Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 57146 |
| ensemblid | ENSG00000011638.11 |
| hgncid | 30136 |
| symbol | LDAF1 |
| name | lipid droplet assembly factor 1 |
| refseq_nuc | NM_001301771.2 |
| refseq_prot | NP_001288700.1 |
| ensembl_nuc | ENST00000233047.9 |
| ensembl_prot | ENSP00000233047.4 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 21158674 |
| end | 21180616 |
| strand | + |
| ver | v1.2 |
| region | chr16:21158674-21180616 |
| region5000 | chr16:21153674-21185616 |
| regionname0 | LDAF1_chr16_21158674_21180616 |
| regionname5000 | LDAF1_chr16_21153674_21185616 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 161 | 360 | 91 | 58 | 166 | 8 | 36 | 128 | LDAF1_chr16_21153674_21185616 | LDAF1 | MAKEE others(156): Show |
chr16 | 21153674 | 21185616 |
| a0002 | 0/0 | 161 | 22 | 1 | 10 | 0 | 5 | 6 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | MAKEE others(156): Show |
chr16 | 21153674 | 21185616 |
| a0003 | 1/0 | 161 | 3 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | MAKEE others(156): Show |
chr16 | 21153674 | 21185616 |
| a0004 | 0/0 | 161 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | MAKEE others(156): Show |
chr16 | 21153674 | 21185616 |
| a0005 | 0/0 | 161 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | MAKEE others(156): Show |
chr16 | 21153674 | 21185616 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 483 | 353 | 89 | 58 | 163 | 8 | 34 | LDAF1_chr16_21153674_21185616 | LDAF1 | ATGGC others(478): Show |
chr16 | 21153674 | 21185616 | ||
| a0001c0005 | 0/0 | 483 | 2 | 0 | 0 | 2 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | ATGGC others(478): Show |
chr16 | 21153674 | 21185616 | ||
| a0001c0006 | 0/0 | 483 | 2 | 0 | 0 | 1 | 0 | 1 | LDAF1_chr16_21153674_21185616 | LDAF1 | ATGGC others(478): Show |
chr16 | 21153674 | 21185616 | ||
| a0001c0007 | 0/0 | 483 | 2 | 2 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | ATGGC others(478): Show |
chr16 | 21153674 | 21185616 | ||
| a0001c0008 | 0/0 | 483 | 1 | 0 | 0 | 0 | 0 | 1 | LDAF1_chr16_21153674_21185616 | LDAF1 | ATGGC others(478): Show |
chr16 | 21153674 | 21185616 | ||
| a0002c0002 | 0/0 | 483 | 22 | 1 | 10 | 0 | 5 | 6 | LDAF1_chr16_21153674_21185616 | LDAF1 | ATGGC others(478): Show |
chr16 | 21153674 | 21185616 | ||
| a0003c0004 | 1/0 | 483 | 3 | 1 | 0 | 0 | 1 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | ATGGC others(478): Show |
chr16 | 21153674 | 21185616 | ||
| a0004c0003 | 0/0 | 483 | 4 | 4 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | ATGGC others(478): Show |
chr16 | 21153674 | 21185616 | ||
| a0005c0009 | 0/0 | 483 | 1 | 1 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | ATGGC others(478): Show |
chr16 | 21153674 | 21185616 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1717 | 334 | 85 | 58 | 149 | 8 | 33 | LDAF1_chr16_21153674_21185616 | LDAF1 | CTCTT others(1712): Show |
chr16 | 21153674 | 21185616 |
| a0001c0001t0003 | 0/0 | 1717 | 9 | 0 | 0 | 8 | 0 | 1 | LDAF1_chr16_21153674_21185616 | LDAF1 | CTCTT others(1712): Show |
chr16 | 21153674 | 21185616 |
| a0001c0001t0004 | 0/0 | 1717 | 3 | 0 | 0 | 3 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | CTCTT others(1712): Show |
chr16 | 21153674 | 21185616 |
| a0001c0001t0005 | 0/0 | 1717 | 3 | 3 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | CTCTT others(1712): Show |
chr16 | 21153674 | 21185616 |
| a0001c0001t0006 | 0/0 | 1717 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | CTCTT others(1712): Show |
chr16 | 21153674 | 21185616 |
| a0001c0001t0011 | 0/0 | 1728 | 1 | 1 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | CTCTT others(1723): Show |
chr16 | 21153674 | 21185616 |
| a0001c0001t0012 | 0/0 | 1717 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | CTCTT others(1712): Show |
chr16 | 21153674 | 21185616 |
| a0001c0001t0013 | 0/0 | 1717 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | CTCTT others(1712): Show |
chr16 | 21153674 | 21185616 |
| a0001c0005t0001 | 0/0 | 1717 | 2 | 0 | 0 | 2 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | CTCTT others(1712): Show |
chr16 | 21153674 | 21185616 |
| a0001c0006t0007 | 0/0 | 1717 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | CTCTT others(1712): Show |
chr16 | 21153674 | 21185616 |
| a0001c0006t0009 | 0/0 | 1717 | 1 | 0 | 0 | 0 | 0 | 1 | LDAF1_chr16_21153674_21185616 | LDAF1 | CTCTT others(1712): Show |
chr16 | 21153674 | 21185616 |
| a0001c0007t0001 | 0/0 | 1717 | 2 | 2 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | CTCTT others(1712): Show |
chr16 | 21153674 | 21185616 |
| a0001c0008t0001 | 0/0 | 1717 | 1 | 0 | 0 | 0 | 0 | 1 | LDAF1_chr16_21153674_21185616 | LDAF1 | CTCTT others(1712): Show |
chr16 | 21153674 | 21185616 |
| a0002c0002t0002 | 0/0 | 1717 | 21 | 1 | 9 | 0 | 5 | 6 | LDAF1_chr16_21153674_21185616 | LDAF1 | CTCTT others(1712): Show |
chr16 | 21153674 | 21185616 |
| a0002c0002t0008 | 0/0 | 1717 | 1 | 0 | 1 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | CTCTT others(1712): Show |
chr16 | 21153674 | 21185616 |
| a0003c0004t0002 | 1/0 | 1717 | 3 | 1 | 0 | 0 | 1 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | CTCTT others(1712): Show |
chr16 | 21153674 | 21185616 |
| a0004c0003t0001 | 0/0 | 1717 | 4 | 4 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | CTCTT others(1712): Show |
chr16 | 21153674 | 21185616 |
| a0005c0009t0010 | 0/0 | 1717 | 1 | 1 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | CTCTT others(1712): Show |
chr16 | 21153674 | 21185616 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 24 | 1 | 10 | 13 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0002 | 0/0 | 22 | 7 | 2 | 10 | 3 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0003 | 0/0 | 15 | 0 | 8 | 2 | 0 | 5 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0004 | 0/0 | 19 | 8 | 2 | 2 | 0 | 7 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0005 | 0/0 | 17 | 1 | 1 | 13 | 0 | 2 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0007 | 0/0 | 9 | 1 | 1 | 6 | 0 | 1 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0008 | 0/0 | 8 | 0 | 2 | 6 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0009 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0011 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0013 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0022 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0048 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0051 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0150 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0003g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0004g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0005g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0005g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0006g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0011g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0012g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0001t0013g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0005t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0006t0007g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0006t0009g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0007t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0007t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0001c0008t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0002c0002t0002g0006 | 0/0 | 10 | 1 | 5 | 0 | 1 | 3 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0002c0002t0002g0028 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0002c0002t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0002c0002t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0002c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0002c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0002c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0002c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0002c0002t0008g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0003c0004t0002g0056 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0003c0004t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0003c0004t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0004c0003t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0004c0003t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0004c0003t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| a0005c0009t0010g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0002 | g0063 | EUR | GBR | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG00140 | hp1 | a0003 | c0004 | t0002 | g0109 | EUR | GBR | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0042 | EUR | FIN | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG00280 | hp2 | a0002 | c0002 | t0002 | g0073 | EUR | FIN | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG00323 | hp1 | a0002 | c0002 | t0002 | g0006 | EUR | FIN | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0055 | EUR | FIN | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | CHS | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | CHS | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG00621 | hp1 | a0001 | c0005 | t0001 | g0046 | EAS | CHS | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG00642 | hp2 | a0002 | c0002 | t0002 | g0006 | AMR | PUR | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | CHS | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG00735 | hp1 | a0002 | c0002 | t0002 | g0075 | AMR | PUR | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG01074 | hp2 | a0002 | c0002 | t0002 | g0062 | AMR | PUR | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG01081 | hp2 | a0002 | c0002 | t0002 | g0006 | AMR | PUR | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG01167 | hp2 | a0002 | c0002 | t0002 | g0057 | AMR | PUR | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG01243 | hp2 | a0002 | c0002 | t0002 | g0006 | AMR | PUR | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG01255 | hp2 | a0002 | c0002 | t0008 | g0006 | AMR | CLM | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG01358 | hp1 | a0002 | c0002 | t0002 | g0006 | AMR | CLM | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG01361 | hp2 | a0002 | c0002 | t0002 | g0006 | AMR | CLM | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG01516 | hp2 | a0002 | c0002 | t0002 | g0028 | EUR | IBS | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG01993 | hp2 | a0002 | c0002 | t0002 | g0028 | AMR | PEL | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02132 | hp2 | a0001 | c0006 | t0007 | g0080 | EAS | KHV | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | CDX | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | CDX | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02523 | hp1 | a0001 | c0001 | t0006 | g0001 | EAS | KHV | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02602 | hp1 | a0002 | c0002 | t0002 | g0006 | SAS | PJL | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02602 | hp2 | a0001 | c0006 | t0009 | g0066 | SAS | PJL | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02615 | hp1 | a0001 | c0001 | t0005 | g0184 | AFR | GWD | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02630 | hp1 | a0003 | c0004 | t0002 | g0118 | AFR | GWD | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02683 | hp1 | a0002 | c0002 | t0002 | g0072 | SAS | PJL | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02735 | hp1 | a0001 | c0008 | t0001 | g0037 | SAS | PJL | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02896 | hp1 | a0001 | c0001 | t0005 | g0050 | AFR | GWD | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0050 | AFR | GWD | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ESN | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02965 | hp1 | a0001 | c0007 | t0001 | g0119 | AFR | ESN | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG03130 | hp1 | a0005 | c0009 | t0010 | g0193 | AFR | ESN | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG03195 | hp1 | a0004 | c0003 | t0001 | g0039 | AFR | ESN | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG03209 | hp1 | a0004 | c0003 | t0001 | g0194 | AFR | MSL | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | MSL | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG03239 | hp1 | a0002 | c0002 | t0002 | g0006 | SAS | PJL | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG03453 | hp1 | a0004 | c0003 | t0001 | g0195 | AFR | MSL | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG03486 | hp1 | a0004 | c0003 | t0001 | g0039 | AFR | MSL | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | MSL | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ESN | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | BEB | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | BEB | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | BEB | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG04115 | hp1 | a0002 | c0002 | t0002 | g0065 | SAS | STU | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | STU | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0153 | SAS | BEB | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG04199 | hp1 | a0002 | c0002 | t0002 | g0067 | SAS | STU | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG04199 | hp2 | a0002 | c0002 | t0002 | g0006 | SAS | STU | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | STU | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | STU | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18522 | hp1 | a0001 | c0001 | t0011 | g0002 | AFR | YRI | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | YRI | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18612 | hp1 | a0001 | c0005 | t0001 | g0046 | EAS | CHB | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | YRI | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18939 | hp1 | a0001 | c0001 | t0004 | g0047 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18946 | hp1 | a0001 | c0001 | t0004 | g0132 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18957 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0102 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18970 | hp1 | a0001 | c0001 | t0013 | g0188 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18979 | hp1 | a0001 | c0001 | t0004 | g0047 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18993 | hp2 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19001 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | LWK | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19030 | hp2 | a0001 | c0007 | t0001 | g0041 | AFR | LWK | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | LWK | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19059 | hp1 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19064 | hp2 | a0001 | c0001 | t0012 | g0012 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19089 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | YRI | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | YRI | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | ASW | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ASW | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA20752 | hp1 | a0002 | c0002 | t0002 | g0074 | EUR | TSI | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | TSI | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0143 | EUR | TSI | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0127 | EUR | TSI | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | GIH | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | GIH | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | MSL | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG06807 | hp1 | a0002 | c0002 | t0002 | g0006 | AFR | USA | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | USA | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | USA | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | USA | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0150 | REF | REF | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| homoSapiens | grch38p0 | a0003 | c0004 | t0002 | g0056 | REF | REF | LDAF1_chr16_21153674_21185616 | LDAF1 | chr16 | 21153674 | 21185616 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:21174018 | A | G | 1 | a0005 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.274A>G | p.Ile92Val | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/5 | 445/1717 | 274/486 | 92/161 | chr16 | 21174018 | |||
| chr16:21174033 | T | C | 1 | a0004 | 4 | HG03195.hp1 HG03209.hp1 HG03453.hp1 others(1): Show |
missense_variant | MODERATE | c.289T>C | p.Phe97Leu | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/5 | 460/1717 | 289/486 | 97/161 | chr16 | 21174033 | |||
| chr16:21174063 | G | A | 1 | a0002 | 22 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(19): Show |
missense_variant | MODERATE | c.319G>A | p.Gly107Ser | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/5 | 490/1717 | 319/486 | 107/161 | chr16 | 21174063 | |||
| chr16:21179530 | G | C | 1 | a0001 | 1 | HG02735.hp1 | missense_variant | MODERATE | c.460G>C | p.Glu154Gln | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 5/5 | 631/1717 | 460/486 | 154/161 | chr16 | 21179530 | |||
| chr16:21179532 | A | C | 3 | a0001 a0004 a0005 |
364 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(361): Show |
missense_variant | MODERATE | c.462A>C | p.Glu154Asp | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 5/5 | 633/1717 | 462/486 | 154/161 | chr16 | 21179532 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:21170496 | C | A | 1 | a0001c0005 | 2 | HG00621.hp1 NA18612.hp1 |
synonymous_variant | LOW | c.156C>A | p.Ala52Ala | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 3/5 | 327/1717 | 156/486 | 52/161 | chr16 | 21170496 | |||
| chr16:21170526 | G | T | 1 | a0001c0007 | 2 | HG02965.hp1 NA19030.hp2 |
synonymous_variant | LOW | c.186G>T | p.Ser62Ser | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 3/5 | 357/1717 | 186/486 | 62/161 | chr16 | 21170526 | |||
| chr16:21170556 | C | T | 1 | a0001c0006 | 2 | HG02132.hp2 HG02602.hp2 |
synonymous_variant | LOW | c.216C>T | p.Ile72Ile | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 3/5 | 387/1717 | 216/486 | 72/161 | chr16 | 21170556 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:21158719 | G | T | 1 | a0001c0001t0013 | 1 | NA18970.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-126G>T | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 1/5 | chr16 | 21158719 | |||||||
| chr16:21158723 | G | A | 1 | a0001c0001t0004 | 3 | NA18939.hp1 NA18946.hp1 NA18979.hp1 |
5_prime_UTR_variant | MODIFIER | c.-122G>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 1/5 | 2460 | chr16 | 21158723 | ||||||
| chr16:21161109 | T | C | 1 | a0001c0001t0006 | 1 | HG02523.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-74T>C | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/5 | chr16 | 21161109 | |||||||
| chr16:21161150 | T | C | 1 | a0001c0006t0007 | 1 | HG02132.hp2 | 5_prime_UTR_variant | MODIFIER | c.-33T>C | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/5 | 33 | chr16 | 21161150 | ||||||
| chr16:21179710 | A | G | 1 | a0001c0001t0005 | 3 | HG02615.hp1 HG02896.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*154A>G | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 5/5 | 154 | chr16 | 21179710 | ||||||
| chr16:21179772 | G | A | 1 | a0002c0002t0008 | 1 | HG01255.hp2 | 3_prime_UTR_variant | MODIFIER | c.*216G>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 5/5 | 216 | chr16 | 21179772 | ||||||
