Search by Gene
| geneid | 60529 |
|---|---|
| ensemblid | ENSG00000052850.8 |
| hgncid | 450 |
| symbol | ALX4 |
| name | ALX homeobox 4 |
| refseq_nuc | NM_021926.4 |
| refseq_prot | NP_068745.2 |
| ensembl_nuc | ENST00000652299.1 |
| ensembl_prot | ENSP00000498217.1 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 44260440 |
| end | 44310139 |
| strand | - |
| ver | v1.2 |
| region | chr11:44260440-44310139 |
| region5000 | chr11:44255440-44315139 |
| regionname0 | ALX4_chr11_44260440_44310139 |
| regionname5000 | ALX4_chr11_44255440_44315139 |
Multiple Alignments (by translate haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
Multiple Alignments (by aa haplotype frequency)
| 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 | regionname | genename | aa |
|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 411 | 216 | 55 | 41 | 92 | 14 | 12 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0002 | 0/0 | 411 | 126 | 1 | 20 | 79 | 4 | 22 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0003 | 0/0 | 411 | 33 | 26 | 4 | 0 | 0 | 3 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0004 | 0/0 | 407 | 10 | 9 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0005 | 0/0 | 411 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0006 | 0/0 | 407 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0007 | 0/0 | 411 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 1236 | 87 | 6 | 19 | 57 | 2 | 3 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| c0002 | 0/1 | 1236 | 78 | 35 | 12 | 18 | 8 | 4 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| c0003 | 0/0 | 1236 | 68 | 1 | 12 | 43 | 1 | 11 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| c0004 | 0/0 | 1236 | 45 | 0 | 7 | 28 | 2 | 8 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| c0005 | 0/0 | 1236 | 23 | 1 | 2 | 17 | 0 | 3 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| c0006 | 0/0 | 1236 | 17 | 16 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| c0007 | 0/0 | 1236 | 14 | 6 | 4 | 0 | 3 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| c0008 | 0/0 | 1236 | 13 | 0 | 1 | 8 | 1 | 3 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| c0009 | 0/0 | 1224 | 8 | 7 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| c0010 | 0/0 | 1236 | 6 | 4 | 2 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| c0011 | 0/0 | 1236 | 3 | 1 | 2 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| c0012 | 0/0 | 1236 | 3 | 0 | 1 | 0 | 1 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| c0013 | 0/0 | 1236 | 2 | 0 | 1 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| c0014 | 0/0 | 1236 | 2 | 2 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| c0015 | 0/0 | 1236 | 2 | 2 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| c0016 | 1/0 | 1236 | 2 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| c0017 | 0/0 | 1236 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| c0018 | 0/0 | 1236 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| c0019 | 0/0 | 1236 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| c0020 | 0/0 | 1236 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| c0021 | 0/0 | 1236 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| c0022 | 0/0 | 1224 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| c0023 | 0/0 | 1224 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| c0024 | 0/0 | 1224 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| c0025 | 0/0 | 1236 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| c0026 | 0/0 | 1236 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| c0027 | 0/0 | 1236 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| c0028 | 0/0 | 1236 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| c0029 | 0/0 | 1236 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| c0030 | 0/0 | 1236 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| c0031 | 0/0 | 1236 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| thapid | 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
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq |
|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 4492 | 100 | 2 | 17 | 63 | 3 | 15 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0002 | 0/0 | 4492 | 38 | 10 | 6 | 19 | 0 | 3 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0003 | 0/0 | 4492 | 34 | 9 | 9 | 7 | 7 | 2 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0004 | 0/0 | 4492 | 30 | 6 | 8 | 15 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0005 | 0/0 | 4492 | 28 | 0 | 0 | 26 | 0 | 2 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0006 | 0/1 | 4492 | 22 | 0 | 3 | 12 | 2 | 4 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0007 | 0/0 | 4492 | 12 | 8 | 1 | 0 | 3 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0008 | 0/0 | 4492 | 11 | 0 | 1 | 10 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0009 | 0/0 | 4492 | 9 | 8 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0010 | 0/0 | 4492 | 8 | 0 | 6 | 2 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0011 | 0/0 | 4488 | 7 | 7 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0012 | 0/0 | 4492 | 5 | 0 | 3 | 2 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0013 | 0/0 | 4492 | 4 | 3 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0014 | 0/0 | 4489 | 4 | 0 | 3 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0015 | 0/0 | 4492 | 3 | 3 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0016 | 0/0 | 4492 | 3 | 3 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0017 | 0/0 | 4492 | 3 | 0 | 2 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0018 | 0/0 | 4492 | 3 | 0 | 0 | 3 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0019 | 0/0 | 4489 | 3 | 1 | 0 | 0 | 1 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0020 | 0/0 | 4492 | 3 | 2 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0021 | 1/0 | 4492 | 2 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0022 | 0/0 | 4492 | 2 | 0 | 0 | 2 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0023 | 0/0 | 4492 | 2 | 2 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0024 | 0/0 | 4492 | 2 | 2 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0025 | 0/0 | 4492 | 2 | 1 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0026 | 0/0 | 4492 | 2 | 2 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0027 | 0/0 | 4489 | 2 | 2 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0028 | 0/0 | 4489 | 2 | 2 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0029 | 0/0 | 4489 | 2 | 2 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0030 | 0/0 | 4489 | 2 | 1 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0031 | 0/0 | 4492 | 2 | 0 | 2 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0032 | 0/0 | 4492 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0033 | 0/0 | 4488 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0034 | 0/0 | 4492 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0035 | 0/0 | 4492 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0036 | 0/0 | 4492 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0037 | 0/0 | 4492 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0038 | 0/0 | 4492 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0039 | 0/0 | 4492 | 1 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0040 | 0/0 | 4492 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0041 | 0/0 | 4492 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0042 | 0/0 | 4492 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0043 | 0/0 | 4492 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0044 | 0/0 | 4492 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0045 | 0/0 | 4492 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0046 | 0/0 | 4492 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0047 | 0/0 | 4492 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0048 | 0/0 | 4492 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0049 | 0/0 | 4492 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0050 | 0/0 | 4492 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0051 | 0/0 | 4492 | 1 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0052 | 0/0 | 4489 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0053 | 0/0 | 4489 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0054 | 0/0 | 4492 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0055 | 0/0 | 4492 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0056 | 0/0 | 4492 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0057 | 0/0 | 4492 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0058 | 0/0 | 4492 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0059 | 0/0 | 4492 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0060 | 0/0 | 4492 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0061 | 0/0 | 4492 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0062 | 0/0 | 4492 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0063 | 0/0 | 4492 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0064 | 0/0 | 4492 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0065 | 0/0 | 4489 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0066 | 0/0 | 4492 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| t0067 | 0/0 | 4488 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| 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 |
|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0004 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0183 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0323 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0356 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0376 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| achapid | ahapid | 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 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | acseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | a0001 | c0001 | 0/0 | 87 | 6 | 19 | 57 | 2 | 3 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0002 | a0001 | c0002 | 0/1 | 78 | 35 | 12 | 18 | 8 | 4 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0005 | a0001 | c0005 | 0/0 | 23 | 1 | 2 | 17 | 0 | 3 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0007 | a0001 | c0007 | 0/0 | 14 | 6 | 4 | 0 | 3 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0011 | a0001 | c0011 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0012 | a0001 | c0012 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0016 | a0001 | c0016 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0026 | a0001 | c0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0027 | a0001 | c0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0028 | a0001 | c0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0029 | a0001 | c0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0030 | a0001 | c0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0031 | a0001 | c0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0002c0003 | a0002 | c0003 | 0/0 | 68 | 1 | 12 | 43 | 1 | 11 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0002c0004 | a0002 | c0004 | 0/0 | 45 | 0 | 7 | 28 | 2 | 8 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0002c0008 | a0002 | c0008 | 0/0 | 13 | 0 | 1 | 8 | 1 | 3 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0003c0006 | a0003 | c0006 | 0/0 | 17 | 16 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0003c0010 | a0003 | c0010 | 0/0 | 6 | 4 | 2 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0003c0013 | a0003 | c0013 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0003c0014 | a0003 | c0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0003c0015 | a0003 | c0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0003c0017 | a0003 | c0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0003c0019 | a0003 | c0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0003c0020 | a0003 | c0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0003c0021 | a0003 | c0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0004c0009 | a0004 | c0009 | 0/0 | 8 | 7 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0004c0023 | a0004 | c0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0004c0024 | a0004 | c0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0005c0025 | a0005 | c0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0006c0022 | a0006 | c0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0007c0018 | a0007 | c0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| acthapid | ahapid | chapid | thapid | 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 | actseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | a0001 | c0001 | t0001 | 0/0 | 46 | 0 | 10 | 31 | 2 | 3 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0001t0002 | a0001 | c0001 | t0002 | 0/0 | 23 | 5 | 5 | 13 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0001t0004 | a0001 | c0001 | t0004 | 0/0 | 10 | 0 | 1 | 9 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0001t0005 | a0001 | c0001 | t0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0001t0006 | a0001 | c0001 | t0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0001t0010 | a0001 | c0001 | t0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0001t0017 | a0001 | c0001 | t0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0001t0018 | a0001 | c0001 | t0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0001t0043 | a0001 | c0001 | t0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0002t0001 | a0001 | c0002 | t0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0002t0002 | a0001 | c0002 | t0002 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0002t0003 | a0001 | c0002 | t0003 | 0/0 | 19 | 2 | 7 | 3 | 6 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0002t0004 | a0001 | c0002 | t0004 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0002t0005 | a0001 | c0002 | t0005 | 0/0 | 8 | 0 | 0 | 6 | 0 | 2 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0002t0006 | a0001 | c0002 | t0006 | 0/1 | 2 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0002t0007 | a0001 | c0002 | t0007 | 0/0 | 7 | 6 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0002t0008 | a0001 | c0002 | t0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0002t0009 | a0001 | c0002 | t0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0002t0011 | a0001 | c0002 | t0011 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0002t0013 | a0001 | c0002 | t0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0002t0015 | a0001 | c0002 | t0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0002t0016 | a0001 | c0002 | t0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0002t0019 | a0001 | c0002 | t0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0002t0020 | a0001 | c0002 | t0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0002t0021 | a0001 | c0002 | t0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0002t0023 | a0001 | c0002 | t0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0002t0025 | a0001 | c0002 | t0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0002t0027 | a0001 | c0002 | t0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0002t0028 | a0001 | c0002 | t0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0002t0030 | a0001 | c0002 | t0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0002t0031 | a0001 | c0002 | t0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0002t0033 | a0001 | c0002 | t0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0002t0036 | a0001 | c0002 | t0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0002t0038 | a0001 | c0002 | t0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0002t0040 | a0001 | c0002 | t0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0002t0052 | a0001 | c0002 | t0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0002t0055 | a0001 | c0002 | t0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0002t0056 | a0001 | c0002 | t0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0002t0057 | a0001 | c0002 | t0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0002t0067 | a0001 | c0002 | t0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0005t0004 | a0001 | c0005 | t0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0005t0005 | a0001 | c0005 | t0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0005t0006 | a0001 | c0005 | t0006 | 0/0 | 11 | 0 | 2 | 8 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0005t0008 | a0001 | c0005 | t0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0005t0058 | a0001 | c0005 | t0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0005t0060 | a0001 | c0005 | t0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0005t0061 | a0001 | c0005 | t0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0005t0064 | a0001 | c0005 | t0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0005t0066 | a0001 | c0005 | t0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0007t0003 | a0001 | c0007 | t0003 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0007t0004 | a0001 | c0007 | t0004 | 0/0 | 7 | 4 | 3 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0007t0007 | a0001 | c0007 | t0007 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0007t0008 | a0001 | c0007 | t0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0007t0016 | a0001 | c0007 | t0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0007t0053 | a0001 | c0007 | t0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0011t0003 | a0001 | c0011 | t0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0011t0020 | a0001 | c0011 | t0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0011t0031 | a0001 | c0011 | t0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0012t0006 | a0001 | c0012 | t0006 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0012t0062 | a0001 | c0012 | t0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0016t0003 | a0001 | c0016 | t0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0016t0021 | a0001 | c0016 | t0021 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0026t0023 | a0001 | c0026 | t0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0027t0050 | a0001 | c0027 | t0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0028t0002 | a0001 | c0028 | t0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0029t0001 | a0001 | c0029 | t0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0030t0026 | a0001 | c0030 | t0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0001c0031t0002 | a0001 | c0031 | t0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0002c0003t0001 | a0002 | c0003 | t0001 | 0/0 | 41 | 0 | 5 | 27 | 1 | 8 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0002c0003t0002 | a0002 | c0003 | t0002 | 0/0 | 5 | 1 | 1 | 3 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0002c0003t0004 | a0002 | c0003 | t0004 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0002c0003t0005 | a0002 | c0003 | t0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0002c0003t0006 | a0002 | c0003 | t0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0002c0003t0010 | a0002 | c0003 | t0010 | 0/0 | 7 | 0 | 5 | 2 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0002c0003t0017 | a0002 | c0003 | t0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0002c0003t0018 | a0002 | c0003 | t0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0002c0003t0041 | a0002 | c0003 | t0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0002c0003t0045 | a0002 | c0003 | t0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0002c0003t0047 | a0002 | c0003 | t0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0002c0003t0049 | a0002 | c0003 | t0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0002c0003t0054 | a0002 | c0003 | t0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0002c0004t0001 | a0002 | c0004 | t0001 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0002c0004t0002 | a0002 | c0004 | t0002 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0002c0004t0003 | a0002 | c0004 | t0003 | 0/0 | 6 | 0 | 1 | 4 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0002c0004t0004 | a0002 | c0004 | t0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0002c0004t0005 | a0002 | c0004 | t0005 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0002c0004t0006 | a0002 | c0004 | t0006 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0002c0004t0007 | a0002 | c0004 | t0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0002c0004t0008 | a0002 | c0004 | t0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0002c0004t0012 | a0002 | c0004 | t0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0002c0004t0014 | a0002 | c0004 | t0014 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0002c0004t0019 | a0002 | c0004 | t0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0002c0004t0020 | a0002 | c0004 | t0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0002c0004t0022 | a0002 | c0004 | t0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0002c0004t0034 | a0002 | c0004 | t0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0002c0004t0035 | a0002 | c0004 | t0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0002c0004t0037 | a0002 | c0004 | t0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0002c0004t0039 | a0002 | c0004 | t0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0002c0004t0046 | a0002 | c0004 | t0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0002c0008t0004 | a0002 | c0008 | t0004 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0002c0008t0005 | a0002 | c0008 | t0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0002c0008t0006 | a0002 | c0008 | t0006 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0002c0008t0012 | a0002 | c0008 | t0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0002c0008t0051 | a0002 | c0008 | t0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0002c0008t0063 | a0002 | c0008 | t0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0003c0006t0003 | a0003 | c0006 | t0003 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0003c0006t0004 | a0003 | c0006 | t0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0003c0006t0007 | a0003 | c0006 | t0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0003c0006t0009 | a0003 | c0006 | t0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0003c0006t0011 | a0003 | c0006 | t0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0003c0006t0013 | a0003 | c0006 | t0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0003c0006t0015 | a0003 | c0006 | t0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0003c0006t0019 | a0003 | c0006 | t0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0003c0006t0024 | a0003 | c0006 | t0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0003c0006t0032 | a0003 | c0006 | t0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0003c0006t0065 | a0003 | c0006 | t0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0003c0010t0001 | a0003 | c0010 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0003c0010t0002 | a0003 | c0010 | t0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0003c0010t0012 | a0003 | c0010 | t0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0003c0010t0042 | a0003 | c0010 | t0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0003c0010t0048 | a0003 | c0010 | t0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0003c0013t0001 | a0003 | c0013 | t0001 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0003c0014t0003 | a0003 | c0014 | t0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0003c0014t0030 | a0003 | c0014 | t0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0003c0015t0029 | a0003 | c0015 | t0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0003c0017t0002 | a0003 | c0017 | t0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0003c0019t0059 | a0003 | c0019 | t0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0003c0020t0026 | a0003 | c0020 | t0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0003c0021t0027 | a0003 | c0021 | t0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0004c0009t0007 | a0004 | c0009 | t0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0004c0009t0009 | a0004 | c0009 | t0009 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0004c0009t0011 | a0004 | c0009 | t0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0004c0009t0013 | a0004 | c0009 | t0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0004c0009t0016 | a0004 | c0009 | t0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0004c0023t0044 | a0004 | c0023 | t0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0004c0024t0001 | a0004 | c0024 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0005c0025t0008 | a0005 | c0025 | t0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0006c0022t0009 | a0006 | c0022 | t0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| a0007c0018t0001 | a0007 | c0018 | t0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | copy fasta |
| actghapid | ahapid | chapid | thapid | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | a0001 | c0001 | t0001 | g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0001g0003 | a0001 | c0001 | t0001 | g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0001g0180 | a0001 | c0001 | t0001 | g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0001g0195 | a0001 | c0001 | t0001 | g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0001g0199 | a0001 | c0001 | t0001 | g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0001g0201 | a0001 | c0001 | t0001 | g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0001g0203 | a0001 | c0001 | t0001 | g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0001g0211 | a0001 | c0001 | t0001 | g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0001g0213 | a0001 | c0001 | t0001 | g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0001g0219 | a0001 | c0001 | t0001 | g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0001g0227 | a0001 | c0001 | t0001 | g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0001g0248 | a0001 | c0001 | t0001 | g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0001g0250 | a0001 | c0001 | t0001 | g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0001g0252 | a0001 | c0001 | t0001 | g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0001g0257 | a0001 | c0001 | t0001 | g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0001g0269 | a0001 | c0001 | t0001 | g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0001g0270 | a0001 | c0001 | t0001 | g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0001g0271 | a0001 | c0001 | t0001 | g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0001g0272 | a0001 | c0001 | t0001 | g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0001g0273 | a0001 | c0001 | t0001 | g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0001g0274 | a0001 | c0001 | t0001 | g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0001g0276 | a0001 | c0001 | t0001 | g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0001g0284 | a0001 | c0001 | t0001 | g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0001g0286 | a0001 | c0001 | t0001 | g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0001g0303 | a0001 | c0001 | t0001 | g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0001g0310 | a0001 | c0001 | t0001 | g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0001g0313 | a0001 | c0001 | t0001 | g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0001g0315 | a0001 | c0001 | t0001 | g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0001g0316 | a0001 | c0001 | t0001 | g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0001g0317 | a0001 | c0001 | t0001 | g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0001g0322 | a0001 | c0001 | t0001 | g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0001g0324 | a0001 | c0001 | t0001 | g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0001g0333 | a0001 | c0001 | t0001 | g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0001g0340 | a0001 | c0001 | t0001 | g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0001g0343 | a0001 | c0001 | t0001 | g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0001g0345 | a0001 | c0001 | t0001 | g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0001g0347 | a0001 | c0001 | t0001 | g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0001g0355 | a0001 | c0001 | t0001 | g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0001g0364 | a0001 | c0001 | t0001 | g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0001g0365 | a0001 | c0001 | t0001 | g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0001g0369 | a0001 | c0001 | t0001 | g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0001g0373 | a0001 | c0001 | t0001 | g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0001g0374 | a0001 | c0001 | t0001 | g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0001g0378 | a0001 | c0001 | t0001 | g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0002g0187 | a0001 | c0001 | t0002 | g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0002g0188 | a0001 | c0001 | t0002 | g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0002g0190 | a0001 | c0001 | t0002 | g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0002g0197 | a0001 | c0001 | t0002 | g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0002g0231 | a0001 | c0001 | t0002 | g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0002g0233 | a0001 | c0001 | t0002 | g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0002g0235 | a0001 | c0001 | t0002 | g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0002g0236 | a0001 | c0001 | t0002 | g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0002g0240 | a0001 | c0001 | t0002 | g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0002g0256 | a0001 | c0001 | t0002 | g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0002g0259 | a0001 | c0001 | t0002 | g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0002g0266 | a0001 | c0001 | t0002 | g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0002g0278 | a0001 | c0001 | t0002 | g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0002g0279 | a0001 | c0001 | t0002 | g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0002g0291 | a0001 | c0001 | t0002 | g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0002g0292 | a0001 | c0001 | t0002 | g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0002g0318 | a0001 | c0001 | t0002 | g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0002g0319 | a0001 | c0001 | t0002 | g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0002g0338 | a0001 | c0001 | t0002 | g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0002g0342 | a0001 | c0001 | t0002 | g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0002g0352 | a0001 | c0001 | t0002 | g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0002g0353 | a0001 | c0001 | t0002 | g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0002g0380 | a0001 | c0001 | t0002 | g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0004g0194 | a0001 | c0001 | t0004 | g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0004g0214 | a0001 | c0001 | t0004 | g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0004g0222 | a0001 | c0001 | t0004 | g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0004g0239 | a0001 | c0001 | t0004 | g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0004g0288 | a0001 | c0001 | t0004 | g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0004g0311 | a0001 | c0001 | t0004 | g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0004g0329 | a0001 | c0001 | t0004 | g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0004g0330 | a0001 | c0001 | t0004 | g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0004g0332 | a0001 | c0001 | t0004 | g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0004g0336 | a0001 | c0001 | t0004 | g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0005g0325 | a0001 | c0001 | t0005 | g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0005g0326 | a0001 | c0001 | t0005 | g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0006g0196 | a0001 | c0001 | t0006 | g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0010g0230 | a0001 | c0001 | t0010 | g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0017g0357 | a0001 | c0001 | t0017 | g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0017g0359 | a0001 | c0001 | t0017 | g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0018g0335 | a0001 | c0001 | t0018 | g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0001t0043g0297 | a0001 | c0001 | t0043 | g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0001g0275 | a0001 | c0002 | t0001 | g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0001g0277 | a0001 | c0002 | t0001 | g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0001g0287 | a0001 | c0002 | t0001 | g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0001g0379 | a0001 | c0002 | t0001 | g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0002g0200 | a0001 | c0002 | t0002 | g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0002g0241 | a0001 | c0002 | t0002 | g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0003g0184 | a0001 | c0002 | t0003 | g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0003g0185 | a0001 | c0002 | t0003 | g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0003g0186 | a0001 | c0002 | t0003 | g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0003g0207 | a0001 | c0002 | t0003 | g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0003g0225 | a0001 | c0002 | t0003 | g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0003g0228 | a0001 | c0002 | t0003 | g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0003g0254 | a0001 | c0002 | t0003 | g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0003g0261 | a0001 | c0002 | t0003 | g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0003g0262 | a0001 | c0002 | t0003 | g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0003g0267 | a0001 | c0002 | t0003 | g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0003g0314 | a0001 | c0002 | t0003 | g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0003g0344 | a0001 | c0002 | t0003 | g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0003g0349 | a0001 | c0002 | t0003 | g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0003g0350 | a0001 | c0002 | t0003 | g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0003g0351 | a0001 | c0002 | t0003 | g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0003g0360 | a0001 | c0002 | t0003 | g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0003g0368 | a0001 | c0002 | t0003 | g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0003g0375 | a0001 | c0002 | t0003 | g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0003g0376 | a0001 | c0002 | t0003 | g0376 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0004g0210 | a0001 | c0002 | t0004 | g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0004g0307 | a0001 | c0002 | t0004 | g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0004g0308 | a0001 | c0002 | t0004 | g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0005g0220 | a0001 | c0002 | t0005 | g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0005g0223 | a0001 | c0002 | t0005 | g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0005g0237 | a0001 | c0002 | t0005 | g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0005g0238 | a0001 | c0002 | t0005 | g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0005g0283 | a0001 | c0002 | t0005 | g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0005g0289 | a0001 | c0002 | t0005 | g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0005g0290 | a0001 | c0002 | t0005 | g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0005g0337 | a0001 | c0002 | t0005 | g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0006g0323 | a0001 | c0002 | t0006 | g0323 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0006g0331 | a0001 | c0002 | t0006 | g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0007g0234 | a0001 | c0002 | t0007 | g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0007g0249 | a0001 | c0002 | t0007 | g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0007g0264 | a0001 | c0002 | t0007 | g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0007g0281 | a0001 | c0002 | t0007 | g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0007g0341 | a0001 | c0002 | t0007 | g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0007g0356 | a0001 | c0002 | t0007 | g0356 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0007g0371 | a0001 | c0002 | t0007 | g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0008g0321 | a0001 | c0002 | t0008 | g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0008g0354 | a0001 | c0002 | t0008 | g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0009g0348 | a0001 | c0002 | t0009 | g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0009g0366 | a0001 | c0002 | t0009 | g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0011g0178 | a0001 | c0002 | t0011 | g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0011g0293 | a0001 | c0002 | t0011 | g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0011g0296 | a0001 | c0002 | t0011 | g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0011g0301 | a0001 | c0002 | t0011 | g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0011g0362 | a0001 | c0002 | t0011 | g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0013g0268 | a0001 | c0002 | t0013 | g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0015g0205 | a0001 | c0002 | t0015 | g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0015g0346 | a0001 | c0002 | t0015 | g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0016g0306 | a0001 | c0002 | t0016 | g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0019g0312 | a0001 | c0002 | t0019 | g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0020g0208 | a0001 | c0002 | t0020 | g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0021g0260 | a0001 | c0002 | t0021 | g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0023g0192 | a0001 | c0002 | t0023 | g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0025g0004 | a0001 | c0002 | t0025 | g0004 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0027g0191 | a0001 | c0002 | t0027 | g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0028g0361 | a0001 | c0002 | t0028 | g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0028g0372 | a0001 | c0002 | t0028 | g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0030g0204 | a0001 | c0002 | t0030 | g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0031g0229 | a0001 | c0002 | t0031 | g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0033g0206 | a0001 | c0002 | t0033 | g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0036g0363 | a0001 | c0002 | t0036 | g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0038g0221 | a0001 | c0002 | t0038 | g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0040g0280 | a0001 | c0002 | t0040 | g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0052g0193 | a0001 | c0002 | t0052 | g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0055g0255 | a0001 | c0002 | t0055 | g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0056g0367 | a0001 | c0002 | t0056 | g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0057g0334 | a0001 | c0002 | t0057 | g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0002t0067g0242 | a0001 | c0002 | t0067 | g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0005t0004g0309 | a0001 | c0005 | t0004 | g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0005t0005g0358 | a0001 | c0005 | t0005 | g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0005t0006g0007 | a0001 | c0005 | t0006 | g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0005t0006g0212 | a0001 | c0005 | t0006 | g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0005t0006g0216 | a0001 | c0005 | t0006 | g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0005t0006g0232 | a0001 | c0005 | t0006 | g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0005t0006g0285 | a0001 | c0005 | t0006 | g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0005t0006g0305 | a0001 | c0005 | t0006 | g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0005t0006g0320 | a0001 | c0005 | t0006 | g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0005t0006g0328 | a0001 | c0005 | t0006 | g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0005t0006g0339 | a0001 | c0005 | t0006 | g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0005t0006g0377 | a0001 | c0005 | t0006 | g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0005t0008g0005 | a0001 | c0005 | t0008 | g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0005t0008g0198 | a0001 | c0005 | t0008 | g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0005t0008g0218 | a0001 | c0005 | t0008 | g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0005t0008g0327 | a0001 | c0005 | t0008 | g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0005t0058g0202 | a0001 | c0005 | t0058 | g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0005t0060g0181 | a0001 | c0005 | t0060 | g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0005t0061g0215 | a0001 | c0005 | t0061 | g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0005t0064g0217 | a0001 | c0005 | t0064 | g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0005t0066g0263 | a0001 | c0005 | t0066 | g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0007t0003g0226 | a0001 | c0007 | t0003 | g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0007t0003g0298 | a0001 | c0007 | t0003 | g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0007t0004g0006 | a0001 | c0007 | t0004 | g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0007t0004g0253 | a0001 | c0007 | t0004 | g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0007t0004g0282 | a0001 | c0007 | t0004 | g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0007t0004g0299 | a0001 | c0007 | t0004 | g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0007t0004g0300 | a0001 | c0007 | t0004 | g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0007t0004g0370 | a0001 | c0007 | t0004 | g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0007t0007g0244 | a0001 | c0007 | t0007 | g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0007t0007g0246 | a0001 | c0007 | t0007 | g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0007t0008g0295 | a0001 | c0007 | t0008 | g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0007t0016g0304 | a0001 | c0007 | t0016 | g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0007t0053g0247 | a0001 | c0007 | t0053 | g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0011t0003g0294 | a0001 | c0011 | t0003 | g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0011t0020g0265 | a0001 | c0011 | t0020 | g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0011t0031g0209 | a0001 | c0011 | t0031 | g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0012t0006g0251 | a0001 | c0012 | t0006 | g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0012t0006g0258 | a0001 | c0012 | t0006 | g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0012t0062g0245 | a0001 | c0012 | t0062 | g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0016t0003g0179 | a0001 | c0016 | t0003 | g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0016t0021g0183 | a0001 | c0016 | t0021 | g0183 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0026t0023g0189 | a0001 | c0026 | t0023 | g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0027t0050g0224 | a0001 | c0027 | t0050 | g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0028t0002g0182 | a0001 | c0028 | t0002 | g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0029t0001g0243 | a0001 | c0029 | t0001 | g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0030t0026g0302 | a0001 | c0030 | t0026 | g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0001c0031t0002g0381 | a0001 | c0031 | t0002 | g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0001g0001 | a0002 | c0003 | t0001 | g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0001g0044 | a0002 | c0003 | t0001 | g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0001g0045 | a0002 | c0003 | t0001 | g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0001g0047 | a0002 | c0003 | t0001 | g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0001g0050 | a0002 | c0003 | t0001 | g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0001g0051 | a0002 | c0003 | t0001 | g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0001g0053 | a0002 | c0003 | t0001 | g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0001g0055 | a0002 | c0003 | t0001 | g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0001g0060 | a0002 | c0003 | t0001 | g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0001g0062 | a0002 | c0003 | t0001 | g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0001g0063 | a0002 | c0003 | t0001 | g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0001g0064 | a0002 | c0003 | t0001 | g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0001g0065 | a0002 | c0003 | t0001 | g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0001g0066 | a0002 | c0003 | t0001 | g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0001g0067 | a0002 | c0003 | t0001 | g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0001g0068 | a0002 | c0003 | t0001 | g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0001g0072 | a0002 | c0003 | t0001 | g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0001g0073 | a0002 | c0003 | t0001 | g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0001g0075 | a0002 | c0003 | t0001 | g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0001g0081 | a0002 | c0003 | t0001 | g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0001g0095 | a0002 | c0003 | t0001 | g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0001g0097 | a0002 | c0003 | t0001 | g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0001g0098 | a0002 | c0003 | t0001 | g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0001g0102 | a0002 | c0003 | t0001 | g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0001g0103 | a0002 | c0003 | t0001 | g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0001g0105 | a0002 | c0003 | t0001 | g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0001g0110 | a0002 | c0003 | t0001 | g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0001g0112 | a0002 | c0003 | t0001 | g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0001g0115 | a0002 | c0003 | t0001 | g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0001g0119 | a0002 | c0003 | t0001 | g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0001g0124 | a0002 | c0003 | t0001 | g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0001g0130 | a0002 | c0003 | t0001 | g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0001g0132 | a0002 | c0003 | t0001 | g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0001g0135 | a0002 | c0003 | t0001 | g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0001g0138 | a0002 | c0003 | t0001 | g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0001g0142 | a0002 | c0003 | t0001 | g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0001g0147 | a0002 | c0003 | t0001 | g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0001g0153 | a0002 | c0003 | t0001 | g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0001g0159 | a0002 | c0003 | t0001 | g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0001g0162 | a0002 | c0003 | t0001 | g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0002g0042 | a0002 | c0003 | t0002 | g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0002g0088 | a0002 | c0003 | t0002 | g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0002g0118 | a0002 | c0003 | t0002 | g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0002g0155 | a0002 | c0003 | t0002 | g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0002g0157 | a0002 | c0003 | t0002 | g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0004g0077 | a0002 | c0003 | t0004 | g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0004g0100 | a0002 | c0003 | t0004 | g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0004g0116 | a0002 | c0003 | t0004 | g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0004g0145 | a0002 | c0003 | t0004 | g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0005g0082 | a0002 | c0003 | t0005 | g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0005g0099 | a0002 | c0003 | t0005 | g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0006g0148 | a0002 | c0003 | t0006 | g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0010g0052 | a0002 | c0003 | t0010 | g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0010g0083 | a0002 | c0003 | t0010 | g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0010g0084 | a0002 | c0003 | t0010 | g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0010g0126 | a0002 | c0003 | t0010 | g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0010g0129 | a0002 | c0003 | t0010 | g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0010g0134 | a0002 | c0003 | t0010 | g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0010g0163 | a0002 | c0003 | t0010 | g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0017g0136 | a0002 | c0003 | t0017 | g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0018g0061 | a0002 | c0003 | t0018 | g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0018g0087 | a0002 | c0003 | t0018 | g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0041g0137 | a0002 | c0003 | t0041 | g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0045g0113 | a0002 | c0003 | t0045 | g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0047g0114 | a0002 | c0003 | t0047 | g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0049g0146 | a0002 | c0003 | t0049 | g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0003t0054g0104 | a0002 | c0003 | t0054 | g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0004t0001g0120 | a0002 | c0004 | t0001 | g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0004t0001g0133 | a0002 | c0004 | t0001 | g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0004t0001g0165 | a0002 | c0004 | t0001 | g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0004t0002g0076 | a0002 | c0004 | t0002 | g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0004t0002g0106 | a0002 | c0004 | t0002 | g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0004t0002g0108 | a0002 | c0004 | t0002 | g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0004t0002g0154 | a0002 | c0004 | t0002 | g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0004t0003g0054 | a0002 | c0004 | t0003 | g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0004t0003g0057 | a0002 | c0004 | t0003 | g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0004t0003g0109 | a0002 | c0004 | t0003 | g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0004t0003g0122 | a0002 | c0004 | t0003 | g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0004t0003g0123 | a0002 | c0004 | t0003 | g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0004t0003g0156 | a0002 | c0004 | t0003 | g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0004t0004g0117 | a0002 | c0004 | t0004 | g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0004t0004g0151 | a0002 | c0004 | t0004 | g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0004t0005g0058 | a0002 | c0004 | t0005 | g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0004t0005g0085 | a0002 | c0004 | t0005 | g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0004t0005g0090 | a0002 | c0004 | t0005 | g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0004t0005g0093 | a0002 | c0004 | t0005 | g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0004t0005g0125 | a0002 | c0004 | t0005 | g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0004t0005g0139 | a0002 | c0004 | t0005 | g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0004t0005g0141 | a0002 | c0004 | t0005 | g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0004t0005g0143 | a0002 | c0004 | t0005 | g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0004t0005g0144 | a0002 | c0004 | t0005 | g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0004t0005g0160 | a0002 | c0004 | t0005 | g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0004t0005g0161 | a0002 | c0004 | t0005 | g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0004t0006g0101 | a0002 | c0004 | t0006 | g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0004t0006g0127 | a0002 | c0004 | t0006 | g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0004t0007g0043 | a0002 | c0004 | t0007 | g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0004t0008g0096 | a0002 | c0004 | t0008 | g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0004t0008g0152 | a0002 | c0004 | t0008 | g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0004t0012g0078 | a0002 | c0004 | t0012 | g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0004t0014g0056 | a0002 | c0004 | t0014 | g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0004t0014g0070 | a0002 | c0004 | t0014 | g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0004t0014g0107 | a0002 | c0004 | t0014 | g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0004t0014g0164 | a0002 | c0004 | t0014 | g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0004t0019g0079 | a0002 | c0004 | t0019 | g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0004t0020g0158 | a0002 | c0004 | t0020 | g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0004t0022g0074 | a0002 | c0004 | t0022 | g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0004t0022g0128 | a0002 | c0004 | t0022 | g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0004t0034g0140 | a0002 | c0004 | t0034 | g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0004t0035g0121 | a0002 | c0004 | t0035 | g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0004t0037g0091 | a0002 | c0004 | t0037 | g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0004t0039g0092 | a0002 | c0004 | t0039 | g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0004t0046g0069 | a0002 | c0004 | t0046 | g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0008t0004g0086 | a0002 | c0008 | t0004 | g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0008t0004g0150 | a0002 | c0008 | t0004 | g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0008t0005g0046 | a0002 | c0008 | t0005 | g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0008t0005g0048 | a0002 | c0008 | t0005 | g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0008t0005g0094 | a0002 | c0008 | t0005 | g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0008t0005g0149 | a0002 | c0008 | t0005 | g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0008t0006g0049 | a0002 | c0008 | t0006 | g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0008t0006g0071 | a0002 | c0008 | t0006 | g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0008t0006g0080 | a0002 | c0008 | t0006 | g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0008t0012g0089 | a0002 | c0008 | t0012 | g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0008t0012g0131 | a0002 | c0008 | t0012 | g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0008t0051g0059 | a0002 | c0008 | t0051 | g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0002c0008t0063g0111 | a0002 | c0008 | t0063 | g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0003c0006t0003g0021 | a0003 | c0006 | t0003 | g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0003c0006t0003g0024 | a0003 | c0006 | t0003 | g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0003c0006t0003g0036 | a0003 | c0006 | t0003 | g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0003c0006t0003g0039 | a0003 | c0006 | t0003 | g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0003c0006t0004g0025 | a0003 | c0006 | t0004 | g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0003c0006t0007g0038 | a0003 | c0006 | t0007 | g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0003c0006t0009g0023 | a0003 | c0006 | t0009 | g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0003c0006t0009g0026 | a0003 | c0006 | t0009 | g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0003c0006t0011g0031 | a0003 | c0006 | t0011 | g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0003c0006t0013g0033 | a0003 | c0006 | t0013 | g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0003c0006t0013g0041 | a0003 | c0006 | t0013 | g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0003c0006t0015g0013 | a0003 | c0006 | t0015 | g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0003c0006t0019g0030 | a0003 | c0006 | t0019 | g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0003c0006t0024g0020 | a0003 | c0006 | t0024 | g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0003c0006t0024g0027 | a0003 | c0006 | t0024 | g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0003c0006t0032g0018 | a0003 | c0006 | t0032 | g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0003c0006t0065g0035 | a0003 | c0006 | t0065 | g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0003c0010t0001g0016 | a0003 | c0010 | t0001 | g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0003c0010t0002g0032 | a0003 | c0010 | t0002 | g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0003c0010t0012g0028 | a0003 | c0010 | t0012 | g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0003c0010t0012g0029 | a0003 | c0010 | t0012 | g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0003c0010t0042g0022 | a0003 | c0010 | t0042 | g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0003c0010t0048g0015 | a0003 | c0010 | t0048 | g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0003c0013t0001g0009 | a0003 | c0013 | t0001 | g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0003c0013t0001g0012 | a0003 | c0013 | t0001 | g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0003c0014t0003g0040 | a0003 | c0014 | t0003 | g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0003c0014t0030g0014 | a0003 | c0014 | t0030 | g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0003c0015t0029g0034 | a0003 | c0015 | t0029 | g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0003c0015t0029g0037 | a0003 | c0015 | t0029 | g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0003c0017t0002g0008 | a0003 | c0017 | t0002 | g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0003c0019t0059g0010 | a0003 | c0019 | t0059 | g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0003c0020t0026g0017 | a0003 | c0020 | t0026 | g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0003c0021t0027g0019 | a0003 | c0021 | t0027 | g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0004c0009t0007g0170 | a0004 | c0009 | t0007 | g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0004c0009t0009g0168 | a0004 | c0009 | t0009 | g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0004c0009t0009g0169 | a0004 | c0009 | t0009 | g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0004c0009t0009g0172 | a0004 | c0009 | t0009 | g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0004c0009t0009g0174 | a0004 | c0009 | t0009 | g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0004c0009t0011g0176 | a0004 | c0009 | t0011 | g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0004c0009t0013g0171 | a0004 | c0009 | t0013 | g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0004c0009t0016g0175 | a0004 | c0009 | t0016 | g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0004c0023t0044g0167 | a0004 | c0023 | t0044 | g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0004c0024t0001g0173 | a0004 | c0024 | t0001 | g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0005c0025t0008g0177 | a0005 | c0025 | t0008 | g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0006c0022t0009g0166 | a0006 | c0022 | t0009 | g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 |
| a0007c0018t0001g0011 | a0007 | c0018 | t0001 | g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0003 | g0186 | EUR | GBR | ALX4_chr11_44255440_44315139 | ALX4 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0252 | EUR | GBR | ALX4_chr11_44255440_44315139 | ALX4 |
| HG00140 | hp1 | a0001 | c0002 | t0007 | g0356 | EUR | GBR | ALX4_chr11_44255440_44315139 | ALX4 |
| HG00140 | hp2 | a0001 | c0002 | t0003 | g0225 | EUR | GBR | ALX4_chr11_44255440_44315139 | ALX4 |
| HG00280 | hp1 | a0002 | c0003 | t0001 | g0130 | EUR | FIN | ALX4_chr11_44255440_44315139 | ALX4 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0317 | EUR | FIN | ALX4_chr11_44255440_44315139 | ALX4 |
| HG00323 | hp1 | a0002 | c0004 | t0039 | g0092 | EUR | FIN | ALX4_chr11_44255440_44315139 | ALX4 |
| HG00323 | hp2 | a0001 | c0002 | t0019 | g0312 | EUR | FIN | ALX4_chr11_44255440_44315139 | ALX4 |
| HG00408 | hp1 | a0001 | c0002 | t0006 | g0331 | EAS | CHS | ALX4_chr11_44255440_44315139 | ALX4 |
| HG00408 | hp2 | a0001 | c0005 | t0006 | g0216 | EAS | CHS | ALX4_chr11_44255440_44315139 | ALX4 |
| HG00423 | hp1 | a0002 | c0004 | t0004 | g0117 | EAS | CHS | ALX4_chr11_44255440_44315139 | ALX4 |
| HG00423 | hp2 | a0002 | c0003 | t0001 | g0045 | EAS | CHS | ALX4_chr11_44255440_44315139 | ALX4 |
| HG00438 | hp1 | a0002 | c0004 | t0005 | g0161 | EAS | CHS | ALX4_chr11_44255440_44315139 | ALX4 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | ALX4_chr11_44255440_44315139 | ALX4 |
| HG00544 | hp1 | a0002 | c0003 | t0001 | g0153 | EAS | CHS | ALX4_chr11_44255440_44315139 | ALX4 |
| HG00544 | hp2 | a0002 | c0004 | t0022 | g0074 | EAS | CHS | ALX4_chr11_44255440_44315139 | ALX4 |
| HG00609 | hp1 | a0001 | c0002 | t0003 | g0314 | EAS | CHS | ALX4_chr11_44255440_44315139 | ALX4 |
| HG00609 | hp2 | a0002 | c0004 | t0035 | g0121 | EAS | CHS | ALX4_chr11_44255440_44315139 | ALX4 |
| HG00621 | hp1 | a0002 | c0004 | t0005 | g0085 | EAS | CHS | ALX4_chr11_44255440_44315139 | ALX4 |
| HG00621 | hp2 | a0002 | c0003 | t0001 | g0072 | EAS | CHS | ALX4_chr11_44255440_44315139 | ALX4 |
| HG00639 | hp1 | a0001 | c0005 | t0006 | g0007 | AMR | PUR | ALX4_chr11_44255440_44315139 | ALX4 |
| HG00639 | hp2 | a0001 | c0002 | t0030 | g0204 | AMR | PUR | ALX4_chr11_44255440_44315139 | ALX4 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | CHS | ALX4_chr11_44255440_44315139 | ALX4 |
| HG00673 | hp2 | a0002 | c0004 | t0005 | g0058 | EAS | CHS | ALX4_chr11_44255440_44315139 | ALX4 |
| HG00738 | hp1 | a0001 | c0007 | t0008 | g0295 | AMR | PUR | ALX4_chr11_44255440_44315139 | ALX4 |
| HG00738 | hp2 | a0001 | c0007 | t0004 | g0253 | AMR | PUR | ALX4_chr11_44255440_44315139 | ALX4 |
| HG00741 | hp1 | a0002 | c0004 | t0006 | g0127 | AMR | PUR | ALX4_chr11_44255440_44315139 | ALX4 |
| HG00741 | hp2 | a0001 | c0002 | t0031 | g0229 | AMR | PUR | ALX4_chr11_44255440_44315139 | ALX4 |
| HG01069 | hp1 | a0002 | c0003 | t0001 | g0098 | AMR | PUR | ALX4_chr11_44255440_44315139 | ALX4 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | ALX4_chr11_44255440_44315139 | ALX4 |
| HG01070 | hp1 | a0001 | c0029 | t0001 | g0243 | AMR | PUR | ALX4_chr11_44255440_44315139 | ALX4 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0373 | AMR | PUR | ALX4_chr11_44255440_44315139 | ALX4 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | ALX4_chr11_44255440_44315139 | ALX4 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0374 | AMR | PUR | ALX4_chr11_44255440_44315139 | ALX4 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0256 | AMR | PUR | ALX4_chr11_44255440_44315139 | ALX4 |
| HG01099 | hp2 | a0001 | c0002 | t0004 | g0308 | AMR | PUR | ALX4_chr11_44255440_44315139 | ALX4 |
| HG01106 | hp1 | a0001 | c0005 | t0006 | g0007 | AMR | PUR | ALX4_chr11_44255440_44315139 | ALX4 |
| HG01106 | hp2 | a0001 | c0002 | t0004 | g0307 | AMR | PUR | ALX4_chr11_44255440_44315139 | ALX4 |
| HG01109 | hp1 | a0003 | c0006 | t0013 | g0033 | AMR | PUR | ALX4_chr11_44255440_44315139 | ALX4 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0235 | AMR | PUR | ALX4_chr11_44255440_44315139 | ALX4 |
| HG01168 | hp1 | a0001 | c0002 | t0003 | g0375 | AMR | PUR | ALX4_chr11_44255440_44315139 | ALX4 |
| HG01168 | hp2 | a0002 | c0004 | t0014 | g0164 | AMR | PUR | ALX4_chr11_44255440_44315139 | ALX4 |
| HG01169 | hp1 | a0002 | c0004 | t0014 | g0070 | AMR | PUR | ALX4_chr11_44255440_44315139 | ALX4 |
| HG01169 | hp2 | a0001 | c0001 | t0004 | g0311 | AMR | PUR | ALX4_chr11_44255440_44315139 | ALX4 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0233 | AMR | PUR | ALX4_chr11_44255440_44315139 | ALX4 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | ALX4_chr11_44255440_44315139 | ALX4 |
| HG01192 | hp1 | a0001 | c0011 | t0003 | g0294 | AMR | PUR | ALX4_chr11_44255440_44315139 | ALX4 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0316 | AMR | PUR | ALX4_chr11_44255440_44315139 | ALX4 |
| HG01243 | hp1 | a0001 | c0002 | t0025 | g0004 | AMR | PUR | ALX4_chr11_44255440_44315139 | ALX4 |
| HG01243 | hp2 | a0004 | c0009 | t0009 | g0168 | AMR | PUR | ALX4_chr11_44255440_44315139 | ALX4 |
| HG01255 | hp1 | a0002 | c0003 | t0001 | g0081 | AMR | CLM | ALX4_chr11_44255440_44315139 | ALX4 |
| HG01255 | hp2 | a0002 | c0004 | t0012 | g0078 | AMR | CLM | ALX4_chr11_44255440_44315139 | ALX4 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | CLM | ALX4_chr11_44255440_44315139 | ALX4 |
| HG01256 | hp2 | a0003 | c0010 | t0012 | g0029 | AMR | CLM | ALX4_chr11_44255440_44315139 | ALX4 |
| HG01257 | hp1 | a0001 | c0002 | t0003 | g0262 | AMR | CLM | ALX4_chr11_44255440_44315139 | ALX4 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0279 | AMR | CLM | ALX4_chr11_44255440_44315139 | ALX4 |
| HG01258 | hp1 | a0001 | c0002 | t0003 | g0261 | AMR | CLM | ALX4_chr11_44255440_44315139 | ALX4 |
| HG01258 | hp2 | a0003 | c0010 | t0012 | g0028 | AMR | CLM | ALX4_chr11_44255440_44315139 | ALX4 |
| HG01261 | hp1 | a0001 | c0002 | t0003 | g0350 | AMR | CLM | ALX4_chr11_44255440_44315139 | ALX4 |
| HG01261 | hp2 | a0002 | c0003 | t0004 | g0145 | AMR | CLM | ALX4_chr11_44255440_44315139 | ALX4 |
| HG01346 | hp1 | a0001 | c0007 | t0004 | g0006 | AMR | CLM | ALX4_chr11_44255440_44315139 | ALX4 |
| HG01346 | hp2 | a0002 | c0004 | t0007 | g0043 | AMR | CLM | ALX4_chr11_44255440_44315139 | ALX4 |
| HG01358 | hp1 | a0001 | c0007 | t0004 | g0006 | AMR | CLM | ALX4_chr11_44255440_44315139 | ALX4 |
| HG01358 | hp2 | a0002 | c0008 | t0004 | g0086 | AMR | CLM | ALX4_chr11_44255440_44315139 | ALX4 |
| HG01361 | hp1 | a0001 | c0001 | t0017 | g0359 | AMR | CLM | ALX4_chr11_44255440_44315139 | ALX4 |
| HG01361 | hp2 | a0002 | c0003 | t0002 | g0118 | AMR | CLM | ALX4_chr11_44255440_44315139 | ALX4 |
| HG01433 | hp1 | a0001 | c0002 | t0003 | g0368 | AMR | CLM | ALX4_chr11_44255440_44315139 | ALX4 |
| HG01433 | hp2 | a0001 | c0011 | t0031 | g0209 | AMR | CLM | ALX4_chr11_44255440_44315139 | ALX4 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | ALX4_chr11_44255440_44315139 | ALX4 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0240 | AMR | CLM | ALX4_chr11_44255440_44315139 | ALX4 |
| HG01515 | hp1 | a0002 | c0004 | t0006 | g0101 | EUR | IBS | ALX4_chr11_44255440_44315139 | ALX4 |
| HG01515 | hp2 | a0001 | c0002 | t0003 | g0185 | EUR | IBS | ALX4_chr11_44255440_44315139 | ALX4 |
| HG01516 | hp1 | a0001 | c0007 | t0007 | g0246 | EUR | IBS | ALX4_chr11_44255440_44315139 | ALX4 |
| HG01516 | hp2 | a0001 | c0002 | t0003 | g0376 | EUR | IBS | ALX4_chr11_44255440_44315139 | ALX4 |
| HG01517 | hp1 | a0001 | c0007 | t0007 | g0244 | EUR | IBS | ALX4_chr11_44255440_44315139 | ALX4 |
| HG01517 | hp2 | a0001 | c0002 | t0003 | g0184 | EUR | IBS | ALX4_chr11_44255440_44315139 | ALX4 |
| HG01884 | hp1 | a0003 | c0010 | t0042 | g0022 | AFR | ACB | ALX4_chr11_44255440_44315139 | ALX4 |
| HG01884 | hp2 | a0003 | c0014 | t0003 | g0040 | AFR | ACB | ALX4_chr11_44255440_44315139 | ALX4 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | ALX4_chr11_44255440_44315139 | ALX4 |
| HG01934 | hp2 | a0002 | c0003 | t0001 | g0110 | AMR | PEL | ALX4_chr11_44255440_44315139 | ALX4 |
| HG01943 | hp1 | a0002 | c0003 | t0010 | g0129 | AMR | PEL | ALX4_chr11_44255440_44315139 | ALX4 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ALX4_chr11_44255440_44315139 | ALX4 |
| HG01952 | hp1 | a0001 | c0001 | t0010 | g0230 | AMR | PEL | ALX4_chr11_44255440_44315139 | ALX4 |
| HG01952 | hp2 | a0002 | c0003 | t0010 | g0083 | AMR | PEL | ALX4_chr11_44255440_44315139 | ALX4 |
| HG01975 | hp1 | a0002 | c0003 | t0010 | g0052 | AMR | PEL | ALX4_chr11_44255440_44315139 | ALX4 |
| HG01975 | hp2 | a0002 | c0003 | t0001 | g0105 | AMR | PEL | ALX4_chr11_44255440_44315139 | ALX4 |
| HG01978 | hp1 | a0002 | c0003 | t0010 | g0084 | AMR | PEL | ALX4_chr11_44255440_44315139 | ALX4 |
