Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55741 |
| ensemblid | ENSG00000088298.13 |
| hgncid | 15877 |
| symbol | EDEM2 |
| name | ER degradation enhancing alpha-mannosidase like protein 2 |
| refseq_nuc | NM_018217.3 |
| refseq_prot | NP_060687.2 |
| ensembl_nuc | ENST00000374492.8 |
| ensembl_prot | ENSP00000363616.3 |
| mane_status | MANE Select |
| chr | chr20 |
| start | 35115364 |
| end | 35147336 |
| strand | - |
| ver | v1.2 |
| region | chr20:35115364-35147336 |
| region5000 | chr20:35110364-35152336 |
| regionname0 | EDEM2_chr20_35115364_35147336 |
| regionname5000 | EDEM2_chr20_35110364_35152336 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 578 | 292 | 90 | 52 | 110 | 8 | 30 | 76 | EDEM2_chr20_35110364_35152336 | EDEM2 | MPFRL others(573): Show |
chr20 | 35110364 | 35152336 |
| a0002 | 0/0 | 578 | 28 | 1 | 6 | 13 | 4 | 4 | 8 | EDEM2_chr20_35110364_35152336 | EDEM2 | MPFRL others(573): Show |
chr20 | 35110364 | 35152336 |
| a0003 | 0/0 | 578 | 8 | 4 | 4 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | MPFRL others(573): Show |
chr20 | 35110364 | 35152336 |
| a0004 | 0/0 | 578 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | MPFRL others(573): Show |
chr20 | 35110364 | 35152336 |
| a0005 | 0/0 | 578 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | MPFRL others(573): Show |
chr20 | 35110364 | 35152336 |
| a0006 | 0/0 | 578 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | MPFRL others(573): Show |
chr20 | 35110364 | 35152336 |
| a0007 | 0/0 | 578 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | MPFRL others(573): Show |
chr20 | 35110364 | 35152336 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1734 | 255 | 56 | 49 | 110 | 8 | 30 | EDEM2_chr20_35110364_35152336 | EDEM2 | ATGCC others(1729): Show |
chr20 | 35110364 | 35152336 | ||
| a0001c0002 | 0/0 | 1734 | 33 | 31 | 2 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | ATGCC others(1729): Show |
chr20 | 35110364 | 35152336 | ||
| a0001c0005 | 0/0 | 1734 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | ATGCC others(1729): Show |
chr20 | 35110364 | 35152336 | ||
| a0001c0006 | 0/0 | 1734 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | ATGCC others(1729): Show |
chr20 | 35110364 | 35152336 | ||
| a0001c0007 | 0/0 | 1734 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | ATGCC others(1729): Show |
chr20 | 35110364 | 35152336 | ||
| a0001c0009 | 0/0 | 1734 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | ATGCC others(1729): Show |
chr20 | 35110364 | 35152336 | ||
| a0002c0003 | 0/0 | 1734 | 28 | 1 | 6 | 13 | 4 | 4 | EDEM2_chr20_35110364_35152336 | EDEM2 | ATGCC others(1729): Show |
chr20 | 35110364 | 35152336 | ||
| a0003c0004 | 0/0 | 1734 | 7 | 3 | 4 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | ATGCC others(1729): Show |
chr20 | 35110364 | 35152336 | ||
| a0003c0008 | 0/0 | 1734 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | ATGCC others(1729): Show |
chr20 | 35110364 | 35152336 | ||
| a0004c0013 | 0/0 | 1734 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | ATGCC others(1729): Show |
chr20 | 35110364 | 35152336 | ||
| a0005c0011 | 0/0 | 1734 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | ATGCC others(1729): Show |
chr20 | 35110364 | 35152336 | ||
| a0006c0012 | 0/0 | 1734 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | ATGCC others(1729): Show |
chr20 | 35110364 | 35152336 | ||
| a0007c0010 | 0/0 | 1734 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | ATGCC others(1729): Show |
chr20 | 35110364 | 35152336 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1884 | 248 | 50 | 49 | 110 | 8 | 29 | EDEM2_chr20_35110364_35152336 | EDEM2 | GAACC others(1879): Show |
chr20 | 35110364 | 35152336 |
| a0001c0001t0002 | 0/0 | 1884 | 7 | 6 | 0 | 0 | 0 | 1 | EDEM2_chr20_35110364_35152336 | EDEM2 | GAACC others(1879): Show |
chr20 | 35110364 | 35152336 |
| a0001c0002t0001 | 0/0 | 1884 | 33 | 31 | 2 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | GAACC others(1879): Show |
chr20 | 35110364 | 35152336 |
| a0001c0005t0001 | 0/0 | 1884 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | GAACC others(1879): Show |
chr20 | 35110364 | 35152336 |
| a0001c0006t0001 | 0/0 | 1884 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | GAACC others(1879): Show |
chr20 | 35110364 | 35152336 |
| a0001c0007t0001 | 0/0 | 1884 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | GAACC others(1879): Show |
chr20 | 35110364 | 35152336 |
| a0001c0009t0001 | 0/0 | 1884 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | GAACC others(1879): Show |
chr20 | 35110364 | 35152336 |
| a0002c0003t0001 | 0/0 | 1884 | 28 | 1 | 6 | 13 | 4 | 4 | EDEM2_chr20_35110364_35152336 | EDEM2 | GAACC others(1879): Show |
chr20 | 35110364 | 35152336 |
| a0003c0004t0001 | 0/0 | 1884 | 7 | 3 | 4 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | GAACC others(1879): Show |
chr20 | 35110364 | 35152336 |
| a0003c0008t0001 | 0/0 | 1884 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | GAACC others(1879): Show |
chr20 | 35110364 | 35152336 |
| a0004c0013t0001 | 0/0 | 1884 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | GAACC others(1879): Show |
chr20 | 35110364 | 35152336 |
| a0005c0011t0001 | 0/0 | 1884 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | GAACC others(1879): Show |
chr20 | 35110364 | 35152336 |
| a0006c0012t0001 | 0/0 | 1884 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | GAACC others(1879): Show |
chr20 | 35110364 | 35152336 |
| a0007c0010t0001 | 0/0 | 1884 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | GAACC others(1879): Show |
chr20 | 35110364 | 35152336 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 29 | 3 | 6 | 15 | 1 | 4 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0004 | 0/0 | 7 | 1 | 1 | 2 | 0 | 3 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0005 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0007 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0008 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0010 | 0/0 | 4 | 2 | 0 | 1 | 0 | 1 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0018 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0083 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0088 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0002g0006 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0002t0001g0003 | 0/0 | 8 | 7 | 1 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0002t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0002t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0002t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0002t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0002t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0002t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0002t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0002t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0002t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0002t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0002t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0002t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0002t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0002t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0002t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0002t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0002t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0002t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0002t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0002t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0005t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0006t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0007t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0001c0009t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0002c0003t0001g0002 | 0/0 | 8 | 1 | 3 | 0 | 2 | 2 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0002c0003t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0002c0003t0001g0032 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0002c0003t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0002c0003t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0002c0003t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0002c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0002c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0002c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0002c0003t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0002c0003t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0002c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0002c0003t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0002c0003t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0002c0003t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0002c0003t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0002c0003t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0002c0003t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0002c0003t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0003c0004t0001g0011 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0003c0004t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0003c0004t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0003c0008t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0004c0013t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0005c0011t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0006c0012t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| a0007c0010t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | GBR | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG00099 | hp2 | a0002 | c0003 | t0001 | g0150 | EUR | GBR | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0136 | EUR | GBR | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0068 | EUR | GBR | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG00280 | hp1 | a0002 | c0003 | t0001 | g0002 | EUR | FIN | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0137 | EUR | FIN | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG00323 | hp1 | a0002 | c0003 | t0001 | g0032 | EUR | FIN | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0145 | EUR | FIN | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG00609 | hp1 | a0004 | c0013 | t0001 | g0125 | EAS | CHS | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG00609 | hp2 | a0002 | c0003 | t0001 | g0024 | EAS | CHS | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG00621 | hp2 | a0002 | c0003 | t0001 | g0024 | EAS | CHS | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG00639 | hp1 | a0002 | c0003 | t0001 | g0002 | AMR | PUR | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | CHS | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG00738 | hp1 | a0003 | c0004 | t0001 | g0034 | AMR | PUR | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0133 | AMR | PUR | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG00741 | hp2 | a0001 | c0006 | t0001 | g0064 | AMR | PUR | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG01167 | hp2 | a0003 | c0004 | t0001 | g0011 | AMR | PUR | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG01168 | hp1 | a0002 | c0003 | t0001 | g0158 | AMR | PUR | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG01169 | hp1 | a0003 | c0004 | t0001 | g0011 | AMR | PUR | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG01192 | hp1 | a0002 | c0003 | t0001 | g0002 | AMR | PUR | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG01243 | hp1 | a0003 | c0004 | t0001 | g0034 | AMR | PUR | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG01257 | hp1 | a0002 | c0003 | t0001 | g0161 | AMR | CLM | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG01258 | hp1 | a0005 | c0011 | t0001 | g0061 | AMR | CLM | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG01346 | hp1 | a0002 | c0003 | t0001 | g0002 | AMR | CLM | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0185 | EUR | IBS | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0029 | EUR | IBS | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0134 | AFR | ACB | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0129 | AFR | ACB | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG01891 | hp2 | a0001 | c0002 | t0001 | g0003 | AFR | ACB | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG01975 | hp2 | a0006 | c0012 | t0001 | g0060 | AMR | PEL | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02056 | hp2 | a0002 | c0003 | t0001 | g0076 | EAS | KHV | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02071 | hp2 | a0002 | c0003 | t0001 | g0160 | EAS | KHV | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0174 | AFR | ACB | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0016 | AFR | ACB | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0003 | AFR | ACB | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0219 | AFR | ACB | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PEL | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0138 | AFR | ACB | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02572 | hp2 | a0003 | c0008 | t0001 | g0162 | AFR | GWD | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02602 | hp1 | a0002 | c0003 | t0001 | g0151 | SAS | PJL | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0176 | AFR | GWD | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | GWD | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | GWD | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0180 | AFR | GWD | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0182 | AFR | GWD | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0041 | AFR | GWD | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0177 | AFR | GWD | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | ESN | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0178 | AFR | ESN | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | ESN | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0168 | AFR | ESN | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ESN | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0003 | AFR | ESN | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG03041 | hp1 | a0001 | c0005 | t0001 | g0179 | AFR | GWD | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0107 | AFR | GWD | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | ESN | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0003 | AFR | ESN | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG03139 | hp2 | a0007 | c0010 | t0001 | g0131 | AFR | ESN | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0139 | AFR | ESN | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ESN | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | MSL | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | MSL | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | MSL | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | MSL | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0016 | AFR | ESN | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG03540 | hp1 | a0003 | c0004 | t0001 | g0011 | AFR | GWD | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0181 | AFR | MSL | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | STU | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG03704 | hp1 | a0002 | c0003 | t0001 | g0002 | SAS | PJL | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | BEB | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | BEB | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG03834 | hp1 | a0002 | c0003 | t0001 | g0002 | SAS | BEB | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | BEB | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG04115 | hp1 | a0002 | c0003 | t0001 | g0152 | SAS | STU | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | STU | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | STU | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | STU | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | STU | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0040 | SAS | STU | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0130 | AFR | YRI | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18522 | hp2 | a0003 | c0004 | t0001 | g0169 | AFR | YRI | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18612 | hp1 | a0002 | c0003 | t0001 | g0175 | EAS | CHB | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHB | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | CHB | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | CHB | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | YRI | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18906 | hp2 | a0003 | c0004 | t0001 | g0011 | AFR | YRI | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18944 | hp1 | a0002 | c0003 | t0001 | g0055 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18957 | hp1 | a0002 | c0003 | t0001 | g0054 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18957 | hp2 | a0002 | c0003 | t0001 | g0081 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18980 | hp1 | a0002 | c0003 | t0001 | g0032 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18982 | hp2 | a0002 | c0003 | t0001 | g0146 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18983 | hp1 | a0002 | c0003 | t0001 | g0056 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA19003 | hp2 | a0002 | c0003 | t0001 | g0048 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0183 | AFR | LWK | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | LWK | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0132 | AFR | LWK | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | LWK | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA19062 | hp1 | a0002 | c0003 | t0001 | g0149 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0016 | AFR | YRI | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | YRI | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA20129 | hp1 | a0002 | c0003 | t0001 | g0002 | AFR | ASW | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ASW | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA20752 | hp2 | a0002 | c0003 | t0001 | g0002 | EUR | TSI | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | GIH | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | GIH | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG01123 | hp1 | a0002 | c0003 | t0001 | g0143 | AMR | CLM | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02109 | hp1 | a0001 | c0009 | t0001 | g0071 | AFR | ACB | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0003 | AFR | ACB | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0184 | AFR | ACB | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0135 | AFR | ACB | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | ACB | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0186 | AFR | MSL | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | MSL | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | USA | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | USA | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | USA | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0128 | AFR | USA | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA21309 | hp1 | a0001 | c0007 | t0001 | g0106 | AFR | LWK | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | LWK | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0088 | REF | REF | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0083 | REF | REF | EDEM2_chr20_35110364_35152336 | EDEM2 | chr20 | 35110364 | 35152336 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:35115514 | C | A | 1 | a0007 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.1656G>T | p.Lys552Asn | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 11/11 | 1734/1884 | 1656/1737 | 552/578 | chr20 | 35115514 | |||
| chr20:35115641 | C | T | 1 | a0003 | 8 | HG00738.hp1 HG01167.hp2 HG01169.hp1 others(5): Show |
missense_variant | MODERATE | c.1529G>A | p.Arg510Gln | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 11/11 | 1607/1884 | 1529/1737 | 510/578 | chr20 | 35115641 | |||
| chr20:35115804 | C | T | 1 | a0002 | 28 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(25): Show |
missense_variant | MODERATE | c.1366G>A | p.Ala456Thr | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 11/11 | 1444/1884 | 1366/1737 | 456/578 | chr20 | 35115804 | |||
| chr20:35131740 | T | C | 1 | a0005 | 1 | HG01258.hp1 | missense_variant | MODERATE | c.746A>G | p.Gln249Arg | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/11 | 824/1884 | 746/1737 | 249/578 | chr20 | 35131740 | |||
| chr20:35134859 | C | A | 1 | a0006 | 1 | HG01975.hp2 | missense_variant | MODERATE | c.581G>T | p.Gly194Val | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 6/11 | 659/1884 | 581/1737 | 194/578 | chr20 | 35134859 | |||
| chr20:35137922 | G | A | 1 | a0004 | 1 | HG00609.hp1 | missense_variant | MODERATE | c.448C>T | p.Leu150Phe | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 5/11 | 526/1884 | 448/1737 | 150/578 | chr20 | 35137922 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:35115511 | G | A | 1 | a0001c0009 | 1 | HG02109.hp1 | synonymous_variant | LOW | c.1659C>T | p.Val553Val | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 11/11 | 1737/1884 | 1659/1737 | 553/578 | chr20 | 35115511 | |||
| chr20:35118706 | G | A | 3 | a0001c0002 a0001c0005 a0003c0004 |
41 | HG00738.hp1 HG00741.hp1 HG01109.hp1 others(38): Show |
synonymous_variant | LOW | c.1128C>T | p.Ser376Ser | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 10/11 | 1206/1884 | 1128/1737 | 376/578 | chr20 | 35118706 | |||
| chr20:35123954 | C | T | 1 | a0001c0007 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.1050G>A | p.Pro350Pro | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 9/11 | 1128/1884 | 1050/1737 | 350/578 | chr20 | 35123954 | |||
| chr20:35131676 | C | G | 1 | a0001c0006 | 1 | HG00741.hp2 | synonymous_variant | LOW | c.810G>C | p.Leu270Leu | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/11 | 888/1884 | 810/1737 | 270/578 | chr20 | 35131676 | |||
| chr20:35134855 | A | G | 1 | a0001c0005 | 1 | HG03041.hp1 | synonymous_variant | LOW | c.585T>C | p.Ile195Ile | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 6/11 | 663/1884 | 585/1737 | 195/578 | chr20 | 35134855 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:35147289 | C | T | 1 | a0001c0001t0002 | 7 | HG02818.hp1 HG02896.hp2 HG02897.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-31G>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 1/11 | 31 | chr20 | 35147289 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:35115946 | A | G | 2 | a0001c0001t0001g0201 a0001c0001t0001g0202 |
2 | HG00673.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.1237-13T>C | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 10/10 | chr20 | 35115946 | |||||||
| chr20:35115984 | T | TA | 27 | a0001c0001t0001g0013 a0001c0001t0001g0052 a0001c0002t0001g0003 others(24): Show |
38 | HG00741.hp1 HG01109.hp1 HG01884.hp2 others(35): Show |
intron_variant | MODIFIER | c.1237-52dupT | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 10/10 | chr20 | 35115984 | |||||||
| chr20:35116305 | T | C | 157 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(154): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.1237-372A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 10/10 | chr20 | 35116305 | |||||||
| chr20:35116426 | C | T | 5 | a0001c0001t0001g0035 a0001c0001t0001g0108 a0001c0001t0001g0118 others(2): Show |
6 | HG01884.hp1 HG02622.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1237-493G>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 10/10 | chr20 | 35116426 | |||||||
| chr20:35116591 | C | A | 1 | a0001c0001t0001g0187 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1237-658G>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 10/10 | chr20 | 35116591 | |||||||
| chr20:35116906 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1237-973G>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 10/10 | chr20 | 35116906 | |||||||
| chr20:35117033 | C | T | 70 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0014 others(67): Show |
112 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.1237-1100G>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 10/10 | chr20 | 35117033 | |||||||
| chr20:35117085 | T | C | 117 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(114): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.1237-1152A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 10/10 | chr20 | 35117085 | |||||||
| chr20:35117269 | G | A | 27 | a0001c0001t0001g0013 a0001c0001t0001g0052 a0001c0002t0001g0003 others(24): Show |
38 | HG00741.hp1 HG01109.hp1 HG01884.hp2 others(35): Show |
intron_variant | MODIFIER | c.1236+1329C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 10/10 | chr20 | 35117269 | |||||||
| chr20:35117423 | C | T | 3 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0220 |
3 | HG02559.hp2 HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1236+1175G>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 10/10 | chr20 | 35117423 | |||||||
| chr20:35117513 | T | C | 2 | a0002c0003t0001g0151 a0002c0003t0001g0152 |
2 | HG02602.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1236+1085A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 10/10 | chr20 | 35117513 | |||||||
| chr20:35117871 | T | C | 2 | a0002c0003t0001g0146 a0002c0003t0001g0149 |
2 | NA18982.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.1236+727A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 10/10 | chr20 | 35117871 | |||||||
| chr20:35117905 | G | C | 159 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(156): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.1236+693C>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 10/10 | chr20 | 35117905 | |||||||
| chr20:35118208 | A | C | 115 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(112): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.1236+390T>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 10/10 | chr20 | 35118208 | |||||||
| chr20:35118350 | C | T | 2 | a0001c0001t0001g0022 a0001c0001t0001g0086 |
3 | HG01071.hp1 HG01361.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1236+248G>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 10/10 | chr20 | 35118350 | |||||||
| chr20:35118365 | A | G | 1 | a0001c0001t0001g0070 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1236+233T>C | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 10/10 | chr20 | 35118365 | |||||||
| chr20:35118384 | T | C | 157 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(154): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.1236+214A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 10/10 | chr20 | 35118384 | |||||||
| chr20:35118573 | T | A | 2 | a0001c0002t0001g0133 a0001c0002t0001g0135 |
