262Tyr | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 1580/8370 | 785/2463 | 262/820 | chr22 | 37374750 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:37373672
|
G | A | 1 | a0001c0010 | 3 | HG01891.hp1 HG02145.hp1 HG03041.hp1 |
synonymous_variant | LOW | c.1863C>T | p.Asp621Asp | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 2658/8370 | 1863/2463 | 621/820 | chr22 | 37373672 | ||
| chr22:37374008
|
G | A | 1 | a0001c0013 | 1 | HG01255.hp1 | synonymous_variant | LOW | c.1527C>T | p.Ala509Ala | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 2322/8370 | 1527/2463 | 509/820 | chr22 | 37374008 | ||
| chr22:37374026
|
G | T | 9 | a0001c0001a0001c0005a0001c0010others(6): Show | 132 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(129): Show |
synonymous_variant | LOW | c.1509C>A | p.Ile503Ile | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 2304/8370 | 1509/2463 | 503/820 | chr22 | 37374026 | ||
| chr22:37374068
|
G | A | 2 | a0001c0008a0001c0018 | 5 | HG02109.hp1 HG02615.hp2 HG02809.hp1 others(2): Show |
synonymous_variant | LOW | c.1467C>T | p.Ala489Ala | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 2262/8370 | 1467/2463 | 489/820 | chr22 | 37374068 | ||
| chr22:37374170
|
G | A | 1 | a0001c0008 | 4 | HG02109.hp1 HG02615.hp2 HG02809.hp1 others(1): Show |
synonymous_variant | LOW | c.1365C>T | p.Ala455Ala | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 2160/8370 | 1365/2463 | 455/820 | chr22 | 37374170 | ||
| chr22:37374317
|
A | G | 12 | a0001c0001a0001c0005a0001c0006others(9): Show | 145 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(142): Show |
synonymous_variant | LOW | c.1218T>C | p.Phe406Phe | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 2013/8370 | 1218/2463 | 406/820 | chr22 | 37374317 | ||
| chr22:37374590
|
G | A | 3 | a0001c0002a0001c0015a0005c0014 | 106 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(103): Show |
synonymous_variant | LOW | c.945C>T | p.Ile315Ile | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 1740/8370 | 945/2463 | 315/820 | chr22 | 37374590 | ||
| chr22:37374743
|
G | A | 1 | a0001c0019 | 1 | HG02717.hp1 | synonymous_variant | LOW | c.792C>T | p.Asp264Asp | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 1587/8370 | 792/2463 | 264/820 | chr22 | 37374743 | ||
| chr22:37374905
|
G | A | 1 | a0001c0020 | 1 | HG02074.hp1 | synonymous_variant | LOW | c.630C>T | p.Tyr210Tyr | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 1425/8370 | 630/2463 | 210/820 | chr22 | 37374905 | ||
| chr22:37375100
|
G | A | 1 | a0001c0015 | 1 | HG02486.hp2 | synonymous_variant | LOW | c.435C>T | p.Thr145Thr | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 1230/8370 | 435/2463 | 145/820 | chr22 | 37375100 | ||
| chr22:37375118
|
G | A | 10 | a0001c0001a0001c0004a0001c0009others(7): Show | 137 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(134): Show |
synonymous_variant | LOW | c.417C>T | p.Ile139Ile | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 1212/8370 | 417/2463 | 139/820 | chr22 | 37375118 | ||
| chr22:37375328
|
G | T | 1 | a0001c0011 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.207C>A | p.Ala69Ala | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 1002/8370 | 207/2463 | 69/820 | chr22 | 37375328 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:37368100
|
G | C | 1 | a0001c0002t0021 | 3 | HG02572.hp1 HG02970.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4972C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 4972 | chr22 | 37368100 | |||||
| chr22:37368114
|
C | A | 1 | a0001c0001t0017 | 3 | HG01516.hp1 HG03195.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4958G>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 4958 | chr22 | 37368114 | |||||
| chr22:37368173
|
C | T | 3 | a0001c0001t0009a0001c0002t0077a0001c0006t0054 | 9 | HG00639.hp2 HG01884.hp1 HG02258.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4899G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 4899 | chr22 | 37368173 | |||||
| chr22:37368213
|
T | C | 43 | a0001c0001t0017a0001c0001t0027a0001c0001t0028others(40): Show | 117 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*4859A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 4859 | chr22 | 37368213 | |||||
| chr22:37368299
|
G | A | 1 | a0001c0003t0094 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4773C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 4773 | chr22 | 37368299 | |||||
| chr22:37368310
|
C | T | 1 | a0001c0002t0021 | 3 | HG02572.hp1 HG02970.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4762G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 4762 | chr22 | 37368310 | |||||
| chr22:37368363
|
T | G | 1 | a0001c0002t0021 | 3 | HG02572.hp1 HG02970.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4709A>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 4709 | chr22 | 37368363 | |||||
| chr22:37368383
|
G | A | 8 | a0001c0002t0066a0001c0002t0067a0001c0003t0081others(5): Show | 10 | HG01168.hp1 HG02109.hp1 HG02615.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4689C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 4689 | chr22 | 37368383 | |||||
| chr22:37368474
|
G | C | 1 | a0001c0001t0027 | 2 | HG02647.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4598C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 4598 | chr22 | 37368474 | |||||
| chr22:37368527
|
C | G | 82 | a0001c0001t0002a0001c0001t0003a0001c0001t0017others(79): Show | 228 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(225): Show |
3_prime_UTR_variant | MODIFIER | c.*4545G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 4545 | chr22 | 37368527 | |||||
| chr22:37368572
|
G | A | 1 | a0001c0002t0089 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4500C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 4500 | chr22 | 37368572 | |||||
| chr22:37368596
|
C | T | 1 | a0001c0003t0020 | 3 | HG00408.hp1 HG00597.hp1 NA18941.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4476G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 4476 | chr22 | 37368596 | |||||
| chr22:37368647
|
C | T | 1 | a0001c0001t0019 | 3 | NA18950.hp1 NA18983.hp2 NA19005.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4425G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 4425 | chr22 | 37368647 | |||||
| chr22:37368845
|
C | A | 1 | a0001c0002t0067 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4227G>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 4227 | chr22 | 37368845 | |||||
| chr22:37368854
|
C | T | 6 | a0001c0001t0065a0001c0002t0006a0001c0002t0031others(3): Show | 19 | HG01081.hp2 HG01167.hp1 HG01168.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*4218G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 4218 | chr22 | 37368854 | |||||
| chr22:37368930
|
T | C | 1 | a0002c0007t0086 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4142A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 4142 | chr22 | 37368930 | |||||
| chr22:37368975
|
C | G | 1 | a0001c0001t0051 | 1 | HG02056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4097G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 4097 | chr22 | 37368975 | |||||
| chr22:37369002
|
T | C | 1 | a0001c0002t0021 | 3 | HG02572.hp1 HG02970.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4070A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 4070 | chr22 | 37369002 | |||||
| chr22:37369117
|
C | T | 2 | a0001c0002t0066a0001c0002t0067 | 2 | HG02818.hp2 HG02895.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3955G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 3955 | chr22 | 37369117 | |||||
| chr22:37369158
|
C | T | 1 | a0001c0002t0031 | 2 | HG01257.hp2 HG01258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3914G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 3914 | chr22 | 37369158 | |||||
| chr22:37369232
|
C | A | 2 | a0001c0002t0036a0001c0002t0082 | 3 | HG02723.hp2 HG03540.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3840G>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 3840 | chr22 | 37369232 | |||||
| chr22:37369335
|
C | G | 1 | a0001c0002t0090 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3737G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 3737 | chr22 | 37369335 | |||||
| chr22:37369444
|
C | T | 1 | a0001c0001t0057 | 1 | HG02148.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3628G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 3628 | chr22 | 37369444 | |||||
| chr22:37369464
|
G | A | 1 | a0001c0003t0073 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3608C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 3608 | chr22 | 37369464 | |||||
| chr22:37369542
|
C | T | 7 | a0001c0002t0066a0001c0002t0067a0001c0003t0092others(4): Show | 9 | HG02109.hp1 HG02615.hp2 HG02809.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3530G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 3530 | chr22 | 37369542 | |||||
| chr22:37369843
|
C | T | 1 | a0001c0003t0092 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3229G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 3229 | chr22 | 37369843 | |||||
| chr22:37369903
|
T | C | 1 | a0001c0001t0064 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3169A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 3169 | chr22 | 37369903 | |||||
| chr22:37370000
|
G | A | 1 | a0001c0002t0078 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3072C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 3072 | chr22 | 37370000 | |||||
| chr22:37370027
|
G | A | 43 | a0001c0001t0017a0001c0001t0028a0001c0001t0060others(40): Show | 119 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(116): Show |
3_prime_UTR_variant | MODIFIER | c.*3045C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 3045 | chr22 | 37370027 | |||||
| chr22:37370048
|
A | C | 14 | a0001c0001t0017a0001c0001t0028a0001c0001t0060others(11): Show | 34 | HG00408.hp2 HG00423.hp2 HG00639.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*3024T>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 3024 | chr22 | 37370048 | |||||
| chr22:37370053
|
T | C | 1 | a0001c0002t0079 | 1 | NA18950.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3019A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 3019 | chr22 | 37370053 | |||||
| chr22:37370088
|
G | A | 1 | a0001c0006t0047 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2984C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 2984 | chr22 | 37370088 | |||||
| chr22:37370156
|
T | C | 23 | a0001c0001t0002a0001c0001t0003a0001c0001t0019others(20): Show | 87 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*2916A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 2916 | chr22 | 37370156 | |||||
| chr22:37370284
|
G | A | 3 | a0001c0008t0015a0001c0008t0046a0001c0011t0059 | 5 | HG02109.hp1 HG02615.hp2 HG02809.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2788C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 2788 | chr22 | 37370284 | |||||
| chr22:37370431
|
G | T | 1 | a0001c0004t0010 | 6 | HG00733.hp1 HG01099.hp2 HG01515.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2641C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 2641 | chr22 | 37370431 | |||||
| chr22:37370504
|
G | A | 1 | a0001c0002t0040 | 1 | NA19080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2568C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 2568 | chr22 | 37370504 | |||||
| chr22:37370517
|
C | T | 1 | a0001c0006t0054 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2555G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 2555 | chr22 | 37370517 | |||||
| chr22:37370542
|
G | A | 2 | a0001c0002t0088a0001c0018t0045 | 2 | HG02258.hp1 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2530C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 2530 | chr22 | 37370542 | |||||
| chr22:37370625
|
G | A | 2 | a0001c0002t0022a0001c0003t0083 | 4 | HG02486.hp1 HG02717.hp2 HG03209.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2447C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 2447 | chr22 | 37370625 | |||||
| chr22:37370653
|
A | G | 49 | a0001c0001t0017a0001c0001t0028a0001c0001t0060others(46): Show | 127 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*2419T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 2419 | chr22 | 37370653 | |||||
| chr22:37370769
|
C | T | 6 | a0001c0001t0065a0001c0002t0006a0001c0002t0031others(3): Show | 20 | HG01081.hp2 HG01167.hp1 HG01168.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2303G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 2303 | chr22 | 37370769 | |||||
| chr22:37370953
|
A | G | 7 | a0001c0001t0025a0001c0001t0027a0001c0001t0050others(4): Show | 15 | HG01433.hp2 HG01891.hp2 HG02258.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2119T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 2119 | chr22 | 37370953 | |||||
| chr22:37370955
|
G | C | 7 | a0001c0001t0025a0001c0001t0027a0001c0001t0050others(4): Show | 15 | HG01433.hp2 HG01891.hp2 HG02258.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2117C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 2117 | chr22 | 37370955 | |||||
| chr22:37370983
|
G | C | 5 | a0001c0001t0027a0001c0001t0050a0001c0002t0021others(2): Show | 8 | HG02258.hp1 HG02572.hp1 HG02622.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2089C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 2089 | chr22 | 37370983 | |||||
| chr22:37371371
|
G | A | 1 | a0001c0001t0065 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1701C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 1701 | chr22 | 37371371 | |||||
| chr22:37371554
|
G | C | 5 | a0001c0001t0025a0001c0001t0027a0001c0002t0088others(2): Show | 7 | HG01433.hp2 HG02258.hp1 HG02559.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1518C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 1518 | chr22 | 37371554 | |||||
| chr22:37371732
|
C | T | 1 | a0001c0003t0041 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1340G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 1340 | chr22 | 37371732 | |||||
| chr22:37371807
|
TG | T | 20 | a0001c0001t0017a0001c0001t0025a0001c0001t0027others(17): Show | 28 | HG01433.hp2 HG01516.hp1 HG01891.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1264delC | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 1264 | chr22 | 37371807 | |||||
| chr22:37371952
|
G | T | 1 | a0001c0003t0034 | 2 | HG03490.hp2 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1120C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 1120 | chr22 | 37371952 | |||||
| chr22:37372210
|
C | T | 1 | a0001c0001t0061 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*862G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 862 | chr22 | 37372210 | |||||
| chr22:37372230
|
C | T | 1 | a0001c0011t0059 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*842G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 842 | chr22 | 37372230 | |||||
| chr22:37372276
|
T | A | 1 | a0001c0002t0095 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*796A>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 796 | chr22 | 37372276 | |||||
| chr22:37372318
|
G | C | 1 | a0001c0008t0046 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*754C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 754 | chr22 | 37372318 | |||||
| chr22:37372427
|
C | T | 1 | a0001c0003t0042 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*645G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 645 | chr22 | 37372427 | |||||
| chr22:37372455
|
G | A | 1 | a0001c0001t0061 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*617C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 617 | chr22 | 37372455 | |||||
| chr22:37372556
|
C | T | 3 | a0001c0002t0066a0001c0002t0067a0001c0002t0068 | 3 | HG02818.hp2 HG02895.hp1 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*516G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 516 | chr22 | 37372556 | |||||
| chr22:37372692
|
C | T | 11 | a0001c0001t0017a0001c0001t0060a0001c0001t0061others(8): Show | 21 | HG01516.hp1 HG01891.hp1 HG01891.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*380G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 380 | chr22 | 37372692 | |||||
| chr22:37372717
|
AC | A | 87 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(84): Show | 254 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(251): Show |
3_prime_UTR_variant | MODIFIER | c.*354delG | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 354 | chr22 | 37372717 | |||||
| chr22:37372761
|
G | A | 1 | a0001c0002t0037 | 2 | HG01256.hp2 HG01361.hp1 |
3_prime_UTR_variant | MODIFIER | c.*311C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 311 | chr22 | 37372761 | |||||
| chr22:37372816
|
C | T | 1 | a0001c0002t0082 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*256G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 256 | chr22 | 37372816 | |||||
| chr22:37373004
|
G | T | 4 | a0001c0003t0012a0001c0003t0034a0001c0003t0081others(1): Show | 8 | HG00140.hp1 HG01168.hp1 HG01255.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*68C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 68 | chr22 | 37373004 | |||||
| chr22:37375612
|
C | T | 1 | a0001c0001t0053 | 1 | NA18943.hp1 | 5_prime_UTR_variant | MODIFIER | c.-78G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 78 | chr22 | 37375612 | |||||
| chr22:37375836
|
C | CCCT | 38 | a0001c0001t0002a0001c0001t0019a0001c0001t0023others(35): Show | 129 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(126): Show |
5_prime_UTR_variant | MODIFIER | c.-305_-303dupAGG | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 303 | chr22 | 37375836 | |||||
| chr22:37375836
|
C | CCCTCCT | 8 | a0001c0001t0025a0001c0001t0026a0001c0003t0070others(5): Show | 12 | HG01433.hp2 HG02015.hp1 HG02055.hp2 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-308_-303dupAGGAGG | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 303 | chr22 | 37375836 | |||||
| chr22:37375836
|
C | CCCTCCTC others(2): Show |
8 | a0001c0001t0024a0001c0002t0066a0001c0002t0067others(5): Show | 9 | HG01099.hp1 HG02818.hp2 HG02895.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-311_-303dupAGGAGG others(3): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 303 | chr22 | 37375836 | |||||
| chr22:37375836
|
C | CCCTCCTC others(5): Show |
1 | a0001c0003t0041 | 1 | HG03209.hp2 | 5_prime_UTR_variant | MODIFIER | c.-314_-303dupAGGAGG others(6): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 303 | chr22 | 37375836 | |||||
| chr22:37375836
|
CCCT | C | 6 | a0001c0001t0017a0001c0001t0060a0001c0001t0061others(3): Show | 10 | HG01109.hp1 HG01516.hp1 HG02486.hp1 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-305_-303delAGG | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 303 | chr22 | 37375836 | |||||
| chr22:37375836
|
CCCTCCT | C | 3 | a0001c0001t0063a0001c0001t0064a0001c0001t0065 | 3 | HG02280.hp1 HG02976.hp1 NA19240.hp1 |
5_prime_UTR_variant | MODIFIER | c.-308_-303delAGGAGG | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 303 | chr22 | 37375836 | |||||
| chr22:37375945
|
A | G | 51 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(48): Show | 151 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(148): Show |
5_prime_UTR_variant | MODIFIER | c.-411T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 411 | chr22 | 37375945 | |||||
| chr22:37375991
|
T | C | 1 | a0001c0001t0096 | 1 | NA18948.hp1 | 5_prime_UTR_variant | MODIFIER | c.-457A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 457 | chr22 | 37375991 | |||||
| chr22:37417780
|
A | T | 6 | a0001c0001t0023a0001c0002t0013a0001c0002t0014others(3): Show | 11 | HG02056.hp1 HG02071.hp2 HG02132.hp1 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-474T>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/3 | 42246 | chr22 | 37417780 | |||||
| chr22:37417885
|
G | A | 1 | a0001c0001t0097 | 1 | HG03540.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-579C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/3 | chr22 | 37417885 | ||||||
| chr22:37427369
|
G | A | 1 | a0001c0001t0098 | 1 | NA18983.hp1 | 5_prime_UTR_variant | MODIFIER | c.-685C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/3 | 51835 | chr22 | 37427369 | |||||
| chr22:37427414
|
G | A | 1 | a0001c0001t0099 | 1 | HG01358.hp2 | 5_prime_UTR_variant | MODIFIER | c.-730C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/3 | 51880 | chr22 | 37427414 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:37376022
|
G | A | 2 | a0001c0002t0031g0174a0001c0002t0031g0175 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-462-26C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37376022 | ||||||
| chr22:37376034
|
T | G | 1 | a0001c0002t0004g0263 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-462-38A>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37376034 | ||||||
| chr22:37376067
|
G | A | 4 | a0001c0001t0027g0204a0001c0001t0027g0216a0001c0001t0050g0145others(1): Show | 4 | HG02622.hp1 HG02647.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-462-71C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37376067 | ||||||
| chr22:37376096
|
G | A | 1 | a0001c0003t0001g0028 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-462-100C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37376096 | ||||||
| chr22:37376126
|
TG | T | 330 | a0001c0001t0002g0029a0001c0001t0002g0041a0001c0001t0002g0052others(327): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.-462-131delC | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37376126 | ||||||
| chr22:37376142
|
A | G | 6 | a0001c0003t0041g0163a0001c0003t0042g0229a0001c0003t0043g0230others(3): Show | 6 | HG02055.hp2 HG03209.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-462-146T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37376142 | ||||||
| chr22:37376240
|
C | T | 1 | a0001c0018t0045g0172 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-462-244G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37376240 | ||||||
| chr22:37376402
|
T | TAC | 6 | a0001c0003t0041g0163a0001c0003t0042g0229a0001c0003t0043g0230others(3): Show | 6 | HG02055.hp2 HG03209.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-462-408_-462-407d others(4): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37376402 | ||||||
| chr22:37376402
|
TAC | T | 131 | a0001c0001t0002g0029a0001c0001t0002g0041a0001c0001t0002g0052others(128): Show | 132 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.-462-408_-462-407d others(4): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37376402 | ||||||
| chr22:37376502
|
A | AAGAATTA others(32): Show |
1 | a0001c0001t0003g0224 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-462-545_-462-507d others(41): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37376502 | ||||||
| chr22:37376829
|
G | T | 241 | a0001c0001t0002g0029a0001c0001t0002g0041a0001c0001t0002g0052others(238): Show | 243 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(240): Show |
intron_variant | MODIFIER | c.-462-833C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37376829 | ||||||
| chr22:37377055
|
C | G | 261 | a0001c0001t0002g0029a0001c0001t0002g0041a0001c0001t0002g0052others(258): Show | 263 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.-462-1059G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37377055 | ||||||
| chr22:37377470
|
A | G | 2 | a0001c0006t0048g0132a0001c0006t0056g0220 | 2 | HG01496.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-462-1474T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37377470 | ||||||
| chr22:37377486
|
A | T | 4 | a0001c0001t0005g0018a0001c0001t0005g0019a0001c0001t0050g0145others(1): Show | 4 | HG02622.hp1 HG02809.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.-462-1490T>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37377486 | ||||||
| chr22:37377608
|
A | G | 252 | a0001c0001t0002g0029a0001c0001t0002g0041a0001c0001t0002g0052others(249): Show | 254 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.-462-1612T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37377608 | ||||||
| chr22:37377672
|
C | T | 4 | a0001c0005t0011g0196a0001c0005t0011g0207a0001c0005t0011g0211others(1): Show | 4 | HG01891.hp2 HG02451.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-462-1676G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37377672 | ||||||
| chr22:37377673
|
G | A | 1 | a0001c0002t0004g0092 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-462-1677C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37377673 | ||||||
| chr22:37377683
|
A | G | 259 | a0001c0001t0002g0029a0001c0001t0002g0041a0001c0001t0002g0052others(256): Show | 261 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.-462-1687T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37377683 | ||||||
| chr22:37377967
|
G | A | 2 | a0001c0001t0064g0310a0001c0001t0065g0169 | 2 | HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-462-1971C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37377967 | ||||||
| chr22:37378004
|
G | A | 108 | a0001c0001t0002g0041a0001c0001t0002g0241a0001c0001t0003g0042others(105): Show | 109 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.-462-2008C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37378004 | ||||||
| chr22:37378045
|
T | C | 139 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0060others(136): Show | 140 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.-462-2049A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37378045 | ||||||
| chr22:37378153
|
G | A | 4 | a0001c0003t0041g0163a0001c0003t0042g0229a0001c0003t0043g0230others(1): Show | 4 | HG03209.hp2 NA18906.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-462-2157C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37378153 | ||||||
| chr22:37378191
|
G | A | 1 | a0001c0001t0002g0281 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-462-2195C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37378191 | ||||||
| chr22:37378200
|
T | C | 3 | a0001c0003t0012g0308a0001c0003t0034g0278a0001c0003t0034g0279 | 3 | HG03490.hp2 HG03492.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.-462-2204A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37378200 | ||||||
