Item | Value |
---|---|
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 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 411 | 216 | 55 | 41 | 92 | 14 | 12 | 79 | ALX4_chr11_44255440_44315139 | ALX4 | MNAET others(406): Show |
chr11 | 44255440 | 44315139 |
a0002 | 0/0 | 411 | 126 | 1 | 20 | 79 | 4 | 22 | 54 | ALX4_chr11_44255440_44315139 | ALX4 | MNAET others(406): Show |
chr11 | 44255440 | 44315139 |
a0003 | 0/0 | 411 | 33 | 26 | 4 | 0 | 0 | 3 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | MNAET others(406): Show |
chr11 | 44255440 | 44315139 |
a0004 | 0/0 | 407 | 11 | 10 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | MNAET others(402): Show |
chr11 | 44255440 | 44315139 |
a0005 | 0/0 | 411 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | MNAET others(406): Show |
chr11 | 44255440 | 44315139 |
a0006 | 0/0 | 411 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | MNAET others(406): Show |
chr11 | 44255440 | 44315139 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1233 | 87 | 6 | 19 | 57 | 2 | 3 | ALX4_chr11_44255440_44315139 | ALX4 | ATGAA others(1228): Show |
chr11 | 44255440 | 44315139 | ||
a0001c0002 | 0/1 | 1233 | 78 | 35 | 12 | 18 | 8 | 4 | ALX4_chr11_44255440_44315139 | ALX4 | ATGAA others(1228): Show |
chr11 | 44255440 | 44315139 | ||
a0001c0005 | 0/0 | 1233 | 23 | 1 | 2 | 17 | 0 | 3 | ALX4_chr11_44255440_44315139 | ALX4 | ATGAA others(1228): Show |
chr11 | 44255440 | 44315139 | ||
a0001c0007 | 0/0 | 1233 | 14 | 6 | 4 | 0 | 3 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | ATGAA others(1228): Show |
chr11 | 44255440 | 44315139 | ||
a0001c0011 | 0/0 | 1233 | 3 | 1 | 2 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | ATGAA others(1228): Show |
chr11 | 44255440 | 44315139 | ||
a0001c0012 | 0/0 | 1233 | 3 | 0 | 1 | 0 | 1 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | ATGAA others(1228): Show |
chr11 | 44255440 | 44315139 | ||
a0001c0016 | 1/0 | 1233 | 2 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | ATGAA others(1228): Show |
chr11 | 44255440 | 44315139 | ||
a0001c0026 | 0/0 | 1233 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | ATGAA others(1228): Show |
chr11 | 44255440 | 44315139 | ||
a0001c0027 | 0/0 | 1233 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | ATGAA others(1228): Show |
chr11 | 44255440 | 44315139 | ||
a0001c0028 | 0/0 | 1233 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | ATGAA others(1228): Show |
chr11 | 44255440 | 44315139 | ||
a0001c0029 | 0/0 | 1233 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | ATGAA others(1228): Show |
chr11 | 44255440 | 44315139 | ||
a0001c0030 | 0/0 | 1233 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | ATGAA others(1228): Show |
chr11 | 44255440 | 44315139 | ||
a0001c0031 | 0/0 | 1233 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | ATGAA others(1228): Show |
chr11 | 44255440 | 44315139 | ||
a0002c0003 | 0/0 | 1233 | 68 | 1 | 12 | 43 | 1 | 11 | ALX4_chr11_44255440_44315139 | ALX4 | ATGAA others(1228): Show |
chr11 | 44255440 | 44315139 | ||
a0002c0004 | 0/0 | 1233 | 45 | 0 | 7 | 28 | 2 | 8 | ALX4_chr11_44255440_44315139 | ALX4 | ATGAA others(1228): Show |
chr11 | 44255440 | 44315139 | ||
a0002c0008 | 0/0 | 1233 | 13 | 0 | 1 | 8 | 1 | 3 | ALX4_chr11_44255440_44315139 | ALX4 | ATGAA others(1228): Show |
chr11 | 44255440 | 44315139 | ||
a0003c0006 | 0/0 | 1233 | 17 | 16 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | ATGAA others(1228): Show |
chr11 | 44255440 | 44315139 | ||
a0003c0010 | 0/0 | 1233 | 6 | 4 | 2 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | ATGAA others(1228): Show |
chr11 | 44255440 | 44315139 | ||
a0003c0013 | 0/0 | 1233 | 2 | 0 | 1 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | ATGAA others(1228): Show |
chr11 | 44255440 | 44315139 | ||
a0003c0014 | 0/0 | 1233 | 2 | 2 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | ATGAA others(1228): Show |
chr11 | 44255440 | 44315139 | ||
a0003c0015 | 0/0 | 1233 | 2 | 2 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | ATGAA others(1228): Show |
chr11 | 44255440 | 44315139 | ||
a0003c0017 | 0/0 | 1233 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | ATGAA others(1228): Show |
chr11 | 44255440 | 44315139 | ||
a0003c0019 | 0/0 | 1233 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | ATGAA others(1228): Show |
chr11 | 44255440 | 44315139 | ||
a0003c0020 | 0/0 | 1233 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | ATGAA others(1228): Show |
chr11 | 44255440 | 44315139 | ||
a0003c0021 | 0/0 | 1233 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | ATGAA others(1228): Show |
chr11 | 44255440 | 44315139 | ||
a0004c0009 | 0/0 | 1221 | 8 | 7 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | ATGAA others(1216): Show |
chr11 | 44255440 | 44315139 | ||
a0004c0022 | 0/0 | 1221 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | ATGAA others(1216): Show |
chr11 | 44255440 | 44315139 | ||
a0004c0023 | 0/0 | 1221 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | ATGAA others(1216): Show |
chr11 | 44255440 | 44315139 | ||
a0004c0024 | 0/0 | 1221 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | ATGAA others(1216): Show |
chr11 | 44255440 | 44315139 | ||
a0005c0018 | 0/0 | 1233 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | ATGAA others(1228): Show |
chr11 | 44255440 | 44315139 | ||
a0006c0025 | 0/0 | 1233 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | ATGAA others(1228): Show |
chr11 | 44255440 | 44315139 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5727 | 46 | 0 | 10 | 31 | 2 | 3 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0001c0001t0002 | 0/0 | 5727 | 23 | 5 | 5 | 13 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0001c0001t0004 | 0/0 | 5727 | 10 | 0 | 1 | 9 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0001c0001t0005 | 0/0 | 5727 | 2 | 0 | 0 | 2 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0001c0001t0006 | 0/0 | 5727 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0001c0001t0010 | 0/0 | 5727 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0001c0001t0017 | 0/0 | 5727 | 2 | 0 | 2 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0001c0001t0018 | 0/0 | 5727 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0001c0001t0043 | 0/0 | 5727 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0001c0002t0001 | 0/0 | 5727 | 4 | 0 | 0 | 4 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0001c0002t0002 | 0/0 | 5727 | 2 | 1 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0001c0002t0003 | 0/0 | 5727 | 19 | 2 | 7 | 3 | 6 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0001c0002t0004 | 0/0 | 5727 | 3 | 1 | 2 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0001c0002t0005 | 0/0 | 5727 | 8 | 0 | 0 | 6 | 0 | 2 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0001c0002t0006 | 0/1 | 5727 | 2 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0001c0002t0007 | 0/0 | 5727 | 7 | 6 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0001c0002t0008 | 0/0 | 5727 | 2 | 0 | 0 | 2 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0001c0002t0009 | 0/0 | 5727 | 2 | 2 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0001c0002t0011 | 0/0 | 5723 | 5 | 5 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5718): Show |
chr11 | 44255440 | 44315139 |
a0001c0002t0013 | 0/0 | 5727 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0001c0002t0015 | 0/0 | 5727 | 2 | 2 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0001c0002t0016 | 0/0 | 5727 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0001c0002t0019 | 0/0 | 5724 | 1 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5719): Show |
chr11 | 44255440 | 44315139 |
a0001c0002t0020 | 0/0 | 5727 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0001c0002t0021 | 0/0 | 5727 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0001c0002t0023 | 0/0 | 5727 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0001c0002t0025 | 0/0 | 5727 | 2 | 1 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0001c0002t0027 | 0/0 | 5724 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5719): Show |
chr11 | 44255440 | 44315139 |
a0001c0002t0028 | 0/0 | 5724 | 2 | 2 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5719): Show |
chr11 | 44255440 | 44315139 |
a0001c0002t0030 | 0/0 | 5724 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5719): Show |
chr11 | 44255440 | 44315139 |
a0001c0002t0031 | 0/0 | 5727 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0001c0002t0033 | 0/0 | 5723 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5718): Show |
chr11 | 44255440 | 44315139 |
a0001c0002t0036 | 0/0 | 5727 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0001c0002t0038 | 0/0 | 5727 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0001c0002t0040 | 0/0 | 5727 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0001c0002t0052 | 0/0 | 5724 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5719): Show |
chr11 | 44255440 | 44315139 |
a0001c0002t0055 | 0/0 | 5727 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0001c0002t0056 | 0/0 | 5727 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0001c0002t0057 | 0/0 | 5727 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0001c0002t0067 | 0/0 | 5723 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5718): Show |
chr11 | 44255440 | 44315139 |
a0001c0005t0004 | 0/0 | 5727 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0001c0005t0005 | 0/0 | 5727 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0001c0005t0006 | 0/0 | 5727 | 11 | 0 | 2 | 8 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0001c0005t0008 | 0/0 | 5727 | 5 | 0 | 0 | 5 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0001c0005t0058 | 0/0 | 5727 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0001c0005t0060 | 0/0 | 5727 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0001c0005t0061 | 0/0 | 5727 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0001c0005t0064 | 0/0 | 5727 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0001c0005t0066 | 0/0 | 5727 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0001c0007t0003 | 0/0 | 5727 | 2 | 1 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0001c0007t0004 | 0/0 | 5727 | 7 | 4 | 3 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0001c0007t0007 | 0/0 | 5727 | 2 | 0 | 0 | 0 | 2 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0001c0007t0008 | 0/0 | 5727 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0001c0007t0016 | 0/0 | 5727 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0001c0007t0053 | 0/0 | 5724 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5719): Show |
chr11 | 44255440 | 44315139 |
a0001c0011t0003 | 0/0 | 5727 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0001c0011t0020 | 0/0 | 5727 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0001c0011t0031 | 0/0 | 5727 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0001c0012t0006 | 0/0 | 5727 | 2 | 0 | 0 | 0 | 1 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0001c0012t0062 | 0/0 | 5727 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0001c0016t0003 | 0/0 | 5727 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0001c0016t0021 | 1/0 | 5727 | 1 | 0 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0001c0026t0023 | 0/0 | 5727 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0001c0027t0050 | 0/0 | 5727 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0001c0028t0002 | 0/0 | 5727 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0001c0029t0001 | 0/0 | 5727 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0001c0030t0026 | 0/0 | 5727 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0001c0031t0002 | 0/0 | 5727 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0002c0003t0001 | 0/0 | 5727 | 41 | 0 | 5 | 27 | 1 | 8 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0002c0003t0002 | 0/0 | 5727 | 5 | 1 | 1 | 3 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0002c0003t0004 | 0/0 | 5727 | 4 | 0 | 1 | 2 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0002c0003t0005 | 0/0 | 5727 | 2 | 0 | 0 | 2 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0002c0003t0006 | 0/0 | 5727 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0002c0003t0010 | 0/0 | 5727 | 7 | 0 | 5 | 2 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0002c0003t0017 | 0/0 | 5727 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0002c0003t0018 | 0/0 | 5727 | 2 | 0 | 0 | 2 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0002c0003t0041 | 0/0 | 5727 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0002c0003t0045 | 0/0 | 5727 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0002c0003t0047 | 0/0 | 5727 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0002c0003t0049 | 0/0 | 5727 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0002c0003t0054 | 0/0 | 5727 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0002c0004t0001 | 0/0 | 5727 | 3 | 0 | 0 | 1 | 0 | 2 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0002c0004t0002 | 0/0 | 5727 | 4 | 0 | 0 | 3 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0002c0004t0003 | 0/0 | 5727 | 6 | 0 | 1 | 4 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0002c0004t0004 | 0/0 | 5727 | 2 | 0 | 0 | 2 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0002c0004t0005 | 0/0 | 5727 | 11 | 0 | 0 | 11 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0002c0004t0006 | 0/0 | 5727 | 2 | 0 | 1 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0002c0004t0007 | 0/0 | 5727 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0002c0004t0008 | 0/0 | 5727 | 2 | 0 | 0 | 2 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0002c0004t0012 | 0/0 | 5727 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0002c0004t0014 | 0/0 | 5724 | 4 | 0 | 3 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5719): Show |
chr11 | 44255440 | 44315139 |
a0002c0004t0019 | 0/0 | 5724 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5719): Show |
chr11 | 44255440 | 44315139 |
a0002c0004t0020 | 0/0 | 5727 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0002c0004t0022 | 0/0 | 5727 | 2 | 0 | 0 | 2 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0002c0004t0034 | 0/0 | 5727 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0002c0004t0035 | 0/0 | 5727 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0002c0004t0037 | 0/0 | 5727 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0002c0004t0039 | 0/0 | 5727 | 1 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0002c0004t0046 | 0/0 | 5727 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0002c0008t0004 | 0/0 | 5727 | 2 | 0 | 1 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0002c0008t0005 | 0/0 | 5727 | 4 | 0 | 0 | 4 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0002c0008t0006 | 0/0 | 5727 | 3 | 0 | 0 | 1 | 0 | 2 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0002c0008t0012 | 0/0 | 5727 | 2 | 0 | 0 | 2 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0002c0008t0051 | 0/0 | 5727 | 1 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0002c0008t0063 | 0/0 | 5727 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0003c0006t0003 | 0/0 | 5727 | 4 | 4 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0003c0006t0004 | 0/0 | 5727 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0003c0006t0007 | 0/0 | 5727 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0003c0006t0009 | 0/0 | 5727 | 2 | 2 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0003c0006t0011 | 0/0 | 5723 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5718): Show |
chr11 | 44255440 | 44315139 |
a0003c0006t0013 | 0/0 | 5727 | 2 | 1 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0003c0006t0015 | 0/0 | 5727 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0003c0006t0019 | 0/0 | 5724 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5719): Show |
chr11 | 44255440 | 44315139 |
a0003c0006t0024 | 0/0 | 5727 | 2 | 2 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0003c0006t0032 | 0/0 | 5727 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0003c0006t0065 | 0/0 | 5724 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5719): Show |
chr11 | 44255440 | 44315139 |
a0003c0010t0001 | 0/0 | 5727 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0003c0010t0002 | 0/0 | 5727 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0003c0010t0012 | 0/0 | 5727 | 2 | 0 | 2 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0003c0010t0042 | 0/0 | 5727 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0003c0010t0048 | 0/0 | 5727 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0003c0013t0001 | 0/0 | 5727 | 2 | 0 | 1 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0003c0014t0003 | 0/0 | 5727 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0003c0014t0030 | 0/0 | 5724 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5719): Show |
chr11 | 44255440 | 44315139 |
a0003c0015t0029 | 0/0 | 5724 | 2 | 2 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5719): Show |
chr11 | 44255440 | 44315139 |
a0003c0017t0002 | 0/0 | 5727 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0003c0019t0059 | 0/0 | 5727 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0003c0020t0026 | 0/0 | 5727 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0003c0021t0027 | 0/0 | 5724 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5719): Show |
chr11 | 44255440 | 44315139 |
a0004c0009t0007 | 0/0 | 5715 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5710): Show |
chr11 | 44255440 | 44315139 |
a0004c0009t0009 | 0/0 | 5715 | 4 | 3 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5710): Show |
chr11 | 44255440 | 44315139 |
a0004c0009t0011 | 0/0 | 5711 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5706): Show |
chr11 | 44255440 | 44315139 |
a0004c0009t0013 | 0/0 | 5715 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5710): Show |
chr11 | 44255440 | 44315139 |
a0004c0009t0016 | 0/0 | 5715 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5710): Show |
chr11 | 44255440 | 44315139 |
a0004c0022t0009 | 0/0 | 5715 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5710): Show |
chr11 | 44255440 | 44315139 |
a0004c0023t0044 | 0/0 | 5715 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5710): Show |
chr11 | 44255440 | 44315139 |
a0004c0024t0001 | 0/0 | 5715 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5710): Show |
chr11 | 44255440 | 44315139 |
a0005c0018t0001 | 0/0 | 5727 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
a0006c0025t0008 | 0/0 | 5727 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | AAACT others(5722): Show |
