Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 129530 |
| ensemblid | ENSG00000144214.10 |
| hgncid | 27014 |
| symbol | LYG1 |
| name | lysozyme g1 |
| refseq_nuc | NM_174898.3 |
| refseq_prot | NP_777558.1 |
| ensembl_nuc | ENST00000308528.9 |
| ensembl_prot | ENSP00000311320.4 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 99284238 |
| end | 99301197 |
| strand | - |
| ver | v1.2 |
| region | chr2:99284238-99301197 |
| region5000 | chr2:99279238-99306197 |
| regionname0 | LYG1_chr2_99284238_99301197 |
| regionname5000 | LYG1_chr2_99279238_99306197 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 194 | 350 | 82 | 80 | 138 | 10 | 38 | 108 | LYG1_chr2_99279238_99306197 | LYG1 | MSALW others(189): Show |
chr2 | 99279238 | 99306197 |
| a0002 | 0/0 | 194 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | MSALW others(189): Show |
chr2 | 99279238 | 99306197 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 582 | 348 | 82 | 79 | 137 | 10 | 38 | LYG1_chr2_99279238_99306197 | LYG1 | ATGTC others(577): Show |
chr2 | 99279238 | 99306197 | ||
| a0001c0003 | 0/0 | 582 | 1 | 0 | 0 | 1 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | ATGTC others(577): Show |
chr2 | 99279238 | 99306197 | ||
| a0001c0005 | 0/0 | 582 | 1 | 0 | 1 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | ATGTC others(577): Show |
chr2 | 99279238 | 99306197 | ||
| a0002c0002 | 0/0 | 582 | 3 | 3 | 0 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | ATGTC others(577): Show |
chr2 | 99279238 | 99306197 | ||
| a0002c0004 | 0/0 | 582 | 1 | 1 | 0 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | ATGTC others(577): Show |
chr2 | 99279238 | 99306197 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1011 | 347 | 81 | 79 | 137 | 10 | 38 | LYG1_chr2_99279238_99306197 | LYG1 | ATAAT others(1006): Show |
chr2 | 99279238 | 99306197 |
| a0001c0001t0002 | 0/0 | 1011 | 1 | 1 | 0 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | ATAAT others(1006): Show |
chr2 | 99279238 | 99306197 |
| a0001c0003t0001 | 0/0 | 1011 | 1 | 0 | 0 | 1 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | ATAAT others(1006): Show |
chr2 | 99279238 | 99306197 |
| a0001c0005t0001 | 0/0 | 1011 | 1 | 0 | 1 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | ATAAT others(1006): Show |
chr2 | 99279238 | 99306197 |
| a0002c0002t0001 | 0/0 | 1011 | 3 | 3 | 0 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | ATAAT others(1006): Show |
chr2 | 99279238 | 99306197 |
| a0002c0004t0001 | 0/0 | 1011 | 1 | 1 | 0 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | ATAAT others(1006): Show |
chr2 | 99279238 | 99306197 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 47 | 1 | 18 | 23 | 2 | 3 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0002 | 0/0 | 36 | 10 | 4 | 14 | 1 | 7 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0003 | 0/1 | 26 | 6 | 7 | 3 | 3 | 6 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0004 | 0/0 | 13 | 2 | 0 | 5 | 0 | 6 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0005 | 1/0 | 11 | 7 | 1 | 0 | 1 | 1 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0006 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0007 | 0/0 | 10 | 0 | 10 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0008 | 0/0 | 8 | 5 | 3 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0009 | 0/0 | 7 | 0 | 3 | 4 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0010 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0011 | 0/0 | 5 | 4 | 0 | 1 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0012 | 0/0 | 5 | 1 | 0 | 4 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 1 | 1 | 0 | 2 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0034 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0003t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0001c0005t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0002c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0002c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0002c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| a0002c0004t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | FIN | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | CHS | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01346 | hp1 | a0001 | c0005 | t0001 | g0069 | AMR | CLM | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0026 | EUR | IBS | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | ACB | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01891 | hp1 | a0002 | c0002 | t0001 | g0051 | AFR | ACB | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02055 | hp1 | a0002 | c0004 | t0001 | g0054 | AFR | ACB | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | CDX | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | CDX | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0138 | AFR | ESN | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ESN | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ESN | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ESN | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | MSL | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | MSL | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG03516 | hp1 | a0002 | c0002 | t0001 | g0056 | AFR | ESN | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | MSL | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | BEB | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | BEB | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | BEB | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | STU | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | BEB | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | STU | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | STU | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | STU | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | YRI | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | YRI | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHB | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | YRI | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | YRI | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA19007 | hp1 | a0001 | c0003 | t0001 | g0109 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | LWK | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | LWK | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | LWK | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | YRI | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ASW | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ASW | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0048 | EUR | TSI | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0084 | EUR | TSI | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | GIH | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0050 | AFR | ACB | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | MSL | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | USA | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | USA | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0003 | REF | REF | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0005 | REF | REF | LYG1_chr2_99279238_99306197 | LYG1 | chr2 | 99279238 | 99306197 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:99284464 | G | C | 1 | a0002 | 4 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(1): Show |
missense_variant | MODERATE | c.514C>G | p.Gln172Glu | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 7/7 | 785/1011 | 514/585 | 172/194 | chr2 | 99284464 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:99291267 | G | T | 1 | a0001c0003 | 1 | NA19007.hp1 | synonymous_variant | LOW | c.303C>A | p.Val101Val | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 5/7 | 574/1011 | 303/585 | 101/194 | chr2 | 99291267 | |||
| chr2:99291387 | G | A | 1 | a0002c0004 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.183C>T | p.Asp61Asp | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 5/7 | 454/1011 | 183/585 | 61/194 | chr2 | 99291387 | |||
| chr2:99292615 | T | A | 1 | a0001c0005 | 1 | HG01346.hp1 | synonymous_variant | LOW | c.69A>T | p.Gly23Gly | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 4/7 | 340/1011 | 69/585 | 23/194 | chr2 | 99292615 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:99301192 | T | A | 1 | a0001c0001t0002 | 1 | HG02965.hp2 | 5_prime_UTR_variant | MODIFIER | c.-266A>T | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 1/7 | 5522 | chr2 | 99301192 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:99284631 | A | T | 1 | a0001c0001t0001g0081 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.466+57T>A | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 6/6 | chr2 | 99284631 | |||||||
| chr2:99284864 | G | A | 1 | a0001c0001t0001g0018 | 3 | HG00408.hp2 NA18949.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.334-44C>T | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 5/6 | chr2 | 99284864 | |||||||
| chr2:99284952 | G | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0111 |
5 | HG02056.hp2 NA18966.hp2 NA18993.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-132C>T | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 5/6 | chr2 | 99284952 | |||||||
| chr2:99285008 | C | G | 5 | a0001c0001t0001g0025 a0001c0001t0001g0039 a0001c0001t0001g0040 others(2): Show |
6 | HG02451.hp2 HG02630.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.334-188G>C | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 5/6 | chr2 | 99285008 | |||||||
| chr2:99285165 | G | A | 4 | a0002c0002t0001g0050 a0002c0002t0001g0051 a0002c0002t0001g0056 others(1): Show |
4 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.334-345C>T | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 5/6 | chr2 | 99285165 | |||||||
| chr2:99285380 | T | TA | 6 | a0001c0001t0001g0013 a0001c0001t0001g0055 a0001c0001t0001g0067 others(3): Show |
10 | HG00597.hp2 HG00621.hp1 HG00621.hp2 others(7): Show |
intron_variant | MODIFIER | c.334-561dupT | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 5/6 | chr2 | 99285380 | |||||||
| chr2:99285380 | TA | T | 8 | a0001c0001t0001g0063 a0001c0001t0001g0066 a0001c0001t0001g0076 others(5): Show |
8 | HG01070.hp1 HG01884.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.334-561delT | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 5/6 | chr2 | 99285380 | |||||||
| chr2:99285581 | C | T | 1 | a0001c0001t0002g0138 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.334-761G>A | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 5/6 | chr2 | 99285581 | |||||||
| chr2:99285584 | A | G | 1 | a0001c0001t0001g0038 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.334-764T>C | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 5/6 | chr2 | 99285584 | |||||||
| chr2:99285603 | T | C | 122 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(119): Show |
309 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(306): Show |
intron_variant | MODIFIER | c.334-783A>G | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 5/6 | chr2 | 99285603 | |||||||
| chr2:99285951 | C | T | 1 | a0001c0001t0002g0138 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.334-1131G>A | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 5/6 | chr2 | 99285951 | |||||||
| chr2:99286239 | A | C | 1 | a0001c0001t0001g0114 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.334-1419T>G | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 5/6 | chr2 | 99286239 | |||||||
| chr2:99286309 | G | C | 1 | a0001c0001t0001g0028 | 2 | HG02572.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.334-1489C>G | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 5/6 | chr2 | 99286309 | |||||||
| chr2:99286579 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.334-1759G>A | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 5/6 | chr2 | 99286579 | |||||||