| chr22:37378238
|
G | T | 4 | a0001c0001t0005g0018a0001c0001t0005g0019a0001c0001t0050g0145others(1): Show | 4 | HG02622.hp1 HG02809.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.-462-2242C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37378238 | ||||||
| chr22:37378318
|
G | A | 122 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0060others(119): Show | 123 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.-462-2322C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37378318 | ||||||
| chr22:37378349
|
A | C | 259 | a0001c0001t0002g0029a0001c0001t0002g0041a0001c0001t0002g0052others(256): Show | 261 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.-462-2353T>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37378349 | ||||||
| chr22:37378500
|
T | C | 259 | a0001c0001t0002g0029a0001c0001t0002g0041a0001c0001t0002g0052others(256): Show | 261 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.-462-2504A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37378500 | ||||||
| chr22:37378527
|
A | G | 5 | a0001c0002t0004g0328a0001c0002t0066g0232a0001c0002t0067g0233others(2): Show | 5 | HG01099.hp1 HG02109.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-462-2531T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37378527 | ||||||
| chr22:37378628
|
C | T | 2 | a0001c0001t0023g0077a0001c0001t0023g0120 | 2 | NA18612.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.-462-2632G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37378628 | ||||||
| chr22:37378703
|
C | T | 5 | a0001c0002t0004g0328a0001c0002t0066g0232a0001c0002t0067g0233others(2): Show | 5 | HG01099.hp1 HG02109.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-462-2707G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37378703 | ||||||
| chr22:37378726
|
C | T | 1 | a0001c0001t0005g0164 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-462-2730G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37378726 | ||||||
| chr22:37378766
|
G | A | 36 | a0001c0001t0002g0041a0001c0001t0002g0241a0001c0001t0003g0273others(33): Show | 36 | HG00423.hp2 HG00639.hp1 HG01256.hp2 others(33): Show |
intron_variant | MODIFIER | c.-462-2770C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37378766 | ||||||
| chr22:37378784
|
C | A | 1 | a0001c0001t0026g0059 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-462-2788G>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37378784 | ||||||
| chr22:37378801
|
G | A | 1 | a0001c0003t0087g0299 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-462-2805C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37378801 | ||||||
| chr22:37378822
|
G | T | 1 | a0001c0003t0083g0219 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-462-2826C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37378822 | ||||||
| chr22:37378839
|
G | T | 2 | a0001c0001t0027g0204a0001c0001t0027g0216 | 2 | HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-462-2843C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37378839 | ||||||
| chr22:37378853
|
T | C | 5 | a0001c0002t0004g0328a0001c0002t0066g0232a0001c0002t0067g0233others(2): Show | 5 | HG01099.hp1 HG02109.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-462-2857A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37378853 | ||||||
| chr22:37378861
|
T | C | 268 | a0001c0001t0002g0029a0001c0001t0002g0041a0001c0001t0002g0052others(265): Show | 270 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(267): Show |
intron_variant | MODIFIER | c.-462-2865A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37378861 | ||||||
| chr22:37379023
|
C | T | 79 | a0001c0001t0003g0042a0001c0001t0003g0054a0001c0001t0003g0084others(76): Show | 80 | HG00140.hp2 HG00438.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.-462-3027G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37379023 | ||||||
| chr22:37379188
|
T | G | 114 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0060others(111): Show | 115 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.-462-3192A>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37379188 | ||||||
| chr22:37379212
|
G | A | 3 | a0001c0001t0005g0164a0001c0001t0027g0204a0001c0001t0027g0216 | 3 | HG02647.hp1 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-462-3216C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37379212 | ||||||
| chr22:37379218
|
A | G | 208 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0060others(205): Show | 210 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.-462-3222T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37379218 | ||||||
| chr22:37379227
|
G | A | 1 | a0001c0002t0006g0195 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-462-3231C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37379227 | ||||||
| chr22:37379294
|
C | T | 2 | a0001c0001t0027g0204a0001c0001t0027g0216 | 2 | HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-462-3298G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37379294 | ||||||
| chr22:37379355
|
G | A | 1 | a0001c0003t0070g0166 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-462-3359C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37379355 | ||||||
| chr22:37379461
|
C | G | 1 | a0001c0002t0032g0037 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-462-3465G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37379461 | ||||||
| chr22:37379641
|
C | T | 2 | a0001c0001t0005g0018a0001c0001t0005g0019 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-462-3645G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37379641 | ||||||
| chr22:37379667
|
G | A | 1 | a0001c0002t0032g0037 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-462-3671C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37379667 | ||||||
| chr22:37379697
|
G | A | 1 | a0001c0001t0003g0086 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-462-3701C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37379697 | ||||||
| chr22:37379718
|
G | C | 2 | a0001c0001t0005g0135a0001c0001t0005g0136 | 2 | HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-462-3722C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37379718 | ||||||
| chr22:37379850
|
C | T | 149 | a0001c0001t0002g0029a0001c0001t0002g0041a0001c0001t0002g0052others(146): Show | 150 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.-462-3854G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37379850 | ||||||
| chr22:37379852
|
G | GGTGCTCC others(6): Show |
1 | a0001c0002t0008g0047 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-462-3869_-462-385 others(17): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37379852 | ||||||
| chr22:37379867
|
C | T | 1 | a0001c0001t0061g0183 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-462-3871G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37379867 | ||||||
| chr22:37379875
|
T | C | 6 | a0001c0001t0002g0262a0001c0001t0002g0285a0001c0001t0002g0298others(3): Show | 6 | NA18945.hp2 NA18964.hp1 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.-462-3879A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37379875 | ||||||
| chr22:37379934
|
C | G | 254 | a0001c0001t0002g0029a0001c0001t0002g0041a0001c0001t0002g0052others(251): Show | 256 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.-462-3938G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37379934 | ||||||
| chr22:37379967
|
C | T | 1 | a0001c0001t0023g0077 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-462-3971G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37379967 | ||||||
| chr22:37379998
|
G | C | 1 | a0001c0003t0006g0121 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-462-4002C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37379998 | ||||||
| chr22:37380265
|
G | A | 1 | a0001c0001t0065g0169 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-462-4269C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37380265 | ||||||
| chr22:37380336
|
T | TCA | 264 | a0001c0001t0002g0029a0001c0001t0002g0041a0001c0001t0002g0052others(261): Show | 266 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(263): Show |
intron_variant | MODIFIER | c.-462-4341_-462-434 others(6): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37380336 | ||||||
| chr22:37380415
|
C | T | 4 | a0001c0003t0001g0177a0001c0003t0001g0200a0001c0003t0001g0201others(1): Show | 4 | HG02145.hp2 HG02630.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-462-4419G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37380415 | ||||||
| chr22:37380485
|
C | G | 1 | a0001c0002t0018g0001 | 2 | HG01261.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.-462-4489G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37380485 | ||||||
| chr22:37380939
|
T | C | 3 | a0001c0003t0001g0011a0001c0003t0001g0028a0001c0003t0001g0083 | 3 | NA18939.hp2 NA18991.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.-462-4943A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37380939 | ||||||
| chr22:37380991
|
A | G | 262 | a0001c0001t0002g0029a0001c0001t0002g0041a0001c0001t0002g0052others(259): Show | 264 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(261): Show |
intron_variant | MODIFIER | c.-462-4995T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37380991 | ||||||
| chr22:37381067
|
G | A | 2 | a0001c0001t0019g0107a0001c0001t0019g0108 | 2 | NA18950.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.-462-5071C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37381067 | ||||||
| chr22:37381304
|
A | G | 1 | a0001c0006t0056g0220 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-462-5308T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37381304 | ||||||
| chr22:37381320
|
CT | C | 235 | a0001c0001t0002g0029a0001c0001t0002g0041a0001c0001t0002g0052others(232): Show | 237 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(234): Show |
intron_variant | MODIFIER | c.-462-5325delA | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37381320 | ||||||
| chr22:37381573
|
T | G | 246 | a0001c0001t0002g0029a0001c0001t0002g0041a0001c0001t0002g0052others(243): Show | 248 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.-462-5577A>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37381573 | ||||||
| chr22:37381632
|
C | T | 1 | a0001c0001t0005g0164 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-462-5636G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37381632 | ||||||
| chr22:37381743
|
C | T | 14 | a0001c0001t0003g0003a0001c0001t0003g0045a0001c0001t0003g0087others(11): Show | 15 | HG01106.hp2 HG01255.hp2 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.-462-5747G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37381743 | ||||||
| chr22:37381883
|
G | A | 2 | a0001c0001t0027g0204a0001c0001t0027g0216 | 2 | HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-462-5887C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37381883 | ||||||
| chr22:37381935
|
G | A | 3 | a0001c0004t0010g0073a0001c0004t0010g0179a0001c0004t0010g0246 | 3 | HG01515.hp2 HG01517.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.-462-5939C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37381935 | ||||||
| chr22:37381955
|
C | CA | 20 | a0001c0002t0006g0264a0001c0002t0007g0106a0001c0003t0001g0002others(17): Show | 21 | HG00099.hp1 HG00408.hp1 HG00609.hp1 others(18): Show |
intron_variant | MODIFIER | c.-462-5960dupT | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37381955 | ||||||
| chr22:37381955
|
C | CAA | 12 | a0001c0002t0007g0129a0001c0003t0001g0026a0001c0003t0001g0030others(9): Show | 12 | HG00408.hp2 HG00642.hp1 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.-462-5961_-462-596 others(6): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37381955 | ||||||
| chr22:37381955
|
CA | C | 6 | a0001c0002t0008g0047a0001c0002t0008g0231a0001c0002t0008g0314others(3): Show | 6 | HG00323.hp2 HG01109.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-462-5960delT | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37381955 | ||||||
| chr22:37381955
|
CAAAAAAA others(1): Show |
C | 64 | a0001c0001t0002g0041a0001c0001t0002g0060a0001c0001t0002g0122others(61): Show | 65 | HG00438.hp1 HG00544.hp1 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.-462-5967_-462-596 others(12): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37381955 | ||||||
| chr22:37381955
|
CAAAAAAA others(2): Show |
C | 176 | a0001c0001t0002g0029a0001c0001t0002g0097a0001c0001t0002g0102others(173): Show | 177 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.-462-5968_-462-596 others(13): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37381955 | ||||||
| chr22:37381955
|
CAAAAAAA others(3): Show |
C | 4 | a0001c0001t0002g0052a0001c0001t0005g0135a0001c0001t0096g0050others(1): Show | 4 | HG02723.hp1 HG03041.hp1 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.-462-5969_-462-596 others(14): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37381955 | ||||||
| chr22:37381955
|
CAAAAAAA others(9): Show |
C | 3 | a0001c0001t0027g0204a0001c0001t0027g0216a0001c0002t0008g0228 | 3 | HG02647.hp1 HG03225.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-462-5975_-462-596 others(20): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37381955 | ||||||
| chr22:37381970
|
AAAAAAAA others(15): Show |
A | 1 | a0001c0001t0005g0164 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-462-5996_-462-597 others(26): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37381970 | ||||||
| chr22:37381980
|
AAAAAAAA others(5): Show |
A | 3 | a0001c0001t0025g0326a0001c0003t0001g0149a0001c0003t0001g0327 | 3 | HG02559.hp2 HG02630.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-462-5996_-462-598 others(16): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37381980 | ||||||
| chr22:37382022
|
C | G | 24 | a0001c0001t0003g0054a0001c0001t0058g0186a0001c0001t0099g0331others(21): Show | 24 | HG00099.hp2 HG01168.hp1 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.-462-6026G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37382022 | ||||||
| chr22:37382055
|
T | C | 264 | a0001c0001t0002g0029a0001c0001t0002g0041a0001c0001t0002g0052others(261): Show | 266 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(263): Show |
intron_variant | MODIFIER | c.-462-6059A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37382055 | ||||||
| chr22:37382114
|
G | A | 1 | a0001c0002t0014g0078 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-462-6118C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37382114 | ||||||
| chr22:37382294
|
CT | C | 233 | a0001c0001t0002g0029a0001c0001t0002g0041a0001c0001t0002g0052others(230): Show | 235 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.-462-6299delA | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37382294 | ||||||
| chr22:37382330
|
T | C | 2 | a0001c0001t0027g0204a0001c0001t0027g0216 | 2 | HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-462-6334A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37382330 | ||||||
| chr22:37382396
|
C | T | 1 | a0001c0002t0066g0232 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-462-6400G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37382396 | ||||||
| chr22:37382433
|
C | T | 235 | a0001c0001t0002g0029a0001c0001t0002g0041a0001c0001t0002g0052others(232): Show | 237 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(234): Show |
intron_variant | MODIFIER | c.-462-6437G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37382433 | ||||||
| chr22:37382436
|
G | T | 235 | a0001c0001t0002g0029a0001c0001t0002g0041a0001c0001t0002g0052others(232): Show | 237 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(234): Show |
intron_variant | MODIFIER | c.-462-6440C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37382436 | ||||||
| chr22:37382534
|
C | T | 236 | a0001c0001t0002g0029a0001c0001t0002g0041a0001c0001t0002g0052others(233): Show | 238 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.-462-6538G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37382534 | ||||||
| chr22:37382552
|
TTTTTTTT others(4): Show |
T | 8 | a0001c0001t0009g0311a0001c0001t0027g0204a0001c0001t0027g0216others(5): Show | 8 | HG02145.hp2 HG02258.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-462-6567_-462-655 others(15): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37382552 | ||||||
| chr22:37382561
|
TTA | T | 9 | a0001c0001t0005g0018a0001c0001t0005g0019a0001c0001t0025g0239others(6): Show | 9 | HG01433.hp2 HG02622.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-462-6567_-462-656 others(6): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37382561 | ||||||
| chr22:37382562
|
T | A | 1 | a0001c0002t0007g0091 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-462-6566A>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37382562 | ||||||
| chr22:37382562
|
TA | T | 205 | a0001c0001t0002g0041a0001c0001t0002g0052a0001c0001t0002g0060others(202): Show | 207 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.-462-6567delT | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37382562 | ||||||
| chr22:37382562
|
TAA | T | 15 | a0001c0001t0002g0097a0001c0001t0003g0005a0001c0001t0003g0244others(12): Show | 15 | HG01099.hp1 HG01167.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.-462-6568_-462-656 others(6): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37382562 | ||||||
| chr22:37382563
|
A | T | 21 | a0001c0001t0002g0029a0001c0001t0002g0130a0001c0001t0002g0241others(18): Show | 21 | HG00423.hp1 HG00621.hp1 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.-462-6567T>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37382563 | ||||||
| chr22:37382564
|
A | T | 226 | a0001c0001t0002g0029a0001c0001t0002g0041a0001c0001t0002g0052others(223): Show | 228 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.-462-6568T>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37382564 | ||||||
| chr22:37382612
|
C | T | 1 | a0001c0002t0008g0228 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-462-6616G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37382612 | ||||||
| chr22:37382616
|
C | G | 238 | a0001c0001t0002g0029a0001c0001t0002g0041a0001c0001t0002g0052others(235): Show | 240 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.-462-6620G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37382616 | ||||||
| chr22:37382772
|
G | C | 15 | a0001c0001t0005g0018a0001c0001t0005g0019a0001c0001t0025g0239others(12): Show | 15 | HG01099.hp1 HG01433.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.-462-6776C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37382772 | ||||||
| chr22:37382782
|
G | C | 1 | a0001c0001t0017g0128 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-462-6786C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37382782 | ||||||
| chr22:37382924
|
C | CT | 4 | a0001c0001t0002g0250a0001c0001t0002g0255a0001c0001t0002g0283others(1): Show | 4 | HG02015.hp1 NA18967.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.-462-6929dupA | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37382924 | ||||||
| chr22:37382931
|
T | C | 15 | a0001c0001t0005g0018a0001c0001t0005g0019a0001c0001t0025g0239others(12): Show | 15 | HG01099.hp1 HG01433.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.-462-6935A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37382931 | ||||||
| chr22:37382953
|
T | C | 2 | a0001c0001t0028g0312a0001c0003t0070g0166 | 2 | HG02630.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.-462-6957A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37382953 | ||||||
| chr22:37383173
|
C | T | 1 | a0001c0001t0017g0128 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-462-7177G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37383173 | ||||||
| chr22:37383178
|
C | A | 1 | a0001c0006t0056g0220 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-462-7182G>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37383178 | ||||||
| chr22:37383179
|
G | A | 239 | a0001c0001t0002g0029a0001c0001t0002g0041a0001c0001t0002g0052others(236): Show | 241 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.-462-7183C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37383179 | ||||||
| chr22:37383220
|
G | A | 1 | a0001c0003t0092g0322 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-462-7224C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37383220 | ||||||
| chr22:37383341
|
G | A | 241 | a0001c0001t0002g0029a0001c0001t0002g0041a0001c0001t0002g0052others(238): Show | 243 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(240): Show |
intron_variant | MODIFIER | c.-462-7345C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37383341 | ||||||
| chr22:37383362
|
G | A | 3 | a0001c0001t0009g0311a0001c0001t0064g0310a0001c0003t0070g0166 | 3 | HG02258.hp2 HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-462-7366C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37383362 | ||||||
| chr22:37383445
|
T | A | 1 | a0001c0001t0005g0044 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-462-7449A>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37383445 | ||||||
| chr22:37383673
|
G | T | 246 | a0001c0001t0002g0029a0001c0001t0002g0041a0001c0001t0002g0052others(243): Show | 248 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.-462-7677C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37383673 | ||||||
| chr22:37383681
|
G | A | 1 | a0001c0006t0056g0220 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-462-7685C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37383681 | ||||||
| chr22:37383789
|
C | G | 261 | a0001c0001t0002g0029a0001c0001t0002g0041a0001c0001t0002g0052others(258): Show | 263 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.-462-7793G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37383789 | ||||||
| chr22:37383911
|
G | A | 1 | a0001c0001t0005g0164 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-462-7915C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37383911 | ||||||
| chr22:37384165
|
G | A | 2 | a0001c0002t0078g0104a0001c0003t0001g0015 | 2 | HG00544.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.-462-8169C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37384165 | ||||||
| chr22:37384184
|
G | T | 1 | a0001c0001t0003g0292 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-462-8188C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37384184 | ||||||
| chr22:37384482
|
G | C | 81 | a0001c0001t0003g0054a0001c0001t0005g0164a0001c0001t0005g0209others(78): Show | 82 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.-462-8486C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37384482 | ||||||
| chr22:37384522
|
T | C | 2 | a0001c0001t0009g0311a0001c0001t0064g0310 | 2 | HG02258.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-462-8526A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37384522 | ||||||
| chr22:37384615
|
C | A | 81 | a0001c0001t0003g0054a0001c0001t0005g0164a0001c0001t0005g0209others(78): Show | 82 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.-462-8619G>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37384615 | ||||||
| chr22:37384643
|
GACCCCTG others(75): Show |
G | 2 | a0001c0003t0001g0061a0001c0003t0001g0125 | 2 | HG00741.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.-462-8729_-462-864 others(86): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37384643 | ||||||
| chr22:37384651
|
GCCTCTCC others(34): Show |
G | 327 | a0001c0001t0002g0029a0001c0001t0002g0041a0001c0001t0002g0052others(324): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.-462-8696_-462-865 others(45): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37384651 | ||||||
| chr22:37384894
|
G | A | 1 | a0001c0006t0001g0277 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-462-8898C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37384894 | ||||||
| chr22:37385084
|
G | T | 257 | a0001c0001t0002g0029a0001c0001t0002g0041a0001c0001t0002g0052others(254): Show | 259 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.-462-9088C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37385084 | ||||||
| chr22:37385169
|
C | T | 1 | a0001c0001t0065g0169 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-462-9173G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37385169 | ||||||
| chr22:37385170
|
G | A | 8 | a0001c0001t0005g0209a0001c0001t0025g0326a0001c0003t0001g0149others(5): Show | 8 | HG01891.hp2 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.-462-9174C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37385170 | ||||||
| chr22:37385220
|
G | A | 2 | a0001c0001t0009g0311a0001c0001t0064g0310 | 2 | HG02258.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-462-9224C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37385220 | ||||||
| chr22:37385313
|
G | A | 2 | a0001c0001t0027g0204a0001c0001t0027g0216 | 2 | HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-462-9317C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37385313 | ||||||
| chr22:37385329
|
A | G | 270 | a0001c0001t0002g0029a0001c0001t0002g0041a0001c0001t0002g0052others(267): Show | 272 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(269): Show |
intron_variant | MODIFIER | c.-462-9333T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37385329 | ||||||
| chr22:37385393
|
T | C | 4 | a0001c0001t0025g0326a0001c0003t0001g0149a0001c0003t0001g0327others(1): Show | 4 | HG01884.hp1 HG02559.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.-462-9397A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37385393 | ||||||
| chr22:37385502
|
C | T | 1 | a0001c0003t0001g0083 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-462-9506G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37385502 | ||||||
| chr22:37385551
|
G | A | 154 | a0001c0001t0002g0029a0001c0001t0002g0041a0001c0001t0002g0052others(151): Show | 155 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.-462-9555C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37385551 | ||||||
| chr22:37385733
|
G | T | 2 | a0001c0001t0027g0204a0001c0001t0027g0216 | 2 | HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-462-9737C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37385733 | ||||||
| chr22:37385834
|
G | T | 264 | a0001c0001t0002g0029a0001c0001t0002g0041a0001c0001t0002g0052others(261): Show | 266 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(263): Show |