chr11 | 44255440 | 44315139 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0001g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0001g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0001g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0002g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0002g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0002g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0002g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0004g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0004g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0004g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0004g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0004g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0004g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0004g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0004g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0004g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0004g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0005g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0005g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0006g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0010g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0017g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0017g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0018g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0001t0043g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0001g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0003g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0003g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0003g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0003g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0003g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0003g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0003g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0003g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0003g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0003g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0003g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0003g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0003g0369 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0003g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0003g0375 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0003g0376 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0003g0377 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0004g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0004g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0004g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0005g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0005g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0005g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0005g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0005g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0005g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0005g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0005g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0006g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0006g0378 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0007g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0007g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0007g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0007g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0007g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0007g0351 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0007g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0008g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0008g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0009g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0009g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0011g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0011g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0011g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0011g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0011g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0013g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0015g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0015g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0016g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0019g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0020g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0021g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0023g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0025g0005 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0027g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0028g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0028g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0030g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0031g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0033g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0036g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0038g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0040g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0052g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0055g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0056g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0057g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0002t0067g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0005t0004g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0005t0005g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0005t0006g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0005t0006g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0005t0006g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0005t0006g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0005t0006g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0005t0006g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0005t0006g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0005t0006g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0005t0006g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0005t0006g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0005t0008g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0005t0008g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0005t0008g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0005t0008g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0005t0058g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0005t0060g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0005t0061g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0005t0064g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0005t0066g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0007t0003g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0007t0003g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0007t0004g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0007t0004g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0007t0004g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0007t0004g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0007t0004g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0007t0004g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0007t0007g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0007t0007g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0007t0008g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0007t0016g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0007t0053g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0011t0003g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0011t0020g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0011t0031g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0012t0006g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0012t0006g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0012t0062g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0016t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0016t0021g0206 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0026t0023g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0027t0050g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0028t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0029t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0030t0026g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0001c0031t0002g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0001g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0004g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0004g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0005g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0005g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0006g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0010g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0010g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0010g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0010g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0010g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0010g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0010g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0017g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0018g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0018g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0041g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0045g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0047g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0049g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0003t0054g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0004t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0004t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0004t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0004t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0004t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0004t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0004t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0004t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0004t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0004t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0004t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0004t0003g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0004t0003g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0004t0004g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0004t0004g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0004t0005g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0004t0005g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0004t0005g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0004t0005g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0004t0005g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0004t0005g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0004t0005g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0004t0005g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0004t0005g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0004t0005g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0004t0005g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0004t0006g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0004t0006g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0004t0007g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0004t0008g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0004t0008g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0004t0012g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0004t0014g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0004t0014g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0004t0014g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0004t0014g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0004t0019g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0004t0020g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0004t0022g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0004t0022g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0004t0034g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0004t0035g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0004t0037g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0004t0039g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0004t0046g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0008t0004g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0008t0004g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0008t0005g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0008t0005g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0008t0005g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0008t0005g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0008t0006g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0008t0006g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0008t0006g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0008t0012g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0008t0012g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0008t0051g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0002c0008t0063g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0003c0006t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0003c0006t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0003c0006t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0003c0006t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0003c0006t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0003c0006t0007g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0003c0006t0009g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0003c0006t0009g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0003c0006t0011g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0003c0006t0013g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0003c0006t0013g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0003c0006t0015g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0003c0006t0019g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0003c0006t0024g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0003c0006t0024g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0003c0006t0032g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0003c0006t0065g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0003c0010t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0003c0010t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0003c0010t0012g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0003c0010t0012g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0003c0010t0042g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0003c0010t0048g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0003c0013t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0003c0013t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0003c0014t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0003c0014t0030g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0003c0015t0029g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0003c0015t0029g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0003c0017t0002g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0003c0019t0059g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0003c0020t0026g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0003c0021t0027g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0004c0009t0007g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0004c0009t0009g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0004c0009t0009g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0004c0009t0009g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0004c0009t0009g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0004c0009t0011g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0004c0009t0013g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0004c0009t0016g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0004c0022t0009g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0004c0023t0044g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0004c0024t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0005c0018t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
a0006c0025t0008g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0003 | g0377 | EUR | GBR | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0235 | EUR | GBR | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG00140 | hp1 | a0001 | c0002 | t0007 | g0351 | EUR | GBR | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG00140 | hp2 | a0001 | c0002 | t0003 | g0213 | EUR | GBR | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG00280 | hp1 | a0002 | c0003 | t0001 | g0133 | EUR | FIN | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0314 | EUR | FIN | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG00323 | hp1 | a0002 | c0004 | t0039 | g0094 | EUR | FIN | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG00323 | hp2 | a0001 | c0002 | t0019 | g0308 | EUR | FIN | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG00408 | hp1 | a0001 | c0002 | t0006 | g0326 | EAS | CHS | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG00408 | hp2 | a0001 | c0005 | t0006 | g0200 | EAS | CHS | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG00423 | hp1 | a0002 | c0004 | t0004 | g0119 | EAS | CHS | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG00423 | hp2 | a0002 | c0003 | t0001 | g0047 | EAS | CHS | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG00438 | hp1 | a0002 | c0004 | t0005 | g0163 | EAS | CHS | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG00544 | hp1 | a0002 | c0003 | t0001 | g0156 | EAS | CHS | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG00544 | hp2 | a0002 | c0004 | t0022 | g0076 | EAS | CHS | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG00609 | hp1 | a0001 | c0002 | t0003 | g0309 | EAS | CHS | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG00609 | hp2 | a0002 | c0004 | t0035 | g0124 | EAS | CHS | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG00621 | hp1 | a0002 | c0004 | t0005 | g0085 | EAS | CHS | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG00621 | hp2 | a0002 | c0003 | t0001 | g0074 | EAS | CHS | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG00639 | hp1 | a0001 | c0005 | t0006 | g0008 | AMR | PUR | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG00639 | hp2 | a0001 | c0002 | t0030 | g0220 | AMR | PUR | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG00673 | hp2 | a0002 | c0004 | t0005 | g0060 | EAS | CHS | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG00738 | hp1 | a0001 | c0007 | t0008 | g0291 | AMR | PUR | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG00738 | hp2 | a0001 | c0007 | t0004 | g0236 | AMR | PUR | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG00741 | hp1 | a0002 | c0004 | t0006 | g0129 | AMR | PUR | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG00741 | hp2 | a0001 | c0002 | t0031 | g0218 | AMR | PUR | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG01069 | hp1 | a0002 | c0003 | t0001 | g0102 | AMR | PUR | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG01070 | hp1 | a0001 | c0029 | t0001 | g0234 | AMR | PUR | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0368 | AMR | PUR | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0370 | AMR | PUR | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0249 | AMR | PUR | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG01099 | hp2 | a0001 | c0002 | t0004 | g0304 | AMR | PUR | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG01106 | hp1 | a0001 | c0005 | t0006 | g0008 | AMR | PUR | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG01106 | hp2 | a0001 | c0002 | t0004 | g0303 | AMR | PUR | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG01109 | hp1 | a0003 | c0006 | t0013 | g0034 | AMR | PUR | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0225 | AMR | PUR | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG01168 | hp1 | a0001 | c0002 | t0003 | g0371 | AMR | PUR | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG01168 | hp2 | a0002 | c0004 | t0014 | g0054 | AMR | PUR | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG01169 | hp1 | a0002 | c0004 | t0014 | g0072 | AMR | PUR | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG01169 | hp2 | a0001 | c0001 | t0004 | g0307 | AMR | PUR | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0224 | AMR | PUR | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG01192 | hp1 | a0001 | c0011 | t0003 | g0290 | AMR | PUR | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0312 | AMR | PUR | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG01243 | hp1 | a0001 | c0002 | t0025 | g0005 | AMR | PUR | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG01243 | hp2 | a0004 | c0009 | t0009 | g0169 | AMR | PUR | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG01255 | hp1 | a0002 | c0003 | t0001 | g0086 | AMR | CLM | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG01255 | hp2 | a0002 | c0004 | t0012 | g0080 | AMR | CLM | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | CLM | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG01256 | hp2 | a0003 | c0010 | t0012 | g0031 | AMR | CLM | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG01257 | hp1 | a0001 | c0002 | t0003 | g0256 | AMR | CLM | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0275 | AMR | CLM | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG01258 | hp1 | a0001 | c0002 | t0003 | g0255 | AMR | CLM | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG01258 | hp2 | a0003 | c0010 | t0012 | g0029 | AMR | CLM | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG01261 | hp1 | a0001 | c0002 | t0003 | g0345 | AMR | CLM | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG01261 | hp2 | a0002 | c0003 | t0004 | g0147 | AMR | CLM | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG01346 | hp1 | a0001 | c0007 | t0004 | g0007 | AMR | CLM | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG01346 | hp2 | a0002 | c0004 | t0007 | g0044 | AMR | CLM | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG01358 | hp1 | a0001 | c0007 | t0004 | g0007 | AMR | CLM | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG01358 | hp2 | a0002 | c0008 | t0004 | g0088 | AMR | CLM | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG01361 | hp1 | a0001 | c0001 | t0017 | g0355 | AMR | CLM | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG01361 | hp2 | a0002 | c0003 | t0002 | g0120 | AMR | CLM | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG01433 | hp1 | a0001 | c0002 | t0003 | g0363 | AMR | CLM | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG01433 | hp2 | a0001 | c0011 | t0031 | g0257 | AMR | CLM | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0232 | AMR | CLM | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG01515 | hp1 | a0002 | c0004 | t0006 | g0097 | EUR | IBS | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG01515 | hp2 | a0001 | c0002 | t0003 | g0376 | EUR | IBS | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG01516 | hp1 | a0001 | c0007 | t0007 | g0238 | EUR | IBS | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG01516 | hp2 | a0001 | c0002 | t0003 | g0369 | EUR | IBS | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG01517 | hp1 | a0001 | c0007 | t0007 | g0239 | EUR | IBS | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG01517 | hp2 | a0001 | c0002 | t0003 | g0375 | EUR | IBS | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG01884 | hp1 | a0003 | c0010 | t0042 | g0023 | AFR | ACB | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG01884 | hp2 | a0003 | c0014 | t0003 | g0041 | AFR | ACB | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG01934 | hp2 | a0002 | c0003 | t0001 | g0112 | AMR | PEL | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG01943 | hp1 | a0002 | c0003 | t0010 | g0132 | AMR | PEL | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG01952 | hp1 | a0001 | c0001 | t0010 | g0219 | AMR | PEL | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG01952 | hp2 | a0002 | c0003 | t0010 | g0082 | AMR | PEL | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG01975 | hp1 | a0002 | c0003 | t0010 | g0055 | AMR | PEL | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG01975 | hp2 | a0002 | c0003 | t0001 | g0107 | AMR | PEL | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG01978 | hp1 | a0002 | c0003 | t0010 | g0084 | AMR | PEL | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG01978 | hp2 | a0002 | c0004 | t0014 | g0046 | AMR | PEL | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02004 | hp1 | a0002 | c0004 | t0003 | g0125 | AMR | PEL | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02004 | hp2 | a0001 | c0012 | t0062 | g0237 | AMR | PEL | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02027 | hp1 | a0002 | c0004 | t0005 | g0095 | EAS | KHV | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | KHV | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02040 | hp1 | a0001 | c0002 | t0001 | g0374 | EAS | KHV | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02040 | hp2 | a0001 | c0005 | t0061 | g0199 | EAS | KHV | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02056 | hp1 | a0002 | c0003 | t0010 | g0128 | EAS | KHV | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02056 | hp2 | a0002 | c0004 | t0034 | g0142 | EAS | KHV | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02071 | hp2 | a0002 | c0003 | t0001 | g0069 | EAS | KHV | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02074 | hp1 | a0002 | c0004 | t0002 | g0157 | EAS | KHV | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02074 | hp2 | a0002 | c0004 | t0004 | g0152 | EAS | KHV | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02080 | hp1 | a0001 | c0002 | t0005 | g0287 | EAS | KHV | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02080 | hp2 | a0002 | c0003 | t0001 | g0135 | EAS | KHV | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02129 | hp1 | a0002 | c0003 | t0049 | g0148 | EAS | KHV | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02129 | hp2 | a0002 | c0003 | t0001 | g0077 | EAS | KHV | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02132 | hp1 | a0002 | c0003 | t0001 | g0144 | EAS | KHV | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02132 | hp2 | a0002 | c0003 | t0001 | g0067 | EAS | KHV | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02145 | hp1 | a0001 | c0026 | t0023 | g0195 | AFR | ACB | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02145 | hp2 | a0001 | c0007 | t0004 | g0365 | AFR | ACB | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02155 | hp1 | a0002 | c0003 | t0001 | g0051 | EAS | CDX | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02155 | hp2 | a0002 | c0004 | t0005 | g0145 | EAS | CDX | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02165 | hp1 | a0002 | c0004 | t0005 | g0162 | EAS | CDX | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02165 | hp2 | a0002 | c0003 | t0001 | g0065 | EAS | CDX | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02257 | hp1 | a0003 | c0014 | t0030 | g0015 | AFR | ACB | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02257 | hp2 | a0001 | c0002 | t0015 | g0222 | AFR | ACB | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02258 | hp1 | a0001 | c0002 | t0033 | g0241 | AFR | ACB | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02258 | hp2 | a0003 | c0006 | t0009 | g0027 | AFR | ACB | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02293 | hp1 | a0003 | c0013 | t0001 | g0013 | AMR | PEL | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02293 | hp2 | a0002 | c0003 | t0001 | g0103 | AMR | PEL | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02300 | hp1 | a0002 | c0003 | t0010 | g0131 | AMR | PEL | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02300 | hp2 | a0001 | c0002 | t0003 | g0263 | AMR | PEL | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02451 | hp1 | a0001 | c0002 | t0007 | g0336 | AFR | ACB | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02451 | hp2 | a0003 | c0006 | t0013 | g0042 | AFR | ACB | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0280 | EAS | KHV | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02523 | hp2 | a0001 | c0001 | t0006 | g0188 | EAS | KHV | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02572 | hp1 | a0001 | c0002 | t0009 | g0343 | AFR | GWD | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02572 | hp2 | a0004 | c0009 | t0007 | g0171 | AFR | GWD | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02602 | hp1 | a0005 | c0018 | t0001 | g0012 | SAS | PJL | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02602 | hp2 | a0002 | c0003 | t0001 | g0100 | SAS | PJL | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02615 | hp1 | a0001 | c0002 | t0003 | g0246 | AFR | GWD | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02615 | hp2 | a0001 | c0002 | t0056 | g0362 | AFR | GWD | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02622 | hp1 | a0001 | c0002 | t0007 | g0259 | AFR | GWD | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02622 | hp2 | a0001 | c0007 | t0016 | g0300 | AFR | GWD | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02630 | hp1 | a0001 | c0002 | t0016 | g0302 | AFR | GWD | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02630 | hp2 | a0001 | c0002 | t0007 | g0245 | AFR | GWD | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02647 | hp1 | a0001 | c0007 | t0003 | g0294 | AFR | GWD | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02647 | hp2 | a0003 | c0006 | t0007 | g0039 | AFR | GWD | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02683 | hp1 | a0002 | c0004 | t0014 | g0109 | SAS | PJL | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02683 | hp2 | a0002 | c0004 | t0019 | g0081 | SAS | PJL | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02698 | hp1 | a0001 | c0002 | t0003 | g0344 | SAS | PJL | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02698 | hp2 | a0002 | c0004 | t0046 | g0070 | SAS | PJL | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02723 | hp1 | a0001 | c0007 | t0004 | g0295 | AFR | GWD | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02723 | hp2 | a0003 | c0006 | t0011 | g0032 | AFR | GWD | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02735 | hp1 | a0002 | c0003 | t0017 | g0138 | SAS | PJL | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02735 | hp2 | a0002 | c0004 | t0001 | g0137 | SAS | PJL | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02809 | hp1 | a0003 | c0020 | t0026 | g0018 | AFR | GWD | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02809 | hp2 | a0003 | c0006 | t0015 | g0014 | AFR | GWD | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02818 | hp1 | a0001 | c0002 | t0055 | g0248 | AFR | GWD | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02818 | hp2 | a0003 | c0006 | t0003 | g0037 | AFR | GWD | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02886 | hp1 | a0003 | c0006 | t0065 | g0036 | AFR | GWD | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02886 | hp2 | a0001 | c0002 | t0003 | g0346 | AFR | GWD | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02895 | hp1 | a0001 | c0002 | t0067 | g0233 | AFR | GWD | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02895 | hp2 | a0003 | c0015 | t0029 | g0035 | AFR | GWD | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02896 | hp1 | a0001 | c0002 | t0011 | g0292 | AFR | GWD | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02896 | hp2 | a0003 | c0006 | t0024 | g0021 | AFR | GWD | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02897 | hp1 | a0001 | c0002 | t0011 | g0289 | AFR | GWD | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02897 | hp2 | a0003 | c0015 | t0029 | g0038 | AFR | GWD | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02922 | hp1 | a0004 | c0009 | t0009 | g0175 | AFR | ESN | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02922 | hp2 | a0001 | c0001 | t0043 | g0293 | AFR | ESN | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0197 | AFR | ESN | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02965 | hp2 | a0003 | c0010 | t0048 | g0016 | AFR | ESN | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02970 | hp1 | a0003 | c0006 | t0024 | g0028 | AFR | ESN | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02970 | hp2 | a0001 | c0028 | t0002 | g0194 | AFR | ESN | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02976 | hp1 | a0001 | c0011 | t0020 | g0261 | AFR | ESN | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02976 | hp2 | a0004 | c0022 | t0009 | g0167 | AFR | ESN | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG03017 | hp1 | a0002 | c0004 | t0020 | g0160 | SAS | PJL | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG03017 | hp2 | a0002 | c0008 | t0006 | g0073 | SAS | PJL | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG03041 | hp1 | a0003 | c0006 | t0003 | g0040 | AFR | GWD | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG03041 | hp2 | a0001 | c0030 | t0026 | g0298 | AFR | GWD | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG03098 | hp1 | a0003 | c0006 | t0009 | g0024 | AFR | MSL | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG03098 | hp2 | a0003 | c0010 | t0002 | g0033 | AFR | MSL | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0347 | AFR | ESN | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG03130 | hp2 | a0001 | c0027 | t0050 | g0212 | AFR | ESN | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG03139 | hp1 | a0001 | c0002 | t0028 | g0367 | AFR | ESN | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG03139 | hp2 | a0004 | c0009 | t0013 | g0172 | AFR | ESN | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG03195 | hp1 | a0001 | c0002 | t0057 | g0332 | AFR | ESN | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0288 | AFR | ESN | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG03209 | hp1 | a0001 | c0002 | t0011 | g0179 | AFR | MSL | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0260 | AFR | MSL | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG03225 | hp1 | a0004 | c0024 | t0001 | g0174 | AFR | MSL | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG03225 | hp2 | a0004 | c0023 | t0044 | g0168 | AFR | MSL | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG03239 | hp1 | a0002 | c0003 | t0001 | g0053 | SAS | PJL | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG03239 | hp2 | a0001 | c0007 | t0053 | g0243 | SAS | PJL | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG03453 | hp1 | a0001 | c0002 | t0007 | g0366 | AFR | MSL | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG03453 | hp2 | a0001 | c0002 | t0040 | g0276 | AFR | MSL | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG03486 | hp1 | a0001 | c0002 | t0013 | g0264 | AFR | MSL | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG03486 | hp2 | a0001 | c0007 | t0004 | g0296 | AFR | MSL | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG03491 | hp1 | a0003 | c0019 | t0059 | g0011 | SAS | PJL | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG03491 | hp2 | a0002 | c0003 | t0001 | g0001 | SAS | PJL | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG03492 | hp1 | a0003 | c0017 | t0002 | g0009 | SAS | PJL | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG03492 | hp2 | a0002 | c0003 | t0001 | g0001 | SAS | PJL | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG03516 | hp1 | a0001 | c0002 | t0021 | g0254 | AFR | ESN | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG03516 | hp2 | a0004 | c0009 | t0011 | g0177 | AFR | ESN | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG03540 | hp1 | a0004 | c0009 | t0016 | g0176 | AFR | GWD | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG03540 | hp2 | a0001 | c0002 | t0015 | g0341 | AFR | GWD | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG03579 | hp1 | a0004 | c0009 | t0009 | g0170 | AFR | MSL | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG03579 | hp2 | a0001 | c0002 | t0007 | g0231 | AFR | MSL | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG03654 | hp1 | a0002 | c0003 | t0054 | g0106 | SAS | PJL | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG03654 | hp2 | a0001 | c0005 | t0058 | g0208 | SAS | PJL | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG03688 | hp1 | a0001 | c0012 | t0006 | g0251 | SAS | STU | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG03688 | hp2 | a0001 | c0005 | t0006 | g0223 | SAS | STU | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG03704 | hp1 | a0002 | c0003 | t0004 | g0108 | SAS | PJL | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG03704 | hp2 | a0001 | c0005 | t0064 | g0205 | SAS | PJL | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | BEB | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG03831 | hp2 | a0001 | c0002 | t0005 | g0285 | SAS | BEB | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0306 | SAS | BEB | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG03942 | hp2 | a0002 | c0004 | t0001 | g0123 | SAS | BEB | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG04115 | hp1 | a0002 | c0003 | t0001 | g0114 | SAS | STU | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG04115 | hp2 | a0002 | c0004 | t0002 | g0098 | SAS | STU | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG04184 | hp1 | a0002 | c0003 | t0001 | g0104 | SAS | BEB | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG04184 | hp2 | a0002 | c0008 | t0063 | g0113 | SAS | BEB | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG04199 | hp1 | a0003 | c0013 | t0001 | g0010 | SAS | STU | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG04199 | hp2 | a0002 | c0008 | t0006 | g0083 | SAS | STU | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG04204 | hp1 | a0002 | c0004 | t0003 | g0159 | SAS | STU | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG04204 | hp2 | a0002 | c0003 | t0001 | g0064 | SAS | STU | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0242 | SAS | STU | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG04228 | hp2 | a0001 | c0002 | t0002 | g0202 | SAS | STU | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18522 | hp1 | a0001 | c0002 | t0052 | g0207 | AFR | YRI | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18522 | hp2 | a0001 | c0002 | t0025 | g0005 | AFR | YRI | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18747 | hp1 | a0001 | c0002 | t0003 | g0339 | EAS | CHB | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18747 | hp2 | a0002 | c0003 | t0001 | g0045 | EAS | CHB | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18906 | hp1 | a0001 | c0016 | t0003 | g0185 | AFR | YRI | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18906 | hp2 | a0001 | c0002 | t0011 | g0297 | AFR | YRI | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18939 | hp1 | a0001 | c0001 | t0004 | g0328 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18939 | hp2 | a0001 | c0001 | t0004 | g0182 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18942 | hp1 | a0002 | c0003 | t0001 | g0056 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18942 | hp2 | a0001 | c0005 | t0006 | g0321 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18943 | hp1 | a0001 | c0001 | t0004 | g0210 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18945 | hp1 | a0001 | c0002 | t0008 | g0311 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18945 | hp2 | a0001 | c0001 | t0004 | g0335 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18946 | hp2 | a0002 | c0003 | t0001 | g0140 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18947 | hp1 | a0002 | c0004 | t0003 | g0122 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18947 | hp2 | a0001 | c0001 | t0004 | g0230 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18948 | hp1 | a0002 | c0003 | t0006 | g0150 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18948 | hp2 | a0002 | c0003 | t0001 | g0075 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18949 | hp1 | a0001 | c0001 | t0004 | g0325 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18949 | hp2 | a0002 | c0004 | t0005 | g0127 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18950 | hp1 | a0002 | c0008 | t0006 | g0052 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18951 | hp1 | a0001 | c0005 | t0006 | g0301 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18952 | hp1 | a0002 | c0003 | t0047 | g0116 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18952 | hp2 | a0002 | c0003 | t0002 | g0043 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0359 