Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 6785 |
| ensemblid | ENSG00000118402.6 |
| hgncid | 14415 |
| symbol | ELOVL4 |
| name | ELOVL fatty acid elongase 4 |
| refseq_nuc | NM_022726.4 |
| refseq_prot | NP_073563.1 |
| ensembl_nuc | ENST00000369816.5 |
| ensembl_prot | ENSP00000358831.4 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 79914814 |
| end | 79947553 |
| strand | - |
| ver | v1.2 |
| region | chr6:79914814-79947553 |
| region5000 | chr6:79909814-79952553 |
| regionname0 | ELOVL4_chr6_79914814_79947553 |
| regionname5000 | ELOVL4_chr6_79909814_79952553 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 314 | 258 | 78 | 55 | 90 | 10 | 23 | 68 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | MGLLD others(309): Show |
chr6 | 79909814 | 79952553 |
| a0002 | 0/0 | 314 | 95 | 18 | 13 | 42 | 2 | 20 | 34 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | MGLLD others(309): Show |
chr6 | 79909814 | 79952553 |
| a0003 | 0/0 | 314 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | MGLLD others(309): Show |
chr6 | 79909814 | 79952553 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 942 | 258 | 78 | 55 | 90 | 10 | 23 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | ATGGG others(937): Show |
chr6 | 79909814 | 79952553 | ||
| a0002c0002 | 0/0 | 942 | 95 | 18 | 13 | 42 | 2 | 20 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | ATGGG others(937): Show |
chr6 | 79909814 | 79952553 | ||
| a0003c0003 | 0/0 | 942 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | ATGGG others(937): Show |
chr6 | 79909814 | 79952553 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3013 | 177 | 28 | 43 | 81 | 5 | 19 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | GCAGA others(3008): Show |
chr6 | 79909814 | 79952553 |
| a0001c0001t0003 | 0/0 | 3013 | 27 | 25 | 2 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | GCAGA others(3008): Show |
chr6 | 79909814 | 79952553 |
| a0001c0001t0004 | 0/1 | 3013 | 22 | 2 | 8 | 3 | 4 | 4 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | GCAGA others(3008): Show |
chr6 | 79909814 | 79952553 |
| a0001c0001t0005 | 0/0 | 3013 | 11 | 11 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | GCAGA others(3008): Show |
chr6 | 79909814 | 79952553 |
| a0001c0001t0007 | 0/0 | 3013 | 5 | 2 | 2 | 0 | 1 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | GCAGA others(3008): Show |
chr6 | 79909814 | 79952553 |
| a0001c0001t0009 | 0/0 | 3026 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | GCAGA others(3021): Show |
chr6 | 79909814 | 79952553 |
| a0001c0001t0010 | 0/0 | 3013 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | GCAGA others(3008): Show |
chr6 | 79909814 | 79952553 |
| a0001c0001t0011 | 0/0 | 3013 | 2 | 0 | 0 | 2 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | GCAGA others(3008): Show |
chr6 | 79909814 | 79952553 |
| a0001c0001t0012 | 0/0 | 3013 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | GCAGA others(3008): Show |
chr6 | 79909814 | 79952553 |
| a0001c0001t0013 | 0/0 | 3013 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | GCAGA others(3008): Show |
chr6 | 79909814 | 79952553 |
| a0001c0001t0015 | 0/0 | 3013 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | GCAGA others(3008): Show |
chr6 | 79909814 | 79952553 |
| a0001c0001t0016 | 0/0 | 3013 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | GCAGA others(3008): Show |
chr6 | 79909814 | 79952553 |
| a0001c0001t0018 | 0/0 | 3013 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | GCAGA others(3008): Show |
chr6 | 79909814 | 79952553 |
| a0001c0001t0019 | 0/0 | 3013 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | GCAGA others(3008): Show |
chr6 | 79909814 | 79952553 |
| a0001c0001t0021 | 0/0 | 3013 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | GCAGA others(3008): Show |
chr6 | 79909814 | 79952553 |
| a0001c0001t0022 | 0/0 | 3013 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | GCAGA others(3008): Show |
chr6 | 79909814 | 79952553 |
| a0001c0001t0023 | 0/0 | 3013 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | GCAGA others(3008): Show |
chr6 | 79909814 | 79952553 |
| a0001c0001t0024 | 0/0 | 3013 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | GCAGA others(3008): Show |
chr6 | 79909814 | 79952553 |
| a0002c0002t0002 | 0/0 | 3011 | 78 | 4 | 12 | 42 | 2 | 18 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | GCAGA others(3006): Show |
chr6 | 79909814 | 79952553 |
| a0002c0002t0006 | 0/0 | 3011 | 10 | 10 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | GCAGA others(3006): Show |
chr6 | 79909814 | 79952553 |
| a0002c0002t0008 | 0/0 | 3013 | 4 | 4 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | GCAGA others(3008): Show |
chr6 | 79909814 | 79952553 |
| a0002c0002t0014 | 0/0 | 3011 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | GCAGA others(3006): Show |
chr6 | 79909814 | 79952553 |
| a0002c0002t0017 | 0/0 | 3011 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | GCAGA others(3006): Show |
chr6 | 79909814 | 79952553 |
| a0002c0002t0020 | 0/0 | 3013 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | GCAGA others(3008): Show |
chr6 | 79909814 | 79952553 |
| a0003c0003t0001 | 0/0 | 3013 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | GCAGA others(3008): Show |
chr6 | 79909814 | 79952553 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 19 | 1 | 6 | 12 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0002 | 1/0 | 18 | 1 | 0 | 13 | 2 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0005 | 0/0 | 6 | 0 | 2 | 0 | 1 | 3 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0035 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0037 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0003g0008 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0003g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0003g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0003g0056 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0003g0057 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0003g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0003g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0004g0006 | 0/0 | 5 | 0 | 1 | 0 | 2 | 2 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0004g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0004g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0004g0062 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0004g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0004g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0004g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0004g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0004g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0004g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0004g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0004g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0004g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0005g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0005g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0005g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0005g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0005g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0005g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0005g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0007g0053 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0007g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0007g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0007g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0009g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0009g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0010g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0010g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0011g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0012g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0013g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0015g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0016g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0018g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0019g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0021g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0022g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0023g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0001c0001t0024g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0002c0002t0002g0003 | 0/0 | 13 | 0 | 0 | 12 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0002c0002t0002g0004 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0002c0002t0002g0007 | 0/0 | 5 | 0 | 3 | 0 | 0 | 2 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0002c0002t0002g0013 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0002c0002t0002g0014 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0002c0002t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0002c0002t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0002c0002t0002g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0002c0002t0002g0025 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0002c0002t0002g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0002c0002t0002g0027 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0002c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0002c0002t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0002c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0002c0002t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0002c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0002c0002t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0002c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0002c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0002c0002t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0002c0002t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0002c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0002c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0002c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0002c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0002c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0002c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0002c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0002c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0002c0002t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0002c0002t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0002c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0002c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0002c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0002c0002t0006g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0002c0002t0006g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0002c0002t0006g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0002c0002t0006g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0002c0002t0006g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0002c0002t0006g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0002c0002t0006g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0002c0002t0008g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0002c0002t0008g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0002c0002t0014g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0002c0002t0017g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0002c0002t0020g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| a0003c0003t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0007 | g0205 | EUR | GBR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG00140 | hp1 | a0002 | c0002 | t0002 | g0087 | EUR | GBR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0017 | EUR | GBR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG00280 | hp2 | a0001 | c0001 | t0004 | g0006 | EUR | FIN | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | FIN | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG00323 | hp2 | a0002 | c0002 | t0002 | g0085 | EUR | FIN | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG00423 | hp1 | a0002 | c0002 | t0002 | g0094 | EAS | CHS | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG00558 | hp1 | a0001 | c0001 | t0011 | g0033 | EAS | CHS | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG00609 | hp1 | a0002 | c0002 | t0002 | g0106 | EAS | CHS | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | CHS | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG00673 | hp2 | a0001 | c0001 | t0004 | g0072 | EAS | CHS | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG00733 | hp1 | a0001 | c0001 | t0004 | g0075 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG00733 | hp2 | a0002 | c0002 | t0002 | g0152 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG00735 | hp1 | a0002 | c0002 | t0002 | g0004 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG01069 | hp2 | a0002 | c0002 | t0002 | g0007 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG01070 | hp2 | a0001 | c0001 | t0007 | g0053 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG01071 | hp2 | a0002 | c0002 | t0002 | g0007 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG01074 | hp2 | a0002 | c0002 | t0002 | g0007 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG01106 | hp1 | a0001 | c0001 | t0004 | g0073 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0219 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG01167 | hp1 | a0002 | c0002 | t0002 | g0027 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG01175 | hp1 | a0001 | c0001 | t0004 | g0070 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0067 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG01256 | hp2 | a0001 | c0001 | t0007 | g0204 | AMR | CLM | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG01257 | hp1 | a0001 | c0001 | t0004 | g0020 | AMR | CLM | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG01258 | hp2 | a0001 | c0001 | t0004 | g0020 | AMR | CLM | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0006 | AMR | CLM | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0223 | AMR | CLM | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG01433 | hp1 | a0002 | c0002 | t0002 | g0093 | AMR | CLM | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG01433 | hp2 | a0002 | c0002 | t0020 | g0112 | AMR | CLM | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0155 | EUR | IBS | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG01515 | hp2 | a0001 | c0001 | t0004 | g0064 | EUR | IBS | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG01884 | hp2 | a0002 | c0002 | t0008 | g0196 | AFR | ACB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG01891 | hp1 | a0001 | c0001 | t0005 | g0049 | AFR | ACB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0216 | AFR | ACB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG01943 | hp1 | a0001 | c0001 | t0004 | g0068 | AMR | PEL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG01943 | hp2 | a0002 | c0002 | t0002 | g0024 | AMR | PEL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG01975 | hp2 | a0002 | c0002 | t0002 | g0026 | AMR | PEL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG01981 | hp1 | a0002 | c0002 | t0002 | g0025 | AMR | PEL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG01993 | hp2 | a0002 | c0002 | t0002 | g0004 | AMR | PEL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02040 | hp1 | a0001 | c0001 | t0004 | g0021 | EAS | KHV | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02040 | hp2 | a0002 | c0002 | t0002 | g0195 | EAS | KHV | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0055 | AFR | ACB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02056 | hp2 | a0002 | c0002 | t0002 | g0022 | EAS | KHV | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02080 | hp2 | a0002 | c0002 | t0002 | g0023 | EAS | KHV | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02129 | hp1 | a0001 | c0001 | t0015 | g0076 | EAS | KHV | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02129 | hp2 | a0001 | c0001 | t0023 | g0131 | EAS | KHV | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02132 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | KHV | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02132 | hp2 | a0001 | c0001 | t0004 | g0021 | EAS | KHV | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0069 | AFR | ACB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02148 | hp1 | a0002 | c0002 | t0002 | g0088 | AMR | PEL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02257 | hp1 | a0002 | c0002 | t0008 | g0011 | AFR | ACB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02257 | hp2 | a0002 | c0002 | t0006 | g0019 | AFR | ACB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0057 | AFR | ACB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02280 | hp1 | a0002 | c0002 | t0006 | g0209 | AFR | ACB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | ACB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02451 | hp1 | a0002 | c0002 | t0006 | g0211 | AFR | ACB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02451 | hp2 | a0001 | c0001 | t0019 | g0118 | AFR | ACB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02523 | hp1 | a0002 | c0002 | t0002 | g0095 | EAS | KHV | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0192 | AFR | GWD | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0222 | AFR | GWD | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0218 | AFR | GWD | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | GWD | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0008 | AFR | GWD | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0193 | AFR | GWD | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0049 | AFR | GWD | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02647 | hp1 | a0001 | c0001 | t0007 | g0053 | AFR | GWD | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | GWD | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02683 | hp1 | a0002 | c0002 | t0002 | g0027 | SAS | PJL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02698 | hp1 | a0002 | c0002 | t0002 | g0100 | SAS | PJL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0051 | AFR | GWD | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02717 | hp2 | a0001 | c0001 | t0007 | g0206 | AFR | GWD | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02723 | hp1 | a0001 | c0001 | t0009 | g0060 | AFR | GWD | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0213 | AFR | GWD | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02735 | hp1 | a0001 | c0001 | t0004 | g0071 | SAS | PJL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02735 | hp2 | a0002 | c0002 | t0002 | g0092 | SAS | PJL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0212 | AFR | GWD | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0221 | AFR | GWD | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02886 | hp1 | a0001 | c0001 | t0005 | g0050 | AFR | GWD | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02886 | hp2 | a0001 | c0001 | t0012 | g0058 | AFR | GWD | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02895 | hp2 | a0002 | c0002 | t0008 | g0011 | AFR | GWD | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02896 | hp1 | a0002 | c0002 | t0002 | g0091 | AFR | GWD | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | GWD | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02897 | hp1 | a0002 | c0002 | t0008 | g0011 | AFR | GWD | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0215 | AFR | GWD | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | ESN | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0057 | AFR | ESN | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0008 | AFR | ESN | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | ESN | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ESN | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02976 | hp2 | a0002 | c0002 | t0006 | g0054 | AFR | ESN | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG03017 | hp1 | a0001 | c0001 | t0004 | g0006 | SAS | PJL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG03017 | hp2 | a0002 | c0002 | t0002 | g0007 | SAS | PJL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0048 | AFR | GWD | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG03041 | hp2 | a0002 | c0002 | t0006 | g0019 | AFR | GWD | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG03098 | hp1 | a0001 | c0001 | t0005 | g0191 | AFR | MSL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | MSL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG03130 | hp1 | a0001 | c0001 | t0005 | g0050 | AFR | ESN | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0008 | AFR | ESN | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0051 | AFR | ESN | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ESN | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0214 | AFR | ESN | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG03209 | hp1 | a0001 | c0001 | t0013 | g0061 | AFR | MSL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG03209 | hp2 | a0002 | c0002 | t0006 | g0208 | AFR | MSL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | MSL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG03225 | hp2 | a0001 | c0001 | t0022 | g0116 | AFR | MSL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG03239 | hp1 | a0002 | c0002 | t0002 | g0007 | SAS | PJL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | MSL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | MSL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG03486 | hp1 | a0002 | c0002 | t0006 | g0019 | AFR | MSL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0217 | AFR | MSL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0006 | SAS | PJL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG03492 | hp2 | a0002 | c0002 | t0002 | g0014 | SAS | PJL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ESN | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0056 | AFR | ESN | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG03540 | hp1 | a0001 | c0001 | t0009 | g0059 | AFR | GWD | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0220 | AFR | GWD | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG03579 | hp1 | a0001 | c0001 | t0010 | g0197 | AFR | MSL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | MSL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG03654 | hp1 | a0002 | c0002 | t0002 | g0003 | SAS | PJL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG03669 | hp1 | a0002 | c0002 | t0002 | g0080 | SAS | PJL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | STU | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG03704 | hp1 | a0002 | c0002 | t0002 | g0013 | SAS | PJL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG03710 | hp1 | a0002 | c0002 | t0002 | g0014 | SAS | PJL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG03831 | hp1 | a0002 | c0002 | t0002 | g0202 | SAS | BEB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG03831 | hp2 | a0001 | c0001 | t0004 | g0066 | SAS | BEB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG03834 | hp1 | a0002 | c0002 | t0002 | g0101 | SAS | BEB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | BEB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | BEB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG03927 | hp2 | a0002 | c0002 | t0002 | g0099 | SAS | BEB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | BEB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG03942 | hp2 | a0002 | c0002 | t0002 | g0084 | SAS | BEB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | STU | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG04115 | hp2 | a0002 | c0002 | t0014 | g0065 | SAS | STU | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | BEB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG04184 | hp2 | a0002 | c0002 | t0017 | g0086 | SAS | BEB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG04199 | hp1 | a0002 | c0002 | t0002 | g0083 | SAS | STU | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG04199 | hp2 | a0002 | c0002 | t0002 | g0090 | SAS | STU | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG04204 | hp1 | a0002 | c0002 | t0002 | g0111 | SAS | STU | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG04204 | hp2 | a0003 | c0003 | t0001 | g0181 | SAS | STU | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG04228 | hp1 | a0002 | c0002 | t0002 | g0014 | SAS | STU | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | STU | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA18522 | hp1 | a0002 | c0002 | t0006 | g0054 | AFR | YRI | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | YRI | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA18747 | hp2 | a0002 | c0002 | t0002 | g0024 | EAS | CHB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA18906 | hp1 | a0002 | c0002 | t0006 | g0210 | AFR | YRI | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA18906 | hp2 | a0001 | c0001 | t0016 | g0190 | AFR | YRI | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA18941 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA18941 | hp2 | a0001 | c0001 | t0018 | g0126 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA18942 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA18943 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA18950 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA18951 | hp2 | a0002 | c0002 | t0002 | g0107 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA18952 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA18957 | hp1 | a0002 | c0002 | t0002 | g0105 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA18959 | hp2 | a0002 | c0002 | t0002 | g0102 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA18966 | hp1 | a0002 | c0002 | t0002 | g0104 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA18969 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA18975 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA18982 | hp1 | a0001 | c0001 | t0011 | g0033 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA18983 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA18987 | hp1 | a0001 | c0001 | t0021 | g0161 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA18989 | hp1 | a0002 | c0002 | t0002 | g0110 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA18993 | hp2 | a0002 | c0002 | t0002 | g0013 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA18999 | hp1 | a0002 | c0002 | t0002 | g0108 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA19001 | hp1 | a0002 | c0002 | t0002 | g0022 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA19006 | hp1 | a0002 | c0002 | t0002 | g0082 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA19007 | hp1 | a0002 | c0002 | t0002 | g0103 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA19009 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA19010 | hp1 | a0002 | c0002 | t0002 | g0200 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA19030 | hp1 | a0001 | c0001 | t0024 | g0203 | AFR | LWK | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA19030 | hp2 | a0001 | c0001 | t0010 | g0198 | AFR | LWK | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | LWK | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | LWK | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA19054 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA19058 | hp2 | a0002 | c0002 | t0002 | g0026 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA19062 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA19063 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA19066 | hp1 | a0002 | c0002 | t0002 | g0025 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA19072 | hp2 | a0002 | c0002 | t0002 | g0013 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA19074 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA19076 | hp2 | a0002 | c0002 | t0002 | g0081 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA19081 | hp1 | a0002 | c0002 | t0002 | g0109 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA19082 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA19083 | hp2 | a0002 | c0002 | t0002 | g0023 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA19088 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA19089 | hp2 | a0002 | c0002 | t0002 | g0089 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA19091 | hp2 | a0002 | c0002 | t0002 | g0096 | EAS | JPT | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0056 | AFR | YRI | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | YRI | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA20805 | hp1 | a0001 | c0001 | t0004 | g0006 | EUR | TSI | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA20805 | hp2 | a0001 | c0001 | t0004 | g0063 | EUR | TSI | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | GIH | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | GIH | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | ACB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0055 | AFR | ACB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG02559 | hp2 | a0002 | c0002 | t0006 | g0207 | AFR | ACB | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG03471 | hp1 | a0002 | c0002 | t0002 | g0113 | AFR | MSL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0048 | AFR | MSL | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0074 | AFR | USA | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | USA | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA20300 | hp1 | a0002 | c0002 | t0002 | g0097 | AFR | USA | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | USA | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA21309 | hp1 | a0002 | c0002 | t0002 | g0098 | AFR | LWK | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | LWK | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0004 | g0062 | REF | REF | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0002 | REF | REF | ELOVL4_chr6_79909814_79952553 | ELOVL4 | chr6 | 79909814 | 79952553 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:79916658 | T | C | 1 | a0002 | 95 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(92): Show |
