Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 948 |
| ensemblid | ENSG00000135218.19 |
| hgncid | 1663 |
| symbol | CD36 |
| name | CD36 molecule |
| refseq_nuc | NM_001001548.3 |
| refseq_prot | NP_001001548.1 |
| ensembl_nuc | ENST00000447544.7 |
| ensembl_prot | ENSP00000415743.2 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 80638642 |
| end | 80679274 |
| strand | + |
| ver | v1.2 |
| region | chr7:80638642-80679274 |
| region5000 | chr7:80633642-80684274 |
| regionname0 | CD36_chr7_80638642_80679274 |
| regionname5000 | CD36_chr7_80633642_80684274 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 472 | 371 | 81 | 67 | 169 | 14 | 38 | 130 | CD36_chr7_80633642_80684274 | CD36 | MGCDR others(467): Show |
chr7 | 80633642 | 80684274 |
| a0002 | 0/0 | 324 | 11 | 11 | 0 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | MGCDR others(319): Show |
chr7 | 80633642 | 80684274 |
| a0003 | 0/0 | 472 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | CD36_chr7_80633642_80684274 | CD36 | MGCDR others(467): Show |
chr7 | 80633642 | 80684274 |
| a0004 | 0/0 | 411 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CD36_chr7_80633642_80684274 | CD36 | MGCDR others(406): Show |
chr7 | 80633642 | 80684274 |
| a0005 | 0/0 | 472 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | MGCDR others(467): Show |
chr7 | 80633642 | 80684274 |
| a0006 | 0/0 | 472 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | MGCDR others(467): Show |
chr7 | 80633642 | 80684274 |
| a0007 | 0/0 | 472 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | MGCDR others(467): Show |
chr7 | 80633642 | 80684274 |
| a0008 | 0/0 | 472 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | MGCDR others(467): Show |
chr7 | 80633642 | 80684274 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1416 | 366 | 80 | 65 | 169 | 13 | 37 | CD36_chr7_80633642_80684274 | CD36 | ATGGG others(1411): Show |
chr7 | 80633642 | 80684274 | ||
| a0001c0004 | 0/0 | 1416 | 3 | 0 | 2 | 0 | 1 | 0 | CD36_chr7_80633642_80684274 | CD36 | ATGGG others(1411): Show |
chr7 | 80633642 | 80684274 | ||
| a0001c0007 | 0/0 | 1416 | 1 | 0 | 0 | 0 | 0 | 1 | CD36_chr7_80633642_80684274 | CD36 | ATGGG others(1411): Show |
chr7 | 80633642 | 80684274 | ||
| a0001c0008 | 0/0 | 1416 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | ATGGG others(1411): Show |
chr7 | 80633642 | 80684274 | ||
| a0002c0002 | 0/0 | 1416 | 11 | 11 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | ATGGG others(1411): Show |
chr7 | 80633642 | 80684274 | ||
| a0003c0003 | 0/0 | 1416 | 4 | 0 | 0 | 4 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | ATGGG others(1411): Show |
chr7 | 80633642 | 80684274 | ||
| a0004c0005 | 0/0 | 1402 | 2 | 0 | 0 | 2 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | ATGGG others(1397): Show |
chr7 | 80633642 | 80684274 | ||
| a0005c0010 | 0/0 | 1416 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | ATGGG others(1411): Show |
chr7 | 80633642 | 80684274 | ||
| a0006c0009 | 0/0 | 1416 | 1 | 0 | 1 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | ATGGG others(1411): Show |
chr7 | 80633642 | 80684274 | ||
| a0007c0006 | 0/0 | 1416 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | ATGGG others(1411): Show |
chr7 | 80633642 | 80684274 | ||
| a0008c0011 | 0/0 | 1416 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | ATGGG others(1411): Show |
chr7 | 80633642 | 80684274 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4589 | 80 | 4 | 18 | 43 | 4 | 11 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4584): Show |
chr7 | 80633642 | 80684274 |
| a0001c0001t0002 | 0/0 | 4598 | 33 | 7 | 6 | 13 | 3 | 4 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4593): Show |
chr7 | 80633642 | 80684274 |
| a0001c0001t0003 | 0/0 | 4596 | 34 | 5 | 7 | 19 | 0 | 3 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4591): Show |
chr7 | 80633642 | 80684274 |
| a0001c0001t0004 | 0/0 | 4591 | 28 | 0 | 0 | 27 | 0 | 1 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4586): Show |
chr7 | 80633642 | 80684274 |
| a0001c0001t0005 | 0/1 | 4596 | 26 | 1 | 8 | 13 | 1 | 2 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4591): Show |
chr7 | 80633642 | 80684274 |
| a0001c0001t0006 | 0/0 | 4591 | 20 | 2 | 0 | 16 | 0 | 2 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4586): Show |
chr7 | 80633642 | 80684274 |
| a0001c0001t0007 | 1/0 | 4598 | 16 | 7 | 2 | 3 | 0 | 3 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4593): Show |
chr7 | 80633642 | 80684274 |
| a0001c0001t0008 | 0/0 | 4589 | 20 | 3 | 3 | 7 | 2 | 5 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4584): Show |
chr7 | 80633642 | 80684274 |
| a0001c0001t0009 | 0/0 | 4594 | 11 | 4 | 7 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4589): Show |
chr7 | 80633642 | 80684274 |
| a0001c0001t0010 | 0/0 | 4596 | 8 | 0 | 0 | 8 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4591): Show |
chr7 | 80633642 | 80684274 |
| a0001c0001t0011 | 0/0 | 4594 | 6 | 6 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4589): Show |
chr7 | 80633642 | 80684274 |
| a0001c0001t0012 | 0/0 | 4595 | 5 | 5 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4590): Show |
chr7 | 80633642 | 80684274 |
| a0001c0001t0013 | 0/0 | 4596 | 4 | 0 | 0 | 4 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4591): Show |
chr7 | 80633642 | 80684274 |
| a0001c0001t0014 | 0/0 | 4600 | 4 | 3 | 0 | 0 | 0 | 1 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4595): Show |
chr7 | 80633642 | 80684274 |
| a0001c0001t0015 | 0/0 | 4590 | 4 | 3 | 1 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4585): Show |
chr7 | 80633642 | 80684274 |
| a0001c0001t0016 | 0/0 | 4594 | 4 | 4 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4589): Show |
chr7 | 80633642 | 80684274 |
| a0001c0001t0017 | 0/0 | 4589 | 3 | 0 | 0 | 3 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4584): Show |
chr7 | 80633642 | 80684274 |
| a0001c0001t0018 | 0/0 | 4590 | 3 | 0 | 3 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4585): Show |
chr7 | 80633642 | 80684274 |
| a0001c0001t0019 | 0/0 | 4595 | 3 | 3 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4590): Show |
chr7 | 80633642 | 80684274 |
| a0001c0001t0020 | 0/0 | 4596 | 2 | 2 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4591): Show |
chr7 | 80633642 | 80684274 |
| a0001c0001t0021 | 0/0 | 4600 | 3 | 3 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4595): Show |
chr7 | 80633642 | 80684274 |
| a0001c0001t0022 | 0/0 | 4590 | 2 | 0 | 0 | 1 | 0 | 1 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4585): Show |
chr7 | 80633642 | 80684274 |
| a0001c0001t0023 | 0/0 | 4589 | 2 | 0 | 2 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4584): Show |
chr7 | 80633642 | 80684274 |
| a0001c0001t0024 | 0/0 | 4596 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4591): Show |
chr7 | 80633642 | 80684274 |
| a0001c0001t0025 | 0/0 | 4595 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4590): Show |
chr7 | 80633642 | 80684274 |
| a0001c0001t0026 | 0/0 | 4594 | 2 | 2 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4589): Show |
chr7 | 80633642 | 80684274 |
| a0001c0001t0027 | 0/0 | 4591 | 2 | 1 | 1 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4586): Show |
chr7 | 80633642 | 80684274 |
| a0001c0001t0028 | 0/0 | 4596 | 2 | 0 | 0 | 0 | 2 | 0 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4591): Show |
chr7 | 80633642 | 80684274 |
| a0001c0001t0029 | 0/0 | 4595 | 2 | 0 | 1 | 0 | 0 | 1 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4590): Show |
chr7 | 80633642 | 80684274 |
| a0001c0001t0030 | 0/0 | 4591 | 2 | 0 | 0 | 2 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4586): Show |
chr7 | 80633642 | 80684274 |
| a0001c0001t0031 | 0/0 | 4595 | 2 | 2 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4590): Show |
chr7 | 80633642 | 80684274 |
| a0001c0001t0032 | 0/0 | 4589 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4584): Show |
chr7 | 80633642 | 80684274 |
| a0001c0001t0033 | 0/0 | 4593 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4588): Show |
chr7 | 80633642 | 80684274 |
| a0001c0001t0034 | 0/0 | 4591 | 1 | 0 | 0 | 0 | 0 | 1 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4586): Show |
chr7 | 80633642 | 80684274 |
| a0001c0001t0035 | 0/0 | 4596 | 1 | 0 | 1 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4591): Show |
chr7 | 80633642 | 80684274 |
| a0001c0001t0036 | 0/0 | 4591 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4586): Show |
chr7 | 80633642 | 80684274 |
| a0001c0001t0037 | 0/0 | 4590 | 1 | 0 | 1 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4585): Show |
chr7 | 80633642 | 80684274 |
| a0001c0001t0038 | 0/0 | 4589 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4584): Show |
chr7 | 80633642 | 80684274 |
| a0001c0001t0039 | 0/0 | 4589 | 1 | 0 | 0 | 0 | 0 | 1 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4584): Show |
chr7 | 80633642 | 80684274 |
| a0001c0001t0040 | 0/0 | 4590 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4585): Show |
chr7 | 80633642 | 80684274 |
| a0001c0001t0041 | 0/0 | 4589 | 1 | 0 | 1 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4584): Show |
chr7 | 80633642 | 80684274 |
| a0001c0001t0042 | 0/0 | 4589 | 1 | 0 | 0 | 0 | 1 | 0 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4584): Show |
chr7 | 80633642 | 80684274 |