| HG01978 | hp2 | a0002 | c0004 | t0014 | g0056 | AMR | PEL | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02004 | hp1 | a0002 | c0004 | t0003 | g0122 | AMR | PEL | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02004 | hp2 | a0001 | c0012 | t0062 | g0245 | AMR | PEL | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02027 | hp1 | a0002 | c0004 | t0005 | g0093 | EAS | KHV | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | KHV | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0379 | EAS | KHV | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02040 | hp2 | a0001 | c0005 | t0061 | g0215 | EAS | KHV | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02056 | hp1 | a0002 | c0003 | t0010 | g0126 | EAS | KHV | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02056 | hp2 | a0002 | c0004 | t0034 | g0140 | EAS | KHV | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02071 | hp2 | a0002 | c0003 | t0001 | g0068 | EAS | KHV | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02074 | hp1 | a0002 | c0004 | t0002 | g0154 | EAS | KHV | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02074 | hp2 | a0002 | c0004 | t0004 | g0151 | EAS | KHV | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02080 | hp1 | a0001 | c0002 | t0005 | g0290 | EAS | KHV | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02080 | hp2 | a0002 | c0003 | t0001 | g0135 | EAS | KHV | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02129 | hp1 | a0002 | c0003 | t0049 | g0146 | EAS | KHV | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02129 | hp2 | a0002 | c0003 | t0001 | g0075 | EAS | KHV | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02132 | hp1 | a0002 | c0003 | t0001 | g0142 | EAS | KHV | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02132 | hp2 | a0002 | c0003 | t0001 | g0067 | EAS | KHV | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02145 | hp1 | a0001 | c0026 | t0023 | g0189 | AFR | ACB | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02145 | hp2 | a0001 | c0007 | t0004 | g0370 | AFR | ACB | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02155 | hp1 | a0002 | c0003 | t0001 | g0050 | EAS | CDX | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02155 | hp2 | a0002 | c0004 | t0005 | g0143 | EAS | CDX | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02165 | hp1 | a0002 | c0004 | t0005 | g0160 | EAS | CDX | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02165 | hp2 | a0002 | c0003 | t0001 | g0065 | EAS | CDX | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02257 | hp1 | a0003 | c0014 | t0030 | g0014 | AFR | ACB | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02257 | hp2 | a0001 | c0002 | t0015 | g0205 | AFR | ACB | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02258 | hp1 | a0001 | c0002 | t0033 | g0206 | AFR | ACB | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02258 | hp2 | a0003 | c0006 | t0009 | g0026 | AFR | ACB | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02293 | hp1 | a0003 | c0013 | t0001 | g0012 | AMR | PEL | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02293 | hp2 | a0002 | c0003 | t0001 | g0102 | AMR | PEL | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02300 | hp1 | a0002 | c0003 | t0010 | g0134 | AMR | PEL | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02300 | hp2 | a0001 | c0002 | t0003 | g0267 | AMR | PEL | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02451 | hp1 | a0001 | c0002 | t0007 | g0341 | AFR | ACB | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02451 | hp2 | a0003 | c0006 | t0013 | g0041 | AFR | ACB | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0291 | EAS | KHV | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02523 | hp2 | a0001 | c0001 | t0006 | g0196 | EAS | KHV | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02572 | hp1 | a0001 | c0002 | t0009 | g0348 | AFR | GWD | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02572 | hp2 | a0004 | c0009 | t0007 | g0170 | AFR | GWD | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02602 | hp1 | a0007 | c0018 | t0001 | g0011 | SAS | PJL | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02602 | hp2 | a0002 | c0003 | t0001 | g0095 | SAS | PJL | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02615 | hp1 | a0001 | c0002 | t0003 | g0207 | AFR | GWD | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02615 | hp2 | a0001 | c0002 | t0056 | g0367 | AFR | GWD | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02622 | hp1 | a0001 | c0002 | t0007 | g0264 | AFR | GWD | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02622 | hp2 | a0001 | c0007 | t0016 | g0304 | AFR | GWD | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02630 | hp1 | a0001 | c0002 | t0016 | g0306 | AFR | GWD | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02630 | hp2 | a0001 | c0002 | t0007 | g0249 | AFR | GWD | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02647 | hp1 | a0001 | c0007 | t0003 | g0298 | AFR | GWD | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02647 | hp2 | a0003 | c0006 | t0007 | g0038 | AFR | GWD | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02683 | hp1 | a0002 | c0004 | t0014 | g0107 | SAS | PJL | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02683 | hp2 | a0002 | c0004 | t0019 | g0079 | SAS | PJL | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02698 | hp1 | a0001 | c0002 | t0003 | g0349 | SAS | PJL | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02698 | hp2 | a0002 | c0004 | t0046 | g0069 | SAS | PJL | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02723 | hp1 | a0001 | c0007 | t0004 | g0299 | AFR | GWD | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02723 | hp2 | a0003 | c0006 | t0011 | g0031 | AFR | GWD | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02735 | hp1 | a0002 | c0003 | t0017 | g0136 | SAS | PJL | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02735 | hp2 | a0002 | c0004 | t0001 | g0133 | SAS | PJL | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02809 | hp1 | a0003 | c0020 | t0026 | g0017 | AFR | GWD | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02809 | hp2 | a0003 | c0006 | t0015 | g0013 | AFR | GWD | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02818 | hp1 | a0001 | c0002 | t0055 | g0255 | AFR | GWD | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02818 | hp2 | a0003 | c0006 | t0003 | g0036 | AFR | GWD | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02886 | hp1 | a0003 | c0006 | t0065 | g0035 | AFR | GWD | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02886 | hp2 | a0001 | c0002 | t0003 | g0351 | AFR | GWD | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02895 | hp1 | a0001 | c0002 | t0067 | g0242 | AFR | GWD | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02895 | hp2 | a0003 | c0015 | t0029 | g0034 | AFR | GWD | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02896 | hp1 | a0001 | c0002 | t0011 | g0296 | AFR | GWD | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02896 | hp2 | a0003 | c0006 | t0024 | g0020 | AFR | GWD | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02897 | hp1 | a0001 | c0002 | t0011 | g0293 | AFR | GWD | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02897 | hp2 | a0003 | c0015 | t0029 | g0037 | AFR | GWD | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02922 | hp1 | a0004 | c0009 | t0009 | g0174 | AFR | ESN | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02922 | hp2 | a0001 | c0001 | t0043 | g0297 | AFR | ESN | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0190 | AFR | ESN | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02965 | hp2 | a0003 | c0010 | t0048 | g0015 | AFR | ESN | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02970 | hp1 | a0003 | c0006 | t0024 | g0027 | AFR | ESN | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02970 | hp2 | a0001 | c0028 | t0002 | g0182 | AFR | ESN | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02976 | hp1 | a0001 | c0011 | t0020 | g0265 | AFR | ESN | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02976 | hp2 | a0006 | c0022 | t0009 | g0166 | AFR | ESN | ALX4_chr11_44255440_44315139 | ALX4 |
| HG03017 | hp1 | a0002 | c0004 | t0020 | g0158 | SAS | PJL | ALX4_chr11_44255440_44315139 | ALX4 |
| HG03017 | hp2 | a0002 | c0008 | t0006 | g0071 | SAS | PJL | ALX4_chr11_44255440_44315139 | ALX4 |
| HG03041 | hp1 | a0003 | c0006 | t0003 | g0039 | AFR | GWD | ALX4_chr11_44255440_44315139 | ALX4 |
| HG03041 | hp2 | a0001 | c0030 | t0026 | g0302 | AFR | GWD | ALX4_chr11_44255440_44315139 | ALX4 |
| HG03098 | hp1 | a0003 | c0006 | t0009 | g0023 | AFR | MSL | ALX4_chr11_44255440_44315139 | ALX4 |
| HG03098 | hp2 | a0003 | c0010 | t0002 | g0032 | AFR | MSL | ALX4_chr11_44255440_44315139 | ALX4 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0352 | AFR | ESN | ALX4_chr11_44255440_44315139 | ALX4 |
| HG03130 | hp2 | a0001 | c0027 | t0050 | g0224 | AFR | ESN | ALX4_chr11_44255440_44315139 | ALX4 |
| HG03139 | hp1 | a0001 | c0002 | t0028 | g0372 | AFR | ESN | ALX4_chr11_44255440_44315139 | ALX4 |
| HG03139 | hp2 | a0004 | c0009 | t0013 | g0171 | AFR | ESN | ALX4_chr11_44255440_44315139 | ALX4 |
| HG03195 | hp1 | a0001 | c0002 | t0057 | g0334 | AFR | ESN | ALX4_chr11_44255440_44315139 | ALX4 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0292 | AFR | ESN | ALX4_chr11_44255440_44315139 | ALX4 |
| HG03209 | hp1 | a0001 | c0002 | t0011 | g0178 | AFR | MSL | ALX4_chr11_44255440_44315139 | ALX4 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0187 | AFR | MSL | ALX4_chr11_44255440_44315139 | ALX4 |
| HG03225 | hp1 | a0004 | c0024 | t0001 | g0173 | AFR | MSL | ALX4_chr11_44255440_44315139 | ALX4 |
| HG03225 | hp2 | a0004 | c0023 | t0044 | g0167 | AFR | MSL | ALX4_chr11_44255440_44315139 | ALX4 |
| HG03239 | hp1 | a0002 | c0003 | t0001 | g0051 | SAS | PJL | ALX4_chr11_44255440_44315139 | ALX4 |
| HG03239 | hp2 | a0001 | c0007 | t0053 | g0247 | SAS | PJL | ALX4_chr11_44255440_44315139 | ALX4 |
| HG03453 | hp1 | a0001 | c0002 | t0007 | g0371 | AFR | MSL | ALX4_chr11_44255440_44315139 | ALX4 |
| HG03453 | hp2 | a0001 | c0002 | t0040 | g0280 | AFR | MSL | ALX4_chr11_44255440_44315139 | ALX4 |
| HG03486 | hp1 | a0001 | c0002 | t0013 | g0268 | AFR | MSL | ALX4_chr11_44255440_44315139 | ALX4 |
| HG03486 | hp2 | a0001 | c0007 | t0004 | g0300 | AFR | MSL | ALX4_chr11_44255440_44315139 | ALX4 |
| HG03491 | hp1 | a0003 | c0019 | t0059 | g0010 | SAS | PJL | ALX4_chr11_44255440_44315139 | ALX4 |
| HG03491 | hp2 | a0002 | c0003 | t0001 | g0001 | SAS | PJL | ALX4_chr11_44255440_44315139 | ALX4 |
| HG03492 | hp1 | a0003 | c0017 | t0002 | g0008 | SAS | PJL | ALX4_chr11_44255440_44315139 | ALX4 |
| HG03492 | hp2 | a0002 | c0003 | t0001 | g0001 | SAS | PJL | ALX4_chr11_44255440_44315139 | ALX4 |
| HG03516 | hp1 | a0001 | c0002 | t0021 | g0260 | AFR | ESN | ALX4_chr11_44255440_44315139 | ALX4 |
| HG03516 | hp2 | a0004 | c0009 | t0011 | g0176 | AFR | ESN | ALX4_chr11_44255440_44315139 | ALX4 |
| HG03540 | hp1 | a0004 | c0009 | t0016 | g0175 | AFR | GWD | ALX4_chr11_44255440_44315139 | ALX4 |
| HG03540 | hp2 | a0001 | c0002 | t0015 | g0346 | AFR | GWD | ALX4_chr11_44255440_44315139 | ALX4 |
| HG03579 | hp1 | a0004 | c0009 | t0009 | g0169 | AFR | MSL | ALX4_chr11_44255440_44315139 | ALX4 |
| HG03579 | hp2 | a0001 | c0002 | t0007 | g0234 | AFR | MSL | ALX4_chr11_44255440_44315139 | ALX4 |
| HG03654 | hp1 | a0002 | c0003 | t0054 | g0104 | SAS | PJL | ALX4_chr11_44255440_44315139 | ALX4 |
| HG03654 | hp2 | a0001 | c0005 | t0058 | g0202 | SAS | PJL | ALX4_chr11_44255440_44315139 | ALX4 |
| HG03688 | hp1 | a0001 | c0012 | t0006 | g0258 | SAS | STU | ALX4_chr11_44255440_44315139 | ALX4 |
| HG03688 | hp2 | a0001 | c0005 | t0006 | g0232 | SAS | STU | ALX4_chr11_44255440_44315139 | ALX4 |
| HG03704 | hp1 | a0002 | c0003 | t0004 | g0100 | SAS | PJL | ALX4_chr11_44255440_44315139 | ALX4 |
| HG03704 | hp2 | a0001 | c0005 | t0064 | g0217 | SAS | PJL | ALX4_chr11_44255440_44315139 | ALX4 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | BEB | ALX4_chr11_44255440_44315139 | ALX4 |
| HG03831 | hp2 | a0001 | c0002 | t0005 | g0289 | SAS | BEB | ALX4_chr11_44255440_44315139 | ALX4 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0310 | SAS | BEB | ALX4_chr11_44255440_44315139 | ALX4 |
| HG03942 | hp2 | a0002 | c0004 | t0001 | g0120 | SAS | BEB | ALX4_chr11_44255440_44315139 | ALX4 |
| HG04115 | hp1 | a0002 | c0003 | t0001 | g0112 | SAS | STU | ALX4_chr11_44255440_44315139 | ALX4 |
| HG04115 | hp2 | a0002 | c0004 | t0002 | g0106 | SAS | STU | ALX4_chr11_44255440_44315139 | ALX4 |
| HG04184 | hp1 | a0002 | c0003 | t0001 | g0103 | SAS | BEB | ALX4_chr11_44255440_44315139 | ALX4 |
| HG04184 | hp2 | a0002 | c0008 | t0063 | g0111 | SAS | BEB | ALX4_chr11_44255440_44315139 | ALX4 |
| HG04199 | hp1 | a0003 | c0013 | t0001 | g0009 | SAS | STU | ALX4_chr11_44255440_44315139 | ALX4 |
| HG04199 | hp2 | a0002 | c0008 | t0006 | g0080 | SAS | STU | ALX4_chr11_44255440_44315139 | ALX4 |
| HG04204 | hp1 | a0002 | c0004 | t0003 | g0156 | SAS | STU | ALX4_chr11_44255440_44315139 | ALX4 |
| HG04204 | hp2 | a0002 | c0003 | t0001 | g0062 | SAS | STU | ALX4_chr11_44255440_44315139 | ALX4 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | STU | ALX4_chr11_44255440_44315139 | ALX4 |
| HG04228 | hp2 | a0001 | c0002 | t0002 | g0200 | SAS | STU | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18522 | hp1 | a0001 | c0002 | t0052 | g0193 | AFR | YRI | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18522 | hp2 | a0001 | c0002 | t0025 | g0004 | AFR | YRI | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18747 | hp1 | a0001 | c0002 | t0003 | g0344 | EAS | CHB | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18747 | hp2 | a0002 | c0003 | t0001 | g0044 | EAS | CHB | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18906 | hp1 | a0001 | c0016 | t0003 | g0179 | AFR | YRI | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18906 | hp2 | a0001 | c0002 | t0011 | g0301 | AFR | YRI | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18939 | hp1 | a0001 | c0001 | t0004 | g0332 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18939 | hp2 | a0001 | c0001 | t0004 | g0194 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18942 | hp1 | a0002 | c0003 | t0001 | g0053 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18942 | hp2 | a0001 | c0005 | t0006 | g0328 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18943 | hp1 | a0001 | c0001 | t0004 | g0222 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18945 | hp1 | a0001 | c0002 | t0008 | g0321 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18945 | hp2 | a0001 | c0001 | t0004 | g0336 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0345 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18946 | hp2 | a0002 | c0003 | t0001 | g0138 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18947 | hp1 | a0002 | c0004 | t0003 | g0123 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18947 | hp2 | a0001 | c0001 | t0004 | g0239 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18948 | hp1 | a0002 | c0003 | t0006 | g0148 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18948 | hp2 | a0002 | c0003 | t0001 | g0073 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18949 | hp1 | a0001 | c0001 | t0004 | g0330 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18949 | hp2 | a0002 | c0004 | t0005 | g0125 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18950 | hp1 | a0002 | c0008 | t0006 | g0049 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18951 | hp1 | a0001 | c0005 | t0006 | g0305 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18952 | hp1 | a0002 | c0003 | t0047 | g0114 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18952 | hp2 | a0002 | c0003 | t0002 | g0042 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0364 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0380 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18954 | hp1 | a0002 | c0004 | t0008 | g0096 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18954 | hp2 | a0001 | c0005 | t0006 | g0212 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18959 | hp1 | a0002 | c0004 | t0037 | g0091 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18959 | hp2 | a0001 | c0005 | t0006 | g0285 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18961 | hp1 | a0001 | c0002 | t0036 | g0363 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18962 | hp1 | a0001 | c0005 | t0008 | g0005 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18964 | hp2 | a0002 | c0004 | t0001 | g0165 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18966 | hp1 | a0001 | c0005 | t0004 | g0309 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18966 | hp2 | a0002 | c0003 | t0001 | g0055 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18968 | hp1 | a0002 | c0003 | t0010 | g0163 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18968 | hp2 | a0002 | c0008 | t0005 | g0149 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18969 | hp1 | a0001 | c0002 | t0005 | g0237 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18969 | hp2 | a0002 | c0004 | t0003 | g0054 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0277 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18971 | hp1 | a0001 | c0001 | t0004 | g0214 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18971 | hp2 | a0002 | c0004 | t0008 | g0152 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18973 | hp1 | a0002 | c0003 | t0001 | g0063 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18974 | hp1 | a0002 | c0008 | t0005 | g0046 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18974 | hp2 | a0002 | c0004 | t0022 | g0128 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18977 | hp1 | a0002 | c0004 | t0003 | g0109 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0353 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18979 | hp2 | a0001 | c0002 | t0008 | g0354 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18980 | hp1 | a0002 | c0003 | t0002 | g0088 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18982 | hp1 | a0002 | c0003 | t0004 | g0077 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18982 | hp2 | a0001 | c0001 | t0018 | g0335 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0287 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18983 | hp2 | a0002 | c0008 | t0012 | g0131 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18984 | hp1 | a0002 | c0003 | t0005 | g0099 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18985 | hp2 | a0002 | c0003 | t0001 | g0119 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18990 | hp1 | a0002 | c0004 | t0005 | g0144 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18990 | hp2 | a0002 | c0008 | t0004 | g0150 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18991 | hp1 | a0001 | c0002 | t0005 | g0283 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18991 | hp2 | a0001 | c0001 | t0005 | g0326 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18993 | hp2 | a0001 | c0002 | t0005 | g0238 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18995 | hp2 | a0001 | c0001 | t0005 | g0325 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0318 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18998 | hp1 | a0002 | c0003 | t0004 | g0116 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18998 | hp2 | a0001 | c0005 | t0008 | g0005 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18999 | hp1 | a0001 | c0005 | t0008 | g0198 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19000 | hp2 | a0002 | c0003 | t0001 | g0060 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19001 | hp1 | a0005 | c0025 | t0008 | g0177 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19001 | hp2 | a0002 | c0003 | t0001 | g0159 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19002 | hp2 | a0002 | c0003 | t0001 | g0147 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19004 | hp1 | a0002 | c0003 | t0005 | g0082 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19004 | hp2 | a0001 | c0005 | t0008 | g0218 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19005 | hp1 | a0002 | c0003 | t0001 | g0064 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19005 | hp2 | a0002 | c0004 | t0002 | g0108 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0365 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19007 | hp2 | a0001 | c0005 | t0060 | g0181 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19009 | hp1 | a0001 | c0005 | t0006 | g0377 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0378 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19010 | hp1 | a0001 | c0005 | t0006 | g0339 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19011 | hp1 | a0002 | c0003 | t0018 | g0061 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0347 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19012 | hp1 | a0002 | c0004 | t0005 | g0090 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19012 | hp2 | a0001 | c0002 | t0005 | g0337 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19030 | hp1 | a0003 | c0006 | t0003 | g0024 | AFR | LWK | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19030 | hp2 | a0001 | c0002 | t0007 | g0281 | AFR | LWK | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0342 | AFR | LWK | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19043 | hp2 | a0001 | c0031 | t0002 | g0381 | AFR | LWK | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19057 | hp1 | a0002 | c0004 | t0002 | g0076 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19060 | hp1 | a0002 | c0003 | t0018 | g0087 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19060 | hp2 | a0002 | c0003 | t0045 | g0113 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0275 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19063 | hp2 | a0001 | c0002 | t0038 | g0221 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19064 | hp1 | a0002 | c0008 | t0012 | g0089 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0355 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19065 | hp2 | a0002 | c0004 | t0005 | g0139 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19066 | hp1 | a0002 | c0003 | t0001 | g0047 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19066 | hp2 | a0002 | c0004 | t0005 | g0141 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19068 | hp1 | a0002 | c0003 | t0001 | g0124 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19070 | hp2 | a0002 | c0003 | t0001 | g0115 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19074 | hp1 | a0001 | c0005 | t0008 | g0327 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19074 | hp2 | a0001 | c0001 | t0004 | g0288 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0338 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19078 | hp1 | a0001 | c0005 | t0005 | g0358 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19078 | hp2 | a0002 | c0003 | t0041 | g0137 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19079 | hp1 | a0002 | c0004 | t0003 | g0057 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19079 | hp2 | a0002 | c0008 | t0005 | g0094 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0319 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19080 | hp2 | a0002 | c0008 | t0005 | g0048 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19081 | hp2 | a0002 | c0003 | t0002 | g0157 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19085 | hp1 | a0001 | c0002 | t0003 | g0228 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19086 | hp1 | a0001 | c0005 | t0006 | g0320 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19086 | hp2 | a0001 | c0001 | t0004 | g0329 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19088 | hp1 | a0001 | c0002 | t0005 | g0223 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19088 | hp2 | a0002 | c0003 | t0001 | g0066 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0369 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19089 | hp2 | a0002 | c0003 | t0001 | g0097 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19091 | hp2 | a0002 | c0003 | t0001 | g0132 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19240 | hp1 | a0003 | c0006 | t0004 | g0025 | AFR | YRI | ALX4_chr11_44255440_44315139 | ALX4 |
| NA19240 | hp2 | a0001 | c0002 | t0004 | g0210 | AFR | YRI | ALX4_chr11_44255440_44315139 | ALX4 |
| NA20129 | hp1 | a0003 | c0021 | t0027 | g0019 | AFR | ASW | ALX4_chr11_44255440_44315139 | ALX4 |
| NA20129 | hp2 | a0004 | c0009 | t0009 | g0172 | AFR | ASW | ALX4_chr11_44255440_44315139 | ALX4 |
| NA20752 | hp1 | a0001 | c0012 | t0006 | g0251 | EUR | TSI | ALX4_chr11_44255440_44315139 | ALX4 |
| NA20752 | hp2 | a0002 | c0008 | t0051 | g0059 | EUR | TSI | ALX4_chr11_44255440_44315139 | ALX4 |
| NA20805 | hp1 | a0001 | c0002 | t0003 | g0254 | EUR | TSI | ALX4_chr11_44255440_44315139 | ALX4 |
| NA20805 | hp2 | a0001 | c0007 | t0003 | g0226 | EUR | TSI | ALX4_chr11_44255440_44315139 | ALX4 |
| NA20905 | hp1 | a0001 | c0002 | t0005 | g0220 | SAS | GIH | ALX4_chr11_44255440_44315139 | ALX4 |
| NA20905 | hp2 | a0002 | c0003 | t0001 | g0162 | SAS | GIH | ALX4_chr11_44255440_44315139 | ALX4 |
| HG01123 | hp1 | a0001 | c0002 | t0003 | g0360 | AMR | CLM | ALX4_chr11_44255440_44315139 | ALX4 |
| HG01123 | hp2 | a0001 | c0001 | t0017 | g0357 | AMR | CLM | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02109 | hp1 | a0001 | c0002 | t0028 | g0361 | AFR | ACB | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02109 | hp2 | a0001 | c0002 | t0027 | g0191 | AFR | ACB | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02486 | hp1 | a0001 | c0002 | t0011 | g0362 | AFR | ACB | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02486 | hp2 | a0001 | c0002 | t0009 | g0366 | AFR | ACB | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02559 | hp1 | a0001 | c0005 | t0066 | g0263 | AFR | ACB | ALX4_chr11_44255440_44315139 | ALX4 |
| HG02559 | hp2 | a0003 | c0010 | t0001 | g0016 | AFR | ACB | ALX4_chr11_44255440_44315139 | ALX4 |
| HG03471 | hp1 | a0001 | c0007 | t0004 | g0282 | AFR | MSL | ALX4_chr11_44255440_44315139 | ALX4 |
| HG03471 | hp2 | a0003 | c0006 | t0032 | g0018 | AFR | MSL | ALX4_chr11_44255440_44315139 | ALX4 |
| HG06807 | hp1 | a0001 | c0002 | t0002 | g0241 | AFR | USA | ALX4_chr11_44255440_44315139 | ALX4 |
| HG06807 | hp2 | a0001 | c0002 | t0020 | g0208 | AFR | USA | ALX4_chr11_44255440_44315139 | ALX4 |
| NA20300 | hp1 | a0003 | c0006 | t0003 | g0021 | AFR | USA | ALX4_chr11_44255440_44315139 | ALX4 |
| NA20300 | hp2 | a0001 | c0002 | t0023 | g0192 | AFR | USA | ALX4_chr11_44255440_44315139 | ALX4 |
| NA21309 | hp1 | a0003 | c0006 | t0019 | g0030 | AFR | LWK | ALX4_chr11_44255440_44315139 | ALX4 |
| NA21309 | hp2 | a0002 | c0003 | t0002 | g0155 | AFR | LWK | ALX4_chr11_44255440_44315139 | ALX4 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0006 | g0323 | REF | REF | ALX4_chr11_44255440_44315139 | ALX4 |
| homoSapiens_grch38 | hp1 | a0001 | c0016 | t0021 | g0183 | REF | REF | ALX4_chr11_44255440_44315139 | ALX4 |
| chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:44264957
|
T | C | 1 | a0007 | 1 | HG02602.hp1 | missense_variant | MODERATE | c.1133A>G | p.Asn378Ser | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 4/4 | 1210/5727 | 1133/1236 | 378/411 | chr11 | 44264957 | ||
| chr11:44309603
|
A | T | 1 | a0006 | 1 | HG02976.hp2 | missense_variant | MODERATE | c.460T>A | p.Cys154Ser | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/4 | 537/5727 | 460/1236 | 154/411 | chr11 | 44309603 | ||
| chr11:44309710
|
G | T | 1 | a0005 | 1 | NA19001.hp1 | missense_variant | MODERATE | c.353C>A | p.Ala118Glu | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/4 | 430/5727 | 353/1236 | 118/411 | chr11 | 44309710 | ||
| chr11:44309737
|
TGCTGCGG others(5): Show |
T | 2 | a0004a0006 | 11 | HG01243.hp2 HG02572.hp2 HG02922.hp1 others(8): Show |
disruptive_inframe_deletion | MODERATE | c.314_325delCGCAGCCG others(4): Show |
p.Pro105_Gln108del | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/4 | 402/5727 | 314/1236 | 105/411 | chr11 | 44309737 | ||
| chr11:44309759
|
G | A | 1 | a0002 | 126 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(123): Show |
missense_variant | MODERATE | c.304C>T | p.Pro102Ser | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/4 | 381/5727 | 304/1236 | 102/411 | chr11 | 44309759 | ||
| chr11:44309959
|
C | G | 3 | a0002a0003a0007 | 160 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(157): Show |
missense_variant | MODERATE | c.104G>C | p.Arg35Thr | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/4 | 181/5727 | 104/1236 | 35/411 | chr11 | 44309959 |
| chr:pos | ref | alt | # # of chapid
|
chapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:44265016
|
G | A | 10 | a0001c0001a0001c0027a0001c0028others(7): Show | 169 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(166): Show |
synonymous_variant | LOW | c.1074C>T | p.His358His | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 4/4 | 1151/5727 | 1074/1236 | 358/411 | chr11 | 44265016 | ||
| chr11:44265172
|
C | T | 2 | a0001c0030a0003c0020 | 2 | HG02809.hp1 HG03041.hp2 |
synonymous_variant | LOW | c.918G>A | p.Pro306Pro | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 4/4 | 995/5727 | 918/1236 | 306/411 | chr11 | 44265172 | ||
| chr11:44267521
|
G | A | 6 | a0001c0005a0001c0012a0002c0008others(3): Show | 43 | HG00408.hp2 HG00639.hp1 HG01106.hp1 others(40): Show |
synonymous_variant | LOW | c.879C>T | p.Leu293Leu | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 3/4 | 956/5727 | 879/1236 | 293/411 | chr11 | 44267521 | ||
| chr11:44275396
|
C | T | 4 | a0001c0007a0001c0012a0001c0029others(1): Show | 19 | HG00738.hp1 HG00738.hp2 HG01070.hp1 others(16): Show |
synonymous_variant | LOW | c.729G>A | p.Ala243Ala | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/4 | 806/5727 | 729/1236 | 243/411 | chr11 | 44275396 | ||
| chr11:44275504
|
T | C | 28 | a0001c0001a0001c0002a0001c0005others(25): Show | 384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
synonymous_variant | LOW | c.621A>G | p.Ser207Ser | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/4 | 698/5727 | 621/1236 | 207/411 | chr11 | 44275504 | ||
| chr11:44275531
|
G | T | 4 | a0001c0011a0001c0027a0003c0014others(1): Show | 7 | HG01192.hp1 HG01433.hp2 HG01884.hp2 others(4): Show |
synonymous_variant | LOW | c.594C>A | p.Leu198Leu | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/4 | 671/5727 | 594/1236 | 198/411 | chr11 | 44275531 | ||
| chr11:44275636
|
C | T | 1 | a0001c0026 | 1 | HG02145.hp1 | synonymous_variant | LOW | c.489G>A | p.Glu163Glu | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/4 | 566/5727 | 489/1236 | 163/411 | chr11 | 44275636 | ||
| chr11:44309703
|
C | A | 1 | a0001c0031 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.360G>T | p.Pro120Pro | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/4 | 437/5727 | 360/1236 | 120/411 | chr11 | 44309703 | ||
| chr11:44309994
|
C | G | 4 | a0003c0013a0003c0017a0003c0019others(1): Show | 5 | HG02293.hp1 HG02602.hp1 HG03491.hp1 others(2): Show |
synonymous_variant | LOW | c.69G>C | p.Pro23Pro | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/4 | 146/5727 | 69/1236 | 23/411 | chr11 | 44309994 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:44260570
|
A | G | 122 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(119): Show | 362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
3_prime_UTR_variant | MODIFIER | c.*4284T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 4/4 | 4284 | chr11 | 44260570 | |||||
| chr11:44261042
|
C | T | 1 | a0002c0003t0047 | 1 | NA18952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3812G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 4/4 | 3812 | chr11 | 44261042 | |||||
| chr11:44261081
|
T | C | 1 | a0001c0002t0025 | 2 | HG01243.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3773A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 4/4 | 3773 | chr11 | 44261081 | |||||
| chr11:44261085
|
A | G | 1 | a0001c0002t0025 | 2 | HG01243.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3769T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 4/4 | 3769 | chr11 | 44261085 | |||||
| chr11:44261258
|
G | C | 7 | a0001c0002t0023a0001c0002t0030a0001c0002t0055others(4): Show | 7 | HG00639.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3596C>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 4/4 | 3596 | chr11 | 44261258 | |||||
| chr11:44261449
|
C | T | 2 | a0001c0001t0017a0002c0003t0017 | 3 | HG01123.hp2 HG01361.hp1 HG02735.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3405G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 4/4 | 3405 | chr11 | 44261449 | |||||
| chr11:44261469
|
G | A | 1 | a0001c0002t0038 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3385C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 4/4 | 3385 | chr11 | 44261469 | |||||
| chr11:44261553
|
C | A | 1 | a0003c0010t0048 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3301G>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 4/4 | 3301 | chr11 | 44261553 | |||||
| chr11:44261688
|
G | A | 25 | a0001c0001t0001a0001c0001t0010a0001c0001t0017others(22): Show | 124 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*3166C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 4/4 | 3166 | chr11 | 44261688 | |||||
| chr11:44261731
|
C | T | 1 | a0001c0005t0066 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3123G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 4/4 | 3123 | chr11 | 44261731 | |||||
| chr11:44261747
|
T | C | 123 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(120): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
3_prime_UTR_variant | MODIFIER | c.*3107A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 4/4 | 3107 | chr11 | 44261747 | |||||
| chr11:44261773
|
G | A | 2 | a0001c0001t0018a0002c0003t0018 | 3 | NA18982.hp2 NA19011.hp1 NA19060.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3081C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 4/4 | 3081 | chr11 | 44261773 | |||||
| chr11:44261842
|
G | C | 6 | a0001c0002t0008a0001c0005t0008a0001c0007t0008others(3): Show | 12 | HG00738.hp1 NA18945.hp1 NA18954.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3012C>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 4/4 | 3012 | chr11 | 44261842 | |||||
| chr11:44262022
|
T | G | 26 | a0001c0001t0001a0001c0001t0010a0001c0001t0017others(23): Show | 125 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*2832A>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 4/4 | 2832 | chr11 | 44262022 | |||||
| chr11:44262026
|
G | A | 1 | a0003c0006t0024 | 2 | HG02896.hp2 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2828C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 4/4 | 2828 | chr11 | 44262026 | |||||
| chr11:44262090
|
G | A | 1 | a0002c0003t0049 | 1 | HG02129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2764C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 4/4 | 2764 | chr11 | 44262090 | |||||
| chr11:44262104
|
C | T | 1 | a0001c0005t0061 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2750G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 4/4 | 2750 | chr11 | 44262104 | |||||
| chr11:44262172
|
G | A | 98 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(95): Show | 287 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(284): Show |
3_prime_UTR_variant | MODIFIER | c.*2682C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 4/4 | 2682 | chr11 | 44262172 | |||||
| chr11:44262347
|