2 | HG00741.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1236+25A>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 10/10 | chr20 | 35118573 | |||||||
| chr20:35118772 | T | A | 117 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(114): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.1115-53A>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 9/10 | chr20 | 35118772 | |||||||
| chr20:35118831 | A | G | 9 | a0001c0002t0001g0107 a0001c0002t0001g0128 a0001c0002t0001g0129 others(6): Show |
9 | HG00741.hp1 HG01884.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1115-112T>C | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 9/10 | chr20 | 35118831 | |||||||
| chr20:35119019 | C | T | 117 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(114): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.1115-300G>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 9/10 | chr20 | 35119019 | |||||||
| chr20:35119033 | T | C | 1 | a0001c0002t0001g0129 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1115-314A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 9/10 | chr20 | 35119033 | |||||||
| chr20:35119083 | T | TAAC | 157 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(154): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.1115-367_1115-365d others(5): Show |
EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 9/10 | chr20 | 35119083 | |||||||
| chr20:35119132 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1115-413A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 9/10 | chr20 | 35119132 | |||||||
| chr20:35119332 | T | C | 118 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(115): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.1115-613A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 9/10 | chr20 | 35119332 | |||||||
| chr20:35119374 | C | T | 36 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(33): Show |
50 | HG01074.hp2 HG01081.hp2 HG01099.hp1 others(47): Show |
intron_variant | MODIFIER | c.1115-655G>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 9/10 | chr20 | 35119374 | |||||||
| chr20:35119557 | C | T | 1 | a0001c0002t0001g0184 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1115-838G>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 9/10 | chr20 | 35119557 | |||||||
| chr20:35119831 | T | C | 9 | a0001c0002t0001g0107 a0001c0002t0001g0128 a0001c0002t0001g0129 others(6): Show |
9 | HG00741.hp1 HG01884.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1115-1112A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 9/10 | chr20 | 35119831 | |||||||
| chr20:35120078 | T | C | 1 | a0001c0001t0001g0103 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1115-1359A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 9/10 | chr20 | 35120078 | |||||||
| chr20:35120186 | C | T | 92 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(89): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.1115-1467G>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 9/10 | chr20 | 35120186 | |||||||
| chr20:35120196 | G | A | 1 | a0001c0001t0001g0109 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1115-1477C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 9/10 | chr20 | 35120196 | |||||||
| chr20:35120220 | C | G | 118 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(115): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.1115-1501G>C | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 9/10 | chr20 | 35120220 | |||||||
| chr20:35120276 | T | C | 17 | a0001c0002t0001g0003 a0001c0002t0001g0016 a0001c0002t0001g0138 others(14): Show |
26 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.1115-1557A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 9/10 | chr20 | 35120276 | |||||||
| chr20:35120585 | G | A | 1 | a0004c0013t0001g0125 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1115-1866C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 9/10 | chr20 | 35120585 | |||||||
| chr20:35120593 | CT | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(131): Show |
205 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.1115-1875delA | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 9/10 | chr20 | 35120593 | |||||||
| chr20:35120596 | T | C | 1 | a0001c0001t0001g0069 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1115-1877A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 9/10 | chr20 | 35120596 | |||||||
| chr20:35120597 | T | C | 88 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(85): Show |
143 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.1115-1878A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 9/10 | chr20 | 35120597 | |||||||
| chr20:35120598 | T | C | 3 | a0001c0001t0001g0063 a0001c0001t0001g0065 a0002c0003t0001g0150 |
3 | HG00099.hp2 HG01993.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.1115-1879A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 9/10 | chr20 | 35120598 | |||||||
| chr20:35120661 | G | A | 1 | a0001c0007t0001g0106 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1115-1942C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 9/10 | chr20 | 35120661 | |||||||
| chr20:35120794 | C | T | 26 | a0001c0002t0001g0003 a0001c0002t0001g0016 a0001c0002t0001g0107 others(23): Show |
35 | HG00741.hp1 HG01109.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.1115-2075G>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 9/10 | chr20 | 35120794 | |||||||
| chr20:35120834 | T | C | 92 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(89): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.1115-2115A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 9/10 | chr20 | 35120834 | |||||||
| chr20:35121054 | C | T | 26 | a0001c0002t0001g0003 a0001c0002t0001g0016 a0001c0002t0001g0107 others(23): Show |
35 | HG00741.hp1 HG01109.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.1115-2335G>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 9/10 | chr20 | 35121054 | |||||||
| chr20:35121068 | A | G | 118 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(115): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.1115-2349T>C | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 9/10 | chr20 | 35121068 | |||||||
| chr20:35121087 | T | G | 92 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(89): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.1115-2368A>C | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 9/10 | chr20 | 35121087 | |||||||
| chr20:35121269 | G | C | 2 | a0001c0001t0001g0140 a0001c0001t0001g0153 |
2 | HG02615.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1115-2550C>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 9/10 | chr20 | 35121269 | |||||||
| chr20:35121404 | C | A | 1 | a0001c0007t0001g0106 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1114+2486G>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 9/10 | chr20 | 35121404 | |||||||
| chr20:35121476 | A | C | 118 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(115): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.1114+2414T>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 9/10 | chr20 | 35121476 | |||||||
| chr20:35121545 | T | C | 3 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 |
3 | HG02630.hp2 HG02809.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1114+2345A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 9/10 | chr20 | 35121545 | |||||||
| chr20:35121601 | G | C | 2 | a0001c0001t0001g0020 a0001c0001t0001g0087 |
3 | NA18965.hp1 NA18966.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.1114+2289C>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 9/10 | chr20 | 35121601 | |||||||
| chr20:35121785 | C | G | 1 | a0001c0001t0001g0072 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1114+2105G>C | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 9/10 | chr20 | 35121785 | |||||||
| chr20:35121799 | GT | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(135): Show |
207 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.1114+2090delA | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 9/10 | chr20 | 35121799 | |||||||
| chr20:35121799 | GTT | G | 17 | a0001c0002t0001g0003 a0001c0002t0001g0016 a0001c0002t0001g0138 others(14): Show |
26 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.1114+2089_1114+209 others(6): Show |
EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 9/10 | chr20 | 35121799 | |||||||
| chr20:35121905 | C | T | 1 | a0007c0010t0001g0131 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1114+1985G>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 9/10 | chr20 | 35121905 | |||||||
| chr20:35121917 | G | A | 3 | a0001c0001t0001g0030 a0001c0001t0001g0116 a0001c0001t0001g0171 |
4 | HG02602.hp2 HG02698.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.1114+1973C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 9/10 | chr20 | 35121917 | |||||||
| chr20:35122043 | G | C | 176 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(173): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.1114+1847C>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 9/10 | chr20 | 35122043 | |||||||
| chr20:35122180 | G | A | 2 | a0001c0001t0001g0126 a0001c0001t0001g0127 |
2 | NA19011.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1114+1710C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 9/10 | chr20 | 35122180 | |||||||
| chr20:35122575 | T | A | 1 | a0001c0001t0001g0203 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1114+1315A>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 9/10 | chr20 | 35122575 | |||||||
| chr20:35122796 | A | G | 1 | a0001c0001t0001g0209 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1114+1094T>C | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 9/10 | chr20 | 35122796 | |||||||
| chr20:35123155 | A | G | 1 | a0001c0001t0001g0126 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1114+735T>C | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 9/10 | chr20 | 35123155 | |||||||
| chr20:35123368 | G | A | 25 | a0001c0002t0001g0003 a0001c0002t0001g0016 a0001c0002t0001g0107 others(22): Show |
34 | HG00741.hp1 HG01109.hp1 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.1114+522C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 9/10 | chr20 | 35123368 | |||||||
| chr20:35123462 | C | T | 2 | a0002c0003t0001g0054 a0002c0003t0001g0055 |
2 | NA18944.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.1114+428G>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 9/10 | chr20 | 35123462 | |||||||
| chr20:35123522 | G | A | 26 | a0001c0002t0001g0003 a0001c0002t0001g0016 a0001c0002t0001g0107 others(23): Show |
35 | HG00741.hp1 HG01109.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.1114+368C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 9/10 | chr20 | 35123522 | |||||||
| chr20:35123540 | C | T | 26 | a0001c0002t0001g0003 a0001c0002t0001g0016 a0001c0002t0001g0107 others(23): Show |
35 | HG00741.hp1 HG01109.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.1114+350G>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 9/10 | chr20 | 35123540 | |||||||
| chr20:35123588 | A | G | 118 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(115): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.1114+302T>C | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 9/10 | chr20 | 35123588 | |||||||
| chr20:35123621 | A | G | 26 | a0001c0002t0001g0003 a0001c0002t0001g0016 a0001c0002t0001g0107 others(23): Show |
35 | HG00741.hp1 HG01109.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.1114+269T>C | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 9/10 | chr20 | 35123621 | |||||||
| chr20:35123698 | G | T | 1 | a0007c0010t0001g0131 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1114+192C>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 9/10 | chr20 | 35123698 | |||||||
| chr20:35123762 | C | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0052 |
4 | HG02572.hp1 HG02895.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1114+128G>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 9/10 | chr20 | 35123762 | |||||||
| chr20:35123821 | T | A | 118 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(115): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.1114+69A>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 9/10 | chr20 | 35123821 | |||||||
| chr20:35123858 | T | C | 26 | a0001c0002t0001g0003 a0001c0002t0001g0016 a0001c0002t0001g0107 others(23): Show |
35 | HG00741.hp1 HG01109.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.1114+32A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 9/10 | chr20 | 35123858 | |||||||
| chr20:35124109 | A | T | 26 | a0001c0002t0001g0003 a0001c0002t0001g0016 a0001c0002t0001g0107 others(23): Show |
35 | HG00741.hp1 HG01109.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.970-75T>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 8/10 | chr20 | 35124109 | |||||||
| chr20:35124267 | A | T | 26 | a0001c0002t0001g0003 a0001c0002t0001g0016 a0001c0002t0001g0107 others(23): Show |
35 | HG00741.hp1 HG01109.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.970-233T>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 8/10 | chr20 | 35124267 | |||||||
| chr20:35124301 | G | C | 4 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0072 others(1): Show |
6 | HG01106.hp1 HG01255.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.970-267C>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 8/10 | chr20 | 35124301 | |||||||