| chr16:21179878 | C | T | 1 | a0001c0001t0012 | 1 | NA19064.hp2 | 3_prime_UTR_variant | MODIFIER | c.*322C>T | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 5/5 | 322 | chr16 | 21179878 | ||||||
| chr16:21180062 | T | G | 1 | a0001c0006t0009 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*506T>G | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 5/5 | 506 | chr16 | 21180062 | ||||||
| chr16:21180227 | C | CT | 5 | a0001c0001t0001 a0001c0001t0005 a0001c0005t0001 others(2): Show |
83 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*693dupT | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 5/5 | 694 | INFO_REALIGN_3_PRIME | chr16 | 21180227 | |||||
| chr16:21180227 | C | CTT | 5 | a0001c0001t0001 a0001c0001t0003 a0001c0006t0007 others(2): Show |
52 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*692_*693dupTT | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 5/5 | 694 | INFO_REALIGN_3_PRIME | chr16 | 21180227 | |||||
| chr16:21180227 | C | CTTT | 2 | a0001c0001t0001 a0001c0001t0003 |
9 | HG01123.hp2 HG02738.hp2 HG04184.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*691_*693dupTTT | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 5/5 | 694 | INFO_REALIGN_3_PRIME | chr16 | 21180227 | |||||
| chr16:21180290 | T | C | 15 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(12): Show |
364 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(361): Show |
3_prime_UTR_variant | MODIFIER | c.*734T>C | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 5/5 | 734 | chr16 | 21180290 | ||||||
| chr16:21180291 | G | A | 1 | a0005c0009t0010 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*735G>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 5/5 | 735 | chr16 | 21180291 | ||||||
| chr16:21180367 | G | A | 1 | a0001c0001t0005 | 3 | HG02615.hp1 HG02896.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*811G>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 5/5 | 811 | chr16 | 21180367 | ||||||
| chr16:21180400 | T | TTTTTTTT others(4): Show |
1 | a0001c0001t0011 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*853_*863dupGTATTT others(5): Show |
LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 5/5 | 864 | INFO_REALIGN_3_PRIME | chr16 | 21180400 | |||||
| chr16:21180598 | A | G | 1 | a0001c0001t0003 | 9 | HG04184.hp2 NA18944.hp2 NA18957.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1042A>G | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 5/5 | 1042 | chr16 | 21180598 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:21158748 | T | C | 1 | a0001c0001t0001g0052 | 1 | HG02809.hp2 | splice_donor_variant&intron_variant | HIGH | c.-99+2T>C | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 1/4 | chr16 | 21158748 | |||||||
| chr16:21158902 | G | A | 3 | a0001c0001t0001g0013 a0001c0001t0001g0053 a0001c0001t0001g0054 |
6 | HG01109.hp1 HG01256.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-99+156G>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 1/4 | chr16 | 21158902 | |||||||
| chr16:21158916 | A | G | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
339 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(336): Show |
intron_variant | MODIFIER | c.-99+170A>G | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 1/4 | chr16 | 21158916 | |||||||
| chr16:21158987 | C | T | 1 | a0001c0001t0001g0196 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-99+241C>T | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 1/4 | chr16 | 21158987 | |||||||
| chr16:21159071 | C | A | 3 | a0001c0001t0001g0030 a0001c0001t0001g0078 a0001c0001t0001g0079 |
4 | HG01884.hp1 HG02145.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.-99+325C>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 1/4 | chr16 | 21159071 | |||||||
| chr16:21159118 | A | G | 5 | a0001c0001t0001g0030 a0001c0001t0001g0078 a0001c0001t0001g0079 others(2): Show |
6 | HG01884.hp1 HG02145.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.-99+372A>G | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 1/4 | chr16 | 21159118 | |||||||
| chr16:21159177 | C | G | 1 | a0005c0009t0010g0193 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-99+431C>G | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 1/4 | chr16 | 21159177 | |||||||
| chr16:21159247 | A | G | 1 | a0001c0001t0001g0051 | 2 | HG02735.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.-99+501A>G | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 1/4 | chr16 | 21159247 | |||||||
| chr16:21159484 | C | G | 9 | a0001c0001t0001g0025 a0001c0001t0001g0185 a0001c0001t0001g0186 others(6): Show |
11 | HG00438.hp1 HG00609.hp1 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.-99+738C>G | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 1/4 | chr16 | 21159484 | |||||||
| chr16:21159564 | A | G | 2 | a0001c0001t0005g0050 a0001c0001t0005g0184 |
3 | HG02615.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-99+818A>G | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 1/4 | chr16 | 21159564 | |||||||
| chr16:21159906 | G | A | 1 | a0001c0006t0007g0080 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-99+1160G>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 1/4 | chr16 | 21159906 | |||||||
| chr16:21160079 | G | A | 3 | a0001c0001t0001g0016 a0001c0001t0001g0081 a0001c0001t0001g0082 |
5 | HG00597.hp1 NA18964.hp2 NA19009.hp2 others(2): Show |
intron_variant | MODIFIER | c.-98-1006G>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 1/4 | chr16 | 21160079 | |||||||
| chr16:21160135 | A | G | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(98): Show |
196 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.-98-950A>G | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 1/4 | chr16 | 21160135 | |||||||
| chr16:21160185 | C | CAGG | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(120): Show |
230 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.-98-899_-98-897dup others(3): Show |
LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21160185 | ||||||
| chr16:21160212 | A | C | 1 | a0001c0001t0001g0183 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-98-873A>C | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 1/4 | chr16 | 21160212 | |||||||
| chr16:21160260 | A | AT | 31 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0036 others(28): Show |
61 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.-98-815dupT | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21160260 | ||||||
| chr16:21160498 | G | T | 1 | a0001c0001t0001g0054 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-98-587G>T | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 1/4 | chr16 | 21160498 | |||||||
| chr16:21160552 | A | C | 42 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0013 others(39): Show |
77 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.-98-533A>C | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 1/4 | chr16 | 21160552 | |||||||
| chr16:21160578 | AG | A | 3 | a0001c0001t0001g0041 a0001c0007t0001g0041 a0001c0007t0001g0119 |
3 | HG02280.hp1 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-98-505delG | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21160578 | ||||||
| chr16:21160651 | A | C | 1 | a0002c0002t0002g0075 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-98-434A>C | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 1/4 | chr16 | 21160651 | |||||||
| chr16:21160799 | G | A | 1 | a0001c0001t0001g0120 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-98-286G>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 1/4 | chr16 | 21160799 | |||||||
| chr16:21160853 | G | T | 1 | a0001c0001t0001g0192 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-98-232G>T | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 1/4 | chr16 | 21160853 | |||||||
| chr16:21160942 | G | A | 23 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0036 others(20): Show |
50 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.-98-143G>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 1/4 | chr16 | 21160942 | |||||||
| chr16:21161361 | G | A | 1 | a0005c0009t0010g0193 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.96+83G>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21161361 | |||||||
| chr16:21161408 | C | T | 1 | a0001c0001t0001g0054 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.96+130C>T | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21161408 | |||||||
| chr16:21161796 | G | A | 23 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0036 others(20): Show |
50 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.96+518G>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21161796 | |||||||
| chr16:21161816 | T | C | 114 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(111): Show |
217 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.96+538T>C | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21161816 | |||||||
| chr16:21162237 | A | G | 1 | a0001c0001t0001g0181 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.96+959A>G | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21162237 | |||||||
| chr16:21162250 | A | G | 41 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0013 others(38): Show |
76 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.96+972A>G | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21162250 | |||||||
| chr16:21162251 | A | G | 1 | a0001c0001t0003g0102 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.96+973A>G | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21162251 | |||||||
| chr16:21162306 | C | T | 1 | a0004c0003t0001g0195 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.96+1028C>T | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21162306 | |||||||
| chr16:21162328 | A | T | 1 | a0001c0001t0001g0049 | 2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.96+1050A>T | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21162328 | |||||||