C | T | 5 | a0001c0002t0008a0001c0005t0008a0001c0007t0008others(2): Show | 11 | HG00738.hp1 NA18945.hp1 NA18954.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2507G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 4/4 | 2507 | chr11 | 44262347 | |||||
| chr11:44262375
|
A | G | 27 | a0001c0001t0001a0001c0001t0010a0001c0001t0017others(24): Show | 127 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*2479T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 4/4 | 2479 | chr11 | 44262375 | |||||
| chr11:44262376
|
A | G | 1 | a0002c0003t0045 | 1 | NA19060.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2478T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 4/4 | 2478 | chr11 | 44262376 | |||||
| chr11:44262628
|
C | T | 2 | a0001c0001t0010a0002c0003t0010 | 8 | HG01943.hp1 HG01952.hp1 HG01952.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2226G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 4/4 | 2226 | chr11 | 44262628 | |||||
| chr11:44262726
|
A | G | 1 | a0001c0005t0060 | 1 | NA19007.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2128T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 4/4 | 2128 | chr11 | 44262726 | |||||
| chr11:44262744
|
T | C | 135 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(132): Show | 383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
3_prime_UTR_variant | MODIFIER | c.*2110A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 4/4 | 2110 | chr11 | 44262744 | |||||
| chr11:44262842
|
T | C | 1 | a0001c0005t0066 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2012A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 4/4 | 2012 | chr11 | 44262842 | |||||
| chr11:44262953
|
T | C | 3 | a0001c0002t0016a0001c0007t0016a0004c0009t0016 | 3 | HG02622.hp2 HG02630.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1901A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 4/4 | 1901 | chr11 | 44262953 | |||||
| chr11:44262958
|
T | C | 8 | a0001c0002t0007a0001c0002t0031a0001c0002t0057others(5): Show | 15 | HG00140.hp1 HG00741.hp2 HG01346.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1896A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 4/4 | 1896 | chr11 | 44262958 | |||||
| chr11:44263141
|
C | G | 2 | a0001c0002t0027a0003c0021t0027 | 2 | HG02109.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1713G>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 4/4 | 1713 | chr11 | 44263141 | |||||
| chr11:44263155
|
C | A | 17 | a0001c0001t0002a0001c0001t0005a0001c0001t0043others(14): Show | 69 | HG00438.hp1 HG00621.hp1 HG00673.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*1699G>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 4/4 | 1699 | chr11 | 44263155 | |||||
| chr11:44263225
|
G | A | 1 | a0001c0005t0066 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1629C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 4/4 | 1629 | chr11 | 44263225 | |||||
| chr11:44263255
|
G | A | 1 | a0002c0008t0063 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1599C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 4/4 | 1599 | chr11 | 44263255 | |||||
| chr11:44263322
|
C | T | 1 | a0003c0019t0059 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1532G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 4/4 | 1532 | chr11 | 44263322 | |||||
| chr11:44263330
|
G | A | 1 | a0002c0004t0034 | 1 | HG02056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1524C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 4/4 | 1524 | chr11 | 44263330 | |||||
| chr11:44263407
|
C | T | 10 | a0001c0002t0015a0001c0002t0023a0001c0002t0025others(7): Show | 12 | HG01243.hp1 HG02145.hp1 HG02257.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1447G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 4/4 | 1447 | chr11 | 44263407 | |||||
| chr11:44263509
|
C | T | 2 | a0001c0005t0066a0003c0006t0024 | 3 | HG02559.hp1 HG02896.hp2 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1345G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 4/4 | 1345 | chr11 | 44263509 | |||||
| chr11:44263517
|
G | T | 1 | a0001c0005t0058 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1337C>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 4/4 | 1337 | chr11 | 44263517 | |||||
| chr11:44263627
|
C | T | 4 | a0001c0002t0013a0001c0002t0040a0003c0006t0013others(1): Show | 5 | HG01109.hp1 HG02451.hp2 HG03139.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1227G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 4/4 | 1227 | chr11 | 44263627 | |||||
| chr11:44263723
|
A | G | 7 | a0001c0001t0005a0001c0002t0005a0001c0005t0005others(4): Show | 29 | HG00438.hp1 HG00621.hp1 HG00673.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1131T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 4/4 | 1131 | chr11 | 44263723 | |||||
| chr11:44263766
|
C | T | 1 | a0003c0010t0042 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1088G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 4/4 | 1088 | chr11 | 44263766 | |||||
| chr11:44263857
|
G | C | 2 | a0001c0001t0043a0003c0010t0042 | 2 | HG01884.hp1 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*997C>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 4/4 | 997 | chr11 | 44263857 | |||||
| chr11:44263881
|
C | T | 11 | a0001c0001t0002a0001c0001t0043a0001c0002t0002others(8): Show | 41 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*973G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 4/4 | 973 | chr11 | 44263881 | |||||
| chr11:44263882
|
G | A | 1 | a0002c0004t0014 | 4 | HG01168.hp2 HG01169.hp1 HG01978.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*972C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 4/4 | 972 | chr11 | 44263882 | |||||
| chr11:44263891
|
C | T | 1 | a0001c0002t0052 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*963G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 4/4 | 963 | chr11 | 44263891 | |||||
| chr11:44263931
|
G | A | 4 | a0001c0002t0013a0001c0002t0040a0003c0006t0013others(1): Show | 5 | HG01109.hp1 HG02451.hp2 HG03139.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*923C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 4/4 | 923 | chr11 | 44263931 | |||||
| chr11:44263932
|
A | C | 4 | a0001c0002t0013a0001c0002t0040a0003c0006t0013others(1): Show | 5 | HG01109.hp1 HG02451.hp2 HG03139.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*922T>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 4/4 | 922 | chr11 | 44263932 | |||||
| chr11:44263952
|
C | T | 2 | a0001c0005t0066a0003c0006t0024 | 3 | HG02559.hp1 HG02896.hp2 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*902G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 4/4 | 902 | chr11 | 44263952 | |||||
| chr11:44264044
|
CCTT | C | 18 | a0001c0002t0011a0001c0002t0019a0001c0002t0027others(15): Show | 27 | HG00323.hp2 HG00639.hp2 HG01168.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*807_*809delAAG | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 4/4 | 807 | chr11 | 44264044 | |||||
| chr11:44264291
|
G | A | 1 | a0002c0003t0054 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*563C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 4/4 | 563 | chr11 | 44264291 | |||||
| chr11:44264307
|
T | C | 126 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(123): Show | 347 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(344): Show |
3_prime_UTR_variant | MODIFIER | c.*547A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 4/4 | 547 | chr11 | 44264307 | |||||
| chr11:44264337
|
G | A | 99 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(96): Show | 305 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(302): Show |
3_prime_UTR_variant | MODIFIER | c.*517C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 4/4 | 517 | chr11 | 44264337 | |||||
| chr11:44264417
|
G | A | 1 | a0001c0005t0064 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*437C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 4/4 | 437 | chr11 | 44264417 | |||||
| chr11:44264588
|
A | C | 9 | a0001c0001t0005a0001c0002t0005a0001c0002t0036others(6): Show | 31 | HG00438.hp1 HG00609.hp2 HG00621.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*266T>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 4/4 | 266 | chr11 | 44264588 | |||||
| chr11:44264626
|
G | A | 27 | a0001c0001t0006a0001c0002t0006a0001c0002t0007others(24): Show | 49 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*228C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 4/4 | 228 | chr11 | 44264626 | |||||
| chr11:44264663
|
CA | C | 5 | a0001c0002t0011a0001c0002t0033a0001c0002t0067others(2): Show | 9 | HG02258.hp1 HG02486.hp1 HG02723.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*190delT | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 4/4 | 190 | chr11 | 44264663 | |||||
| chr11:44264698
|
C | T | 3 | a0001c0002t0015a0003c0006t0015a0003c0006t0032 | 4 | HG02257.hp2 HG02809.hp2 HG03471.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*156G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 4/4 | 156 | chr11 | 44264698 | |||||
| chr11:44264699
|
G | A | 1 | a0003c0006t0065 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*155C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 4/4 | 155 | chr11 | 44264699 | |||||
| chr11:44264809
|
G | A | 1 | a0001c0005t0066 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*45C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 4/4 | 45 | chr11 | 44264809 | |||||
| chr11:44264830
|
T | C | 1 | a0001c0002t0067 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*24A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 4/4 | 24 | chr11 | 44264830 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:44265231
|
G | A | 1 | a0001c0002t0052g0193 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.907-48C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 3/3 | chr11 | 44265231 | ||||||
| chr11:44265255
|
C | T | 15 | a0001c0002t0003g0225a0001c0002t0004g0210a0001c0002t0028g0361others(12): Show | 16 | HG00140.hp2 HG00738.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.907-72G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 3/3 | chr11 | 44265255 | ||||||
| chr11:44265308
|
T | C | 4 | a0001c0002t0030g0204a0003c0006t0024g0020a0003c0006t0024g0027others(1): Show | 4 | HG00639.hp2 HG02257.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.907-125A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 3/3 | chr11 | 44265308 | ||||||
| chr11:44265369
|
G | A | 41 | a0001c0001t0001g0271a0001c0001t0001g0343a0001c0001t0002g0187others(38): Show | 41 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(38): Show |
intron_variant | MODIFIER | c.907-186C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 3/3 | chr11 | 44265369 | ||||||
| chr11:44265478
|
T | C | 82 | a0001c0001t0001g0271a0001c0001t0001g0343a0001c0001t0002g0187others(79): Show | 82 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.907-295A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 3/3 | chr11 | 44265478 | ||||||
| chr11:44265498
|
G | T | 115 | a0001c0001t0001g0271a0001c0001t0001g0343a0001c0001t0002g0187others(112): Show | 116 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.907-315C>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 3/3 | chr11 | 44265498 | ||||||
| chr11:44265599
|
C | T | 78 | a0001c0001t0001g0271a0001c0001t0001g0343a0001c0001t0002g0187others(75): Show | 78 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.907-416G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 3/3 | chr11 | 44265599 | ||||||
| chr11:44265636
|
G | C | 1 | a0001c0002t0052g0193 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.907-453C>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 3/3 | chr11 | 44265636 | ||||||
| chr11:44265666
|
G | A | 1 | a0002c0004t0001g0133 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.907-483C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 3/3 | chr11 | 44265666 | ||||||
| chr11:44265742
|
A | G | 129 | a0001c0001t0001g0271a0001c0001t0001g0343a0001c0001t0002g0187others(126): Show | 129 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.907-559T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 3/3 | chr11 | 44265742 | ||||||
| chr11:44265753
|
T | G | 5 | a0001c0002t0015g0205a0001c0002t0015g0346a0001c0002t0025g0004others(2): Show | 6 | HG01243.hp1 HG02257.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.907-570A>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 3/3 | chr11 | 44265753 | ||||||
| chr11:44265803
|
T | G | 103 | a0001c0001t0001g0271a0001c0001t0001g0343a0001c0001t0002g0187others(100): Show | 103 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.907-620A>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 3/3 | chr11 | 44265803 | ||||||
| chr11:44265832
|
G | A | 7 | a0001c0002t0008g0321a0001c0002t0008g0354a0002c0004t0002g0076others(4): Show | 7 | HG00423.hp1 NA18945.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.907-649C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 3/3 | chr11 | 44265832 | ||||||
| chr11:44265844
|
T | C | 314 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0180others(311): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(318): Show |
intron_variant | MODIFIER | c.907-661A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 3/3 | chr11 | 44265844 | ||||||
| chr11:44265972
|
TG | T | 35 | a0001c0001t0001g0271a0001c0001t0001g0343a0001c0001t0002g0187others(32): Show | 35 | HG01099.hp1 HG01175.hp1 HG01257.hp2 others(32): Show |
intron_variant | MODIFIER | c.907-790delC | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 3/3 | chr11 | 44265972 | ||||||
| chr11:44266075
|
G | A | 2 | a0003c0006t0013g0033a0003c0006t0013g0041 | 2 | HG01109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.907-892C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 3/3 | chr11 | 44266075 | ||||||
| chr11:44266097
|
G | A | 1 | a0002c0003t0006g0148 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.907-914C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 3/3 | chr11 | 44266097 | ||||||
| chr11:44266120
|
T | C | 34 | a0001c0002t0003g0184a0001c0002t0003g0185a0001c0002t0003g0186others(31): Show | 34 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.907-937A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 3/3 | chr11 | 44266120 | ||||||
| chr11:44266131
|
G | A | 253 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0180others(250): Show | 260 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.907-948C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 3/3 | chr11 | 44266131 | ||||||
| chr11:44266144
|
C | T | 1 | a0001c0002t0016g0306 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.907-961G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 3/3 | chr11 | 44266144 | ||||||
| chr11:44266449
|
C | T | 7 | a0001c0002t0008g0321a0001c0002t0008g0354a0002c0004t0002g0076others(4): Show | 7 | HG00423.hp1 NA18945.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.906+1045G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 3/3 | chr11 | 44266449 | ||||||
| chr11:44266500
|
G | C | 39 | a0001c0002t0003g0184a0001c0002t0003g0185a0001c0002t0003g0186others(36): Show | 39 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.906+994C>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 3/3 | chr11 | 44266500 | ||||||
| chr11:44266510
|
A | G | 39 | a0001c0002t0003g0184a0001c0002t0003g0185a0001c0002t0003g0186others(36): Show | 39 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.906+984T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 3/3 | chr11 | 44266510 | ||||||
| chr11:44266617
|
A | T | 39 | a0001c0002t0003g0184a0001c0002t0003g0185a0001c0002t0003g0186others(36): Show | 39 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.906+877T>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 3/3 | chr11 | 44266617 | ||||||
| chr11:44266865
|
G | C | 39 | a0001c0002t0003g0184a0001c0002t0003g0185a0001c0002t0003g0186others(36): Show | 39 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.906+629C>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 3/3 | chr11 | 44266865 | ||||||
| chr11:44267168
|
G | A | 2 | a0001c0001t0002g0266a0001c0001t0002g0319 | 2 | NA18984.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.906+326C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 3/3 | chr11 | 44267168 | ||||||
| chr11:44267199
|
C | G | 1 | a0001c0002t0003g0351 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.906+295G>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 3/3 | chr11 | 44267199 | ||||||
| chr11:44267257
|
T | C | 2 | a0003c0006t0003g0039a0003c0014t0003g0040 | 2 | HG01884.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.906+237A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 3/3 | chr11 | 44267257 | ||||||
| chr11:44267296
|
C | T | 1 | a0001c0002t0033g0206 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.906+198G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 3/3 | chr11 | 44267296 | ||||||
| chr11:44267360
|
C | T | 1 | a0002c0003t0001g0098 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.906+134G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 3/3 | chr11 | 44267360 | ||||||
| chr11:44267394
|
C | T | 1 | a0001c0005t0060g0181 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.906+100G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 3/3 | chr11 | 44267394 | ||||||
| chr11:44267408
|
G | A | 6 | a0001c0002t0005g0337a0001c0002t0015g0205a0001c0002t0015g0346others(3): Show | 7 | HG01243.hp1 HG02257.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.906+86C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 3/3 | chr11 | 44267408 | ||||||
| chr11:44267437
|
C | A | 1 | a0001c0002t0013g0268 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.906+57G>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 3/3 | chr11 | 44267437 | ||||||
| chr11:44267450
|
C | T | 1 | a0003c0006t0009g0026 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.906+44G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 3/3 | chr11 | 44267450 | ||||||
| chr11:44267462
|
G | A | 5 | a0001c0002t0015g0205a0001c0002t0015g0346a0001c0002t0025g0004others(2): Show | 6 | HG01243.hp1 HG02257.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.906+32C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 3/3 | chr11 | 44267462 | ||||||
| chr11:44267633
|
C | T | 14 | a0001c0002t0011g0178a0001c0002t0011g0301a0001c0002t0027g0191others(11): Show | 14 | HG01168.hp2 HG01169.hp1 HG01978.hp2 others(11): Show |
intron_variant | MODIFIER | c.778-11G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44267633 | ||||||
| chr11:44267739
|
A | G | 303 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0180others(300): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(307): Show |
intron_variant | MODIFIER | c.778-117T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44267739 | ||||||
| chr11:44267762
|
C | G | 231 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0180others(228): Show | 238 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.778-140G>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44267762 | ||||||
| chr11:44267818
|
G | A | 1 | a0001c0001t0006g0196 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.778-196C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44267818 | ||||||
| chr11:44267833
|
C | G | 1 | a0006c0022t0009g0166 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.778-211G>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44267833 | ||||||
| chr11:44267885
|
G | C | 256 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0180others(253): Show | 263 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.778-263C>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44267885 | ||||||
| chr11:44267958
|
C | A | 1 | a0001c0001t0001g0227 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.778-336G>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44267958 | ||||||
| chr11:44268024
|
A | G | 1 | a0002c0003t0001g0097 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.778-402T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44268024 | ||||||
| chr11:44268086
|
C | G | 223 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0180others(220): Show | 229 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.778-464G>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44268086 | ||||||
| chr11:44268480
|
C | T | 1 | a0001c0002t0056g0367 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.778-858G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44268480 | ||||||
| chr11:44268516
|
T | C | 41 | a0001c0002t0003g0184a0001c0002t0003g0185a0001c0002t0003g0186others(38): Show | 41 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.778-894A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44268516 | ||||||
| chr11:44268576
|
T | C | 288 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0180others(285): Show | 294 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.778-954A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44268576 | ||||||
| chr11:44268699
|
T | A | 3 | a0002c0004t0002g0076a0002c0004t0002g0108a0002c0004t0008g0152 | 3 | NA18971.hp2 NA19005.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.778-1077A>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44268699 | ||||||
| chr11:44268753
|
C | T | 248 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0180others(245): Show | 254 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.778-1131G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44268753 | ||||||
| chr11:44268831
|
T | C | 289 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0180others(286): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.778-1209A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44268831 | ||||||
| chr11:44268915
|
T | C | 288 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0180others(285): Show | 294 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.778-1293A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44268915 | ||||||
| chr11:44268989
|
T | C | 1 | a0001c0002t0013g0268 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.778-1367A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44268989 | ||||||
| chr11:44268995
|
C | A | 39 | a0001c0002t0003g0184a0001c0002t0003g0185a0001c0002t0003g0186others(36): Show | 39 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.778-1373G>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44268995 | ||||||
| chr11:44269007
|
C | G | 2 | a0001c0002t0040g0280a0004c0009t0013g0171 | 2 | HG03139.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.778-1385G>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44269007 | ||||||
| chr11:44269037
|
C | T | 19 | a0001c0001t0001g0252a0001c0002t0011g0178a0001c0002t0011g0301others(16): Show | 20 | HG00099.hp2 HG00323.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.778-1415G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44269037 | ||||||
| chr11:44269103
|
T | C | 1 | a0001c0002t0056g0367 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.778-1481A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44269103 | ||||||
| chr11:44269123
|
G | T | 1 | a0001c0002t0013g0268 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.778-1501C>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44269123 | ||||||
| chr11:44269246
|
G | C | 2 | a0002c0004t0002g0076a0002c0004t0008g0152 | 2 | NA18971.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.778-1624C>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44269246 | ||||||
| chr11:44269277
|
G | A | 1 | a0004c0009t0009g0168 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.778-1655C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44269277 | ||||||
| chr11:44269516
|
G | A | 56 | a0001c0002t0003g0267a0001c0002t0009g0366a0001c0002t0040g0280others(53): Show | 58 | HG00408.hp2 HG00639.hp1 HG01106.hp1 others(55): Show |
intron_variant | MODIFIER | c.778-1894C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44269516 | ||||||
| chr11:44269571
|
T | C | 59 | a0001c0002t0003g0267a0001c0002t0009g0366a0001c0002t0040g0280others(56): Show | 61 | HG00408.hp2 HG00639.hp1 HG01106.hp1 others(58): Show |
intron_variant | MODIFIER | c.778-1949A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44269571 | ||||||
| chr11:44269588
|
A | G | 27 | a0001c0002t0005g0220a0001c0002t0005g0223a0001c0002t0005g0237others(24): Show | 27 | HG00423.hp1 HG00438.hp1 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.778-1966T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44269588 | ||||||
| chr11:44269606
|
G | A | 11 | a0001c0001t0001g0252a0001c0002t0011g0178a0001c0002t0011g0301others(8): Show | 11 | HG00099.hp2 HG00323.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.778-1984C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44269606 | ||||||
| chr11:44269610
|
C | T | 18 | a0001c0001t0001g0252a0001c0002t0011g0178a0001c0002t0011g0301others(15): Show | 19 | HG00099.hp2 HG00323.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.778-1988G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44269610 | ||||||
| chr11:44269836
|
A | G | 1 | a0001c0002t0006g0331 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.778-2214T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44269836 | ||||||
| chr11:44269905
|
C | T | 2 | a0001c0030t0026g0302a0003c0020t0026g0017 | 2 | HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.778-2283G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44269905 | ||||||
| chr11:44269934
|
A | G | 252 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0180others(249): Show | 258 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.778-2312T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44269934 | ||||||
| chr11:44270045
|
C | T | 19 | a0001c0001t0002g0190a0001c0001t0002g0235a0001c0001t0002g0240others(16): Show | 20 | HG00738.hp2 HG00741.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.778-2423G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44270045 | ||||||
| chr11:44270182
|
C | T | 12 | a0001c0001t0001g0252a0001c0002t0011g0178a0001c0002t0011g0301others(9): Show | 13 | HG00099.hp2 HG00323.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.778-2560G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44270182 | ||||||
| chr11:44270184
|
C | T | 12 | a0001c0001t0001g0252a0001c0002t0011g0178a0001c0002t0011g0301others(9): Show | 13 | HG00099.hp2 HG00323.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.778-2562G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44270184 | ||||||
| chr11:44270236
|
G | A | 40 | a0001c0002t0003g0267a0001c0002t0040g0280a0001c0005t0004g0309others(37): Show | 42 | HG00408.hp2 HG00639.hp1 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.778-2614C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44270236 | ||||||
| chr11:44270341
|
TGA | T | 30 | a0001c0001t0002g0279a0001c0002t0003g0184a0001c0002t0003g0185others(27): Show | 30 | HG00323.hp1 HG00544.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.778-2721_778-2720d others(4): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44270341 | ||||||
| chr11:44270376
|
G | A | 1 | a0001c0002t0052g0193 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.778-2754C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44270376 | ||||||
| chr11:44270603
|
C | T | 3 | a0001c0002t0011g0293a0001c0002t0011g0296a0003c0020t0026g0017 | 3 | HG02809.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.778-2981G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44270603 | ||||||
| chr11:44270617
|
C | T | 1 | a0001c0002t0006g0331 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.778-2995G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44270617 | ||||||
| chr11:44270671
|
C | A | 301 | a0001c0001t0001g0002a0001c0001t0001g0180a0001c0001t0001g0195others(298): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.778-3049G>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44270671 | ||||||
| chr11:44270898
|
G | A | 1 | a0001c0002t0003g0267 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.778-3276C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44270898 | ||||||
| chr11:44270966
|
G | A | 1 | a0002c0004t0005g0139 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.778-3344C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44270966 | ||||||
| chr11:44271036
|
C | T | 3 | a0001c0002t0015g0346a0003c0006t0015g0013a0003c0006t0032g0018 | 3 | HG02809.hp2 HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.778-3414G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44271036 | ||||||
| chr11:44271157
|
A | AC | 157 | a0001c0001t0001g0003a0001c0001t0001g0199a0001c0001t0001g0203others(154): Show | 160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.778-3536dupG | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44271157 | ||||||
| chr11:44271163
|
C | A | 1 | a0002c0003t0010g0163 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.778-3541G>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44271163 | ||||||
| chr11:44271163
|
C | CA | 217 | a0001c0001t0001g0002a0001c0001t0001g0180a0001c0001t0001g0195others(214): Show | 221 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.778-3542_778-3541i others(3): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44271163 | ||||||
| chr11:44271165
|
A | G | 1 | a0003c0006t0009g0023 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.778-3543T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44271165 | ||||||
| chr11:44271172
|
T | C | 2 | a0001c0002t0004g0210a0001c0002t0016g0306 | 2 | HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.778-3550A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44271172 | ||||||
| chr11:44271197
|
G | A | 52 | a0001c0001t0002g0233a0001c0001t0002g0256a0001c0002t0003g0261others(49): Show | 52 | HG00738.hp1 HG00738.hp2 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.778-3575C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44271197 | ||||||
| chr11:44271268
|
A | T | 117 | a0001c0001t0001g0180a0001c0001t0001g0195a0001c0001t0001g0211others(114): Show | 119 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.778-3646T>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44271268 | ||||||
| chr11:44271286
|
A | G | 3 | a0001c0002t0009g0366a0001c0002t0025g0004a0001c0005t0066g0263 | 4 | HG01243.hp1 HG02486.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.778-3664T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44271286 | ||||||
| chr11:44271314
|
G | A | 7 | a0001c0002t0013g0268a0004c0009t0009g0168a0004c0009t0009g0169others(4): Show | 7 | HG01243.hp2 HG02922.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.778-3692C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44271314 | ||||||
| chr11:44271344
|
G | A | 1 | a0003c0021t0027g0019 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.778-3722C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44271344 | ||||||
| chr11:44271366
|
T | C | 7 | a0001c0002t0013g0268a0004c0009t0009g0168a0004c0009t0009g0169others(4): Show | 7 | HG01243.hp2 HG02922.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.778-3744A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44271366 | ||||||
| chr11:44271456
|
C | T | 1 | a0002c0004t0020g0158 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.778-3834G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44271456 | ||||||
| chr11:44271500
|
C | T | 1 | a0003c0010t0048g0015 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.777+3848G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44271500 | ||||||
| chr11:44271591
|
T | C | 1 | a0003c0010t0001g0016 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.777+3757A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44271591 | ||||||
| chr11:44271712
|
G | A | 5 | a0001c0002t0004g0210a0001c0002t0007g0234a0001c0002t0007g0371others(2): Show | 5 | HG02615.hp2 HG03195.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.777+3636C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44271712 | ||||||
| chr11:44271716
|
G | A | 2 | a0002c0003t0001g0001a0002c0003t0010g0126 | 3 | HG02056.hp1 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.777+3632C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44271716 | ||||||
| chr11:44271780
|
C | T | 7 | a0001c0001t0002g0352a0001c0002t0015g0346a0003c0006t0009g0026others(4): Show | 7 | HG02258.hp2 HG02809.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.777+3568G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44271780 | ||||||
| chr11:44271781
|
G | A | 1 | a0002c0004t0003g0156 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.777+3567C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44271781 | ||||||
| chr11:44271798
|
T | C | 1 | a0001c0027t0050g0224 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.777+3550A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44271798 | ||||||
| chr11:44271799
|
T | C | 1 | a0001c0002t0009g0348 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.777+3549A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44271799 | ||||||
| chr11:44271847
|
C | T | 7 | a0001c0002t0009g0366a0001c0002t0025g0004a0001c0002t0040g0280others(4): Show | 8 | HG01243.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.777+3501G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44271847 | ||||||
| chr11:44271862
|
A | G | 364 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0180others(361): Show | 371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.777+3486T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44271862 | ||||||
| chr11:44271884
|
A | C | 109 | a0001c0001t0001g0248a0001c0001t0001g0257a0001c0001t0001g0271others(106): Show | 111 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.777+3464T>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44271884 | ||||||
| chr11:44271979
|
A | C | 114 | a0001c0001t0001g0248a0001c0001t0001g0257a0001c0001t0001g0271others(111): Show | 116 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.777+3369T>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44271979 | ||||||
| chr11:44272005
|
C | T | 4 | a0001c0011t0020g0265a0001c0027t0050g0224a0003c0014t0003g0040others(1): Show | 4 | HG01884.hp2 HG02809.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.777+3343G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44272005 | ||||||
| chr11:44272137
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.777+3211G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44272137 | ||||||
| chr11:44272205
|
G | A | 7 | a0001c0001t0001g0252a0001c0001t0043g0297a0001c0002t0015g0205others(4): Show | 7 | HG00099.hp2 HG01256.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.777+3143C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44272205 | ||||||
| chr11:44272276
|
T | TG | 359 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0180others(356): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.777+3071dupC | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44272276 | ||||||
| chr11:44272364