| chr2:99286596 | C | T | 1 | a0001c0001t0001g0100 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.334-1776G>A | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 5/6 | chr2 | 99286596 | |||||||
| chr2:99286612 | G | C | 1 | a0001c0001t0001g0041 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.334-1792C>G | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 5/6 | chr2 | 99286612 | |||||||
| chr2:99286757 | T | G | 1 | a0001c0001t0001g0021 | 3 | HG03130.hp1 NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.334-1937A>C | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 5/6 | chr2 | 99286757 | |||||||
| chr2:99286860 | A | G | 1 | a0001c0001t0001g0052 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.334-2040T>C | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 5/6 | chr2 | 99286860 | |||||||
| chr2:99286905 | T | C | 1 | a0001c0001t0001g0037 | 2 | NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.334-2085A>G | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 5/6 | chr2 | 99286905 | |||||||
| chr2:99286912 | A | C | 1 | a0001c0001t0001g0037 | 2 | NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.334-2092T>G | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 5/6 | chr2 | 99286912 | |||||||
| chr2:99286929 | A | C | 1 | a0001c0001t0001g0094 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.334-2109T>G | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 5/6 | chr2 | 99286929 | |||||||
| chr2:99287045 | G | T | 1 | a0001c0001t0002g0138 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.334-2225C>A | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 5/6 | chr2 | 99287045 | |||||||
| chr2:99287204 | A | G | 1 | a0001c0001t0001g0110 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.334-2384T>C | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 5/6 | chr2 | 99287204 | |||||||
| chr2:99287320 | G | C | 1 | a0001c0001t0002g0138 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.334-2500C>G | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 5/6 | chr2 | 99287320 | |||||||
| chr2:99287422 | G | A | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG01074.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.334-2602C>T | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 5/6 | chr2 | 99287422 | |||||||
| chr2:99287490 | G | A | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(117): Show |
307 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(304): Show |
intron_variant | MODIFIER | c.334-2670C>T | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 5/6 | chr2 | 99287490 | |||||||
| chr2:99287584 | T | G | 1 | a0001c0001t0001g0068 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.334-2764A>C | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 5/6 | chr2 | 99287584 | |||||||
| chr2:99287620 | C | T | 1 | a0002c0002t0001g0056 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.334-2800G>A | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 5/6 | chr2 | 99287620 | |||||||
| chr2:99287669 | A | G | 4 | a0001c0001t0001g0020 a0001c0001t0001g0076 a0001c0001t0001g0077 others(1): Show |
6 | HG01070.hp1 HG01071.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.334-2849T>C | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 5/6 | chr2 | 99287669 | |||||||
| chr2:99287705 | G | C | 1 | a0001c0001t0001g0023 | 3 | NA18939.hp2 NA19000.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.334-2885C>G | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 5/6 | chr2 | 99287705 | |||||||
| chr2:99287762 | T | C | 1 | a0001c0001t0001g0028 | 2 | HG02572.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.334-2942A>G | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 5/6 | chr2 | 99287762 | |||||||
| chr2:99287873 | G | T | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(117): Show |
307 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(304): Show |
intron_variant | MODIFIER | c.334-3053C>A | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 5/6 | chr2 | 99287873 | |||||||
| chr2:99287988 | T | A | 2 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.334-3168A>T | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 5/6 | chr2 | 99287988 | |||||||
| chr2:99287989 | A | T | 2 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.334-3169T>A | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 5/6 | chr2 | 99287989 | |||||||
| chr2:99288200 | A | C | 1 | a0001c0001t0001g0112 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.333+3037T>G | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 5/6 | chr2 | 99288200 | |||||||
| chr2:99288354 | A | G | 4 | a0001c0001t0001g0020 a0001c0001t0001g0076 a0001c0001t0001g0077 others(1): Show |
6 | HG01070.hp1 HG01071.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.333+2883T>C | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 5/6 | chr2 | 99288354 | |||||||
| chr2:99288527 | T | C | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(117): Show |
307 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(304): Show |
intron_variant | MODIFIER | c.333+2710A>G | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 5/6 | chr2 | 99288527 | |||||||
| chr2:99288551 | CTCTTG | C | 25 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(22): Show |
76 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.333+2681_333+2685d others(7): Show |
LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 5/6 | chr2 | 99288551 | |||||||
| chr2:99288610 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.333+2627G>A | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 5/6 | chr2 | 99288610 | |||||||
| chr2:99288654 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.333+2583G>A | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 5/6 | chr2 | 99288654 | |||||||