intron_variant | MODIFIER | c.-462-9838C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37385834 | ||||||
| chr22:37386146
|
C | T | 1 | a0001c0001t0003g0287 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-462-10150G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37386146 | ||||||
| chr22:37386209
|
C | T | 1 | a0001c0003t0006g0121 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-462-10213G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37386209 | ||||||
| chr22:37386216
|
A | G | 276 | a0001c0001t0002g0029a0001c0001t0002g0041a0001c0001t0002g0052others(273): Show | 278 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(275): Show |
intron_variant | MODIFIER | c.-462-10220T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37386216 | ||||||
| chr22:37386522
|
C | T | 1 | a0001c0003t0001g0303 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-462-10526G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37386522 | ||||||
| chr22:37386527
|
G | T | 1 | a0003c0017t0002g0046 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-462-10531C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37386527 | ||||||
| chr22:37386703
|
G | A | 1 | a0001c0001t0003g0185 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-462-10707C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37386703 | ||||||
| chr22:37386898
|
G | T | 139 | a0001c0001t0002g0041a0001c0001t0002g0060a0001c0001t0002g0241others(136): Show | 139 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.-462-10902C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37386898 | ||||||
| chr22:37387033
|
C | T | 1 | a0001c0003t0092g0322 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-462-11037G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37387033 | ||||||
| chr22:37387106
|
T | C | 7 | a0001c0001t0005g0164a0001c0001t0050g0145a0001c0002t0069g0009others(4): Show | 7 | HG01099.hp1 HG02109.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-462-11110A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37387106 | ||||||
| chr22:37387230
|
C | T | 1 | a0001c0002t0033g0023 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-462-11234G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37387230 | ||||||
| chr22:37387311
|
G | A | 72 | a0001c0001t0002g0122a0001c0001t0002g0241a0001c0001t0002g0248others(69): Show | 72 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.-462-11315C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37387311 | ||||||
| chr22:37387363
|
T | C | 12 | a0001c0001t0005g0164a0001c0001t0009g0167a0001c0001t0009g0168others(9): Show | 12 | HG02109.hp2 HG02280.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.-462-11367A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37387363 | ||||||
| chr22:37387636
|
G | A | 1 | a0001c0003t0001g0149 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-462-11640C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37387636 | ||||||
| chr22:37387650
|
G | A | 1 | a0001c0006t0056g0220 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-462-11654C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37387650 | ||||||
| chr22:37387693
|
C | T | 1 | a0001c0001t0027g0216 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-462-11697G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37387693 | ||||||
| chr22:37387980
|
C | T | 1 | a0001c0003t0041g0163 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-462-11984G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37387980 | ||||||
| chr22:37388012
|
C | G | 1 | a0001c0003t0001g0141 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-462-12016G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37388012 | ||||||
| chr22:37388121
|
C | T | 12 | a0001c0001t0003g0045a0001c0001t0003g0178a0001c0001t0003g0242others(9): Show | 12 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.-462-12125G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37388121 | ||||||
| chr22:37388189
|
G | T | 16 | a0001c0001t0003g0045a0001c0001t0003g0178a0001c0001t0003g0242others(13): Show | 16 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.-462-12193C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37388189 | ||||||
| chr22:37388250
|
C | T | 1 | a0001c0002t0018g0176 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-462-12254G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37388250 | ||||||
| chr22:37388470
|
C | G | 13 | a0001c0001t0002g0300a0001c0001t0003g0045a0001c0001t0003g0178others(10): Show | 13 | HG00323.hp1 HG00597.hp2 HG00639.hp1 others(10): Show |
intron_variant | MODIFIER | c.-462-12474G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37388470 | ||||||
| chr22:37388476
|
T | C | 1 | a0001c0003t0006g0121 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-462-12480A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37388476 | ||||||
| chr22:37388477
|
A | C | 20 | a0001c0001t0005g0018a0001c0001t0005g0019a0001c0001t0005g0070others(17): Show | 20 | HG01109.hp1 HG01433.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.-462-12481T>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37388477 | ||||||
| chr22:37388483
|
G | A | 5 | a0001c0001t0005g0135a0001c0001t0005g0136a0001c0002t0021g0134others(2): Show | 5 | HG02572.hp1 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-462-12487C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37388483 | ||||||
| chr22:37388611
|
C | T | 4 | a0001c0001t0005g0044a0001c0001t0005g0164a0001c0002t0018g0176others(1): Show | 4 | HG02965.hp1 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-462-12615G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37388611 | ||||||
| chr22:37388769
|
G | A | 1 | a0001c0003t0041g0163 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-462-12773C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37388769 | ||||||
| chr22:37388970
|
A | G | 1 | a0001c0002t0069g0009 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-462-12974T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37388970 | ||||||
| chr22:37388996
|
T | A | 1 | a0001c0003t0041g0163 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-462-13000A>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37388996 | ||||||
| chr22:37389206
|
G | C | 5 | a0001c0002t0008g0228a0001c0002t0066g0232a0001c0002t0067g0233others(2): Show | 5 | HG02818.hp2 HG02895.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.-462-13210C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37389206 | ||||||
| chr22:37389378
|
C | T | 2 | a0001c0002t0007g0187a0001c0002t0007g0188 | 2 | HG02738.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.-462-13382G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37389378 | ||||||
| chr22:37389550
|
C | T | 1 | a0001c0001t0026g0059 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-462-13554G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37389550 | ||||||
| chr22:37389600
|
C | T | 11 | a0001c0002t0008g0231a0001c0002t0008g0314a0001c0002t0021g0197others(8): Show | 11 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-462-13604G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37389600 | ||||||
| chr22:37389729
|
C | A | 1 | a0001c0001t0050g0145 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-462-13733G>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37389729 | ||||||
| chr22:37389760
|
T | C | 1 | a0001c0006t0047g0203 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-462-13764A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37389760 | ||||||
| chr22:37389836
|
G | A | 4 | a0001c0001t0003g0042a0001c0001t0003g0084a0001c0001t0003g0086others(1): Show | 4 | HG00642.hp1 HG01257.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.-462-13840C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37389836 | ||||||
| chr22:37389950
|
G | C | 1 | a0001c0001t0061g0183 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-462-13954C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37389950 | ||||||
| chr22:37389988
|
C | T | 3 | a0001c0010t0016g0288a0001c0010t0016g0295a0001c0010t0016g0296 | 3 | HG01891.hp1 HG02145.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-462-13992G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37389988 | ||||||
| chr22:37390049
|
T | A | 6 | a0001c0001t0005g0209a0001c0001t0009g0210a0001c0005t0011g0196others(3): Show | 6 | HG00639.hp2 HG01891.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-462-14053A>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37390049 | ||||||
| chr22:37390175
|
G | C | 11 | a0001c0002t0008g0231a0001c0002t0008g0314a0001c0002t0021g0197others(8): Show | 11 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-462-14179C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37390175 | ||||||
| chr22:37390261
|
G | A | 1 | a0001c0002t0006g0301 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-462-14265C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37390261 | ||||||
| chr22:37390551
|
G | C | 1 | a0001c0003t0041g0163 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-462-14555C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37390551 | ||||||
| chr22:37390607
|
A | AG | 330 | a0001c0001t0002g0029a0001c0001t0002g0041a0001c0001t0002g0052others(327): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.-462-14612dupC | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37390607 | ||||||
| chr22:37390667
|
C | T | 2 | a0001c0001t0009g0311a0001c0001t0064g0310 | 2 | HG02258.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-462-14671G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37390667 | ||||||
| chr22:37390670
|
G | C | 153 | a0001c0001t0002g0029a0001c0001t0002g0097a0001c0001t0002g0102others(150): Show | 154 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.-462-14674C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37390670 | ||||||
| chr22:37390805
|
A | G | 1 | a0001c0002t0018g0176 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-462-14809T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37390805 | ||||||
| chr22:37390938
|
G | A | 1 | a0001c0003t0041g0163 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-462-14942C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37390938 | ||||||
| chr22:37391089
|
G | A | 1 | a0001c0001t0003g0269 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-462-15093C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37391089 | ||||||
| chr22:37391181
|
G | A | 172 | a0001c0001t0002g0029a0001c0001t0002g0097a0001c0001t0002g0102others(169): Show | 173 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(170): Show |
intron_variant | MODIFIER | c.-462-15185C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37391181 | ||||||
| chr22:37391273
|
G | A | 6 | a0001c0001t0009g0167a0001c0001t0009g0168a0001c0001t0009g0171others(3): Show | 6 | HG02109.hp2 HG02622.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-462-15277C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37391273 | ||||||
| chr22:37391285
|
A | G | 175 | a0001c0001t0002g0029a0001c0001t0002g0097a0001c0001t0002g0102others(172): Show | 176 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.-462-15289T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37391285 | ||||||
| chr22:37391340
|
C | T | 1 | a0001c0002t0032g0037 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-462-15344G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37391340 | ||||||
| chr22:37391347
|
G | A | 1 | a0001c0001t0002g0306 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-462-15351C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37391347 | ||||||
| chr22:37391739
|
C | T | 2 | a0001c0002t0004g0038a0005c0014t0004g0032 | 2 | NA19068.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.-462-15743G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37391739 | ||||||
| chr22:37391842
|
A | T | 1 | a0003c0017t0002g0046 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-462-15846T>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37391842 | ||||||
| chr22:37391899
|
G | A | 1 | a0001c0002t0004g0173 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-462-15903C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37391899 | ||||||
| chr22:37391916
|
G | A | 2 | a0001c0001t0005g0044a0001c0002t0068g0133 | 2 | HG02965.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-462-15920C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37391916 | ||||||
| chr22:37392053
|
A | G | 1 | a0001c0001t0027g0216 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-462-16057T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37392053 | ||||||
| chr22:37392135
|
C | G | 6 | a0001c0001t0005g0018a0001c0001t0005g0019a0001c0001t0005g0044others(3): Show | 6 | HG01109.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-462-16139G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37392135 | ||||||
| chr22:37392166
|
T | A | 13 | a0001c0001t0003g0045a0001c0001t0003g0178a0001c0001t0003g0242others(10): Show | 13 | HG00597.hp2 HG00639.hp1 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.-462-16170A>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37392166 | ||||||
| chr22:37392318
|
C | CT | 114 | a0001c0001t0002g0052a0001c0001t0002g0111a0001c0001t0002g0122others(111): Show | 114 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.-462-16323dupA | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37392318 | ||||||
| chr22:37392318
|
C | CTT | 9 | a0001c0001t0005g0135a0001c0001t0005g0136a0001c0001t0017g0128others(6): Show | 9 | HG00140.hp2 HG02572.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.-462-16324_-462-16 others(8): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37392318 | ||||||
| chr22:37392318
|
CT | C | 18 | a0001c0001t0002g0105a0001c0001t0002g0284a0001c0001t0005g0070others(15): Show | 18 | HG00140.hp1 HG01109.hp1 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.-462-16323delA | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37392318 | ||||||
| chr22:37392325
|
T | TC | 10 | a0001c0001t0003g0045a0001c0001t0003g0178a0001c0001t0003g0242others(7): Show | 10 | HG00597.hp2 HG00639.hp1 HG00733.hp2 others(7): Show |
intron_variant | MODIFIER | c.-462-16330_-462-16 others(7): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37392325 | ||||||
| chr22:37392326
|
T | C | 1 | a0004c0012t0001g0243 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-462-16330A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37392326 | ||||||
| chr22:37392350
|
C | T | 9 | a0001c0002t0008g0231a0001c0002t0008g0314a0001c0002t0021g0197others(6): Show | 9 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-462-16354G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37392350 | ||||||
| chr22:37392410
|
C | A | 1 | a0001c0002t0013g0075 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-462-16414G>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37392410 | ||||||
| chr22:37392466
|
C | T | 4 | a0001c0001t0009g0017a0001c0001t0063g0325a0001c0002t0022g0156others(1): Show | 4 | HG01884.hp1 HG02280.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-462-16470G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37392466 | ||||||
| chr22:37392520
|
A | G | 3 | a0001c0001t0053g0090a0001c0003t0001g0109a0001c0009t0002g0112 | 3 | NA18939.hp1 NA18943.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.-462-16524T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37392520 | ||||||
| chr22:37392600
|
A | G | 141 | a0001c0001t0002g0029a0001c0001t0002g0097a0001c0001t0002g0102others(138): Show | 142 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.-462-16604T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37392600 | ||||||
| chr22:37392607
|
C | T | 12 | a0001c0002t0004g0199a0001c0002t0008g0231a0001c0002t0008g0314others(9): Show | 12 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.-462-16611G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37392607 | ||||||
| chr22:37392684
|
A | T | 5 | a0001c0002t0022g0315a0001c0008t0015g0160a0001c0008t0015g0161others(2): Show | 5 | HG02109.hp1 HG02615.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-462-16688T>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37392684 | ||||||
| chr22:37392812
|
T | A | 3 | a0001c0001t0025g0326a0001c0003t0001g0149a0001c0003t0001g0327 | 3 | HG02559.hp2 HG02630.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-462-16816A>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37392812 | ||||||
| chr22:37392875
|
G | A | 1 | a0002c0007t0086g0316 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-462-16879C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37392875 | ||||||
| chr22:37392902
|
C | A | 1 | a0005c0014t0004g0032 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-462-16906G>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37392902 | ||||||
| chr22:37392913
|
T | A | 1 | a0001c0002t0014g0031 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-462-16917A>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37392913 | ||||||
| chr22:37393066
|
G | A | 156 | a0001c0001t0002g0029a0001c0001t0002g0097a0001c0001t0002g0102others(153): Show | 157 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.-462-17070C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37393066 | ||||||
| chr22:37393246
|
C | T | 1 | a0001c0001t0003g0292 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-462-17250G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37393246 | ||||||
| chr22:37393267
|
G | A | 4 | a0001c0001t0009g0017a0001c0001t0063g0325a0001c0002t0022g0156others(1): Show | 4 | HG01884.hp1 HG02280.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-462-17271C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37393267 | ||||||
| chr22:37393281
|
G | C | 1 | a0001c0003t0041g0163 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-462-17285C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37393281 | ||||||
| chr22:37393422
|
C | T | 1 | a0001c0006t0001g0277 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-462-17426G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37393422 | ||||||
| chr22:37393502
|
G | A | 108 | a0001c0001t0002g0029a0001c0001t0002g0097a0001c0001t0002g0102others(105): Show | 109 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.-462-17506C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37393502 | ||||||
| chr22:37393589
|
G | A | 1 | a0001c0002t0089g0131 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-462-17593C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37393589 | ||||||
| chr22:37393672
|
G | C | 3 | a0001c0003t0042g0229a0001c0003t0043g0230a0001c0003t0044g0329 | 3 | NA18906.hp1 NA20129.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-462-17676C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37393672 | ||||||
| chr22:37393676
|
T | C | 19 | a0001c0001t0005g0135a0001c0001t0005g0136a0001c0001t0017g0128others(16): Show | 19 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.-462-17680A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37393676 | ||||||
| chr22:37393739
|
C | T | 4 | a0001c0001t0097g0324a0001c0002t0008g0314a0001c0002t0018g0176others(1): Show | 4 | HG02559.hp1 HG03540.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.-462-17743G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37393739 | ||||||
| chr22:37393740
|
G | A | 2 | a0001c0003t0001g0118a0002c0007t0086g0316 | 2 | HG01433.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-462-17744C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37393740 | ||||||
| chr22:37393778
|
G | A | 5 | a0001c0001t0005g0044a0001c0001t0097g0324a0001c0002t0018g0176others(2): Show | 5 | HG02965.hp1 HG03471.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.-462-17782C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37393778 | ||||||
| chr22:37393888
|
C | T | 2 | a0001c0002t0031g0174a0001c0002t0031g0175 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-462-17892G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37393888 | ||||||
| chr22:37394060
|
C | T | 76 | a0001c0001t0002g0029a0001c0001t0002g0097a0001c0001t0002g0102others(73): Show | 77 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.-462-18064G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37394060 | ||||||
| chr22:37394071
|
A | C | 154 | a0001c0001t0002g0029a0001c0001t0002g0097a0001c0001t0002g0102others(151): Show | 155 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.-462-18075T>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37394071 | ||||||
| chr22:37394164
|
G | A | 6 | a0001c0002t0008g0228a0001c0002t0066g0232a0001c0003t0042g0229others(3): Show | 6 | HG02895.hp1 HG03098.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.-462-18168C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37394164 | ||||||
| chr22:37394175
|
C | A | 7 | a0001c0001t0003g0217a0001c0001t0017g0208a0001c0001t0017g0319others(4): Show | 7 | HG01496.hp1 HG01516.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-462-18179G>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37394175 | ||||||
| chr22:37394228
|
C | T | 1 | a0001c0001t0027g0216 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-462-18232G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37394228 | ||||||
| chr22:37394245
|
C | T | 1 | a0001c0001t0025g0239 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-462-18249G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37394245 | ||||||
| chr22:37394254
|
C | A | 102 | a0001c0001t0002g0029a0001c0001t0002g0097a0001c0001t0002g0102others(99): Show | 103 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.-462-18258G>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37394254 | ||||||
| chr22:37394337
|
G | A | 7 | a0001c0001t0003g0217a0001c0001t0017g0208a0001c0001t0017g0319others(4): Show | 7 | HG01496.hp1 HG01516.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-462-18341C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37394337 | ||||||
| chr22:37394377
|
A | G | 1 | a0001c0005t0011g0207 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-462-18381T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37394377 | ||||||
| chr22:37394378
|
T | C | 6 | a0001c0001t0005g0135a0001c0001t0005g0136a0001c0001t0017g0128others(3): Show | 6 | HG02572.hp1 HG02647.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-462-18382A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37394378 | ||||||
| chr22:37394463
|
G | A | 84 | a0001c0001t0002g0052a0001c0001t0002g0111a0001c0001t0002g0122others(81): Show | 84 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.-462-18467C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37394463 | ||||||
| chr22:37394540
|
C | G | 1 | a0001c0001t0009g0171 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-462-18544G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37394540 | ||||||
| chr22:37394562
|
C | T | 7 | a0001c0002t0004g0254a0001c0002t0006g0247a0001c0002t0006g0253others(4): Show | 7 | HG01168.hp2 HG01169.hp1 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.-462-18566G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37394562 | ||||||
| chr22:37394592
|
G | A | 8 | a0001c0001t0003g0217a0001c0001t0017g0208a0001c0001t0017g0319others(5): Show | 8 | HG01496.hp1 HG01516.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.-462-18596C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37394592 | ||||||
| chr22:37394624
|
C | T | 4 | a0001c0001t0009g0017a0001c0001t0063g0325a0001c0002t0022g0156others(1): Show | 4 | HG01884.hp1 HG02280.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-462-18628G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37394624 | ||||||
| chr22:37394649
|
C | T | 17 | a0001c0001t0097g0324a0001c0002t0004g0199a0001c0002t0008g0231others(14): Show | 17 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.-462-18653G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37394649 | ||||||
| chr22:37394778
|
A | G | 5 | a0001c0002t0008g0228a0001c0002t0066g0232a0001c0003t0042g0229others(2): Show | 5 | HG02895.hp1 HG03471.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.-462-18782T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37394778 | ||||||
| chr22:37394789
|
CCGACCTT others(66): Show |
C | 1 | a0005c0014t0004g0032 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-462-18866_-462-18 others(79): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37394789 | ||||||
| chr22:37394920
|
T | A | 1 | a0001c0003t0083g0219 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-462-18924A>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37394920 | ||||||
| chr22:37394923
|
C | T | 113 | a0001c0001t0002g0029a0001c0001t0002g0097a0001c0001t0002g0102others(110): Show | 114 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.-462-18927G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37394923 | ||||||
| chr22:37394933
|
T | C | 13 | a0001c0001t0005g0018a0001c0001t0005g0019a0001c0001t0009g0227others(10): Show | 13 | HG01891.hp1 HG02145.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-462-18937A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37394933 | ||||||
| chr22:37394957
|
G | T | 1 | a0001c0002t0008g0231 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-462-18961C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37394957 | ||||||
| chr22:37395029
|
C | T | 4 | a0001c0001t0002g0281a0001c0001t0023g0120a0001c0002t0004g0038others(1): Show | 4 | NA18960.hp1 NA18966.hp2 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.-462-19033G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37395029 | ||||||
| chr22:37395048
|
T | C | 7 | a0001c0001t0003g0217a0001c0001t0017g0208a0001c0001t0017g0319others(4): Show | 7 | HG01496.hp1 HG01516.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-462-19052A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37395048 | ||||||
| chr22:37395106
|
A | AAAAT | 104 | a0001c0001t0002g0052a0001c0001t0002g0111a0001c0001t0002g0122others(101): Show | 104 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.-462-19114_-462-19 others(10): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37395106 | ||||||
| chr22:37395106
|
A | AAAATAAA others(1): Show |
10 | a0001c0002t0004g0238a0001c0002t0004g0263a0001c0002t0006g0253others(7): Show | 10 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(7): Show |