missense_variant | MODERATE | c.895A>G | p.Met299Val | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 6/6 | 1169/3013 | 895/945 | 299/314 | chr6 | 79916658 | |||
| chr6:79916753 | A | G | 1 | a0003 | 1 | HG04204.hp2 | missense_variant | MODERATE | c.800T>C | p.Ile267Thr | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 6/6 | 1074/3013 | 800/945 | 267/314 | chr6 | 79916753 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:79914849 | A | T | 1 | a0001c0001t0021 | 1 | NA18987.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1759T>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 6/6 | 1759 | chr6 | 79914849 | ||||||
| chr6:79914939 | A | C | 5 | a0002c0002t0002 a0002c0002t0006 a0002c0002t0014 others(2): Show |
91 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*1669T>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 6/6 | 1669 | chr6 | 79914939 | ||||||
| chr6:79915057 | T | C | 2 | a0001c0001t0005 a0001c0001t0009 |
13 | HG01891.hp1 HG02572.hp1 HG02622.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1551A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 6/6 | 1551 | chr6 | 79915057 | ||||||
| chr6:79915542 | A | C | 2 | a0001c0001t0007 a0001c0001t0022 |
6 | HG00099.hp1 HG01070.hp2 HG01256.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1066T>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 6/6 | 1066 | chr6 | 79915542 | ||||||
| chr6:79915560 | C | T | 1 | a0001c0001t0019 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1048G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 6/6 | 1048 | chr6 | 79915560 | ||||||
| chr6:79915588 | T | C | 1 | a0002c0002t0017 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1020A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 6/6 | 1020 | chr6 | 79915588 | ||||||
| chr6:79915812 | CAT | C | 4 | a0002c0002t0002 a0002c0002t0006 a0002c0002t0014 others(1): Show |
90 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*794_*795delAT | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 6/6 | 794 | chr6 | 79915812 | ||||||
| chr6:79915941 | A | G | 5 | a0002c0002t0002 a0002c0002t0006 a0002c0002t0008 others(2): Show |
94 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*667T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 6/6 | 667 | chr6 | 79915941 | ||||||
| chr6:79915999 | C | T | 2 | a0001c0001t0007 a0001c0001t0022 |
6 | HG00099.hp1 HG01070.hp2 HG01256.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*609G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 6/6 | 609 | chr6 | 79915999 | ||||||
| chr6:79916099 | G | A | 1 | a0001c0001t0016 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*509C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 6/6 | 509 | chr6 | 79916099 | ||||||
| chr6:79916231 | A | T | 1 | a0001c0001t0011 | 2 | HG00558.hp1 NA18982.hp1 |
3_prime_UTR_variant | MODIFIER | c.*377T>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 6/6 | 377 | chr6 | 79916231 | ||||||
| chr6:79916247 | G | A | 2 | a0001c0001t0007 a0001c0001t0022 |
6 | HG00099.hp1 HG01070.hp2 HG01256.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*361C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 6/6 | 361 | chr6 | 79916247 | ||||||
| chr6:79916248 | T | C | 1 | a0001c0001t0023 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*360A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 6/6 | 360 | chr6 | 79916248 | ||||||
| chr6:79916400 | T | A | 1 | a0001c0001t0024 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*208A>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 6/6 | 208 | chr6 | 79916400 | ||||||
| chr6:79916401 | A | T | 1 | a0001c0001t0018 | 1 | NA18941.hp2 | 3_prime_UTR_variant | MODIFIER | c.*207T>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 6/6 | 207 | chr6 | 79916401 | ||||||
| chr6:79916404 | A | C | 1 | a0001c0001t0010 | 2 | HG03579.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*204T>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 6/6 | 204 | chr6 | 79916404 | ||||||
| chr6:79916466 | C | G | 5 | a0002c0002t0002 a0002c0002t0006 a0002c0002t0008 others(2): Show |
94 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*142G>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 6/6 | 142 | chr6 | 79916466 | ||||||
| chr6:79916600 | A | G | 1 | a0001c0001t0016 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 6/6 | 8 | chr6 | 79916600 | ||||||
| chr6:79947309 | A | C | 1 | a0001c0001t0015 | 1 | HG02129.hp1 | 5_prime_UTR_variant | MODIFIER | c.-30T>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/6 | 30 | chr6 | 79947309 | ||||||
| chr6:79947316 | G | A | 1 | a0001c0001t0024 | 1 | NA19030.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-37C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/6 | chr6 | 79947316 | |||||||
| chr6:79947369 | C | G | 2 | a0001c0001t0004 a0002c0002t0014 |
22 | HG00280.hp2 HG00673.hp2 HG00733.hp1 others(19): Show |
5_prime_UTR_variant | MODIFIER | c.-90G>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/6 | 90 | chr6 | 79947369 | ||||||
| chr6:79947377 | G | A | 1 | a0001c0001t0012 | 1 | HG02886.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-98C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/6 | chr6 | 79947377 | |||||||
| chr6:79947382 | C | G | 1 | a0001c0001t0013 | 1 | HG03209.hp1 | 5_prime_UTR_variant | MODIFIER | c.-103G>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/6 | 103 | chr6 | 79947382 | ||||||
| chr6:79947515 | G | A | 5 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0009 others(2): Show |
45 | HG00099.hp1 HG01070.hp2 HG01109.hp2 others(42): Show |
5_prime_UTR_variant | MODIFIER | c.-236C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/6 | 236 | chr6 | 79947515 | ||||||
| chr6:79947538 | C | CGCTGCAC others(6): Show |
1 | a0001c0001t0009 | 2 | HG02723.hp1 HG03540.hp1 |
5_prime_UTR_variant | MODIFIER | c.-272_-260dupAGACTG others(7): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/6 | 260 | chr6 | 79947538 | ||||||
| chr6:79947547 | A | C | 1 | a0001c0001t0012 | 1 | HG02886.hp2 | 5_prime_UTR_variant | MODIFIER | c.-268T>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/6 | 268 | chr6 | 79947547 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:79917069 | T | C | 1 | a0001c0001t0007g0206 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.670-186A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 5/5 | chr6 | 79917069 | |||||||
| chr6:79917131 | AT | A | 83 | a0001c0001t0001g0039 a0001c0001t0001g0077 a0001c0001t0001g0153 others(80): Show |
131 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.670-249delA | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 5/5 | chr6 | 79917131 | |||||||
| chr6:79917139 | T | A | 1 | a0001c0001t0010g0198 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.670-256A>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 5/5 | chr6 | 79917139 | |||||||
| chr6:79917585 | C | T | 9 | a0001c0001t0005g0048 a0001c0001t0005g0049 a0001c0001t0005g0050 others(6): Show |
13 | HG01891.hp1 HG02572.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.670-702G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 5/5 | chr6 | 79917585 | |||||||
| chr6:79917688 | G | T | 1 | a0001c0001t0001g0138 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.670-805C>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 5/5 | chr6 | 79917688 | |||||||
| chr6:79917794 | T | C | 1 | a0001c0001t0001g0201 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.670-911A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 5/5 | chr6 | 79917794 | |||||||
| chr6:79917828 | A | G | 2 | a0002c0002t0008g0011 a0002c0002t0008g0196 |
4 | HG01884.hp2 HG02257.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.670-945T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 5/5 | chr6 | 79917828 | |||||||
| chr6:79917916 | G | C | 19 | a0001c0001t0001g0039 a0001c0001t0001g0153 a0001c0001t0001g0154 others(16): Show |
30 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.670-1033C>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 5/5 | chr6 | 79917916 | |||||||
| chr6:79918199 | A | G | 1 | a0001c0001t0001g0009 | 4 | HG01070.hp1 HG01071.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.669+1221T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 5/5 | chr6 | 79918199 | |||||||
| chr6:79918316 | T | G | 1 | a0003c0003t0001g0181 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.669+1104A>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 5/5 | chr6 | 79918316 | |||||||
| chr6:79918435 | C | T | 58 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0007 others(55): Show |
94 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.669+985G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 5/5 | chr6 | 79918435 | |||||||
| chr6:79918606 | A | G | 4 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0155 others(1): Show |
9 | HG01070.hp1 HG01071.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.669+814T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 5/5 | chr6 | 79918606 | |||||||
| chr6:79918639 | T | C | 5 | a0001c0001t0007g0053 a0001c0001t0007g0204 a0001c0001t0007g0205 others(2): Show |
6 | HG00099.hp1 HG01070.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.669+781A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 5/5 | chr6 | 79918639 | |||||||
| chr6:79918983 | T | A | 2 | a0002c0002t0006g0207 a0002c0002t0006g0209 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.669+437A>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 5/5 | chr6 | 79918983 | |||||||
| chr6:79919030 | A | G | 1 | a0001c0001t0013g0061 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.669+390T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 5/5 | chr6 | 79919030 | |||||||
| chr6:79919042 | A | G | 79 | a0001c0001t0001g0039 a0001c0001t0001g0077 a0001c0001t0001g0153 others(76): Show |
126 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.669+378T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 5/5 | chr6 | 79919042 | |||||||
| chr6:79919110 | A | ACATAAAT | 190 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(187): Show |
296 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(293): Show |
intron_variant | MODIFIER | c.669+309_669+310ins others(7): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 5/5 | chr6 | 79919110 | |||||||
| chr6:79919127 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.669+293C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 5/5 | chr6 | 79919127 | |||||||
| chr6:79919131 | T | G | 2 | a0001c0001t0001g0167 a0001c0001t0001g0170 |
2 | HG03654.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.669+289A>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 5/5 | chr6 | 79919131 | |||||||
| chr6:79919194 | G | GCTATGTC others(313): Show |
1 | a0002c0002t0002g0113 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.669+225_669+226ins others(320): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 5/5 | chr6 | 79919194 | |||||||
| chr6:79919265 | A | T | 57 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0007 others(54): Show |
91 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.669+155T>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 5/5 | chr6 | 79919265 | |||||||
| chr6:79919290 | C | T | 1 | a0001c0001t0001g0134 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.669+130G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 5/5 | chr6 | 79919290 | |||||||
| chr6:79919362 | T | A | 3 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 |
3 | HG02486.hp1 HG02922.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.669+58A>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 5/5 | chr6 | 79919362 | |||||||
| chr6:79919369 | TA | T | 2 | a0002c0002t0008g0011 a0002c0002t0008g0196 |
4 | HG01884.hp2 HG02257.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.669+50delT | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 5/5 | chr6 | 79919369 | |||||||
| chr6:79919399 | C | T | 1 | a0002c0002t0002g0107 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.669+21G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 5/5 | chr6 | 79919399 | |||||||
| chr6:79919638 | T | A | 1 | a0001c0001t0001g0186 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.542-91A>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 4/5 | chr6 | 79919638 | |||||||
| chr6:79919801 | G | T | 1 | a0001c0001t0001g0077 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.542-254C>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 4/5 | chr6 | 79919801 | |||||||
| chr6:79919924 | G | A | 1 | a0001c0001t0016g0190 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.542-377C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 4/5 | chr6 | 79919924 | |||||||
| chr6:79920128 | T | G | 19 | a0001c0001t0001g0039 a0001c0001t0001g0153 a0001c0001t0001g0154 others(16): Show |
30 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.542-581A>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 4/5 | chr6 | 79920128 | |||||||
| chr6:79920337 | T | G | 59 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0007 others(56): Show |
95 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.542-790A>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 4/5 | chr6 | 79920337 | |||||||
| chr6:79920411 | A | G | 2 | a0002c0002t0008g0011 a0002c0002t0008g0196 |
4 | HG01884.hp2 HG02257.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.542-864T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 4/5 | chr6 | 79920411 | |||||||
| chr6:79920569 | G | C | 4 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0155 others(1): Show |
9 | HG01070.hp1 HG01071.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.542-1022C>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 4/5 | chr6 | 79920569 | |||||||