| a0001c0001t0043 | 0/0 | 4596 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4591): Show |
chr7 | 80633642 | 80684274 |
| a0001c0001t0044 | 0/0 | 4598 | 1 | 0 | 1 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4593): Show |
chr7 | 80633642 | 80684274 |
| a0001c0001t0045 | 0/0 | 4596 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4591): Show |
chr7 | 80633642 | 80684274 |
| a0001c0001t0046 | 0/0 | 4597 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4592): Show |
chr7 | 80633642 | 80684274 |
| a0001c0001t0047 | 0/0 | 4599 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4594): Show |
chr7 | 80633642 | 80684274 |
| a0001c0001t0048 | 0/0 | 4596 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4591): Show |
chr7 | 80633642 | 80684274 |
| a0001c0001t0049 | 0/0 | 4595 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4590): Show |
chr7 | 80633642 | 80684274 |
| a0001c0001t0050 | 0/0 | 4592 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4587): Show |
chr7 | 80633642 | 80684274 |
| a0001c0001t0051 | 0/0 | 4595 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4590): Show |
chr7 | 80633642 | 80684274 |
| a0001c0001t0052 | 0/0 | 4596 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4591): Show |
chr7 | 80633642 | 80684274 |
| a0001c0001t0054 | 0/0 | 4601 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4596): Show |
chr7 | 80633642 | 80684274 |
| a0001c0001t0055 | 0/0 | 4591 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4586): Show |
chr7 | 80633642 | 80684274 |
| a0001c0001t0056 | 0/0 | 4590 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4585): Show |
chr7 | 80633642 | 80684274 |
| a0001c0001t0057 | 0/0 | 4594 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4589): Show |
chr7 | 80633642 | 80684274 |
| a0001c0001t0058 | 0/0 | 4590 | 1 | 0 | 1 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4585): Show |
chr7 | 80633642 | 80684274 |
| a0001c0001t0059 | 0/0 | 4595 | 1 | 0 | 0 | 0 | 0 | 1 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4590): Show |
chr7 | 80633642 | 80684274 |
| a0001c0001t0060 | 0/0 | 4596 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4591): Show |
chr7 | 80633642 | 80684274 |
| a0001c0001t0061 | 0/0 | 4599 | 1 | 0 | 1 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4594): Show |
chr7 | 80633642 | 80684274 |
| a0001c0001t0062 | 0/0 | 4594 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4589): Show |
chr7 | 80633642 | 80684274 |
| a0001c0001t0063 | 0/0 | 4589 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4584): Show |
chr7 | 80633642 | 80684274 |
| a0001c0004t0001 | 0/0 | 4589 | 3 | 0 | 2 | 0 | 1 | 0 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4584): Show |
chr7 | 80633642 | 80684274 |
| a0001c0007t0024 | 0/0 | 4596 | 1 | 0 | 0 | 0 | 0 | 1 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4591): Show |
chr7 | 80633642 | 80684274 |
| a0001c0008t0007 | 0/0 | 4598 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4593): Show |
chr7 | 80633642 | 80684274 |
| a0002c0002t0002 | 0/0 | 4598 | 5 | 5 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4593): Show |
chr7 | 80633642 | 80684274 |
| a0002c0002t0007 | 0/0 | 4598 | 5 | 5 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4593): Show |
chr7 | 80633642 | 80684274 |
| a0002c0002t0025 | 0/0 | 4595 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4590): Show |
chr7 | 80633642 | 80684274 |
| a0003c0003t0001 | 0/0 | 4589 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4584): Show |
chr7 | 80633642 | 80684274 |
| a0003c0003t0006 | 0/0 | 4591 | 3 | 0 | 0 | 3 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4586): Show |
chr7 | 80633642 | 80684274 |
| a0004c0005t0004 | 0/0 | 4577 | 2 | 0 | 0 | 2 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4572): Show |
chr7 | 80633642 | 80684274 |
| a0005c0010t0006 | 0/0 | 4591 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4586): Show |
chr7 | 80633642 | 80684274 |
| a0006c0009t0001 | 0/0 | 4589 | 1 | 0 | 1 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4584): Show |
chr7 | 80633642 | 80684274 |
| a0007c0006t0020 | 0/0 | 4596 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4591): Show |
chr7 | 80633642 | 80684274 |
| a0008c0011t0053 | 0/0 | 4598 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | AGGAC others(4593): Show |
chr7 | 80633642 | 80684274 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0001g0003 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0001g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0002g0001 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0002g0016 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0002g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0002g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0002g0025 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0002g0042 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0003g0005 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0003g0013 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0003g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0003g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0003g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0004g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0004g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0004g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0004g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0004g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0004g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0004g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0004g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0004g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0004g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0005g0001 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0005g0017 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0005g0024 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0005g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0005g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0005g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0005g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0005g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0005g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0005g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0005g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0005g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0005g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0005g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0005g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0005g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0005g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0006g0002 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0006g0006 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0006g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0006g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0006g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0006g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0006g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0006g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0006g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0006g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0007g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0007g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0007g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0007g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0007g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0007g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0007g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0007g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0007g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0007g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0007g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0007g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0007g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0007g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0007g0260 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0007g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0008g0041 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0008g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0008g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0008g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0008g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0008g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0008g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0008g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0008g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0008g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0008g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0008g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0008g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0008g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0008g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0008g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0008g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0008g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0009g0010 