intron_variant | MODIFIER | c.-462-19118_-462-19 others(14): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37395106 | ||||||
| chr22:37395106
|
AAAAT | A | 22 | a0001c0001t0002g0119a0001c0001t0003g0140a0001c0001t0005g0148others(19): Show | 22 | HG00438.hp2 HG01109.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.-462-19114_-462-19 others(10): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37395106 | ||||||
| chr22:37395106
|
AAAATAAA others(1): Show |
A | 87 | a0001c0001t0002g0029a0001c0001t0002g0097a0001c0001t0002g0102others(84): Show | 88 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.-462-19118_-462-19 others(14): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37395106 | ||||||
| chr22:37395106
|
AAAATAAA others(5): Show |
A | 23 | a0001c0001t0005g0018a0001c0001t0005g0019a0001c0001t0005g0135others(20): Show | 23 | HG01884.hp1 HG01891.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.-462-19122_-462-19 others(18): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37395106 | ||||||
| chr22:37395106
|
AAAATAAA others(13): Show |
A | 1 | a0001c0001t0017g0128 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-462-19130_-462-19 others(26): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37395106 | ||||||
| chr22:37395130
|
TA | T | 7 | a0001c0001t0003g0217a0001c0001t0017g0208a0001c0001t0017g0319others(4): Show | 7 | HG01496.hp1 HG01516.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-462-19135delT | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37395130 | ||||||
| chr22:37395140
|
A | C | 1 | a0001c0002t0068g0133 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-462-19144T>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37395140 | ||||||
| chr22:37395145
|
A | G | 15 | a0001c0001t0005g0070a0001c0001t0005g0148a0001c0001t0005g0150others(12): Show | 15 | HG01109.hp1 HG01433.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.-462-19149T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37395145 | ||||||
| chr22:37395150
|
T | G | 42 | a0001c0001t0003g0217a0001c0001t0005g0018a0001c0001t0005g0019others(39): Show | 42 | HG01109.hp2 HG01496.hp1 HG01516.hp1 others(39): Show |
intron_variant | MODIFIER | c.-462-19154A>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37395150 | ||||||
| chr22:37395270
|
T | C | 1 | a0001c0002t0004g0139 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-462-19274A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37395270 | ||||||
| chr22:37395422
|
G | C | 13 | a0001c0002t0004g0199a0001c0002t0008g0231a0001c0002t0008g0314others(10): Show | 13 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.-462-19426C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37395422 | ||||||
| chr22:37395482
|
T | C | 1 | a0001c0001t0027g0216 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-462-19486A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37395482 | ||||||
| chr22:37395545
|
C | G | 1 | a0001c0001t0027g0216 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-462-19549G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37395545 | ||||||
| chr22:37395613
|
C | T | 1 | a0001c0001t0027g0216 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-462-19617G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37395613 | ||||||
| chr22:37395718
|
G | A | 1 | a0001c0002t0008g0049 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-462-19722C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37395718 | ||||||
| chr22:37395752
|
G | A | 7 | a0001c0001t0003g0217a0001c0001t0017g0208a0001c0001t0017g0319others(4): Show | 7 | HG01496.hp1 HG01516.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-462-19756C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37395752 | ||||||
| chr22:37395798
|
G | A | 1 | a0002c0007t0086g0316 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-462-19802C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37395798 | ||||||
| chr22:37395806
|
C | T | 7 | a0001c0001t0003g0217a0001c0001t0017g0208a0001c0001t0017g0319others(4): Show | 7 | HG01496.hp1 HG01516.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-462-19810G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37395806 | ||||||
| chr22:37395856
|
G | A | 10 | a0001c0001t0009g0167a0001c0001t0009g0168a0001c0001t0009g0171others(7): Show | 10 | HG02109.hp2 HG02602.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-462-19860C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37395856 | ||||||
| chr22:37395941
|
C | T | 1 | a0001c0001t0097g0324 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-462-19945G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37395941 | ||||||
| chr22:37396076
|
C | T | 1 | a0001c0001t0027g0216 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-462-20080G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37396076 | ||||||
| chr22:37396267
|
G | A | 7 | a0001c0001t0003g0217a0001c0001t0017g0208a0001c0001t0017g0319others(4): Show | 7 | HG01496.hp1 HG01516.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-462-20271C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37396267 | ||||||
| chr22:37396351
|
C | T | 13 | a0001c0001t0005g0164a0001c0002t0004g0199a0001c0002t0008g0231others(10): Show | 13 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.-462-20355G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37396351 | ||||||
| chr22:37396373
|
G | A | 32 | a0001c0001t0005g0018a0001c0001t0005g0019a0001c0001t0005g0135others(29): Show | 32 | HG01109.hp2 HG01891.hp1 HG02145.hp1 others(29): Show |
intron_variant | MODIFIER | c.-462-20377C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37396373 | ||||||
| chr22:37396411
|
C | A | 1 | a0001c0001t0002g0248 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-462-20415G>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37396411 | ||||||
| chr22:37396418
|
C | T | 1 | a0001c0002t0008g0314 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-462-20422G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37396418 | ||||||
| chr22:37396454
|
G | A | 5 | a0001c0002t0008g0228a0001c0002t0066g0232a0001c0003t0042g0229others(2): Show | 5 | HG02895.hp1 HG03471.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.-462-20458C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37396454 | ||||||
| chr22:37396473
|
C | T | 85 | a0001c0001t0002g0029a0001c0001t0002g0097a0001c0001t0002g0102others(82): Show | 86 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.-462-20477G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37396473 | ||||||
| chr22:37396537
|
C | T | 86 | a0001c0001t0002g0029a0001c0001t0002g0097a0001c0001t0002g0102others(83): Show | 87 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.-462-20541G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37396537 | ||||||
| chr22:37396550
|
A | G | 86 | a0001c0001t0002g0029a0001c0001t0002g0097a0001c0001t0002g0102others(83): Show | 87 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.-462-20554T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37396550 | ||||||
| chr22:37396599
|
G | A | 86 | a0001c0001t0002g0029a0001c0001t0002g0097a0001c0001t0002g0102others(83): Show | 87 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.-462-20603C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37396599 | ||||||
| chr22:37396621
|
G | A | 1 | a0003c0017t0002g0046 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-462-20625C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37396621 | ||||||
| chr22:37396634
|
C | T | 1 | a0001c0001t0025g0239 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-462-20638G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37396634 | ||||||
| chr22:37396635
|
G | A | 5 | a0001c0002t0008g0228a0001c0002t0066g0232a0001c0003t0042g0229others(2): Show | 5 | HG02895.hp1 HG03471.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.-462-20639C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37396635 | ||||||
| chr22:37396779
|
G | A | 1 | a0002c0007t0086g0316 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-462-20783C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37396779 | ||||||
| chr22:37396887
|
G | A | 2 | a0001c0001t0005g0044a0001c0002t0068g0133 | 2 | HG02965.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-463+20882C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37396887 | ||||||
| chr22:37396947
|
T | G | 1 | a0001c0001t0027g0216 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-463+20822A>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37396947 | ||||||
| chr22:37396968
|
C | T | 1 | a0001c0002t0006g0280 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-463+20801G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37396968 | ||||||
| chr22:37396969
|
G | C | 1 | a0002c0007t0072g0323 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-463+20800C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37396969 | ||||||
| chr22:37397040
|
C | G | 89 | a0001c0001t0002g0029a0001c0001t0002g0097a0001c0001t0002g0102others(86): Show | 90 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.-463+20729G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37397040 | ||||||
| chr22:37397109
|
G | T | 3 | a0001c0001t0005g0018a0001c0001t0005g0019a0001c0001t0025g0239 | 3 | HG01433.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-463+20660C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37397109 | ||||||
| chr22:37397126
|
C | T | 91 | a0001c0001t0002g0052a0001c0001t0002g0123a0001c0001t0002g0240others(88): Show | 91 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.-463+20643G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37397126 | ||||||
| chr22:37397156
|
A | C | 4 | a0001c0008t0015g0160a0001c0008t0015g0161a0001c0008t0015g0170others(1): Show | 4 | HG02109.hp1 HG02615.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-463+20613T>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37397156 | ||||||
| chr22:37397240
|
C | T | 82 | a0001c0001t0002g0029a0001c0001t0002g0097a0001c0001t0002g0102others(79): Show | 83 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.-463+20529G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37397240 | ||||||
| chr22:37397289
|
T | C | 156 | a0001c0001t0002g0029a0001c0001t0002g0097a0001c0001t0002g0102others(153): Show | 157 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.-463+20480A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37397289 | ||||||
| chr22:37397290
|
G | A | 79 | a0001c0001t0002g0029a0001c0001t0002g0097a0001c0001t0002g0102others(76): Show | 80 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.-463+20479C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37397290 | ||||||
| chr22:37397368
|
A | G | 41 | a0001c0001t0002g0275a0001c0001t0003g0003a0001c0001t0003g0180others(38): Show | 42 | HG00099.hp2 HG00423.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.-463+20401T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37397368 | ||||||
| chr22:37397475
|
C | T | 46 | a0001c0001t0002g0300a0001c0001t0003g0003a0001c0001t0003g0180others(43): Show | 47 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.-463+20294G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37397475 | ||||||
| chr22:37397476
|
G | A | 1 | a0001c0001t0017g0319 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-463+20293C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37397476 | ||||||
| chr22:37397510
|
A | T | 55 | a0001c0001t0003g0003a0001c0001t0003g0180a0001c0001t0003g0185others(52): Show | 56 | HG00099.hp2 HG00423.hp2 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.-463+20259T>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37397510 | ||||||
| chr22:37397613
|
T | G | 116 | a0001c0001t0002g0300a0001c0001t0002g0306a0001c0001t0003g0003others(113): Show | 117 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.-463+20156A>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37397613 | ||||||
| chr22:37397695
|
C | A | 7 | a0001c0001t0005g0018a0001c0001t0005g0019a0001c0001t0009g0017others(4): Show | 7 | HG01884.hp1 HG02622.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-463+20074G>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37397695 | ||||||
| chr22:37397710
|
C | T | 1 | a0001c0002t0008g0231 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-463+20059G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37397710 | ||||||
| chr22:37397787
|
GGA | G | 36 | a0001c0001t0003g0003a0001c0001t0003g0180a0001c0001t0003g0185others(33): Show | 37 | HG00099.hp2 HG00423.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.-463+19980_-463+19 others(8): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37397787 | ||||||
| chr22:37397799
|
G | GT | 3 | a0001c0001t0005g0018a0001c0001t0005g0019a0002c0007t0086g0316 | 3 | HG02895.hp2 HG02897.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-463+19969_-463+19 others(7): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37397799 | ||||||
| chr22:37397800
|
C | T | 3 | a0001c0001t0005g0018a0001c0001t0005g0019a0002c0007t0086g0316 | 3 | HG02895.hp2 HG02897.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-463+19969G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37397800 | ||||||
| chr22:37397803
|
CCGGGCTG others(21): Show |
C | 1 | a0001c0001t0027g0204 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-463+19938_-463+19 others(34): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37397803 | ||||||
| chr22:37397805
|
G | A | 1 | a0001c0011t0059g0218 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-463+19964C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37397805 | ||||||
| chr22:37397841
|
G | A | 1 | a0001c0001t0005g0154 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-463+19928C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37397841 | ||||||
| chr22:37397882
|
T | C | 7 | a0001c0001t0003g0224a0001c0001t0005g0018a0001c0001t0005g0019others(4): Show | 7 | HG02486.hp2 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-463+19887A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37397882 | ||||||
| chr22:37397907
|
C | CCT | 7 | a0001c0001t0003g0224a0001c0001t0005g0018a0001c0001t0005g0019others(4): Show | 7 | HG02486.hp2 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-463+19860_-463+19 others(8): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37397907 | ||||||
| chr22:37398014
|
G | A | 7 | a0001c0001t0003g0224a0001c0001t0005g0018a0001c0001t0005g0019others(4): Show | 7 | HG02486.hp2 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-463+19755C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37398014 | ||||||
| chr22:37398025
|
A | G | 8 | a0001c0001t0005g0209a0001c0001t0009g0210a0001c0001t0017g0208others(5): Show | 8 | HG00639.hp2 HG01891.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-463+19744T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37398025 | ||||||
| chr22:37398028
|
C | G | 6 | a0001c0001t0003g0178a0001c0001t0003g0242a0001c0001t0003g0244others(3): Show | 6 | HG00140.hp1 HG00733.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.-463+19741G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37398028 | ||||||
| chr22:37398056
|
C | T | 11 | a0001c0001t0003g0224a0001c0001t0005g0018a0001c0001t0005g0019others(8): Show | 11 | HG02109.hp1 HG02486.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-463+19713G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37398056 | ||||||
| chr22:37398059
|
T | A | 4 | a0001c0008t0015g0160a0001c0008t0015g0161a0001c0008t0015g0170others(1): Show | 4 | HG02109.hp1 HG02615.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-463+19710A>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37398059 | ||||||
| chr22:37398062
|
G | A | 11 | a0001c0001t0003g0224a0001c0001t0005g0018a0001c0001t0005g0019others(8): Show | 11 | HG02145.hp2 HG02486.hp2 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.-463+19707C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37398062 | ||||||
| chr22:37398190
|
G | A | 1 | a0001c0002t0006g0266 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-463+19579C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37398190 | ||||||
| chr22:37398229
|
T | C | 185 | a0001c0001t0002g0052a0001c0001t0002g0111a0001c0001t0002g0123others(182): Show | 186 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.-463+19540A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37398229 | ||||||
| chr22:37398253
|
A | C | 26 | a0001c0001t0003g0217a0001c0001t0003g0224a0001c0001t0005g0018others(23): Show | 26 | HG01516.hp1 HG01891.hp1 HG02145.hp1 others(23): Show |
intron_variant | MODIFIER | c.-463+19516T>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37398253 | ||||||
| chr22:37398259
|
T | G | 1 | a0001c0001t0027g0216 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-463+19510A>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37398259 | ||||||
| chr22:37398299
|
A | ACGGCCTC others(4): Show |
1 | a0005c0014t0004g0032 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-463+19469_-463+19 others(17): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37398299 | ||||||
| chr22:37398300
|
T | A | 1 | a0005c0014t0004g0032 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-463+19469A>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37398300 | ||||||
| chr22:37398300
|
T | C | 2 | a0001c0002t0008g0231a0001c0003t0041g0163 | 2 | HG01109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-463+19469A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37398300 | ||||||
| chr22:37398319
|
C | G | 26 | a0001c0001t0003g0217a0001c0001t0003g0224a0001c0001t0005g0018others(23): Show | 26 | HG01516.hp1 HG01891.hp1 HG02145.hp1 others(23): Show |
intron_variant | MODIFIER | c.-463+19450G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37398319 | ||||||
| chr22:37398335
|
C | A | 1 | a0001c0002t0007g0072 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-463+19434G>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37398335 | ||||||
| chr22:37398443
|
G | A | 33 | a0001c0001t0003g0217a0001c0001t0003g0224a0001c0001t0005g0018others(30): Show | 33 | HG00639.hp2 HG01516.hp1 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.-463+19326C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37398443 | ||||||
| chr22:37398473
|
G | A | 1 | a0001c0005t0011g0211 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-463+19296C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37398473 | ||||||
| chr22:37398563
|
G | A | 24 | a0001c0001t0003g0217a0001c0001t0003g0224a0001c0001t0009g0227others(21): Show | 24 | HG01516.hp1 HG01891.hp1 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.-463+19206C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37398563 | ||||||
| chr22:37398582
|
C | T | 24 | a0001c0001t0003g0217a0001c0001t0003g0224a0001c0001t0009g0227others(21): Show | 24 | HG01516.hp1 HG01891.hp1 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.-463+19187G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37398582 | ||||||
| chr22:37398583
|
G | A | 1 | a0001c0003t0001g0024 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-463+19186C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37398583 | ||||||
| chr22:37398635
|
T | A | 19 | a0001c0001t0003g0217a0001c0001t0009g0227a0001c0001t0017g0319others(16): Show | 19 | HG01516.hp1 HG01891.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.-463+19134A>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37398635 | ||||||
| chr22:37398636
|
C | T | 19 | a0001c0001t0003g0217a0001c0001t0009g0227a0001c0001t0017g0319others(16): Show | 19 | HG01516.hp1 HG01891.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.-463+19133G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37398636 | ||||||
| chr22:37398664
|
G | A | 1 | a0001c0003t0001g0015 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-463+19105C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37398664 | ||||||
| chr22:37398668
|
T | G | 5 | a0001c0001t0003g0224a0001c0002t0074g0223a0001c0003t0093g0318others(2): Show | 5 | HG02486.hp2 HG03098.hp1 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.-463+19101A>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37398668 | ||||||
| chr22:37398742
|
C | T | 1 | a0001c0001t0005g0225 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-463+19027G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37398742 | ||||||
| chr22:37398764
|
CAT | C | 5 | a0001c0001t0003g0224a0001c0002t0074g0223a0001c0003t0093g0318others(2): Show | 5 | HG02486.hp2 HG03098.hp1 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.-463+19003_-463+19 others(8): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37398764 | ||||||
| chr22:37398800
|
C | T | 1 | a0001c0001t0027g0216 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-463+18969G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37398800 | ||||||
| chr22:37398811
|
G | A | 57 | a0001c0001t0002g0298a0001c0001t0002g0300a0001c0001t0002g0306others(54): Show | 58 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.-463+18958C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37398811 | ||||||
| chr22:37398814
|
C | T | 7 | a0001c0001t0003g0224a0001c0002t0018g0176a0001c0002t0069g0009others(4): Show | 7 | HG01099.hp1 HG02486.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.-463+18955G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37398814 | ||||||
| chr22:37398893
|
C | A | 1 | a0001c0005t0011g0196 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-463+18876G>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37398893 | ||||||
| chr22:37398990
|
A | G | 2 | a0001c0001t0097g0324a0001c0002t0021g0147 | 2 | HG03540.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-463+18779T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37398990 | ||||||
| chr22:37399063
|
T | C | 2 | a0001c0003t0001g0030a0001c0003t0001g0066 | 2 | HG02074.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.-463+18706A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399063 | ||||||
| chr22:37399078
|
A | T | 1 | a0001c0009t0055g0013 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-463+18691T>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399078 | ||||||
| chr22:37399109
|
A | G | 3 | a0001c0001t0029g0098a0001c0001t0029g0114a0001c0001t0051g0025 | 3 | HG00621.hp2 HG02056.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.-463+18660T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399109 | ||||||
| chr22:37399118
|
T | C | 18 | a0001c0001t0003g0217a0001c0001t0009g0227a0001c0001t0017g0319others(15): Show | 18 | HG01516.hp1 HG01891.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.-463+18651A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399118 | ||||||
| chr22:37399119
|
G | C | 1 | a0001c0003t0083g0219 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-463+18650C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399119 | ||||||
| chr22:37399132
|
C | G | 120 | a0001c0001t0002g0052a0001c0001t0002g0111a0001c0001t0002g0123others(117): Show | 120 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.-463+18637G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399132 | ||||||
| chr22:37399189
|
G | A | 120 | a0001c0001t0002g0052a0001c0001t0002g0111a0001c0001t0002g0123others(117): Show | 120 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.-463+18580C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399189 | ||||||
| chr22:37399221
|
C | G | 2 | a0001c0002t0018g0176a0001c0002t0069g0009 | 2 | HG01099.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-463+18548G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399221 | ||||||
| chr22:37399243
|
A | G | 141 | a0001c0001t0002g0052a0001c0001t0002g0111a0001c0001t0002g0123others(138): Show | 141 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.-463+18526T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399243 | ||||||
| chr22:37399253
|
G | C | 1 | a0005c0014t0004g0032 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-463+18516C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399253 | ||||||
| chr22:37399472
|
A | AGACCACC others(32): Show |
1 | a0001c0002t0007g0072 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-463+18258_-463+18 others(45): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399472 | ||||||
| chr22:37399472
|
A | AGACCACC others(71): Show |
1 | a0001c0001t0002g0041 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-463+18219_-463+18 others(84): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399472 | ||||||
| chr22:37399472
|
A | AGACCACC others(110): Show |
3 | a0001c0001t0005g0152a0001c0001t0005g0154a0001c0002t0077g0159 | 3 | HG02896.hp1 HG02970.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-463+18296_-463+18 others(123): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399472 | ||||||
| chr22:37399472
|
A | AGACCACC others(149): Show |
3 | a0001c0001t0005g0150a0001c0001t0005g0151a0001c0001t0005g0155 | 3 | HG02965.hp2 HG03130.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-463+18296_-463+18 others(162): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399472 | ||||||
| chr22:37399472
|
AGACCACC others(71): Show |
A | 23 | a0001c0001t0003g0217a0001c0001t0009g0227a0001c0001t0017g0319others(20): Show | 23 | HG01516.hp1 HG01891.hp1 HG01928.hp2 others(20): Show |
intron_variant | MODIFIER | c.-463+18219_-463+18 others(84): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399472 | ||||||
| chr22:37399480
|
G | GGCCCACC others(32): Show |
31 | a0001c0001t0005g0044a0001c0001t0005g0148a0001c0001t0005g0202others(28): Show | 31 | HG00423.hp2 HG00639.hp2 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.-463+18250_-463+18 others(45): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399480 | ||||||
| chr22:37399480
|
G | GGCCCACC others(149): Show |
1 | a0001c0003t0001g0268 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-463+18288_-463+18 others(162): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399480 | ||||||
| chr22:37399480
|
GGCCCACC others(32): Show |
G | 73 | a0001c0001t0002g0052a0001c0001t0002g0111a0001c0001t0002g0123others(70): Show | 73 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.-463+18250_-463+18 others(45): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399480 | ||||||