| chr6:79920609 | C | T | 2 | a0001c0001t0001g0121 a0001c0001t0001g0137 |
2 | HG02818.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.541+1016G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 4/5 | chr6 | 79920609 | |||||||
| chr6:79920669 | T | G | 1 | a0002c0002t0006g0209 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.541+956A>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 4/5 | chr6 | 79920669 | |||||||
| chr6:79920671 | T | C | 4 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0155 others(1): Show |
9 | HG01070.hp1 HG01071.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.541+954A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 4/5 | chr6 | 79920671 | |||||||
| chr6:79921039 | C | T | 1 | a0001c0001t0003g0214 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.541+586G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 4/5 | chr6 | 79921039 | |||||||
| chr6:79921097 | G | A | 3 | a0001c0001t0001g0150 a0001c0001t0003g0212 a0001c0001t0024g0203 |
3 | HG01175.hp2 HG02809.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.541+528C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 4/5 | chr6 | 79921097 | |||||||
| chr6:79921202 | T | C | 88 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0039 others(85): Show |
141 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.541+423A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 4/5 | chr6 | 79921202 | |||||||
| chr6:79921227 | C | T | 1 | a0001c0001t0001g0077 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.541+398G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 4/5 | chr6 | 79921227 | |||||||
| chr6:79921283 | A | C | 1 | a0001c0001t0001g0077 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.541+342T>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 4/5 | chr6 | 79921283 | |||||||
| chr6:79921369 | G | A | 3 | a0001c0001t0003g0056 a0001c0001t0003g0057 a0001c0001t0003g0219 |
5 | HG01109.hp2 HG02258.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.541+256C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 4/5 | chr6 | 79921369 | |||||||
| chr6:79921456 | T | C | 1 | a0001c0001t0001g0012 | 3 | HG01109.hp1 HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.541+169A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 4/5 | chr6 | 79921456 | |||||||
| chr6:79921459 | C | CA | 16 | a0001c0001t0001g0030 a0001c0001t0001g0034 a0001c0001t0001g0035 others(13): Show |
19 | HG00597.hp2 HG01175.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.541+165dupT | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 4/5 | chr6 | 79921459 | |||||||
| chr6:79921459 | C | CAA | 15 | a0001c0001t0001g0038 a0001c0001t0001g0041 a0001c0001t0001g0078 others(12): Show |
21 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(18): Show |
intron_variant | MODIFIER | c.541+164_541+165dup others(2): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 4/5 | chr6 | 79921459 | |||||||
| chr6:79921459 | CA | C | 22 | a0001c0001t0001g0015 a0001c0001t0001g0032 a0001c0001t0001g0129 others(19): Show |
31 | HG00733.hp2 HG00738.hp2 HG01169.hp1 others(28): Show |
intron_variant | MODIFIER | c.541+165delT | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 4/5 | chr6 | 79921459 | |||||||
| chr6:79921459 | CAA | C | 44 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0007 others(41): Show |
77 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.541+164_541+165del others(2): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 4/5 | chr6 | 79921459 | |||||||
| chr6:79921459 | CAAAAA | C | 10 | a0001c0001t0001g0042 a0001c0001t0001g0045 a0001c0001t0001g0047 others(7): Show |
13 | HG00438.hp2 HG00642.hp1 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.541+161_541+165del others(5): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 4/5 | chr6 | 79921459 | |||||||
| chr6:79921459 | CAAAAAA | C | 27 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0017 others(24): Show |
41 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.541+160_541+165del others(6): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 4/5 | chr6 | 79921459 | |||||||
| chr6:79921459 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0164 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.541+156_541+165del others(10): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 4/5 | chr6 | 79921459 | |||||||
| chr6:79921459 | CAAAAAAA others(4): Show |
C | 6 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0121 others(3): Show |
11 | HG01070.hp1 HG01071.hp1 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.541+155_541+165del others(11): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 4/5 | chr6 | 79921459 | |||||||
| chr6:79921459 | CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0001g0155 a0001c0001t0003g0222 |
2 | HG01515.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.541+154_541+165del others(12): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 4/5 | chr6 | 79921459 | |||||||
| chr6:79921459 | CAAAAAAA others(6): Show |
C | 5 | a0001c0001t0007g0053 a0001c0001t0007g0204 a0001c0001t0007g0205 others(2): Show |
6 | HG00099.hp1 HG01070.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.541+153_541+165del others(13): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 4/5 | chr6 | 79921459 | |||||||
| chr6:79921459 | CAAAAAAA others(10): Show |
C | 2 | a0002c0002t0008g0011 a0002c0002t0008g0196 |
4 | HG01884.hp2 HG02257.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.541+149_541+165del others(17): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 4/5 | chr6 | 79921459 | |||||||
| chr6:79921565 | C | T | 3 | a0001c0001t0001g0012 a0001c0001t0004g0063 a0001c0001t0004g0064 |
5 | HG01109.hp1 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.541+60G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 4/5 | chr6 | 79921565 | |||||||
| chr6:79921869 | G | C | 1 | a0001c0001t0007g0204 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.370-73C>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79921869 | |||||||
| chr6:79921913 | G | T | 57 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0007 others(54): Show |
91 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.370-117C>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79921913 | |||||||
| chr6:79921914 | G | C | 57 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0007 others(54): Show |
91 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.370-118C>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79921914 | |||||||
| chr6:79921961 | TG | T | 17 | a0001c0001t0001g0153 a0001c0001t0001g0201 a0001c0001t0003g0008 others(14): Show |
27 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.370-166delC | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79921961 | |||||||
| chr6:79922039 | C | T | 1 | a0001c0001t0001g0176 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.370-243G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79922039 | |||||||
| chr6:79922115 | C | T | 3 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 |
3 | HG02486.hp1 HG02922.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.370-319G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79922115 | |||||||
| chr6:79922177 | C | T | 1 | a0001c0001t0001g0038 | 2 | HG01346.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.370-381G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79922177 | |||||||
| chr6:79922214 | T | C | 59 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0007 others(56): Show |
95 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.370-418A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79922214 | |||||||
| chr6:79922457 | G | C | 1 | a0002c0002t0002g0080 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.370-661C>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79922457 | |||||||
| chr6:79922460 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.370-664T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79922460 | |||||||
| chr6:79922533 | A | T | 3 | a0001c0001t0001g0028 a0001c0001t0001g0136 a0001c0001t0018g0126 |
4 | NA18940.hp2 NA18941.hp2 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.370-737T>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79922533 | |||||||
| chr6:79922812 | T | C | 59 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0007 others(56): Show |
95 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.370-1016A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79922812 | |||||||
| chr6:79922854 | GAAAC | G | 2 | a0001c0001t0001g0039 a0001c0001t0001g0154 |
3 | HG02109.hp2 HG03098.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.370-1062_370-1059d others(6): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79922854 | |||||||
| chr6:79922904 | A | T | 55 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0007 others(52): Show |
89 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.370-1108T>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79922904 | |||||||
| chr6:79922922 | T | G | 3 | a0001c0001t0003g0218 a0001c0001t0003g0220 a0001c0001t0003g0221 |
3 | HG02615.hp1 HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.370-1126A>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79922922 | |||||||
| chr6:79923074 | C | A | 2 | a0002c0002t0008g0011 a0002c0002t0008g0196 |
4 | HG01884.hp2 HG02257.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.370-1278G>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79923074 | |||||||
| chr6:79923095 | A | G | 5 | a0001c0001t0007g0053 a0001c0001t0007g0204 a0001c0001t0007g0205 others(2): Show |
6 | HG00099.hp1 HG01070.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.370-1299T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79923095 | |||||||
| chr6:79923226 | C | T | 2 | a0002c0002t0002g0103 a0002c0002t0002g0106 |
2 | HG00609.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.370-1430G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79923226 | |||||||
| chr6:79923232 | G | A | 5 | a0001c0001t0007g0053 a0001c0001t0007g0204 a0001c0001t0007g0205 others(2): Show |
6 | HG00099.hp1 HG01070.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.370-1436C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79923232 | |||||||
| chr6:79923386 | TGTAA | T | 59 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0007 others(56): Show |
95 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.369+1562_369+1565d others(6): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79923386 | |||||||
| chr6:79923475 | G | C | 17 | a0001c0001t0001g0153 a0001c0001t0001g0201 a0001c0001t0003g0008 others(14): Show |
27 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.369+1477C>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79923475 | |||||||
| chr6:79923493 | T | C | 20 | a0001c0001t0001g0039 a0001c0001t0001g0077 a0001c0001t0001g0153 others(17): Show |
31 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.369+1459A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79923493 | |||||||
| chr6:79923534 | T | G | 4 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0155 others(1): Show |
9 | HG01070.hp1 HG01071.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.369+1418A>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79923534 | |||||||
| chr6:79923625 | C | A | 87 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0039 others(84): Show |
140 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.369+1327G>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79923625 | |||||||
| chr6:79923714 | A | G | 2 | a0001c0001t0001g0031 a0001c0001t0001g0135 |
3 | NA18942.hp2 NA18943.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.369+1238T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79923714 | |||||||
| chr6:79923895 | C | T | 1 | a0001c0001t0001g0159 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.369+1057G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79923895 | |||||||
| chr6:79923939 | G | A | 17 | a0001c0001t0001g0153 a0001c0001t0001g0201 a0001c0001t0003g0008 others(14): Show |
27 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.369+1013C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79923939 | |||||||
| chr6:79924012 | G | GTT | 57 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0007 others(54): Show |
91 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.369+938_369+939dup others(2): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79924012 | |||||||
| chr6:79924107 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.369+845G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79924107 | |||||||
| chr6:79924197 | C | A | 1 | a0001c0001t0001g0132 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.369+755G>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79924197 | |||||||
| chr6:79924270 | T | C | 1 | a0001c0001t0016g0190 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.369+682A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79924270 | |||||||
| chr6:79924293 | C | T | 4 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0155 others(1): Show |
9 | HG01070.hp1 HG01071.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.369+659G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79924293 | |||||||
| chr6:79924427 | T | C | 1 | a0001c0001t0001g0154 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.369+525A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79924427 | |||||||
| chr6:79924558 | A | G | 2 | a0002c0002t0008g0011 a0002c0002t0008g0196 |
4 | HG01884.hp2 HG02257.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.369+394T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79924558 | |||||||
| chr6:79924565 | G | A | 57 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0007 others(54): Show |
91 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.369+387C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79924565 | |||||||
| chr6:79924711 | C | T | 1 | a0001c0001t0022g0116 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.369+241G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79924711 | |||||||
| chr6:79924752 | T | C | 59 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0007 others(56): Show |
95 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.369+200A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79924752 | |||||||
| chr6:79924805 | A | G | 19 | a0001c0001t0001g0039 a0001c0001t0001g0153 a0001c0001t0001g0154 others(16): Show |
30 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.369+147T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79924805 | |||||||