|
T | G | 1 | a0001c0002t0008g0354 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.777+2984A>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44272364 | ||||||
| chr11:44272419
|
G | A | 1 | a0001c0001t0002g0352 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.777+2929C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44272419 | ||||||
| chr11:44272475
|
G | A | 113 | a0001c0001t0001g0248a0001c0001t0001g0257a0001c0001t0001g0271others(110): Show | 116 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.777+2873C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44272475 | ||||||
| chr11:44272502
|
TA | T | 84 | a0001c0001t0001g0003a0001c0001t0001g0199a0001c0001t0001g0203others(81): Show | 85 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.777+2845delT | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44272502 | ||||||
| chr11:44272502
|
TAA | T | 113 | a0001c0001t0001g0248a0001c0001t0001g0257a0001c0001t0001g0271others(110): Show | 116 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.777+2844_777+2845d others(4): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44272502 | ||||||
| chr11:44272738
|
G | T | 1 | a0001c0005t0006g0232 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.777+2610C>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44272738 | ||||||
| chr11:44272776
|
T | A | 6 | a0001c0001t0001g0310a0001c0002t0003g0267a0003c0013t0001g0009others(3): Show | 6 | HG02300.hp2 HG02602.hp1 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.777+2572A>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44272776 | ||||||
| chr11:44272780
|
A | G | 1 | a0001c0002t0011g0301 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.777+2568T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44272780 | ||||||
| chr11:44272823
|
TA | T | 61 | a0001c0001t0001g0003a0001c0001t0001g0199a0001c0001t0001g0203others(58): Show | 62 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.777+2524delT | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44272823 | ||||||
| chr11:44273069
|
G | A | 2 | a0003c0006t0013g0033a0003c0006t0013g0041 | 2 | HG01109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.777+2279C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44273069 | ||||||
| chr11:44273085
|
G | A | 80 | a0001c0001t0001g0003a0001c0001t0001g0199a0001c0001t0001g0203others(77): Show | 81 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(78): Show |
intron_variant | MODIFIER | c.777+2263C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44273085 | ||||||
| chr11:44273089
|
A | T | 3 | a0004c0009t0007g0170a0004c0009t0013g0171a0004c0009t0016g0175 | 3 | HG02572.hp2 HG03139.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.777+2259T>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44273089 | ||||||
| chr11:44273190
|
TA | T | 176 | a0001c0001t0001g0003a0001c0001t0001g0199a0001c0001t0001g0203others(173): Show | 178 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.777+2157delT | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44273190 | ||||||
| chr11:44273190
|
TAA | T | 127 | a0001c0001t0001g0002a0001c0001t0001g0201a0001c0001t0001g0219others(124): Show | 131 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.777+2156_777+2157d others(4): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44273190 | ||||||
| chr11:44273193
|
A | T | 17 | a0001c0001t0001g0252a0001c0001t0043g0297a0001c0002t0004g0210others(14): Show | 17 | HG00099.hp2 HG00639.hp2 HG01258.hp2 others(14): Show |
intron_variant | MODIFIER | c.777+2155T>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44273193 | ||||||
| chr11:44273194
|
A | T | 1 | a0003c0010t0012g0029 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.777+2154T>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44273194 | ||||||
| chr11:44273458
|
G | A | 1 | a0001c0001t0002g0256 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.777+1890C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44273458 | ||||||
| chr11:44273499
|
G | A | 21 | a0001c0001t0001g0252a0001c0001t0043g0297a0001c0002t0004g0210others(18): Show | 21 | HG00099.hp2 HG00639.hp2 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.777+1849C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44273499 | ||||||
| chr11:44273585
|
C | T | 1 | a0002c0003t0005g0082 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.777+1763G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44273585 | ||||||
| chr11:44273606
|
G | A | 1 | a0001c0002t0052g0193 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.777+1742C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44273606 | ||||||
| chr11:44273631
|
G | A | 1 | a0003c0006t0032g0018 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.777+1717C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44273631 | ||||||
| chr11:44273779
|
C | T | 182 | a0001c0001t0001g0003a0001c0001t0001g0199a0001c0001t0001g0203others(179): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.777+1569G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44273779 | ||||||
| chr11:44273814
|
G | A | 5 | a0001c0005t0006g0377a0002c0003t0001g0102a0002c0003t0001g0115others(2): Show | 5 | HG02293.hp2 NA18983.hp2 NA19009.hp1 others(2): Show |
intron_variant | MODIFIER | c.777+1534C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44273814 | ||||||
| chr11:44273859
|
G | A | 1 | a0003c0014t0030g0014 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.777+1489C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44273859 | ||||||
| chr11:44273996
|
C | T | 8 | a0001c0001t0001g0250a0001c0001t0017g0357a0001c0002t0006g0323others(5): Show | 8 | HG00140.hp1 HG00741.hp2 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.777+1352G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44273996 | ||||||
| chr11:44274193
|
G | A | 1 | a0002c0003t0001g0142 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.777+1155C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44274193 | ||||||
| chr11:44274285
|
C | T | 4 | a0001c0011t0020g0265a0001c0027t0050g0224a0003c0014t0003g0040others(1): Show | 4 | HG01884.hp2 HG02809.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.777+1063G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44274285 | ||||||
| chr11:44274357
|
C | T | 193 | a0001c0001t0001g0003a0001c0001t0001g0199a0001c0001t0001g0203others(190): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.777+991G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44274357 | ||||||
| chr11:44274452
|
T | G | 189 | a0001c0001t0001g0003a0001c0001t0001g0199a0001c0001t0001g0203others(186): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.777+896A>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44274452 | ||||||
| chr11:44274453
|
C | T | 3 | a0004c0009t0007g0170a0004c0009t0013g0171a0004c0009t0016g0175 | 3 | HG02572.hp2 HG03139.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.777+895G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44274453 | ||||||
| chr11:44274463
|
G | C | 2 | a0002c0003t0001g0068a0002c0004t0037g0091 | 2 | HG02071.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.777+885C>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44274463 | ||||||
| chr11:44274493
|
T | C | 2 | a0001c0001t0004g0330a0001c0001t0004g0332 | 2 | NA18939.hp1 NA18949.hp1 |
intron_variant | MODIFIER | c.777+855A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44274493 | ||||||
| chr11:44274601
|
G | T | 1 | a0001c0001t0001g0303 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.777+747C>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44274601 | ||||||
| chr11:44274618
|
A | G | 1 | a0004c0009t0011g0176 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.777+730T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44274618 | ||||||
| chr11:44274638
|
G | A | 1 | a0001c0002t0052g0193 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.777+710C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44274638 | ||||||
| chr11:44274663
|
T | C | 182 | a0001c0001t0001g0003a0001c0001t0001g0199a0001c0001t0001g0203others(179): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.777+685A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44274663 | ||||||
| chr11:44274840
|
C | T | 186 | a0001c0001t0001g0003a0001c0001t0001g0199a0001c0001t0001g0203others(183): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.777+508G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44274840 | ||||||
| chr11:44274878
|
G | A | 5 | a0003c0006t0003g0039a0003c0006t0009g0023a0003c0006t0011g0031others(2): Show | 5 | HG01109.hp1 HG02451.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.777+470C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44274878 | ||||||
| chr11:44274931
|
C | T | 369 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0180others(366): Show | 376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.777+417G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44274931 | ||||||
| chr11:44274943
|
G | A | 193 | a0001c0001t0001g0003a0001c0001t0001g0199a0001c0001t0001g0203others(190): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.777+405C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44274943 | ||||||
| chr11:44274988
|
C | G | 1 | a0001c0001t0001g0310 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.777+360G>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44274988 | ||||||
| chr11:44275041
|
T | C | 359 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0180others(356): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.777+307A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44275041 | ||||||
| chr11:44275076
|
C | A | 1 | a0001c0002t0030g0204 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.777+272G>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44275076 | ||||||
| chr11:44275133
|
G | A | 1 | a0001c0005t0064g0217 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.777+215C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44275133 | ||||||
| chr11:44275278
|
C | T | 169 | a0001c0001t0001g0003a0001c0001t0001g0199a0001c0001t0001g0203others(166): Show | 173 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.777+70G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44275278 | ||||||
| chr11:44275294
|
G | A | 7 | a0001c0001t0002g0352a0001c0002t0015g0346a0003c0006t0009g0026others(4): Show | 7 | HG02258.hp2 HG02809.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.777+54C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44275294 | ||||||
| chr11:44275703
|
A | G | 359 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0180others(356): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.467-45T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44275703 | ||||||
| chr11:44275733
|
G | A | 1 | a0001c0001t0001g0378 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.467-75C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44275733 | ||||||
| chr11:44275742
|
G | A | 1 | a0001c0002t0021g0260 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.467-84C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44275742 | ||||||
| chr11:44275793
|
C | A | 376 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0180others(373): Show | 383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
intron_variant | MODIFIER | c.467-135G>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44275793 | ||||||
| chr11:44275917
|
G | A | 2 | a0001c0011t0003g0294a0001c0011t0031g0209 | 2 | HG01192.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.467-259C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44275917 | ||||||
| chr11:44275928
|
G | A | 106 | a0001c0001t0001g0248a0001c0001t0001g0257a0001c0001t0001g0271others(103): Show | 108 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.467-270C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44275928 | ||||||
| chr11:44275934
|
A | G | 7 | a0001c0002t0009g0366a0001c0002t0025g0004a0001c0002t0040g0280others(4): Show | 8 | HG01243.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.467-276T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44275934 | ||||||
| chr11:44276058
|
G | A | 21 | a0001c0001t0002g0187a0001c0001t0002g0342a0001c0001t0002g0352others(18): Show | 21 | HG01123.hp1 HG01361.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.467-400C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44276058 | ||||||
| chr11:44276076
|
T | A | 1 | a0002c0003t0001g0124 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.467-418A>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44276076 | ||||||
| chr11:44276125
|
G | C | 363 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0180others(360): Show | 370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.467-467C>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44276125 | ||||||
| chr11:44276222
|
G | A | 1 | a0001c0011t0020g0265 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.467-564C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44276222 | ||||||
| chr11:44276229
|
A | T | 1 | a0002c0003t0001g0073 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.467-571T>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44276229 | ||||||
| chr11:44276339
|
G | C | 1 | a0002c0003t0001g0098 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.467-681C>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44276339 | ||||||
| chr11:44276359
|
ACT | A | 12 | a0001c0001t0001g0252a0001c0001t0043g0297a0001c0002t0004g0210others(9): Show | 12 | HG00099.hp2 HG01256.hp2 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.467-703_467-702del others(2): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44276359 | ||||||
| chr11:44276379
|
G | A | 101 | a0001c0001t0001g0002a0001c0001t0001g0201a0001c0001t0001g0219others(98): Show | 103 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.467-721C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44276379 | ||||||
| chr11:44276400
|
G | A | 1 | a0006c0022t0009g0166 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.467-742C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44276400 | ||||||
| chr11:44276443
|
G | C | 1 | a0001c0001t0001g0203 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.467-785C>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44276443 | ||||||
| chr11:44276588
|
C | T | 6 | a0002c0003t0001g0062a0002c0003t0001g0130a0002c0004t0003g0122others(3): Show | 6 | HG00280.hp1 HG01358.hp2 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.467-930G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44276588 | ||||||
| chr11:44276592
|
C | T | 8 | a0001c0007t0003g0298a0001c0007t0004g0253a0001c0007t0004g0282others(5): Show | 8 | HG00738.hp2 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.467-934G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44276592 | ||||||
| chr11:44276749
|
C | T | 1 | a0002c0003t0001g0062 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.467-1091G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44276749 | ||||||
| chr11:44276834
|
C | T | 7 | a0001c0002t0009g0366a0001c0002t0025g0004a0001c0002t0040g0280others(4): Show | 8 | HG01243.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.467-1176G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44276834 | ||||||
| chr11:44276904
|
C | T | 10 | a0001c0001t0001g0252a0001c0001t0043g0297a0001c0002t0004g0210others(7): Show | 10 | HG00099.hp2 HG01256.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.467-1246G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44276904 | ||||||
| chr11:44276926
|
C | G | 1 | a0004c0009t0013g0171 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.467-1268G>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44276926 | ||||||
| chr11:44276935
|
A | G | 1 | a0004c0009t0013g0171 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.467-1277T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44276935 | ||||||
| chr11:44276947
|
T | C | 2 | a0001c0007t0008g0295a0001c0029t0001g0243 | 2 | HG00738.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.467-1289A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44276947 | ||||||
| chr11:44277049
|
G | T | 11 | a0001c0001t0001g0252a0001c0001t0043g0297a0001c0002t0004g0210others(8): Show | 11 | HG00099.hp2 HG01256.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.467-1391C>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44277049 | ||||||
| chr11:44277068
|
C | A | 1 | a0002c0004t0005g0090 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.467-1410G>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44277068 | ||||||
| chr11:44277070
|
C | T | 1 | a0004c0009t0011g0176 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.467-1412G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44277070 | ||||||
| chr11:44277071
|
G | A | 280 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0201others(277): Show | 285 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.467-1413C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44277071 | ||||||
| chr11:44277164
|
T | C | 2 | a0001c0011t0003g0294a0001c0011t0031g0209 | 2 | HG01192.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.467-1506A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44277164 | ||||||
| chr11:44277190
|
A | G | 1 | a0002c0003t0001g0095 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.467-1532T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44277190 | ||||||
| chr11:44277291
|
G | A | 2 | a0001c0011t0003g0294a0001c0011t0031g0209 | 2 | HG01192.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.467-1633C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44277291 | ||||||
| chr11:44277313
|
G | A | 1 | a0001c0002t0005g0223 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.467-1655C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44277313 | ||||||
| chr11:44277378
|
G | A | 1 | a0001c0002t0007g0356 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.467-1720C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44277378 | ||||||
| chr11:44277450
|
C | T | 1 | a0002c0004t0006g0127 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.467-1792G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44277450 | ||||||
| chr11:44277511
|
C | T | 4 | a0001c0011t0020g0265a0001c0027t0050g0224a0003c0014t0003g0040others(1): Show | 4 | HG01884.hp2 HG02809.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.467-1853G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44277511 | ||||||
| chr11:44277688
|
G | A | 2 | a0001c0002t0021g0260a0001c0031t0002g0381 | 2 | HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.467-2030C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44277688 | ||||||
| chr11:44277712
|
C | G | 6 | a0001c0011t0003g0294a0001c0011t0020g0265a0001c0011t0031g0209others(3): Show | 6 | HG01192.hp1 HG01433.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.467-2054G>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44277712 | ||||||
| chr11:44277875
|
C | A | 1 | a0001c0002t0011g0178 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.467-2217G>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44277875 | ||||||
| chr11:44277941
|
G | T | 13 | a0001c0001t0001g0252a0001c0001t0043g0297a0001c0002t0004g0210others(10): Show | 13 | HG00099.hp2 HG01256.hp2 HG01258.hp2 others(10): Show |
intron_variant | MODIFIER | c.467-2283C>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44277941 | ||||||
| chr11:44278011
|
GT | G | 114 | a0001c0001t0001g0003a0001c0001t0001g0203a0001c0001t0001g0227others(111): Show | 116 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(113): Show |
intron_variant | MODIFIER | c.467-2354delA | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44278011 | ||||||
| chr11:44278119
|
G | A | 1 | a0002c0004t0004g0151 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.467-2461C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44278119 | ||||||
| chr11:44278121
|
C | T | 4 | a0002c0003t0006g0148a0002c0004t0005g0090a0002c0004t0005g0093others(1): Show | 4 | HG00438.hp1 HG02027.hp1 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.467-2463G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44278121 | ||||||
| chr11:44278163
|
C | T | 8 | a0004c0009t0007g0170a0004c0009t0009g0168a0004c0009t0009g0169others(5): Show | 8 | HG01243.hp2 HG02572.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.467-2505G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44278163 | ||||||
| chr11:44278235
|
G | A | 16 | a0001c0002t0013g0268a0002c0003t0001g0062a0002c0003t0001g0130others(13): Show | 16 | HG00280.hp1 HG01243.hp2 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.467-2577C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44278235 | ||||||
| chr11:44278267
|
G | GT | 13 | a0001c0001t0001g0252a0001c0001t0043g0297a0001c0002t0004g0210others(10): Show | 13 | HG00099.hp2 HG01256.hp2 HG01258.hp2 others(10): Show |
intron_variant | MODIFIER | c.467-2610_467-2609i others(3): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44278267 | ||||||
| chr11:44278291
|
G | A | 114 | a0001c0001t0001g0248a0001c0001t0001g0257a0001c0001t0001g0271others(111): Show | 116 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.467-2633C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44278291 | ||||||
| chr11:44278359
|
C | G | 326 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0201others(323): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.467-2701G>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44278359 | ||||||
| chr11:44278492
|
C | T | 280 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0201others(277): Show | 286 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.467-2834G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44278492 | ||||||
| chr11:44278507
|
C | T | 1 | a0001c0027t0050g0224 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.467-2849G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44278507 | ||||||
| chr11:44278806
|
A | G | 1 | a0001c0002t0007g0356 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.467-3148T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44278806 | ||||||
| chr11:44278932
|
T | C | 2 | a0002c0003t0005g0082a0002c0003t0005g0099 | 2 | NA18984.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.467-3274A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44278932 | ||||||
| chr11:44279225
|
G | A | 5 | a0003c0006t0009g0026a0003c0006t0015g0013a0003c0006t0032g0018others(2): Show | 5 | HG02258.hp2 HG02809.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.467-3567C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44279225 | ||||||
| chr11:44279320
|
C | T | 1 | a0002c0003t0001g0147 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.467-3662G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44279320 | ||||||
| chr11:44279359
|
CCT | C | 3 | a0003c0006t0003g0039a0003c0006t0013g0033a0003c0006t0013g0041 | 3 | HG01109.hp1 HG02451.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.467-3703_467-3702d others(4): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44279359 | ||||||
| chr11:44279505
|
G | A | 1 | a0007c0018t0001g0011 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.467-3847C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44279505 | ||||||
| chr11:44279535
|
G | GACGCAGA others(6): Show |
5 | a0002c0003t0001g0130a0002c0004t0003g0122a0002c0004t0003g0156others(2): Show | 5 | HG00280.hp1 HG01358.hp2 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.467-3878_467-3877i others(15): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44279535 | ||||||
| chr11:44279536
|
C | T | 5 | a0002c0003t0001g0130a0002c0004t0003g0122a0002c0004t0003g0156others(2): Show | 5 | HG00280.hp1 HG01358.hp2 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.467-3878G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44279536 | ||||||
| chr11:44279602
|
A | C | 1 | a0002c0004t0002g0106 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.467-3944T>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44279602 | ||||||
| chr11:44279644
|
C | T | 3 | a0001c0011t0020g0265a0001c0027t0050g0224a0003c0020t0026g0017 | 3 | HG02809.hp1 HG02976.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.467-3986G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44279644 | ||||||
| chr11:44279736
|
G | A | 4 | a0001c0001t0043g0297a0001c0002t0015g0205a0003c0006t0003g0021others(1): Show | 4 | HG01884.hp1 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.467-4078C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44279736 | ||||||
| chr11:44279743
|
C | T | 5 | a0002c0003t0001g0130a0002c0004t0003g0122a0002c0004t0003g0156others(2): Show | 5 | HG00280.hp1 HG01358.hp2 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.467-4085G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44279743 | ||||||
| chr11:44279825
|
C | T | 7 | a0001c0001t0001g0252a0001c0001t0043g0297a0001c0002t0015g0205others(4): Show | 7 | HG00099.hp2 HG01256.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.467-4167G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44279825 | ||||||
| chr11:44279837
|
G | A | 1 | a0002c0003t0001g0098 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.467-4179C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44279837 | ||||||
| chr11:44279903
|
C | A | 25 | a0001c0001t0001g0252a0001c0001t0043g0297a0001c0002t0004g0210others(22): Show | 25 | HG00099.hp2 HG00280.hp1 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.467-4245G>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44279903 | ||||||
| chr11:44279921
|
G | A | 2 | a0001c0002t0003g0261a0001c0002t0003g0262 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.467-4263C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44279921 | ||||||
| chr11:44279964
|
C | T | 1 | a0001c0001t0002g0342 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.467-4306G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44279964 | ||||||
| chr11:44280038
|
A | G | 1 | a0003c0021t0027g0019 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.467-4380T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44280038 | ||||||
| chr11:44280112
|
G | A | 3 | a0002c0003t0010g0126a0002c0004t0014g0070a0002c0004t0014g0164 | 3 | HG01168.hp2 HG01169.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.467-4454C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44280112 | ||||||
| chr11:44280118
|
A | T | 2 | a0001c0002t0004g0307a0001c0002t0004g0308 | 2 | HG01099.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.467-4460T>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44280118 | ||||||
| chr11:44280263
|
G | A | 299 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0201others(296): Show | 306 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(303): Show |
intron_variant | MODIFIER | c.467-4605C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44280263 | ||||||
| chr11:44280312
|
G | T | 1 | a0001c0002t0001g0379 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.467-4654C>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44280312 | ||||||
| chr11:44280365
|
G | A | 1 | a0001c0002t0007g0234 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.467-4707C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44280365 | ||||||
| chr11:44280420
|
G | A | 11 | a0001c0002t0009g0366a0001c0002t0025g0004a0001c0002t0052g0193others(8): Show | 12 | HG00280.hp1 HG01192.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.467-4762C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44280420 | ||||||
| chr11:44280456
|
C | T | 1 | a0004c0009t0013g0171 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.467-4798G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44280456 | ||||||
| chr11:44280464
|
G | A | 1 | a0002c0004t0005g0058 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.467-4806C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44280464 | ||||||
| chr11:44280531
|
C | G | 2 | a0003c0015t0029g0034a0003c0015t0029g0037 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.467-4873G>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44280531 | ||||||
| chr11:44280603
|
A | G | 3 | a0001c0002t0007g0234a0001c0002t0007g0371a0001c0002t0057g0334 | 3 | HG03195.hp1 HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.467-4945T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44280603 | ||||||
| chr11:44280604
|
T | C | 230 | a0001c0001t0001g0002a0001c0001t0001g0201a0001c0001t0001g0219others(227): Show | 234 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.467-4946A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44280604 | ||||||
| chr11:44280694
|
T | C | 114 | a0001c0001t0001g0002a0001c0001t0001g0201a0001c0001t0001g0219others(111): Show | 116 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.467-5036A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44280694 | ||||||
| chr11:44280730
|
C | T | 2 | a0001c0011t0003g0294a0001c0011t0031g0209 | 2 | HG01192.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.467-5072G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44280730 | ||||||
| chr11:44280761
|
T | C | 250 | a0001c0001t0001g0002a0001c0001t0001g0201a0001c0001t0001g0219others(247): Show | 254 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(251): Show |
intron_variant | MODIFIER | c.467-5103A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44280761 | ||||||
| chr11:44280788
|
G | A | 100 | a0001c0001t0001g0002a0001c0001t0001g0201a0001c0001t0001g0219others(97): Show | 102 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.467-5130C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44280788 | ||||||
| chr11:44280841
|
C | G | 1 | a0001c0002t0013g0268 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.467-5183G>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44280841 | ||||||
| chr11:44281136
|
G | A | 243 | a0001c0001t0001g0002a0001c0001t0001g0201a0001c0001t0001g0219others(240): Show | 247 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(244): Show |
intron_variant | MODIFIER | c.467-5478C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44281136 | ||||||
| chr11:44281197
|
G | C | 2 | a0001c0001t0017g0357a0001c0002t0006g0323 | 2 | HG01123.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.467-5539C>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44281197 | ||||||
| chr11:44281315
|
C | T | 24 | a0001c0001t0001g0003a0001c0001t0001g0203a0001c0001t0001g0227others(21): Show | 25 | HG00609.hp1 HG01069.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.467-5657G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44281315 | ||||||
| chr11:44281344
|
C | T | 1 | a0001c0001t0001g0248 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.467-5686G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44281344 | ||||||
| chr11:44281357
|
G | T | 3 | a0002c0003t0002g0118a0002c0004t0007g0043a0002c0008t0051g0059 | 3 | HG01346.hp2 HG01361.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.467-5699C>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44281357 | ||||||
| chr11:44281375
|
G | A | 1 | a0001c0001t0001g0211 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.467-5717C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44281375 | ||||||
| chr11:44281486
|
C | G | 6 | a0001c0001t0002g0190a0001c0002t0040g0280a0001c0002t0052g0193others(3): Show | 6 | HG02559.hp1 HG02886.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.467-5828G>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44281486 | ||||||
| chr11:44281521
|
A | G | 1 | a0003c0020t0026g0017 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.467-5863T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44281521 | ||||||
| chr11:44281569
|
C | T | 1 | a0002c0003t0001g0081 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.467-5911G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44281569 | ||||||
| chr11:44281575
|
G | A | 1 | a0002c0003t0001g0102 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.467-5917C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44281575 | ||||||
| chr11:44281584
|
G | A | 1 | a0002c0003t0001g0153 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.467-5926C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44281584 | ||||||
| chr11:44281609
|
G | A | 7 | a0001c0007t0003g0298a0001c0007t0004g0282a0001c0007t0004g0299others(4): Show | 7 | HG02145.hp2 HG02622.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.467-5951C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44281609 | ||||||
| chr11:44281620
|
G | C | 1 | a0001c0001t0002g0352 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.467-5962C>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44281620 | ||||||
| chr11:44281671
|
G | A | 1 | a0001c0001t0017g0359 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.467-6013C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44281671 | ||||||
| chr11:44281857
|
C | T | 108 | a0001c0001t0001g0002a0001c0001t0001g0201a0001c0001t0001g0219others(105): Show | 110 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.467-6199G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44281857 | ||||||
| chr11:44281924
|
G | C | 1 | a0001c0012t0006g0251 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.467-6266C>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44281924 | ||||||
| chr11:44282326
|
G | A | 13 | a0001c0001t0001g0373a0001c0001t0001g0374a0001c0002t0003g0184others(10): Show | 13 | HG00099.hp1 HG01069.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.467-6668C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44282326 | ||||||
| chr11:44282352
|
AC | A | 108 | a0001c0001t0001g0002a0001c0001t0001g0201a0001c0001t0001g0219others(105): Show | 110 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.467-6695delG | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44282352 | ||||||
| chr11:44282454
|
C | A | 126 | a0001c0001t0001g0248a0001c0001t0001g0250a0001c0001t0001g0252others(123): Show | 128 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.467-6796G>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44282454 | ||||||
| chr11:44282551
|
A | T | 13 | a0001c0001t0001g0373a0001c0001t0001g0374a0001c0002t0003g0184others(10): Show | 13 | HG00099.hp1 HG01069.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.467-6893T>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44282551 | ||||||
| chr11:44282558
|
C | T | 1 | a0002c0003t0001g0119 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.467-6900G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44282558 | ||||||
| chr11:44282603
|
C | T | 1 | a0002c0008t0004g0086 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.467-6945G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44282603 | ||||||
| chr11:44282687
|
G | T | 1 | a0001c0002t0013g0268 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.467-7029C>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44282687 | ||||||
| chr11:44282726
|