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0379 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18954 | hp1 | a0002 | c0004 | t0008 | g0099 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18954 | hp2 | a0001 | c0005 | t0006 | g0183 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18959 | hp1 | a0002 | c0004 | t0037 | g0093 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18959 | hp2 | a0001 | c0005 | t0006 | g0286 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18961 | hp1 | a0001 | c0002 | t0036 | g0358 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18962 | hp1 | a0001 | c0005 | t0008 | g0006 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18964 | hp2 | a0002 | c0004 | t0001 | g0166 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18966 | hp1 | a0001 | c0005 | t0004 | g0305 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18966 | hp2 | a0002 | c0003 | t0001 | g0058 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18968 | hp1 | a0002 | c0003 | t0010 | g0165 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18968 | hp2 | a0002 | c0008 | t0005 | g0151 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18969 | hp1 | a0001 | c0002 | t0005 | g0228 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18969 | hp2 | a0002 | c0004 | t0003 | g0057 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18970 | hp2 | a0001 | c0002 | t0001 | g0273 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18971 | hp1 | a0001 | c0001 | t0004 | g0196 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18971 | hp2 | a0002 | c0004 | t0008 | g0158 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18973 | hp1 | a0002 | c0003 | t0001 | g0068 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18974 | hp1 | a0002 | c0008 | t0005 | g0048 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18974 | hp2 | a0002 | c0004 | t0022 | g0130 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18977 | hp1 | a0002 | c0004 | t0003 | g0111 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0348 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18979 | hp2 | a0001 | c0002 | t0008 | g0349 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18980 | hp1 | a0002 | c0003 | t0002 | g0090 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18982 | hp1 | a0002 | c0003 | t0004 | g0079 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18982 | hp2 | a0001 | c0001 | t0018 | g0334 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18983 | hp1 | a0001 | c0002 | t0001 | g0283 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18983 | hp2 | a0002 | c0008 | t0012 | g0134 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18984 | hp1 | a0002 | c0003 | t0005 | g0105 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18985 | hp2 | a0002 | c0003 | t0001 | g0121 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18990 | hp1 | a0002 | c0004 | t0005 | g0146 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18990 | hp2 | a0002 | c0008 | t0004 | g0153 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18991 | hp1 | a0001 | c0002 | t0005 | g0281 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18991 | hp2 | a0001 | c0001 | t0005 | g0323 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18993 | hp2 | a0001 | c0002 | t0005 | g0229 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18995 | hp2 | a0001 | c0001 | t0005 | g0322 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18997 | hp2 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18998 | hp1 | a0002 | c0003 | t0004 | g0118 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18998 | hp2 | a0001 | c0005 | t0008 | g0006 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18999 | hp1 | a0001 | c0005 | t0008 | g0191 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19000 | hp2 | a0002 | c0003 | t0001 | g0062 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19001 | hp1 | a0006 | c0025 | t0008 | g0178 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19001 | hp2 | a0002 | c0003 | t0001 | g0161 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19002 | hp2 | a0002 | c0003 | t0001 | g0149 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19004 | hp1 | a0002 | c0003 | t0005 | g0087 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19004 | hp2 | a0001 | c0005 | t0008 | g0204 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19005 | hp1 | a0002 | c0003 | t0001 | g0071 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19005 | hp2 | a0002 | c0004 | t0002 | g0110 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0360 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19007 | hp2 | a0001 | c0005 | t0060 | g0187 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19009 | hp1 | a0001 | c0005 | t0006 | g0372 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0373 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19010 | hp1 | a0001 | c0005 | t0006 | g0331 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19011 | hp1 | a0002 | c0003 | t0018 | g0063 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19012 | hp1 | a0002 | c0004 | t0005 | g0092 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19012 | hp2 | a0001 | c0002 | t0005 | g0329 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19030 | hp1 | a0003 | c0006 | t0003 | g0025 | AFR | LWK | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19030 | hp2 | a0001 | c0002 | t0007 | g0277 | AFR | LWK | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0337 | AFR | LWK | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19043 | hp2 | a0001 | c0031 | t0002 | g0380 | AFR | LWK | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19057 | hp1 | a0002 | c0004 | t0002 | g0078 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19060 | hp1 | a0002 | c0003 | t0018 | g0089 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19060 | hp2 | a0002 | c0003 | t0045 | g0115 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19063 | hp1 | a0001 | c0002 | t0001 | g0271 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19063 | hp2 | a0001 | c0002 | t0038 | g0209 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19064 | hp1 | a0002 | c0008 | t0012 | g0091 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0350 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19065 | hp2 | a0002 | c0004 | t0005 | g0141 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19066 | hp1 | a0002 | c0003 | t0001 | g0049 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19066 | hp2 | a0002 | c0004 | t0005 | g0143 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19068 | hp1 | a0002 | c0003 | t0001 | g0126 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19070 | hp2 | a0002 | c0003 | t0001 | g0117 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19074 | hp1 | a0001 | c0005 | t0008 | g0320 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19074 | hp2 | a0001 | c0001 | t0004 | g0284 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0330 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19078 | hp1 | a0001 | c0005 | t0005 | g0353 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19078 | hp2 | a0002 | c0003 | t0041 | g0139 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19079 | hp1 | a0002 | c0004 | t0003 | g0059 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19079 | hp2 | a0002 | c0008 | t0005 | g0096 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0316 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19080 | hp2 | a0002 | c0008 | t0005 | g0050 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19081 | hp2 | a0002 | c0003 | t0002 | g0154 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19085 | hp1 | a0001 | c0002 | t0003 | g0217 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19086 | hp1 | a0001 | c0005 | t0006 | g0317 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19086 | hp2 | a0001 | c0001 | t0004 | g0324 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19088 | hp1 | a0001 | c0002 | t0005 | g0211 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19088 | hp2 | a0002 | c0003 | t0001 | g0066 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0364 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19089 | hp2 | a0002 | c0003 | t0001 | g0101 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19091 | hp2 | a0002 | c0003 | t0001 | g0136 | EAS | JPT | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19240 | hp1 | a0003 | c0006 | t0004 | g0026 | AFR | YRI | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA19240 | hp2 | a0001 | c0002 | t0004 | g0193 | AFR | YRI | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA20129 | hp1 | a0003 | c0021 | t0027 | g0020 | AFR | ASW | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA20129 | hp2 | a0004 | c0009 | t0009 | g0173 | AFR | ASW | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA20752 | hp1 | a0001 | c0012 | t0006 | g0244 | EUR | TSI | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA20752 | hp2 | a0002 | c0008 | t0051 | g0061 | EUR | TSI | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA20805 | hp1 | a0001 | c0002 | t0003 | g0247 | EUR | TSI | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA20805 | hp2 | a0001 | c0007 | t0003 | g0214 | EUR | TSI | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA20905 | hp1 | a0001 | c0002 | t0005 | g0203 | SAS | GIH | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA20905 | hp2 | a0002 | c0003 | t0001 | g0164 | SAS | GIH | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG01123 | hp1 | a0001 | c0002 | t0003 | g0354 | AMR | CLM | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG01123 | hp2 | a0001 | c0001 | t0017 | g0352 | AMR | CLM | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02109 | hp1 | a0001 | c0002 | t0028 | g0356 | AFR | ACB | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02109 | hp2 | a0001 | c0002 | t0027 | g0198 | AFR | ACB | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02486 | hp1 | a0001 | c0002 | t0011 | g0357 | AFR | ACB | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02486 | hp2 | a0001 | c0002 | t0009 | g0361 | AFR | ACB | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02559 | hp1 | a0001 | c0005 | t0066 | g0258 | AFR | ACB | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG02559 | hp2 | a0003 | c0010 | t0001 | g0017 | AFR | ACB | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG03471 | hp1 | a0001 | c0007 | t0004 | g0278 | AFR | MSL | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG03471 | hp2 | a0003 | c0006 | t0032 | g0019 | AFR | MSL | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG06807 | hp1 | a0001 | c0002 | t0002 | g0227 | AFR | USA | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
HG06807 | hp2 | a0001 | c0002 | t0020 | g0252 | AFR | USA | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA20300 | hp1 | a0003 | c0006 | t0003 | g0022 | AFR | USA | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA20300 | hp2 | a0001 | c0002 | t0023 | g0201 | AFR | USA | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA21309 | hp1 | a0003 | c0006 | t0019 | g0030 | AFR | LWK | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
NA21309 | hp2 | a0002 | c0003 | t0002 | g0155 | AFR | LWK | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
homoSapiens | chm13v2 | a0001 | c0002 | t0006 | g0378 | REF | REF | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
homoSapiens | grch38p0 | a0001 | c0016 | t0021 | g0206 | REF | REF | ALX4_chr11_44255440_44315139 | ALX4 | chr11 | 44255440 | 44315139 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:44264957 | T | C | 1 | a0005 | 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 | a0004 | 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 | a0006 | 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 | 1 | a0004 | 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 | a0002 a0003 a0005 |
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 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:44265016 | G | A | 10 | a0001c0001 a0001c0027 a0001c0028 others(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 | a0001c0030 a0003c0020 |
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 | a0001c0005 a0001c0012 a0002c0008 others(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 | a0001c0007 a0001c0012 a0001c0029 others(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 | a0001c0001 a0001c0002 a0001c0005 others(25): Show |
383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): 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 | a0001c0011 a0001c0027 a0003c0014 others(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 | a0003c0013 a0003c0017 a0003c0019 others(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 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:44260570 | A | G | 122 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(119): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): 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 | a0001c0002t0023 a0001c0002t0030 a0001c0002t0055 others(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 | a0001c0001t0017 a0002c0003t0017 |
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 | a0001c0001t0001 a0001c0001t0010 a0001c0001t0017 others(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 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(120): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): 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 | a0001c0001t0018 a0002c0003t0018 |
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 | a0001c0002t0008 a0001c0005t0008 a0001c0007t0008 others(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 | a0001c0001t0001 a0001c0001t0010 a0001c0001t0017 others(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 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(95): Show |
286 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(283): 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 | a0001c0002t0008 a0001c0005t0008 a0001c0007t0008 others(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 | a0001c0001t0001 a0001c0001t0010 a0001c0001t0017 others(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 | a0001c0001t0010 a0002c0003t0010 |
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 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(132): Show |
382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): 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 | a0001c0002t0016 a0001c0007t0016 a0004c0009t0016 |
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 | a0001c0002t0007 a0001c0002t0031 a0001c0002t0057 others(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 | a0001c0002t0027 a0003c0021t0027 |
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 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0043 others(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 | a0001c0002t0015 a0001c0002t0023 a0001c0002t0025 others(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 | a0001c0005t0066 a0003c0006t0024 |
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 | a0001c0002t0013 a0001c0002t0040 a0003c0006t0013 others(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 | a0001c0001t0005 a0001c0002t0005 a0001c0005t0005 others(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 | a0001c0001t0043 a0003c0010t0042 |
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 | a0001c0001t0002 a0001c0001t0043 a0001c0002t0002 others(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 | a0001c0002t0013 a0001c0002t0040 a0003c0006t0013 others(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 | a0001c0002t0013 a0001c0002t0040 a0003c0006t0013 others(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 | a0001c0005t0066 a0003c0006t0024 |
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 | a0001c0002t0011 a0001c0002t0019 a0001c0002t0027 others(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 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(123): Show |
346 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(343): 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 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(96): Show |
304 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(301): 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 | a0001c0001t0005 a0001c0002t0005 a0001c0002t0036 others(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 | a0001c0001t0006 a0001c0002t0006 a0001c0002t0007 others(24): Show |
48 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(45): 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 | a0001c0002t0011 a0001c0002t0033 a0001c0002t0067 others(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 | a0001c0002t0015 a0003c0006t0015 a0003c0006t0032 |
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 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:44265231 | G | A | 1 | a0001c0002t0052g0207 | 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 | a0001c0002t0003g0213 a0001c0002t0004g0193 a0001c0002t0028g0356 others(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 | a0001c0002t0030g0220 a0003c0006t0024g0021 a0003c0006t0024g0028 others(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 | a0001c0001t0001g0267 a0001c0001t0001g0338 a0001c0001t0002g0184 others(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 | 81 | a0001c0001t0001g0267 a0001c0001t0001g0338 a0001c0001t0002g0184 others(78): Show |
81 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.907-295A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 3/3 | chr11 | 44265478 | |||||||
chr11:44265498 | G | T | 114 | a0001c0001t0001g0267 a0001c0001t0001g0338 a0001c0001t0002g0184 others(111): Show |
115 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.907-315C>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 3/3 | chr11 | 44265498 | |||||||
chr11:44265599 | C | T | 77 | a0001c0001t0001g0267 a0001c0001t0001g0338 a0001c0001t0002g0184 others(74): Show |
77 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(74): 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 | a0001c0002t0052g0207 | 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 | a0002c0004t0001g0137 | 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 | 128 | a0001c0001t0001g0267 a0001c0001t0001g0338 a0001c0001t0002g0184 others(125): Show |
128 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(125): 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 | a0001c0002t0015g0222 a0001c0002t0015g0341 a0001c0002t0025g0005 others(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 | 102 | a0001c0001t0001g0267 a0001c0001t0001g0338 a0001c0001t0002g0184 others(99): Show |
102 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(99): 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 | a0001c0002t0008g0311 a0001c0002t0008g0349 a0002c0004t0002g0078 others(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 | 312 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(309): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(317): 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 | a0001c0001t0001g0267 a0001c0001t0001g0338 a0001c0001t0002g0184 others(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 | a0003c0006t0013g0034 a0003c0006t0013g0042 |
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 | a0002c0003t0006g0150 | 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 | 33 | a0001c0002t0003g0217 a0001c0002t0003g0246 a0001c0002t0003g0247 others(30): Show |
33 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.907-937A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 3/3 | chr11 | 44266120 | |||||||