| chr2:99288655 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.333+2582C>T | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 5/6 | chr2 | 99288655 | |||||||
| chr2:99288672 | G | A | 9 | a0001c0001t0001g0004 a0001c0001t0001g0030 a0001c0001t0001g0031 others(6): Show |
23 | HG01168.hp1 HG02135.hp1 HG02451.hp1 others(20): Show |
intron_variant | MODIFIER | c.333+2565C>T | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 5/6 | chr2 | 99288672 | |||||||
| chr2:99288816 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.333+2421G>A | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 5/6 | chr2 | 99288816 | |||||||
| chr2:99288883 | C | T | 1 | a0001c0001t0001g0111 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.333+2354G>A | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 5/6 | chr2 | 99288883 | |||||||
| chr2:99289161 | A | C | 1 | a0001c0001t0001g0065 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.333+2076T>G | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 5/6 | chr2 | 99289161 | |||||||
| chr2:99289302 | A | T | 1 | a0001c0001t0001g0055 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.333+1935T>A | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 5/6 | chr2 | 99289302 | |||||||
| chr2:99289347 | C | T | 2 | a0001c0001t0001g0033 a0001c0001t0001g0035 |
4 | HG01934.hp2 HG01975.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.333+1890G>A | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 5/6 | chr2 | 99289347 | |||||||
| chr2:99289423 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.333+1814A>G | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 5/6 | chr2 | 99289423 | |||||||
| chr2:99289455 | T | TA | 115 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(112): Show |
302 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(299): Show |
intron_variant | MODIFIER | c.333+1781dupT | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 5/6 | chr2 | 99289455 | |||||||
| chr2:99289738 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.333+1499C>T | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 5/6 | chr2 | 99289738 | |||||||
| chr2:99289768 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.333+1469C>T | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 5/6 | chr2 | 99289768 | |||||||
| chr2:99289840 | T | TTTG | 31 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0016 others(28): Show |
91 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.333+1394_333+1396d others(5): Show |
LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 5/6 | chr2 | 99289840 | |||||||
| chr2:99289840 | T | TTTGTTG | 2 | a0001c0001t0001g0019 a0001c0001t0001g0029 |
5 | NA18952.hp2 NA18964.hp2 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.333+1391_333+1396d others(8): Show |
LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 5/6 | chr2 | 99289840 | |||||||
| chr2:99289840 | TTTG | T | 28 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(25): Show |
76 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.333+1394_333+1396d others(5): Show |
LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 5/6 | chr2 | 99289840 | |||||||
| chr2:99289968 | C | T | 1 | a0001c0001t0001g0032 | 2 | NA18950.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.333+1269G>A | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 5/6 | chr2 | 99289968 | |||||||
| chr2:99290078 | G | A | 3 | a0001c0001t0001g0025 a0001c0001t0001g0039 a0001c0001t0001g0040 |
4 | HG02630.hp1 HG02717.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.333+1159C>T | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 5/6 | chr2 | 99290078 | |||||||
| chr2:99290113 | C | T | 33 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0016 others(30): Show |
95 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.333+1124G>A | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 5/6 | chr2 | 99290113 | |||||||
| chr2:99290149 | C | T | 49 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0010 others(46): Show |
120 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.333+1088G>A | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 5/6 | chr2 | 99290149 | |||||||
| chr2:99290642 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.333+595C>T | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 5/6 | chr2 | 99290642 | |||||||
| chr2:99290769 | G | A | 54 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0010 others(51): Show |
127 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.333+468C>T | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 5/6 | chr2 | 99290769 | |||||||
| chr2:99290779 | A | C | 4 | a0001c0001t0001g0020 a0001c0001t0001g0076 a0001c0001t0001g0077 others(1): Show |
6 | HG01070.hp1 HG01071.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.333+458T>G | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 5/6 | chr2 | 99290779 | |||||||
| chr2:99291484 | G | A | 1 | a0001c0001t0002g0138 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.149-63C>T | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 4/6 | chr2 | 99291484 | |||||||
| chr2:99291636 | T | G | 1 | a0001c0001t0001g0062 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.149-215A>C | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 4/6 | chr2 | 99291636 | |||||||
| chr2:99291637 | C | T | 1 | a0001c0001t0001g0062 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.149-216G>A | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 4/6 | chr2 | 99291637 | |||||||
| chr2:99291660 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.149-239G>A | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 4/6 | chr2 | 99291660 | |||||||
| chr2:99291703 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.149-282G>A | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 4/6 | chr2 | 99291703 | |||||||
| chr2:99291814 | A | T | 1 | a0001c0001t0002g0138 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.149-393T>A | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 4/6 | chr2 | 99291814 | |||||||