| chr22:37399480
|
GGCCCACC others(110): Show |
G | 4 | a0001c0002t0021g0197a0001c0003t0001g0177a0001c0003t0001g0200others(1): Show | 4 | HG02145.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-463+18172_-463+18 others(6): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399480 | ||||||
| chr22:37399483
|
CCACCTCT others(30): Show |
C | 1 | a0005c0014t0004g0032 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-463+18249_-463+18 others(43): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399483 | ||||||
| chr22:37399519
|
A | G | 3 | a0001c0002t0007g0187a0001c0002t0007g0188a0001c0002t0008g0231 | 3 | HG01109.hp2 HG02738.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.-463+18250T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399519 | ||||||
| chr22:37399519
|
AGCCCACC others(32): Show |
A | 11 | a0001c0001t0003g0084a0001c0001t0003g0224a0001c0001t0060g0226others(8): Show | 11 | HG01496.hp1 HG02735.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.-463+18211_-463+18 others(45): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399519 | ||||||
| chr22:37399557
|
C | T | 6 | a0001c0001t0005g0018a0001c0001t0005g0019a0001c0001t0009g0017others(3): Show | 6 | HG01884.hp1 HG02622.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-463+18212G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399557 | ||||||
| chr22:37399558
|
G | A | 72 | a0001c0001t0002g0298a0001c0001t0002g0300a0001c0001t0002g0306others(69): Show | 73 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.-463+18211C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399558 | ||||||
| chr22:37399558
|
G | GGCCCACC others(71): Show |
10 | a0001c0001t0005g0148a0001c0001t0005g0202a0001c0001t0025g0239others(7): Show | 10 | HG01109.hp1 HG01433.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.-463+18133_-463+18 others(84): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399558 | ||||||
| chr22:37399558
|
GGCCCACC others(32): Show |
G | 6 | a0001c0001t0003g0140a0001c0001t0005g0164a0001c0003t0001g0055others(3): Show | 6 | HG01346.hp1 HG03209.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.-463+18172_-463+18 others(45): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399558 | ||||||
| chr22:37399581
|
G | GACCACGG others(266): Show |
1 | a0001c0002t0021g0147 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-463+18187_-463+18 others(279): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399581 | ||||||
| chr22:37399581
|
G | GACCACGG others(149): Show |
1 | a0001c0001t0097g0324 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-463+18187_-463+18 others(162): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399581 | ||||||
| chr22:37399659
|
G | A | 3 | a0001c0001t0002g0281a0001c0002t0004g0038a0005c0014t0004g0032 | 3 | NA18966.hp2 NA19068.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.-463+18110C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399659 | ||||||
| chr22:37399664
|
C | T | 1 | a0001c0003t0094g0008 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-463+18105G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399664 | ||||||
| chr22:37399673
|
T | C | 9 | a0001c0001t0005g0209a0001c0001t0009g0210a0001c0001t0017g0208others(6): Show | 9 | HG00639.hp2 HG01891.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.-463+18096A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399673 | ||||||
| chr22:37399716
|
A | G | 86 | a0001c0001t0002g0298a0001c0001t0002g0300a0001c0001t0002g0306others(83): Show | 86 | HG00323.hp1 HG00323.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-463+18053T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399716 | ||||||
| chr22:37399727
|
C | T | 4 | a0001c0001t0003g0224a0001c0002t0074g0223a0001c0003t0093g0318others(1): Show | 4 | HG02486.hp2 NA18906.hp2 NA20905.hp2 others(1): Show |
intron_variant | MODIFIER | c.-463+18042G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399727 | ||||||
| chr22:37399744
|
G | A | 12 | a0001c0001t0005g0209a0001c0001t0009g0210a0001c0001t0017g0208others(9): Show | 12 | HG00639.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.-463+18025C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399744 | ||||||
| chr22:37399853
|
G | A | 1 | a0001c0001t0027g0216 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-463+17916C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399853 | ||||||
| chr22:37399917
|
G | A | 2 | a0001c0001t0065g0169a0001c0018t0045g0172 | 2 | HG02809.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-463+17852C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399917 | ||||||
| chr22:37400094
|
A | G | 12 | a0001c0001t0005g0202a0001c0001t0009g0167a0001c0001t0009g0168others(9): Show | 12 | HG01433.hp2 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.-463+17675T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37400094 | ||||||
| chr22:37400116
|
A | G | 8 | a0001c0001t0009g0167a0001c0001t0009g0168a0001c0001t0009g0171others(5): Show | 8 | HG02109.hp2 HG02622.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.-463+17653T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37400116 | ||||||
| chr22:37400121
|
A | C | 8 | a0001c0001t0009g0167a0001c0001t0009g0168a0001c0001t0009g0171others(5): Show | 8 | HG02109.hp2 HG02622.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.-463+17648T>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37400121 | ||||||
| chr22:37400238
|
C | T | 5 | a0001c0002t0004g0142a0001c0002t0021g0197a0001c0003t0001g0177others(2): Show | 5 | HG02145.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-463+17531G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37400238 | ||||||
| chr22:37400357
|
T | C | 1 | a0001c0001t0003g0224 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-463+17412A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37400357 | ||||||
| chr22:37400370
|
C | G | 1 | a0001c0001t0061g0183 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-463+17399G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37400370 | ||||||
| chr22:37400371
|
C | G | 1 | a0001c0001t0061g0183 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-463+17398G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37400371 | ||||||
| chr22:37400443
|
G | T | 1 | a0005c0014t0004g0032 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-463+17326C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37400443 | ||||||
| chr22:37400585
|
G | A | 2 | a0001c0001t0002g0252a0001c0006t0001g0277 | 2 | HG00558.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.-463+17184C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37400585 | ||||||
| chr22:37400695
|
C | T | 5 | a0001c0001t0005g0164a0001c0001t0005g0225a0001c0002t0008g0228others(2): Show | 5 | HG03041.hp2 HG03453.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.-463+17074G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37400695 | ||||||
| chr22:37400774
|
G | A | 61 | a0001c0001t0002g0298a0001c0001t0002g0300a0001c0001t0002g0306others(58): Show | 61 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.-463+16995C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37400774 | ||||||
| chr22:37400909
|
A | G | 2 | a0001c0002t0007g0187a0001c0002t0007g0188 | 2 | HG02738.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.-463+16860T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37400909 | ||||||
| chr22:37400937
|
G | C | 62 | a0001c0001t0002g0298a0001c0001t0002g0300a0001c0001t0002g0306others(59): Show | 62 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.-463+16832C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37400937 | ||||||
| chr22:37400992
|
G | A | 100 | a0001c0001t0002g0111a0001c0001t0002g0123a0001c0001t0002g0240others(97): Show | 100 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.-463+16777C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37400992 | ||||||
| chr22:37401098
|
A | G | 161 | a0001c0001t0002g0111a0001c0001t0002g0123a0001c0001t0002g0240others(158): Show | 161 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.-463+16671T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37401098 | ||||||
| chr22:37401121
|
C | T | 1 | a0003c0017t0002g0046 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-463+16648G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37401121 | ||||||
| chr22:37401188
|
G | A | 8 | a0001c0001t0005g0209a0001c0001t0009g0210a0001c0001t0017g0208others(5): Show | 8 | HG00639.hp2 HG01891.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-463+16581C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37401188 | ||||||
| chr22:37401345
|
A | G | 5 | a0001c0001t0003g0224a0001c0002t0074g0223a0001c0003t0093g0318others(2): Show | 5 | HG02486.hp2 HG03098.hp1 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.-463+16424T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37401345 | ||||||
| chr22:37401422
|
TC | T | 95 | a0001c0001t0002g0111a0001c0001t0002g0123a0001c0001t0002g0240others(92): Show | 95 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.-463+16346delG | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37401422 | ||||||
| chr22:37401423
|
C | A | 1 | a0005c0014t0004g0032 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-463+16346G>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37401423 | ||||||
| chr22:37401424
|
A | G | 1 | a0005c0014t0004g0032 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-463+16345T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37401424 | ||||||
| chr22:37401522
|
A | G | 8 | a0001c0001t0005g0209a0001c0001t0009g0210a0001c0001t0017g0208others(5): Show | 8 | HG00639.hp2 HG01891.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-463+16247T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37401522 | ||||||
| chr22:37401529
|
A | AGGGAGGA others(17): Show |
1 | a0005c0014t0004g0032 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-463+16216_-463+16 others(30): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37401529 | ||||||
| chr22:37401589
|
C | A | 1 | a0001c0001t0002g0267 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-463+16180G>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37401589 | ||||||
| chr22:37401657
|
G | T | 153 | a0001c0001t0002g0111a0001c0001t0002g0123a0001c0001t0002g0240others(150): Show | 153 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.-463+16112C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37401657 | ||||||
| chr22:37401674
|
C | T | 4 | a0001c0001t0005g0202a0001c0002t0036g0321a0001c0002t0082g0320others(1): Show | 4 | HG02257.hp1 HG02717.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-463+16095G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37401674 | ||||||
| chr22:37401687
|
G | C | 153 | a0001c0001t0002g0111a0001c0001t0002g0123a0001c0001t0002g0240others(150): Show | 153 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.-463+16082C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37401687 | ||||||
| chr22:37401688
|
C | G | 153 | a0001c0001t0002g0111a0001c0001t0002g0123a0001c0001t0002g0240others(150): Show | 153 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.-463+16081G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37401688 | ||||||
| chr22:37401689
|
G | A | 5 | a0001c0001t0005g0018a0001c0001t0005g0019a0001c0001t0009g0017others(2): Show | 5 | HG01884.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-463+16080C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37401689 | ||||||
| chr22:37401702
|
G | T | 1 | a0002c0007t0072g0323 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-463+16067C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37401702 | ||||||
| chr22:37401713
|
G | A | 6 | a0001c0001t0005g0018a0001c0001t0005g0019a0001c0001t0009g0017others(3): Show | 6 | HG01884.hp1 HG02622.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-463+16056C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37401713 | ||||||
| chr22:37401760
|
T | C | 161 | a0001c0001t0002g0111a0001c0001t0002g0123a0001c0001t0002g0240others(158): Show | 161 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.-463+16009A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37401760 | ||||||
| chr22:37401836
|
C | T | 4 | a0001c0001t0005g0135a0001c0001t0005g0136a0001c0001t0017g0128others(1): Show | 4 | HG02647.hp2 HG02717.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-463+15933G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37401836 | ||||||
| chr22:37401837
|
G | A | 6 | a0001c0001t0005g0018a0001c0001t0005g0019a0001c0001t0009g0017others(3): Show | 6 | HG01884.hp1 HG02622.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-463+15932C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37401837 | ||||||
| chr22:37401883
|
C | T | 14 | a0001c0001t0003g0217a0001c0001t0009g0227a0001c0001t0017g0319others(11): Show | 14 | HG01516.hp1 HG02280.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.-463+15886G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37401883 | ||||||
| chr22:37401931
|
C | T | 153 | a0001c0001t0002g0111a0001c0001t0002g0123a0001c0001t0002g0240others(150): Show | 153 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.-463+15838G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37401931 | ||||||
| chr22:37401988
|
A | G | 4 | a0001c0008t0015g0160a0001c0008t0015g0161a0001c0008t0015g0170others(1): Show | 4 | HG02109.hp1 HG02615.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-463+15781T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37401988 | ||||||
| chr22:37402127
|
G | A | 7 | a0001c0001t0005g0164a0001c0002t0004g0142a0001c0002t0021g0197others(4): Show | 7 | HG02145.hp2 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-463+15642C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37402127 | ||||||
| chr22:37402227
|
G | A | 10 | a0001c0001t0005g0148a0001c0001t0005g0150a0001c0001t0005g0151others(7): Show | 10 | HG01109.hp1 HG02055.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.-463+15542C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37402227 | ||||||
| chr22:37402330
|
C | G | 161 | a0001c0001t0002g0111a0001c0001t0002g0123a0001c0001t0002g0240others(158): Show | 161 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.-463+15439G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37402330 | ||||||
| chr22:37402361
|
T | C | 4 | a0001c0001t0005g0225a0001c0002t0008g0228a0001c0003t0042g0229others(1): Show | 4 | HG03041.hp2 HG03471.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-463+15408A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37402361 | ||||||
| chr22:37402543
|
C | A | 161 | a0001c0001t0002g0111a0001c0001t0002g0123a0001c0001t0002g0240others(158): Show | 161 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.-463+15226G>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37402543 | ||||||
| chr22:37402577
|
A | C | 1 | a0001c0003t0012g0308 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-463+15192T>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37402577 | ||||||
| chr22:37402604
|
G | T | 153 | a0001c0001t0002g0111a0001c0001t0002g0123a0001c0001t0002g0240others(150): Show | 153 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.-463+15165C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37402604 | ||||||
| chr22:37402624
|
GT | G | 153 | a0001c0001t0002g0111a0001c0001t0002g0123a0001c0001t0002g0240others(150): Show | 153 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.-463+15144delA | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37402624 | ||||||
| chr22:37402659
|
A | G | 8 | a0001c0001t0005g0209a0001c0001t0009g0210a0001c0001t0017g0208others(5): Show | 8 | HG00639.hp2 HG01891.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-463+15110T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37402659 | ||||||
| chr22:37402676
|
G | A | 8 | a0001c0001t0005g0209a0001c0001t0009g0210a0001c0001t0017g0208others(5): Show | 8 | HG00639.hp2 HG01891.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-463+15093C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37402676 | ||||||
| chr22:37402800
|
G | A | 1 | a0001c0001t0099g0331 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-463+14969C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37402800 | ||||||
| chr22:37402914
|
C | T | 3 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0002t0018g0001 | 4 | HG01167.hp2 HG01169.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.-463+14855G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37402914 | ||||||
| chr22:37402915
|
G | A | 101 | a0001c0001t0002g0111a0001c0001t0002g0123a0001c0001t0002g0240others(98): Show | 101 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.-463+14854C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37402915 | ||||||
| chr22:37402964
|
T | A | 10 | a0001c0001t0005g0148a0001c0001t0005g0150a0001c0001t0005g0151others(7): Show | 10 | HG01109.hp1 HG02055.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.-463+14805A>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37402964 | ||||||
| chr22:37402989
|
G | A | 2 | a0001c0001t0005g0164a0001c0003t0041g0163 | 2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-463+14780C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37402989 | ||||||
| chr22:37403021
|
T | C | 5 | a0001c0002t0004g0142a0001c0002t0021g0197a0001c0003t0001g0177others(2): Show | 5 | HG02145.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-463+14748A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37403021 | ||||||
| chr22:37403061
|
G | C | 153 | a0001c0001t0002g0111a0001c0001t0002g0130a0001c0001t0002g0240others(150): Show | 153 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.-463+14708C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37403061 | ||||||
| chr22:37403096
|
CCAA | C | 4 | a0001c0008t0015g0160a0001c0008t0015g0161a0001c0008t0015g0170others(1): Show | 4 | HG02109.hp1 HG02615.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-463+14670_-463+14 others(9): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37403096 | ||||||
| chr22:37403148
|
G | T | 163 | a0001c0001t0002g0111a0001c0001t0002g0123a0001c0001t0002g0130others(160): Show | 163 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.-463+14621C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37403148 | ||||||
| chr22:37403181
|
C | T | 163 | a0001c0001t0002g0111a0001c0001t0002g0123a0001c0001t0002g0130others(160): Show | 163 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.-463+14588G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37403181 | ||||||
| chr22:37403258
|
G | C | 8 | a0001c0001t0009g0167a0001c0001t0009g0168a0001c0001t0009g0171others(5): Show | 8 | HG02109.hp2 HG02622.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-463+14511C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37403258 | ||||||
| chr22:37403307
|
A | G | 8 | a0001c0001t0005g0209a0001c0001t0009g0210a0001c0001t0017g0208others(5): Show | 8 | HG00639.hp2 HG01891.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-463+14462T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37403307 | ||||||
| chr22:37403329
|
A | G | 163 | a0001c0001t0002g0111a0001c0001t0002g0123a0001c0001t0002g0130others(160): Show | 163 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.-463+14440T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37403329 | ||||||
| chr22:37403406
|
C | T | 1 | a0001c0003t0020g0033 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-463+14363G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37403406 | ||||||
| chr22:37403409
|
G | GCGAGGGG others(1): Show |
162 | a0001c0001t0002g0111a0001c0001t0002g0123a0001c0001t0002g0130others(159): Show | 162 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.-463+14352_-463+14 others(14): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37403409 | ||||||
| chr22:37403467
|
G | T | 11 | a0001c0001t0009g0167a0001c0001t0009g0168a0001c0001t0009g0171others(8): Show | 11 | HG02109.hp2 HG02572.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.-463+14302C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37403467 | ||||||
| chr22:37403498
|
A | G | 163 | a0001c0001t0002g0111a0001c0001t0002g0123a0001c0001t0002g0130others(160): Show | 163 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.-463+14271T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37403498 | ||||||
| chr22:37403592
|
G | A | 1 | a0001c0001t0028g0276 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-463+14177C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37403592 | ||||||
| chr22:37403597
|
C | T | 72 | a0001c0001t0002g0298a0001c0001t0002g0300a0001c0001t0002g0306others(69): Show | 72 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.-463+14172G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37403597 | ||||||
| chr22:37403622
|
C | T | 3 | a0001c0001t0053g0090a0001c0003t0001g0109a0001c0009t0002g0112 | 3 | NA18939.hp1 NA18943.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.-463+14147G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37403622 | ||||||
| chr22:37403624
|
C | T | 81 | a0001c0001t0002g0111a0001c0001t0002g0130a0001c0001t0002g0240others(78): Show | 81 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.-463+14145G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37403624 | ||||||
| chr22:37403779
|
G | A | 1 | a0001c0001t0050g0145 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-463+13990C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37403779 | ||||||
| chr22:37403794
|
G | A | 4 | a0001c0001t0019g0107a0001c0001t0019g0108a0001c0002t0004g0021others(1): Show | 4 | NA18941.hp1 NA18950.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.-463+13975C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37403794 | ||||||
| chr22:37403800
|
A | C | 2 | a0001c0002t0037g0110a0001c0002t0037g0113 | 2 | HG01256.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.-463+13969T>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37403800 | ||||||
| chr22:37403813
|
C | T | 169 | a0001c0001t0002g0111a0001c0001t0002g0123a0001c0001t0002g0130others(166): Show | 169 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.-463+13956G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37403813 | ||||||
| chr22:37403817
|
G | A | 91 | a0001c0001t0002g0111a0001c0001t0002g0123a0001c0001t0002g0130others(88): Show | 91 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.-463+13952C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37403817 | ||||||
| chr22:37403839
|
T | C | 6 | a0001c0001t0005g0018a0001c0001t0005g0019a0001c0001t0009g0017others(3): Show | 6 | HG01884.hp1 HG02622.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-463+13930A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37403839 | ||||||
| chr22:37403844
|
G | T | 169 | a0001c0001t0002g0111a0001c0001t0002g0123a0001c0001t0002g0130others(166): Show | 169 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.-463+13925C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37403844 | ||||||
| chr22:37403960
|
A | G | 122 | a0001c0001t0002g0298a0001c0001t0002g0300a0001c0001t0002g0306others(119): Show | 123 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.-463+13809T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37403960 | ||||||
| chr22:37404037
|
C | T | 2 | a0001c0001t0097g0324a0001c0002t0021g0147 | 2 | HG03540.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-463+13732G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37404037 | ||||||
| chr22:37404073
|
C | A | 2 | a0001c0001t0005g0164a0001c0003t0041g0163 | 2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-463+13696G>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37404073 | ||||||
| chr22:37404129
|
G | A | 97 | a0001c0001t0002g0111a0001c0001t0002g0123a0001c0001t0002g0130others(94): Show | 97 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.-463+13640C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37404129 | ||||||
| chr22:37404135
|
C | T | 62 | a0001c0001t0002g0298a0001c0001t0002g0300a0001c0001t0002g0306others(59): Show | 62 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.-463+13634G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37404135 | ||||||
| chr22:37404265
|
C | T | 1 | a0001c0019t0030g0127 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-463+13504G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37404265 | ||||||
| chr22:37404297
|
C | T | 4 | a0001c0001t0005g0135a0001c0001t0005g0136a0001c0001t0017g0128others(1): Show | 4 | HG02647.hp2 HG02717.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-463+13472G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37404297 | ||||||
| chr22:37404309
|
G | A | 1 | a0002c0007t0086g0316 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-463+13460C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37404309 | ||||||
| chr22:37404383
|
G | A | 4 | a0001c0001t0005g0135a0001c0001t0005g0136a0001c0001t0017g0128others(1): Show | 4 | HG02647.hp2 HG02717.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-463+13386C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37404383 | ||||||
| chr22:37404456
|
G | T | 98 | a0001c0001t0002g0111a0001c0001t0002g0123a0001c0001t0002g0130others(95): Show | 98 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.-463+13313C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37404456 | ||||||
| chr22:37404534
|
T | C | 1 | a0001c0006t0056g0220 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-463+13235A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37404534 | ||||||
| chr22:37404538
|
G | A | 169 | a0001c0001t0002g0111a0001c0001t0002g0123a0001c0001t0002g0130others(166): Show | 169 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.-463+13231C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37404538 | ||||||
| chr22:37404597
|
C | A | 4 | a0001c0008t0015g0160a0001c0008t0015g0161a0001c0008t0015g0170others(1): Show | 4 | HG02109.hp1 HG02615.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-463+13172G>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37404597 | ||||||
| chr22:37404602
|
C | T | 62 | a0001c0001t0002g0298a0001c0001t0002g0300a0001c0001t0002g0306others(59): Show | 62 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.-463+13167G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37404602 | ||||||