chr11:44266131 | G | A | 252 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(249): 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 | a0001c0002t0016g0302 | 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 | a0001c0002t0008g0311 a0001c0002t0008g0349 a0002c0004t0002g0078 others(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 | 38 | a0001c0002t0003g0217 a0001c0002t0003g0246 a0001c0002t0003g0247 others(35): Show |
38 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.906+994C>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 3/3 | chr11 | 44266500 | |||||||
chr11:44266510 | A | G | 38 | a0001c0002t0003g0217 a0001c0002t0003g0246 a0001c0002t0003g0247 others(35): Show |
38 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.906+984T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 3/3 | chr11 | 44266510 | |||||||
chr11:44266617 | A | T | 38 | a0001c0002t0003g0217 a0001c0002t0003g0246 a0001c0002t0003g0247 others(35): Show |
38 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.906+877T>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 3/3 | chr11 | 44266617 | |||||||
chr11:44266865 | G | C | 38 | a0001c0002t0003g0217 a0001c0002t0003g0246 a0001c0002t0003g0247 others(35): Show |
38 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(35): 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 | a0001c0001t0002g0262 a0001c0001t0002g0316 |
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 | a0001c0002t0003g0346 | 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 | a0003c0006t0003g0040 a0003c0014t0003g0041 |
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 | a0001c0002t0033g0241 | 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 | a0002c0003t0001g0102 | 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 | a0001c0005t0060g0187 | 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 | a0001c0002t0005g0329 a0001c0002t0015g0222 a0001c0002t0015g0341 others(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 | a0001c0002t0013g0264 | 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 | a0003c0006t0009g0027 | 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 | a0001c0002t0015g0222 a0001c0002t0015g0341 a0001c0002t0025g0005 others(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 | a0001c0002t0011g0179 a0001c0002t0011g0297 a0001c0002t0027g0198 others(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 | 301 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(298): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(306): Show |
intron_variant | MODIFIER | c.778-117T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44267739 | |||||||
chr11:44267762 | C | G | 230 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(227): 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 | a0001c0001t0006g0188 | 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 | a0004c0022t0009g0167 | 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 | 255 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(252): 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 | a0001c0001t0001g0216 | 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 | a0002c0003t0001g0101 | 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 | 222 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(219): 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 | a0001c0002t0056g0362 | 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 | 40 | a0001c0002t0003g0217 a0001c0002t0003g0246 a0001c0002t0003g0247 others(37): Show |
40 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.778-894A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44268516 | |||||||
chr11:44268576 | T | C | 286 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(283): Show |
293 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(290): 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 | a0002c0004t0002g0078 a0002c0004t0002g0110 a0002c0004t0008g0158 |
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 | 247 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(244): 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 | 287 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(284): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.778-1209A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44268831 | |||||||
chr11:44268915 | T | C | 286 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(283): Show |
293 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(290): 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 | a0001c0002t0013g0264 | 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 | 38 | a0001c0002t0003g0217 a0001c0002t0003g0246 a0001c0002t0003g0247 others(35): Show |
38 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(35): 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 | a0001c0002t0040g0276 a0004c0009t0013g0172 |
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 | a0001c0001t0001g0235 a0001c0002t0011g0179 a0001c0002t0011g0297 others(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 | a0001c0002t0056g0362 | 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 | a0001c0002t0013g0264 | 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 | a0002c0004t0002g0078 a0002c0004t0008g0158 |
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 | a0004c0009t0009g0169 | 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 | a0001c0002t0003g0263 a0001c0002t0009g0361 a0001c0002t0040g0276 others(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 | a0001c0002t0003g0263 a0001c0002t0009g0361 a0001c0002t0040g0276 others(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 | a0001c0002t0005g0203 a0001c0002t0005g0211 a0001c0002t0005g0228 others(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 | a0001c0001t0001g0235 a0001c0002t0011g0179 a0001c0002t0011g0297 others(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 | a0001c0001t0001g0235 a0001c0002t0011g0179 a0001c0002t0011g0297 others(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 | a0001c0002t0006g0326 | 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 | a0001c0030t0026g0298 a0003c0020t0026g0018 |
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 | 251 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(248): 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 | a0001c0001t0002g0197 a0001c0001t0002g0225 a0001c0001t0002g0232 others(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 | a0001c0001t0001g0235 a0001c0002t0011g0179 a0001c0002t0011g0297 others(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 | a0001c0001t0001g0235 a0001c0002t0011g0179 a0001c0002t0011g0297 others(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 | a0001c0002t0003g0263 a0001c0002t0040g0276 a0001c0005t0004g0305 others(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 | 29 | a0001c0001t0002g0275 a0001c0002t0003g0217 a0001c0002t0003g0246 others(26): Show |
29 | HG00323.hp1 HG00544.hp2 HG00609.hp1 others(26): 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 | a0001c0002t0052g0207 | 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 | a0001c0002t0011g0289 a0001c0002t0011g0292 a0003c0020t0026g0018 |
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 | a0001c0002t0006g0326 | 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 | 300 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0180 others(297): 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 | a0001c0002t0003g0263 | 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 | a0002c0004t0005g0141 | 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 | a0001c0002t0015g0341 a0003c0006t0015g0014 a0003c0006t0032g0019 |
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 | 156 | a0001c0001t0001g0004 a0001c0001t0001g0192 a0001c0001t0001g0215 others(153): Show |
159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.778-3536dupG | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44271157 | |||||||
chr11:44271163 | C | A | 1 | a0002c0003t0010g0165 | 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 | 216 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0180 others(213): 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 | a0003c0006t0009g0024 | 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 | a0001c0002t0004g0193 a0001c0002t0016g0302 |
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 | a0001c0001t0002g0224 a0001c0001t0002g0249 a0001c0002t0003g0255 others(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 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0186 others(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 | a0001c0002t0009g0361 a0001c0002t0025g0005 a0001c0005t0066g0258 |
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 | a0001c0002t0013g0264 a0004c0009t0009g0169 a0004c0009t0009g0170 others(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 | a0003c0021t0027g0020 | 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 | a0001c0002t0013g0264 a0004c0009t0009g0169 a0004c0009t0009g0170 others(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 | a0002c0004t0020g0160 | 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 | a0003c0010t0048g0016 | 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 | a0003c0010t0001g0017 | 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 | a0001c0002t0004g0193 a0001c0002t0007g0231 a0001c0002t0007g0366 others(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 | a0002c0003t0001g0001 a0002c0003t0010g0128 |
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 | a0001c0001t0002g0347 a0001c0002t0015g0341 a0003c0006t0009g0027 others(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 | a0002c0004t0003g0159 | 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 | a0001c0027t0050g0212 | 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 | a0001c0002t0009g0343 | 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 | a0001c0002t0009g0361 a0001c0002t0025g0005 a0001c0002t0040g0276 others(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 | 362 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(359): Show |
370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): 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 | a0001c0001t0001g0240 a0001c0001t0001g0250 a0001c0001t0001g0267 others(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 | a0001c0001t0001g0240 a0001c0001t0001g0250 a0001c0001t0001g0267 others(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 | a0001c0011t0020g0261 a0001c0027t0050g0212 a0003c0014t0003g0041 others(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 | a0001c0001t0001g0215 | 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 | a0001c0001t0001g0235 a0001c0001t0043g0293 a0001c0002t0015g0222 others(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 | 357 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(354): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.777+3071dupC | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44272276 | |||||||
chr11:44272364 | T | G | 1 | a0001c0002t0008g0349 | 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 | a0001c0001t0002g0347 | 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 | a0001c0001t0001g0240 a0001c0001t0001g0250 a0001c0001t0001g0267 others(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 | 83 | a0001c0001t0001g0004 a0001c0001t0001g0192 a0001c0001t0001g0215 others(80): Show |
84 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.777+2845delT | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44272502 | |||||||
chr11:44272502 | TAA | T | 113 | a0001c0001t0001g0240 a0001c0001t0001g0250 a0001c0001t0001g0267 others(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 | a0001c0005t0006g0223 | 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 | a0001c0001t0001g0306 a0001c0002t0003g0263 a0003c0013t0001g0010 others(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 | a0001c0002t0011g0297 | 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 | 60 | a0001c0001t0001g0004 a0001c0001t0001g0192 a0001c0001t0001g0215 others(57): Show |
61 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.777+2524delT | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44272823 | |||||||
chr11:44273069 | G | A | 2 | a0003c0006t0013g0034 a0003c0006t0013g0042 |
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 | 79 | a0001c0001t0001g0004 a0001c0001t0001g0192 a0001c0001t0001g0215 others(76): Show |
80 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(77): 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 | a0004c0009t0007g0171 a0004c0009t0013g0172 a0004c0009t0016g0176 |
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 | 175 | a0001c0001t0001g0004 a0001c0001t0001g0192 a0001c0001t0001g0215 others(172): Show |
177 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.777+2157delT | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44273190 | |||||||
chr11:44273190 | TAA | T | 126 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0235 others(123): 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 | a0001c0001t0001g0235 a0001c0001t0043g0293 a0001c0002t0004g0193 others(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 | a0003c0010t0012g0031 | 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 | a0001c0001t0002g0249 | 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 | a0001c0001t0001g0235 a0001c0001t0043g0293 a0001c0002t0004g0193 others(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 | a0002c0003t0005g0087 | 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 | a0001c0002t0052g0207 | 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 | a0003c0006t0032g0019 | 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 | 181 | a0001c0001t0001g0004 a0001c0001t0001g0192 a0001c0001t0001g0215 others(178): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): 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 | a0001c0005t0006g0372 a0002c0003t0001g0103 a0002c0003t0001g0117 others(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 | a0003c0014t0030g0015 | 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 | 7 | a0001c0001t0001g0242 a0001c0001t0017g0352 a0001c0002t0007g0351 others(4): Show |
7 | HG00140.hp1 HG00741.hp2 HG01123.hp2 others(4): 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 | a0002c0003t0001g0144 | 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 | a0001c0011t0020g0261 a0001c0027t0050g0212 a0003c0014t0003g0041 others(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 | 192 | a0001c0001t0001g0004 a0001c0001t0001g0192 a0001c0001t0001g0215 others(189): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.777+991G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44274357 | |||||||
chr11:44274452 | T | G | 188 | a0001c0001t0001g0004 a0001c0001t0001g0192 a0001c0001t0001g0215 others(185): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): 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 | a0004c0009t0007g0171 a0004c0009t0013g0172 a0004c0009t0016g0176 |
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 | a0002c0003t0001g0069 a0002c0004t0037g0093 |
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 | a0001c0001t0004g0325 a0001c0001t0004g0328 |
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 | a0001c0001t0001g0299 | 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 | a0004c0009t0011g0177 | 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 | a0001c0002t0052g0207 | 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 | 181 | a0001c0001t0001g0004 a0001c0001t0001g0192 a0001c0001t0001g0215 others(178): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.777+685A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44274663 | |||||||
chr11:44274840 | C | T | 185 | a0001c0001t0001g0004 a0001c0001t0001g0192 a0001c0001t0001g0215 others(182): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): 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 | a0003c0006t0003g0040 a0003c0006t0009g0024 a0003c0006t0011g0032 others(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 | 367 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(364): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.777+417G>A | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 2/3 | chr11 | 44274931 | |||||||
chr11:44274943 | G | A | 192 | a0001c0001t0001g0004 a0001c0001t0001g0192 a0001c0001t0001g0215 others(189): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): 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 | a0001c0001t0001g0306 | 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 | 357 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(354): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): 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 | a0001c0002t0030g0220 | 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 | a0001c0005t0064g0205 | 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 | 168 | a0001c0001t0001g0004 a0001c0001t0001g0192 a0001c0001t0001g0215 others(165): Show |
172 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(169): 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 | a0001c0001t0002g0347 a0001c0002t0015g0341 a0003c0006t0009g0027 others(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 | 357 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(354): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): 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 | a0001c0001t0001g0373 | 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 | a0001c0002t0021g0254 | 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 | 374 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(371): Show |
382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): 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 | a0001c0011t0003g0290 a0001c0011t0031g0257 |
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 | a0001c0001t0001g0240 a0001c0001t0001g0250 a0001c0001t0001g0267 others(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 | a0001c0002t0009g0361 a0001c0002t0025g0005 a0001c0002t0040g0276 others(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 | a0001c0001t0002g0260 a0001c0001t0002g0337 a0001c0001t0002g0347 others(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 | a0002c0003t0001g0126 | 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 | 361 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(358): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): 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 | a0001c0011t0020g0261 | 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 | a0002c0003t0001g0075 | 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 | a0002c0003t0001g0102 | 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 | a0001c0001t0001g0235 a0001c0001t0043g0293 a0001c0002t0004g0193 others(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 | 100 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0265 others(97): 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 | a0004c0022t0009g0167 | 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 | a0001c0001t0001g0215 | 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 | a0002c0003t0001g0064 a0002c0003t0001g0133 a0002c0004t0003g0125 others(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 | a0001c0007t0003g0294 a0001c0007t0004g0236 a0001c0007t0004g0278 others(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 | a0002c0003t0001g0064 | 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 | a0001c0002t0009g0361 a0001c0002t0025g0005 a0001c0002t0040g0276 others(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 | a0001c0001t0001g0235 a0001c0001t0043g0293 a0001c0002t0004g0193 others(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 | a0004c0009t0013g0172 | 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 | a0004c0009t0013g0172 | 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 | a0001c0007t0008g0291 a0001c0029t0001g0234 |
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 | a0001c0001t0001g0235 a0001c0001t0043g0293 a0001c0002t0004g0193 others(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 | a0002c0004t0005g0092 | 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 | a0004c0009t0011g0177 | 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 | 278 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(275): Show |