| chr2:99291823 | A | T | 1 | a0001c0001t0001g0044 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.149-402T>A | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 4/6 | chr2 | 99291823 | |||||||
| chr2:99291847 | C | A | 1 | a0001c0001t0001g0117 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.149-426G>T | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 4/6 | chr2 | 99291847 | |||||||
| chr2:99291851 | A | G | 1 | a0001c0001t0001g0061 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.149-430T>C | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 4/6 | chr2 | 99291851 | |||||||
| chr2:99291875 | C | T | 2 | a0001c0001t0001g0060 a0001c0001t0001g0071 |
2 | HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.149-454G>A | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 4/6 | chr2 | 99291875 | |||||||
| chr2:99291982 | T | G | 5 | a0001c0001t0001g0006 a0001c0001t0001g0038 a0001c0001t0001g0118 others(2): Show |
15 | HG00408.hp1 HG00673.hp2 HG02155.hp1 others(12): Show |
intron_variant | MODIFIER | c.148+554A>C | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 4/6 | chr2 | 99291982 | |||||||
| chr2:99292190 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.148+346G>A | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 4/6 | chr2 | 99292190 | |||||||
| chr2:99292206 | AC | A | 4 | a0001c0001t0001g0020 a0001c0001t0001g0076 a0001c0001t0001g0077 others(1): Show |
6 | HG01070.hp1 HG01071.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.148+329delG | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 4/6 | chr2 | 99292206 | |||||||
| chr2:99292246 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.148+290A>G | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 4/6 | chr2 | 99292246 | |||||||
| chr2:99292403 | AGCTAAGT others(16): Show |
A | 1 | a0001c0001t0001g0091 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.148+110_148+132del others(23): Show |
LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 4/6 | chr2 | 99292403 | |||||||
| chr2:99292450 | G | T | 1 | a0001c0001t0001g0118 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.148+86C>A | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 4/6 | chr2 | 99292450 | |||||||
| chr2:99292822 | T | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0091 |
4 | NA18939.hp2 NA18997.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.44-182A>G | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 3/6 | chr2 | 99292822 | |||||||
| chr2:99292985 | C | CT | 89 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(86): Show |
243 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.44-346dupA | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 3/6 | chr2 | 99292985 | |||||||
| chr2:99292985 | C | CTT | 15 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(12): Show |
35 | HG00544.hp1 HG00741.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.44-347_44-346dupAA | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 3/6 | chr2 | 99292985 | |||||||
| chr2:99293149 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.44-509C>T | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 3/6 | chr2 | 99293149 | |||||||
| chr2:99293282 | G | A | 1 | a0001c0001t0002g0138 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.44-642C>T | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 3/6 | chr2 | 99293282 | |||||||
| chr2:99293495 | A | G | 25 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(22): Show |
76 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.44-855T>C | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 3/6 | chr2 | 99293495 | |||||||
| chr2:99293663 | G | A | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(117): Show |
307 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(304): Show |
intron_variant | MODIFIER | c.44-1023C>T | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 3/6 | chr2 | 99293663 | |||||||
| chr2:99293745 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.44-1105T>C | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 3/6 | chr2 | 99293745 | |||||||
| chr2:99293811 | T | C | 1 | a0001c0001t0002g0138 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.44-1171A>G | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 3/6 | chr2 | 99293811 | |||||||
| chr2:99293909 | T | TTTAA | 3 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0121 |
3 | HG01168.hp2 HG01169.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.44-1273_44-1270dup others(4): Show |
LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 3/6 | chr2 | 99293909 | |||||||
| chr2:99293935 | T | C | 1 | a0002c0004t0001g0054 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.44-1295A>G | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 3/6 | chr2 | 99293935 | |||||||
| chr2:99294204 | G | A | 2 | a0002c0002t0001g0050 a0002c0002t0001g0051 |
2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.43+1424C>T | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 3/6 | chr2 | 99294204 | |||||||
| chr2:99294298 | A | G | 2 | a0002c0002t0001g0050 a0002c0002t0001g0051 |
2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.43+1330T>C | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 3/6 | chr2 | 99294298 | |||||||
| chr2:99294304 | A | G | 3 | a0001c0001t0001g0022 a0001c0001t0001g0101 a0001c0001t0001g0130 |
5 | NA18939.hp1 NA18941.hp2 NA18945.hp2 others(2): Show |
intron_variant | MODIFIER | c.43+1324T>C | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 3/6 | chr2 | 99294304 | |||||||
| chr2:99294509 | G | T | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(117): Show |
307 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(304): Show |
intron_variant | MODIFIER | c.43+1119C>A | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 3/6 | chr2 | 99294509 | |||||||