| chr22:37404678
|
T | G | 2 | a0001c0001t0058g0186a0001c0003t0081g0182 | 2 | HG00099.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.-463+13091A>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37404678 | ||||||
| chr22:37404723
|
C | T | 6 | a0001c0001t0005g0018a0001c0001t0005g0019a0001c0001t0009g0017others(3): Show | 6 | HG01884.hp1 HG02622.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-463+13046G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37404723 | ||||||
| chr22:37404783
|
T | C | 169 | a0001c0001t0002g0111a0001c0001t0002g0123a0001c0001t0002g0130others(166): Show | 169 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.-463+12986A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37404783 | ||||||
| chr22:37404784
|
G | A | 169 | a0001c0001t0002g0111a0001c0001t0002g0123a0001c0001t0002g0130others(166): Show | 169 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.-463+12985C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37404784 | ||||||
| chr22:37405088
|
GCAT | G | 8 | a0001c0001t0009g0167a0001c0001t0009g0168a0001c0001t0009g0171others(5): Show | 8 | HG02109.hp2 HG02622.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-463+12678_-463+12 others(9): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37405088 | ||||||
| chr22:37405089
|
C | CT | 7 | a0001c0001t0002g0306a0001c0001t0017g0128a0001c0002t0004g0142others(4): Show | 7 | HG01109.hp2 HG02071.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.-463+12679_-463+12 others(7): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37405089 | ||||||
| chr22:37405089
|
C | CTT | 14 | a0001c0001t0005g0018a0001c0001t0005g0019a0001c0001t0005g0164others(11): Show | 14 | HG00639.hp2 HG01884.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.-463+12679_-463+12 others(8): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37405089 | ||||||
| chr22:37405089
|
C | CTTT | 4 | a0001c0001t0002g0240a0001c0001t0025g0239a0001c0003t0001g0268others(1): Show | 4 | HG01433.hp2 HG03490.hp2 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.-463+12679_-463+12 others(9): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37405089 | ||||||
| chr22:37405089
|
C | CTTTT | 79 | a0001c0001t0002g0111a0001c0001t0002g0123a0001c0001t0002g0130others(76): Show | 79 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.-463+12679_-463+12 others(10): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37405089 | ||||||
| chr22:37405089
|
C | CTTTTT | 8 | a0001c0001t0002g0250a0001c0001t0002g0252a0001c0001t0003g0269others(5): Show | 8 | HG00408.hp2 HG01106.hp2 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.-463+12679_-463+12 others(11): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37405089 | ||||||
| chr22:37405089
|
CA | C | 10 | a0001c0001t0005g0148a0001c0001t0005g0150a0001c0001t0005g0151others(7): Show | 10 | HG01109.hp1 HG02572.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.-463+12679delT | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37405089 | ||||||
| chr22:37405090
|
A | AT | 24 | a0001c0001t0002g0097a0001c0001t0003g0003a0001c0001t0003g0054others(21): Show | 25 | HG00099.hp2 HG00438.hp2 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.-463+12678dupA | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37405090 | ||||||
| chr22:37405090
|
A | T | 151 | a0001c0001t0002g0111a0001c0001t0002g0123a0001c0001t0002g0130others(148): Show | 151 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.-463+12679T>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37405090 | ||||||
| chr22:37405090
|
AT | A | 15 | a0001c0001t0002g0052a0001c0001t0003g0086a0001c0001t0009g0227others(12): Show | 15 | HG00423.hp2 HG01255.hp1 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-463+12678delA | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37405090 | ||||||
| chr22:37405118
|
G | A | 4 | a0001c0001t0005g0135a0001c0001t0005g0136a0001c0001t0017g0128others(1): Show | 4 | HG02647.hp2 HG02717.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-463+12651C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37405118 | ||||||
| chr22:37405129
|
C | G | 169 | a0001c0001t0002g0111a0001c0001t0002g0123a0001c0001t0002g0130others(166): Show | 169 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.-463+12640G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37405129 | ||||||
| chr22:37405201
|
T | C | 1 | a0001c0002t0069g0009 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-463+12568A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37405201 | ||||||
| chr22:37405362
|
G | A | 1 | a0002c0007t0086g0316 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-463+12407C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37405362 | ||||||
| chr22:37405510
|
A | T | 1 | a0002c0007t0072g0323 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-463+12259T>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37405510 | ||||||
| chr22:37405519
|
A | G | 3 | a0001c0002t0013g0076a0001c0002t0039g0006a0001c0002t0040g0007 | 3 | HG02071.hp2 NA18949.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.-463+12250T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37405519 | ||||||
| chr22:37405538
|
C | T | 11 | a0001c0001t0009g0167a0001c0001t0009g0168a0001c0001t0009g0171others(8): Show | 11 | HG02109.hp2 HG02572.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.-463+12231G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37405538 | ||||||
| chr22:37405637
|
G | T | 1 | a0001c0010t0016g0288 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-463+12132C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37405637 | ||||||
| chr22:37405721
|
G | C | 107 | a0001c0001t0002g0111a0001c0001t0002g0123a0001c0001t0002g0130others(104): Show | 107 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.-463+12048C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37405721 | ||||||
| chr22:37405781
|
A | T | 1 | a0001c0001t0003g0287 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-463+11988T>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37405781 | ||||||
| chr22:37405837
|
T | TG | 11 | a0001c0001t0003g0224a0001c0001t0005g0164a0001c0002t0008g0231others(8): Show | 11 | HG00733.hp1 HG01099.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-463+11931dupC | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37405837 | ||||||
| chr22:37405840
|
A | G | 60 | a0001c0001t0002g0298a0001c0001t0002g0300a0001c0001t0002g0306others(57): Show | 60 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.-463+11929T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37405840 | ||||||
| chr22:37405992
|
C | T | 2 | a0001c0002t0031g0174a0001c0002t0031g0175 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-463+11777G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37405992 | ||||||
| chr22:37406043
|
G | A | 86 | a0001c0001t0002g0123a0001c0001t0002g0130a0001c0001t0002g0240others(83): Show | 86 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.-463+11726C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37406043 | ||||||
| chr22:37406100
|
C | A | 1 | a0001c0002t0071g0069 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-463+11669G>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37406100 | ||||||
| chr22:37406182
|
G | C | 1 | a0001c0001t0003g0269 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-463+11587C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37406182 | ||||||
| chr22:37406208
|
G | A | 1 | a0001c0001t0025g0239 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-463+11561C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37406208 | ||||||
| chr22:37406307
|
G | A | 90 | a0001c0001t0002g0123a0001c0001t0002g0130a0001c0001t0002g0240others(87): Show | 90 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.-463+11462C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37406307 | ||||||
| chr22:37406326
|
C | T | 3 | a0001c0001t0003g0042a0001c0001t0003g0084a0001c0001t0003g0086 | 3 | HG01257.hp1 HG02735.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.-463+11443G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37406326 | ||||||
| chr22:37406354
|
G | A | 10 | a0001c0001t0005g0148a0001c0001t0005g0150a0001c0001t0005g0151others(7): Show | 10 | HG01109.hp1 HG02055.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.-463+11415C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37406354 | ||||||
| chr22:37406450
|
A | G | 4 | a0001c0008t0015g0160a0001c0008t0015g0161a0001c0008t0015g0170others(1): Show | 4 | HG02109.hp1 HG02615.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-463+11319T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37406450 | ||||||
| chr22:37406523
|
C | T | 1 | a0001c0002t0013g0075 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-463+11246G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37406523 | ||||||
| chr22:37406780
|
C | A | 2 | a0001c0001t0097g0324a0001c0002t0021g0147 | 2 | HG03540.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-463+10989G>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37406780 | ||||||
| chr22:37406856
|
C | T | 8 | a0001c0001t0005g0209a0001c0001t0009g0210a0001c0001t0017g0208others(5): Show | 8 | HG00639.hp2 HG01891.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-463+10913G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37406856 | ||||||
| chr22:37406908
|
G | A | 1 | a0001c0001t0097g0324 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-463+10861C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37406908 | ||||||
| chr22:37407081
|
T | C | 330 | a0001c0001t0002g0029a0001c0001t0002g0041a0001c0001t0002g0052others(327): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.-463+10688A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37407081 | ||||||
| chr22:37407122
|
C | T | 1 | a0001c0002t0008g0231 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-463+10647G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37407122 | ||||||
| chr22:37407123
|
T | G | 1 | a0001c0002t0008g0231 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-463+10646A>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37407123 | ||||||
| chr22:37407124
|
T | C | 1 | a0001c0002t0008g0231 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-463+10645A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37407124 | ||||||
| chr22:37407184
|
T | TC | 64 | a0001c0001t0002g0298a0001c0001t0002g0300a0001c0001t0002g0306others(61): Show | 64 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.-463+10584dupG | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37407184 | ||||||
| chr22:37407225
|
C | T | 1 | a0001c0003t0001g0138 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-463+10544G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37407225 | ||||||
| chr22:37407313
|
G | A | 1 | a0002c0007t0086g0316 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-463+10456C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37407313 | ||||||
| chr22:37407389
|
C | T | 1 | a0001c0002t0004g0027 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-463+10380G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37407389 | ||||||
| chr22:37407435
|
A | G | 67 | a0001c0001t0002g0298a0001c0001t0002g0300a0001c0001t0002g0306others(64): Show | 67 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.-463+10334T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37407435 | ||||||
| chr22:37407474
|
G | A | 1 | a0001c0001t0002g0281 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-463+10295C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37407474 | ||||||
| chr22:37407552
|
C | T | 1 | a0001c0002t0004g0139 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-463+10217G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37407552 | ||||||
| chr22:37407612
|
C | T | 1 | a0001c0002t0018g0176 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-463+10157G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37407612 | ||||||
| chr22:37407628
|
T | A | 1 | a0001c0002t0022g0317 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-463+10141A>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37407628 | ||||||
| chr22:37407649
|
A | G | 2 | a0001c0001t0005g0044a0001c0001t0005g0070 | 2 | HG01884.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-463+10120T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37407649 | ||||||
| chr22:37407680
|
G | A | 48 | a0001c0001t0002g0298a0001c0001t0002g0300a0001c0001t0002g0306others(45): Show | 48 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.-463+10089C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37407680 | ||||||
| chr22:37407733
|
TA | T | 11 | a0001c0001t0005g0148a0001c0001t0005g0150a0001c0001t0005g0151others(8): Show | 11 | HG01109.hp1 HG02055.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.-463+10035delT | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37407733 | ||||||
| chr22:37407820
|
G | A | 4 | a0001c0001t0025g0326a0001c0001t0063g0325a0001c0003t0001g0149others(1): Show | 4 | HG02280.hp1 HG02559.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.-463+9949C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37407820 | ||||||
| chr22:37407850
|
G | A | 11 | a0001c0001t0005g0148a0001c0001t0005g0150a0001c0001t0005g0151others(8): Show | 11 | HG01109.hp1 HG02055.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.-463+9919C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37407850 | ||||||
| chr22:37407850
|
G | T | 87 | a0001c0001t0002g0123a0001c0001t0002g0130a0001c0001t0002g0240others(84): Show | 87 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.-463+9919C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37407850 | ||||||
| chr22:37407851
|
C | T | 8 | a0001c0001t0005g0164a0001c0002t0004g0142a0001c0002t0008g0231others(5): Show | 8 | HG01109.hp2 HG02145.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-463+9918G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37407851 | ||||||
| chr22:37407910
|
G | A | 8 | a0001c0001t0005g0209a0001c0001t0009g0210a0001c0001t0017g0208others(5): Show | 8 | HG00639.hp2 HG01891.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-463+9859C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37407910 | ||||||
| chr22:37407997
|
C | G | 8 | a0001c0001t0005g0209a0001c0001t0009g0210a0001c0001t0017g0208others(5): Show | 8 | HG00639.hp2 HG01891.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-463+9772G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37407997 | ||||||
| chr22:37408007
|
T | C | 1 | a0001c0001t0005g0209 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-463+9762A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37408007 | ||||||
| chr22:37408034
|
T | C | 1 | a0001c0003t0094g0008 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-463+9735A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37408034 | ||||||
| chr22:37408136
|
G | A | 67 | a0001c0001t0002g0298a0001c0001t0002g0300a0001c0001t0002g0306others(64): Show | 67 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.-463+9633C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37408136 | ||||||
| chr22:37408158
|
A | G | 1 | a0001c0002t0004g0249 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-463+9611T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37408158 | ||||||
| chr22:37408229
|
G | A | 2 | a0001c0001t0003g0004a0001c0001t0003g0005 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-463+9540C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37408229 | ||||||
| chr22:37408283
|
C | T | 2 | a0001c0001t0097g0324a0001c0002t0021g0147 | 2 | HG03540.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-463+9486G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37408283 | ||||||
| chr22:37408303
|
G | A | 2 | a0001c0001t0003g0140a0001c0003t0001g0138 | 2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-463+9466C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37408303 | ||||||
| chr22:37408412
|
G | A | 1 | a0001c0001t0050g0145 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-463+9357C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37408412 | ||||||
| chr22:37408682
|
G | A | 6 | a0001c0001t0005g0018a0001c0001t0005g0019a0001c0001t0009g0017others(3): Show | 6 | HG01884.hp1 HG02622.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-463+9087C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37408682 | ||||||
| chr22:37408955
|
G | A | 1 | a0001c0001t0002g0119 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-463+8814C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37408955 | ||||||
| chr22:37409040
|
G | C | 10 | a0001c0001t0005g0164a0001c0002t0004g0142a0001c0002t0008g0231others(7): Show | 10 | HG01109.hp2 HG02145.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.-463+8729C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37409040 | ||||||
| chr22:37409163
|
C | T | 1 | a0001c0001t0027g0216 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-463+8606G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37409163 | ||||||
| chr22:37409223
|
C | A | 2 | a0001c0001t0009g0017a0001c0002t0022g0156 | 2 | HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-463+8546G>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37409223 | ||||||
| chr22:37409239
|
G | A | 6 | a0001c0001t0003g0042a0001c0001t0003g0084a0001c0001t0003g0086others(3): Show | 6 | HG00642.hp1 HG01257.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-463+8530C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37409239 | ||||||
| chr22:37409250
|
G | A | 1 | a0001c0003t0083g0219 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-463+8519C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37409250 | ||||||
| chr22:37409385
|
G | A | 2 | a0001c0001t0097g0324a0001c0002t0021g0147 | 2 | HG03540.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-463+8384C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37409385 | ||||||
| chr22:37409404
|
C | G | 1 | a0001c0001t0027g0216 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-463+8365G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37409404 | ||||||
| chr22:37409450
|
C | T | 3 | a0001c0002t0008g0228a0001c0003t0042g0229a0001c0003t0043g0230 | 3 | HG03471.hp1 NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-463+8319G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37409450 | ||||||
| chr22:37409487
|
G | A | 1 | a0001c0001t0027g0216 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-463+8282C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37409487 | ||||||
| chr22:37409551
|
C | T | 1 | a0001c0002t0007g0205 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-463+8218G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37409551 | ||||||
| chr22:37409677
|
A | G | 72 | a0001c0001t0002g0298a0001c0001t0002g0300a0001c0001t0002g0306others(69): Show | 72 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.-463+8092T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37409677 | ||||||
| chr22:37409705
|
C | T | 1 | a0001c0003t0001g0141 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-463+8064G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37409705 | ||||||
| chr22:37409725
|
T | G | 48 | a0001c0001t0002g0298a0001c0001t0002g0300a0001c0001t0002g0306others(45): Show | 48 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.-463+8044A>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37409725 | ||||||
| chr22:37409813
|
A | T | 1 | a0001c0001t0029g0114 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-463+7956T>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37409813 | ||||||
| chr22:37409835
|
G | A | 78 | a0001c0001t0002g0130a0001c0001t0002g0240a0001c0001t0002g0248others(75): Show | 78 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.-463+7934C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37409835 | ||||||
| chr22:37410136
|
C | T | 2 | a0001c0002t0037g0110a0001c0002t0037g0113 | 2 | HG01256.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.-463+7633G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37410136 | ||||||
| chr22:37410158
|
C | T | 2 | a0001c0001t0097g0324a0001c0002t0021g0147 | 2 | HG03540.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-463+7611G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37410158 | ||||||
| chr22:37410237
|
C | T | 28 | a0001c0001t0003g0003a0001c0001t0003g0180a0001c0001t0003g0185others(25): Show | 29 | HG00099.hp2 HG00423.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.-463+7532G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37410237 | ||||||
| chr22:37410245
|
C | T | 7 | a0001c0002t0004g0142a0001c0002t0008g0314a0001c0002t0021g0197others(4): Show | 7 | HG02145.hp2 HG02559.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-463+7524G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37410245 | ||||||
| chr22:37410308
|
G | A | 5 | a0001c0001t0005g0209a0001c0001t0009g0210a0001c0005t0011g0196others(2): Show | 5 | HG00639.hp2 HG01891.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-463+7461C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37410308 | ||||||
| chr22:37410365
|
T | C | 1 | a0001c0003t0001g0016 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-463+7404A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37410365 | ||||||
| chr22:37410372
|
G | A | 1 | a0001c0001t0003g0087 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-463+7397C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37410372 | ||||||
| chr22:37410422
|
G | A | 4 | a0001c0001t0005g0135a0001c0001t0005g0136a0001c0001t0017g0128others(1): Show | 4 | HG02647.hp2 HG02717.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-463+7347C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37410422 | ||||||
| chr22:37410448
|
G | T | 8 | a0001c0001t0005g0209a0001c0001t0009g0210a0001c0001t0017g0208others(5): Show | 8 | HG00639.hp2 HG01891.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-463+7321C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37410448 | ||||||
| chr22:37410473
|
G | A | 1 | a0001c0004t0010g0307 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-463+7296C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37410473 | ||||||
| chr22:37410560
|
A | C | 1 | a0001c0002t0004g0010 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-463+7209T>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37410560 | ||||||
| chr22:37410755
|
G | A | 6 | a0001c0001t0003g0224a0001c0002t0074g0223a0001c0003t0092g0322others(3): Show | 6 | HG02486.hp2 HG03098.hp1 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.-463+7014C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37410755 | ||||||
| chr22:37410831
|
A | G | 86 | a0001c0001t0002g0298a0001c0001t0002g0300a0001c0001t0002g0306others(83): Show | 86 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.-463+6938T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37410831 | ||||||
| chr22:37410880
|
A | G | 86 | a0001c0001t0002g0298a0001c0001t0002g0300a0001c0001t0002g0306others(83): Show | 86 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.-463+6889T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37410880 | ||||||
| chr22:37410923
|
G | A | 31 | a0001c0001t0002g0298a0001c0001t0002g0300a0001c0001t0002g0306others(28): Show | 31 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.-463+6846C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37410923 | ||||||
| chr22:37410970
|
C | T | 1 | a0002c0007t0072g0323 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-463+6799G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37410970 | ||||||
| chr22:37410974
|
A | G | 1 | a0001c0001t0061g0183 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-463+6795T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37410974 | ||||||
| chr22:37411004
|
G | A | 1 | a0001c0001t0002g0241 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-463+6765C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37411004 | ||||||
| chr22:37411062
|
G | A | 86 | a0001c0001t0002g0298a0001c0001t0002g0300a0001c0001t0002g0306others(83): Show | 86 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.-463+6707C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37411062 | ||||||
| chr22:37411070
|
A | G | 86 | a0001c0001t0002g0298a0001c0001t0002g0300a0001c0001t0002g0306others(83): Show | 86 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.-463+6699T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37411070 | ||||||
| chr22:37411079
|
A | G | 5 | a0001c0002t0018g0176a0001c0002t0021g0197a0001c0003t0001g0177others(2): Show | 5 | HG02145.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-463+6690T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37411079 | ||||||
| chr22:37411264
|
A | C | 90 | a0001c0001t0002g0298a0001c0001t0002g0300a0001c0001t0002g0306others(87): Show | 90 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.-463+6505T>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37411264 | ||||||
| chr22:37411343
|
C | CTT | 9 | a0001c0001t0002g0111a0001c0001t0019g0107a0001c0001t0019g0108others(6): Show | 9 | NA18939.hp1 NA18941.hp1 NA18943.hp1 others(6): Show |
intron_variant | MODIFIER | c.-463+6425_-463+642 others(6): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37411343 | ||||||
| chr22:37411344
|
A | T | 9 | a0001c0001t0002g0111a0001c0001t0019g0107a0001c0001t0019g0108others(6): Show | 9 | NA18939.hp1 NA18941.hp1 NA18943.hp1 others(6): Show |
intron_variant | MODIFIER | c.-463+6425T>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37411344 | ||||||
| chr22:37411405
|
TG | T | 211 | a0001c0001t0002g0123a0001c0001t0002g0130a0001c0001t0002g0240others(208): Show | 212 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.-463+6363delC | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37411405 | ||||||
| chr22:37411417
|
G | C | 5 | a0001c0002t0088g0289a0001c0003t0012g0294a0001c0010t0016g0288others(2): Show | 5 | HG01891.hp1 HG02145.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-463+6352C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37411417 | ||||||
| chr22:37411469
|
G | A | 2 | a0001c0002t0006g0270a0001c0002t0006g0271 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-463+6300C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37411469 | ||||||