| chr6:79924896 | G | A | 20 | a0001c0001t0001g0039 a0001c0001t0001g0077 a0001c0001t0001g0153 others(17): Show |
31 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.369+56C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 3/5 | chr6 | 79924896 | |||||||
| chr6:79925131 | A | G | 79 | a0001c0001t0001g0039 a0001c0001t0001g0077 a0001c0001t0001g0153 others(76): Show |
126 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.289-99T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 2/5 | chr6 | 79925131 | |||||||
| chr6:79925413 | A | T | 1 | a0001c0001t0007g0206 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.289-381T>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 2/5 | chr6 | 79925413 | |||||||
| chr6:79925514 | G | T | 2 | a0001c0001t0001g0031 a0001c0001t0001g0135 |
3 | NA18942.hp2 NA18943.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.289-482C>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 2/5 | chr6 | 79925514 | |||||||
| chr6:79925523 | C | G | 78 | a0001c0001t0001g0039 a0001c0001t0001g0077 a0001c0001t0001g0153 others(75): Show |
125 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.289-491G>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 2/5 | chr6 | 79925523 | |||||||
| chr6:79925568 | T | C | 1 | a0001c0001t0001g0132 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.289-536A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 2/5 | chr6 | 79925568 | |||||||
| chr6:79925735 | T | C | 7 | a0002c0002t0006g0019 a0002c0002t0006g0054 a0002c0002t0006g0207 others(4): Show |
10 | HG02257.hp2 HG02280.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.288+459A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 2/5 | chr6 | 79925735 | |||||||
| chr6:79925878 | G | A | 20 | a0001c0001t0001g0039 a0001c0001t0001g0077 a0001c0001t0001g0153 others(17): Show |
31 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.288+316C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 2/5 | chr6 | 79925878 | |||||||
| chr6:79925917 | C | T | 58 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0007 others(55): Show |
94 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.288+277G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 2/5 | chr6 | 79925917 | |||||||
| chr6:79926005 | C | T | 87 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0039 others(84): Show |
140 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.288+189G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 2/5 | chr6 | 79926005 | |||||||
| chr6:79926385 | T | C | 2 | a0001c0001t0010g0197 a0001c0001t0010g0198 |
2 | HG03579.hp1 NA19030.hp2 |
splice_region_variant&intron_variant | LOW | c.101-4A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79926385 | |||||||
| chr6:79926472 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.101-91A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79926472 | |||||||
| chr6:79926538 | C | A | 1 | a0002c0002t0002g0089 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.101-157G>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79926538 | |||||||
| chr6:79926649 | C | T | 3 | a0001c0001t0001g0043 a0001c0001t0001g0183 a0002c0002t0002g0082 |
4 | HG02258.hp2 HG02809.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-268G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79926649 | |||||||
| chr6:79926665 | G | C | 2 | a0002c0002t0008g0011 a0002c0002t0008g0196 |
4 | HG01884.hp2 HG02257.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-284C>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79926665 | |||||||
| chr6:79926684 | A | T | 56 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0007 others(53): Show |
90 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.101-303T>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79926684 | |||||||
| chr6:79926837 | G | A | 56 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0007 others(53): Show |
90 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.101-456C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79926837 | |||||||
| chr6:79926906 | T | C | 1 | a0001c0001t0001g0173 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.101-525A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79926906 | |||||||
| chr6:79927046 | C | T | 3 | a0001c0001t0003g0056 a0001c0001t0003g0057 a0001c0001t0003g0219 |
5 | HG01109.hp2 HG02258.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.101-665G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79927046 | |||||||
| chr6:79927243 | C | T | 1 | a0001c0001t0004g0020 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.101-862G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79927243 | |||||||
| chr6:79927337 | T | C | 1 | a0001c0001t0001g0012 | 3 | HG01109.hp1 HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.101-956A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79927337 | |||||||
| chr6:79927350 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.101-969T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79927350 | |||||||
| chr6:79927354 | C | T | 19 | a0001c0001t0001g0039 a0001c0001t0001g0153 a0001c0001t0001g0154 others(16): Show |
30 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.101-973G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79927354 | |||||||
| chr6:79927355 | G | A | 2 | a0001c0001t0010g0197 a0001c0001t0010g0198 |
2 | HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.101-974C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79927355 | |||||||
| chr6:79927432 | C | T | 3 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0151 |
3 | HG01074.hp1 HG01192.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.101-1051G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79927432 | |||||||
| chr6:79927447 | T | C | 1 | a0001c0001t0001g0043 | 2 | HG02809.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.101-1066A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79927447 | |||||||
| chr6:79927521 | G | C | 1 | a0001c0001t0001g0178 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.101-1140C>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79927521 | |||||||
| chr6:79927522 | T | C | 20 | a0001c0001t0001g0039 a0001c0001t0001g0077 a0001c0001t0001g0153 others(17): Show |
31 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.101-1141A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79927522 | |||||||
| chr6:79927593 | G | A | 56 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0007 others(53): Show |
90 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.101-1212C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79927593 | |||||||
| chr6:79927629 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.101-1248C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79927629 | |||||||
| chr6:79927780 | CAT | C | 19 | a0001c0001t0001g0039 a0001c0001t0001g0153 a0001c0001t0001g0154 others(16): Show |
30 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.101-1401_101-1400d others(4): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79927780 | |||||||
| chr6:79927818 | T | C | 2 | a0002c0002t0008g0011 a0002c0002t0008g0196 |
4 | HG01884.hp2 HG02257.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-1437A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79927818 | |||||||
| chr6:79928041 | T | C | 1 | a0001c0001t0001g0180 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.101-1660A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79928041 | |||||||
| chr6:79928098 | C | A | 5 | a0001c0001t0007g0053 a0001c0001t0007g0204 a0001c0001t0007g0205 others(2): Show |
6 | HG00099.hp1 HG01070.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.101-1717G>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79928098 | |||||||
| chr6:79928224 | C | A | 163 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0012 others(160): Show |
246 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.101-1843G>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79928224 | |||||||
| chr6:79928348 | C | T | 87 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0039 others(84): Show |
140 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.101-1967G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79928348 | |||||||
| chr6:79928358 | T | C | 4 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0155 others(1): Show |
9 | HG01070.hp1 HG01071.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.101-1977A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79928358 | |||||||
| chr6:79928364 | A | C | 1 | a0001c0001t0001g0009 | 4 | HG01070.hp1 HG01071.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-1983T>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79928364 | |||||||
| chr6:79928403 | C | A | 4 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0155 others(1): Show |
9 | HG01070.hp1 HG01071.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.101-2022G>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79928403 | |||||||
| chr6:79928423 | G | C | 2 | a0002c0002t0008g0011 a0002c0002t0008g0196 |
4 | HG01884.hp2 HG02257.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-2042C>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79928423 | |||||||
| chr6:79928426 | T | A | 20 | a0001c0001t0001g0039 a0001c0001t0001g0077 a0001c0001t0001g0153 others(17): Show |
31 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.101-2045A>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79928426 | |||||||
| chr6:79928516 | T | C | 4 | a0001c0001t0001g0038 a0001c0001t0001g0164 a0001c0001t0004g0073 others(1): Show |
5 | HG00733.hp1 HG01106.hp1 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.101-2135A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79928516 | |||||||
| chr6:79928626 | T | C | 19 | a0001c0001t0001g0039 a0001c0001t0001g0153 a0001c0001t0001g0154 others(16): Show |
30 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.101-2245A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79928626 | |||||||
| chr6:79928636 | T | C | 56 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0007 others(53): Show |
90 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.101-2255A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79928636 | |||||||
| chr6:79928727 | G | GT | 48 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0016 others(45): Show |
67 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.101-2347dupA | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79928727 | |||||||
| chr6:79928727 | G | GTT | 21 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0043 others(18): Show |
27 | HG00140.hp2 HG00735.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.101-2348_101-2347d others(4): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79928727 | |||||||
| chr6:79928727 | G | GTTT | 7 | a0001c0001t0001g0042 a0001c0001t0001g0046 a0001c0001t0001g0186 others(4): Show |
10 | HG00738.hp1 HG00741.hp2 HG01943.hp2 others(7): Show |
intron_variant | MODIFIER | c.101-2349_101-2347d others(5): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79928727 | |||||||
| chr6:79928727 | G | GTTTT | 29 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0002c0002t0002g0003 others(26): Show |
55 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.101-2350_101-2347d others(6): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79928727 | |||||||
| chr6:79928727 | G | GTTTTT | 23 | a0001c0001t0003g0057 a0001c0001t0003g0215 a0001c0001t0003g0219 others(20): Show |
30 | HG00733.hp2 HG01109.hp2 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.101-2351_101-2347d others(7): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79928727 | |||||||
| chr6:79928727 | G | GTTTTTT | 16 | a0001c0001t0001g0153 a0001c0001t0003g0008 a0001c0001t0003g0010 others(13): Show |
25 | HG01891.hp2 HG01981.hp1 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.101-2352_101-2347d others(8): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79928727 | |||||||
| chr6:79928727 | G | GTTTTTTT others(3): Show |
1 | a0001c0001t0001g0154 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.101-2356_101-2347d others(12): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79928727 | |||||||
| chr6:79928742 | T | G | 1 | a0001c0001t0001g0141 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.101-2361A>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79928742 | |||||||
| chr6:79928755 | T | TA | 3 | a0001c0001t0001g0044 a0001c0001t0001g0176 a0001c0001t0001g0179 |
4 | NA18940.hp1 NA18994.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-2375dupT | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79928755 | |||||||
| chr6:79928770 | C | G | 2 | a0002c0002t0008g0011 a0002c0002t0008g0196 |
4 | HG01884.hp2 HG02257.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-2389G>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79928770 | |||||||
| chr6:79928847 | C | T | 1 | a0001c0001t0004g0074 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.101-2466G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79928847 | |||||||
| chr6:79928952 | C | T | 17 | a0001c0001t0001g0153 a0001c0001t0001g0201 a0001c0001t0003g0008 others(14): Show |
27 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.101-2571G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79928952 | |||||||
| chr6:79928984 | C | A | 1 | a0002c0002t0002g0202 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.101-2603G>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79928984 | |||||||
| chr6:79929125 | G | C | 1 | a0001c0001t0001g0144 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.101-2744C>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79929125 | |||||||
| chr6:79929169 | AG | A | 56 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0007 others(53): Show |
90 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.101-2789delC | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79929169 | |||||||
| chr6:79929310 | C | T | 22 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0001g0041 others(19): Show |
31 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.101-2929G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79929310 | |||||||
| chr6:79929354 | C | A | 2 | a0001c0001t0001g0177 a0001c0001t0001g0178 |
2 | HG02015.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.101-2973G>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79929354 | |||||||
| chr6:79929389 | C | T | 75 | a0001c0001t0001g0039 a0001c0001t0001g0153 a0001c0001t0001g0154 others(72): Show |
120 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.101-3008G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79929389 | |||||||