| chr16:21162354 | T | A | 1 | a0001c0001t0003g0102 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.96+1076T>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21162354 | |||||||
| chr16:21162402 | GT | G | 173 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(170): Show |
341 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(338): Show |
intron_variant | MODIFIER | c.96+1126delT | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21162402 | ||||||
| chr16:21162528 | T | C | 2 | a0001c0001t0001g0031 a0001c0001t0001g0087 |
3 | HG02647.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.96+1250T>C | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21162528 | |||||||
| chr16:21162619 | C | T | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(98): Show |
196 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.96+1341C>T | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21162619 | |||||||
| chr16:21162716 | A | G | 1 | a0001c0001t0001g0180 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.96+1438A>G | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21162716 | |||||||
| chr16:21162845 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.96+1567C>T | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21162845 | |||||||
| chr16:21162866 | A | G | 3 | a0001c0001t0001g0030 a0001c0001t0001g0078 a0001c0001t0001g0079 |
4 | HG01884.hp1 HG02145.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.96+1588A>G | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21162866 | |||||||
| chr16:21162894 | G | A | 3 | a0001c0001t0001g0030 a0001c0001t0001g0078 a0001c0001t0001g0079 |
4 | HG01884.hp1 HG02145.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.96+1616G>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21162894 | |||||||
| chr16:21163026 | T | A | 19 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0014 others(16): Show |
50 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.96+1748T>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21163026 | |||||||
| chr16:21163041 | G | A | 2 | a0001c0001t0001g0121 a0001c0001t0001g0122 |
2 | HG02698.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.96+1763G>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21163041 | |||||||
| chr16:21163154 | A | C | 1 | a0001c0001t0001g0077 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.96+1876A>C | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21163154 | |||||||
| chr16:21163344 | A | G | 1 | a0001c0001t0001g0190 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.96+2066A>G | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21163344 | |||||||
| chr16:21163386 | C | T | 1 | a0001c0001t0001g0179 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.96+2108C>T | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21163386 | |||||||
| chr16:21163412 | G | A | 1 | a0001c0001t0001g0014 | 4 | NA18964.hp1 NA19062.hp2 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+2134G>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21163412 | |||||||
| chr16:21163481 | C | G | 1 | a0001c0001t0001g0086 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.96+2203C>G | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21163481 | |||||||
| chr16:21163518 | G | A | 2 | a0001c0001t0001g0083 a0001c0001t0001g0123 |
2 | HG00408.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.96+2240G>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21163518 | |||||||
| chr16:21163559 | C | T | 2 | a0001c0001t0001g0076 a0001c0001t0001g0077 |
2 | HG02738.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.96+2281C>T | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21163559 | |||||||
| chr16:21163616 | G | C | 1 | a0001c0001t0001g0053 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.96+2338G>C | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21163616 | |||||||
| chr16:21163854 | T | TTTTG | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(143): Show |
280 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.96+2588_96+2591dup others(4): Show |
LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21163854 | ||||||
| chr16:21163859 | T | TTTGG | 2 | a0001c0001t0001g0020 a0001c0001t0001g0124 |
4 | NA18947.hp1 NA18954.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.96+2584_96+2585ins others(4): Show |
LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21163859 | ||||||
| chr16:21163900 | C | T | 23 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0036 others(20): Show |
50 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.96+2622C>T | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21163900 | |||||||
| chr16:21163941 | A | G | 2 | a0002c0002t0002g0073 a0002c0002t0002g0074 |
2 | HG00280.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.96+2663A>G | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21163941 | |||||||
| chr16:21163953 | C | A | 31 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0036 others(28): Show |
61 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.96+2675C>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21163953 | |||||||
| chr16:21163982 | G | A | 1 | a0001c0001t0001g0103 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.96+2704G>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21163982 | |||||||
| chr16:21164035 | T | C | 173 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(170): Show |
341 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(338): Show |
intron_variant | MODIFIER | c.96+2757T>C | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21164035 | |||||||
| chr16:21164273 | T | C | 2 | a0001c0001t0001g0042 a0001c0001t0001g0043 |
4 | HG00280.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.96+2995T>C | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21164273 | |||||||
| chr16:21164723 | T | C | 3 | a0001c0001t0001g0030 a0001c0001t0001g0078 a0001c0001t0001g0079 |
4 | HG01884.hp1 HG02145.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.96+3445T>C | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21164723 | |||||||
| chr16:21164858 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.96+3580G>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21164858 | |||||||
| chr16:21164858 | G | T | 1 | a0001c0001t0001g0177 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.96+3580G>T | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21164858 | |||||||
| chr16:21164911 | G | A | 1 | a0001c0001t0001g0125 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.96+3633G>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21164911 | |||||||
| chr16:21165104 | G | GAATCTTG others(16): Show |
1 | a0001c0001t0003g0102 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.96+3833_96+3834ins others(23): Show |
LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21165104 | ||||||
| chr16:21165163 | G | A | 2 | a0001c0001t0001g0116 a0001c0001t0001g0117 |
2 | HG02055.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.96+3885G>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21165163 | |||||||
| chr16:21165184 | G | A | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(104): Show |
208 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.96+3906G>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21165184 | |||||||
| chr16:21165219 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.96+3941G>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21165219 | |||||||
| chr16:21165501 | A | T | 173 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(170): Show |
341 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(338): Show |
intron_variant | MODIFIER | c.96+4223A>T | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21165501 | |||||||
| chr16:21165595 | C | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(104): Show |
208 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.96+4317C>T | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21165595 | |||||||
| chr16:21165646 | C | T | 3 | a0001c0001t0001g0030 a0001c0001t0001g0078 a0001c0001t0001g0079 |
4 | HG01884.hp1 HG02145.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.96+4368C>T | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21165646 | |||||||
| chr16:21165743 | T | C | 3 | a0001c0001t0001g0030 a0001c0001t0001g0078 a0001c0001t0001g0079 |
4 | HG01884.hp1 HG02145.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.96+4465T>C | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21165743 | |||||||
| chr16:21165840 | GAAAC | G | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(104): Show |
208 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.96+4566_96+4569del others(4): Show |
LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21165840 | ||||||
| chr16:21165921 | G | A | 1 | a0004c0003t0001g0039 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.97-4516G>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21165921 | |||||||
| chr16:21165951 | C | G | 1 | a0001c0001t0001g0176 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.97-4486C>G | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21165951 | |||||||
| chr16:21165953 | G | A | 1 | a0001c0001t0001g0127 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.97-4484G>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21165953 | |||||||
| chr16:21165972 | G | A | 19 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0014 others(16): Show |
50 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.97-4465G>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21165972 | |||||||
| chr16:21166000 | C | A | 1 | a0001c0001t0001g0044 | 2 | NA18944.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.97-4437C>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21166000 | |||||||