| chr22:37411580
|
C | CG | 330 | a0001c0001t0002g0029a0001c0001t0002g0041a0001c0001t0002g0052others(327): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.-463+6188dupC | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37411580 | ||||||
| chr22:37411591
|
A | AG | 330 | a0001c0001t0002g0029a0001c0001t0002g0041a0001c0001t0002g0052others(327): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.-463+6177dupC | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37411591 | ||||||
| chr22:37411710
|
A | C | 5 | a0001c0001t0005g0018a0001c0001t0005g0019a0001c0001t0009g0017others(2): Show | 5 | HG01884.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-463+6059T>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37411710 | ||||||
| chr22:37412011
|
G | A | 11 | a0001c0001t0005g0209a0001c0001t0009g0210a0001c0001t0017g0208others(8): Show | 11 | HG00639.hp2 HG01891.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-463+5758C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37412011 | ||||||
| chr22:37412082
|
G | C | 84 | a0001c0001t0002g0298a0001c0001t0002g0300a0001c0001t0002g0306others(81): Show | 84 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.-463+5687C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37412082 | ||||||
| chr22:37412173
|
G | C | 78 | a0001c0001t0002g0298a0001c0001t0002g0300a0001c0001t0002g0306others(75): Show | 78 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.-463+5596C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37412173 | ||||||
| chr22:37412244
|
C | G | 1 | a0001c0003t0041g0163 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-463+5525G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37412244 | ||||||
| chr22:37412277
|
C | CA | 6 | a0001c0001t0005g0070a0001c0001t0009g0227a0001c0002t0004g0199others(3): Show | 7 | HG01884.hp2 HG02886.hp1 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.-463+5491dupT | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37412277 | ||||||
| chr22:37412277
|
C | CAAAAA | 20 | a0001c0001t0005g0150a0001c0001t0005g0225a0001c0001t0009g0210others(17): Show | 20 | HG00639.hp2 HG01891.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.-463+5487_-463+549 others(9): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37412277 | ||||||
| chr22:37412277
|
C | CAAAAAA | 21 | a0001c0001t0005g0018a0001c0001t0005g0148a0001c0001t0005g0151others(18): Show | 21 | HG01109.hp1 HG01109.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.-463+5486_-463+549 others(10): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37412277 | ||||||
| chr22:37412277
|
C | CAAAAAAA | 7 | a0001c0001t0005g0019a0001c0001t0005g0154a0001c0001t0009g0017others(4): Show | 7 | HG01884.hp1 HG02622.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-463+5485_-463+549 others(11): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37412277 | ||||||
| chr22:37412277
|
CA | C | 84 | a0001c0001t0002g0052a0001c0001t0002g0123a0001c0001t0002g0130others(81): Show | 84 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.-463+5491delT | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37412277 | ||||||
| chr22:37412292
|
A | AAAAAAG | 26 | a0001c0001t0002g0298a0001c0001t0002g0300a0001c0001t0005g0135others(23): Show | 26 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(23): Show |
intron_variant | MODIFIER | c.-463+5476_-463+547 others(10): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37412292 | ||||||
| chr22:37412292
|
A | G | 4 | a0001c0001t0019g0107a0001c0001t0019g0108a0001c0002t0004g0021others(1): Show | 4 | NA18941.hp1 NA18950.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.-463+5477T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37412292 | ||||||
| chr22:37412309
|
G | A | 84 | a0001c0001t0002g0298a0001c0001t0002g0300a0001c0001t0002g0306others(81): Show | 84 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.-463+5460C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37412309 | ||||||
| chr22:37412310
|
G | GA | 10 | a0001c0001t0002g0126a0001c0001t0003g0193a0001c0001t0003g0292others(7): Show | 10 | HG00735.hp1 HG00735.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.-463+5458dupT | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37412310 | ||||||
| chr22:37412375
|
C | T | 1 | a0001c0006t0048g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-463+5394G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37412375 | ||||||
| chr22:37412379
|
G | A | 1 | a0001c0001t0002g0241 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-463+5390C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37412379 | ||||||
| chr22:37412575
|
G | A | 2 | a0001c0002t0004g0297a0001c0002t0079g0237 | 2 | HG00597.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.-463+5194C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37412575 | ||||||
| chr22:37412719
|
C | T | 1 | a0001c0002t0004g0089 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-463+5050G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37412719 | ||||||
| chr22:37412845
|
A | G | 84 | a0001c0001t0002g0298a0001c0001t0002g0300a0001c0001t0002g0306others(81): Show | 84 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.-463+4924T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37412845 | ||||||
| chr22:37412872
|
T | C | 171 | a0001c0001t0002g0123a0001c0001t0002g0130a0001c0001t0002g0240others(168): Show | 171 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.-463+4897A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37412872 | ||||||
| chr22:37412928
|
C | T | 1 | a0001c0003t0094g0008 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-463+4841G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37412928 | ||||||
| chr22:37412952
|
T | C | 71 | a0001c0001t0002g0298a0001c0001t0002g0300a0001c0001t0002g0306others(68): Show | 71 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.-463+4817A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37412952 | ||||||
| chr22:37412966
|
G | C | 1 | a0001c0002t0004g0146 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-463+4803C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37412966 | ||||||
| chr22:37413102
|
G | A | 31 | a0001c0001t0002g0298a0001c0001t0002g0300a0001c0001t0002g0306others(28): Show | 31 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.-463+4667C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37413102 | ||||||
| chr22:37413199
|
G | A | 76 | a0001c0001t0002g0123a0001c0001t0002g0130a0001c0001t0002g0240others(73): Show | 76 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.-463+4570C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37413199 | ||||||
| chr22:37413396
|
G | A | 76 | a0001c0001t0002g0123a0001c0001t0002g0130a0001c0001t0002g0240others(73): Show | 76 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.-463+4373C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37413396 | ||||||
| chr22:37413403
|
CAA | C | 60 | a0001c0001t0002g0298a0001c0001t0002g0300a0001c0001t0002g0306others(57): Show | 60 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.-463+4364_-463+436 others(6): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37413403 | ||||||
| chr22:37413439
|
G | A | 81 | a0001c0001t0002g0123a0001c0001t0002g0130a0001c0001t0002g0240others(78): Show | 81 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.-463+4330C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37413439 | ||||||
| chr22:37413440
|
T | C | 1 | a0001c0006t0001g0277 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-463+4329A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37413440 | ||||||
| chr22:37413463
|
G | A | 21 | a0001c0001t0005g0209a0001c0001t0009g0167a0001c0001t0009g0168others(18): Show | 21 | HG00639.hp2 HG01891.hp2 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.-463+4306C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37413463 | ||||||
| chr22:37413563
|
C | A | 31 | a0001c0001t0002g0298a0001c0001t0002g0300a0001c0001t0002g0306others(28): Show | 31 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.-463+4206G>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37413563 | ||||||
| chr22:37413568
|
T | TA | 20 | a0001c0001t0003g0224a0001c0001t0003g0287a0001c0001t0005g0148others(17): Show | 20 | HG01109.hp1 HG02055.hp1 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.-463+4200dupT | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37413568 | ||||||
| chr22:37413568
|
TA | T | 23 | a0001c0001t0002g0284a0001c0001t0002g0298a0001c0001t0002g0300others(20): Show | 23 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.-463+4200delT | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37413568 | ||||||
| chr22:37413612
|
TG | T | 6 | a0001c0001t0005g0018a0001c0001t0005g0019a0001c0001t0009g0017others(3): Show | 6 | HG01884.hp1 HG02622.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-463+4156delC | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37413612 | ||||||
| chr22:37413616
|
G | A | 67 | a0001c0001t0002g0298a0001c0001t0002g0300a0001c0001t0002g0306others(64): Show | 67 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.-463+4153C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37413616 | ||||||
| chr22:37413732
|
G | A | 103 | a0001c0001t0002g0123a0001c0001t0002g0130a0001c0001t0002g0240others(100): Show | 103 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.-463+4037C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37413732 | ||||||
| chr22:37413783
|
T | G | 1 | a0001c0002t0021g0134 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-463+3986A>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37413783 | ||||||
| chr22:37413814
|
G | A | 1 | a0001c0001t0098g0330 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-463+3955C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37413814 | ||||||
| chr22:37413877
|
G | A | 1 | a0001c0001t0017g0128 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-463+3892C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37413877 | ||||||
| chr22:37413915
|
G | A | 1 | a0001c0004t0010g0307 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-463+3854C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37413915 | ||||||
| chr22:37413960
|
G | A | 8 | a0001c0001t0009g0167a0001c0001t0009g0168a0001c0001t0009g0171others(5): Show | 8 | HG02109.hp2 HG02622.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-463+3809C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37413960 | ||||||
| chr22:37414004
|
G | A | 6 | a0001c0001t0005g0018a0001c0001t0005g0019a0001c0001t0009g0017others(3): Show | 6 | HG01884.hp1 HG02622.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-463+3765C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37414004 | ||||||
| chr22:37414044
|
T | A | 9 | a0001c0001t0005g0164a0001c0002t0008g0231a0001c0002t0018g0176others(6): Show | 9 | HG01109.hp2 HG02145.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.-463+3725A>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37414044 | ||||||
| chr22:37414136
|
T | C | 59 | a0001c0001t0002g0298a0001c0001t0002g0300a0001c0001t0002g0306others(56): Show | 59 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.-463+3633A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37414136 | ||||||
| chr22:37414257
|
T | G | 13 | a0001c0001t0005g0209a0001c0001t0009g0210a0001c0001t0017g0208others(10): Show | 13 | HG00639.hp2 HG01891.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.-463+3512A>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37414257 | ||||||
| chr22:37414329
|
G | A | 6 | a0001c0001t0005g0018a0001c0001t0005g0019a0001c0001t0009g0017others(3): Show | 6 | HG01884.hp1 HG02622.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-463+3440C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37414329 | ||||||
| chr22:37414363
|
G | A | 2 | a0001c0002t0031g0174a0001c0002t0031g0175 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-463+3406C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37414363 | ||||||
| chr22:37414417
|
C | G | 59 | a0001c0001t0002g0298a0001c0001t0002g0300a0001c0001t0002g0306others(56): Show | 59 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.-463+3352G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37414417 | ||||||
| chr22:37414452
|
A | T | 59 | a0001c0001t0002g0298a0001c0001t0002g0300a0001c0001t0002g0306others(56): Show | 59 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.-463+3317T>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37414452 | ||||||
| chr22:37414575
|
C | A | 1 | a0001c0001t0005g0155 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-463+3194G>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37414575 | ||||||
| chr22:37414653
|
G | A | 68 | a0001c0001t0002g0298a0001c0001t0002g0300a0001c0001t0002g0306others(65): Show | 68 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.-463+3116C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37414653 | ||||||
| chr22:37414668
|
C | A | 71 | a0001c0001t0002g0130a0001c0001t0002g0240a0001c0001t0002g0248others(68): Show | 71 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.-463+3101G>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37414668 | ||||||
| chr22:37414713
|
T | C | 1 | a0001c0002t0004g0085 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-463+3056A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37414713 | ||||||
| chr22:37414738
|
A | G | 81 | a0001c0001t0002g0298a0001c0001t0002g0300a0001c0001t0002g0306others(78): Show | 81 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.-463+3031T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37414738 | ||||||
| chr22:37414807
|
C | G | 9 | a0001c0001t0005g0164a0001c0002t0008g0231a0001c0002t0018g0176others(6): Show | 9 | HG01109.hp2 HG02145.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.-463+2962G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37414807 | ||||||
| chr22:37414826
|
G | A | 13 | a0001c0001t0005g0209a0001c0001t0009g0210a0001c0001t0017g0208others(10): Show | 13 | HG00639.hp2 HG01891.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.-463+2943C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37414826 | ||||||
| chr22:37414990
|
G | C | 1 | a0001c0002t0021g0147 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-463+2779C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37414990 | ||||||
| chr22:37415185
|
GTCC | G | 67 | a0001c0001t0002g0298a0001c0001t0002g0300a0001c0001t0002g0306others(64): Show | 67 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.-463+2581_-463+258 others(7): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37415185 | ||||||
| chr22:37415200
|
T | G | 174 | a0001c0001t0002g0123a0001c0001t0002g0130a0001c0001t0002g0240others(171): Show | 174 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.-463+2569A>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37415200 | ||||||
| chr22:37415239
|
G | T | 2 | a0001c0002t0033g0023a0001c0003t0001g0024 | 2 | HG02015.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.-463+2530C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37415239 | ||||||
| chr22:37415395
|
G | A | 2 | a0001c0001t0097g0324a0001c0002t0021g0147 | 2 | HG03540.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-463+2374C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37415395 | ||||||
| chr22:37415595
|
C | G | 2 | a0001c0002t0033g0023a0001c0003t0001g0024 | 2 | HG02015.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.-463+2174G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37415595 | ||||||
| chr22:37415599
|
G | A | 3 | a0001c0003t0012g0308a0001c0003t0034g0278a0001c0003t0034g0279 | 3 | HG03490.hp2 HG03492.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.-463+2170C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37415599 | ||||||
| chr22:37415737
|
T | C | 35 | a0001c0001t0003g0224a0001c0001t0005g0018a0001c0001t0005g0019others(32): Show | 35 | HG01109.hp1 HG01109.hp2 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.-463+2032A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37415737 | ||||||
| chr22:37415790
|
A | G | 19 | a0001c0001t0003g0224a0001c0001t0005g0018a0001c0001t0005g0019others(16): Show | 19 | HG01109.hp2 HG01884.hp1 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.-463+1979T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37415790 | ||||||
| chr22:37415797
|
C | T | 5 | a0001c0002t0088g0289a0001c0003t0012g0294a0001c0010t0016g0288others(2): Show | 5 | HG01891.hp1 HG02145.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-463+1972G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37415797 | ||||||
| chr22:37415806
|
C | T | 10 | a0001c0001t0005g0018a0001c0001t0005g0019a0001c0001t0009g0017others(7): Show | 10 | HG01884.hp1 HG02622.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.-463+1963G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37415806 | ||||||
| chr22:37415833
|
G | A | 20 | a0001c0001t0003g0224a0001c0001t0005g0018a0001c0001t0005g0019others(17): Show | 20 | HG01109.hp2 HG01884.hp1 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.-463+1936C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37415833 | ||||||
| chr22:37415895
|
G | A | 1 | a0001c0002t0006g0280 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-463+1874C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37415895 | ||||||
| chr22:37415919
|
T | C | 1 | a0002c0007t0072g0323 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-463+1850A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37415919 | ||||||
| chr22:37415969
|
A | T | 21 | a0001c0001t0002g0097a0001c0001t0002g0102a0001c0001t0002g0105others(18): Show | 21 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(18): Show |
intron_variant | MODIFIER | c.-463+1800T>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37415969 | ||||||
| chr22:37415986
|
A | G | 22 | a0001c0001t0003g0224a0001c0001t0005g0018a0001c0001t0005g0019others(19): Show | 22 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.-463+1783T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37415986 | ||||||
| chr22:37416105
|
G | A | 10 | a0001c0001t0005g0018a0001c0001t0005g0019a0001c0001t0009g0017others(7): Show | 10 | HG01109.hp2 HG01884.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-463+1664C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37416105 | ||||||
| chr22:37416127
|
C | T | 1 | a0001c0001t0005g0044 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-463+1642G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37416127 | ||||||
| chr22:37416131
|
G | A | 104 | a0001c0001t0002g0123a0001c0001t0002g0130a0001c0001t0002g0240others(101): Show | 104 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.-463+1638C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37416131 | ||||||
| chr22:37416240
|
G | A | 1 | a0001c0001t0027g0216 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-463+1529C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37416240 | ||||||
| chr22:37416341
|
C | T | 41 | a0001c0001t0003g0003a0001c0001t0003g0180a0001c0001t0003g0185others(38): Show | 42 | HG00099.hp2 HG00423.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.-463+1428G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37416341 | ||||||
| chr22:37416359
|
T | C | 1 | a0001c0002t0018g0176 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-463+1410A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37416359 | ||||||
| chr22:37416456
|
C | T | 5 | a0001c0001t0003g0042a0001c0001t0003g0084a0001c0001t0003g0086others(2): Show | 5 | HG01257.hp1 HG02451.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.-463+1313G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37416456 | ||||||
| chr22:37416541
|
G | A | 3 | a0001c0002t0036g0321a0001c0002t0082g0320a0001c0003t0083g0219 | 3 | HG02717.hp2 HG03540.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-463+1228C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37416541 | ||||||
| chr22:37416646
|
C | T | 1 | a0001c0002t0069g0009 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-463+1123G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37416646 | ||||||
| chr22:37416710
|
C | G | 3 | a0001c0002t0021g0134a0001c0002t0068g0133a0001c0006t0048g0132 | 3 | HG02572.hp1 HG02965.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-463+1059G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37416710 | ||||||
| chr22:37416872
|
A | G | 158 | a0001c0001t0002g0029a0001c0001t0002g0041a0001c0001t0002g0052others(155): Show | 160 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.-463+897T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37416872 | ||||||
| chr22:37416916
|
T | C | 1 | a0001c0002t0069g0009 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-463+853A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37416916 | ||||||
| chr22:37416980
|
T | C | 261 | a0001c0001t0002g0029a0001c0001t0002g0041a0001c0001t0002g0052others(258): Show | 264 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(261): Show |
intron_variant | MODIFIER | c.-463+789A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37416980 | ||||||
| chr22:37417040
|
G | A | 1 | a0001c0001t0002g0281 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-463+729C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37417040 | ||||||
| chr22:37417049
|
C | T | 1 | a0002c0007t0086g0316 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-463+720G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37417049 | ||||||
| chr22:37417069
|
A | G | 1 | a0001c0003t0038g0074 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-463+700T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37417069 | ||||||
| chr22:37417122
|
GCCTCT | G | 4 | a0001c0001t0005g0225a0001c0002t0008g0228a0001c0003t0042g0229others(1): Show | 4 | HG03041.hp2 HG03471.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-463+642_-463+646d others(7): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37417122 | ||||||
| chr22:37417130
|
T | C | 1 | a0001c0003t0094g0008 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-463+639A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37417130 | ||||||
| chr22:37417392
|
A | T | 8 | a0001c0001t0009g0167a0001c0001t0009g0168a0001c0001t0009g0171others(5): Show | 8 | HG02109.hp2 HG02622.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-463+377T>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37417392 | ||||||
| chr22:37417448
|
G | T | 1 | a0001c0001t0005g0225 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-463+321C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37417448 | ||||||
| chr22:37417567
|
C | T | 2 | a0001c0002t0008g0314a0001c0002t0022g0315 | 2 | HG02559.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-463+202G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37417567 | ||||||
| chr22:37417650
|
A | C | 1 | a0001c0001t0002g0248 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-463+119T>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37417650 | ||||||
| chr22:37417754
|
G | A | 1 | a0001c0002t0006g0195 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-463+15C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37417754 | ||||||
| chr22:37418043
|
C | T | 1 | a0001c0003t0092g0322 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-613-124G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37418043 | ||||||
| chr22:37418119
|
G | C | 11 | a0001c0001t0023g0077a0001c0001t0023g0120a0001c0002t0013g0075others(8): Show | 11 | HG02056.hp1 HG02071.hp2 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.-613-200C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37418119 | ||||||
| chr22:37418316
|
T | C | 13 | a0001c0001t0005g0209a0001c0001t0009g0210a0001c0001t0017g0208others(10): Show | 13 | HG00639.hp2 HG01891.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.-613-397A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37418316 | ||||||
| chr22:37418521
|
C | T | 1 | a0001c0002t0036g0165 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-613-602G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37418521 | ||||||
| chr22:37418524
|
G | C | 12 | a0001c0001t0005g0209a0001c0001t0009g0210a0001c0001t0017g0208others(9): Show | 12 | HG00639.hp2 HG01891.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.-613-605C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37418524 | ||||||
| chr22:37418668
|
C | T | 1 | a0001c0003t0041g0163 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-613-749G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37418668 | ||||||
| chr22:37418884
|
A | G | 89 | a0001c0001t0002g0123a0001c0001t0002g0130a0001c0001t0002g0240others(86): Show | 89 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.-613-965T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37418884 | ||||||
| chr22:37418938
|
G | A | 4 | a0001c0002t0008g0081a0001c0002t0008g0093a0001c0003t0001g0082others(1): Show | 4 | NA18943.hp2 NA18969.hp2 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.-613-1019C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37418938 | ||||||
| chr22:37419000
|
A | G | 101 | a0001c0001t0002g0123a0001c0001t0002g0130a0001c0001t0002g0240others(98): Show | 101 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.-613-1081T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37419000 | ||||||
| chr22:37419069
|
G | C | 2 | a0001c0001t0097g0324a0001c0002t0021g0147 | 2 | HG03540.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-613-1150C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37419069 | ||||||
| chr22:37419078
|
A | G | 1 | a0001c0015t0080g0222 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-613-1159T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37419078 | ||||||
| chr22:37419334
|
AAC | A | 10 | a0001c0001t0005g0018a0001c0001t0005g0019a0001c0001t0009g0017others(7): Show | 10 | HG01109.hp2 HG01884.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-613-1417_-613-141 others(6): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37419334 | ||||||
| chr22:37419469
|
T | C | 1 | a0001c0003t0094g0008 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-613-1550A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37419469 | ||||||
| chr22:37419844
|