| chr2:99294513 | CTTTT | C | 66 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(63): Show |
180 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.43+1111_43+1114del others(4): Show |
LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 3/6 | chr2 | 99294513 | |||||||
| chr2:99294593 | TCCTTGGT others(5): Show |
T | 1 | a0001c0001t0001g0099 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.43+1023_43+1034del others(12): Show |
LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 3/6 | chr2 | 99294593 | |||||||
| chr2:99294620 | C | CCCTAG | 4 | a0001c0001t0001g0020 a0001c0001t0001g0076 a0001c0001t0001g0077 others(1): Show |
6 | HG01070.hp1 HG01071.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.43+1003_43+1007dup others(5): Show |
LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 3/6 | chr2 | 99294620 | |||||||
| chr2:99294647 | A | G | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(117): Show |
307 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(304): Show |
intron_variant | MODIFIER | c.43+981T>C | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 3/6 | chr2 | 99294647 | |||||||
| chr2:99294886 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.43+742C>T | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 3/6 | chr2 | 99294886 | |||||||
| chr2:99295101 | C | CA | 5 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0082 others(2): Show |
17 | HG00544.hp2 HG01070.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.43+526dupT | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 3/6 | chr2 | 99295101 | |||||||
| chr2:99295118 | A | T | 1 | a0001c0001t0001g0095 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.43+510T>A | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 3/6 | chr2 | 99295118 | |||||||
| chr2:99295139 | G | A | 2 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.43+489C>T | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 3/6 | chr2 | 99295139 | |||||||
| chr2:99295230 | T | C | 1 | a0001c0001t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.43+398A>G | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 3/6 | chr2 | 99295230 | |||||||
| chr2:99295740 | T | C | 1 | a0001c0001t0002g0138 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-32-38A>G | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 2/6 | chr2 | 99295740 | |||||||
| chr2:99295844 | GA | G | 51 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0010 others(48): Show |
124 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.-32-143delT | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 2/6 | chr2 | 99295844 | |||||||
| chr2:99295941 | T | C | 1 | a0001c0001t0001g0088 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-32-239A>G | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 2/6 | chr2 | 99295941 | |||||||
| chr2:99296002 | A | G | 1 | a0001c0001t0002g0138 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-32-300T>C | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 2/6 | chr2 | 99296002 | |||||||
| chr2:99296046 | T | C | 1 | a0001c0001t0001g0103 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-32-344A>G | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 2/6 | chr2 | 99296046 | |||||||
| chr2:99296238 | C | T | 1 | a0001c0001t0001g0028 | 2 | HG02572.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-32-536G>A | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 2/6 | chr2 | 99296238 | |||||||
| chr2:99296351 | A | G | 1 | a0001c0001t0001g0094 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-32-649T>C | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 2/6 | chr2 | 99296351 | |||||||
| chr2:99296421 | A | C | 1 | a0001c0001t0001g0091 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-32-719T>G | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 2/6 | chr2 | 99296421 | |||||||
| chr2:99296761 | A | C | 1 | a0001c0001t0001g0091 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-32-1059T>G | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 2/6 | chr2 | 99296761 | |||||||
| chr2:99297082 | T | C | 1 | a0001c0001t0001g0074 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-33+1377A>G | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 2/6 | chr2 | 99297082 | |||||||
| chr2:99297133 | G | A | 1 | a0002c0004t0001g0054 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-33+1326C>T | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 2/6 | chr2 | 99297133 | |||||||
| chr2:99297216 | C | T | 1 | a0001c0001t0001g0084 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-33+1243G>A | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 2/6 | chr2 | 99297216 | |||||||
| chr2:99297223 | GCTCAGAT others(7): Show |
G | 2 | a0002c0002t0001g0050 a0002c0002t0001g0051 |
2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.-33+1222_-33+1235d others(16): Show |
LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 2/6 | chr2 | 99297223 | |||||||
| chr2:99297242 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-33+1217T>C | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 2/6 | chr2 | 99297242 | |||||||
| chr2:99297264 | C | G | 1 | a0002c0002t0001g0050 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-33+1195G>C | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 2/6 | chr2 | 99297264 | |||||||
| chr2:99297302 | C | T | 1 | a0001c0001t0001g0091 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-33+1157G>A | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 2/6 | chr2 | 99297302 | |||||||
| chr2:99297535 | G | T | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(117): Show |
307 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(304): Show |
intron_variant | MODIFIER | c.-33+924C>A | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 2/6 | chr2 | 99297535 | |||||||