| chr20:35124345 | A | C | 92 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(89): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.970-311T>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 8/10 | chr20 | 35124345 | |||||||
| chr20:35124366 | G | A | 4 | a0001c0001t0001g0029 a0001c0001t0001g0113 a0001c0001t0001g0120 others(1): Show |
5 | HG01074.hp2 HG01099.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.970-332C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 8/10 | chr20 | 35124366 | |||||||
| chr20:35124534 | T | C | 1 | a0001c0001t0001g0192 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.970-500A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 8/10 | chr20 | 35124534 | |||||||
| chr20:35124724 | T | C | 1 | a0001c0001t0001g0136 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.970-690A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 8/10 | chr20 | 35124724 | |||||||
| chr20:35125019 | A | G | 1 | a0001c0002t0001g0180 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.970-985T>C | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 8/10 | chr20 | 35125019 | |||||||
| chr20:35125078 | C | A | 1 | a0001c0001t0001g0192 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.970-1044G>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 8/10 | chr20 | 35125078 | |||||||
| chr20:35125112 | C | T | 118 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(115): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.970-1078G>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 8/10 | chr20 | 35125112 | |||||||
| chr20:35125201 | C | CT | 5 | a0001c0001t0001g0029 a0001c0001t0001g0101 a0001c0001t0001g0113 others(2): Show |
6 | HG01074.hp2 HG01175.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.969+1049dupA | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 8/10 | chr20 | 35125201 | |||||||
| chr20:35125201 | CT | C | 89 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0014 others(86): Show |
140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.969+1049delA | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 8/10 | chr20 | 35125201 | |||||||
| chr20:35125201 | CTT | C | 24 | a0001c0001t0001g0008 a0001c0001t0001g0073 a0001c0001t0001g0084 others(21): Show |
37 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.969+1048_969+1049d others(4): Show |
EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 8/10 | chr20 | 35125201 | |||||||
| chr20:35125237 | G | A | 92 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(89): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.969+1014C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 8/10 | chr20 | 35125237 | |||||||
| chr20:35125252 | A | G | 118 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(115): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.969+999T>C | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 8/10 | chr20 | 35125252 | |||||||
| chr20:35125446 | G | A | 3 | a0003c0004t0001g0011 a0003c0004t0001g0034 a0003c0004t0001g0169 |
7 | HG00738.hp1 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.969+805C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 8/10 | chr20 | 35125446 | |||||||
| chr20:35125448 | A | G | 92 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(89): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.969+803T>C | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 8/10 | chr20 | 35125448 | |||||||
| chr20:35125460 | C | A | 4 | a0001c0002t0001g0180 a0001c0002t0001g0181 a0001c0002t0001g0182 others(1): Show |
4 | HG02717.hp2 HG02723.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.969+791G>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 8/10 | chr20 | 35125460 | |||||||
| chr20:35125481 | T | C | 1 | a0001c0001t0001g0192 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.969+770A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 8/10 | chr20 | 35125481 | |||||||
| chr20:35125679 | C | A | 27 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0012 others(24): Show |
45 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.969+572G>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 8/10 | chr20 | 35125679 | |||||||
| chr20:35125705 | G | A | 2 | a0001c0001t0001g0077 a0001c0001t0001g0191 |
2 | NA18970.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.969+546C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 8/10 | chr20 | 35125705 | |||||||
| chr20:35125747 | T | C | 3 | a0001c0002t0001g0139 a0001c0002t0001g0184 a0007c0010t0001g0131 |
3 | HG02486.hp1 HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.969+504A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 8/10 | chr20 | 35125747 | |||||||
| chr20:35125836 | G | A | 92 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(89): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.969+415C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 8/10 | chr20 | 35125836 | |||||||
| chr20:35125871 | T | C | 118 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(115): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.969+380A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 8/10 | chr20 | 35125871 | |||||||
| chr20:35126160 | T | C | 157 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(154): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.969+91A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 8/10 | chr20 | 35126160 | |||||||
| chr20:35126172 | A | C | 157 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(154): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.969+79T>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 8/10 | chr20 | 35126172 | |||||||
| chr20:35126384 | G | A | 92 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(89): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.845-9C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35126384 | |||||||
| chr20:35126399 | T | C | 1 | a0001c0001t0001g0165 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.845-24A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35126399 | |||||||
| chr20:35126566 | C | T | 5 | a0001c0001t0001g0147 a0001c0001t0001g0172 a0001c0001t0001g0173 others(2): Show |
6 | HG00323.hp1 NA18612.hp1 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.845-191G>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35126566 | |||||||
| chr20:35126585 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.845-210C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35126585 | |||||||
| chr20:35126783 | A | G | 13 | a0001c0001t0001g0015 a0001c0001t0001g0037 a0001c0001t0001g0111 others(10): Show |
16 | HG00323.hp2 HG01261.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.845-408T>C | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35126783 | |||||||
| chr20:35126908 | A | G | 1 | a0002c0003t0001g0151 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.845-533T>C | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35126908 | |||||||
| chr20:35127002 | T | C | 93 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(90): Show |
148 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.845-627A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35127002 | |||||||
| chr20:35127171 | G | A | 2 | a0001c0001t0001g0035 a0001c0001t0001g0108 |
3 | HG02622.hp2 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.845-796C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35127171 | |||||||
| chr20:35127264 | G | A | 93 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(90): Show |
148 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.845-889C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35127264 | |||||||
| chr20:35127481 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.845-1106C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35127481 | |||||||
| chr20:35127621 | T | C | 3 | a0001c0002t0001g0139 a0001c0002t0001g0184 a0007c0010t0001g0131 |
3 | HG02486.hp1 HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.845-1246A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35127621 | |||||||
| chr20:35127763 | A | G | 26 | a0001c0002t0001g0003 a0001c0002t0001g0016 a0001c0002t0001g0107 others(23): Show |
35 | HG00741.hp1 HG01109.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.845-1388T>C | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35127763 | |||||||
| chr20:35127789 | T | C | 26 | a0001c0002t0001g0003 a0001c0002t0001g0016 a0001c0002t0001g0107 others(23): Show |
35 | HG00741.hp1 HG01109.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.845-1414A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35127789 | |||||||
| chr20:35127883 | G | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0052 |
4 | HG02572.hp1 HG02895.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.845-1508C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35127883 | |||||||
| chr20:35127919 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.845-1544G>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35127919 | |||||||
| chr20:35127974 | G | T | 92 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(89): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.845-1599C>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35127974 | |||||||
| chr20:35128026 | T | A | 1 | a0001c0001t0001g0187 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.845-1651A>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35128026 | |||||||
| chr20:35128041 | G | A | 5 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0199 others(2): Show |
5 | NA18966.hp1 NA18994.hp1 NA19059.hp2 others(2): Show |
intron_variant | MODIFIER | c.845-1666C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35128041 | |||||||
| chr20:35128042 | C | T | 1 | a0001c0001t0001g0021 | 2 | HG00673.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.845-1667G>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35128042 | |||||||
| chr20:35128111 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.845-1736G>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35128111 | |||||||
| chr20:35128112 | G | A | 1 | a0001c0002t0001g0183 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.845-1737C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35128112 | |||||||
| chr20:35128113 | T | C | 1 | a0001c0001t0001g0084 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.845-1738A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35128113 | |||||||
| chr20:35128150 | G | C | 1 | a0001c0001t0001g0049 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.845-1775C>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35128150 | |||||||
| chr20:35128151 | C | T | 1 | a0001c0001t0001g0049 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.845-1776G>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35128151 | |||||||
| chr20:35128199 | G | A | 8 | a0001c0002t0001g0107 a0001c0002t0001g0129 a0001c0002t0001g0130 others(5): Show |
8 | HG00741.hp1 HG01884.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.845-1824C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35128199 | |||||||
| chr20:35128254 | GCGCCTGT others(740): Show |
G | 13 | a0001c0001t0001g0015 a0001c0001t0001g0037 a0001c0001t0001g0111 others(10): Show |
16 | HG00323.hp2 HG01261.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.845-2626_845-1880d others(2): Show |
EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35128254 | |||||||
| chr20:35128343 | A | G | 1 | a0002c0003t0001g0024 | 2 | HG00609.hp2 HG00621.hp2 |
intron_variant | MODIFIER | c.845-1968T>C | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35128343 | |||||||
| chr20:35128460 | A | G | 157 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(154): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.845-2085T>C | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35128460 | |||||||
| chr20:35128497 | C | T | 1 | a0001c0002t0001g0133 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.845-2122G>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35128497 | |||||||
| chr20:35128564 | C | CT | 66 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0014 others(63): Show |
103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.845-2190dupA | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35128564 | |||||||
| chr20:35128565 | T | TA | 39 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0013 others(36): Show |
57 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.845-2191dupT | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35128565 | |||||||
| chr20:35128565 | TA | T | 6 | a0001c0001t0001g0210 a0001c0001t0001g0215 a0001c0001t0001g0217 others(3): Show |
6 | HG02486.hp1 HG02559.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.845-2191delT | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35128565 | |||||||
| chr20:35128566 | A | T | 2 | a0001c0001t0001g0028 a0001c0001t0001g0059 |
2 | HG01168.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.845-2191T>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35128566 | |||||||
| chr20:35128795 | G | A | 161 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(158): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.845-2420C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35128795 | |||||||
| chr20:35128837 | A | T | 5 | a0001c0001t0001g0001 a0001c0001t0001g0073 a0001c0001t0001g0080 others(2): Show |