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0009g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0009g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0009g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0009g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0009g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0009g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0010g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0010g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0010g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0010g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0011g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0011g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0011g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0011g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0012g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0012g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0013g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0013g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0013g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0013g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0014g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0014g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0014g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0014g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0015g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0015g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0015g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0016g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0016g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0017g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0017g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0018g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0018g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0018g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0019g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0019g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0019g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0020g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0020g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0021g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0021g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0021g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0022g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0022g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0023g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0024g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0025g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0026g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0026g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0027g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0028g0046 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0029g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0029g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0030g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0030g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0031g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0031g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0032g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0033g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0034g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0035g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0036g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0037g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0038g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0039g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0040g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0041g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0042g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0043g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0044g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0045g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0046g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0047g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0048g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0049g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0050g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0051g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0052g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0054g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0055g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0056g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0057g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0058g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0059g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0060g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0061g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0062g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0001t0063g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0004t0001g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0004t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0007t0024g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0001c0008t0007g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0002c0002t0002g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0002c0002t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0002c0002t0007g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0002c0002t0007g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0002c0002t0007g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0002c0002t0007g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0002c0002t0025g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0003c0003t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0003c0003t0006g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0003c0003t0006g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0004c0005t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0004c0005t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0005c0010t0006g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0006c0009t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0007c0006t0020g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| a0008c0011t0053g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0171 | EUR | GBR | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG00099 | hp2 | a0001 | c0001 | t0008 | g0228 | EUR | GBR | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG00140 | hp1 | a0001 | c0001 | t0008 | g0041 | EUR | GBR | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG00140 | hp2 | a0001 | c0001 | t0042 | g0033 | EUR | GBR | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | FIN | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0016 | EUR | FIN | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG00423 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | CHS | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | CHS | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG00438 | hp1 | a0001 | c0001 | t0043 | g0135 | EAS | CHS | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | CHS | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG00544 | hp1 | a0001 | c0001 | t0013 | g0112 | EAS | CHS | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG00544 | hp2 | a0001 | c0001 | t0005 | g0234 | EAS | CHS | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | CHS | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | CHS | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG00609 | hp1 | a0001 | c0001 | t0007 | g0149 | EAS | CHS | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | CHS | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG00621 | hp1 | a0001 | c0001 | t0007 | g0111 | EAS | CHS | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG00621 | hp2 | a0001 | c0001 | t0008 | g0202 | EAS | CHS | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG00639 | hp1 | a0001 | c0001 | t0007 | g0261 | AMR | PUR | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0025 | AMR | PUR | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0042 | AMR | PUR | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG00673 | hp1 | a0005 | c0010 | t0006 | g0176 | EAS | CHS | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG00673 | hp2 | a0001 | c0001 | t0004 | g0058 | EAS | CHS | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG00733 | hp1 | a0001 | c0001 | t0009 | g0231 | AMR | PUR | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG00738 | hp1 | a0001 | c0001 | t0005 | g0245 | AMR | PUR | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG01069 | hp2 | a0001 | c0001 | t0008 | g0044 | AMR | PUR | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG01071 | hp1 | a0001 | c0001 | t0009 | g0010 | AMR | PUR | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG01071 | hp2 | a0001 | c0001 | t0008 | g0044 | AMR | PUR | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0218 | AMR | PUR | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG01074 | hp2 | a0001 | c0001 | t0029 | g0241 | AMR | PUR | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG01081 | hp1 | a0001 | c0001 | t0008 | g0272 | AMR | PUR | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG01081 | hp2 | a0001 | c0001 | t0009 | g0010 | AMR | PUR | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG01099 | hp1 | a0001 | c0001 | t0037 | g0270 | AMR | PUR | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG01099 | hp2 | a0001 | c0001 | t0009 | g0010 | AMR | PUR | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG01106 | hp1 | a0001 | c0001 | t0005 | g0045 | AMR | PUR | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG01106 | hp2 | a0001 | c0001 | t0023 | g0008 | AMR | PUR | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG01168 | hp1 | a0006 | c0009 | t0001 | g0191 | AMR | PUR | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG01168 | hp2 | a0001 | c0001 | t0005 | g0045 | AMR | PUR | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG01175 | hp1 | a0001 | c0001 | t0061 | g0246 | AMR | PUR | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG01243 | hp1 | a0001 | c0001 | t0027 | g0027 | AMR | PUR | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG01243 | hp2 | a0001 | c0001 | t0041 | g0157 | AMR | PUR | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG01255 | hp1 | a0001 | c0001 | t0015 | g0201 | AMR | CLM | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | CLM | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG01256 | hp1 | a0001 | c0001 | t0005 | g0017 | AMR | CLM | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | CLM | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG01257 | hp1 | a0001 | c0004 | t0001 | g0039 | AMR | CLM | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG01258 | hp1 | a0001 | c0004 | t0001 | g0039 | AMR | CLM | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | CLM | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG01261 | hp1 | a0001 | c0001 | t0009 | g0010 | AMR | CLM | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG01261 | hp2 | a0001 | c0001 | t0007 | g0189 | AMR | CLM | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG01346 | hp1 | a0001 | c0001 | t0005 | g0217 | AMR | CLM | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | CLM | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG01358 | hp1 | a0001 | c0001 | t0005 | g0017 | AMR | CLM | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0128 | AMR | CLM | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG01361 | hp2 | a0001 | c0001 | t0023 | g0008 | AMR | CLM | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG01433 | hp1 | a0001 | c0001 | t0009 | g0230 | AMR | CLM | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0125 | AMR | CLM | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0013 | AMR | CLM | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG01496 | hp2 | a0001 | c0001 | t0018 | g0008 | AMR | CLM | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0037 | EUR | IBS | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG01515 | hp2 | a0001 | c0001 | t0028 | g0046 | EUR | IBS | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0016 | EUR | IBS | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG01517 | hp2 | a0001 | c0001 | t0028 | g0046 | EUR | IBS | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG01891 | hp1 | a0001 | c0001 | t0015 | g0200 | AFR | ACB | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG01891 | hp2 | a0002 | c0002 | t0002 | g0205 | AFR | ACB | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0013 | AMR | PEL | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG01928 | hp2 | a0001 | c0001 | t0058 | g0139 | AMR | PEL | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG01934 | hp2 | a0001 | c0001 | t0018 | g0167 | AMR | PEL | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG01943 | hp2 | a0001 | c0001 | t0005 | g0001 | AMR | PEL | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | PEL | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0013 | AMR | PEL | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG01993 | hp1 | a0001 | c0001 | t0009 | g0010 | AMR | PEL | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG01993 | hp2 | a0001 | c0001 | t0035 | g0090 | AMR | PEL | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02027 | hp1 | a0001 | c0001 | t0010 | g0224 | EAS | KHV | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02027 | hp2 | a0001 | c0001 | t0006 | g0006 | EAS | KHV | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02040 | hp1 | a0001 | c0001 | t0030 | g0251 | EAS | KHV | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02055 | hp1 | a0001 | c0001 | t0012 | g0029 | AFR | ACB | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02055 | hp2 | a0001 | c0001 | t0031 | g0197 | AFR | ACB | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0096 | EAS | KHV | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0152 | EAS | KHV | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02074 | hp1 | a0001 | c0001 | t0005 | g0236 | EAS | KHV | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02080 | hp1 | a0001 | c0001 | t0005 | g0252 | EAS | KHV | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02129 | hp2 | a0001 | c0001 | t0008 | g0250 | EAS | KHV | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02135 | hp2 | a0001 | c0001 | t0032 | g0095 | EAS | KHV | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02145 | hp2 | a0001 | c0001 | t0007 | g0123 | AFR | ACB | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02148 | hp1 | a0001 | c0001 | t0044 | g0013 | AMR | PEL | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02155 | hp2 | a0001 | c0001 | t0006 | g0022 | EAS | CDX | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02165 | hp2 | a0001 | c0001 | t0005 | g0043 | EAS | CDX | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02257 | hp1 | a0001 | c0001 | t0015 | g0040 | AFR | ACB | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02257 | hp2 | a0001 | c0001 | t0027 | g0027 | AFR | ACB | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0029 | AFR | ACB | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0262 | AFR | ACB | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02273 | hp2 | a0001 | c0001 | t0005 | g0017 | AMR | PEL | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0265 | AFR | ACB | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0163 | AMR | PEL | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02300 | hp2 | a0001 | c0001 | t0018 | g0057 | AMR | PEL | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0129 | EAS | KHV | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02523 | hp2 | a0001 | c0001 | t0008 | g0249 | EAS | KHV | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02572 | hp1 | a0001 | c0001 | t0008 | g0211 | AFR | GWD | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02572 | hp2 | a0001 | c0001 | t0009 | g0140 | AFR | GWD | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0275 | SAS | PJL | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02615 | hp2 | a0001 | c0001 | t0051 | g0094 | AFR | GWD | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02622 | hp1 | a0001 | c0008 | t0007 | g0122 | AFR | GWD | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02622 | hp2 | a0001 | c0001 | t0016 | g0011 | AFR | GWD | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02630 | hp1 | a0001 | c0001 | t0019 | g0277 | AFR | GWD | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02630 | hp2 | a0001 | c0001 | t0046 | g0124 | AFR | GWD | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02647 | hp1 | a0001 | c0001 | t0007 | g0259 | AFR | GWD | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0107 | AFR | GWD | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02683 | hp2 | a0001 | c0001 | t0008 | g0219 | SAS | PJL | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02717 | hp1 | a0001 | c0001 | t0007 | g0088 | AFR | GWD | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02717 | hp2 | a0001 | c0001 | t0006 | g0188 | AFR | GWD | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02723 | hp1 | a0001 | c0001 | t0047 | g0132 | AFR | GWD | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0199 | AFR | GWD | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0186 | SAS | PJL | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0240 | SAS | PJL | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02809 | hp1 | a0001 | c0001 | t0025 | g0145 | AFR | GWD | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02809 | hp2 | a0001 | c0001 | t0011 | g0026 | AFR | GWD | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02818 | hp1 | a0001 | c0001 | t0052 | g0266 | AFR | GWD | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02818 | hp2 | a0002 | c0002 | t0025 | g0255 | AFR | GWD | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02886 | hp1 | a0001 | c0001 | t0007 | g0118 | AFR | GWD | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02886 | hp2 | a0001 | c0001 | t0008 | g0196 | AFR | GWD | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | GWD | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0126 | AFR | GWD | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02896 | hp1 | a0001 | c0001 | t0009 | g0198 | AFR | GWD | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02896 | hp2 | a0001 | c0001 | t0016 | g0011 | AFR | GWD | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | GWD | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02897 | hp2 | a0001 | c0001 | t0016 | g0011 | AFR | GWD | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02922 | hp1 | a0002 | c0002 | t0002 | g0015 | AFR | ESN | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02922 | hp2 | a0001 | c0001 | t0009 | g0011 | AFR | ESN | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02965 | hp1 | a0002 | c0002 | t0007 | g0278 | AFR | ESN | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02965 | hp2 | a0002 | c0002 | t0002 | g0015 | AFR | ESN | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02970 | hp1 | a0002 | c0002 | t0007 | g0048 | AFR | ESN | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02970 | hp2 | a0001 | c0001 | t0031 | g0248 | AFR | ESN | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02976 | hp1 | a0002 | c0002 | t0002 | g0015 | AFR | ESN | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02976 | hp2 | a0001 | c0001 | t0033 | g0049 | AFR | ESN | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG03017 | hp1 | a0001 | c0001 | t0014 | g0115 | SAS | PJL | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG03041 | hp1 | a0001 | c0001 | t0057 | g0050 | AFR | GWD | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG03041 | hp2 | a0001 | c0001 | t0040 | g0133 | AFR | GWD | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG03098 | hp1 | a0001 | c0001 | t0015 | g0040 | AFR | MSL | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG03098 | hp2 | a0007 | c0006 | t0020 | g0195 | AFR | MSL | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0204 | AFR | ESN | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG03130 | hp2 | a0001 | c0001 | t0014 | g0084 | AFR | ESN | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG03139 | hp1 | a0001 | c0001 | t0056 | g0051 | AFR | ESN | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG03139 | hp2 | a0001 | c0001 | t0024 | g0254 | AFR | ESN | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG03195 | hp1 | a0008 | c0011 | t0053 | g0269 | AFR | ESN | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG03195 | hp2 | a0002 | c0002 | t0007 | g0264 | AFR | ESN | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG03209 | hp1 | a0001 | c0001 | t0011 | g0032 | AFR | MSL | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG03209 | hp2 | a0001 | c0001 | t0019 | g0267 | AFR | MSL | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | MSL | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG03225 | hp2 | a0001 | c0001 | t0009 | g0082 | AFR | MSL | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG03239 | hp1 | a0001 | c0001 | t0008 | g0247 | SAS | PJL | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG03239 | hp2 | a0001 | c0001 | t0008 | g0041 | SAS | PJL | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG03453 | hp1 | a0001 | c0001 | t0012 | g0014 | AFR | MSL | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG03453 | hp2 | a0001 | c0001 | t0019 | g0276 | AFR | MSL | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG03486 | hp1 | a0001 | c0001 | t0026 | g0256 | AFR | MSL | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG03486 | hp2 | a0001 | c0001 | t0016 | g0054 | AFR | MSL | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG03516 | hp1 | a0002 | c0002 | t0002 | g0015 | AFR | ESN | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG03516 | hp2 | a0001 | c0001 | t0012 | g0014 | AFR | ESN | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG03540 | hp1 | a0001 | c0001 | t0011 | g0026 | AFR | GWD | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG03540 | hp2 | a0001 | c0001 | t0054 | g0222 | AFR | GWD | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG03579 | hp1 | a0001 | c0001 | t0007 | g0166 | AFR | MSL | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG03579 | hp2 | a0001 | c0001 | t0005 | g0242 | AFR | MSL | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG03654 | hp1 | a0001 | c0001 | t0008 | g0229 | SAS | PJL | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0177 | SAS | PJL | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG03669 | hp2 | a0001 | c0001 | t0007 | g0148 | SAS | PJL | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG03688 | hp1 | a0001 | c0001 | t0006 | g0002 | SAS | STU | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG03688 | hp2 | a0001 | c0001 | t0008 | g0210 | SAS | STU | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG03704 | hp2 | a0001 | c0007 | t0024 | g0183 | SAS | PJL | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG03710 | hp1 | a0001 | c0001 | t0029 | g0238 | SAS | PJL | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0223 | SAS | BEB | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG03831 | hp2 | a0001 | c0001 | t0007 | g0169 | SAS | BEB | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG03834 | hp1 | a0001 | c0001 | t0004 | g0059 | SAS | BEB | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0159 | SAS | BEB | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0244 | SAS | STU | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0237 | SAS | STU | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG04184 | hp1 | a0001 | c0001 | t0022 | g0271 | SAS | BEB | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG04184 | hp2 | a0001 | c0001 | t0007 | g0147 | SAS | BEB | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | STU | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | STU | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG04204 | hp1 | a0001 | c0001 | t0039 | g0106 | SAS | STU | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG04204 | hp2 | a0001 | c0001 | t0005 | g0243 | SAS | STU | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG04228 | hp1 | a0001 | c0001 | t0059 | g0215 | SAS | STU | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG04228 | hp2 | a0001 | c0001 | t0005 | g0220 | SAS | STU | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18522 | hp1 | a0001 | c0001 | t0014 | g0190 | AFR | YRI | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18522 | hp2 | a0002 | c0002 | t0007 | g0263 | AFR | YRI | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18612 | hp1 | a0001 | c0001 | t0006 | g0022 | EAS | CHB | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18612 | hp2 | a0001 | c0001 | t0005 | g0226 | EAS | CHB | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18906 | hp1 | a0002 | c0002 | t0007 | g0048 | AFR | YRI | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18906 | hp2 | a0001 | c0001 | t0062 | g0209 | AFR | YRI | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18940 | hp1 | a0001 | c0001 | t0006 | g0092 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18940 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18945 | hp1 | a0001 | c0001 | t0013 | g0170 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18945 | hp2 | a0001 | c0001 | t0004 | g0018 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18946 | hp2 | a0001 | c0001 | t0055 | g0221 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18948 | hp2 | a0001 | c0001 | t0005 | g0047 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18951 | hp2 | a0001 | c0001 | t0008 | g0212 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18953 | hp1 | a0001 | c0001 | t0004 | g0079 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18953 | hp2 | a0001 | c0001 | t0010 | g0009 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18956 | hp1 | a0004 | c0005 | t0004 | g0080 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18957 | hp1 | a0001 | c0001 | t0006 | g0006 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18960 | hp2 | a0001 | c0001 | t0004 | g0097 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18961 | hp1 | a0001 | c0001 | t0010 | g0207 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0134 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18962 | hp1 | a0001 | c0001 | t0006 | g0182 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18963 | hp2 | a0001 | c0001 | t0006 | g0073 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18964 | hp1 | a0001 | c0001 | t0008 | g0216 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18964 | hp2 | a0001 | c0001 | t0004 | g0072 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0116 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18965 | hp2 | a0001 | c0001 | t0010 | g0009 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18966 | hp1 | a0001 | c0001 | t0036 | g0074 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18966 | hp2 | a0001 | c0001 | t0030 | g0208 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18967 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18968 | hp1 | a0001 | c0001 | t0005 | g0043 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18968 | hp2 | a0001 | c0001 | t0004 | g0018 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18969 | hp1 | a0003 | c0003 | t0006 | g0034 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18969 | hp2 | a0001 | c0001 | t0048 | g0068 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18971 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18971 | hp2 | a0001 | c0001 | t0010 | g0009 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18974 | hp2 | a0001 | c0001 | t0010 | g0227 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18975 | hp2 | a0001 | c0001 | t0007 | g0021 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18978 | hp1 | a0004 | c0005 | t0004 | g0077 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18980 | hp1 | a0001 | c0001 | t0006 | g0002 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18980 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18981 | hp2 | a0003 | c0003 | t0006 | g0151 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18982 | hp2 | a0001 | c0001 | t0017 | g0083 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18983 | hp1 | a0001 | c0001 | t0004 | g0018 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18983 | hp2 | a0001 | c0001 | t0017 | g0002 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18984 | hp1 | a0001 | c0001 | t0006 | g0006 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18984 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18985 | hp1 | a0001 | c0001 | t0008 | g0233 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18985 | hp2 | a0001 | c0001 | t0006 | g0006 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18988 | hp2 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18990 | hp1 | a0001 | c0001 | t0010 | g0009 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18990 | hp2 | a0001 | c0001 | t0004 | g0165 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18991 | hp1 | a0001 | c0001 | t0005 | g0213 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18995 | hp2 | a0001 | c0001 | t0006 | g0038 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18998 | hp1 | a0001 | c0001 | t0006 | g0006 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18999 | hp1 | a0001 | c0001 | t0004 | g0064 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA19000 | hp1 | a0003 | c0003 | t0001 | g0150 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA19000 | hp2 | a0001 | c0001 | t0038 | g0113 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA19001 | hp2 | a0001 | c0001 | t0050 | g0180 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA19002 | hp1 | a0001 | c0001 | t0004 | g0075 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA19004 | hp2 | a0001 | c0001 | t0006 | g0006 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA19006 | hp1 | a0001 | c0001 | t0004 | g0028 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA19006 | hp2 | a0001 | c0001 | t0003 | g0142 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA19007 | hp1 | a0003 | c0003 | t0006 | g0034 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA19007 | hp2 | a0001 | c0001 | t0005 | g0225 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA19010 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA19010 | hp2 | a0001 | c0001 | t0004 | g0158 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA19011 | hp2 | a0001 | c0001 | t0022 | g0076 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA19012 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA19012 | hp2 | a0001 | c0001 | t0006 | g0022 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA19030 | hp1 | a0001 | c0001 | t0021 | g0141 | AFR | LWK | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA19030 | hp2 | a0001 | c0001 | t0007 | g0052 | AFR | LWK | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA19043 | hp1 | a0001 | c0001 | t0012 | g0014 | AFR | LWK | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA19043 | hp2 | a0001 | c0001 | t0020 | g0203 | AFR | LWK | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA19057 | hp1 | a0001 | c0001 | t0004 | g0063 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA19057 | hp2 | a0001 | c0001 | t0060 | g0235 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA19058 | hp1 | a0001 | c0001 | t0063 | g0214 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA19060 | hp1 | a0001 | c0001 | t0004 | g0098 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA19064 | hp2 | a0001 | c0001 | t0004 | g0060 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA19065 | hp1 | a0001 | c0001 | t0004 | g0071 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA19065 | hp2 | a0001 | c0001 | t0004 | g0178 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA19066 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA19066 | hp2 | a0001 | c0001 | t0017 | g0002 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA19067 | hp2 | a0001 | c0001 | t0004 | g0070 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA19074 | hp1 | a0001 | c0001 | t0006 | g0193 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA19077 | hp2 | a0001 | c0001 | t0045 | g0021 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA19079 | hp2 | a0001 | c0001 | t0004 | g0162 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA19080 | hp2 | a0001 | c0001 | t0013 | g0153 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA19084 | hp2 | a0001 | c0001 | t0010 | g0009 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA19086 | hp2 | a0001 | c0001 | t0008 | g0253 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA19087 | hp2 | a0001 | c0001 | t0004 | g0028 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA19088 | hp2 | a0001 | c0001 | t0004 | g0078 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA19090 | hp1 | a0001 | c0001 | t0013 | g0093 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA19240 | hp1 | a0001 | c0001 | t0049 | g0155 | AFR | YRI | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA19240 | hp2 | a0001 | c0001 | t0011 | g0258 | AFR | YRI | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA20129 | hp1 | a0001 | c0001 | t0026 | g0257 | AFR | ASW | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | ASW | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0175 | EUR | TSI | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA20752 | hp2 | a0001 | c0001 | t0005 | g0024 | EUR | TSI | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0042 | EUR | TSI | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA20805 | hp2 | a0001 | c0004 | t0001 | g0187 | EUR | TSI | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA20905 | hp1 | a0001 | c0001 | t0034 | g0160 | SAS | GIH | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA20905 | hp2 | a0001 | c0001 | t0006 | g0002 | SAS | GIH | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02109 | hp1 | a0001 | c0001 | t0007 | g0164 | AFR | ACB | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02109 | hp2 | a0001 | c0001 | t0011 | g0032 | AFR | ACB | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02486 | hp1 | a0001 | c0001 | t0008 | g0279 | AFR | ACB | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02486 | hp2 | a0001 | c0001 | t0011 | g0268 | AFR | ACB | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02559 | hp1 | a0001 | c0001 | t0021 | g0053 | AFR | ACB | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG02559 | hp2 | a0001 | c0001 | t0012 | g0014 | AFR | ACB | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG03471 | hp1 | a0001 | c0001 | t0021 | g0206 | AFR | MSL | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0232 | AFR | MSL | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | USA | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| HG06807 | hp2 | a0001 | c0001 | t0020 | g0194 | AFR | USA | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18955 | hp1 | a0001 | c0001 | t0006 | g0038 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA18955 | hp2 | a0001 | c0001 | t0004 | g0056 | EAS | JPT | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA21309 | hp1 | a0001 | c0001 | t0006 | g0156 | AFR | LWK | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| NA21309 | hp2 | a0001 | c0001 | t0014 | g0119 | AFR | LWK | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0005 | g0024 | REF | REF | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0007 | g0260 | REF | REF | CD36_chr7_80633642_80684274 | CD36 | chr7 | 80633642 | 80684274 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:80656577 | A | G | 1 | a0008 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.158A>G | p.Asn53Ser | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 4/15 | 446/4598 | 158/1419 | 53/472 | chr7 | 80656577 | |||
| chr7:80656687 | C | T | 1 | a0003 | 4 | NA18969.hp1 NA18981.hp2 NA19000.hp1 others(1): Show |
missense_variant | MODERATE | c.268C>T | p.Pro90Ser | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 4/15 | 556/4598 | 268/1419 | 90/472 | chr7 | 80656687 | |||
| chr7:80661161 | C | T | 1 | a0005 | 1 | HG00673.hp1 | missense_variant | MODERATE | c.380C>T | p.Ser127Leu | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 5/15 | 668/4598 | 380/1419 | 127/472 | chr7 | 80661161 | |||
| chr7:80669964 | T | G | 1 | a0007 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.760T>G | p.Phe254Val | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 9/15 | 1048/4598 | 760/1419 | 254/472 | chr7 | 80669964 | |||
| chr7:80671133 | T | G | 1 | a0002 | 11 | HG01891.hp2 HG02818.hp2 HG02922.hp1 others(8): Show |
stop_gained | HIGH | c.975T>G | p.Tyr325* | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 10/15 | 1263/4598 | 975/1419 | 325/472 | chr7 | 80671133 | |||
| chr7:80672783 | C | G | 1 | a0006 | 1 | HG01168.hp1 | missense_variant | MODERATE | c.1139C>G | p.Thr380Ser | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 12/15 | 1427/4598 | 1139/1419 | 380/472 | chr7 | 80672783 | |||
| chr7:80673379 | CTATATTG others(7): Show |
C | 1 | a0004 | 2 | NA18956.hp1 NA18978.hp1 |
frameshift_variant | HIGH | c.1226_1239delATATTG others(8): Show |