| chr6:79929411 | T | C | 1 | a0001c0001t0016g0190 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.101-3030A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79929411 | |||||||
| chr6:79929429 | C | G | 1 | a0001c0001t0003g0216 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.101-3048G>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79929429 | |||||||
| chr6:79929604 | T | C | 32 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0017 others(29): Show |
48 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.101-3223A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79929604 | |||||||
| chr6:79929732 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.101-3351C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79929732 | |||||||
| chr6:79929797 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.101-3416G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79929797 | |||||||
| chr6:79929799 | A | G | 1 | a0001c0001t0001g0179 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.101-3418T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79929799 | |||||||
| chr6:79929881 | T | C | 1 | a0001c0001t0001g0179 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.101-3500A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79929881 | |||||||
| chr6:79930000 | C | T | 19 | a0001c0001t0001g0039 a0001c0001t0001g0153 a0001c0001t0001g0154 others(16): Show |
30 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.101-3619G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79930000 | |||||||
| chr6:79930073 | C | T | 87 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0039 others(84): Show |
140 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.101-3692G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79930073 | |||||||
| chr6:79930105 | C | T | 2 | a0001c0001t0010g0197 a0001c0001t0010g0198 |
2 | HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.101-3724G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79930105 | |||||||
| chr6:79930249 | A | T | 1 | a0002c0002t0002g0081 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.101-3868T>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79930249 | |||||||
| chr6:79930446 | C | T | 2 | a0001c0001t0001g0028 a0001c0001t0018g0126 |
3 | NA18940.hp2 NA18941.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.101-4065G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79930446 | |||||||
| chr6:79930592 | T | A | 1 | a0001c0001t0001g0077 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.101-4211A>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79930592 | |||||||
| chr6:79930613 | C | G | 1 | a0001c0001t0001g0125 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.101-4232G>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79930613 | |||||||
| chr6:79930676 | G | T | 7 | a0001c0001t0005g0048 a0001c0001t0005g0049 a0001c0001t0005g0050 others(4): Show |
11 | HG01891.hp1 HG02572.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.101-4295C>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79930676 | |||||||
| chr6:79931130 | G | A | 33 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0001g0041 others(30): Show |
46 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.101-4749C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79931130 | |||||||
| chr6:79931154 | T | C | 1 | a0001c0001t0005g0193 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.101-4773A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79931154 | |||||||
| chr6:79931234 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.101-4853C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79931234 | |||||||
| chr6:79931294 | C | T | 1 | a0001c0001t0001g0077 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.101-4913G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79931294 | |||||||
| chr6:79931384 | G | A | 1 | a0001c0001t0004g0074 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.101-5003C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79931384 | |||||||
| chr6:79931437 | C | G | 9 | a0001c0001t0005g0048 a0001c0001t0005g0049 a0001c0001t0005g0050 others(6): Show |
13 | HG01891.hp1 HG02572.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.101-5056G>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79931437 | |||||||
| chr6:79931689 | G | C | 4 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0155 others(1): Show |
9 | HG01070.hp1 HG01071.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.101-5308C>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79931689 | |||||||
| chr6:79931715 | G | GA | 2 | a0001c0001t0001g0045 a0001c0001t0001g0180 |
3 | HG00642.hp1 HG01123.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.101-5335dupT | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79931715 | |||||||
| chr6:79931785 | A | T | 1 | a0002c0002t0006g0054 | 2 | HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.101-5404T>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79931785 | |||||||
| chr6:79931806 | T | C | 1 | a0001c0001t0001g0077 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.101-5425A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79931806 | |||||||
| chr6:79931986 | T | G | 3 | a0001c0001t0003g0056 a0001c0001t0003g0057 a0001c0001t0003g0219 |
5 | HG01109.hp2 HG02258.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.101-5605A>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79931986 | |||||||
| chr6:79932328 | G | T | 19 | a0002c0002t0002g0004 a0002c0002t0002g0007 a0002c0002t0002g0022 others(16): Show |
34 | HG00140.hp1 HG00323.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.101-5947C>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79932328 | |||||||
| chr6:79932438 | G | A | 4 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0155 others(1): Show |
9 | HG01070.hp1 HG01071.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.101-6057C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79932438 | |||||||
| chr6:79932529 | G | C | 2 | a0002c0002t0008g0011 a0002c0002t0008g0196 |
4 | HG01884.hp2 HG02257.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-6148C>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79932529 | |||||||
| chr6:79932551 | C | CA | 18 | a0001c0001t0001g0036 a0001c0001t0001g0142 a0001c0001t0001g0143 others(15): Show |
29 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.101-6171dupT | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79932551 | |||||||
| chr6:79932551 | C | CAA | 58 | a0001c0001t0003g0220 a0001c0001t0003g0221 a0002c0002t0002g0003 others(55): Show |
92 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.101-6172_101-6171d others(4): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79932551 | |||||||
| chr6:79932564 | T | G | 3 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 |
3 | HG02486.hp1 HG02922.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.101-6183A>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79932564 | |||||||
| chr6:79932566 | G | A | 1 | a0001c0001t0007g0205 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.101-6185C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79932566 | |||||||
| chr6:79932842 | TG | T | 20 | a0001c0001t0001g0039 a0001c0001t0001g0077 a0001c0001t0001g0153 others(17): Show |
31 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.101-6462delC | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79932842 | |||||||
| chr6:79932862 | G | C | 2 | a0002c0002t0008g0011 a0002c0002t0008g0196 |
4 | HG01884.hp2 HG02257.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-6481C>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79932862 | |||||||
| chr6:79932870 | G | T | 2 | a0001c0001t0009g0059 a0001c0001t0009g0060 |
2 | HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.101-6489C>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79932870 | |||||||
| chr6:79932892 | CTT | C | 5 | a0001c0001t0007g0053 a0001c0001t0007g0204 a0001c0001t0007g0205 others(2): Show |
6 | HG00099.hp1 HG01070.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.101-6513_101-6512d others(4): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79932892 | |||||||
| chr6:79932948 | C | G | 79 | a0001c0001t0001g0039 a0001c0001t0001g0077 a0001c0001t0001g0153 others(76): Show |
126 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.101-6567G>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79932948 | |||||||
| chr6:79933045 | T | C | 1 | a0001c0001t0001g0037 | 2 | HG01081.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.101-6664A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79933045 | |||||||
| chr6:79933220 | T | G | 1 | a0002c0002t0006g0211 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.101-6839A>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79933220 | |||||||
| chr6:79933220 | T | TTTTG | 20 | a0001c0001t0001g0153 a0001c0001t0001g0201 a0001c0001t0003g0008 others(17): Show |
32 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.101-6843_101-6840d others(6): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79933220 | |||||||
| chr6:79933220 | TTTTGTTT others(1): Show |
T | 4 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0155 others(1): Show |
9 | HG01070.hp1 HG01071.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.101-6847_101-6840d others(10): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79933220 | |||||||
| chr6:79933328 | G | T | 79 | a0001c0001t0001g0039 a0001c0001t0001g0077 a0001c0001t0001g0153 others(76): Show |
126 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.101-6947C>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79933328 | |||||||
| chr6:79933333 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.101-6952G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79933333 | |||||||
| chr6:79933419 | C | T | 65 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0017 others(62): Show |
94 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.101-7038G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79933419 | |||||||
| chr6:79933569 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.101-7188C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79933569 | |||||||
| chr6:79933833 | A | G | 79 | a0001c0001t0001g0039 a0001c0001t0001g0077 a0001c0001t0001g0153 others(76): Show |
126 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.101-7452T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79933833 | |||||||
| chr6:79933957 | T | C | 17 | a0001c0001t0001g0153 a0001c0001t0001g0201 a0001c0001t0003g0008 others(14): Show |
27 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.101-7576A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79933957 | |||||||
| chr6:79934259 | G | A | 20 | a0001c0001t0001g0039 a0001c0001t0001g0077 a0001c0001t0001g0153 others(17): Show |
31 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.101-7878C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79934259 | |||||||
| chr6:79934320 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.101-7939C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79934320 | |||||||
| chr6:79934336 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.101-7955C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79934336 | |||||||
| chr6:79934457 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.101-8076C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79934457 | |||||||
| chr6:79934698 | C | G | 2 | a0002c0002t0008g0011 a0002c0002t0008g0196 |
4 | HG01884.hp2 HG02257.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-8317G>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79934698 | |||||||
| chr6:79934738 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.101-8357A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79934738 | |||||||
| chr6:79934773 | A | G | 1 | a0001c0001t0001g0123 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.101-8392T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79934773 | |||||||
| chr6:79934809 | A | G | 1 | a0001c0001t0001g0166 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.101-8428T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79934809 | |||||||
| chr6:79934972 | A | C | 1 | a0002c0002t0002g0084 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.101-8591T>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79934972 | |||||||
| chr6:79935105 | T | C | 16 | a0002c0002t0002g0003 a0002c0002t0002g0013 a0002c0002t0002g0089 others(13): Show |
30 | HG00423.hp1 HG00609.hp1 HG02040.hp2 others(27): Show |
intron_variant | MODIFIER | c.101-8724A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79935105 | |||||||
| chr6:79935167 | C | T | 78 | a0001c0001t0001g0039 a0001c0001t0001g0077 a0001c0001t0001g0153 others(75): Show |
125 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.101-8786G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79935167 | |||||||
| chr6:79935314 | T | C | 1 | a0001c0001t0001g0189 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.101-8933A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79935314 | |||||||
| chr6:79935462 | G | T | 1 | a0001c0001t0001g0123 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.101-9081C>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79935462 | |||||||
| chr6:79935524 | A | G | 3 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 |
3 | HG02486.hp1 HG02922.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.101-9143T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79935524 | |||||||
| chr6:79935743 | T | A | 58 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0007 others(55): Show |
94 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.101-9362A>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79935743 | |||||||
| chr6:79935788 | T | C | 1 | a0001c0001t0016g0190 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.101-9407A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79935788 | |||||||
| chr6:79935885 | T | C | 2 | a0001c0001t0001g0052 a0001c0001t0001g0146 |
3 | HG00423.hp2 HG00609.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.101-9504A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79935885 | |||||||
| chr6:79936017 | G | T | 2 | a0002c0002t0008g0011 a0002c0002t0008g0196 |
4 | HG01884.hp2 HG02257.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-9636C>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79936017 | |||||||
| chr6:79936044 | G | A | 1 | a0002c0002t0002g0110 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.101-9663C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79936044 | |||||||