9 | HG00438.hp1 HG00597.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.845-2462T>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35128837 | |||||||
| chr20:35128839 | A | G | 1 | a0001c0001t0001g0001 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.845-2464T>C | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35128839 | |||||||
| chr20:35128876 | T | C | 4 | a0001c0002t0001g0168 a0003c0004t0001g0011 a0003c0004t0001g0034 others(1): Show |
8 | HG00738.hp1 HG01167.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.845-2501A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35128876 | |||||||
| chr20:35128936 | C | T | 157 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(154): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.845-2561G>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35128936 | |||||||
| chr20:35128965 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.845-2590G>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35128965 | |||||||
| chr20:35129041 | G | A | 4 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0220 others(1): Show |
4 | HG02486.hp1 HG02559.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.844+2601C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35129041 | |||||||
| chr20:35129276 | G | T | 1 | a0001c0001t0001g0167 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.844+2366C>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35129276 | |||||||
| chr20:35129401 | T | C | 1 | a0001c0001t0001g0030 | 2 | HG02602.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.844+2241A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35129401 | |||||||
| chr20:35129442 | G | A | 53 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(50): Show |
74 | HG00323.hp2 HG00738.hp1 HG01074.hp2 others(71): Show |
intron_variant | MODIFIER | c.844+2200C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35129442 | |||||||
| chr20:35129570 | CA | C | 83 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(80): Show |
113 | HG00323.hp2 HG00738.hp1 HG00741.hp1 others(110): Show |
intron_variant | MODIFIER | c.844+2071delT | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35129570 | |||||||
| chr20:35129625 | T | C | 1 | a0001c0001t0001g0206 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.844+2017A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35129625 | |||||||
| chr20:35129645 | G | A | 1 | a0001c0001t0001g0075 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.844+1997C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35129645 | |||||||
| chr20:35129653 | A | G | 1 | a0001c0001t0001g0199 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.844+1989T>C | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35129653 | |||||||
| chr20:35129977 | A | T | 1 | a0001c0001t0001g0033 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.844+1665T>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35129977 | |||||||
| chr20:35130180 | A | G | 1 | a0001c0002t0001g0138 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.844+1462T>C | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35130180 | |||||||
| chr20:35130184 | T | C | 174 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(171): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.844+1458A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35130184 | |||||||
| chr20:35130199 | T | C | 1 | a0001c0001t0001g0042 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.844+1443A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35130199 | |||||||
| chr20:35130254 | G | C | 2 | a0001c0001t0001g0013 a0001c0001t0001g0052 |
4 | HG02572.hp1 HG02895.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.844+1388C>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35130254 | |||||||
| chr20:35130695 | T | C | 4 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0220 others(1): Show |
4 | HG02486.hp1 HG02559.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.844+947A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35130695 | |||||||
| chr20:35130826 | C | T | 25 | a0001c0001t0001g0166 a0001c0002t0001g0003 a0001c0002t0001g0016 others(22): Show |
34 | HG00741.hp1 HG01109.hp1 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.844+816G>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35130826 | |||||||
| chr20:35130903 | G | A | 174 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(171): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.844+739C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35130903 | |||||||
| chr20:35130971 | T | G | 4 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0220 others(1): Show |
4 | HG02486.hp1 HG02559.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.844+671A>C | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35130971 | |||||||
| chr20:35131010 | T | C | 23 | a0001c0002t0001g0003 a0001c0002t0001g0016 a0001c0002t0001g0107 others(20): Show |
32 | HG00741.hp1 HG01109.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.844+632A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35131010 | |||||||
| chr20:35131161 | C | T | 2 | a0001c0001t0001g0013 a0001c0001t0001g0052 |
4 | HG02572.hp1 HG02895.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.844+481G>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35131161 | |||||||
| chr20:35131190 | C | G | 78 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(75): Show |
108 | HG00323.hp2 HG00738.hp1 HG00741.hp1 others(105): Show |
intron_variant | MODIFIER | c.844+452G>C | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35131190 | |||||||
| chr20:35131215 | G | GGC | 3 | a0001c0001t0001g0038 a0001c0001t0001g0197 a0001c0001t0001g0205 |
4 | NA18941.hp2 NA18955.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.844+425_844+426dup others(2): Show |
EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35131215 | |||||||
| chr20:35131341 | C | T | 14 | a0001c0002t0001g0003 a0001c0002t0001g0016 a0001c0002t0001g0138 others(11): Show |
23 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.844+301G>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35131341 | |||||||
| chr20:35131379 | C | T | 4 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0220 others(1): Show |
4 | HG02486.hp1 HG02559.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.844+263G>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35131379 | |||||||
| chr20:35131380 | G | A | 24 | a0001c0001t0001g0084 a0001c0001t0001g0091 a0001c0001t0001g0147 others(21): Show |
33 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.844+262C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35131380 | |||||||
| chr20:35131597 | G | A | 78 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(75): Show |
108 | HG00323.hp2 HG00738.hp1 HG00741.hp1 others(105): Show |
intron_variant | MODIFIER | c.844+45C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 7/10 | chr20 | 35131597 | |||||||
| chr20:35131884 | T | C | 78 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(75): Show |
108 | HG00323.hp2 HG00738.hp1 HG00741.hp1 others(105): Show |
intron_variant | MODIFIER | c.703-101A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 6/10 | chr20 | 35131884 | |||||||
| chr20:35131929 | G | T | 1 | a0001c0002t0001g0186 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.703-146C>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 6/10 | chr20 | 35131929 | |||||||
| chr20:35132142 | T | C | 11 | a0001c0001t0001g0015 a0001c0001t0001g0037 a0001c0001t0001g0140 others(8): Show |
14 | HG00323.hp2 HG01261.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.703-359A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 6/10 | chr20 | 35132142 | |||||||
| chr20:35132230 | C | A | 53 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(50): Show |
74 | HG00323.hp2 HG00738.hp1 HG01074.hp2 others(71): Show |
intron_variant | MODIFIER | c.703-447G>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 6/10 | chr20 | 35132230 | |||||||
| chr20:35132354 | G | T | 45 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0015 others(42): Show |
59 | HG00323.hp2 HG00738.hp1 HG01074.hp2 others(56): Show |
intron_variant | MODIFIER | c.703-571C>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 6/10 | chr20 | 35132354 | |||||||
| chr20:35132360 | T | C | 2 | a0001c0001t0001g0187 a0001c0002t0001g0139 |
2 | HG02258.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.703-577A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 6/10 | chr20 | 35132360 | |||||||
| chr20:35132437 | G | T | 79 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(76): Show |
109 | HG00323.hp2 HG00738.hp1 HG00741.hp1 others(106): Show |
intron_variant | MODIFIER | c.703-654C>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 6/10 | chr20 | 35132437 | |||||||
| chr20:35132583 | G | A | 12 | a0001c0002t0001g0003 a0001c0002t0001g0016 a0001c0002t0001g0138 others(9): Show |
21 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.703-800C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 6/10 | chr20 | 35132583 | |||||||
| chr20:35132653 | C | CA | 77 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0014 others(74): Show |
122 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.703-871dupT | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 6/10 | chr20 | 35132653 | |||||||
| chr20:35132691 | T | C | 44 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0033 others(41): Show |
64 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.703-908A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 6/10 | chr20 | 35132691 | |||||||
| chr20:35132780 | C | G | 1 | a0001c0001t0001g0187 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.703-997G>C | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 6/10 | chr20 | 35132780 | |||||||
| chr20:35132786 | C | A | 1 | a0001c0001t0001g0119 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.703-1003G>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 6/10 | chr20 | 35132786 | |||||||
| chr20:35132789 | T | C | 41 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(38): Show |
55 | HG00741.hp1 HG01074.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.703-1006A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 6/10 | chr20 | 35132789 | |||||||
| chr20:35132923 | C | T | 14 | a0001c0001t0001g0013 a0001c0001t0001g0052 a0001c0001t0001g0108 others(11): Show |
16 | HG00741.hp1 HG01884.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.703-1140G>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 6/10 | chr20 | 35132923 | |||||||
| chr20:35133040 | C | T | 11 | a0001c0001t0001g0108 a0001c0002t0001g0107 a0001c0002t0001g0128 others(8): Show |
11 | HG00741.hp1 HG01891.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.703-1257G>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 6/10 | chr20 | 35133040 | |||||||
| chr20:35133117 | T | C | 26 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0029 others(23): Show |
38 | HG01074.hp2 HG01081.hp2 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.703-1334A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 6/10 | chr20 | 35133117 | |||||||
| chr20:35133207 | C | T | 1 | a0001c0001t0001g0198 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.703-1424G>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 6/10 | chr20 | 35133207 | |||||||
| chr20:35133249 | C | T | 12 | a0001c0001t0001g0108 a0001c0002t0001g0107 a0001c0002t0001g0128 others(9): Show |
12 | HG00741.hp1 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.703-1466G>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 6/10 | chr20 | 35133249 | |||||||
| chr20:35133371 | T | C | 1 | a0001c0001t0001g0109 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.702+1367A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 6/10 | chr20 | 35133371 | |||||||
| chr20:35133458 | C | G | 29 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(26): Show |
43 | HG01074.hp2 HG01081.hp2 HG01099.hp1 others(40): Show |
intron_variant | MODIFIER | c.702+1280G>C | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 6/10 | chr20 | 35133458 | |||||||
| chr20:35133461 | C | CG | 9 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0025 others(6): Show |
15 | HG01934.hp1 HG01943.hp1 HG01993.hp2 others(12): Show |
intron_variant | MODIFIER | c.702+1276dupC | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 6/10 | chr20 | 35133461 | |||||||
| chr20:35133524 | T | C | 1 | a0001c0001t0001g0077 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.702+1214A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 6/10 | chr20 | 35133524 | |||||||
| chr20:35133530 | G | A | 29 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(26): Show |
43 | HG01074.hp2 HG01081.hp2 HG01099.hp1 others(40): Show |
intron_variant | MODIFIER | c.702+1208C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 6/10 | chr20 | 35133530 | |||||||
| chr20:35133536 | G | A | 1 | a0001c0001t0001g0188 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.702+1202C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 6/10 | chr20 | 35133536 | |||||||
| chr20:35133553 | A | G | 41 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(38): Show |
55 | HG00741.hp1 HG01074.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.702+1185T>C | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 6/10 | chr20 | 35133553 | |||||||
| chr20:35133623 | C | T | 27 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0029 others(24): Show |