C | G | 2 | a0001c0001t0003g0004a0001c0001t0003g0005 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-613-1925G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37419844 | ||||||
| chr22:37419908
|
C | G | 261 | a0001c0001t0002g0029a0001c0001t0002g0041a0001c0001t0002g0052others(258): Show | 264 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(261): Show |
intron_variant | MODIFIER | c.-613-1989G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37419908 | ||||||
| chr22:37420056
|
C | A | 5 | a0001c0002t0088g0289a0001c0003t0012g0294a0001c0010t0016g0288others(2): Show | 5 | HG01891.hp1 HG02145.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-613-2137G>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37420056 | ||||||
| chr22:37420079
|
C | A | 1 | a0001c0001t0003g0292 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-613-2160G>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37420079 | ||||||
| chr22:37420163
|
G | C | 1 | a0001c0001t0003g0087 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-613-2244C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37420163 | ||||||
| chr22:37420343
|
C | G | 1 | a0001c0002t0007g0309 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-613-2424G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37420343 | ||||||
| chr22:37420435
|
G | A | 1 | a0001c0001t0002g0041 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-613-2516C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37420435 | ||||||
| chr22:37420661
|
G | C | 1 | a0001c0003t0001g0138 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-613-2742C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37420661 | ||||||
| chr22:37420708
|
AG | A | 91 | a0001c0001t0002g0130a0001c0001t0002g0240a0001c0001t0002g0248others(88): Show | 91 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.-613-2790delC | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37420708 | ||||||
| chr22:37420794
|
A | G | 12 | a0001c0001t0003g0224a0001c0001t0017g0319a0001c0001t0097g0324others(9): Show | 12 | HG01516.hp1 HG02486.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.-613-2875T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37420794 | ||||||
| chr22:37420824
|
T | A | 11 | a0001c0001t0003g0224a0001c0001t0017g0319a0001c0001t0097g0324others(8): Show | 11 | HG01516.hp1 HG02486.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.-613-2905A>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37420824 | ||||||
| chr22:37420899
|
G | A | 70 | a0001c0001t0002g0130a0001c0001t0002g0240a0001c0001t0002g0248others(67): Show | 70 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.-613-2980C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37420899 | ||||||
| chr22:37420938
|
T | C | 1 | a0001c0009t0055g0013 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-613-3019A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37420938 | ||||||
| chr22:37420959
|
A | G | 1 | a0001c0001t0003g0206 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-613-3040T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37420959 | ||||||
| chr22:37421008
|
G | C | 14 | a0001c0001t0002g0298a0001c0001t0002g0300a0001c0001t0002g0306others(11): Show | 14 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(11): Show |
intron_variant | MODIFIER | c.-613-3089C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37421008 | ||||||
| chr22:37421633
|
G | A | 14 | a0001c0001t0005g0018a0001c0001t0005g0019a0001c0001t0009g0017others(11): Show | 14 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.-613-3714C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37421633 | ||||||
| chr22:37421686
|
G | A | 1 | a0001c0001t0025g0239 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-613-3767C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37421686 | ||||||
| chr22:37421756
|
G | A | 2 | a0001c0001t0002g0122a0001c0003t0006g0121 | 2 | HG00741.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.-613-3837C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37421756 | ||||||
| chr22:37421782
|
C | T | 1 | a0001c0001t0002g0041 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-613-3863G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37421782 | ||||||
| chr22:37421823
|
G | A | 7 | a0001c0001t0005g0135a0001c0001t0005g0136a0001c0001t0005g0202others(4): Show | 7 | HG02055.hp2 HG02257.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-613-3904C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37421823 | ||||||
| chr22:37421848
|
C | A | 9 | a0001c0001t0005g0018a0001c0001t0005g0019a0001c0001t0009g0017others(6): Show | 9 | HG01109.hp2 HG01884.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-613-3929G>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37421848 | ||||||
| chr22:37421973
|
G | T | 11 | a0001c0001t0003g0224a0001c0001t0017g0319a0001c0001t0097g0324others(8): Show | 11 | HG01516.hp1 HG02486.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.-613-4054C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37421973 | ||||||
| chr22:37422067
|
A | G | 1 | a0001c0003t0001g0094 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-613-4148T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37422067 | ||||||
| chr22:37422073
|
C | T | 210 | a0001c0001t0002g0123a0001c0001t0002g0130a0001c0001t0002g0240others(207): Show | 211 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.-613-4154G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37422073 | ||||||
| chr22:37422201
|
G | C | 80 | a0001c0001t0002g0123a0001c0001t0002g0130a0001c0001t0002g0240others(77): Show | 80 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.-613-4282C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37422201 | ||||||
| chr22:37422292
|
G | T | 78 | a0001c0001t0002g0123a0001c0001t0002g0130a0001c0001t0002g0240others(75): Show | 78 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.-613-4373C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37422292 | ||||||
| chr22:37422340
|
T | C | 1 | a0001c0003t0001g0040 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-613-4421A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37422340 | ||||||
| chr22:37422379
|
C | T | 92 | a0001c0001t0002g0130a0001c0001t0002g0240a0001c0001t0002g0248others(89): Show | 92 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.-613-4460G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37422379 | ||||||
| chr22:37422380
|
GT | G | 23 | a0001c0001t0003g0224a0001c0001t0005g0018a0001c0001t0005g0019others(20): Show | 23 | HG01109.hp2 HG01516.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.-613-4462delA | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37422380 | ||||||
| chr22:37422435
|
A | G | 99 | a0001c0001t0002g0123a0001c0001t0002g0130a0001c0001t0002g0240others(96): Show | 99 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.-613-4516T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37422435 | ||||||
| chr22:37422469
|
G | A | 1 | a0001c0002t0004g0085 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-613-4550C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37422469 | ||||||
| chr22:37422596
|
T | C | 1 | a0001c0003t0041g0163 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-613-4677A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37422596 | ||||||
| chr22:37422887
|
G | A | 9 | a0001c0001t0017g0319a0001c0002t0008g0314a0001c0002t0022g0315others(6): Show | 9 | HG01516.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-614+4411C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37422887 | ||||||
| chr22:37422943
|
C | CG | 44 | a0001c0001t0002g0029a0001c0001t0003g0180a0001c0001t0003g0217others(41): Show | 44 | HG00423.hp2 HG00733.hp2 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.-614+4354dupC | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37422943 | ||||||
| chr22:37422943
|
CG | C | 19 | a0001c0001t0002g0284a0001c0001t0002g0285a0001c0001t0003g0086others(16): Show | 19 | HG01099.hp2 HG01257.hp1 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.-614+4354delC | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37422943 | ||||||
| chr22:37422943
|
CGGGG | C | 20 | a0001c0001t0005g0018a0001c0001t0005g0019a0001c0001t0005g0135others(17): Show | 20 | HG01516.hp1 HG01884.hp1 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.-614+4351_-614+435 others(8): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37422943 | ||||||
| chr22:37422945
|
G | C | 4 | a0001c0002t0088g0289a0001c0010t0016g0288a0001c0010t0016g0295others(1): Show | 4 | HG01891.hp1 HG02145.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.-614+4353C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37422945 | ||||||
| chr22:37422945
|
G | GC | 7 | a0001c0001t0053g0090a0001c0002t0004g0089a0001c0002t0004g0092others(4): Show | 7 | HG00735.hp1 HG02602.hp1 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.-614+4352_-614+435 others(5): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37422945 | ||||||
| chr22:37422946
|
G | C | 41 | a0001c0001t0002g0097a0001c0001t0002g0102a0001c0001t0002g0105others(38): Show | 41 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.-614+4352C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37422946 | ||||||
| chr22:37422947
|
G | C | 1 | a0001c0002t0021g0147 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-614+4351C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37422947 | ||||||
| chr22:37422948
|
G | C | 1 | a0001c0003t0001g0016 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-614+4350C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37422948 | ||||||
| chr22:37422948
|
G | T | 1 | a0001c0002t0004g0027 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-614+4350C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37422948 | ||||||
| chr22:37422949
|
G | T | 1 | a0001c0002t0069g0009 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-614+4349C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37422949 | ||||||
| chr22:37422950
|
G | A | 5 | a0001c0001t0017g0319a0001c0002t0036g0321a0001c0002t0082g0320others(2): Show | 5 | HG01516.hp1 HG03239.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-614+4348C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37422950 | ||||||
| chr22:37422953
|
G | C | 1 | a0001c0001t0050g0145 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-614+4345C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37422953 | ||||||
| chr22:37422955
|
G | C | 1 | a0001c0001t0002g0123 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-614+4343C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37422955 | ||||||
| chr22:37422983
|
G | A | 11 | a0001c0001t0005g0018a0001c0001t0005g0019a0001c0001t0005g0135others(8): Show | 11 | HG01884.hp1 HG02572.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.-614+4315C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37422983 | ||||||
| chr22:37423137
|
G | A | 3 | a0001c0001t0005g0202a0001c0001t0027g0204a0001c0006t0047g0203 | 3 | HG02055.hp2 HG02257.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-614+4161C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37423137 | ||||||
| chr22:37423308
|
G | A | 1 | a0001c0002t0077g0159 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-614+3990C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37423308 | ||||||
| chr22:37423376
|
A | C | 2 | a0001c0002t0008g0314a0001c0002t0022g0315 | 2 | HG02559.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-614+3922T>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37423376 | ||||||
| chr22:37423604
|
C | T | 1 | a0001c0003t0001g0026 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-614+3694G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37423604 | ||||||
| chr22:37423687
|
T | A | 3 | a0001c0001t0005g0202a0001c0001t0027g0204a0001c0006t0047g0203 | 3 | HG02055.hp2 HG02257.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-614+3611A>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37423687 | ||||||
| chr22:37423754
|
A | T | 1 | a0001c0001t0051g0025 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-614+3544T>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37423754 | ||||||
| chr22:37423795
|
G | C | 1 | a0001c0001t0005g0164 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-614+3503C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37423795 | ||||||
| chr22:37423911
|
G | C | 1 | a0001c0002t0004g0290 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-614+3387C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37423911 | ||||||
| chr22:37423947
|
G | T | 5 | a0001c0001t0003g0242a0001c0001t0003g0244a0001c0003t0012g0245others(2): Show | 5 | HG00140.hp1 HG00733.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.-614+3351C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37423947 | ||||||
| chr22:37424039
|
G | A | 22 | a0001c0001t0005g0148a0001c0001t0005g0150a0001c0001t0005g0151others(19): Show | 22 | HG01109.hp1 HG01516.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.-614+3259C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37424039 | ||||||
| chr22:37424377
|
T | C | 9 | a0001c0001t0017g0319a0001c0002t0008g0314a0001c0002t0022g0315others(6): Show | 9 | HG01516.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-614+2921A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37424377 | ||||||
| chr22:37424545
|
A | AC | 330 | a0001c0001t0002g0029a0001c0001t0002g0041a0001c0001t0002g0052others(327): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.-614+2752dupG | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37424545 | ||||||
| chr22:37424592
|
A | C | 2 | a0001c0001t0017g0128a0001c0019t0030g0127 | 2 | HG02717.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-614+2706T>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37424592 | ||||||
| chr22:37424630
|
G | A | 3 | a0001c0001t0002g0126a0001c0003t0001g0124a0001c0003t0001g0125 | 3 | HG00735.hp2 HG00741.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.-614+2668C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37424630 | ||||||
| chr22:37424680
|
CG | C | 81 | a0001c0001t0002g0130a0001c0001t0002g0248a0001c0001t0002g0250others(78): Show | 81 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.-614+2617delC | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37424680 | ||||||
| chr22:37424682
|
G | T | 24 | a0001c0001t0002g0298a0001c0001t0002g0300a0001c0001t0002g0306others(21): Show | 24 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.-614+2616C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37424682 | ||||||
| chr22:37424684
|
G | GC | 3 | a0001c0001t0005g0202a0001c0001t0027g0204a0001c0006t0047g0203 | 3 | HG02055.hp2 HG02257.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-614+2613_-614+261 others(5): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37424684 | ||||||
| chr22:37424684
|
G | T | 2 | a0001c0002t0033g0023a0001c0003t0001g0024 | 2 | HG02015.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.-614+2614C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37424684 | ||||||
| chr22:37424713
|
A | AGACAGC | 3 | a0001c0001t0005g0202a0001c0001t0027g0204a0001c0006t0047g0203 | 3 | HG02055.hp2 HG02257.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-614+2579_-614+258 others(10): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37424713 | ||||||
| chr22:37424776
|
C | T | 68 | a0001c0001t0002g0240a0001c0001t0002g0241a0001c0001t0002g0248others(65): Show | 68 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.-614+2522G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37424776 | ||||||
| chr22:37424814
|
G | A | 1 | a0001c0003t0012g0308 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-614+2484C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37424814 | ||||||
| chr22:37424947
|
G | A | 1 | a0001c0002t0007g0309 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-614+2351C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37424947 | ||||||
| chr22:37424947
|
G | GC | 9 | a0001c0001t0017g0319a0001c0002t0008g0314a0001c0002t0022g0315others(6): Show | 9 | HG01516.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-614+2350dupG | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37424947 | ||||||
| chr22:37424949
|
C | T | 1 | a0001c0001t0005g0148 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-614+2349G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37424949 | ||||||
| chr22:37425055
|
T | G | 1 | a0001c0002t0004g0199 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-614+2243A>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37425055 | ||||||
| chr22:37425245
|
A | C | 25 | a0001c0001t0005g0148a0001c0001t0005g0150a0001c0001t0005g0151others(22): Show | 25 | HG01109.hp1 HG02055.hp1 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.-614+2053T>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37425245 | ||||||
| chr22:37425402
|
G | A | 1 | a0001c0001t0097g0324 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-614+1896C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37425402 | ||||||
| chr22:37425587
|
GC | G | 68 | a0001c0001t0003g0003a0001c0001t0003g0178a0001c0001t0003g0180others(65): Show | 69 | HG00099.hp2 HG00423.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.-614+1710delG | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37425587 | ||||||
| chr22:37425777
|
A | G | 1 | a0001c0003t0001g0177 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-614+1521T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37425777 | ||||||
| chr22:37425783
|
A | G | 1 | a0001c0002t0069g0009 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-614+1515T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37425783 | ||||||
| chr22:37425830
|
C | T | 1 | a0001c0002t0021g0147 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-614+1468G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37425830 | ||||||
| chr22:37425870
|
T | TAC | 4 | a0001c0001t0003g0140a0001c0002t0004g0139a0001c0002t0006g0137others(1): Show | 4 | HG03490.hp1 HG03831.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.-614+1426_-614+142 others(6): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37425870 | ||||||
| chr22:37425870
|
T | TACAC | 14 | a0001c0001t0005g0164a0001c0001t0050g0145a0001c0001t0099g0331others(11): Show | 14 | HG00140.hp2 HG01257.hp2 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-614+1424_-614+142 others(8): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37425870 | ||||||
| chr22:37425870
|
T | TACACAC | 47 | a0001c0001t0003g0003a0001c0001t0003g0178a0001c0001t0003g0180others(44): Show | 48 | HG00099.hp2 HG00642.hp2 HG01168.hp1 others(45): Show |
intron_variant | MODIFIER | c.-614+1422_-614+142 others(10): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37425870 | ||||||
| chr22:37425870
|
T | TACACACA others(1): Show |
73 | a0001c0001t0002g0240a0001c0001t0002g0241a0001c0001t0002g0248others(70): Show | 73 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.-614+1420_-614+142 others(12): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37425870 | ||||||
| chr22:37425870
|
T | TACACACA others(3): Show |
28 | a0001c0001t0002g0298a0001c0001t0002g0300a0001c0001t0002g0306others(25): Show | 28 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.-614+1418_-614+142 others(14): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37425870 | ||||||
| chr22:37425870
|
T | TACACACA others(5): Show |
2 | a0001c0002t0066g0232a0001c0006t0056g0220 | 2 | HG01496.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.-614+1416_-614+142 others(16): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37425870 | ||||||
| chr22:37425870
|
T | TACACACA others(7): Show |
4 | a0001c0001t0009g0311a0001c0001t0028g0312a0001c0001t0064g0310others(1): Show | 4 | HG02258.hp2 HG02818.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-614+1414_-614+142 others(18): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37425870 | ||||||
| chr22:37425870
|
TAC | T | 9 | a0001c0001t0017g0319a0001c0002t0004g0021a0001c0002t0008g0314others(6): Show | 9 | HG01516.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-614+1426_-614+142 others(6): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37425870 | ||||||
| chr22:37425945
|
G | A | 1 | a0001c0003t0001g0141 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-614+1353C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37425945 | ||||||
| chr22:37425957
|
G | A | 1 | a0001c0001t0003g0221 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-614+1341C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37425957 | ||||||
| chr22:37426013
|
A | C | 179 | a0001c0001t0002g0240a0001c0001t0002g0241a0001c0001t0002g0248others(176): Show | 180 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.-614+1285T>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37426013 | ||||||
| chr22:37426103
|
G | T | 1 | a0001c0002t0079g0237 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-614+1195C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37426103 | ||||||
| chr22:37426178
|
C | T | 169 | a0001c0001t0002g0240a0001c0001t0002g0241a0001c0001t0002g0248others(166): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.-614+1120G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37426178 | ||||||
| chr22:37426281
|
C | T | 1 | a0001c0002t0004g0010 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-614+1017G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37426281 | ||||||
| chr22:37426288
|
C | T | 25 | a0001c0001t0005g0148a0001c0001t0005g0150a0001c0001t0005g0151others(22): Show | 25 | HG01109.hp1 HG02055.hp1 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.-614+1010G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37426288 | ||||||
| chr22:37426338
|
A | G | 141 | a0001c0001t0002g0029a0001c0001t0002g0041a0001c0001t0002g0052others(138): Show | 143 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.-614+960T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37426338 | ||||||
| chr22:37426340
|
GCA | G | 4 | a0001c0001t0005g0018a0001c0001t0005g0019a0001c0001t0009g0017others(1): Show | 4 | HG01884.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-614+956_-614+957d others(4): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37426340 | ||||||
| chr22:37426344
|
A | ACG | 9 | a0001c0002t0004g0010a0001c0002t0004g0014a0001c0002t0004g0146others(6): Show | 9 | HG00544.hp1 HG00621.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-614+952_-614+953d others(4): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37426344 | ||||||
| chr22:37426344
|
ACG | A | 12 | a0001c0001t0003g0224a0001c0001t0005g0225a0001c0001t0009g0227others(9): Show | 12 | HG01109.hp2 HG02486.hp2 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.-614+952_-614+953d others(4): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37426344 | ||||||
| chr22:37426356
|
G | GCA | 9 | a0001c0001t0017g0319a0001c0002t0008g0314a0001c0002t0022g0315others(6): Show | 9 | HG01516.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-614+940_-614+941d others(4): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37426356 | ||||||
| chr22:37426356
|
GCA | G | 77 | a0001c0001t0002g0240a0001c0001t0002g0241a0001c0001t0002g0248others(74): Show | 77 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.-614+940_-614+941d others(4): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37426356 | ||||||
| chr22:37426358
|
A | G | 3 | a0001c0002t0069g0009a0001c0002t0090g0235a0001c0004t0010g0236 | 3 | HG01099.hp1 HG01099.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.-614+940T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37426358 | ||||||
| chr22:37426451
|
A | G | 330 | a0001c0001t0002g0029a0001c0001t0002g0041a0001c0001t0002g0052others(327): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.-614+847T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37426451 | ||||||
| chr22:37426517
|
C | T | 1 | a0001c0003t0001g0234 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-614+781G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37426517 | ||||||
| chr22:37426615
|
A | G | 2 | a0001c0001t0050g0145a0001c0003t0094g0008 | 2 | HG02622.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.-614+683T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37426615 | ||||||
| chr22:37426632
|
C | T | 1 | a0001c0003t0001g0234 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-614+666G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37426632 | ||||||
| chr22:37426650
|
AACAC | A | 90 | a0001c0001t0002g0240a0001c0001t0002g0241a0001c0001t0002g0248others(87): Show | 90 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.-614+644_-614+647d others(6): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37426650 | ||||||
| chr22:37426800
|
A | G | 2 | a0001c0002t0039g0006a0001c0002t0040g0007 | 2 | NA18949.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.-614+498T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37426800 | ||||||
| chr22:37427023
|
T | C | 1 | a0002c0007t0072g0323 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-614+275A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37427023 | ||||||
| chr22:37427057
|
G | GCCTCCGC others(18): Show |
1 | a0001c0001t0097g0324 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-614+216_-614+240d others(27): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37427057 | ||||||
| chr22:37427068
|
C | A | 1 | a0001c0003t0044g0329 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-614+230G>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37427068 | ||||||
| chr22:37427122
|
G | A | 5 | a0001c0001t0025g0326a0001c0001t0063g0325a0001c0002t0004g0328others(2): Show | 5 | HG02109.hp2 HG02280.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.-614+176C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37427122 | ||||||
| chr22:37427169
|
C | T | 3 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0002t0018g0001 | 4 | HG01167.hp2 HG01169.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.-614+129G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37427169 | ||||||
| chr22:37427253
|
CCGGT | C | 186 | a0001c0001t0002g0240a0001c0001t0002g0241a0001c0001t0002g0248others(183): Show | 187 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.-614+41_-614+44del others(4): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37427253 |