| chr6:79936059 | G | T | 87 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0039 others(84): Show |
140 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.101-9678C>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79936059 | |||||||
| chr6:79936502 | A | G | 4 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0155 others(1): Show |
9 | HG01070.hp1 HG01071.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.101-10121T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79936502 | |||||||
| chr6:79936623 | C | T | 3 | a0001c0001t0001g0150 a0001c0001t0003g0212 a0001c0001t0024g0203 |
3 | HG01175.hp2 HG02809.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.101-10242G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79936623 | |||||||
| chr6:79936642 | T | G | 79 | a0001c0001t0001g0039 a0001c0001t0001g0077 a0001c0001t0001g0153 others(76): Show |
126 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.101-10261A>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79936642 | |||||||
| chr6:79936807 | C | T | 4 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0155 others(1): Show |
9 | HG01070.hp1 HG01071.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.100+10373G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79936807 | |||||||
| chr6:79936825 | A | G | 1 | a0001c0001t0001g0077 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.100+10355T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79936825 | |||||||
| chr6:79936898 | T | C | 2 | a0002c0002t0008g0011 a0002c0002t0008g0196 |
4 | HG01884.hp2 HG02257.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+10282A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79936898 | |||||||
| chr6:79937000 | G | C | 57 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0007 others(54): Show |
91 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.100+10180C>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79937000 | |||||||
| chr6:79937056 | A | C | 59 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0007 others(56): Show |
95 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.100+10124T>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79937056 | |||||||
| chr6:79937087 | C | A | 3 | a0002c0002t0002g0025 a0002c0002t0002g0026 a0002c0002t0002g0088 |
5 | HG01975.hp2 HG01981.hp1 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+10093G>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79937087 | |||||||
| chr6:79937165 | C | G | 1 | a0001c0001t0001g0122 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.100+10015G>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79937165 | |||||||
| chr6:79937175 | A | G | 84 | a0001c0001t0001g0039 a0001c0001t0001g0077 a0001c0001t0001g0153 others(81): Show |
132 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.100+10005T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79937175 | |||||||
| chr6:79937220 | A | G | 4 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0155 others(1): Show |
9 | HG01070.hp1 HG01071.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.100+9960T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79937220 | |||||||
| chr6:79937274 | G | A | 4 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0155 others(1): Show |
9 | HG01070.hp1 HG01071.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.100+9906C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79937274 | |||||||
| chr6:79937462 | G | T | 5 | a0001c0001t0007g0053 a0001c0001t0007g0204 a0001c0001t0007g0205 others(2): Show |
6 | HG00099.hp1 HG01070.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.100+9718C>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79937462 | |||||||
| chr6:79937550 | G | A | 2 | a0001c0001t0010g0197 a0001c0001t0010g0198 |
2 | HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.100+9630C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79937550 | |||||||
| chr6:79937568 | G | A | 57 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0007 others(54): Show |
91 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.100+9612C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79937568 | |||||||
| chr6:79937595 | C | T | 2 | a0002c0002t0008g0011 a0002c0002t0008g0196 |
4 | HG01884.hp2 HG02257.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+9585G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79937595 | |||||||
| chr6:79937618 | T | TAG | 7 | a0001c0001t0005g0048 a0001c0001t0005g0049 a0001c0001t0005g0050 others(4): Show |
11 | HG01891.hp1 HG02572.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.100+9560_100+9561d others(4): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79937618 | |||||||
| chr6:79937665 | G | T | 8 | a0001c0001t0001g0153 a0001c0001t0003g0008 a0001c0001t0003g0010 others(5): Show |
16 | HG02055.hp1 HG02109.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.100+9515C>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79937665 | |||||||
| chr6:79937829 | T | C | 1 | a0003c0003t0001g0181 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.100+9351A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79937829 | |||||||
| chr6:79937905 | A | G | 3 | a0001c0001t0003g0223 a0001c0001t0004g0020 a0001c0001t0004g0068 |
4 | HG01257.hp1 HG01258.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+9275T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79937905 | |||||||
| chr6:79937936 | C | T | 2 | a0002c0002t0008g0011 a0002c0002t0008g0196 |
4 | HG01884.hp2 HG02257.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+9244G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79937936 | |||||||
| chr6:79937944 | G | A | 2 | a0001c0001t0001g0009 a0001c0001t0001g0155 |
5 | HG01070.hp1 HG01071.hp1 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.100+9236C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79937944 | |||||||
| chr6:79937983 | C | A | 2 | a0002c0002t0008g0011 a0002c0002t0008g0196 |
4 | HG01884.hp2 HG02257.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+9197G>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79937983 | |||||||
| chr6:79938455 | G | T | 59 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0007 others(56): Show |
95 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.100+8725C>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79938455 | |||||||
| chr6:79938468 | T | C | 1 | a0001c0001t0001g0156 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.100+8712A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79938468 | |||||||
| chr6:79938628 | T | C | 2 | a0002c0002t0008g0011 a0002c0002t0008g0196 |
4 | HG01884.hp2 HG02257.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+8552A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79938628 | |||||||
| chr6:79938799 | C | T | 1 | a0002c0002t0002g0113 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+8381G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79938799 | |||||||
| chr6:79938802 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.100+8378A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79938802 | |||||||
| chr6:79938813 | A | G | 88 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0039 others(85): Show |
141 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.100+8367T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79938813 | |||||||
| chr6:79938960 | C | A | 1 | a0001c0001t0007g0206 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.100+8220G>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79938960 | |||||||
| chr6:79938970 | G | A | 83 | a0001c0001t0001g0039 a0001c0001t0001g0077 a0001c0001t0001g0153 others(80): Show |
131 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.100+8210C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79938970 | |||||||
| chr6:79939042 | T | C | 1 | a0001c0001t0001g0165 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.100+8138A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79939042 | |||||||
| chr6:79939142 | C | T | 1 | a0002c0002t0002g0096 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.100+8038G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79939142 | |||||||
| chr6:79939390 | C | G | 19 | a0001c0001t0001g0039 a0001c0001t0001g0153 a0001c0001t0001g0154 others(16): Show |
30 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.100+7790G>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79939390 | |||||||
| chr6:79939419 | T | C | 2 | a0002c0002t0008g0011 a0002c0002t0008g0196 |
4 | HG01884.hp2 HG02257.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+7761A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79939419 | |||||||
| chr6:79939455 | A | G | 1 | a0001c0001t0001g0077 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.100+7725T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79939455 | |||||||
| chr6:79939503 | C | CTTTA | 74 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0001g0041 others(71): Show |
104 | HG00140.hp1 HG00280.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.100+7673_100+7676d others(6): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79939503 | |||||||
| chr6:79939503 | C | CTTTATTT others(1): Show |
15 | a0001c0001t0001g0159 a0001c0001t0004g0075 a0001c0001t0005g0049 others(12): Show |
24 | HG00323.hp2 HG00733.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.100+7669_100+7676d others(10): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79939503 | |||||||
| chr6:79939503 | C | CTTTATTT others(5): Show |
3 | a0001c0001t0001g0188 a0001c0001t0005g0051 a0001c0001t0005g0193 |
4 | HG02622.hp2 HG02717.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+7665_100+7676d others(14): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79939503 | |||||||
| chr6:79939503 | CTTTA | C | 5 | a0001c0001t0007g0053 a0001c0001t0007g0204 a0001c0001t0007g0205 others(2): Show |
6 | HG00099.hp1 HG01070.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.100+7673_100+7676d others(6): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79939503 | |||||||
| chr6:79939503 | CTTTATTT others(5): Show |
C | 4 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0155 others(1): Show |
9 | HG01070.hp1 HG01071.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.100+7665_100+7676d others(14): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79939503 | |||||||
| chr6:79939680 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.100+7500C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79939680 | |||||||
| chr6:79939712 | T | C | 88 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0039 others(85): Show |
141 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.100+7468A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79939712 | |||||||
| chr6:79939732 | T | C | 17 | a0001c0001t0001g0153 a0001c0001t0001g0201 a0001c0001t0003g0008 others(14): Show |
27 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.100+7448A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79939732 | |||||||
| chr6:79939997 | A | G | 1 | a0001c0001t0001g0077 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.100+7183T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79939997 | |||||||
| chr6:79940005 | C | T | 124 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0038 others(121): Show |
190 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.100+7175G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79940005 | |||||||
| chr6:79940166 | T | C | 1 | a0001c0001t0001g0160 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.100+7014A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79940166 | |||||||
| chr6:79940300 | C | T | 1 | a0001c0001t0003g0222 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.100+6880G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79940300 | |||||||
| chr6:79940314 | A | G | 1 | a0001c0001t0001g0077 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.100+6866T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79940314 | |||||||
| chr6:79940317 | T | C | 4 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0155 others(1): Show |
9 | HG01070.hp1 HG01071.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.100+6863A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79940317 | |||||||
| chr6:79940374 | T | C | 5 | a0001c0001t0007g0053 a0001c0001t0007g0204 a0001c0001t0007g0205 others(2): Show |
6 | HG00099.hp1 HG01070.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.100+6806A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79940374 | |||||||
| chr6:79940394 | G | A | 4 | a0001c0001t0001g0153 a0001c0001t0003g0010 a0001c0001t0003g0213 others(1): Show |
7 | HG02109.hp1 HG02280.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.100+6786C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79940394 | |||||||
| chr6:79940405 | T | C | 2 | a0002c0002t0008g0011 a0002c0002t0008g0196 |
4 | HG01884.hp2 HG02257.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+6775A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79940405 | |||||||
| chr6:79940453 | C | T | 2 | a0001c0001t0001g0039 a0001c0001t0001g0154 |
3 | HG02109.hp2 HG03098.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.100+6727G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79940453 | |||||||
| chr6:79940663 | T | C | 1 | a0002c0002t0002g0087 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.100+6517A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79940663 | |||||||
| chr6:79940676 | G | A | 1 | a0001c0001t0005g0193 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.100+6504C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79940676 | |||||||
| chr6:79940694 | A | G | 84 | a0001c0001t0001g0039 a0001c0001t0001g0077 a0001c0001t0001g0153 others(81): Show |
132 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.100+6486T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79940694 | |||||||
| chr6:79940742 | C | T | 2 | a0001c0001t0001g0121 a0002c0002t0002g0091 |
2 | HG02896.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.100+6438G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79940742 | |||||||
| chr6:79940829 | T | A | 4 | a0001c0001t0001g0018 a0001c0001t0001g0047 a0001c0001t0001g0189 others(1): Show |
7 | HG02129.hp1 NA18962.hp1 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.100+6351A>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79940829 | |||||||
| chr6:79940929 | A | AGAC | 4 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0155 others(1): Show |
9 | HG01070.hp1 HG01071.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.100+6248_100+6250d others(5): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79940929 | |||||||
| chr6:79941012 | TA | T | 21 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0001g0041 others(18): Show |