39 | HG01074.hp2 HG01081.hp2 HG01099.hp1 others(36): Show |
intron_variant | MODIFIER | c.702+1115G>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 6/10 | chr20 | 35133623 | |||||||
| chr20:35133668 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.702+1070A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 6/10 | chr20 | 35133668 | |||||||
| chr20:35133742 | C | T | 12 | a0001c0001t0001g0108 a0001c0002t0001g0107 a0001c0002t0001g0128 others(9): Show |
12 | HG00741.hp1 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.702+996G>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 6/10 | chr20 | 35133742 | |||||||
| chr20:35133746 | C | T | 4 | a0001c0001t0001g0140 a0001c0001t0001g0153 a0001c0001t0001g0154 others(1): Show |
4 | HG01261.hp2 HG02615.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.702+992G>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 6/10 | chr20 | 35133746 | |||||||
| chr20:35133747 | G | A | 12 | a0001c0001t0001g0108 a0001c0002t0001g0107 a0001c0002t0001g0128 others(9): Show |
12 | HG00741.hp1 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.702+991C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 6/10 | chr20 | 35133747 | |||||||
| chr20:35133952 | A | G | 1 | a0001c0001t0001g0062 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.702+786T>C | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 6/10 | chr20 | 35133952 | |||||||
| chr20:35133980 | A | G | 1 | a0005c0011t0001g0061 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.702+758T>C | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 6/10 | chr20 | 35133980 | |||||||
| chr20:35133988 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.702+750A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 6/10 | chr20 | 35133988 | |||||||
| chr20:35134187 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.702+551A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 6/10 | chr20 | 35134187 | |||||||
| chr20:35134354 | G | T | 1 | a0001c0001t0001g0218 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.702+384C>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 6/10 | chr20 | 35134354 | |||||||
| chr20:35134387 | G | C | 1 | a0001c0001t0001g0079 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.702+351C>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 6/10 | chr20 | 35134387 | |||||||
| chr20:35134423 | G | T | 1 | a0001c0002t0001g0139 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.702+315C>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 6/10 | chr20 | 35134423 | |||||||
| chr20:35134470 | C | T | 3 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 |
3 | HG02630.hp2 HG02809.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.702+268G>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 6/10 | chr20 | 35134470 | |||||||
| chr20:35134471 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.702+267C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 6/10 | chr20 | 35134471 | |||||||
| chr20:35134665 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.702+73T>C | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 6/10 | chr20 | 35134665 | |||||||
| chr20:35135060 | A | G | 41 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(38): Show |
55 | HG00741.hp1 HG01074.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.491-111T>C | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 5/10 | chr20 | 35135060 | |||||||
| chr20:35135085 | A | G | 1 | a0001c0001t0001g0197 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.491-136T>C | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 5/10 | chr20 | 35135085 | |||||||
| chr20:35135088 | A | AT | 80 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0014 others(77): Show |
127 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.491-140dupA | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 5/10 | chr20 | 35135088 | |||||||
| chr20:35135360 | TC | T | 3 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0002t0001g0219 |
3 | HG02258.hp1 HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.491-412delG | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 5/10 | chr20 | 35135360 | |||||||
| chr20:35135479 | T | G | 2 | a0001c0001t0001g0013 a0001c0001t0001g0052 |
4 | HG02572.hp1 HG02895.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.491-530A>C | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 5/10 | chr20 | 35135479 | |||||||
| chr20:35135628 | G | T | 1 | a0001c0002t0001g0139 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.491-679C>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 5/10 | chr20 | 35135628 | |||||||
| chr20:35135638 | G | A | 3 | a0001c0001t0001g0080 a0002c0003t0001g0151 a0002c0003t0001g0152 |
3 | HG01261.hp1 HG02602.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.491-689C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 5/10 | chr20 | 35135638 | |||||||
| chr20:35135652 | A | AAATAAT | 41 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(38): Show |
55 | HG00741.hp1 HG01074.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.491-709_491-704dup others(6): Show |
EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 5/10 | chr20 | 35135652 | |||||||
| chr20:35135927 | G | A | 1 | a0001c0002t0001g0184 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.491-978C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 5/10 | chr20 | 35135927 | |||||||
| chr20:35136007 | T | C | 177 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(174): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.491-1058A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 5/10 | chr20 | 35136007 | |||||||
| chr20:35136418 | C | T | 26 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0029 others(23): Show |
38 | HG01074.hp2 HG01081.hp2 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.490+1462G>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 5/10 | chr20 | 35136418 | |||||||
| chr20:35136549 | G | C | 1 | a0001c0001t0001g0207 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.490+1331C>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 5/10 | chr20 | 35136549 | |||||||
| chr20:35136754 | G | GA | 70 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0014 others(67): Show |
117 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.490+1125dupT | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 5/10 | chr20 | 35136754 | |||||||
| chr20:35136754 | G | GAA | 10 | a0001c0001t0001g0086 a0001c0001t0001g0089 a0001c0001t0001g0101 others(7): Show |
11 | HG00609.hp2 HG00621.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.490+1124_490+1125d others(4): Show |
EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 5/10 | chr20 | 35136754 | |||||||
| chr20:35136754 | GA | G | 21 | a0001c0001t0001g0013 a0001c0001t0001g0052 a0001c0001t0001g0108 others(18): Show |
23 | HG00323.hp2 HG00741.hp1 HG01257.hp1 others(20): Show |
intron_variant | MODIFIER | c.490+1125delT | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 5/10 | chr20 | 35136754 | |||||||
| chr20:35136754 | GAA | G | 26 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0029 others(23): Show |
38 | HG01074.hp2 HG01081.hp2 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.490+1124_490+1125d others(4): Show |
EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 5/10 | chr20 | 35136754 | |||||||
| chr20:35136919 | T | C | 1 | a0001c0001t0001g0090 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.490+961A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 5/10 | chr20 | 35136919 | |||||||
| chr20:35136955 | A | G | 41 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(38): Show |
55 | HG00741.hp1 HG01074.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.490+925T>C | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 5/10 | chr20 | 35136955 | |||||||
| chr20:35137017 | C | A | 3 | a0001c0001t0002g0006 a0001c0001t0002g0040 a0001c0001t0002g0041 |
7 | HG02818.hp1 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.490+863G>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 5/10 | chr20 | 35137017 | |||||||
| chr20:35137151 | C | A | 1 | a0001c0001t0001g0170 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.490+729G>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 5/10 | chr20 | 35137151 | |||||||
| chr20:35137183 | C | T | 1 | a0001c0002t0001g0178 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.490+697G>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 5/10 | chr20 | 35137183 | |||||||
| chr20:35137404 | A | G | 41 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(38): Show |
55 | HG00741.hp1 HG01074.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.490+476T>C | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 5/10 | chr20 | 35137404 | |||||||
| chr20:35137610 | A | T | 11 | a0001c0001t0001g0108 a0001c0002t0001g0107 a0001c0002t0001g0128 others(8): Show |
11 | HG00741.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.490+270T>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 5/10 | chr20 | 35137610 | |||||||
| chr20:35137684 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.490+196G>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 5/10 | chr20 | 35137684 | |||||||
| chr20:35138347 | T | C | 41 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(38): Show |
55 | HG00741.hp1 HG01074.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.365-342A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35138347 | |||||||
| chr20:35138356 | C | T | 12 | a0001c0002t0001g0003 a0001c0002t0001g0016 a0001c0002t0001g0138 others(9): Show |
21 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.365-351G>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35138356 | |||||||
| chr20:35138520 | A | G | 164 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(161): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.365-515T>C | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35138520 | |||||||
| chr20:35138580 | C | CT | 8 | a0001c0001t0001g0013 a0001c0001t0001g0052 a0001c0001t0001g0085 others(5): Show |
10 | HG01099.hp1 HG02145.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.365-576dupA | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35138580 | |||||||
| chr20:35138648 | C | T | 43 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0033 others(40): Show |
62 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.365-643G>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35138648 | |||||||
| chr20:35138666 | G | A | 1 | a0001c0002t0001g0134 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.365-661C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35138666 | |||||||
| chr20:35138684 | G | A | 1 | a0001c0001t0001g0035 | 2 | HG02622.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.365-679C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35138684 | |||||||
| chr20:35138733 | C | T | 23 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0029 others(20): Show |
34 | HG01074.hp2 HG01081.hp2 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.365-728G>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35138733 | |||||||
| chr20:35138745 | A | T | 1 | a0007c0010t0001g0131 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.365-740T>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35138745 | |||||||
| chr20:35138828 | C | T | 29 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(26): Show |
43 | HG01074.hp2 HG01081.hp2 HG01099.hp1 others(40): Show |
intron_variant | MODIFIER | c.365-823G>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35138828 | |||||||
| chr20:35138930 | A | G | 1 | a0001c0001t0001g0193 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.365-925T>C | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35138930 | |||||||
| chr20:35139037 | C | A | 1 | a0001c0002t0001g0181 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.365-1032G>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35139037 | |||||||
| chr20:35139070 | C | T | 29 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(26): Show |
43 | HG01074.hp2 HG01081.hp2 HG01099.hp1 others(40): Show |
intron_variant | MODIFIER | c.365-1065G>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35139070 | |||||||
| chr20:35139157 | C | T | 1 | a0002c0003t0001g0143 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.365-1152G>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35139157 | |||||||
| chr20:35139220 | A | G | 41 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(38): Show |
55 | HG00741.hp1 HG01074.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.365-1215T>C | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35139220 | |||||||
| chr20:35139247 | A | G | 177 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(174): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.365-1242T>C | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35139247 | |||||||
| chr20:35139318 | T | C | 177 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(174): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.365-1313A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35139318 | |||||||
| chr20:35139349 | C | CA | 18 | a0001c0001t0001g0025 a0001c0001t0001g0038 a0001c0001t0001g0039 others(15): Show |
30 | HG01109.hp1 HG01891.hp2 HG02027.hp1 others(27): Show |
intron_variant | MODIFIER | c.365-1345dupT | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35139349 | |||||||