| chr2:99297618 | T | A | 1 | a0001c0001t0001g0091 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-33+841A>T | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 2/6 | chr2 | 99297618 | |||||||
| chr2:99297619 | G | T | 1 | a0001c0001t0001g0091 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-33+840C>A | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 2/6 | chr2 | 99297619 | |||||||
| chr2:99297675 | T | C | 1 | a0001c0001t0001g0091 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-33+784A>G | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 2/6 | chr2 | 99297675 | |||||||
| chr2:99297680 | A | G | 1 | a0001c0001t0001g0059 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-33+779T>C | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 2/6 | chr2 | 99297680 | |||||||
| chr2:99297715 | T | G | 1 | a0001c0001t0002g0138 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-33+744A>C | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 2/6 | chr2 | 99297715 | |||||||
| chr2:99297720 | C | CT | 53 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0010 others(50): Show |
126 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.-33+738dupA | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 2/6 | chr2 | 99297720 | |||||||
| chr2:99297772 | T | C | 1 | a0001c0001t0001g0019 | 3 | NA18952.hp2 NA19005.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.-33+687A>G | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 2/6 | chr2 | 99297772 | |||||||
| chr2:99297778 | G | C | 1 | a0001c0001t0002g0138 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-33+681C>G | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 2/6 | chr2 | 99297778 | |||||||
| chr2:99297846 | C | T | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | HG01261.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-33+613G>A | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 2/6 | chr2 | 99297846 | |||||||
| chr2:99298202 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-33+257G>A | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 2/6 | chr2 | 99298202 | |||||||
| chr2:99298243 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-33+216G>A | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 2/6 | chr2 | 99298243 | |||||||
| chr2:99298272 | C | T | 1 | a0001c0001t0002g0138 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-33+187G>A | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 2/6 | chr2 | 99298272 | |||||||
| chr2:99298320 | T | G | 1 | a0001c0001t0001g0092 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-33+139A>C | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 2/6 | chr2 | 99298320 | |||||||
| chr2:99298406 | G | A | 1 | a0001c0001t0001g0091 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-33+53C>T | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 2/6 | chr2 | 99298406 | |||||||
| chr2:99298704 | G | A | 3 | a0001c0001t0001g0022 a0001c0001t0001g0101 a0001c0001t0001g0130 |
5 | NA18939.hp1 NA18941.hp2 NA18945.hp2 others(2): Show |
intron_variant | MODIFIER | c.-123-155C>T | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 1/6 | chr2 | 99298704 | |||||||
| chr2:99298717 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-123-168C>T | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 1/6 | chr2 | 99298717 | |||||||
| chr2:99298718 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-123-169A>G | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 1/6 | chr2 | 99298718 | |||||||
| chr2:99298812 | G | T | 1 | a0001c0001t0001g0105 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-123-263C>A | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 1/6 | chr2 | 99298812 | |||||||
| chr2:99298897 | T | A | 1 | a0001c0001t0001g0038 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-123-348A>T | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 1/6 | chr2 | 99298897 | |||||||
| chr2:99298899 | A | T | 1 | a0001c0001t0001g0038 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-123-350T>A | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 1/6 | chr2 | 99298899 | |||||||
| chr2:99298903 | T | A | 1 | a0001c0001t0001g0038 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-123-354A>T | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 1/6 | chr2 | 99298903 | |||||||
| chr2:99298928 | T | A | 1 | a0001c0001t0001g0125 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-123-379A>T | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 1/6 | chr2 | 99298928 | |||||||
| chr2:99299084 | G | A | 1 | a0002c0002t0001g0056 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-123-535C>T | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 1/6 | chr2 | 99299084 | |||||||
| chr2:99299117 | G | C | 1 | a0001c0001t0001g0102 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-123-568C>G | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 1/6 | chr2 | 99299117 | |||||||
| chr2:99299151 | T | A | 1 | a0001c0001t0001g0126 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-123-602A>T | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 1/6 | chr2 | 99299151 | |||||||
| chr2:99299264 | C | T | 1 | a0001c0001t0001g0091 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-123-715G>A | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 1/6 | chr2 | 99299264 | |||||||
| chr2:99299268 | T | C | 1 | a0001c0001t0001g0091 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-123-719A>G | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 1/6 | chr2 | 99299268 | |||||||
| chr2:99299284 | C | CT | 7 | a0001c0001t0001g0043 a0001c0001t0001g0076 a0001c0001t0001g0077 others(4): Show |
7 | HG01070.hp1 HG01071.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.-123-736dupA | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 1/6 | chr2 | 99299284 | |||||||
| chr2:99299284 | CT | C | 5 | a0001c0001t0001g0031 a0001c0001t0001g0036 a0001c0001t0001g0089 others(2): Show |