30 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(27): Show |
intron_variant | MODIFIER | c.100+6167delT | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79941012 | |||||||
| chr6:79941147 | T | G | 2 | a0001c0001t0001g0039 a0001c0001t0001g0154 |
3 | HG02109.hp2 HG03098.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.100+6033A>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79941147 | |||||||
| chr6:79941153 | G | A | 1 | a0002c0002t0002g0089 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.100+6027C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79941153 | |||||||
| chr6:79941154 | A | G | 1 | a0002c0002t0002g0089 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.100+6026T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79941154 | |||||||
| chr6:79941583 | C | T | 1 | a0002c0002t0002g0090 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.100+5597G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79941583 | |||||||
| chr6:79941598 | G | A | 3 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 |
3 | HG02486.hp1 HG02922.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.100+5582C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79941598 | |||||||
| chr6:79941678 | A | T | 1 | a0002c0002t0002g0089 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.100+5502T>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79941678 | |||||||
| chr6:79941711 | C | A | 1 | a0002c0002t0002g0089 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.100+5469G>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79941711 | |||||||
| chr6:79941712 | A | C | 1 | a0002c0002t0002g0089 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.100+5468T>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79941712 | |||||||
| chr6:79941771 | T | C | 1 | a0001c0001t0003g0212 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.100+5409A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79941771 | |||||||
| chr6:79941861 | G | A | 1 | a0002c0002t0002g0111 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.100+5319C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79941861 | |||||||
| chr6:79941894 | T | C | 1 | a0001c0001t0016g0190 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.100+5286A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79941894 | |||||||
| chr6:79941899 | A | G | 4 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0155 others(1): Show |
9 | HG01070.hp1 HG01071.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.100+5281T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79941899 | |||||||
| chr6:79941961 | T | C | 1 | a0001c0001t0001g0077 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.100+5219A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79941961 | |||||||
| chr6:79942084 | G | C | 5 | a0001c0001t0007g0053 a0001c0001t0007g0204 a0001c0001t0007g0205 others(2): Show |
6 | HG00099.hp1 HG01070.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.100+5096C>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79942084 | |||||||
| chr6:79942185 | G | C | 19 | a0002c0002t0002g0004 a0002c0002t0002g0007 a0002c0002t0002g0022 others(16): Show |
34 | HG00140.hp1 HG00323.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.100+4995C>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79942185 | |||||||
| chr6:79942226 | C | T | 1 | a0001c0001t0001g0120 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.100+4954G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79942226 | |||||||
| chr6:79942245 | C | T | 1 | a0001c0001t0003g0212 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.100+4935G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79942245 | |||||||
| chr6:79942356 | T | C | 1 | a0002c0002t0002g0080 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.100+4824A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79942356 | |||||||
| chr6:79942414 | T | C | 1 | a0001c0001t0001g0077 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.100+4766A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79942414 | |||||||
| chr6:79942512 | G | T | 78 | a0001c0001t0001g0039 a0001c0001t0001g0077 a0001c0001t0001g0153 others(75): Show |
125 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.100+4668C>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79942512 | |||||||
| chr6:79942760 | A | T | 59 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0007 others(56): Show |
95 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.100+4420T>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79942760 | |||||||
| chr6:79942846 | G | C | 1 | a0001c0001t0001g0077 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.100+4334C>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79942846 | |||||||
| chr6:79942952 | G | A | 7 | a0001c0001t0005g0048 a0001c0001t0005g0049 a0001c0001t0005g0050 others(4): Show |
11 | HG01891.hp1 HG02572.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.100+4228C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79942952 | |||||||
| chr6:79943176 | T | A | 4 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0155 others(1): Show |
9 | HG01070.hp1 HG01071.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.100+4004A>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79943176 | |||||||
| chr6:79943228 | G | C | 19 | a0001c0001t0001g0039 a0001c0001t0001g0153 a0001c0001t0001g0154 others(16): Show |
30 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.100+3952C>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79943228 | |||||||
| chr6:79943437 | C | G | 4 | a0001c0001t0001g0117 a0001c0001t0001g0119 a0001c0001t0001g0199 others(1): Show |
4 | HG00741.hp1 HG02055.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+3743G>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79943437 | |||||||
| chr6:79943442 | A | G | 57 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0007 others(54): Show |
91 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.100+3738T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79943442 | |||||||
| chr6:79943460 | G | T | 3 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 |
3 | HG02486.hp1 HG02922.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.100+3720C>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79943460 | |||||||
| chr6:79943461 | G | T | 1 | a0001c0001t0001g0157 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.100+3719C>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79943461 | |||||||
| chr6:79943465 | A | C | 1 | a0001c0001t0003g0213 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.100+3715T>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79943465 | |||||||
| chr6:79943549 | G | A | 1 | a0002c0002t0002g0113 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+3631C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79943549 | |||||||
| chr6:79943656 | C | A | 19 | a0001c0001t0001g0039 a0001c0001t0001g0153 a0001c0001t0001g0154 others(16): Show |
30 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.100+3524G>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79943656 | |||||||
| chr6:79943674 | A | C | 59 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0007 others(56): Show |
95 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.100+3506T>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79943674 | |||||||
| chr6:79943778 | C | T | 4 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0155 others(1): Show |
9 | HG01070.hp1 HG01071.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.100+3402G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79943778 | |||||||
| chr6:79943820 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.100+3360A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79943820 | |||||||
| chr6:79943925 | A | G | 78 | a0001c0001t0001g0039 a0001c0001t0001g0153 a0001c0001t0001g0154 others(75): Show |
125 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.100+3255T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79943925 | |||||||
| chr6:79943933 | A | G | 78 | a0001c0001t0001g0039 a0001c0001t0001g0153 a0001c0001t0001g0154 others(75): Show |
125 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.100+3247T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79943933 | |||||||
| chr6:79943941 | GAA | G | 19 | a0002c0002t0002g0004 a0002c0002t0002g0007 a0002c0002t0002g0022 others(16): Show |
34 | HG00140.hp1 HG00323.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.100+3237_100+3238d others(4): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79943941 | |||||||
| chr6:79944200 | A | T | 1 | a0002c0002t0002g0089 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.100+2980T>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79944200 | |||||||
| chr6:79944388 | A | G | 1 | a0001c0001t0001g0038 | 2 | HG01346.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.100+2792T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79944388 | |||||||
| chr6:79944916 | T | C | 163 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0012 others(160): Show |
246 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.100+2264A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79944916 | |||||||
| chr6:79944929 | C | T | 5 | a0001c0001t0007g0053 a0001c0001t0007g0204 a0001c0001t0007g0205 others(2): Show |
6 | HG00099.hp1 HG01070.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.100+2251G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79944929 | |||||||
| chr6:79944987 | C | CA | 15 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0034 others(12): Show |
22 | HG00741.hp1 HG01257.hp2 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.100+2192dupT | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79944987 | |||||||
| chr6:79944987 | CA | C | 38 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0035 others(35): Show |
45 | HG00280.hp2 HG00558.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.100+2192delT | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79944987 | |||||||
| chr6:79944987 | CAA | C | 29 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0017 others(26): Show |
43 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.100+2191_100+2192d others(4): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79944987 | |||||||
| chr6:79944987 | CAAAAAAA others(1): Show |
C | 59 | a0001c0001t0001g0077 a0001c0001t0004g0006 a0002c0002t0002g0003 others(56): Show |
93 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.100+2185_100+2192d others(10): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79944987 | |||||||
| chr6:79944987 | CAAAAAAA others(3): Show |
C | 22 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0039 others(19): Show |
38 | HG01070.hp1 HG01071.hp1 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.100+2183_100+2192d others(12): Show |
ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79944987 | |||||||
| chr6:79945133 | A | G | 1 | a0002c0002t0002g0080 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.100+2047T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79945133 | |||||||
| chr6:79945224 | G | A | 1 | a0002c0002t0002g0088 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.100+1956C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79945224 | |||||||
| chr6:79945282 | A | T | 2 | a0001c0001t0001g0115 a0001c0001t0004g0066 |
2 | HG03704.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.100+1898T>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79945282 | |||||||
| chr6:79945707 | A | T | 1 | a0001c0001t0001g0114 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.100+1473T>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79945707 | |||||||
| chr6:79945797 | C | CA | 62 | a0001c0001t0001g0077 a0001c0001t0001g0194 a0001c0001t0010g0197 others(59): Show |
98 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.100+1382dupT | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79945797 | |||||||
| chr6:79945834 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.100+1346C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79945834 | |||||||
| chr6:79946164 | G | A | 1 | a0002c0002t0002g0200 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.100+1016C>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79946164 | |||||||
| chr6:79946381 | T | C | 1 | a0001c0001t0001g0052 | 2 | HG00609.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.100+799A>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79946381 | |||||||
| chr6:79946392 | A | G | 19 | a0001c0001t0001g0079 a0002c0002t0002g0004 a0002c0002t0002g0007 others(16): Show |
34 | HG00140.hp1 HG00323.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.100+788T>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79946392 | |||||||
| chr6:79946394 | GA | G | 56 | a0001c0001t0001g0012 a0001c0001t0001g0079 a0002c0002t0002g0003 others(53): Show |
92 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.100+785delT | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79946394 | |||||||
| chr6:79946511 | C | T | 3 | a0001c0001t0001g0078 a0001c0001t0004g0063 a0001c0001t0004g0064 |
3 | HG00558.hp2 HG01515.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.100+669G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79946511 | |||||||
| chr6:79946516 | C | G | 1 | a0001c0001t0001g0077 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.100+664G>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79946516 | |||||||
| chr6:79946670 | C | G | 2 | a0001c0001t0009g0059 a0001c0001t0009g0060 |
2 | HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.100+510G>C | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79946670 | |||||||
| chr6:79946714 | G | C | 1 | a0001c0001t0001g0201 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.100+466C>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79946714 | |||||||
| chr6:79946798 | A | C | 2 | a0001c0001t0012g0058 a0002c0002t0008g0011 |
4 | HG02257.hp1 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+382T>G | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79946798 | |||||||
| chr6:79946972 | C | A | 1 | a0002c0002t0002g0202 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.100+208G>T | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79946972 | |||||||
| chr6:79947028 | C | T | 4 | a0001c0001t0007g0053 a0001c0001t0007g0204 a0001c0001t0007g0205 others(1): Show |
5 | HG00099.hp1 HG01070.hp2 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.100+152G>A | ELOVL4 | ENSG00000118402.6 | transcript | ENST00000369816.5 | protein_coding | 1/5 | chr6 | 79947028 |