284 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(281): 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 | a0001c0011t0003g0290 a0001c0011t0031g0257 |
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 | a0002c0003t0001g0100 | 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 | a0001c0011t0003g0290 a0001c0011t0031g0257 |
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 | a0001c0002t0005g0211 | 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 | a0001c0002t0007g0351 | 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 | a0002c0004t0006g0129 | 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 | a0001c0011t0020g0261 a0001c0027t0050g0212 a0003c0014t0003g0041 others(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 | a0001c0002t0021g0254 a0001c0031t0002g0380 |
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 | a0001c0011t0003g0290 a0001c0011t0020g0261 a0001c0011t0031g0257 others(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 | a0001c0002t0011g0179 | 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 | a0001c0001t0001g0235 a0001c0001t0043g0293 a0001c0002t0004g0193 others(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 | 113 | a0001c0001t0001g0004 a0001c0001t0001g0215 a0001c0001t0001g0216 others(110): Show |
115 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(112): Show |
intron_variant | MODIFIER | c.467-2354delA | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44278011 | |||||||
chr11:44278119 | G | A | 1 | a0002c0004t0004g0152 | 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 | a0002c0003t0006g0150 a0002c0004t0005g0092 a0002c0004t0005g0095 others(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 | a0004c0009t0007g0171 a0004c0009t0009g0169 a0004c0009t0009g0170 others(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 | a0001c0002t0013g0264 a0002c0003t0001g0064 a0002c0003t0001g0133 others(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 | a0001c0001t0001g0235 a0001c0001t0043g0293 a0001c0002t0004g0193 others(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 | a0001c0001t0001g0240 a0001c0001t0001g0250 a0001c0001t0001g0267 others(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 | 324 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(321): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.467-2701G>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44278359 | |||||||
chr11:44278492 | C | T | 278 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(275): Show |
285 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(282): 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 | a0001c0027t0050g0212 | 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 | a0001c0002t0007g0351 | 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 | a0002c0003t0005g0087 a0002c0003t0005g0105 |
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 | a0003c0006t0009g0027 a0003c0006t0015g0014 a0003c0006t0032g0019 others(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 | a0002c0003t0001g0149 | 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 | a0003c0006t0003g0040 a0003c0006t0013g0034 a0003c0006t0013g0042 |
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 | a0005c0018t0001g0012 | 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 | a0002c0003t0001g0133 a0002c0004t0003g0125 a0002c0004t0003g0159 others(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 | a0002c0003t0001g0133 a0002c0004t0003g0125 a0002c0004t0003g0159 others(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 | a0002c0004t0002g0098 | 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 | a0001c0011t0020g0261 a0001c0027t0050g0212 a0003c0020t0026g0018 |
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 | a0001c0001t0043g0293 a0001c0002t0015g0222 a0003c0006t0003g0022 others(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 | a0002c0003t0001g0133 a0002c0004t0003g0125 a0002c0004t0003g0159 others(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 | a0001c0001t0001g0235 a0001c0001t0043g0293 a0001c0002t0015g0222 others(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 | a0002c0003t0001g0102 | 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 | a0001c0001t0001g0235 a0001c0001t0043g0293 a0001c0002t0004g0193 others(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 | a0001c0002t0003g0255 a0001c0002t0003g0256 |
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 | a0001c0001t0002g0337 | 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 | a0003c0021t0027g0020 | 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 | a0002c0003t0010g0128 a0002c0004t0014g0054 a0002c0004t0014g0072 |
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 | a0001c0002t0004g0303 a0001c0002t0004g0304 |
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 | 297 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(294): Show |
305 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(302): 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 | a0001c0002t0001g0374 | 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 | a0001c0002t0007g0231 | 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 | a0001c0002t0009g0361 a0001c0002t0025g0005 a0001c0002t0052g0207 others(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 | a0004c0009t0013g0172 | 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 | a0002c0004t0005g0060 | 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 | a0003c0015t0029g0035 a0003c0015t0029g0038 |
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 | a0001c0002t0007g0231 a0001c0002t0007g0366 a0001c0002t0057g0332 |
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 | 229 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0240 others(226): 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 | 113 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0265 others(110): 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 | a0001c0011t0003g0290 a0001c0011t0031g0257 |
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 | 249 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0240 others(246): 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 | 99 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0265 others(96): 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 | a0001c0002t0013g0264 | 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 | 242 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0235 others(239): 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 | 1 | a0001c0001t0017g0352 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.467-5539C>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44281197 | |||||||
chr11:44281315 | C | T | 24 | a0001c0001t0001g0004 a0001c0001t0001g0215 a0001c0001t0001g0216 others(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 | a0001c0001t0001g0240 | 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 | a0002c0003t0002g0120 a0002c0004t0007g0044 a0002c0008t0051g0061 |
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 | a0001c0001t0001g0181 | 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 | a0001c0001t0002g0197 a0001c0002t0040g0276 a0001c0002t0052g0207 others(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 | a0003c0020t0026g0018 | 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 | a0002c0003t0001g0086 | 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 | a0002c0003t0001g0103 | 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 | a0002c0003t0001g0156 | 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 | a0001c0007t0003g0294 a0001c0007t0004g0278 a0001c0007t0004g0295 others(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 | a0001c0001t0002g0347 | 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 | a0001c0001t0017g0355 | 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 | 107 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0265 others(104): 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 | a0001c0012t0006g0244 | 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 | a0001c0001t0001g0368 a0001c0001t0001g0370 a0001c0002t0003g0344 others(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 | 107 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0265 others(104): 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 | a0001c0001t0001g0235 a0001c0001t0001g0240 a0001c0001t0001g0242 others(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 | a0001c0001t0001g0368 a0001c0001t0001g0370 a0001c0002t0003g0344 others(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 | a0002c0003t0001g0121 | 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 | a0002c0008t0004g0088 | 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 | a0001c0002t0013g0264 | 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 | 109 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0265 others(106): 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 | a0001c0002t0009g0361 a0001c0002t0025g0005 a0001c0002t0056g0362 |
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 | a0001c0027t0050g0212 | 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 | a0002c0003t0001g0071 | 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 | a0001c0001t0001g0186 a0001c0001t0002g0184 a0001c0005t0060g0187 |
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 | a0001c0027t0050g0212 | 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 | a0001c0002t0013g0264 | 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 | a0001c0001t0001g0269 a0001c0001t0002g0197 a0001c0001t0004g0182 others(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 | 110 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0265 others(107): 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 | a0001c0027t0050g0212 | 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 | a0001c0002t0007g0259 a0001c0002t0007g0336 a0001c0002t0011g0289 others(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 | a0003c0006t0009g0027 a0003c0006t0015g0014 a0003c0006t0032g0019 others(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 | a0003c0015t0029g0035 a0003c0015t0029g0038 |
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 | a0002c0003t0001g0133 a0002c0004t0003g0125 a0002c0004t0003g0159 others(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 | a0004c0009t0007g0171 a0004c0009t0009g0169 a0004c0009t0009g0170 others(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 | a0001c0002t0013g0264 | 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 | a0002c0003t0001g0156 | 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 | a0001c0001t0001g0235 a0001c0001t0001g0242 a0001c0001t0002g0224 others(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 | 56 | a0001c0001t0001g0004 a0001c0001t0001g0215 a0001c0001t0001g0216 others(53): Show |
59 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(56): 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 | a0002c0003t0001g0126 | 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 | a0001c0027t0050g0212 | 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 | a0001c0001t0001g0319 | 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 | a0001c0027t0050g0212 | 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 | a0001c0002t0005g0228 | 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 | a0001c0001t0001g0368 a0001c0001t0001g0370 a0001c0002t0003g0344 others(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 | a0002c0003t0047g0116 | 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 | a0001c0002t0009g0361 a0001c0002t0025g0005 a0001c0002t0056g0362 |
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 | a0001c0001t0001g0235 a0001c0001t0001g0240 a0001c0001t0001g0242 others(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 | a0002c0004t0001g0137 | 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 | a0001c0002t0003g0246 | 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 | a0004c0009t0007g0171 a0004c0009t0009g0169 a0004c0009t0009g0170 others(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 | a0001c0001t0002g0197 a0001c0002t0040g0276 a0001c0005t0066g0258 others(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 | 328 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(325): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): 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 | a0001c0027t0050g0212 | 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 | a0001c0002t0007g0259 a0001c0002t0013g0264 a0001c0027t0050g0212 |
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 | 254 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0216 others(251): 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 | 124 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0265 others(121): 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 | a0001c0002t0052g0207 a0003c0006t0009g0027 a0003c0006t0015g0014 others(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 | a0001c0001t0002g0197 a0001c0002t0011g0289 a0001c0002t0011g0292 others(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 | a0002c0004t0037g0093 | 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 | a0003c0006t0009g0027 a0003c0006t0015g0014 a0003c0006t0032g0019 others(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 | a0002c0008t0005g0048 | 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 | a0001c0002t0052g0207 a0004c0009t0007g0171 a0004c0009t0009g0169 others(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 | a0001c0002t0007g0245 | 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 | a0002c0004t0002g0078 | 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 | a0001c0001t0001g0267 | 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 | a0001c0002t0013g0264 a0001c0002t0052g0207 a0004c0009t0007g0171 others(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 | a0001c0002t0013g0264 a0001c0002t0052g0207 a0004c0009t0007g0171 others(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 | a0003c0013t0001g0013 | 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 | a0004c0009t0013g0172 | 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 | a0001c0001t0002g0197 a0001c0002t0040g0276 |
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 | a0002c0003t0017g0138 | 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 | a0002c0003t0001g0140 | 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 | a0002c0003t0001g0114 | 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 | a0001c0002t0003g0263 a0001c0005t0058g0208 |
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 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0342 others(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 | 291 | a0001c0001t0001g0004 a0001c0001t0001g0215 a0001c0001t0001g0216 others(288): Show |
296 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(293): Show |
intron_variant | MODIFIER | c.467-11948delC | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44287605 | |||||||
chr11:44287605 | AGAAAAG | A | 5 | a0003c0006t0009g0027 a0003c0006t0015g0014 a0003c0006t0032g0019 others(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 | 64 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0180 others(61): 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 | a0001c0001t0002g0347 | 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 | a0001c0002t0003g0213 a0001c0002t0019g0308 |
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 | a0001c0001t0002g0347 | 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 | a0001c0001t0001g0250 a0001c0001t0001g0267 a0001c0001t0001g0279 others(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 | a0001c0002t0025g0005 a0001c0011t0020g0261 a0003c0006t0009g0027 others(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 | a0001c0001t0002g0347 | 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 | a0001c0002t0013g0264 a0001c0002t0052g0207 a0004c0009t0007g0171 others(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 | a0001c0001t0002g0347 | 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 | a0003c0006t0024g0021 a0003c0006t0024g0028 a0003c0010t0001g0017 others(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 | a0002c0004t0014g0109 | 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 | a0001c0001t0001g0180 | 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 | a0001c0002t0013g0264 a0001c0002t0052g0207 a0004c0009t0007g0171 others(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 | a0001c0002t0003g0213 a0001c0002t0019g0308 |
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 | 376 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(373): Show |
384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): 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 | a0001c0001t0001g0306 a0003c0013t0001g0010 a0003c0013t0001g0013 others(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 | a0001c0002t0040g0276 | 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 | a0001c0001t0002g0348 a0001c0002t0005g0211 |
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 | a0001c0001t0004g0324 a0001c0001t0004g0325 a0001c0001t0004g0328 others(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 | a0001c0001t0001g0265 a0001c0001t0001g0266 |
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 | a0001c0001t0002g0274 | 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 | a0002c0004t0005g0060 | 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 | a0001c0001t0043g0293 a0001c0002t0015g0222 a0001c0005t0066g0258 others(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 | a0002c0004t0005g0127 | 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 | a0001c0001t0001g0235 a0001c0001t0001g0240 a0001c0001t0001g0242 others(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 | a0001c0005t0006g0008 | 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 | a0002c0003t0001g0049 | 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 | 339 | a0001c0001t0001g0004 a0001c0001t0001g0215 a0001c0001t0001g0216 others(336): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): 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 | a0001c0029t0001g0234 | 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 | a0001c0001t0002g0347 a0001c0002t0013g0264 a0001c0002t0016g0302 others(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 | a0001c0001t0001g0235 a0001c0001t0001g0240 a0001c0001t0001g0242 others(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 | a0001c0001t0001g0364 | 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 | a0001c0002t0003g0255 a0001c0002t0003g0256 |
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 | a0001c0002t0002g0227 | 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 | a0001c0001t0001g0235 a0001c0001t0001g0240 a0001c0001t0001g0242 others(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 | a0001c0001t0001g0235 a0001c0001t0001g0240 a0001c0001t0001g0242 others(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 | 51 | a0001c0001t0001g0004 a0001c0001t0001g0215 a0001c0001t0001g0216 others(48): Show |
54 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(51): 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 | a0001c0007t0007g0238 a0001c0007t0007g0239 a0001c0011t0003g0290 others(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 | a0001c0001t0001g0368 a0001c0001t0001g0370 a0001c0002t0003g0344 others(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 | 80 | a0001c0001t0001g0004 a0001c0001t0001g0215 a0001c0001t0001g0216 others(77): Show |