| chr20:35139349 | C | CAA | 12 | a0001c0001t0001g0108 a0001c0002t0001g0107 a0001c0002t0001g0128 others(9): Show |
12 | HG01884.hp2 HG01891.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.365-1346_365-1345d others(4): Show |
EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35139349 | |||||||
| chr20:35139349 | CA | C | 28 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(25): Show |
42 | HG01074.hp2 HG01081.hp2 HG01099.hp1 others(39): Show |
intron_variant | MODIFIER | c.365-1345delT | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35139349 | |||||||
| chr20:35139473 | AC | A | 41 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0033 others(38): Show |
60 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.365-1469delG | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35139473 | |||||||
| chr20:35139628 | C | T | 17 | a0001c0001t0001g0008 a0001c0001t0001g0147 a0001c0001t0001g0148 others(14): Show |
29 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.365-1623G>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35139628 | |||||||
| chr20:35139708 | T | C | 1 | a0002c0003t0001g0160 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.365-1703A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35139708 | |||||||
| chr20:35139851 | CA | C | 75 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0014 others(72): Show |
118 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.365-1847delT | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35139851 | |||||||
| chr20:35139975 | A | T | 1 | a0001c0002t0001g0139 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.365-1970T>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35139975 | |||||||
| chr20:35139976 | G | T | 41 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(38): Show |
55 | HG00741.hp1 HG01074.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.365-1971C>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35139976 | |||||||
| chr20:35140095 | G | T | 2 | a0001c0001t0001g0191 a0001c0001t0001g0192 |
2 | NA18970.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.365-2090C>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35140095 | |||||||
| chr20:35140131 | A | G | 1 | a0001c0001t0001g0218 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.365-2126T>C | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35140131 | |||||||
| chr20:35140187 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.365-2182T>C | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35140187 | |||||||
| chr20:35140210 | C | T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0031 a0001c0001t0001g0110 others(2): Show |
11 | HG02015.hp2 HG02027.hp2 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.364+2163G>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35140210 | |||||||
| chr20:35140223 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.364+2150G>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35140223 | |||||||
| chr20:35140226 | G | A | 4 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0220 others(1): Show |
4 | HG02258.hp1 HG02559.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.364+2147C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35140226 | |||||||
| chr20:35140292 | T | C | 1 | a0001c0002t0001g0139 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.364+2081A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35140292 | |||||||
| chr20:35140399 | G | A | 10 | a0001c0001t0001g0108 a0001c0002t0001g0107 a0001c0002t0001g0128 others(7): Show |
10 | HG00741.hp1 HG01884.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.364+1974C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35140399 | |||||||
| chr20:35140432 | C | T | 23 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0029 others(20): Show |
34 | HG01074.hp2 HG01081.hp2 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.364+1941G>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35140432 | |||||||
| chr20:35140560 | G | A | 1 | a0001c0001t0001g0084 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.364+1813C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35140560 | |||||||
| chr20:35140791 | G | A | 1 | a0001c0001t0001g0172 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.364+1582C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35140791 | |||||||
| chr20:35140875 | T | C | 30 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0033 others(27): Show |
45 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.364+1498A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35140875 | |||||||
| chr20:35140895 | G | A | 1 | a0007c0010t0001g0131 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.364+1478C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35140895 | |||||||
| chr20:35140946 | C | A | 1 | a0001c0002t0001g0139 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.364+1427G>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35140946 | |||||||
| chr20:35141119 | C | CA | 74 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0012 others(71): Show |
110 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.364+1253dupT | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35141119 | |||||||
| chr20:35141119 | C | CAA | 12 | a0001c0001t0001g0017 a0001c0001t0001g0039 a0001c0001t0001g0091 others(9): Show |
15 | HG02055.hp1 HG02080.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.364+1252_364+1253d others(4): Show |
EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35141119 | |||||||
| chr20:35141119 | CA | C | 10 | a0001c0001t0001g0047 a0001c0001t0001g0050 a0001c0001t0001g0058 others(7): Show |
10 | HG01081.hp2 HG01099.hp2 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.364+1253delT | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35141119 | |||||||
| chr20:35141119 | CAAAAAAA others(7): Show |
C | 3 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 |
3 | HG02630.hp2 HG02809.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.364+1240_364+1253d others(16): Show |
EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35141119 | |||||||
| chr20:35141119 | CAAAAAAA others(10): Show |
C | 2 | a0001c0001t0001g0049 a0001c0001t0001g0109 |
2 | NA18940.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.364+1237_364+1253d others(19): Show |
EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35141119 | |||||||
| chr20:35141131 | A | C | 1 | a0001c0001t0001g0172 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.364+1242T>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35141131 | |||||||
| chr20:35141344 | T | G | 42 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0012 others(39): Show |
65 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.364+1029A>C | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35141344 | |||||||
| chr20:35141384 | A | C | 1 | a0003c0008t0001g0162 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.364+989T>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35141384 | |||||||
| chr20:35141473 | T | G | 1 | a0001c0002t0001g0139 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.364+900A>C | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35141473 | |||||||
| chr20:35141477 | G | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0052 |
4 | HG02572.hp1 HG02895.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.364+896C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35141477 | |||||||
| chr20:35141571 | T | C | 1 | a0001c0007t0001g0106 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.364+802A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35141571 | |||||||
| chr20:35141589 | A | G | 1 | a0001c0001t0001g0190 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.364+784T>C | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35141589 | |||||||
| chr20:35141593 | T | C | 1 | a0001c0001t0001g0190 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.364+780A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35141593 | |||||||
| chr20:35141639 | A | C | 40 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(37): Show |
54 | HG00741.hp1 HG01074.hp2 HG01081.hp2 others(51): Show |
intron_variant | MODIFIER | c.364+734T>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35141639 | |||||||
| chr20:35141674 | C | G | 41 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(38): Show |
55 | HG00741.hp1 HG01074.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.364+699G>C | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35141674 | |||||||
| chr20:35141676 | G | A | 41 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(38): Show |
55 | HG00741.hp1 HG01074.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.364+697C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35141676 | |||||||
| chr20:35141738 | T | TCCAATTC others(15): Show |
1 | a0007c0010t0001g0131 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.364+613_364+634dup others(22): Show |
EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35141738 | |||||||
| chr20:35141786 | C | A | 41 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(38): Show |
55 | HG00741.hp1 HG01074.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.364+587G>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35141786 | |||||||
| chr20:35141787 | C | A | 41 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(38): Show |
55 | HG00741.hp1 HG01074.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.364+586G>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35141787 | |||||||
| chr20:35141788 | A | G | 41 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(38): Show |
55 | HG00741.hp1 HG01074.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.364+585T>C | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35141788 | |||||||
| chr20:35141789 | C | G | 41 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(38): Show |
55 | HG00741.hp1 HG01074.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.364+584G>C | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35141789 | |||||||
| chr20:35141791 | T | C | 41 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(38): Show |
55 | HG00741.hp1 HG01074.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.364+582A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35141791 | |||||||
| chr20:35141792 | G | C | 41 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(38): Show |
55 | HG00741.hp1 HG01074.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.364+581C>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35141792 | |||||||
| chr20:35141793 | G | C | 41 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(38): Show |
55 | HG00741.hp1 HG01074.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.364+580C>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35141793 | |||||||
| chr20:35141794 | G | A | 41 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(38): Show |
55 | HG00741.hp1 HG01074.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.364+579C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35141794 | |||||||
| chr20:35141977 | G | A | 1 | a0001c0002t0001g0184 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.364+396C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35141977 | |||||||
| chr20:35142232 | G | C | 6 | a0001c0001t0001g0012 a0001c0001t0001g0036 a0001c0001t0001g0209 others(3): Show |
10 | HG00558.hp1 HG02027.hp1 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.364+141C>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35142232 | |||||||
| chr20:35142235 | G | A | 1 | a0002c0003t0001g0161 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.364+138C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35142235 | |||||||
| chr20:35142247 | C | T | 1 | a0001c0002t0001g0139 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.364+126G>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35142247 | |||||||
| chr20:35142263 | C | G | 1 | a0001c0001t0001g0057 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.364+110G>C | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 4/10 | chr20 | 35142263 | |||||||
| chr20:35142527 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.259-49C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 3/10 | chr20 | 35142527 | |||||||
| chr20:35142575 | C | T | 1 | a0001c0001t0001g0214 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.259-97G>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 3/10 | chr20 | 35142575 | |||||||
| chr20:35142584 | C | T | 30 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0033 others(27): Show |
45 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.259-106G>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 3/10 | chr20 | 35142584 | |||||||
| chr20:35142661 | A | G | 146 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(143): Show |
215 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.259-183T>C | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 3/10 | chr20 | 35142661 | |||||||
| chr20:35142746 | T | A | 1 | a0001c0001t0001g0028 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.259-268A>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 3/10 | chr20 | 35142746 | |||||||
| chr20:35142775 | CG | C | 3 | a0001c0001t0002g0006 a0001c0001t0002g0040 a0001c0001t0002g0041 |
7 | HG02818.hp1 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.259-298delC | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 3/10 | chr20 | 35142775 | |||||||