| chr16:21166182 | T | C | 2 | a0001c0001t0005g0050 a0001c0001t0005g0184 |
3 | HG02615.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.97-4255T>C | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21166182 | |||||||
| chr16:21166589 | C | T | 3 | a0001c0001t0001g0175 a0004c0003t0001g0194 a0004c0003t0001g0195 |
3 | HG03209.hp1 HG03453.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.97-3848C>T | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21166589 | |||||||
| chr16:21166755 | A | T | 1 | a0001c0001t0001g0175 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.97-3682A>T | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21166755 | |||||||
| chr16:21166972 | T | A | 5 | a0001c0001t0001g0030 a0001c0001t0001g0040 a0001c0001t0001g0078 others(2): Show |
7 | HG01884.hp1 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.97-3465T>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21166972 | |||||||
| chr16:21167006 | G | C | 1 | a0001c0001t0001g0026 | 2 | HG00733.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.97-3431G>C | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21167006 | |||||||
| chr16:21167045 | G | A | 1 | a0005c0009t0010g0193 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.97-3392G>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21167045 | |||||||
| chr16:21167317 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.97-3120C>T | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21167317 | |||||||
| chr16:21167416 | A | G | 1 | a0002c0002t0002g0072 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.97-3021A>G | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21167416 | |||||||
| chr16:21167538 | C | G | 2 | a0001c0001t0001g0024 a0001c0001t0001g0174 |
4 | HG02165.hp2 NA18965.hp1 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.97-2899C>G | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21167538 | |||||||
| chr16:21167696 | G | GTTTTTCT others(6): Show |
1 | a0001c0001t0001g0092 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.97-2736_97-2735ins others(13): Show |
LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21167696 | ||||||
| chr16:21167696 | G | GTTTTTTT others(2): Show |
8 | a0001c0001t0001g0013 a0001c0001t0001g0053 a0001c0001t0001g0104 others(5): Show |
12 | HG01081.hp1 HG01109.hp1 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.97-2736_97-2728dup others(9): Show |
LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21167696 | ||||||
| chr16:21167696 | G | GTTTTTTT others(3): Show |
23 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0030 others(20): Show |
51 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.97-2737_97-2728dup others(10): Show |
LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21167696 | ||||||
| chr16:21167696 | G | GTTTTTTT others(4): Show |
6 | a0001c0001t0001g0038 a0001c0001t0001g0077 a0001c0001t0001g0079 others(3): Show |
8 | HG02257.hp2 HG02738.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.97-2738_97-2728dup others(11): Show |
LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21167696 | ||||||
| chr16:21167696 | G | GTTTTTTT others(5): Show |
5 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0093 others(2): Show |
7 | HG00558.hp2 HG01070.hp1 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.97-2739_97-2728dup others(12): Show |
LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21167696 | ||||||
| chr16:21167696 | G | GTTTTTTT others(8): Show |
5 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0190 others(2): Show |
5 | HG00438.hp1 HG02080.hp1 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.97-2729_97-2728ins others(15): Show |
LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21167696 | ||||||
| chr16:21167696 | G | GTTTTTTT others(6): Show |
25 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0014 others(22): Show |
64 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.97-2740_97-2728dup others(13): Show |
LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21167696 | ||||||
| chr16:21167696 | G | GTTTTTTT others(7): Show |
21 | a0001c0001t0001g0019 a0001c0001t0001g0031 a0001c0001t0001g0032 others(18): Show |
27 | HG00438.hp2 HG00673.hp1 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.97-2728_97-2727ins others(14): Show |
LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21167696 | ||||||
| chr16:21167696 | G | GTTTTTTT others(8): Show |
59 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(56): Show |
143 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.97-2728_97-2727ins others(15): Show |
LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21167696 | ||||||
| chr16:21167696 | G | GTTTTTTT others(9): Show |
35 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0016 others(32): Show |
53 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.97-2728_97-2727ins others(16): Show |
LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21167696 | ||||||
| chr16:21167696 | G | GTTTTTTT others(10): Show |
5 | a0001c0001t0001g0023 a0001c0001t0001g0170 a0001c0001t0001g0171 others(2): Show |
7 | HG00408.hp1 HG03942.hp1 HG04115.hp2 others(4): Show |
intron_variant | MODIFIER | c.97-2728_97-2727ins others(17): Show |
LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21167696 | ||||||
| chr16:21167699 | T | TTTTTTTT others(5): Show |
2 | a0004c0003t0001g0194 a0004c0003t0001g0195 |
2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.97-2731_97-2730ins others(12): Show |
LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21167699 | ||||||
| chr16:21167728 | G | T | 1 | a0001c0001t0001g0186 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.97-2709G>T | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21167728 | |||||||
| chr16:21167733 | G | A | 1 | a0004c0003t0001g0039 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.97-2704G>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21167733 | |||||||
| chr16:21167899 | G | A | 1 | a0004c0003t0001g0195 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.97-2538G>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21167899 | |||||||
| chr16:21167912 | G | A | 1 | a0001c0001t0003g0153 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.97-2525G>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21167912 | |||||||
| chr16:21167984 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.97-2453C>T | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21167984 | |||||||
| chr16:21168157 | A | G | 40 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0013 others(37): Show |
74 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.97-2280A>G | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21168157 | |||||||
| chr16:21168345 | A | C | 1 | a0002c0002t0002g0065 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.97-2092A>C | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21168345 | |||||||
| chr16:21168414 | T | C | 2 | a0001c0001t0001g0133 a0001c0001t0001g0154 |
2 | NA18990.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.97-2023T>C | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21168414 | |||||||
| chr16:21168475 | TTAATAAT others(8): Show |
T | 1 | a0004c0003t0001g0039 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.97-1942_97-1928del others(15): Show |
LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21168475 | ||||||
| chr16:21168522 | AAAT | A | 4 | a0001c0001t0001g0013 a0001c0001t0001g0053 a0001c0001t0001g0054 others(1): Show |
7 | HG01109.hp1 HG01256.hp2 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.97-1910_97-1908del others(3): Show |
LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21168522 | ||||||
| chr16:21168536 | T | A | 1 | a0001c0001t0001g0092 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.97-1901T>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21168536 | |||||||
| chr16:21168547 | ATAT | A | 3 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0155 |
3 | HG02040.hp2 HG02055.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.97-1886_97-1884del others(3): Show |
LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21168547 | ||||||
| chr16:21168627 | T | C | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.97-1810T>C | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21168627 | |||||||
| chr16:21168698 | TTTATATA others(3): Show |
T | 7 | a0001c0001t0001g0030 a0001c0001t0001g0040 a0001c0001t0001g0078 others(4): Show |
9 | HG01884.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.97-1729_97-1720del others(10): Show |
LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21168698 | ||||||
| chr16:21168699 | TTA | T | 5 | a0001c0001t0001g0004 a0001c0001t0001g0129 a0001c0001t0001g0137 others(2): Show |
10 | HG01099.hp2 HG02109.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.97-1731_97-1730del others(2): Show |
LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21168699 | ||||||
| chr16:21168707 | AATT | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0084 |
5 | HG02109.hp1 HG02280.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.97-1727_97-1725del others(3): Show |
LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21168707 | ||||||
| chr16:21168709 | TTA | T | 4 | a0001c0001t0001g0133 a0001c0001t0001g0151 a0001c0001t0001g0152 others(1): Show |
4 | NA18939.hp2 NA18990.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.97-1718_97-1717del others(2): Show |
LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21168709 | ||||||
| chr16:21168779 | T | G | 1 | a0005c0009t0010g0193 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.97-1658T>G | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21168779 | |||||||
| chr16:21168826 | T | C | 21 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0014 others(18): Show |