83 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(80): 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 | a0003c0006t0009g0027 a0003c0006t0015g0014 a0003c0006t0032g0019 others(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 | a0001c0001t0002g0347 | 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 | a0001c0001t0001g0235 a0001c0001t0001g0240 a0001c0001t0001g0242 others(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 | a0001c0001t0001g0235 a0001c0001t0001g0240 a0001c0001t0001g0242 others(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 | a0001c0001t0001g0235 a0001c0001t0001g0240 a0001c0001t0001g0242 others(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 | a0001c0001t0001g0235 a0001c0001t0001g0240 a0001c0001t0001g0242 others(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 | a0003c0020t0026g0018 | 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 | a0001c0002t0007g0277 | 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 | a0001c0001t0001g0235 a0001c0001t0001g0240 a0001c0001t0001g0242 others(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 | a0001c0001t0001g0235 a0001c0001t0001g0240 a0001c0001t0001g0242 others(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 | a0001c0001t0002g0347 a0001c0002t0016g0302 |
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 | a0004c0009t0013g0172 | 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 | a0001c0001t0001g0235 a0001c0001t0001g0240 a0001c0001t0001g0242 others(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 | a0001c0001t0001g0235 a0001c0001t0001g0240 a0001c0001t0001g0242 others(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 | a0001c0001t0001g0235 a0001c0001t0001g0240 a0001c0001t0001g0242 others(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 | a0001c0001t0001g0235 a0001c0001t0001g0240 a0001c0001t0001g0242 others(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 | a0001c0002t0025g0005 a0001c0011t0020g0261 a0003c0020t0026g0018 |
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 | a0001c0001t0001g0235 a0001c0001t0001g0240 a0001c0001t0001g0242 others(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 | a0001c0001t0001g0235 a0001c0001t0001g0240 a0001c0001t0001g0242 others(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 | a0001c0001t0043g0293 a0001c0002t0015g0222 a0001c0005t0066g0258 others(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 | a0001c0001t0001g0235 a0001c0001t0001g0240 a0001c0001t0001g0242 others(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 | a0002c0004t0014g0054 a0002c0004t0014g0072 |
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 | a0002c0004t0002g0098 | 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 | a0001c0002t0013g0264 | 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 | a0001c0001t0001g0235 a0001c0001t0001g0240 a0001c0001t0001g0242 others(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 | 131 | a0001c0001t0001g0004 a0001c0001t0001g0216 a0001c0001t0001g0268 others(128): Show |
135 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.467-16720delA | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44292377 | |||||||
chr11:44292377 | ATT | A | 194 | a0001c0001t0001g0235 a0001c0001t0001g0240 a0001c0001t0001g0242 others(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 | a0001c0001t0001g0215 a0001c0001t0001g0319 a0001c0002t0036g0358 others(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 | 129 | a0001c0001t0001g0004 a0001c0001t0001g0216 a0001c0001t0001g0268 others(126): Show |
133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): 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 | a0001c0001t0001g0235 a0001c0001t0001g0240 a0001c0001t0001g0242 others(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 | a0001c0002t0007g0336 | 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 | 376 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(373): Show |
384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.467-16804C>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44292462 | |||||||
chr11:44292465 | T | C | 337 | a0001c0001t0001g0004 a0001c0001t0001g0215 a0001c0001t0001g0216 others(334): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.467-16807A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44292465 | |||||||
chr11:44292534 | G | A | 337 | a0001c0001t0001g0004 a0001c0001t0001g0215 a0001c0001t0001g0216 others(334): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): 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 | a0001c0001t0002g0347 a0001c0002t0013g0264 a0001c0002t0016g0302 others(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 | a0002c0003t0004g0108 | 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 | a0001c0001t0001g0368 a0001c0001t0001g0370 a0001c0002t0003g0344 others(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 | a0002c0003t0001g0149 a0002c0008t0004g0153 a0002c0008t0005g0050 others(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 | a0001c0005t0066g0258 a0003c0006t0003g0025 a0003c0006t0003g0037 others(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 | a0001c0001t0001g0364 a0001c0002t0008g0311 a0001c0002t0008g0349 |
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 | a0001c0002t0040g0276 | 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 | 163 | a0001c0001t0001g0004 a0001c0001t0001g0215 a0001c0001t0001g0216 others(160): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): 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 | a0001c0001t0002g0260 a0001c0002t0007g0336 a0001c0002t0009g0343 others(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 | a0001c0001t0001g0368 a0001c0001t0001g0370 a0001c0002t0003g0344 others(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 | 336 | a0001c0001t0001g0004 a0001c0001t0001g0215 a0001c0001t0001g0216 others(333): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): 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 | a0001c0031t0002g0380 | 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 | a0001c0001t0001g0180 a0001c0001t0001g0190 a0001c0001t0002g0262 others(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 | a0001c0001t0004g0182 a0001c0005t0006g0183 a0001c0005t0061g0199 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0186 a0001c0001t0001g0269 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0216 a0001c0001t0001g0265 others(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 | 72 | a0001c0001t0001g0003 a0001c0001t0001g0215 a0001c0001t0001g0250 others(69): Show |
74 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(71): 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 | a0001c0001t0001g0327 a0001c0001t0001g0368 a0001c0001t0001g0370 others(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 | a0001c0001t0002g0288 a0001c0002t0003g0345 a0001c0002t0003g0346 others(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 | a0001c0001t0043g0293 a0001c0031t0002g0380 a0003c0006t0003g0022 others(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 | a0001c0002t0015g0222 | 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 | a0001c0001t0001g0235 a0001c0007t0004g0236 |
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 | a0001c0001t0002g0347 a0003c0006t0015g0014 a0003c0006t0032g0019 others(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 | a0001c0001t0001g0242 a0001c0002t0030g0220 a0001c0002t0055g0248 others(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 | a0001c0001t0001g0240 a0001c0001t0002g0224 a0001c0002t0007g0245 others(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 | a0001c0001t0001g0267 a0003c0006t0009g0027 |
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 | a0001c0002t0011g0357 a0001c0002t0015g0341 a0001c0007t0003g0214 others(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 | a0001c0002t0025g0005 a0001c0011t0020g0261 a0002c0003t0017g0138 others(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 | a0001c0001t0001g0235 a0001c0001t0001g0240 a0001c0001t0001g0242 others(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 | a0002c0004t0012g0080 | 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 | a0001c0001t0001g0235 a0001c0001t0001g0240 a0001c0001t0001g0242 others(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 | a0002c0004t0012g0080 a0004c0022t0009g0167 |
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 | a0002c0003t0001g0100 | 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 | a0001c0002t0028g0356 a0002c0003t0001g0064 a0002c0003t0001g0133 others(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 | 274 | a0001c0001t0001g0004 a0001c0001t0001g0215 a0001c0001t0001g0216 others(271): Show |
279 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(276): 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 | a0001c0001t0001g0235 a0001c0001t0001g0240 a0001c0001t0001g0242 others(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 | a0001c0002t0013g0264 a0001c0002t0052g0207 a0004c0009t0007g0171 others(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 | 317 | a0001c0001t0001g0004 a0001c0001t0001g0215 a0001c0001t0001g0216 others(314): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): 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 | a0003c0006t0003g0040 a0003c0006t0013g0034 a0003c0006t0013g0042 others(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 | a0001c0001t0002g0347 | 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 | a0001c0001t0001g0368 a0001c0001t0001g0370 a0001c0001t0002g0347 others(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 | 145 | a0001c0001t0001g0004 a0001c0001t0001g0215 a0001c0001t0001g0216 others(142): Show |
149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): 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 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0342 others(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 | a0001c0002t0007g0277 a0001c0002t0040g0276 a0003c0006t0009g0027 others(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 | 318 | a0001c0001t0001g0004 a0001c0001t0001g0215 a0001c0001t0001g0216 others(315): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): 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 | a0001c0002t0001g0271 a0001c0002t0001g0273 |
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 | a0001c0002t0007g0277 a0001c0002t0040g0276 |
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 | 152 | a0001c0001t0001g0004 a0001c0001t0001g0215 a0001c0001t0001g0216 others(149): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): 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 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0342 others(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 | a0001c0005t0006g0372 | 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 | a0001c0005t0006g0372 | 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 | a0001c0002t0007g0259 a0001c0002t0011g0179 a0001c0002t0025g0005 others(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 | a0003c0006t0009g0027 a0003c0006t0015g0014 a0003c0006t0032g0019 others(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 | a0001c0027t0050g0212 | 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 | a0001c0001t0002g0347 | 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 | a0001c0002t0007g0259 a0001c0002t0011g0179 a0001c0002t0025g0005 others(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 | a0002c0003t0001g0001 a0002c0003t0004g0147 a0002c0003t0049g0148 |
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 | a0001c0001t0002g0347 | 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 | a0001c0002t0023g0201 a0001c0002t0027g0198 |
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 | a0001c0027t0050g0212 | 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 | 24 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0180 others(21): 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 | a0001c0001t0001g0190 a0001c0001t0002g0262 a0001c0001t0004g0196 others(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 | a0001c0002t0027g0198 | 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 | a0001c0001t0001g0265 a0001c0001t0001g0342 a0001c0001t0001g0359 others(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 | 175 | a0001c0001t0001g0004 a0001c0001t0001g0215 a0001c0001t0001g0216 others(172): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): 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 | a0001c0001t0002g0197 | 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 | a0001c0001t0002g0347 | 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 | a0001c0002t0009g0361 a0001c0002t0016g0302 a0001c0002t0056g0362 others(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 | a0002c0003t0001g0064 a0002c0003t0010g0128 a0002c0004t0014g0054 others(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 | a0001c0002t0007g0259 a0001c0002t0011g0179 a0001c0002t0025g0005 others(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 | a0001c0030t0026g0298 | 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 | 329 | a0001c0001t0001g0004 a0001c0001t0001g0215 a0001c0001t0001g0216 others(326): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.466+14228T>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44295369 | |||||||
chr11:44295715 | C | T | 160 | a0001c0001t0001g0004 a0001c0001t0001g0215 a0001c0001t0001g0216 others(157): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): 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 | a0001c0001t0001g0368 a0001c0001t0001g0370 a0001c0002t0003g0344 others(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 | a0001c0001t0004g0324 | 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 | a0001c0001t0004g0324 | 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 | a0001c0001t0002g0347 | 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 | a0001c0001t0001g0359 | 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 | a0001c0002t0013g0264 | 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 | 147 | a0001c0001t0001g0004 a0001c0001t0001g0215 a0001c0001t0001g0216 others(144): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.466+13702T>C | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44295895 | |||||||
chr11:44295927 | C | T | 160 | a0001c0001t0001g0004 a0001c0001t0001g0215 a0001c0001t0001g0216 others(157): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): 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 | a0003c0006t0009g0027 a0003c0006t0015g0014 a0003c0006t0032g0019 others(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 | a0003c0006t0003g0025 | 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 | a0001c0001t0001g0368 a0001c0001t0001g0370 a0001c0002t0003g0344 others(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 | a0001c0001t0002g0260 a0001c0002t0007g0336 a0001c0002t0009g0343 others(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 | a0001c0001t0002g0347 a0001c0002t0007g0259 a0001c0002t0011g0179 others(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 | a0001c0001t0001g0215 | 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 | a0001c0001t0002g0347 a0001c0002t0007g0259 a0001c0002t0011g0179 others(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 | a0003c0006t0009g0027 a0003c0006t0015g0014 a0003c0006t0032g0019 others(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 | a0003c0013t0001g0010 a0003c0013t0001g0013 a0003c0017t0002g0009 others(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 | 160 | a0001c0001t0001g0004 a0001c0001t0001g0215 a0001c0001t0001g0216 others(157): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): 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 | a0001c0027t0050g0212 | 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 | a0001c0001t0002g0260 a0001c0002t0007g0336 a0001c0002t0009g0343 others(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 | a0001c0001t0002g0347 a0001c0002t0007g0259 a0001c0002t0011g0179 others(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 | a0002c0004t0014g0054 a0002c0004t0014g0072 |
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 | a0001c0002t0038g0209 | 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 | a0002c0003t0002g0120 | 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 | 153 | a0001c0001t0001g0004 a0001c0001t0001g0215 a0001c0001t0001g0216 others(150): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): 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 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0342 others(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 | a0001c0001t0001g0368 a0001c0001t0001g0370 a0001c0001t0010g0219 others(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 | 129 | a0001c0001t0001g0004 a0001c0001t0001g0215 a0001c0001t0001g0216 others(126): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): 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 | a0001c0001t0004g0324 a0001c0001t0004g0325 a0001c0002t0007g0259 others(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 | a0001c0001t0002g0347 a0001c0002t0007g0259 a0001c0002t0011g0179 others(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 | a0002c0003t0004g0079 | 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 | 166 | a0001c0001t0001g0004 a0001c0001t0001g0215 a0001c0001t0001g0216 others(163): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): 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 | a0001c0001t0004g0324 | 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 | a0002c0004t0005g0092 | 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 | 339 | a0001c0001t0001g0004 a0001c0001t0001g0215 a0001c0001t0001g0216 others(336): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): 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 | a0001c0007t0008g0291 | 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 | a0001c0002t0007g0259 a0001c0002t0011g0179 |
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 | a0001c0002t0003g0375 a0001c0002t0003g0376 a0001c0002t0003g0377 others(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 | a0001c0001t0002g0347 a0001c0002t0007g0259 a0001c0002t0011g0179 others(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 | a0001c0001t0001g0368 a0001c0001t0001g0370 a0001c0002t0003g0344 others(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 | 140 | a0001c0001t0001g0004 a0001c0001t0001g0215 a0001c0001t0001g0216 others(137): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): 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 | a0001c0002t0007g0277 | 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 | a0001c0001t0002g0347 a0001c0002t0007g0259 a0001c0002t0011g0179 others(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 | a0003c0010t0042g0023 | 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 | a0001c0001t0001g0368 a0001c0001t0001g0370 a0001c0002t0003g0344 others(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 | a0001c0001t0002g0347 a0001c0002t0007g0259 a0001c0002t0011g0179 others(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 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0342 others(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 | a0002c0003t0002g0090 a0002c0008t0012g0091 |
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 | a0001c0002t0009g0361 a0001c0002t0056g0362 |
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 | 339 | a0001c0001t0001g0004 a0001c0001t0001g0215 a0001c0001t0001g0216 others(336): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): 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 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0342 others(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 | a0004c0009t0007g0171 | 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 | a0001c0002t0011g0179 | 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 | a0001c0001t0002g0189 | 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 | 322 | a0001c0001t0001g0004 a0001c0001t0001g0215 a0001c0001t0001g0216 others(319): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.466+10802delT | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44298794 | |||||||