7 | HG01099.hp1 HG01168.hp1 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.-123-736delA | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 1/6 | chr2 | 99299284 | |||||||
| chr2:99299504 | C | A | 2 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-123-955G>T | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 1/6 | chr2 | 99299504 | |||||||
| chr2:99299668 | G | A | 2 | a0001c0001t0001g0047 a0001c0001t0001g0090 |
2 | HG02451.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-123-1119C>T | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 1/6 | chr2 | 99299668 | |||||||
| chr2:99299681 | T | C | 1 | a0001c0001t0001g0091 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-123-1132A>G | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 1/6 | chr2 | 99299681 | |||||||
| chr2:99299682 | C | T | 1 | a0001c0001t0001g0091 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-123-1133G>A | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 1/6 | chr2 | 99299682 | |||||||
| chr2:99299723 | A | T | 1 | a0001c0001t0001g0091 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-123-1174T>A | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 1/6 | chr2 | 99299723 | |||||||
| chr2:99299725 | T | A | 1 | a0001c0001t0001g0091 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-123-1176A>T | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 1/6 | chr2 | 99299725 | |||||||
| chr2:99299748 | A | T | 1 | a0001c0001t0002g0138 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-123-1199T>A | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 1/6 | chr2 | 99299748 | |||||||
| chr2:99299779 | T | C | 33 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0016 others(30): Show |
95 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.-123-1230A>G | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 1/6 | chr2 | 99299779 | |||||||
| chr2:99299780 | A | T | 66 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(63): Show |
180 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.-123-1231T>A | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 1/6 | chr2 | 99299780 | |||||||
| chr2:99300053 | T | C | 1 | a0001c0001t0001g0092 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-124+997A>G | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 1/6 | chr2 | 99300053 | |||||||
| chr2:99300075 | T | G | 25 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(22): Show |
76 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-124+975A>C | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 1/6 | chr2 | 99300075 | |||||||
| chr2:99300081 | CT | C | 47 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0010 others(44): Show |
121 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.-124+968delA | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 1/6 | chr2 | 99300081 | |||||||
| chr2:99300113 | G | A | 3 | a0001c0001t0001g0037 a0001c0001t0001g0131 a0001c0001t0001g0134 |
4 | HG02055.hp2 HG02615.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-124+937C>T | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 1/6 | chr2 | 99300113 | |||||||
| chr2:99300157 | T | A | 1 | a0001c0001t0001g0132 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-124+893A>T | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 1/6 | chr2 | 99300157 | |||||||
| chr2:99300340 | T | C | 1 | a0001c0001t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-124+710A>G | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 1/6 | chr2 | 99300340 | |||||||
| chr2:99300430 | C | T | 2 | a0001c0001t0001g0048 a0001c0001t0001g0049 |
2 | HG01106.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-124+620G>A | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 1/6 | chr2 | 99300430 | |||||||
| chr2:99300432 | T | G | 1 | a0001c0001t0001g0038 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-124+618A>C | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 1/6 | chr2 | 99300432 | |||||||
| chr2:99300444 | C | G | 1 | a0001c0001t0001g0047 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-124+606G>C | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 1/6 | chr2 | 99300444 | |||||||
| chr2:99300457 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-124+593C>T | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 1/6 | chr2 | 99300457 | |||||||
| chr2:99300497 | C | T | 7 | a0001c0001t0001g0026 a0001c0001t0001g0041 a0001c0001t0001g0042 others(4): Show |
8 | HG00639.hp2 HG01074.hp1 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.-124+553G>A | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 1/6 | chr2 | 99300497 | |||||||
| chr2:99300522 | C | T | 3 | a0001c0001t0001g0025 a0001c0001t0001g0039 a0001c0001t0001g0040 |
4 | HG02630.hp1 HG02717.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-124+528G>A | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 1/6 | chr2 | 99300522 | |||||||
| chr2:99300563 | T | C | 1 | a0001c0001t0001g0134 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-124+487A>G | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 1/6 | chr2 | 99300563 | |||||||
| chr2:99300645 | A | G | 1 | a0001c0001t0001g0038 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-124+405T>C | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 1/6 | chr2 | 99300645 | |||||||
| chr2:99300771 | A | T | 1 | a0001c0001t0001g0038 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-124+279T>A | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 1/6 | chr2 | 99300771 | |||||||
| chr2:99300930 | G | A | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | HG02886.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.-124+120C>T | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 1/6 | chr2 | 99300930 | |||||||
| chr2:99301016 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-124+34C>T | LYG1 | ENSG00000144214.10 | transcript | ENST00000308528.9 | protein_coding | 1/6 | chr2 | 99301016 |