51 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.97-1611T>C | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21168826 | |||||||
| chr16:21168839 | A | G | 1 | a0001c0001t0001g0064 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.97-1598A>G | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21168839 | |||||||
| chr16:21168912 | T | TTATTTAT others(15): Show |
1 | a0001c0001t0001g0169 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.97-1510_97-1489dup others(22): Show |
LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21168912 | ||||||
| chr16:21168920 | A | G | 8 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0087 others(5): Show |
11 | HG01884.hp2 HG02615.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.97-1517A>G | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21168920 | |||||||
| chr16:21168930 | T | G | 1 | a0005c0009t0010g0193 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.97-1507T>G | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21168930 | |||||||
| chr16:21168958 | ATATAATA others(8): Show |
A | 8 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0087 others(5): Show |
11 | HG01884.hp2 HG02615.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.97-1474_97-1460del others(15): Show |
LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21168958 | ||||||
| chr16:21168963 | ATATAT | A | 43 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(40): Show |
80 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.97-1463_97-1459del others(5): Show |
LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21168963 | ||||||
| chr16:21168990 | CAT | C | 43 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0016 others(40): Show |
78 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.97-1441_97-1440del others(2): Show |
LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21168990 | ||||||
| chr16:21169186 | C | T | 1 | a0001c0001t0001g0043 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.97-1251C>T | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21169186 | |||||||
| chr16:21169313 | T | C | 2 | a0001c0001t0001g0121 a0001c0001t0001g0122 |
2 | HG02698.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.97-1124T>C | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21169313 | |||||||
| chr16:21169485 | T | G | 2 | a0004c0003t0001g0194 a0004c0003t0001g0195 |
2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.97-952T>G | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21169485 | |||||||
| chr16:21169561 | G | A | 1 | a0001c0001t0001g0054 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.97-876G>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21169561 | |||||||
| chr16:21169596 | A | C | 1 | a0001c0001t0001g0162 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.97-841A>C | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21169596 | |||||||
| chr16:21169598 | C | A | 1 | a0001c0001t0001g0162 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.97-839C>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21169598 | |||||||
| chr16:21169599 | A | G | 1 | a0001c0001t0001g0162 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.97-838A>G | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21169599 | |||||||
| chr16:21169600 | C | G | 1 | a0001c0001t0001g0162 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.97-837C>G | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21169600 | |||||||
| chr16:21169602 | C | T | 1 | a0001c0001t0001g0162 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.97-835C>T | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21169602 | |||||||
| chr16:21169603 | C | T | 1 | a0001c0001t0001g0162 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.97-834C>T | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21169603 | |||||||
| chr16:21169604 | C | G | 1 | a0001c0001t0001g0162 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.97-833C>G | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21169604 | |||||||
| chr16:21169606 | G | A | 1 | a0001c0001t0001g0162 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.97-831G>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21169606 | |||||||
| chr16:21169607 | C | T | 1 | a0001c0001t0001g0162 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.97-830C>T | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21169607 | |||||||
| chr16:21169614 | C | T | 12 | a0001c0001t0001g0069 a0002c0002t0002g0006 a0002c0002t0002g0028 others(9): Show |
22 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(19): Show |
intron_variant | MODIFIER | c.97-823C>T | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21169614 | |||||||
| chr16:21169734 | T | C | 5 | a0001c0001t0001g0013 a0001c0001t0001g0053 a0001c0001t0001g0054 others(2): Show |
8 | HG01109.hp1 HG01256.hp2 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.97-703T>C | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21169734 | |||||||
| chr16:21169739 | C | T | 2 | a0001c0001t0001g0161 a0001c0001t0003g0153 |
2 | HG02523.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.97-698C>T | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21169739 | |||||||
| chr16:21169831 | G | T | 1 | a0001c0001t0001g0101 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.97-606G>T | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21169831 | |||||||
| chr16:21169915 | C | CT | 114 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(111): Show |
218 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.97-507dupT | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21169915 | ||||||
| chr16:21170091 | C | A | 1 | a0005c0009t0010g0193 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.97-346C>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21170091 | |||||||
| chr16:21170097 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.97-340G>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21170097 | |||||||
| chr16:21170138 | G | T | 1 | a0001c0001t0001g0090 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.97-299G>T | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21170138 | |||||||
| chr16:21170228 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.97-209C>T | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21170228 | |||||||
| chr16:21170304 | G | A | 2 | a0001c0001t0001g0116 a0001c0001t0001g0117 |
2 | HG02055.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.97-133G>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21170304 | |||||||
| chr16:21170340 | C | T | 2 | a0001c0001t0001g0013 a0001c0001t0001g0053 |
5 | HG01109.hp1 HG01256.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.97-97C>T | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21170340 | |||||||
| chr16:21170400 | T | C | 1 | a0005c0009t0010g0193 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.97-37T>C | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 2/4 | chr16 | 21170400 | |||||||
| chr16:21170790 | G | T | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.265+185G>T | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 3/4 | chr16 | 21170790 | |||||||
| chr16:21171286 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.265+681A>G | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 3/4 | chr16 | 21171286 | |||||||
| chr16:21171714 | T | C | 1 | a0001c0001t0001g0044 | 2 | NA18944.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.265+1109T>C | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 3/4 | chr16 | 21171714 | |||||||
| chr16:21171768 | T | G | 1 | a0001c0001t0001g0092 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.265+1163T>G | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 3/4 | chr16 | 21171768 | |||||||
| chr16:21171769 | A | T | 1 | a0001c0001t0001g0092 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.265+1164A>T | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 3/4 | chr16 | 21171769 | |||||||
| chr16:21171770 | C | G | 1 | a0001c0001t0001g0092 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.265+1165C>G | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 3/4 | chr16 | 21171770 | |||||||
| chr16:21171865 | G | A | 41 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0016 others(38): Show |
75 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.265+1260G>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 3/4 | chr16 | 21171865 | |||||||
| chr16:21171989 | C | T | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(98): Show |
197 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.265+1384C>T | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 3/4 | chr16 | 21171989 | |||||||
| chr16:21172008 | G | A | 1 | a0001c0006t0007g0080 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.265+1403G>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 3/4 | chr16 | 21172008 | |||||||
| chr16:21172148 | T | TA | 7 | a0001c0001t0001g0018 a0001c0001t0001g0070 a0001c0001t0001g0092 others(4): Show |
9 | HG00408.hp2 HG01934.hp2 HG04115.hp2 others(6): Show |
intron_variant | MODIFIER | c.265+1558dupA | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 21172148 | ||||||
| chr16:21172148 | TA | T | 14 | a0001c0001t0001g0037 a0001c0001t0001g0048 a0001c0001t0001g0094 others(11): Show |
15 | HG00099.hp1 HG01169.hp1 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.265+1558delA | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 21172148 | ||||||
| chr16:21172166 | G | T | 1 | a0001c0001t0001g0162 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.265+1561G>T | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 3/4 | chr16 | 21172166 | |||||||
| chr16:21172202 | C | T | 2 | a0001c0001t0001g0116 a0001c0001t0001g0117 |