| chr20:35142811 | G | A | 1 | a0001c0001t0001g0093 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.259-333C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 3/10 | chr20 | 35142811 | |||||||
| chr20:35142841 | C | T | 41 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(38): Show |
55 | HG00741.hp1 HG01074.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.259-363G>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 3/10 | chr20 | 35142841 | |||||||
| chr20:35142888 | C | CCT | 41 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(38): Show |
55 | HG00741.hp1 HG01074.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.259-411_259-410ins others(2): Show |
EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 3/10 | chr20 | 35142888 | |||||||
| chr20:35142956 | C | A | 13 | a0001c0001t0001g0014 a0001c0001t0001g0047 a0001c0001t0001g0094 others(10): Show |
15 | HG00099.hp1 HG00738.hp2 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.259-478G>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 3/10 | chr20 | 35142956 | |||||||
| chr20:35143041 | C | T | 1 | a0001c0001t0001g0053 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.259-563G>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 3/10 | chr20 | 35143041 | |||||||
| chr20:35143042 | G | A | 1 | a0001c0001t0001g0105 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.259-564C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 3/10 | chr20 | 35143042 | |||||||
| chr20:35143045 | C | T | 5 | a0001c0001t0001g0187 a0001c0001t0001g0217 a0001c0001t0001g0218 others(2): Show |
5 | HG02258.hp1 HG02258.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.259-567G>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 3/10 | chr20 | 35143045 | |||||||
| chr20:35143207 | G | A | 41 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(38): Show |
55 | HG00741.hp1 HG01074.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.259-729C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 3/10 | chr20 | 35143207 | |||||||
| chr20:35143219 | T | C | 1 | a0001c0001t0001g0213 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.259-741A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 3/10 | chr20 | 35143219 | |||||||
| chr20:35143442 | G | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0052 |
4 | HG02572.hp1 HG02895.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.259-964C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 3/10 | chr20 | 35143442 | |||||||
| chr20:35143447 | T | C | 3 | a0001c0001t0002g0006 a0001c0001t0002g0040 a0001c0001t0002g0041 |
7 | HG02818.hp1 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.259-969A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 3/10 | chr20 | 35143447 | |||||||
| chr20:35143519 | C | T | 5 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0188 others(2): Show |
11 | HG00408.hp2 HG02080.hp2 NA18950.hp2 others(8): Show |
intron_variant | MODIFIER | c.259-1041G>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 3/10 | chr20 | 35143519 | |||||||
| chr20:35143634 | A | T | 40 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(37): Show |
54 | HG00741.hp1 HG01074.hp2 HG01081.hp2 others(51): Show |
intron_variant | MODIFIER | c.259-1156T>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 3/10 | chr20 | 35143634 | |||||||
| chr20:35143681 | T | A | 26 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0029 others(23): Show |
38 | HG01074.hp2 HG01081.hp2 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.259-1203A>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 3/10 | chr20 | 35143681 | |||||||
| chr20:35143818 | G | A | 1 | a0002c0003t0001g0048 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.258+1161C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 3/10 | chr20 | 35143818 | |||||||
| chr20:35143822 | T | C | 41 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0012 others(38): Show |
64 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.258+1157A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 3/10 | chr20 | 35143822 | |||||||
| chr20:35144062 | C | A | 1 | a0001c0002t0001g0132 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.258+917G>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 3/10 | chr20 | 35144062 | |||||||
| chr20:35144290 | T | C | 4 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0220 others(1): Show |
4 | HG02258.hp1 HG02559.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.258+689A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 3/10 | chr20 | 35144290 | |||||||
| chr20:35144326 | A | ATATTATT others(193): Show |
1 | a0001c0001t0001g0142 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.258+652_258+653ins others(200): Show |
EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 3/10 | chr20 | 35144326 | |||||||
| chr20:35144403 | G | A | 1 | a0001c0002t0001g0139 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.258+576C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 3/10 | chr20 | 35144403 | |||||||
| chr20:35144437 | A | C | 1 | a0001c0002t0001g0139 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.258+542T>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 3/10 | chr20 | 35144437 | |||||||
| chr20:35144566 | T | G | 40 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(37): Show |
54 | HG00741.hp1 HG01074.hp2 HG01081.hp2 others(51): Show |
intron_variant | MODIFIER | c.258+413A>C | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 3/10 | chr20 | 35144566 | |||||||
| chr20:35144641 | C | T | 1 | a0001c0002t0001g0139 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.258+338G>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 3/10 | chr20 | 35144641 | |||||||
| chr20:35144774 | T | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0052 |
4 | HG02572.hp1 HG02895.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.258+205A>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 3/10 | chr20 | 35144774 | |||||||
| chr20:35144775 | T | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0052 |
4 | HG02572.hp1 HG02895.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.258+204A>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 3/10 | chr20 | 35144775 | |||||||
| chr20:35144883 | G | A | 2 | a0001c0001t0001g0172 a0001c0001t0001g0173 |
2 | NA18951.hp1 NA19059.hp1 |
intron_variant | MODIFIER | c.258+96C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 3/10 | chr20 | 35144883 | |||||||
| chr20:35145044 | G | A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0123 a0001c0001t0001g0124 |
4 | HG02027.hp2 HG02040.hp1 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.219-26C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 2/10 | chr20 | 35145044 | |||||||
| chr20:35145222 | T | A | 3 | a0001c0002t0001g0133 a0001c0002t0001g0134 a0001c0002t0001g0135 |
3 | HG00741.hp1 HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.219-204A>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 2/10 | chr20 | 35145222 | |||||||
| chr20:35145266 | C | T | 2 | a0001c0001t0001g0013 a0001c0001t0001g0052 |
4 | HG02572.hp1 HG02895.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.219-248G>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 2/10 | chr20 | 35145266 | |||||||
| chr20:35145275 | T | C | 44 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0033 others(41): Show |
64 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.219-257A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 2/10 | chr20 | 35145275 | |||||||
| chr20:35145377 | G | A | 40 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0012 others(37): Show |
63 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.219-359C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 2/10 | chr20 | 35145377 | |||||||
| chr20:35145560 | T | C | 1 | a0001c0002t0001g0186 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.219-542A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 2/10 | chr20 | 35145560 | |||||||
| chr20:35145611 | T | C | 2 | a0001c0001t0001g0035 a0001c0002t0001g0174 |
3 | HG02145.hp1 HG02622.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.219-593A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 2/10 | chr20 | 35145611 | |||||||
| chr20:35145719 | G | A | 1 | a0002c0003t0001g0175 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.219-701C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 2/10 | chr20 | 35145719 | |||||||
| chr20:35145838 | G | A | 27 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0029 others(24): Show |
38 | HG01074.hp2 HG01081.hp2 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.219-820C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 2/10 | chr20 | 35145838 | |||||||
| chr20:35145901 | C | G | 102 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(99): Show |
154 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.219-883G>C | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 2/10 | chr20 | 35145901 | |||||||
| chr20:35145959 | G | A | 1 | a0004c0013t0001g0125 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.218+866C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 2/10 | chr20 | 35145959 | |||||||
| chr20:35145990 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.218+835C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 2/10 | chr20 | 35145990 | |||||||
| chr20:35146002 | C | CA | 10 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0002t0001g0128 others(7): Show |
10 | HG00741.hp1 HG01884.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.218+822dupT | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 2/10 | chr20 | 35146002 | |||||||
| chr20:35146002 | CA | C | 12 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(9): Show |
12 | HG01081.hp1 HG01081.hp2 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.218+822delT | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 2/10 | chr20 | 35146002 | |||||||
| chr20:35146002 | CAA | C | 78 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(75): Show |
120 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.218+821_218+822del others(2): Show |
EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 2/10 | chr20 | 35146002 | |||||||
| chr20:35146002 | CAAA | C | 20 | a0001c0001t0001g0036 a0001c0001t0001g0141 a0001c0001t0001g0185 others(17): Show |
30 | HG01109.hp1 HG01515.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.218+820_218+822del others(3): Show |
EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 2/10 | chr20 | 35146002 | |||||||
| chr20:35146002 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0140 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.218+813_218+822del others(10): Show |
EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 2/10 | chr20 | 35146002 | |||||||
| chr20:35146042 | T | C | 2 | a0001c0001t0001g0136 a0001c0001t0001g0137 |
2 | HG00140.hp1 HG00280.hp2 |
intron_variant | MODIFIER | c.218+783A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 2/10 | chr20 | 35146042 | |||||||
| chr20:35146209 | A | G | 102 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(99): Show |
154 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.218+616T>C | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 2/10 | chr20 | 35146209 | |||||||
| chr20:35146284 | G | A | 1 | a0001c0001t0002g0041 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.218+541C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 2/10 | chr20 | 35146284 | |||||||
| chr20:35146373 | A | G | 1 | a0001c0001t0001g0042 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.218+452T>C | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 2/10 | chr20 | 35146373 | |||||||
| chr20:35146458 | C | G | 54 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0012 others(51): Show |
86 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.218+367G>C | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 2/10 | chr20 | 35146458 | |||||||
| chr20:35146490 | T | C | 102 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(99): Show |
154 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.218+335A>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 2/10 | chr20 | 35146490 | |||||||
| chr20:35146603 | C | T | 1 | a0001c0002t0001g0139 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.218+222G>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 2/10 | chr20 | 35146603 | |||||||
| chr20:35146661 | A | G | 44 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0033 others(41): Show |
64 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.218+164T>C | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 2/10 | chr20 | 35146661 | |||||||
| chr20:35146690 | G | A | 102 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(99): Show |
154 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.218+135C>T | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 2/10 | chr20 | 35146690 | |||||||
| chr20:35147022 | C | T | 1 | a0001c0002t0001g0138 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.108-87G>A | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 1/10 | chr20 | 35147022 | |||||||
| chr20:35147102 | G | C | 103 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(100): Show |
155 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.107+50C>G | EDEM2 | ENSG00000088298.13 | transcript | ENST00000374492.8 | protein_coding | 1/10 | chr20 | 35147102 |