chr11:44298794 | CAA | C | 16 | a0001c0001t0001g0368 a0001c0001t0001g0370 a0001c0001t0004g0324 others(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 | a0003c0006t0013g0034 a0003c0006t0013g0042 a0003c0010t0002g0033 |
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 | a0001c0002t0007g0259 a0001c0002t0011g0179 |
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 | a0001c0001t0002g0249 | 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 | a0001c0001t0002g0347 a0001c0002t0040g0276 |
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 | a0001c0002t0011g0357 | 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 | a0002c0004t0014g0109 | 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 | a0003c0020t0026g0018 | 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 | a0001c0002t0055g0248 | 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 | a0001c0001t0002g0347 a0001c0002t0040g0276 |
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 | a0002c0003t0004g0147 | 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 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0340 others(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 | 135 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0180 others(132): Show |
138 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.466+10242dupA | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44299354 | |||||||
chr11:44299354 | G | GTT | 18 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(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 | a0001c0001t0001g0368 a0001c0001t0001g0370 a0001c0002t0003g0345 others(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 | a0001c0001t0001g0368 a0001c0001t0001g0370 a0001c0002t0003g0344 others(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 | a0004c0009t0007g0171 a0004c0009t0009g0169 a0004c0009t0009g0170 others(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 | a0002c0003t0002g0120 a0002c0004t0007g0044 a0002c0008t0051g0061 |
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 | a0003c0006t0009g0027 a0003c0006t0015g0014 a0003c0006t0032g0019 others(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 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0340 others(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 | a0001c0001t0002g0347 a0001c0002t0040g0276 |
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 | a0002c0004t0002g0110 | 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 | a0001c0002t0007g0259 a0001c0002t0007g0277 a0001c0002t0009g0361 others(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 | a0001c0001t0002g0249 | 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 | a0001c0002t0003g0263 a0001c0005t0058g0208 |
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 | 139 | a0001c0001t0001g0004 a0001c0001t0001g0215 a0001c0001t0001g0216 others(136): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): 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 | a0001c0002t0038g0209 | 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 | a0002c0003t0002g0120 a0002c0004t0007g0044 a0002c0008t0051g0061 |
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 | a0001c0002t0013g0264 a0004c0009t0007g0171 a0004c0009t0009g0169 others(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 | a0001c0005t0004g0305 | 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 | a0003c0006t0009g0027 a0003c0006t0015g0014 a0003c0006t0032g0019 others(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 | a0002c0003t0010g0165 | 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 | a0001c0007t0016g0300 | 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 | a0002c0003t0001g0077 | 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 | a0001c0001t0002g0347 | 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 | a0001c0002t0025g0005 a0001c0011t0020g0261 |
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 | a0003c0006t0009g0027 | 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 | a0001c0001t0002g0347 | 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 | a0001c0005t0005g0353 | 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 | a0001c0002t0013g0264 a0004c0009t0007g0171 a0004c0009t0009g0169 others(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 | a0001c0005t0004g0305 | 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 | a0002c0003t0001g0056 a0002c0003t0001g0058 a0002c0004t0003g0057 |
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 | a0002c0008t0006g0073 | 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 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0340 others(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 | a0001c0027t0050g0212 | 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 | a0002c0004t0002g0078 | 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 | a0001c0001t0001g0368 a0001c0001t0001g0370 a0001c0002t0003g0344 others(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 | a0001c0002t0030g0220 | 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 | a0003c0006t0011g0032 | 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 | a0002c0003t0002g0154 | 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 | a0001c0002t0003g0369 | 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 | a0001c0002t0016g0302 a0001c0005t0066g0258 a0003c0006t0003g0022 others(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 | a0001c0027t0050g0212 | 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 | a0001c0007t0016g0300 | 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 | a0001c0002t0025g0005 a0001c0011t0020g0261 |
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 | a0001c0005t0006g0008 | 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 | a0001c0002t0013g0264 a0004c0009t0007g0171 a0004c0009t0009g0169 others(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 | a0001c0007t0004g0007 | 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 | a0001c0002t0025g0005 a0001c0011t0020g0261 |
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 | a0001c0001t0001g0186 a0001c0001t0002g0184 a0001c0005t0060g0187 |
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 | a0002c0004t0004g0119 | 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 | a0001c0002t0025g0005 a0001c0011t0020g0261 |
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 | a0001c0002t0040g0276 | 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 | a0001c0001t0001g0368 a0001c0001t0001g0370 a0001c0002t0003g0344 others(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 | a0001c0001t0001g0215 | 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 | a0001c0016t0003g0185 | 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 | a0001c0001t0001g0338 a0001c0002t0003g0339 |
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 | a0001c0005t0058g0208 | 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 | a0001c0001t0001g0299 | 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 | a0002c0004t0005g0146 | 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 | a0001c0001t0001g0235 a0001c0001t0001g0240 a0001c0001t0001g0242 others(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 | a0003c0017t0002g0009 a0005c0018t0001g0012 |
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 | a0001c0002t0021g0254 a0001c0031t0002g0380 |
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 | a0002c0003t0001g0056 | 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 | a0001c0002t0025g0005 a0001c0011t0020g0261 |
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 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0340 others(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 | a0001c0001t0004g0210 | 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 | a0003c0006t0009g0027 a0003c0006t0015g0014 a0003c0006t0032g0019 others(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 | a0001c0001t0002g0379 | 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 | a0001c0002t0003g0263 a0001c0005t0058g0208 |
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 | a0003c0006t0015g0014 a0003c0006t0032g0019 a0003c0021t0027g0020 |
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 | a0001c0001t0001g0250 | 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 | a0001c0001t0001g0368 a0001c0001t0001g0370 a0001c0002t0003g0344 others(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 | 327 | a0001c0001t0001g0004 a0001c0001t0001g0215 a0001c0001t0001g0216 others(324): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): 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 | a0001c0002t0003g0263 a0001c0005t0058g0208 |
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 | a0001c0007t0003g0214 | 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 | a0002c0003t0001g0140 a0002c0003t0001g0144 a0002c0004t0003g0111 others(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 | a0004c0009t0007g0171 a0004c0009t0009g0169 a0004c0009t0009g0170 others(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 | a0001c0002t0007g0259 | 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 | 142 | a0001c0001t0001g0004 a0001c0001t0001g0215 a0001c0001t0001g0216 others(139): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): 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 | a0003c0006t0009g0027 a0003c0006t0015g0014 a0003c0006t0032g0019 others(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 | a0002c0004t0005g0145 | 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 | a0001c0001t0002g0184 | 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 | a0001c0012t0006g0251 | 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 | a0001c0005t0006g0183 | 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 | a0001c0002t0038g0209 | 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 | a0002c0003t0001g0074 a0002c0003t0001g0112 a0002c0003t0010g0055 |
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 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0004g0182 |
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 | a0001c0002t0009g0361 a0001c0002t0056g0362 |
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 | a0001c0002t0015g0341 a0001c0002t0020g0252 |
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 | a0001c0002t0003g0213 a0001c0002t0019g0308 |
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 | a0003c0013t0001g0010 a0003c0013t0001g0013 a0003c0017t0002g0009 others(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 | a0001c0002t0007g0259 a0001c0002t0011g0179 |
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 | a0001c0001t0002g0347 | 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 | a0001c0005t0004g0305 | 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 | a0001c0001t0001g0267 | 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 | a0001c0001t0004g0210 | 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 | 315 | a0001c0001t0001g0004 a0001c0001t0001g0215 a0001c0001t0001g0216 others(312): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): 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 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0004g0307 others(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 | a0002c0004t0005g0145 | 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 | a0002c0003t0001g0045 | 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 | a0003c0006t0009g0024 a0003c0006t0013g0034 a0003c0006t0013g0042 others(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 | a0002c0008t0051g0061 | 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 | a0002c0003t0001g0056 a0002c0003t0001g0058 a0002c0003t0001g0075 others(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 | a0002c0004t0022g0076 | 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 | a0001c0002t0009g0361 a0001c0002t0056g0362 |
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 | a0002c0008t0063g0113 | 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 | a0002c0003t0004g0118 | 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 | a0001c0007t0016g0300 | 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 | a0003c0020t0026g0018 | 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 | a0001c0001t0002g0260 a0001c0002t0009g0343 |
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 | a0002c0004t0005g0060 | 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 | 142 | a0001c0001t0001g0004 a0001c0001t0001g0215 a0001c0001t0001g0216 others(139): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.466+3350A>G | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44306247 | |||||||
chr11:44306268 | T | C | 314 | a0001c0001t0001g0004 a0001c0001t0001g0215 a0001c0001t0001g0216 others(311): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): 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 | a0004c0009t0007g0171 a0004c0009t0009g0169 a0004c0009t0009g0170 others(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 | a0001c0002t0003g0377 | 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 | a0001c0001t0001g0368 a0001c0001t0001g0370 a0001c0001t0002g0347 others(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 | a0003c0006t0007g0039 | 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 | 150 | a0001c0001t0001g0004 a0001c0001t0001g0215 a0001c0001t0001g0216 others(147): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): 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 | a0004c0009t0007g0171 a0004c0009t0009g0169 a0004c0009t0009g0170 others(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 | a0002c0003t0001g0114 | 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 | a0001c0002t0007g0259 a0001c0002t0011g0179 |
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 | a0001c0002t0009g0361 a0001c0002t0056g0362 |
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 | a0001c0001t0001g0342 a0001c0001t0001g0359 a0001c0001t0001g0360 others(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 | 334 | a0001c0001t0001g0004 a0001c0001t0001g0215 a0001c0001t0001g0216 others(331): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): 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 | a0004c0009t0007g0171 a0004c0009t0009g0169 a0004c0009t0009g0170 others(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 | a0003c0006t0003g0025 a0003c0006t0003g0037 a0003c0006t0004g0026 others(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 | a0002c0004t0007g0044 | 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 | a0001c0001t0002g0379 | 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 | a0004c0023t0044g0168 | 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 | a0002c0003t0045g0115 a0002c0004t0005g0146 |
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 | a0002c0003t0047g0116 | 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 | a0001c0002t0009g0361 a0001c0002t0056g0362 a0001c0027t0050g0212 |
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 | a0001c0002t0025g0005 a0001c0011t0020g0261 |
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 | a0001c0002t0021g0254 a0001c0031t0002g0380 |
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 | a0003c0006t0003g0022 a0003c0006t0003g0025 a0003c0006t0003g0037 others(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 | a0003c0020t0026g0018 | 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 | a0001c0002t0005g0211 | 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 | 148 | a0001c0001t0001g0004 a0001c0001t0001g0215 a0001c0001t0001g0216 others(145): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): 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 | a0002c0004t0020g0160 | 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 | a0006c0025t0008g0178 | 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 | a0002c0004t0005g0162 | 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 | a0001c0002t0003g0255 a0001c0002t0003g0256 |
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 | a0001c0002t0003g0375 a0001c0002t0003g0376 a0001c0002t0003g0377 others(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 | a0001c0002t0016g0302 a0001c0005t0066g0258 |
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 | 146 | a0001c0001t0001g0004 a0001c0001t0001g0215 a0001c0001t0001g0216 others(143): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): 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 | a0001c0002t0013g0264 | 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 | a0002c0003t0001g0117 a0002c0004t0003g0059 |
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 | a0002c0003t0001g0001 a0002c0003t0001g0045 a0002c0003t0001g0047 others(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 | 338 | a0001c0001t0001g0004 a0001c0001t0001g0215 a0001c0001t0001g0216 others(335): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): 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 | a0002c0003t0001g0062 a0002c0003t0001g0064 a0002c0003t0001g0065 others(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 | a0002c0003t0001g0077 | 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 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0267 others(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 | a0002c0003t0001g0161 | 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 |
63 | a0001c0001t0001g0306 a0001c0001t0001g0310 a0001c0001t0001g0312 others(60): Show |
65 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(62): 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 | a0001c0001t0001g0350 a0001c0001t0001g0359 a0001c0001t0001g0360 others(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 | a0001c0001t0001g0364 a0001c0001t0001g0368 a0001c0001t0001g0370 others(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 | a0001c0001t0001g0373 a0001c0005t0006g0372 |
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 | a0001c0002t0001g0374 | 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 | a0002c0003t0001g0001 a0002c0003t0001g0086 a0002c0003t0001g0100 others(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 | a0002c0003t0001g0117 a0002c0003t0001g0121 a0002c0003t0001g0126 others(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 | a0002c0003t0001g0149 a0002c0003t0001g0156 a0002c0003t0002g0154 others(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 | a0002c0003t0001g0164 a0002c0003t0010g0165 a0002c0004t0005g0162 others(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 | a0001c0002t0003g0375 a0001c0002t0003g0376 a0001c0002t0003g0377 |
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 | a0002c0003t0001g0045 a0002c0003t0001g0047 a0002c0003t0001g0049 others(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 | a0001c0001t0002g0260 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0180 a0001c0001t0001g0192 others(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 | a0002c0004t0014g0054 | 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 | a0002c0004t0014g0054 | 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 | 347 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(344): Show |
354 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(351): 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 | a0001c0001t0002g0184 a0001c0001t0002g0197 a0001c0002t0023g0201 others(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 | a0001c0002t0004g0193 | 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 | a0001c0001t0002g0379 | 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 | a0001c0001t0002g0379 | 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 | a0002c0004t0001g0166 | 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 | a0002c0003t0002g0043 | 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 | a0001c0002t0011g0179 | 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 | a0001c0001t0002g0379 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.466+57A>T | ALX4 | ENSG00000052850.8 | transcript | ENST00000652299.1 | protein_coding | 1/3 | chr11 | 44309540 |