T | C | 110 | a0001c0001t0001g0002a0001c0001t0001g0201a0001c0001t0001g0219others(107): Show | 112 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.467-7068A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44282726 | ||||||
| chr11:44282834
|
G | T | 3 | a0001c0002t0009g0366a0001c0002t0025g0004a0001c0002t0056g0367 | 4 | HG01243.hp1 HG02486.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.467-7176C>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44282834 | ||||||
| chr11:44282888
|
T | A | 1 | a0001c0027t0050g0224 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.467-7230A>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44282888 | ||||||
| chr11:44283064
|
C | T | 1 | a0002c0003t0001g0064 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.467-7406G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44283064 | ||||||
| chr11:44283083
|
C | A | 3 | a0001c0001t0001g0180a0001c0001t0002g0188a0001c0005t0060g0181 | 3 | NA19002.hp1 NA19007.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.467-7425G>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44283083 | ||||||
| chr11:44283101
|
G | A | 1 | a0001c0027t0050g0224 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.467-7443C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44283101 | ||||||
| chr11:44283103
|
C | T | 1 | a0001c0002t0013g0268 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.467-7445G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44283103 | ||||||
| chr11:44283247
|
C | CA | 23 | a0001c0001t0001g0272a0001c0001t0002g0190a0001c0001t0004g0194others(20): Show | 24 | HG01175.hp2 HG01243.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.467-7590dupT | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44283247 | ||||||
| chr11:44283247
|
CA | C | 111 | a0001c0001t0001g0002a0001c0001t0001g0201a0001c0001t0001g0219others(108): Show | 114 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.467-7590delT | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44283247 | ||||||
| chr11:44283291
|
T | A | 1 | a0001c0027t0050g0224 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.467-7633A>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44283291 | ||||||
| chr11:44283337
|
T | C | 7 | a0001c0002t0007g0264a0001c0002t0007g0341a0001c0002t0011g0293others(4): Show | 7 | HG02145.hp1 HG02451.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.467-7679A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44283337 | ||||||
| chr11:44283471
|
C | T | 4 | a0003c0006t0009g0026a0003c0006t0015g0013a0003c0006t0032g0018others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.467-7813G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44283471 | ||||||
| chr11:44283667
|
G | A | 2 | a0003c0015t0029g0034a0003c0015t0029g0037 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.467-8009C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44283667 | ||||||
| chr11:44283721
|
AC | A | 5 | a0002c0003t0001g0130a0002c0004t0003g0122a0002c0004t0003g0156others(2): Show | 5 | HG00280.hp1 HG01358.hp2 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.467-8064delG | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44283721 | ||||||
| chr11:44283852
|
C | T | 10 | a0004c0009t0007g0170a0004c0009t0009g0168a0004c0009t0009g0169others(7): Show | 10 | HG01243.hp2 HG02572.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.467-8194G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44283852 | ||||||
| chr11:44283875
|
T | C | 1 | a0001c0002t0013g0268 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.467-8217A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44283875 | ||||||
| chr11:44283989
|
T | C | 1 | a0002c0003t0001g0153 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.467-8331A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44283989 | ||||||
| chr11:44284003
|
T | C | 23 | a0001c0001t0001g0250a0001c0001t0001g0252a0001c0001t0002g0233others(20): Show | 24 | HG00099.hp2 HG00738.hp1 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.467-8345A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44284003 | ||||||
| chr11:44284217
|
T | G | 57 | a0001c0001t0001g0003a0001c0001t0001g0203a0001c0001t0001g0227others(54): Show | 60 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.467-8559A>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44284217 | ||||||
| chr11:44284463
|
A | G | 1 | a0002c0003t0001g0124 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.467-8805T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44284463 | ||||||
| chr11:44284569
|
C | A | 1 | a0001c0027t0050g0224 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.467-8911G>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44284569 | ||||||
| chr11:44284574
|
G | T | 1 | a0001c0001t0001g0324 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.467-8916C>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44284574 | ||||||
| chr11:44284595
|
C | A | 1 | a0001c0027t0050g0224 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.467-8937G>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44284595 | ||||||
| chr11:44284618
|
C | T | 1 | a0001c0002t0005g0237 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.467-8960G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44284618 | ||||||
| chr11:44284627
|
C | T | 13 | a0001c0001t0001g0373a0001c0001t0001g0374a0001c0002t0003g0184others(10): Show | 13 | HG00099.hp1 HG01069.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.467-8969G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44284627 | ||||||
| chr11:44284637
|
C | T | 1 | a0002c0003t0047g0114 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.467-8979G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44284637 | ||||||
| chr11:44284697
|
C | T | 3 | a0001c0002t0009g0366a0001c0002t0025g0004a0001c0002t0056g0367 | 4 | HG01243.hp1 HG02486.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.467-9039G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44284697 | ||||||
| chr11:44284831
|
C | T | 119 | a0001c0001t0001g0248a0001c0001t0001g0250a0001c0001t0001g0252others(116): Show | 121 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.467-9173G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44284831 | ||||||
| chr11:44284832
|
G | A | 1 | a0002c0004t0001g0133 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.467-9174C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44284832 | ||||||
| chr11:44284911
|
A | G | 1 | a0001c0002t0003g0207 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.467-9253T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44284911 | ||||||
| chr11:44284918
|
TAC | T | 10 | a0004c0009t0007g0170a0004c0009t0009g0168a0004c0009t0009g0169others(7): Show | 10 | HG01243.hp2 HG02572.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.467-9262_467-9261d others(4): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44284918 | ||||||
| chr11:44284924
|
C | T | 5 | a0001c0001t0002g0190a0001c0002t0040g0280a0001c0005t0066g0263others(2): Show | 5 | HG02559.hp1 HG02886.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.467-9266G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44284924 | ||||||
| chr11:44285029
|
C | A | 330 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0180others(327): Show | 337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.467-9371G>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44285029 | ||||||
| chr11:44285098
|
G | T | 1 | a0001c0027t0050g0224 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.467-9440C>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44285098 | ||||||
| chr11:44285328
|
C | T | 3 | a0001c0002t0007g0264a0001c0002t0013g0268a0001c0027t0050g0224 | 3 | HG02622.hp1 HG03130.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.467-9670G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44285328 | ||||||
| chr11:44285332
|
C | T | 255 | a0001c0001t0001g0002a0001c0001t0001g0201a0001c0001t0001g0219others(252): Show | 259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.467-9674G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44285332 | ||||||
| chr11:44285357
|
C | T | 125 | a0001c0001t0001g0002a0001c0001t0001g0201a0001c0001t0001g0219others(122): Show | 127 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.467-9699G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44285357 | ||||||
| chr11:44285406
|
A | G | 16 | a0001c0002t0052g0193a0003c0006t0009g0026a0003c0006t0015g0013others(13): Show | 16 | HG01243.hp2 HG01884.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.467-9748T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44285406 | ||||||
| chr11:44285468
|
C | T | 9 | a0001c0001t0002g0190a0001c0002t0011g0293a0001c0002t0011g0296others(6): Show | 9 | HG02559.hp1 HG02818.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.467-9810G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44285468 | ||||||
| chr11:44285501
|
A | G | 1 | a0002c0004t0037g0091 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.467-9843T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44285501 | ||||||
| chr11:44285697
|
T | A | 5 | a0003c0006t0009g0026a0003c0006t0015g0013a0003c0006t0032g0018others(2): Show | 5 | HG01884.hp2 HG02258.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.467-10039A>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44285697 | ||||||
| chr11:44285975
|
G | A | 1 | a0002c0008t0005g0046 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.467-10317C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44285975 | ||||||
| chr11:44286092
|
T | C | 11 | a0001c0002t0052g0193a0004c0009t0007g0170a0004c0009t0009g0168others(8): Show | 11 | HG01243.hp2 HG02572.hp2 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.467-10434A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44286092 | ||||||
| chr11:44286212
|
G | A | 1 | a0001c0002t0007g0249 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.467-10554C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44286212 | ||||||
| chr11:44286306
|
T | C | 1 | a0002c0004t0002g0076 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.467-10648A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44286306 | ||||||
| chr11:44286343
|
G | A | 1 | a0001c0001t0001g0271 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.467-10685C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44286343 | ||||||
| chr11:44286389
|
T | C | 12 | a0001c0002t0013g0268a0001c0002t0052g0193a0004c0009t0007g0170others(9): Show | 12 | HG01243.hp2 HG02572.hp2 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.467-10731A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44286389 | ||||||
| chr11:44286511
|
T | C | 12 | a0001c0002t0013g0268a0001c0002t0052g0193a0004c0009t0007g0170others(9): Show | 12 | HG01243.hp2 HG02572.hp2 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.467-10853A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44286511 | ||||||
| chr11:44286688
|
G | A | 1 | a0003c0013t0001g0012 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.467-11030C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44286688 | ||||||
| chr11:44286801
|
T | C | 1 | a0004c0009t0013g0171 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.467-11143A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44286801 | ||||||
| chr11:44286926
|
A | G | 2 | a0001c0001t0002g0190a0001c0002t0040g0280 | 2 | HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.467-11268T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44286926 | ||||||
| chr11:44286945
|
C | T | 1 | a0002c0003t0017g0136 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.467-11287G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44286945 | ||||||
| chr11:44287115
|
C | T | 1 | a0002c0003t0001g0138 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.467-11457G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44287115 | ||||||
| chr11:44287308
|
A | T | 1 | a0002c0003t0001g0112 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.467-11650T>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44287308 | ||||||
| chr11:44287385
|
A | G | 2 | a0001c0002t0003g0267a0001c0005t0058g0202 | 2 | HG02300.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.467-11727T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44287385 | ||||||
| chr11:44287604
|
AAG | A | 10 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0347others(7): Show | 10 | HG01517.hp1 HG02895.hp2 HG03041.hp2 others(7): Show |
intron_variant | MODIFIER | c.467-11948_467-1194 others(6): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44287604 | ||||||
| chr11:44287605
|
AG | A | 292 | a0001c0001t0001g0003a0001c0001t0001g0203a0001c0001t0001g0227others(289): Show | 297 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.467-11948delC | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44287605 | ||||||
| chr11:44287605
|
AGAAAAG | A | 5 | a0003c0006t0009g0026a0003c0006t0015g0013a0003c0006t0032g0018others(2): Show | 5 | HG01884.hp2 HG02258.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.467-11953_467-1194 others(10): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44287605 | ||||||
| chr11:44287606
|
G | A | 65 | a0001c0001t0001g0002a0001c0001t0001g0195a0001c0001t0001g0199others(62): Show | 67 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.467-11948C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44287606 | ||||||
| chr11:44287689
|
C | T | 1 | a0001c0001t0002g0352 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.467-12031G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44287689 | ||||||
| chr11:44288107
|
C | T | 2 | a0001c0002t0003g0225a0001c0002t0019g0312 | 2 | HG00140.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.467-12449G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44288107 | ||||||
| chr11:44288421
|
A | C | 1 | a0001c0001t0002g0352 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.467-12763T>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44288421 | ||||||
| chr11:44288425
|
G | T | 21 | a0001c0001t0001g0257a0001c0001t0001g0271a0001c0001t0001g0284others(18): Show | 21 | HG01256.hp1 HG02523.hp1 NA18939.hp1 others(18): Show |
intron_variant | MODIFIER | c.467-12767C>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44288425 | ||||||
| chr11:44288473
|
C | G | 8 | a0001c0002t0025g0004a0001c0011t0020g0265a0003c0006t0009g0026others(5): Show | 9 | HG01243.hp1 HG01884.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.467-12815G>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44288473 | ||||||
| chr11:44288540
|
G | A | 1 | a0001c0001t0002g0352 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.467-12882C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44288540 | ||||||
| chr11:44288584
|
C | T | 12 | a0001c0002t0013g0268a0001c0002t0052g0193a0004c0009t0007g0170others(9): Show | 12 | HG01243.hp2 HG02572.hp2 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.467-12926G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44288584 | ||||||
| chr11:44288669
|
C | T | 1 | a0001c0001t0002g0352 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.467-13011G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44288669 | ||||||
| chr11:44288670
|
G | A | 5 | a0003c0006t0024g0020a0003c0006t0024g0027a0003c0010t0001g0016others(2): Show | 5 | HG02257.hp1 HG02559.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.467-13012C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44288670 | ||||||
| chr11:44288899
|
C | T | 1 | a0002c0004t0014g0107 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.467-13241G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44288899 | ||||||
| chr11:44288914
|
C | T | 1 | a0001c0001t0001g0195 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.467-13256G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44288914 | ||||||
| chr11:44288950
|
C | T | 12 | a0001c0002t0013g0268a0001c0002t0052g0193a0004c0009t0007g0170others(9): Show | 12 | HG01243.hp2 HG02572.hp2 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.467-13292G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44288950 | ||||||
| chr11:44288956
|
T | C | 2 | a0001c0002t0003g0225a0001c0002t0019g0312 | 2 | HG00140.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.467-13298A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44288956 | ||||||
| chr11:44289055
|
C | G | 378 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0180others(375): Show | 385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.467-13397G>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44289055 | ||||||
| chr11:44289119
|
C | T | 6 | a0001c0001t0001g0310a0003c0013t0001g0009a0003c0013t0001g0012others(3): Show | 6 | HG02293.hp1 HG02602.hp1 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.467-13461G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44289119 | ||||||
| chr11:44289138
|
G | T | 1 | a0001c0002t0040g0280 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.467-13480C>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44289138 | ||||||
| chr11:44289163
|
T | A | 2 | a0001c0001t0002g0353a0001c0002t0005g0223 | 2 | NA18979.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.467-13505A>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44289163 | ||||||
| chr11:44289183
|
G | A | 5 | a0001c0001t0004g0329a0001c0001t0004g0330a0001c0001t0004g0332others(2): Show | 5 | NA18939.hp1 NA18945.hp2 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.467-13525C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44289183 | ||||||
| chr11:44289382
|
G | T | 2 | a0001c0001t0001g0269a0001c0001t0001g0270 | 2 | NA18961.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.467-13724C>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44289382 | ||||||
| chr11:44289519
|
A | T | 1 | a0001c0001t0002g0278 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.467-13861T>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44289519 | ||||||
| chr11:44289569
|
G | A | 1 | a0002c0004t0005g0058 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.467-13911C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44289569 | ||||||
| chr11:44289952
|
G | T | 21 | a0001c0001t0043g0297a0001c0002t0015g0205a0001c0005t0066g0263others(18): Show | 21 | HG01109.hp1 HG01256.hp2 HG01258.hp2 others(18): Show |
intron_variant | MODIFIER | c.467-14294C>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44289952 | ||||||
| chr11:44289983
|
G | A | 1 | a0002c0004t0005g0125 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.467-14325C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44289983 | ||||||
| chr11:44289987
|
C | A | 250 | a0001c0001t0001g0248a0001c0001t0001g0250a0001c0001t0001g0252others(247): Show | 252 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(249): Show |
intron_variant | MODIFIER | c.467-14329G>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44289987 | ||||||
| chr11:44290090
|
T | A | 1 | a0001c0005t0006g0007 | 2 | HG00639.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.467-14432A>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44290090 | ||||||
| chr11:44290181
|
G | C | 1 | a0002c0003t0001g0047 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.467-14523C>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44290181 | ||||||
| chr11:44290255
|
A | G | 340 | a0001c0001t0001g0003a0001c0001t0001g0203a0001c0001t0001g0227others(337): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.467-14597T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44290255 | ||||||
| chr11:44290290
|
C | T | 1 | a0001c0029t0001g0243 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.467-14632G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44290290 | ||||||
| chr11:44290388
|
GC | G | 16 | a0001c0001t0002g0352a0001c0002t0013g0268a0001c0002t0016g0306others(13): Show | 16 | HG01243.hp2 HG02572.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.467-14731delG | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44290388 | ||||||
| chr11:44290418
|
C | A | 251 | a0001c0001t0001g0248a0001c0001t0001g0250a0001c0001t0001g0252others(248): Show | 253 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.467-14760G>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44290418 | ||||||
| chr11:44290555
|
G | T | 1 | a0001c0001t0001g0369 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.467-14897C>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44290555 | ||||||
| chr11:44290761
|
G | A | 2 | a0001c0002t0003g0261a0001c0002t0003g0262 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.467-15103C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44290761 | ||||||
| chr11:44290909
|
C | T | 1 | a0001c0002t0002g0241 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.467-15251G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44290909 | ||||||
| chr11:44291006
|
C | T | 251 | a0001c0001t0001g0248a0001c0001t0001g0250a0001c0001t0001g0252others(248): Show | 253 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.467-15348G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44291006 | ||||||
| chr11:44291014
|
T | C | 251 | a0001c0001t0001g0248a0001c0001t0001g0250a0001c0001t0001g0252others(248): Show | 253 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.467-15356A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44291014 | ||||||
| chr11:44291016
|
C | T | 52 | a0001c0001t0001g0003a0001c0001t0001g0203a0001c0001t0001g0227others(49): Show | 55 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(52): Show |
intron_variant | MODIFIER | c.467-15358G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44291016 | ||||||
| chr11:44291020
|
C | G | 4 | a0001c0007t0007g0244a0001c0007t0007g0246a0001c0011t0003g0294others(1): Show | 4 | HG01192.hp1 HG01516.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.467-15362G>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44291020 | ||||||
| chr11:44291055
|
C | T | 13 | a0001c0001t0001g0373a0001c0001t0001g0374a0001c0002t0003g0184others(10): Show | 13 | HG00099.hp1 HG01070.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.467-15397G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44291055 | ||||||
| chr11:44291098
|
T | G | 81 | a0001c0001t0001g0003a0001c0001t0001g0203a0001c0001t0001g0227others(78): Show | 84 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(81): Show |
intron_variant | MODIFIER | c.467-15440A>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44291098 | ||||||
| chr11:44291232
|
T | TA | 5 | a0003c0006t0009g0026a0003c0006t0015g0013a0003c0006t0032g0018others(2): Show | 5 | HG01884.hp2 HG02258.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.467-15575dupT | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44291232 | ||||||
| chr11:44291246
|
A | T | 1 | a0001c0001t0002g0352 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.467-15588T>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44291246 | ||||||
| chr11:44291259
|
C | T | 251 | a0001c0001t0001g0248a0001c0001t0001g0250a0001c0001t0001g0252others(248): Show | 253 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.467-15601G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44291259 | ||||||
| chr11:44291289
|
A | G | 251 | a0001c0001t0001g0248a0001c0001t0001g0250a0001c0001t0001g0252others(248): Show | 253 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.467-15631T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44291289 | ||||||
| chr11:44291331
|
C | T | 251 | a0001c0001t0001g0248a0001c0001t0001g0250a0001c0001t0001g0252others(248): Show | 253 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.467-15673G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44291331 | ||||||
| chr11:44291348
|
C | G | 251 | a0001c0001t0001g0248a0001c0001t0001g0250a0001c0001t0001g0252others(248): Show | 253 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.467-15690G>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44291348 | ||||||
| chr11:44291366
|
C | T | 1 | a0003c0020t0026g0017 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.467-15708G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44291366 | ||||||
| chr11:44291367
|
G | A | 1 | a0001c0002t0007g0281 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.467-15709C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44291367 | ||||||
| chr11:44291414
|
C | CTTTTCTT others(1): Show |
250 | a0001c0001t0001g0248a0001c0001t0001g0250a0001c0001t0001g0252others(247): Show | 252 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(249): Show |
intron_variant | MODIFIER | c.467-15757_467-1575 others(12): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44291414 | ||||||
| chr11:44291418
|
C | T | 251 | a0001c0001t0001g0248a0001c0001t0001g0250a0001c0001t0001g0252others(248): Show | 253 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.467-15760G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44291418 | ||||||
| chr11:44291454
|
G | A | 2 | a0001c0001t0002g0352a0001c0002t0016g0306 | 2 | HG02630.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.467-15796C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44291454 | ||||||
| chr11:44291468
|
G | T | 1 | a0004c0009t0013g0171 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.467-15810C>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44291468 | ||||||
| chr11:44291469
|
T | C | 259 | a0001c0001t0001g0248a0001c0001t0001g0250a0001c0001t0001g0252others(256): Show | 262 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(259): Show |
intron_variant | MODIFIER | c.467-15811A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44291469 | ||||||
| chr11:44291566
|
A | G | 251 | a0001c0001t0001g0248a0001c0001t0001g0250a0001c0001t0001g0252others(248): Show | 253 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.467-15908T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44291566 | ||||||
| chr11:44291605
|
C | G | 251 | a0001c0001t0001g0248a0001c0001t0001g0250a0001c0001t0001g0252others(248): Show | 253 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.467-15947G>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44291605 | ||||||
| chr11:44291641
|
A | G | 251 | a0001c0001t0001g0248a0001c0001t0001g0250a0001c0001t0001g0252others(248): Show | 253 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.467-15983T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44291641 | ||||||
| chr11:44291649
|
G | A | 3 | a0001c0002t0025g0004a0001c0011t0020g0265a0003c0020t0026g0017 | 4 | HG01243.hp1 HG02809.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.467-15991C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44291649 | ||||||
| chr11:44291658
|
A | G | 251 | a0001c0001t0001g0248a0001c0001t0001g0250a0001c0001t0001g0252others(248): Show | 253 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.467-16000T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44291658 | ||||||
| chr11:44291666
|
G | A | 251 | a0001c0001t0001g0248a0001c0001t0001g0250a0001c0001t0001g0252others(248): Show | 253 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.467-16008C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44291666 | ||||||
| chr11:44291712
|
T | C | 17 | a0001c0001t0043g0297a0001c0002t0015g0205a0001c0005t0066g0263others(14): Show | 17 | HG01256.hp2 HG01258.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.467-16054A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44291712 | ||||||
| chr11:44291900
|
C | A | 251 | a0001c0001t0001g0248a0001c0001t0001g0250a0001c0001t0001g0252others(248): Show | 253 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.467-16242G>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44291900 | ||||||
| chr11:44291939
|
C | T | 2 | a0002c0004t0014g0070a0002c0004t0014g0164 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.467-16281G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44291939 | ||||||
| chr11:44292049
|
C | T | 1 | a0002c0004t0002g0106 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.467-16391G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44292049 | ||||||
| chr11:44292052
|
C | T | 1 | a0001c0002t0013g0268 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.467-16394G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44292052 | ||||||
| chr11:44292284
|
C | T | 251 | a0001c0001t0001g0248a0001c0001t0001g0250a0001c0001t0001g0252others(248): Show | 253 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.467-16626G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44292284 | ||||||
| chr11:44292377
|
AT | A | 132 | a0001c0001t0001g0003a0001c0001t0001g0227a0001c0001t0001g0272others(129): Show | 136 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.467-16720delA | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44292377 | ||||||
| chr11:44292377
|
ATT | A | 194 | a0001c0001t0001g0248a0001c0001t0001g0250a0001c0001t0001g0252others(191): Show | 196 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.467-16721_467-1672 others(6): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44292377 | ||||||
| chr11:44292378
|
T | A | 14 | a0001c0001t0001g0203a0001c0001t0001g0324a0001c0002t0036g0363others(11): Show | 14 | HG01433.hp2 HG02129.hp2 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.467-16720A>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44292378 | ||||||
| chr11:44292379
|
T | A | 130 | a0001c0001t0001g0003a0001c0001t0001g0227a0001c0001t0001g0272others(127): Show | 134 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.467-16721A>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44292379 | ||||||
| chr11:44292380
|
T | A | 193 | a0001c0001t0001g0248a0001c0001t0001g0250a0001c0001t0001g0252others(190): Show | 195 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.467-16722A>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44292380 | ||||||
| chr11:44292381
|
T | A | 1 | a0001c0002t0007g0341 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.467-16723A>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44292381 | ||||||
| chr11:44292462
|
G | C | 378 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0180others(375): Show | 385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.467-16804C>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44292462 | ||||||
| chr11:44292465
|
T | C | 338 | a0001c0001t0001g0003a0001c0001t0001g0203a0001c0001t0001g0227others(335): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.467-16807A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44292465 | ||||||
| chr11:44292534
|
G | A | 338 | a0001c0001t0001g0003a0001c0001t0001g0203a0001c0001t0001g0227others(335): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.467-16876C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44292534 | ||||||
| chr11:44292579
|
C | T | 16 | a0001c0001t0002g0352a0001c0002t0013g0268a0001c0002t0016g0306others(13): Show | 16 | HG01243.hp2 HG02572.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.467-16921G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44292579 | ||||||
| chr11:44292596
|
T | C | 1 | a0002c0003t0004g0100 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.467-16938A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44292596 | ||||||
| chr11:44292677
|
G | A | 13 | a0001c0001t0001g0373a0001c0001t0001g0374a0001c0002t0003g0184others(10): Show | 13 | HG00099.hp1 HG01070.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.466+16920C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44292677 | ||||||
| chr11:44292716
|
T | G | 4 | a0002c0003t0001g0147a0002c0008t0004g0150a0002c0008t0005g0048others(1): Show | 4 | NA18990.hp2 NA19002.hp2 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.466+16881A>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44292716 | ||||||
| chr11:44292738
|
A | T | 5 | a0001c0005t0066g0263a0003c0006t0003g0024a0003c0006t0003g0036others(2): Show | 5 | HG02559.hp1 HG02818.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.466+16859T>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44292738 | ||||||
| chr11:44292809
|
C | G | 3 | a0001c0001t0001g0369a0001c0002t0008g0321a0001c0002t0008g0354 | 3 | NA18945.hp1 NA18979.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.466+16788G>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44292809 | ||||||
| chr11:44292816
|
C | A | 1 | a0001c0002t0040g0280 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.466+16781G>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44292816 | ||||||
| chr11:44292822
|
A | G | 164 | a0001c0001t0001g0003a0001c0001t0001g0203a0001c0001t0001g0227others(161): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.466+16775T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44292822 | ||||||
| chr11:44292859
|
G | A | 9 | a0001c0001t0002g0187a0001c0002t0007g0341a0001c0002t0009g0348others(6): Show | 9 | HG02109.hp1 HG02451.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.466+16738C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44292859 | ||||||
| chr11:44292942
|
T | C | 13 | a0001c0001t0001g0373a0001c0001t0001g0374a0001c0002t0003g0184others(10): Show | 13 | HG00099.hp1 HG01070.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.466+16655A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44292942 | ||||||
| chr11:44292946
|
T | A | 337 | a0001c0001t0001g0003a0001c0001t0001g0203a0001c0001t0001g0227others(334): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.466+16651A>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44292946 | ||||||
| chr11:44293092
|
G | C | 1 | a0001c0031t0002g0381 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.466+16505C>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44293092 | ||||||
| chr11:44293099
|
A | AGAAG | 6 | a0001c0001t0001g0195a0001c0001t0001g0213a0001c0001t0002g0266others(3): Show | 6 | HG02071.hp1 HG03704.hp2 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.466+16494_466+1649 others(8): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44293099 | ||||||
| chr11:44293099
|
A | AGAAGGAA others(5): Show |
3 | a0001c0001t0004g0194a0001c0005t0006g0212a0001c0005t0061g0215 | 3 | HG02040.hp2 NA18939.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.466+16486_466+1649 others(16): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44293099 | ||||||
| chr11:44293099
|
AGAAG | A | 81 | a0001c0001t0001g0180a0001c0001t0001g0219a0001c0001t0001g0272others(78): Show | 81 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.466+16494_466+1649 others(8): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44293099 | ||||||
| chr11:44293099
|
AGAAGGAA others(1): Show |
A | 58 | a0001c0001t0001g0003a0001c0001t0001g0227a0001c0001t0001g0269others(55): Show | 60 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(57): Show |
intron_variant | MODIFIER | c.466+16490_466+1649 others(12): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44293099 | ||||||
| chr11:44293099
|
AGAAGGAA others(5): Show |
A | 73 | a0001c0001t0001g0201a0001c0001t0001g0203a0001c0001t0001g0257others(70): Show | 75 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.466+16486_466+1649 others(16): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44293099 | ||||||