2 | HG02055.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.265+1597C>T | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 3/4 | chr16 | 21172202 | |||||||
| chr16:21172231 | A | G | 1 | a0001c0001t0001g0162 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.265+1626A>G | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 3/4 | chr16 | 21172231 | |||||||
| chr16:21172232 | G | A | 1 | a0001c0001t0001g0162 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.265+1627G>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 3/4 | chr16 | 21172232 | |||||||
| chr16:21172242 | T | C | 2 | a0001c0001t0001g0045 a0001c0001t0001g0141 |
3 | HG02809.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.265+1637T>C | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 3/4 | chr16 | 21172242 | |||||||
| chr16:21172304 | G | A | 1 | a0001c0001t0001g0164 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.265+1699G>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 3/4 | chr16 | 21172304 | |||||||
| chr16:21172308 | A | G | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.266-1702A>G | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 3/4 | chr16 | 21172308 | |||||||
| chr16:21172489 | A | C | 1 | a0001c0001t0001g0124 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.266-1521A>C | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 3/4 | chr16 | 21172489 | |||||||
| chr16:21172592 | A | C | 2 | a0001c0001t0001g0013 a0001c0001t0001g0053 |
5 | HG01109.hp1 HG01256.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.266-1418A>C | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 3/4 | chr16 | 21172592 | |||||||
| chr16:21172718 | C | A | 37 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0013 others(34): Show |
70 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.266-1292C>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 3/4 | chr16 | 21172718 | |||||||
| chr16:21172834 | G | C | 1 | a0001c0001t0001g0086 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.266-1176G>C | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 3/4 | chr16 | 21172834 | |||||||
| chr16:21172861 | T | C | 1 | a0001c0001t0001g0095 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.266-1149T>C | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 3/4 | chr16 | 21172861 | |||||||
| chr16:21172866 | G | T | 1 | a0001c0001t0001g0060 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.266-1144G>T | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 3/4 | chr16 | 21172866 | |||||||
| chr16:21172956 | A | G | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(129): Show |
266 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.266-1054A>G | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 3/4 | chr16 | 21172956 | |||||||
| chr16:21173058 | G | A | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(104): Show |
205 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.266-952G>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 3/4 | chr16 | 21173058 | |||||||
| chr16:21173384 | G | A | 2 | a0004c0003t0001g0194 a0004c0003t0001g0195 |
2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.266-626G>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 3/4 | chr16 | 21173384 | |||||||
| chr16:21173484 | C | G | 1 | a0001c0001t0001g0191 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.266-526C>G | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 3/4 | chr16 | 21173484 | |||||||
| chr16:21173556 | A | C | 27 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0036 others(24): Show |
55 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.266-454A>C | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 3/4 | chr16 | 21173556 | |||||||
| chr16:21173703 | A | ACT | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(171): Show |
342 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(339): Show |
intron_variant | MODIFIER | c.266-306_266-305dup others(2): Show |
LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 21173703 | ||||||
| chr16:21173823 | A | G | 1 | a0001c0001t0001g0069 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.266-187A>G | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 3/4 | chr16 | 21173823 | |||||||
| chr16:21173981 | C | T | 1 | a0005c0009t0010g0193 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.266-29C>T | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 3/4 | chr16 | 21173981 | |||||||
| chr16:21174349 | C | A | 2 | a0001c0001t0001g0045 a0001c0001t0001g0141 |
3 | HG02809.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.404+201C>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | chr16 | 21174349 | |||||||
| chr16:21174350 | C | A | 2 | a0001c0001t0001g0045 a0001c0001t0001g0141 |
3 | HG02809.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.404+202C>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | chr16 | 21174350 | |||||||
| chr16:21174372 | TTTTTTG | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0081 |
4 | HG00597.hp1 NA19009.hp2 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.404+226_404+231del others(6): Show |
LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 21174372 | ||||||
| chr16:21174380 | A | G | 2 | a0001c0001t0001g0016 a0001c0001t0001g0081 |
4 | HG00597.hp1 NA19009.hp2 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.404+232A>G | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | chr16 | 21174380 | |||||||
| chr16:21174477 | A | T | 39 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0020 others(36): Show |
74 | HG00408.hp2 HG00621.hp2 HG00733.hp1 others(71): Show |
intron_variant | MODIFIER | c.404+329A>T | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | chr16 | 21174477 | |||||||
| chr16:21174494 | G | A | 1 | a0004c0003t0001g0039 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.404+346G>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | chr16 | 21174494 | |||||||
| chr16:21174686 | T | C | 1 | a0001c0001t0001g0055 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.404+538T>C | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | chr16 | 21174686 | |||||||
| chr16:21174690 | A | C | 1 | a0001c0001t0001g0166 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.404+542A>C | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | chr16 | 21174690 | |||||||
| chr16:21174858 | G | A | 2 | a0001c0001t0001g0088 a0001c0001t0001g0147 |
2 | HG02132.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.404+710G>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | chr16 | 21174858 | |||||||
| chr16:21174890 | C | T | 2 | a0001c0001t0004g0047 a0001c0001t0004g0132 |
3 | NA18939.hp1 NA18946.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.404+742C>T | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | chr16 | 21174890 | |||||||
| chr16:21175022 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.404+874C>T | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | chr16 | 21175022 | |||||||
| chr16:21175353 | G | A | 4 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0005g0050 others(1): Show |
5 | HG02055.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.404+1205G>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | chr16 | 21175353 | |||||||
| chr16:21175406 | CAA | C | 5 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0055 others(2): Show |
8 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(5): Show |
intron_variant | MODIFIER | c.404+1259_404+1260d others(4): Show |
LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | chr16 | 21175406 | |||||||
| chr16:21175573 | C | T | 7 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0017 others(4): Show |
16 | HG01109.hp1 HG01256.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.404+1425C>T | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | chr16 | 21175573 | |||||||
| chr16:21175790 | A | G | 1 | a0001c0001t0001g0173 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.404+1642A>G | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | chr16 | 21175790 | |||||||
| chr16:21175958 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.404+1810C>T | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | chr16 | 21175958 | |||||||
| chr16:21175989 | C | A | 4 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0005g0050 others(1): Show |
5 | HG02055.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.404+1841C>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | chr16 | 21175989 | |||||||
| chr16:21175994 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.404+1846G>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | chr16 | 21175994 | |||||||
| chr16:21176136 | G | A | 4 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0005g0050 others(1): Show |
5 | HG02055.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.404+1988G>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | chr16 | 21176136 | |||||||
| chr16:21176276 | A | G | 17 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0018 others(14): Show |
44 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.404+2128A>G | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | chr16 | 21176276 | |||||||
| chr16:21176365 | T | C | 1 | a0001c0001t0001g0054 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.404+2217T>C | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | chr16 | 21176365 | |||||||
| chr16:21176437 | G | C | 1 | a0001c0001t0001g0096 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.404+2289G>C | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | chr16 | 21176437 | |||||||
| chr16:21176452 | A | G | 1 | a0001c0001t0003g0110 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.404+2304A>G | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | chr16 | 21176452 | |||||||