p.Tyr409fs | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 13/15 | 1514/4598 | 1226/1419 | 409/472 | INFO_REALIGN_3_PRIME | chr7 | 80673379 | ||
| chr7:80673381 | ATATTGTG others(5): Show |
A | 1 | a0001 | 2 | HG00544.hp1 NA19090.hp1 |
conservative_inframe_deletion | MODERATE | c.1228_1239delATTGTG others(6): Show |
p.Ile410_Ile413del | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 13/15 | 1516/4598 | 1228/1419 | 410/472 | INFO_REALIGN_3_PRIME | chr7 | 80673381 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:80663133 | G | A | 1 | a0001c0004 | 3 | HG01257.hp1 HG01258.hp1 NA20805.hp2 |
synonymous_variant | LOW | c.573G>A | p.Pro191Pro | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 6/15 | 861/4598 | 573/1419 | 191/472 | chr7 | 80663133 | |||
| chr7:80671037 | T | C | 1 | a0001c0007 | 1 | HG03704.hp2 | synonymous_variant | LOW | c.879T>C | p.Phe293Phe | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 10/15 | 1167/4598 | 879/1419 | 293/472 | chr7 | 80671037 | |||
| chr7:80672796 | A | C | 1 | a0001c0008 | 1 | HG02622.hp1 | synonymous_variant | LOW | c.1152A>C | p.Ala384Ala | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 12/15 | 1440/4598 | 1152/1419 | 384/472 | chr7 | 80672796 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:80646121 | T | A | 1 | a0001c0001t0032 | 1 | HG02135.hp2 | 5_prime_UTR_variant | MODIFIER | c.-150T>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 2/15 | 620 | chr7 | 80646121 | ||||||
| chr7:80646139 | A | C | 25 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0008 others(22): Show |
134 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(131): Show |
5_prime_UTR_variant | MODIFIER | c.-132A>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 2/15 | 602 | chr7 | 80646139 | ||||||
| chr7:80646675 | T | G | 1 | a0001c0001t0028 | 2 | HG01515.hp2 HG01517.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-66T>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/15 | chr7 | 80646675 | |||||||
| chr7:80676471 | C | T | 1 | a0001c0001t0027 | 2 | HG01243.hp1 HG02257.hp2 |
3_prime_UTR_variant | MODIFIER | c.*88C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 2324 | chr7 | 80676471 | ||||||
| chr7:80676591 | C | T | 1 | a0008c0011t0053 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*208C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 2444 | chr7 | 80676591 | ||||||
| chr7:80676597 | A | G | 1 | a0001c0001t0063 | 1 | NA19058.hp1 | 3_prime_UTR_variant | MODIFIER | c.*214A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 2450 | chr7 | 80676597 | ||||||
| chr7:80676617 | A | G | 2 | a0001c0001t0052 a0001c0001t0062 |
2 | HG02818.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*234A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 2470 | chr7 | 80676617 | ||||||
| chr7:80676710 | T | A | 1 | a0001c0001t0034 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*327T>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 2563 | chr7 | 80676710 | ||||||
| chr7:80676807 | C | CT | 5 | a0001c0001t0019 a0001c0001t0049 a0001c0001t0050 others(2): Show |
7 | HG01175.hp1 HG02615.hp2 HG02630.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*436dupT | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 2673 | INFO_REALIGN_3_PRIME | chr7 | 80676807 | |||||
| chr7:80676916 | G | A | 1 | a0001c0001t0049 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*533G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 2769 | chr7 | 80676916 | ||||||
| chr7:80676924 | T | C | 1 | a0001c0001t0035 | 1 | HG01993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*541T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 2777 | chr7 | 80676924 | ||||||
| chr7:80676955 | G | A | 33 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(30): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
3_prime_UTR_variant | MODIFIER | c.*572G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 2808 | chr7 | 80676955 | ||||||
| chr7:80677034 | C | G | 32 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(29): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
3_prime_UTR_variant | MODIFIER | c.*651C>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 2887 | chr7 | 80677034 | ||||||
| chr7:80677087 | A | C | 1 | a0001c0001t0048 | 1 | NA18969.hp2 | 3_prime_UTR_variant | MODIFIER | c.*704A>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 2940 | chr7 | 80677087 | ||||||
| chr7:80677091 | C | A | 1 | a0001c0001t0027 | 2 | HG01243.hp1 HG02257.hp2 |
3_prime_UTR_variant | MODIFIER | c.*708C>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 2944 | chr7 | 80677091 | ||||||
| chr7:80677293 | G | C | 1 | a0001c0001t0059 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*910G>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 3146 | chr7 | 80677293 | ||||||
| chr7:80677342 | G | A | 1 | a0001c0001t0017 | 3 | NA18982.hp2 NA18983.hp2 NA19066.hp2 |
3_prime_UTR_variant | MODIFIER | c.*959G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 3195 | chr7 | 80677342 | ||||||
| chr7:80677435 | C | T | 26 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0008 others(23): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
3_prime_UTR_variant | MODIFIER | c.*1052C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 3288 | chr7 | 80677435 | ||||||
| chr7:80677496 | C | T | 1 | a0001c0001t0042 | 1 | HG00140.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1113C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 3349 | chr7 | 80677496 | ||||||
| chr7:80677610 | T | A | 1 | a0001c0001t0043 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1227T>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 3463 | chr7 | 80677610 | ||||||
| chr7:80677612 | T | A | 1 | a0001c0001t0043 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1229T>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 3465 | chr7 | 80677612 | ||||||
| chr7:80677613 | C | A | 1 | a0001c0001t0043 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1230C>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 3466 | chr7 | 80677613 | ||||||
| chr7:80677614 | C | G | 1 | a0001c0001t0043 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1231C>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 3467 | chr7 | 80677614 | ||||||
| chr7:80677617 | G | C | 1 | a0001c0001t0043 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1234G>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 3470 | chr7 | 80677617 | ||||||
| chr7:80677620 | A | G | 1 | a0001c0001t0043 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1237A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 3473 | chr7 | 80677620 | ||||||
| chr7:80677624 | A | C | 1 | a0001c0001t0043 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1241A>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 3477 | chr7 | 80677624 | ||||||
| chr7:80677625 | T | A | 1 | a0001c0001t0043 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1242T>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 3478 | chr7 | 80677625 | ||||||
| chr7:80677630 | A | T | 1 | a0001c0001t0043 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1247A>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 3483 | chr7 | 80677630 | ||||||
| chr7:80677632 | G | T | 1 | a0001c0001t0043 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1249G>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 3485 | chr7 | 80677632 | ||||||
| chr7:80677633 | A | C | 1 | a0001c0001t0043 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1250A>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 3486 | chr7 | 80677633 | ||||||
| chr7:80677635 | A | T | 1 | a0001c0001t0043 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1252A>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 3488 | chr7 | 80677635 | ||||||
| chr7:80677640 | T | A | 1 | a0001c0001t0043 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1257T>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 3493 | chr7 | 80677640 | ||||||
| chr7:80677641 | G | T | 1 | a0001c0001t0043 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1258G>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 3494 | chr7 | 80677641 | ||||||
| chr7:80677646 | C | T | 1 | a0001c0001t0043 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1263C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 3499 | chr7 | 80677646 | ||||||
| chr7:80677649 | G | C | 1 | a0001c0001t0043 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1266G>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 3502 | chr7 | 80677649 | ||||||
| chr7:80677652 | C | G | 1 | a0001c0001t0043 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1269C>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 3505 | chr7 | 80677652 | ||||||
| chr7:80677653 | T | G | 1 | a0001c0001t0043 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1270T>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 3506 | chr7 | 80677653 | ||||||
| chr7:80677654 | T | A | 1 | a0001c0001t0043 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1271T>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 3507 | chr7 | 80677654 | ||||||
| chr7:80677656 | T | A | 1 | a0001c0001t0043 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1273T>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 3509 | chr7 | 80677656 | ||||||
| chr7:80677678 | T | C | 2 | a0001c0001t0024 a0001c0007t0024 |