| chr11:44293099
|
AGAAGGAA others(9): Show |
A | 26 | a0001c0001t0001g0333a0001c0001t0001g0373a0001c0001t0001g0374others(23): Show | 26 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.466+16482_466+1649 others(20): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44293099 | ||||||
| chr11:44293099
|
AGAAGGAA others(13): Show |
A | 9 | a0001c0001t0002g0292a0001c0002t0003g0184a0001c0002t0003g0185others(6): Show | 9 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.466+16478_466+1649 others(24): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44293099 | ||||||
| chr11:44293099
|
AGAAGGAA others(17): Show |
A | 10 | a0001c0001t0043g0297a0001c0031t0002g0381a0003c0006t0003g0021others(7): Show | 10 | HG01109.hp1 HG01884.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.466+16474_466+1649 others(28): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44293099 | ||||||
| chr11:44293099
|
AGAAGGAA others(29): Show |
A | 1 | a0001c0002t0015g0205 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.466+16462_466+1649 others(40): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44293099 | ||||||
| chr11:44293148
|
GAAGGAAG others(6): Show |
G | 2 | a0001c0001t0001g0252a0001c0007t0004g0253 | 2 | HG00099.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.466+16436_466+1644 others(17): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44293148 | ||||||
| chr11:44293148
|
GAAGGAAG others(17): Show |
G | 4 | a0001c0001t0002g0352a0003c0006t0015g0013a0003c0006t0032g0018others(1): Show | 4 | HG02809.hp2 HG03130.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.466+16425_466+1644 others(28): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44293148 | ||||||
| chr11:44293152
|
GAAGGAAG others(2): Show |
G | 4 | a0001c0001t0001g0250a0001c0002t0030g0204a0001c0002t0055g0255others(1): Show | 4 | HG00639.hp2 HG02818.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.466+16436_466+1644 others(13): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44293152 | ||||||
| chr11:44293156
|
GAAGGA | G | 8 | a0001c0001t0001g0248a0001c0001t0002g0233a0001c0002t0007g0249others(5): Show | 8 | HG00738.hp1 HG01070.hp1 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.466+16436_466+1644 others(9): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44293156 | ||||||
| chr11:44293156
|
GAAGGAAG others(9): Show |
G | 2 | a0001c0001t0001g0271a0003c0006t0009g0026 | 2 | HG02258.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.466+16425_466+1644 others(20): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44293156 | ||||||
| chr11:44293160
|
GA | G | 15 | a0001c0002t0011g0362a0001c0002t0015g0346a0001c0007t0003g0226others(12): Show | 15 | HG01192.hp1 HG01516.hp1 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.466+16436delT | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44293160 | ||||||
| chr11:44293160
|
GAAGGAAG others(5): Show |
G | 4 | a0001c0002t0025g0004a0001c0011t0020g0265a0002c0003t0017g0136others(1): Show | 5 | HG01243.hp1 HG01884.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.466+16425_466+1643 others(16): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44293160 | ||||||
| chr11:44293165
|
A | C | 29 | a0001c0001t0001g0248a0001c0001t0001g0250a0001c0001t0001g0252others(26): Show | 29 | HG00099.hp2 HG00639.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.466+16432T>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44293165 | ||||||
| chr11:44293166
|
A | G | 1 | a0002c0004t0012g0078 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.466+16431T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44293166 | ||||||
| chr11:44293167
|
GGAA | G | 29 | a0001c0001t0001g0248a0001c0001t0001g0250a0001c0001t0001g0252others(26): Show | 29 | HG00099.hp2 HG00639.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.466+16427_466+1642 others(7): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44293167 | ||||||
| chr11:44293168
|
G | C | 2 | a0002c0004t0012g0078a0006c0022t0009g0166 | 2 | HG01255.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.466+16429C>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44293168 | ||||||
| chr11:44293170
|
A | AGGAAGGA others(17): Show |
1 | a0002c0003t0001g0095 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.466+16426_466+1642 others(28): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44293170 | ||||||
| chr11:44293170
|
A | AGGAG | 11 | a0001c0002t0028g0361a0002c0003t0001g0062a0002c0003t0001g0130others(8): Show | 11 | HG00280.hp1 HG00741.hp1 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.466+16426_466+1642 others(8): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44293170 | ||||||
| chr11:44293170
|
A | G | 275 | a0001c0001t0001g0003a0001c0001t0001g0203a0001c0001t0001g0227others(272): Show | 280 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.466+16427T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44293170 | ||||||
| chr11:44293176
|
C | G | 31 | a0001c0001t0001g0248a0001c0001t0001g0250a0001c0001t0001g0252others(28): Show | 31 | HG00099.hp2 HG00639.hp2 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.466+16421G>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44293176 | ||||||
| chr11:44293180
|
C | CAGGG | 12 | a0001c0002t0013g0268a0001c0002t0052g0193a0004c0009t0007g0170others(9): Show | 12 | HG01243.hp2 HG02572.hp2 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.466+16413_466+1641 others(8): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44293180 | ||||||
| chr11:44293180
|
C | G | 318 | a0001c0001t0001g0003a0001c0001t0001g0203a0001c0001t0001g0227others(315): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.466+16417G>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44293180 | ||||||
| chr11:44293250
|
A | T | 4 | a0003c0006t0003g0039a0003c0006t0013g0033a0003c0006t0013g0041others(1): Show | 4 | HG01109.hp1 HG02451.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.466+16347T>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44293250 | ||||||
| chr11:44293271
|
A | T | 1 | a0001c0001t0002g0352 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.466+16326T>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44293271 | ||||||
| chr11:44293420
|
G | GA | 13 | a0001c0001t0001g0373a0001c0001t0001g0374a0001c0001t0002g0352others(10): Show | 14 | HG01070.hp2 HG01071.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.466+16176dupT | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44293420 | ||||||
| chr11:44293422
|
A | AG | 146 | a0001c0001t0001g0003a0001c0001t0001g0203a0001c0001t0001g0227others(143): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.466+16174_466+1617 others(5): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44293422 | ||||||
| chr11:44293426
|
A | AT | 171 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0347others(168): Show | 172 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.466+16170_466+1617 others(5): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44293426 | ||||||
| chr11:44293428
|
A | AT | 7 | a0001c0002t0007g0281a0001c0002t0040g0280a0003c0006t0009g0026others(4): Show | 7 | HG01884.hp2 HG02258.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.466+16168_466+1616 others(5): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44293428 | ||||||
| chr11:44293428
|
A | T | 319 | a0001c0001t0001g0003a0001c0001t0001g0203a0001c0001t0001g0227others(316): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.466+16169T>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44293428 | ||||||
| chr11:44293550
|
C | T | 1 | a0001c0001t0001g0002 | 2 | NA18951.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.466+16047G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44293550 | ||||||
| chr11:44293610
|
C | T | 2 | a0001c0002t0001g0275a0001c0002t0001g0277 | 2 | NA18970.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.466+15987G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44293610 | ||||||
| chr11:44293618
|
G | A | 2 | a0001c0002t0007g0281a0001c0002t0040g0280 | 2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.466+15979C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44293618 | ||||||
| chr11:44293840
|
A | G | 153 | a0001c0001t0001g0003a0001c0001t0001g0203a0001c0001t0001g0227others(150): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.466+15757T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44293840 | ||||||
| chr11:44293891
|
G | A | 11 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0347others(8): Show | 11 | HG02074.hp2 NA18953.hp1 NA18961.hp2 others(8): Show |
intron_variant | MODIFIER | c.466+15706C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44293891 | ||||||
| chr11:44293924
|
G | T | 1 | a0001c0005t0006g0377 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.466+15673C>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44293924 | ||||||
| chr11:44293925
|
G | T | 1 | a0001c0005t0006g0377 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.466+15672C>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44293925 | ||||||
| chr11:44293977
|
A | G | 4 | a0001c0002t0007g0264a0001c0002t0011g0178a0001c0002t0025g0004others(1): Show | 5 | HG01243.hp1 HG02622.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.466+15620T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44293977 | ||||||
| chr11:44294009
|
AC | A | 5 | a0003c0006t0009g0026a0003c0006t0015g0013a0003c0006t0032g0018others(2): Show | 5 | HG01884.hp2 HG02258.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.466+15587delG | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44294009 | ||||||
| chr11:44294157
|
C | T | 1 | a0001c0027t0050g0224 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.466+15440G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44294157 | ||||||
| chr11:44294343
|
C | T | 1 | a0001c0001t0002g0352 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.466+15254G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44294343 | ||||||
| chr11:44294373
|
A | G | 4 | a0001c0002t0007g0264a0001c0002t0011g0178a0001c0002t0025g0004others(1): Show | 5 | HG01243.hp1 HG02622.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.466+15224T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44294373 | ||||||
| chr11:44294460
|
A | T | 3 | a0002c0003t0001g0001a0002c0003t0004g0145a0002c0003t0049g0146 | 4 | HG01261.hp2 HG02129.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.466+15137T>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44294460 | ||||||
| chr11:44294512
|
A | T | 1 | a0001c0001t0002g0352 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.466+15085T>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44294512 | ||||||
| chr11:44294566
|
G | A | 2 | a0001c0002t0023g0192a0001c0002t0027g0191 | 2 | HG02109.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.466+15031C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44294566 | ||||||
| chr11:44294804
|
C | T | 1 | a0001c0027t0050g0224 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.466+14793G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44294804 | ||||||
| chr11:44294828
|
C | CTATT | 25 | a0001c0001t0001g0002a0001c0001t0001g0195a0001c0001t0001g0199others(22): Show | 26 | HG00438.hp2 HG00673.hp1 HG02486.hp2 others(23): Show |
intron_variant | MODIFIER | c.466+14765_466+1476 others(8): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44294828 | ||||||
| chr11:44294828
|
C | CTATTTAT others(1): Show |
8 | a0001c0001t0001g0213a0001c0001t0002g0266a0001c0001t0004g0214others(5): Show | 8 | HG00408.hp2 HG02040.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.466+14761_466+1476 others(12): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44294828 | ||||||
| chr11:44294828
|
C | CTATTTAT others(5): Show |
1 | a0001c0002t0027g0191 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.466+14757_466+1476 others(16): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44294828 | ||||||
| chr11:44294828
|
CTATT | C | 138 | a0001c0001t0001g0269a0001c0001t0001g0347a0001c0001t0001g0364others(135): Show | 139 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.466+14765_466+1476 others(8): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44294828 | ||||||
| chr11:44294828
|
CTATTTAT others(1): Show |
C | 176 | a0001c0001t0001g0003a0001c0001t0001g0203a0001c0001t0001g0227others(173): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.466+14761_466+1476 others(12): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44294828 | ||||||
| chr11:44294985
|
G | T | 1 | a0001c0001t0002g0190 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.466+14612C>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44294985 | ||||||
| chr11:44295048
|
A | T | 1 | a0001c0001t0002g0352 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.466+14549T>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44295048 | ||||||
| chr11:44295103
|
G | A | 27 | a0001c0002t0009g0366a0001c0002t0016g0306a0001c0002t0056g0367others(24): Show | 27 | HG01109.hp1 HG01256.hp2 HG01258.hp2 others(24): Show |
intron_variant | MODIFIER | c.466+14494C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44295103 | ||||||
| chr11:44295126
|
C | T | 4 | a0002c0003t0001g0062a0002c0003t0010g0126a0002c0004t0014g0070others(1): Show | 4 | HG01168.hp2 HG01169.hp1 HG02056.hp1 others(1): Show |
intron_variant | MODIFIER | c.466+14471G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44295126 | ||||||
| chr11:44295197
|
C | T | 4 | a0001c0002t0007g0264a0001c0002t0011g0178a0001c0002t0025g0004others(1): Show | 5 | HG01243.hp1 HG02622.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.466+14400G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44295197 | ||||||
| chr11:44295206
|
A | G | 1 | a0001c0030t0026g0302 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.466+14391T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44295206 | ||||||
| chr11:44295369
|
A | C | 330 | a0001c0001t0001g0003a0001c0001t0001g0203a0001c0001t0001g0227others(327): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.466+14228T>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44295369 | ||||||
| chr11:44295715
|
C | T | 161 | a0001c0001t0001g0003a0001c0001t0001g0203a0001c0001t0001g0227others(158): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.466+13882G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44295715 | ||||||
| chr11:44295727
|
G | T | 10 | a0001c0001t0001g0373a0001c0001t0001g0374a0001c0002t0003g0349others(7): Show | 10 | HG01070.hp2 HG01071.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.466+13870C>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44295727 | ||||||
| chr11:44295765
|
G | T | 1 | a0001c0001t0004g0329 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.466+13832C>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44295765 | ||||||
| chr11:44295766
|
T | C | 1 | a0001c0001t0004g0329 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.466+13831A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44295766 | ||||||
| chr11:44295778
|
G | A | 1 | a0001c0001t0002g0352 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.466+13819C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44295778 | ||||||
| chr11:44295828
|
C | T | 1 | a0001c0001t0001g0364 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.466+13769G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44295828 | ||||||
| chr11:44295876
|
C | T | 1 | a0001c0002t0013g0268 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.466+13721G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44295876 | ||||||
| chr11:44295895
|
A | G | 148 | a0001c0001t0001g0003a0001c0001t0001g0203a0001c0001t0001g0227others(145): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.466+13702T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44295895 | ||||||
| chr11:44295927
|
C | T | 161 | a0001c0001t0001g0003a0001c0001t0001g0203a0001c0001t0001g0227others(158): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.466+13670G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44295927 | ||||||
| chr11:44295972
|
C | T | 5 | a0003c0006t0009g0026a0003c0006t0015g0013a0003c0006t0032g0018others(2): Show | 5 | HG01884.hp2 HG02258.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.466+13625G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44295972 | ||||||
| chr11:44295998
|
A | C | 1 | a0003c0006t0003g0024 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.466+13599T>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44295998 | ||||||
| chr11:44296030
|
G | A | 10 | a0001c0001t0001g0373a0001c0001t0001g0374a0001c0002t0003g0349others(7): Show | 10 | HG01070.hp2 HG01071.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.466+13567C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44296030 | ||||||
| chr11:44296059
|
G | C | 9 | a0001c0001t0002g0187a0001c0002t0007g0341a0001c0002t0009g0348others(6): Show | 9 | HG02109.hp1 HG02451.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.466+13538C>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44296059 | ||||||
| chr11:44296110
|
G | A | 4 | a0001c0001t0002g0352a0001c0002t0007g0264a0001c0002t0011g0178others(1): Show | 4 | HG02622.hp1 HG03130.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.466+13487C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44296110 | ||||||
| chr11:44296132
|
G | C | 1 | a0001c0001t0001g0203 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.466+13465C>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44296132 | ||||||
| chr11:44296146
|
T | C | 4 | a0001c0001t0002g0352a0001c0002t0007g0264a0001c0002t0011g0178others(1): Show | 4 | HG02622.hp1 HG03130.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.466+13451A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44296146 | ||||||
| chr11:44296201
|
C | G | 5 | a0003c0006t0009g0026a0003c0006t0015g0013a0003c0006t0032g0018others(2): Show | 5 | HG01884.hp2 HG02258.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.466+13396G>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44296201 | ||||||
| chr11:44296281
|
C | G | 5 | a0003c0013t0001g0009a0003c0013t0001g0012a0003c0017t0002g0008others(2): Show | 5 | HG02293.hp1 HG02602.hp1 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.466+13316G>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44296281 | ||||||
| chr11:44296312
|
C | A | 161 | a0001c0001t0001g0003a0001c0001t0001g0203a0001c0001t0001g0227others(158): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.466+13285G>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44296312 | ||||||
| chr11:44296355
|
A | G | 1 | a0001c0027t0050g0224 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.466+13242T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44296355 | ||||||
| chr11:44296389
|
A | T | 9 | a0001c0001t0002g0187a0001c0002t0007g0341a0001c0002t0009g0348others(6): Show | 9 | HG02109.hp1 HG02451.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.466+13208T>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44296389 | ||||||
| chr11:44296691
|
G | GA | 4 | a0001c0001t0002g0352a0001c0002t0007g0264a0001c0002t0011g0178others(1): Show | 4 | HG02622.hp1 HG03130.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.466+12905dupT | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44296691 | ||||||
| chr11:44296737
|
G | A | 2 | a0002c0004t0014g0070a0002c0004t0014g0164 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.466+12860C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44296737 | ||||||
| chr11:44296745
|
A | T | 1 | a0001c0002t0038g0221 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.466+12852T>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44296745 | ||||||
| chr11:44296822
|
A | C | 1 | a0002c0003t0002g0118 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.466+12775T>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44296822 | ||||||
| chr11:44296934
|
G | A | 154 | a0001c0001t0001g0003a0001c0001t0001g0203a0001c0001t0001g0227others(151): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.466+12663C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44296934 | ||||||
| chr11:44297009
|
CA | C | 132 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0347others(129): Show | 133 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.466+12587delT | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44297009 | ||||||
| chr11:44297009
|
CAA | C | 47 | a0001c0001t0001g0373a0001c0001t0001g0374a0001c0001t0010g0230others(44): Show | 47 | HG00323.hp1 HG00438.hp1 HG01070.hp2 others(44): Show |
intron_variant | MODIFIER | c.466+12586_466+1258 others(6): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44297009 | ||||||
| chr11:44297009
|
CAAA | C | 130 | a0001c0001t0001g0003a0001c0001t0001g0203a0001c0001t0001g0227others(127): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.466+12585_466+1258 others(7): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44297009 | ||||||
| chr11:44297009
|
CAAAA | C | 20 | a0001c0001t0004g0329a0001c0001t0004g0330a0001c0002t0007g0264others(17): Show | 20 | HG01070.hp1 HG01243.hp2 HG02572.hp2 others(17): Show |
intron_variant | MODIFIER | c.466+12584_466+1258 others(8): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44297009 | ||||||
| chr11:44297108
|
C | T | 4 | a0001c0001t0002g0352a0001c0002t0007g0264a0001c0002t0011g0178others(1): Show | 4 | HG02622.hp1 HG03130.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.466+12489G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44297108 | ||||||
| chr11:44297182
|
A | G | 1 | a0002c0003t0004g0077 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.466+12415T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44297182 | ||||||
| chr11:44297236
|
G | A | 167 | a0001c0001t0001g0003a0001c0001t0001g0203a0001c0001t0001g0227others(164): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.466+12361C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44297236 | ||||||
| chr11:44297236
|
G | T | 1 | a0001c0001t0004g0329 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.466+12361C>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44297236 | ||||||
| chr11:44297517
|
A | C | 1 | a0001c0001t0001g0002 | 2 | NA18951.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.466+12080T>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44297517 | ||||||
| chr11:44297586
|
C | T | 1 | a0002c0004t0005g0090 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.466+12011G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44297586 | ||||||
| chr11:44297722
|
TAATAA | T | 340 | a0001c0001t0001g0003a0001c0001t0001g0203a0001c0001t0001g0227others(337): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.466+11870_466+1187 others(9): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44297722 | ||||||
| chr11:44297808
|
C | T | 1 | a0001c0007t0008g0295 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.466+11789G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44297808 | ||||||
| chr11:44297948
|
C | T | 2 | a0001c0002t0007g0264a0001c0002t0011g0178 | 2 | HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.466+11649G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44297948 | ||||||
| chr11:44297967
|
A | G | 4 | a0001c0002t0003g0184a0001c0002t0003g0185a0001c0002t0003g0186others(1): Show | 4 | HG00099.hp1 HG01433.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.466+11630T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44297967 | ||||||
| chr11:44298051
|
A | G | 4 | a0001c0001t0002g0352a0001c0002t0007g0264a0001c0002t0011g0178others(1): Show | 4 | HG02622.hp1 HG03130.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.466+11546T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44298051 | ||||||
| chr11:44298063
|
A | T | 10 | a0001c0001t0001g0373a0001c0001t0001g0374a0001c0002t0003g0349others(7): Show | 10 | HG01070.hp2 HG01071.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.466+11534T>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44298063 | ||||||
| chr11:44298107
|
C | G | 141 | a0001c0001t0001g0003a0001c0001t0001g0203a0001c0001t0001g0227others(138): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.466+11490G>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44298107 | ||||||
| chr11:44298138
|
C | T | 1 | a0001c0002t0007g0281 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.466+11459G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44298138 | ||||||
| chr11:44298155
|
A | G | 4 | a0001c0001t0002g0352a0001c0002t0007g0264a0001c0002t0011g0178others(1): Show | 4 | HG02622.hp1 HG03130.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.466+11442T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44298155 | ||||||
| chr11:44298188
|
T | C | 1 | a0003c0010t0042g0022 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.466+11409A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44298188 | ||||||
| chr11:44298231
|
C | A | 10 | a0001c0001t0001g0373a0001c0001t0001g0374a0001c0002t0003g0349others(7): Show | 10 | HG01070.hp2 HG01071.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.466+11366G>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44298231 | ||||||
| chr11:44298252
|
C | T | 4 | a0001c0001t0002g0352a0001c0002t0007g0264a0001c0002t0011g0178others(1): Show | 4 | HG02622.hp1 HG03130.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.466+11345G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44298252 | ||||||
| chr11:44298355
|
T | C | 198 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0347others(195): Show | 200 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(197): Show |
intron_variant | MODIFIER | c.466+11242A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44298355 | ||||||
| chr11:44298521
|
G | T | 2 | a0002c0003t0002g0088a0002c0008t0012g0089 | 2 | NA18980.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.466+11076C>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44298521 | ||||||
| chr11:44298540
|
G | A | 2 | a0001c0002t0009g0366a0001c0002t0056g0367 | 2 | HG02486.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.466+11057C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44298540 | ||||||
| chr11:44298608
|
G | A | 340 | a0001c0001t0001g0003a0001c0001t0001g0203a0001c0001t0001g0227others(337): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.466+10989C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44298608 | ||||||
| chr11:44298622
|
C | T | 166 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0347others(163): Show | 167 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.466+10975G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44298622 | ||||||
| chr11:44298623
|
G | A | 1 | a0004c0009t0007g0170 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.466+10974C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44298623 | ||||||
| chr11:44298734
|
A | T | 1 | a0001c0002t0011g0178 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.466+10863T>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44298734 | ||||||
| chr11:44298764
|
C | T | 1 | a0001c0001t0002g0197 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.466+10833G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44298764 | ||||||
| chr11:44298794
|
CA | C | 323 | a0001c0001t0001g0003a0001c0001t0001g0203a0001c0001t0001g0227others(320): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.466+10802delT | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44298794 | ||||||
| chr11:44298794
|
CAA | C | 16 | a0001c0001t0001g0373a0001c0001t0001g0374a0001c0001t0004g0329others(13): Show | 16 | HG01070.hp2 HG01071.hp2 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.466+10801_466+1080 others(6): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44298794 | ||||||
| chr11:44298829
|
G | A | 3 | a0003c0006t0013g0033a0003c0006t0013g0041a0003c0010t0002g0032 | 3 | HG01109.hp1 HG02451.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.466+10768C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44298829 | ||||||
| chr11:44298904
|
A | G | 2 | a0001c0002t0007g0264a0001c0002t0011g0178 | 2 | HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.466+10693T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44298904 | ||||||
| chr11:44298991
|
T | C | 1 | a0001c0001t0002g0256 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.466+10606A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44298991 | ||||||
| chr11:44299020
|
G | T | 2 | a0001c0001t0002g0352a0001c0002t0040g0280 | 2 | HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.466+10577C>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44299020 | ||||||
| chr11:44299175
|
T | G | 1 | a0001c0002t0011g0362 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.466+10422A>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44299175 | ||||||
| chr11:44299178
|
G | A | 1 | a0002c0004t0014g0107 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.466+10419C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44299178 | ||||||
| chr11:44299280
|
G | T | 1 | a0003c0020t0026g0017 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.466+10317C>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44299280 | ||||||
| chr11:44299301
|
T | C | 1 | a0001c0002t0055g0255 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.466+10296A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44299301 | ||||||
| chr11:44299320
|
T | A | 2 | a0001c0001t0002g0352a0001c0002t0040g0280 | 2 | HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.466+10277A>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44299320 | ||||||
| chr11:44299350
|
C | T | 1 | a0002c0003t0004g0145 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.466+10247G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44299350 | ||||||
| chr11:44299351
|
A | G | 173 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0345others(170): Show | 174 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.466+10246T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44299351 | ||||||
| chr11:44299354
|
G | GT | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0180others(133): Show | 139 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.466+10242dupA | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44299354 | ||||||
| chr11:44299354
|
G | GTT | 18 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273others(15): Show | 18 | HG00408.hp1 HG00609.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.466+10241_466+1024 others(6): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44299354 | ||||||
| chr11:44299354
|
GTTT | G | 8 | a0001c0001t0001g0373a0001c0001t0001g0374a0001c0002t0003g0350others(5): Show | 8 | HG01070.hp2 HG01071.hp2 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.466+10240_466+1024 others(7): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44299354 | ||||||
| chr11:44299517
|
C | A | 10 | a0001c0001t0001g0373a0001c0001t0001g0374a0001c0002t0003g0349others(7): Show | 10 | HG01070.hp2 HG01071.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.466+10080G>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44299517 | ||||||
| chr11:44299517
|
C | T | 9 | a0004c0009t0007g0170a0004c0009t0009g0168a0004c0009t0009g0169others(6): Show | 9 | HG01243.hp2 HG02572.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.466+10080G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44299517 | ||||||
| chr11:44299635
|
C | T | 3 | a0002c0003t0002g0118a0002c0004t0007g0043a0002c0008t0051g0059 | 3 | HG01346.hp2 HG01361.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.466+9962G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44299635 | ||||||
| chr11:44299636
|
G | C | 5 | a0003c0006t0009g0026a0003c0006t0015g0013a0003c0006t0032g0018others(2): Show | 5 | HG01884.hp2 HG02258.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.466+9961C>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44299636 | ||||||
| chr11:44299649
|
T | C | 200 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0345others(197): Show | 202 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.466+9948A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44299649 | ||||||
| chr11:44299650
|
G | A | 2 | a0001c0001t0002g0352a0001c0002t0040g0280 | 2 | HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.466+9947C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44299650 | ||||||
| chr11:44299658
|
C | A | 1 | a0002c0004t0002g0108 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.466+9939G>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44299658 | ||||||
| chr11:44299784
|
C | T | 5 | a0001c0002t0007g0264a0001c0002t0007g0281a0001c0002t0009g0366others(2): Show | 5 | HG02486.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.466+9813G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44299784 | ||||||
| chr11:44299799
|
G | A | 1 | a0001c0001t0002g0256 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.466+9798C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44299799 | ||||||
| chr11:44299811
|
C | T | 2 | a0001c0002t0003g0267a0001c0005t0058g0202 | 2 | HG02300.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.466+9786G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44299811 | ||||||
| chr11:44299958
|
C | A | 140 | a0001c0001t0001g0003a0001c0001t0001g0203a0001c0001t0001g0227others(137): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.466+9639G>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44299958 | ||||||
| chr11:44300090
|
A | C | 1 | a0001c0002t0038g0221 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.466+9507T>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44300090 | ||||||
| chr11:44300265
|
C | G | 3 | a0002c0003t0002g0118a0002c0004t0007g0043a0002c0008t0051g0059 | 3 | HG01346.hp2 HG01361.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.466+9332G>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44300265 | ||||||
| chr11:44300301
|
A | G | 12 | a0001c0002t0013g0268a0004c0009t0007g0170a0004c0009t0009g0168others(9): Show | 12 | HG01243.hp2 HG02572.hp2 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.466+9296T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44300301 | ||||||
| chr11:44300463
|
C | T | 1 | a0001c0005t0004g0309 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.466+9134G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44300463 | ||||||
| chr11:44300614
|
A | G | 5 | a0003c0006t0009g0026a0003c0006t0015g0013a0003c0006t0032g0018others(2): Show | 5 | HG01884.hp2 HG02258.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.466+8983T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44300614 | ||||||
| chr11:44300616
|
G | A | 1 | a0002c0003t0010g0163 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.466+8981C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44300616 | ||||||
| chr11:44300681
|
G | T | 1 | a0001c0007t0016g0304 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.466+8916C>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44300681 | ||||||