| chr16:21176513 | C | T | 2 | a0001c0001t0001g0098 a0001c0001t0001g0100 |
2 | NA18949.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.404+2365C>T | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | chr16 | 21176513 | |||||||
| chr16:21176898 | T | TG | 3 | a0001c0001t0001g0139 a0001c0001t0001g0145 a0001c0001t0001g0187 |
3 | HG02074.hp1 NA18975.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.405-2575dupG | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 21176898 | ||||||
| chr16:21176900 | G | GA | 14 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0031 others(11): Show |
23 | HG01081.hp1 HG01109.hp1 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.405-2560dupA | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 21176900 | ||||||
| chr16:21176900 | GA | G | 21 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0018 others(18): Show |
49 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(46): Show |
intron_variant | MODIFIER | c.405-2560delA | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 21176900 | ||||||
| chr16:21176901 | A | G | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(97): Show |
200 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.405-2574A>G | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | chr16 | 21176901 | |||||||
| chr16:21176902 | A | G | 2 | a0001c0001t0001g0146 a0001c0007t0001g0119 |
2 | HG02630.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.405-2573A>G | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | chr16 | 21176902 | |||||||
| chr16:21177170 | C | T | 4 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0005g0050 others(1): Show |
5 | HG02055.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.405-2305C>T | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | chr16 | 21177170 | |||||||
| chr16:21177178 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.405-2297C>T | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | chr16 | 21177178 | |||||||
| chr16:21177185 | G | A | 4 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0005g0050 others(1): Show |
5 | HG02055.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.405-2290G>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | chr16 | 21177185 | |||||||
| chr16:21177291 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.405-2184C>T | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | chr16 | 21177291 | |||||||
| chr16:21177311 | T | G | 4 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0005g0050 others(1): Show |
5 | HG02055.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.405-2164T>G | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | chr16 | 21177311 | |||||||
| chr16:21177328 | G | A | 187 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(184): Show |
364 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(361): Show |
intron_variant | MODIFIER | c.405-2147G>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | chr16 | 21177328 | |||||||
| chr16:21177331 | A | AGTGATAG others(307): Show |
2 | a0001c0001t0005g0050 a0001c0001t0005g0184 |
3 | HG02615.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.405-2131_405-2130i others(316): Show |
LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 21177331 | ||||||
| chr16:21177331 | A | AGTGATAG others(308): Show |
2 | a0001c0001t0001g0116 a0001c0001t0001g0117 |
2 | HG02055.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.405-2131_405-2130i others(317): Show |
LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 21177331 | ||||||
| chr16:21177429 | A | G | 1 | a0002c0002t0002g0062 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.405-2046A>G | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | chr16 | 21177429 | |||||||
| chr16:21177546 | G | A | 43 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(40): Show |
97 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.405-1929G>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | chr16 | 21177546 | |||||||
| chr16:21177566 | G | A | 1 | a0001c0006t0007g0080 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.405-1909G>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | chr16 | 21177566 | |||||||
| chr16:21177619 | C | CT | 60 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(57): Show |
120 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.405-1836dupT | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 21177619 | ||||||
| chr16:21177619 | C | CTT | 14 | a0001c0001t0001g0011 a0001c0001t0001g0030 a0001c0001t0001g0035 others(11): Show |
22 | HG00423.hp2 HG00673.hp1 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.405-1837_405-1836d others(4): Show |
LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 21177619 | ||||||
| chr16:21177671 | T | TGCA | 43 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(40): Show |
97 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.405-1802_405-1800d others(5): Show |
LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 21177671 | ||||||
| chr16:21177742 | C | T | 1 | a0001c0006t0007g0080 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.405-1733C>T | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | chr16 | 21177742 | |||||||
| chr16:21177824 | G | C | 17 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0018 others(14): Show |
44 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.405-1651G>C | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | chr16 | 21177824 | |||||||
| chr16:21177854 | G | C | 1 | a0001c0001t0001g0167 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.405-1621G>C | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | chr16 | 21177854 | |||||||
| chr16:21178002 | A | G | 17 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0018 others(14): Show |
44 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.405-1473A>G | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | chr16 | 21178002 | |||||||
| chr16:21178170 | G | A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0103 a0001c0001t0001g0114 others(1): Show |
11 | HG00558.hp1 HG00597.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.405-1305G>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | chr16 | 21178170 | |||||||
| chr16:21178243 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.405-1232C>T | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | chr16 | 21178243 | |||||||
| chr16:21178378 | G | C | 2 | a0001c0001t0001g0088 a0001c0001t0001g0091 |
2 | HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.405-1097G>C | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | chr16 | 21178378 | |||||||
| chr16:21178439 | A | G | 2 | a0001c0001t0001g0147 a0001c0001t0001g0148 |
2 | HG02132.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.405-1036A>G | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | chr16 | 21178439 | |||||||
| chr16:21178629 | A | G | 187 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(184): Show |
364 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(361): Show |
intron_variant | MODIFIER | c.405-846A>G | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | chr16 | 21178629 | |||||||
| chr16:21178642 | C | A | 2 | a0001c0001t0001g0076 a0001c0001t0001g0077 |
2 | HG02738.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.405-833C>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | chr16 | 21178642 | |||||||
| chr16:21178771 | G | A | 27 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0026 others(24): Show |
39 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.405-704G>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | chr16 | 21178771 | |||||||
| chr16:21178792 | T | A | 2 | a0001c0001t0005g0050 a0001c0001t0005g0184 |
3 | HG02615.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.405-683T>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | chr16 | 21178792 | |||||||
| chr16:21178816 | T | G | 1 | a0001c0001t0001g0143 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.405-659T>G | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | chr16 | 21178816 | |||||||
| chr16:21178948 | C | T | 2 | a0001c0001t0005g0050 a0001c0001t0005g0184 |
3 | HG02615.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.405-527C>T | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | chr16 | 21178948 | |||||||
| chr16:21178992 | A | G | 1 | a0001c0006t0007g0080 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.405-483A>G | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | chr16 | 21178992 | |||||||
| chr16:21179023 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.405-452G>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | chr16 | 21179023 | |||||||
| chr16:21179048 | A | G | 1 | a0002c0002t0002g0028 | 2 | HG01516.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.405-427A>G | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | chr16 | 21179048 | |||||||
| chr16:21179176 | G | A | 2 | a0001c0001t0005g0050 a0001c0001t0005g0184 |
3 | HG02615.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.405-299G>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | chr16 | 21179176 | |||||||
| chr16:21179334 | A | G | 1 | a0001c0001t0001g0136 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.405-141A>G | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | chr16 | 21179334 | |||||||
| chr16:21179354 | G | A | 2 | a0001c0001t0001g0088 a0001c0001t0001g0091 |
2 | HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.405-121G>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | chr16 | 21179354 | |||||||
| chr16:21179470 | G | A | 2 | a0001c0001t0005g0050 a0001c0001t0005g0184 |
3 | HG02615.hp1 HG02896.hp1 HG02897.hp2 |
splice_region_variant&intron_variant | LOW | c.405-5G>A | LDAF1 | ENSG00000011638.11 | transcript | ENST00000233047.9 | protein_coding | 4/4 | chr16 | 21179470 |