| chr11:44300848
|
A | T | 1 | a0002c0003t0001g0075 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.466+8749T>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44300848 | ||||||
| chr11:44300932
|
G | A | 1 | a0001c0001t0002g0352 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.466+8665C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44300932 | ||||||
| chr11:44300941
|
C | T | 2 | a0001c0002t0025g0004a0001c0011t0020g0265 | 3 | HG01243.hp1 HG02976.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.466+8656G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44300941 | ||||||
| chr11:44301198
|
G | T | 1 | a0003c0006t0009g0026 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.466+8399C>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44301198 | ||||||
| chr11:44301459
|
T | A | 1 | a0001c0001t0002g0352 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.466+8138A>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44301459 | ||||||
| chr11:44301478
|
T | C | 1 | a0001c0005t0005g0358 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.466+8119A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44301478 | ||||||
| chr11:44301509
|
C | T | 12 | a0001c0002t0013g0268a0004c0009t0007g0170a0004c0009t0009g0168others(9): Show | 12 | HG01243.hp2 HG02572.hp2 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.466+8088G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44301509 | ||||||
| chr11:44301517
|
C | A | 1 | a0001c0005t0004g0309 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.466+8080G>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44301517 | ||||||
| chr11:44301552
|
G | A | 3 | a0002c0003t0001g0053a0002c0003t0001g0055a0002c0004t0003g0054 | 3 | NA18942.hp1 NA18966.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.466+8045C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44301552 | ||||||
| chr11:44301619
|
G | C | 1 | a0002c0008t0006g0071 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.466+7978C>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44301619 | ||||||
| chr11:44301643
|
T | C | 169 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0345others(166): Show | 170 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.466+7954A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44301643 | ||||||
| chr11:44301836
|
A | G | 1 | a0001c0027t0050g0224 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.466+7761T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44301836 | ||||||
| chr11:44301898
|
C | T | 1 | a0002c0004t0002g0076 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.466+7699G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44301898 | ||||||
| chr11:44301912
|
G | A | 10 | a0001c0001t0001g0373a0001c0001t0001g0374a0001c0002t0003g0349others(7): Show | 10 | HG01070.hp2 HG01071.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.466+7685C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44301912 | ||||||
| chr11:44301924
|
G | T | 1 | a0001c0002t0030g0204 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.466+7673C>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44301924 | ||||||
| chr11:44301955
|
G | A | 1 | a0003c0006t0011g0031 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.466+7642C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44301955 | ||||||
| chr11:44301974
|
G | A | 1 | a0002c0003t0002g0157 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.466+7623C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44301974 | ||||||
| chr11:44302180
|
G | A | 1 | a0001c0002t0003g0376 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.466+7417C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44302180 | ||||||
| chr11:44302279
|
C | T | 25 | a0001c0002t0016g0306a0001c0005t0066g0263a0003c0006t0003g0021others(22): Show | 25 | HG01109.hp1 HG01256.hp2 HG01258.hp2 others(22): Show |
intron_variant | MODIFIER | c.466+7318G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44302279 | ||||||
| chr11:44302286
|
G | A | 1 | a0001c0027t0050g0224 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.466+7311C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44302286 | ||||||
| chr11:44302468
|
C | A | 1 | a0001c0007t0016g0304 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.466+7129G>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44302468 | ||||||
| chr11:44302623
|
A | T | 2 | a0001c0002t0025g0004a0001c0011t0020g0265 | 3 | HG01243.hp1 HG02976.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.466+6974T>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44302623 | ||||||
| chr11:44302630
|
C | T | 1 | a0001c0005t0006g0007 | 2 | HG00639.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.466+6967G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44302630 | ||||||
| chr11:44302643
|
TGAGCCTG others(8): Show |
T | 12 | a0001c0002t0013g0268a0004c0009t0007g0170a0004c0009t0009g0168others(9): Show | 12 | HG01243.hp2 HG02572.hp2 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.466+6939_466+6953d others(17): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44302643 | ||||||
| chr11:44302701
|
C | T | 1 | a0001c0007t0004g0006 | 2 | HG01346.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.466+6896G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44302701 | ||||||
| chr11:44302736
|
C | T | 2 | a0001c0002t0025g0004a0001c0011t0020g0265 | 3 | HG01243.hp1 HG02976.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.466+6861G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44302736 | ||||||
| chr11:44302755
|
C | G | 3 | a0001c0001t0001g0180a0001c0001t0002g0188a0001c0005t0060g0181 | 3 | NA19002.hp1 NA19007.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.466+6842G>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44302755 | ||||||
| chr11:44302788
|
C | T | 1 | a0002c0004t0004g0117 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.466+6809G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44302788 | ||||||
| chr11:44302844
|
G | A | 2 | a0001c0002t0025g0004a0001c0011t0020g0265 | 3 | HG01243.hp1 HG02976.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.466+6753C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44302844 | ||||||
| chr11:44302856
|
G | A | 1 | a0001c0002t0040g0280 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.466+6741C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44302856 | ||||||
| chr11:44302897
|
C | T | 10 | a0001c0001t0001g0373a0001c0001t0001g0374a0001c0002t0003g0349others(7): Show | 10 | HG01070.hp2 HG01071.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.466+6700G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44302897 | ||||||
| chr11:44302941
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.466+6656G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44302941 | ||||||
| chr11:44302972
|
C | T | 1 | a0001c0016t0003g0179 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.466+6625G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44302972 | ||||||
| chr11:44302995
|
G | A | 2 | a0001c0001t0001g0343a0001c0002t0003g0344 | 2 | NA18747.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.466+6602C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44302995 | ||||||
| chr11:44303003
|
A | G | 1 | a0001c0005t0058g0202 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.466+6594T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44303003 | ||||||
| chr11:44303022
|
G | A | 1 | a0001c0001t0001g0303 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.466+6575C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44303022 | ||||||
| chr11:44303028
|
G | A | 1 | a0002c0004t0005g0144 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.466+6569C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44303028 | ||||||
| chr11:44303033
|
G | A | 85 | a0001c0001t0001g0248a0001c0001t0001g0250a0001c0001t0001g0252others(82): Show | 86 | HG00099.hp2 HG00408.hp1 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.466+6564C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44303033 | ||||||
| chr11:44303045
|
C | T | 2 | a0003c0017t0002g0008a0007c0018t0001g0011 | 2 | HG02602.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.466+6552G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44303045 | ||||||
| chr11:44303185
|
C | A | 2 | a0001c0002t0021g0260a0001c0031t0002g0381 | 2 | HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.466+6412G>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44303185 | ||||||
| chr11:44303202
|
C | T | 1 | a0002c0003t0001g0053 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.466+6395G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44303202 | ||||||
| chr11:44303356
|
C | T | 2 | a0001c0002t0025g0004a0001c0011t0020g0265 | 3 | HG01243.hp1 HG02976.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.466+6241G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44303356 | ||||||
| chr11:44303357
|
G | C | 132 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0345others(129): Show | 133 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.466+6240C>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44303357 | ||||||
| chr11:44303368
|
C | T | 1 | a0001c0001t0004g0222 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.466+6229G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44303368 | ||||||
| chr11:44303416
|
C | T | 5 | a0003c0006t0009g0026a0003c0006t0015g0013a0003c0006t0032g0018others(2): Show | 5 | HG01884.hp2 HG02258.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.466+6181G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44303416 | ||||||
| chr11:44303439
|
C | G | 1 | a0001c0001t0002g0380 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.466+6158G>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44303439 | ||||||
| chr11:44303479
|
C | G | 2 | a0001c0002t0003g0267a0001c0005t0058g0202 | 2 | HG02300.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.466+6118G>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44303479 | ||||||
| chr11:44303511
|
T | C | 3 | a0003c0006t0015g0013a0003c0006t0032g0018a0003c0021t0027g0019 | 3 | HG02809.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.466+6086A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44303511 | ||||||
| chr11:44303579
|
G | A | 1 | a0001c0001t0001g0257 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.466+6018C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44303579 | ||||||
| chr11:44303598
|
C | T | 10 | a0001c0001t0001g0373a0001c0001t0001g0374a0001c0002t0003g0349others(7): Show | 10 | HG01070.hp2 HG01071.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.466+5999G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44303598 | ||||||
| chr11:44303687
|
C | G | 328 | a0001c0001t0001g0003a0001c0001t0001g0203a0001c0001t0001g0227others(325): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.466+5910G>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44303687 | ||||||
| chr11:44303808
|
T | G | 2 | a0001c0002t0003g0267a0001c0005t0058g0202 | 2 | HG02300.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.466+5789A>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44303808 | ||||||
| chr11:44303857
|
C | T | 1 | a0001c0007t0003g0226 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.466+5740G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44303857 | ||||||
| chr11:44304075
|
G | A | 6 | a0002c0003t0001g0138a0002c0003t0001g0142a0002c0004t0003g0109others(3): Show | 6 | HG02056.hp2 HG02132.hp1 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.466+5522C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44304075 | ||||||
| chr11:44304095
|
TG | T | 10 | a0004c0009t0007g0170a0004c0009t0009g0168a0004c0009t0009g0169others(7): Show | 10 | HG01243.hp2 HG02572.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.466+5501delC | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44304095 | ||||||
| chr11:44304097
|
G | A | 1 | a0001c0002t0007g0264 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.466+5500C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44304097 | ||||||
| chr11:44304150
|
T | G | 143 | a0001c0001t0001g0003a0001c0001t0001g0203a0001c0001t0001g0227others(140): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.466+5447A>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44304150 | ||||||
| chr11:44304153
|
C | T | 5 | a0003c0006t0009g0026a0003c0006t0015g0013a0003c0006t0032g0018others(2): Show | 5 | HG01884.hp2 HG02258.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.466+5444G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44304153 | ||||||
| chr11:44304156
|
G | T | 1 | a0002c0004t0005g0143 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.466+5441C>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44304156 | ||||||
| chr11:44304283
|
C | T | 1 | a0001c0001t0002g0188 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.466+5314G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44304283 | ||||||
| chr11:44304292
|
G | C | 1 | a0001c0012t0006g0258 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.466+5305C>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44304292 | ||||||
| chr11:44304306
|
A | G | 1 | a0001c0005t0006g0212 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.466+5291T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44304306 | ||||||
| chr11:44304406
|
T | A | 1 | a0001c0002t0038g0221 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.466+5191A>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44304406 | ||||||
| chr11:44304452
|
C | A | 3 | a0002c0003t0001g0072a0002c0003t0001g0110a0002c0003t0010g0052 | 3 | HG00621.hp2 HG01934.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.466+5145G>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44304452 | ||||||
| chr11:44304500
|
C | T | 3 | a0001c0001t0001g0195a0001c0001t0001g0211a0001c0001t0004g0194 | 3 | HG00438.hp2 NA18939.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.466+5097G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44304500 | ||||||
| chr11:44304501
|
C | G | 2 | a0001c0002t0009g0366a0001c0002t0056g0367 | 2 | HG02486.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.466+5096G>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44304501 | ||||||
| chr11:44304641
|
C | A | 2 | a0001c0002t0015g0346a0001c0002t0020g0208 | 2 | HG03540.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.466+4956G>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44304641 | ||||||
| chr11:44304779
|
G | T | 2 | a0001c0002t0003g0225a0001c0002t0019g0312 | 2 | HG00140.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.466+4818C>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44304779 | ||||||
| chr11:44304849
|
C | T | 5 | a0003c0013t0001g0009a0003c0013t0001g0012a0003c0017t0002g0008others(2): Show | 5 | HG02293.hp1 HG02602.hp1 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.466+4748G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44304849 | ||||||
| chr11:44304870
|
C | T | 2 | a0001c0002t0007g0264a0001c0002t0011g0178 | 2 | HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.466+4727G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44304870 | ||||||
| chr11:44304924
|
C | T | 1 | a0001c0001t0002g0352 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.466+4673G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44304924 | ||||||
| chr11:44304993
|
C | G | 1 | a0001c0005t0004g0309 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.466+4604G>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44304993 | ||||||
| chr11:44305132
|
C | T | 1 | a0001c0001t0001g0271 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.466+4465G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44305132 | ||||||
| chr11:44305258
|
G | A | 1 | a0001c0001t0004g0222 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.466+4339C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44305258 | ||||||
| chr11:44305262
|
A | G | 316 | a0001c0001t0001g0003a0001c0001t0001g0203a0001c0001t0001g0227others(313): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.466+4335T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44305262 | ||||||
| chr11:44305309
|
G | C | 128 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0004g0311others(125): Show | 129 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.466+4288C>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44305309 | ||||||
| chr11:44305335
|
T | C | 1 | a0002c0004t0005g0143 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.466+4262A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44305335 | ||||||
| chr11:44305415
|
C | T | 1 | a0002c0003t0001g0044 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.466+4182G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44305415 | ||||||
| chr11:44305449
|
G | C | 4 | a0003c0006t0009g0023a0003c0006t0013g0033a0003c0006t0013g0041others(1): Show | 4 | HG01109.hp1 HG02451.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.466+4148C>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44305449 | ||||||
| chr11:44305584
|
C | G | 1 | a0002c0008t0051g0059 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.466+4013G>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44305584 | ||||||
| chr11:44305617
|
C | A | 4 | a0002c0003t0001g0053a0002c0003t0001g0055a0002c0003t0001g0073others(1): Show | 4 | NA18942.hp1 NA18948.hp2 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.466+3980G>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44305617 | ||||||
| chr11:44305739
|
T | C | 1 | a0002c0004t0022g0074 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.466+3858A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44305739 | ||||||
| chr11:44305751
|
C | T | 2 | a0001c0002t0009g0366a0001c0002t0056g0367 | 2 | HG02486.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.466+3846G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44305751 | ||||||
| chr11:44305874
|
G | A | 1 | a0002c0008t0063g0111 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.466+3723C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44305874 | ||||||
| chr11:44305943
|
C | T | 1 | a0002c0003t0004g0116 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.466+3654G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44305943 | ||||||
| chr11:44305997
|
G | C | 1 | a0001c0007t0016g0304 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.466+3600C>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44305997 | ||||||
| chr11:44306004
|
C | T | 1 | a0003c0020t0026g0017 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.466+3593G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44306004 | ||||||
| chr11:44306006
|
C | T | 2 | a0001c0001t0002g0187a0001c0002t0009g0348 | 2 | HG02572.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.466+3591G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44306006 | ||||||
| chr11:44306036
|
C | T | 1 | a0002c0004t0005g0058 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.466+3561G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44306036 | ||||||
| chr11:44306247
|
T | C | 143 | a0001c0001t0001g0003a0001c0001t0001g0203a0001c0001t0001g0227others(140): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.466+3350A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44306247 | ||||||
| chr11:44306268
|
T | C | 315 | a0001c0001t0001g0003a0001c0001t0001g0203a0001c0001t0001g0227others(312): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.466+3329A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44306268 | ||||||
| chr11:44306281
|
G | T | 11 | a0004c0009t0007g0170a0004c0009t0009g0168a0004c0009t0009g0169others(8): Show | 11 | HG01243.hp2 HG02572.hp2 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.466+3316C>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44306281 | ||||||
| chr11:44306367
|
G | A | 1 | a0001c0002t0003g0186 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.466+3230C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44306367 | ||||||
| chr11:44306552
|
T | C | 11 | a0001c0001t0001g0373a0001c0001t0001g0374a0001c0001t0002g0352others(8): Show | 11 | HG01070.hp2 HG01071.hp2 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.466+3045A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44306552 | ||||||
| chr11:44306768
|
C | T | 1 | a0003c0006t0007g0038 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.466+2829G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44306768 | ||||||
| chr11:44306877
|
T | C | 151 | a0001c0001t0001g0003a0001c0001t0001g0203a0001c0001t0001g0227others(148): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.466+2720A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44306877 | ||||||
| chr11:44307064
|
T | A | 11 | a0004c0009t0007g0170a0004c0009t0009g0168a0004c0009t0009g0169others(8): Show | 11 | HG01243.hp2 HG02572.hp2 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.466+2533A>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44307064 | ||||||
| chr11:44307130
|
C | A | 1 | a0002c0003t0001g0112 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.466+2467G>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44307130 | ||||||
| chr11:44307131
|
G | A | 2 | a0001c0002t0007g0264a0001c0002t0011g0178 | 2 | HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.466+2466C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44307131 | ||||||
| chr11:44307189
|
G | A | 2 | a0001c0002t0009g0366a0001c0002t0056g0367 | 2 | HG02486.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.466+2408C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44307189 | ||||||
| chr11:44307393
|
G | A | 6 | a0001c0001t0001g0347a0001c0001t0001g0364a0001c0001t0001g0365others(3): Show | 6 | NA18951.hp1 NA18953.hp1 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.466+2204C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44307393 | ||||||
| chr11:44307617
|
T | C | 335 | a0001c0001t0001g0003a0001c0001t0001g0203a0001c0001t0001g0227others(332): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.466+1980A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44307617 | ||||||
| chr11:44307658
|
C | T | 11 | a0004c0009t0007g0170a0004c0009t0009g0168a0004c0009t0009g0169others(8): Show | 11 | HG01243.hp2 HG02572.hp2 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.466+1939G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44307658 | ||||||
| chr11:44307659
|
G | A | 6 | a0003c0006t0003g0024a0003c0006t0003g0036a0003c0006t0004g0025others(3): Show | 6 | HG02818.hp2 HG02886.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.466+1938C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44307659 | ||||||
| chr11:44307721
|
G | T | 1 | a0002c0004t0007g0043 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.466+1876C>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44307721 | ||||||
| chr11:44307743
|
A | T | 1 | a0001c0001t0002g0380 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.466+1854T>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44307743 | ||||||
| chr11:44307806
|
A | C | 1 | a0004c0023t0044g0167 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.466+1791T>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44307806 | ||||||
| chr11:44307812
|
G | A | 2 | a0002c0003t0045g0113a0002c0004t0005g0144 | 2 | NA18990.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.466+1785C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44307812 | ||||||
| chr11:44307894
|
G | A | 1 | a0002c0003t0047g0114 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.466+1703C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44307894 | ||||||
| chr11:44307924
|
A | G | 3 | a0001c0002t0009g0366a0001c0002t0056g0367a0001c0027t0050g0224 | 3 | HG02486.hp2 HG02615.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.466+1673T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44307924 | ||||||
| chr11:44308063
|
G | A | 2 | a0001c0002t0025g0004a0001c0011t0020g0265 | 3 | HG01243.hp1 HG02976.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.466+1534C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44308063 | ||||||
| chr11:44308185
|
G | C | 2 | a0001c0002t0021g0260a0001c0031t0002g0381 | 2 | HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.466+1412C>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44308185 | ||||||
| chr11:44308234
|
T | C | 29 | a0003c0006t0003g0021a0003c0006t0003g0024a0003c0006t0003g0036others(26): Show | 29 | HG01109.hp1 HG01256.hp2 HG01258.hp2 others(26): Show |
intron_variant | MODIFIER | c.466+1363A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44308234 | ||||||
| chr11:44308235
|
A | T | 1 | a0003c0020t0026g0017 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.466+1362T>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44308235 | ||||||
| chr11:44308285
|
T | G | 1 | a0001c0002t0005g0223 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.466+1312A>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44308285 | ||||||
| chr11:44308288
|
A | G | 149 | a0001c0001t0001g0003a0001c0001t0001g0203a0001c0001t0001g0227others(146): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.466+1309T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44308288 | ||||||
| chr11:44308332
|
T | C | 1 | a0002c0004t0020g0158 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.466+1265A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44308332 | ||||||
| chr11:44308430
|
G | C | 1 | a0005c0025t0008g0177 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.466+1167C>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44308430 | ||||||
| chr11:44308454
|
C | G | 1 | a0002c0004t0005g0160 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.466+1143G>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44308454 | ||||||
| chr11:44308649
|
G | A | 2 | a0001c0002t0003g0261a0001c0002t0003g0262 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.466+948C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44308649 | ||||||
| chr11:44308710
|
G | A | 4 | a0001c0002t0003g0184a0001c0002t0003g0185a0001c0002t0003g0186others(1): Show | 4 | HG00099.hp1 HG01433.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.466+887C>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44308710 | ||||||
| chr11:44308778
|
A | G | 2 | a0001c0002t0016g0306a0001c0005t0066g0263 | 2 | HG02559.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.466+819T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44308778 | ||||||
| chr11:44308951
|
G | T | 147 | a0001c0001t0001g0003a0001c0001t0001g0203a0001c0001t0001g0227others(144): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.466+646C>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44308951 | ||||||
| chr11:44309024
|
C | T | 1 | a0001c0002t0013g0268 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.466+573G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44309024 | ||||||
| chr11:44309046
|
C | T | 2 | a0002c0003t0001g0115a0002c0004t0003g0057 | 2 | NA19070.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.466+551G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44309046 | ||||||
| chr11:44309060
|
C | T | 169 | a0002c0003t0001g0001a0002c0003t0001g0044a0002c0003t0001g0045others(166): Show | 170 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.466+537G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44309060 | ||||||
| chr11:44309138
|
T | C | 339 | a0001c0001t0001g0003a0001c0001t0001g0203a0001c0001t0001g0227others(336): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.466+459A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44309138 | ||||||
| chr11:44309149
|
T | TGCTGTCC others(17): Show |
18 | a0002c0003t0001g0060a0002c0003t0001g0062a0002c0003t0001g0063others(15): Show | 18 | HG00544.hp2 HG00621.hp2 HG00673.hp2 others(15): Show |
intron_variant | MODIFIER | c.466+424_466+447dup others(24): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44309149 | ||||||
| chr11:44309149
|
T | TGCTGTCC others(41): Show |
1 | a0002c0003t0001g0075 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.466+447_466+448ins others(48): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44309149 | ||||||
| chr11:44309154
|
T | TCCCGCAG others(1): Show |
59 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0271others(56): Show | 60 | HG00738.hp1 HG01069.hp2 HG01071.hp1 others(57): Show |
intron_variant | MODIFIER | c.466+435_466+442dup others(8): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44309154 | ||||||
| chr11:44309154
|
T | TCCCGCAG others(42): Show |
1 | a0002c0003t0001g0159 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.466+442_466+443ins others(49): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44309154 | ||||||
| chr11:44309154
|
T | TCCCGCAG others(9): Show |
64 | a0001c0001t0001g0310a0001c0001t0001g0313a0001c0001t0001g0315others(61): Show | 66 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.466+427_466+442dup others(16): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44309154 | ||||||
| chr11:44309154
|
T | TCCCGCAG others(17): Show |
20 | a0001c0001t0001g0355a0001c0001t0001g0364a0001c0001t0001g0365others(17): Show | 20 | HG00140.hp1 HG01123.hp1 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.466+419_466+442dup others(24): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44309154 | ||||||
| chr11:44309154
|
T | TCCCGCAG others(25): Show |
10 | a0001c0001t0001g0369a0001c0001t0001g0373a0001c0001t0001g0374others(7): Show | 10 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.466+442_466+443ins others(32): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44309154 | ||||||
| chr11:44309154
|
T | TCCCGCAG others(33): Show |
2 | a0001c0001t0001g0378a0001c0005t0006g0377 | 2 | NA19009.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.466+442_466+443ins others(40): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44309154 | ||||||
| chr11:44309154
|
T | TCCCGCAG others(41): Show |
1 | a0001c0002t0001g0379 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.466+442_466+443ins others(48): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44309154 | ||||||
| chr11:44309154
|
T | TCCCGCAG others(25): Show |
41 | a0002c0003t0001g0001a0002c0003t0001g0081a0002c0003t0001g0095others(38): Show | 42 | HG00323.hp1 HG00621.hp1 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.466+442_466+443ins others(32): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44309154 | ||||||
| chr11:44309154
|
T | TCCCGCAG others(33): Show |
31 | a0002c0003t0001g0115a0002c0003t0001g0119a0002c0003t0001g0124others(28): Show | 31 | HG00280.hp1 HG00423.hp1 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.466+442_466+443ins others(40): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44309154 | ||||||
| chr11:44309154
|
T | TCCCGCAG others(41): Show |
12 | a0002c0003t0001g0147a0002c0003t0001g0153a0002c0003t0002g0155others(9): Show | 12 | HG00544.hp1 HG02074.hp1 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.466+442_466+443ins others(48): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44309154 | ||||||
| chr11:44309154
|
T | TCCCGCAG others(49): Show |
4 | a0002c0003t0001g0162a0002c0003t0010g0163a0002c0004t0005g0160others(1): Show | 4 | HG00438.hp1 HG02165.hp1 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.466+442_466+443ins others(56): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44309154 | ||||||
| chr11:44309156
|
CCGCAGCC others(17): Show |
C | 3 | a0001c0002t0003g0184a0001c0002t0003g0185a0001c0002t0003g0186 | 3 | HG00099.hp1 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.466+417_466+440del others(24): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44309156 | ||||||
| chr11:44309162
|
C | CCCCGCAG others(9): Show |
13 | a0002c0003t0001g0044a0002c0003t0001g0045a0002c0003t0001g0047others(10): Show | 13 | HG00423.hp2 HG01346.hp2 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.466+434_466+435ins others(16): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44309162 | ||||||
| chr11:44309164
|
CCGCAGCC others(9): Show |
C | 1 | a0001c0001t0002g0187 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.466+417_466+432del others(16): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44309164 | ||||||
| chr11:44309172
|
CCGCAGCC others(1): Show |
C | 16 | a0001c0001t0001g0195a0001c0001t0001g0199a0001c0001t0001g0201others(13): Show | 16 | HG00639.hp2 HG01433.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.466+417_466+424del others(8): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44309172 | ||||||
| chr11:44309176
|
A | T | 1 | a0002c0004t0014g0164 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.466+421T>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44309176 | ||||||
| chr11:44309177
|
G | GTCCCGCA others(19): Show |
1 | a0002c0004t0014g0164 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.466+419_466+420ins others(26): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44309177 | ||||||
| chr11:44309180
|
T | C | 348 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0211others(345): Show | 355 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(352): Show |
intron_variant | MODIFIER | c.466+417A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44309180 | ||||||
| chr11:44309180
|
T | TCGCAGCC others(9): Show |
6 | a0001c0001t0002g0188a0001c0001t0002g0190a0001c0002t0023g0192others(3): Show | 6 | HG02109.hp2 HG02145.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.466+401_466+416dup others(16): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44309180 | ||||||
| chr11:44309180
|
T | TCGCAGCC others(17): Show |
1 | a0001c0002t0004g0210 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.466+393_466+416dup others(24): Show |
ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44309180 | ||||||
| chr11:44309213
|
C | G | 1 | a0001c0001t0002g0380 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.466+384G>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44309213 | ||||||
| chr11:44309214
|
G | C | 1 | a0001c0001t0002g0380 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.466+383C>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44309214 | ||||||
| chr11:44309239
|
C | A | 1 | a0002c0004t0001g0165 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.466+358G>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44309239 | ||||||
| chr11:44309317
|
C | G | 1 | a0002c0003t0002g0042 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.466+280G>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44309317 | ||||||
| chr11:44309352
|
C | T | 1 | a0001c0002t0011g0178 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.466+245G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44309352 | ||||||
| chr11:44309540
|
T | A | 1 | a0001c0001t0002g0380 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.466+57A>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44309540 |