2 | HG03139.hp2 HG03704.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1295T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 3531 | chr7 | 80677678 | ||||||
| chr7:80677713 | T | C | 1 | a0001c0001t0036 | 1 | NA18966.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1330T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 3566 | chr7 | 80677713 | ||||||
| chr7:80677817 | T | G | 2 | a0001c0001t0020 a0007c0006t0020 |
3 | HG03098.hp2 HG06807.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1434T>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 3670 | chr7 | 80677817 | ||||||
| chr7:80677908 | G | T | 22 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0008 others(19): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
3_prime_UTR_variant | MODIFIER | c.*1525G>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 3761 | chr7 | 80677908 | ||||||
| chr7:80678081 | A | ATG | 4 | a0001c0001t0014 a0001c0001t0021 a0001c0001t0047 others(1): Show |
9 | HG02559.hp1 HG02723.hp1 HG03017.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1729_*1730dupTG | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 3967 | INFO_REALIGN_3_PRIME | chr7 | 80678081 | |||||
| chr7:80678081 | ATG | A | 17 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0010 others(14): Show |
90 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*1729_*1730delTG | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 3965 | INFO_REALIGN_3_PRIME | chr7 | 80678081 | |||||
| chr7:80678081 | ATGTG | A | 13 | a0001c0001t0009 a0001c0001t0011 a0001c0001t0016 others(10): Show |
35 | HG00733.hp1 HG01071.hp1 HG01081.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*1727_*1730delTGTG | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 3963 | INFO_REALIGN_3_PRIME | chr7 | 80678081 | |||||
| chr7:80678081 | ATGTGTGT others(1): Show |
A | 14 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0022 others(11): Show |
66 | HG00673.hp1 HG00673.hp2 HG01099.hp1 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*1723_*1730delTGTG others(4): Show |
CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 3959 | INFO_REALIGN_3_PRIME | chr7 | 80678081 | |||||
| chr7:80678081 | ATGTGTGT others(3): Show |
A | 17 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0015 others(14): Show |
125 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*1721_*1730delTGTG others(6): Show |
CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 3957 | INFO_REALIGN_3_PRIME | chr7 | 80678081 | |||||
| chr7:80678104 | T | G | 1 | a0001c0001t0044 | 1 | HG02148.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1721T>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 3957 | chr7 | 80678104 | ||||||
| chr7:80678149 | G | A | 1 | a0001c0001t0045 | 1 | NA19077.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1766G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 4002 | chr7 | 80678149 | ||||||
| chr7:80678186 | G | A | 19 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0008 others(16): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
3_prime_UTR_variant | MODIFIER | c.*1803G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 4039 | chr7 | 80678186 | ||||||
| chr7:80678208 | G | A | 1 | a0001c0001t0058 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1825G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 4061 | chr7 | 80678208 | ||||||
| chr7:80678308 | C | T | 26 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0008 others(23): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
3_prime_UTR_variant | MODIFIER | c.*1925C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 4161 | chr7 | 80678308 | ||||||
| chr7:80678310 | G | C | 1 | a0001c0001t0051 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1927G>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 4163 | chr7 | 80678310 | ||||||
| chr7:80678365 | A | G | 1 | a0001c0001t0027 | 2 | HG01243.hp1 HG02257.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1982A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 4218 | chr7 | 80678365 | ||||||
| chr7:80678539 | G | T | 1 | a0001c0001t0039 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2156G>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 4392 | chr7 | 80678539 | ||||||
| chr7:80678655 | C | T | 1 | a0001c0001t0023 | 2 | HG01106.hp2 HG01361.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2272C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 4508 | chr7 | 80678655 | ||||||
| chr7:80678798 | C | T | 7 | a0001c0001t0019 a0001c0001t0037 a0001c0001t0049 others(4): Show |
9 | HG01099.hp1 HG02615.hp2 HG02630.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2415C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 4651 | chr7 | 80678798 | ||||||
| chr7:80678826 | G | C | 1 | a0008c0011t0053 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2443G>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 4679 | chr7 | 80678826 | ||||||
| chr7:80678842 | C | CA | 29 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(26): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
3_prime_UTR_variant | MODIFIER | c.*2471dupA | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 4708 | INFO_REALIGN_3_PRIME | chr7 | 80678842 | |||||
| chr7:80678842 | C | CAA | 4 | a0001c0001t0015 a0001c0001t0018 a0001c0001t0040 others(1): Show |
9 | HG01255.hp1 HG01496.hp2 HG01891.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2470_*2471dupAA | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 4708 | INFO_REALIGN_3_PRIME | chr7 | 80678842 | |||||
| chr7:80678842 | CA | C | 3 | a0001c0001t0012 a0001c0001t0046 a0001c0001t0047 |
7 | HG02055.hp1 HG02559.hp2 HG02630.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2471delA | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 4707 | INFO_REALIGN_3_PRIME | chr7 | 80678842 | |||||
| chr7:80678855 | C | A | 37 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(34): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
3_prime_UTR_variant | MODIFIER | c.*2472C>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 4708 | chr7 | 80678855 | ||||||
| chr7:80678883 | G | A | 3 | a0001c0001t0010 a0001c0001t0013 a0001c0001t0048 |
13 | HG00544.hp1 HG02027.hp1 NA18945.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2500G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 4736 | chr7 | 80678883 | ||||||
| chr7:80678924 | G | A | 1 | a0001c0001t0054 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2541G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 4777 | chr7 | 80678924 | ||||||
| chr7:80678969 | G | C | 1 | a0008c0011t0053 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2586G>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 4822 | chr7 | 80678969 | ||||||
| chr7:80678986 | T | C | 2 | a0001c0001t0016 a0001c0001t0026 |
6 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2603T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 4839 | chr7 | 80678986 | ||||||
| chr7:80679080 | A | G | 1 | a0001c0001t0038 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2697A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 4933 | chr7 | 80679080 | ||||||
| chr7:80679164 | T | A | 7 | a0001c0001t0019 a0001c0001t0037 a0001c0001t0049 others(4): Show |
9 | HG01099.hp1 HG02615.hp2 HG02630.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2781T>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 5017 | chr7 | 80679164 | ||||||
| chr7:80679191 | G | A | 1 | a0001c0001t0060 | 1 | NA19057.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2808G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 5044 | chr7 | 80679191 | ||||||
| chr7:80679218 | A | C | 1 | a0001c0001t0049 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2835A>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 15/15 | 5071 | chr7 | 80679218 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:80638799 | C | T | 4 | a0001c0001t0008g0279 a0001c0001t0019g0276 a0001c0001t0019g0277 others(1): Show |
4 | HG02486.hp1 HG02630.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-184+53C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80638799 | |||||||
| chr7:80638823 | T | G | 3 | a0001c0001t0011g0026 a0001c0001t0027g0027 a0001c0001t0033g0049 |
5 | HG01243.hp1 HG02257.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-184+77T>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80638823 | |||||||
| chr7:80638866 | A | AAAAGGTA others(284): Show |
1 | a0001c0001t0001g0275 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-184+141_-184+142i others(293): Show |
CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 80638866 | ||||||
| chr7:80639103 | G | T | 1 | a0001c0001t0001g0274 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-184+357G>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80639103 | |||||||
| chr7:80639104 | C | T | 1 | a0001c0001t0001g0274 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-184+358C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80639104 | |||||||
| chr7:80639243 | G | T | 1 | a0001c0001t0001g0273 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-184+497G>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80639243 | |||||||
| chr7:80639402 | A | G | 1 | a0001c0001t0008g0272 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-184+656A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80639402 | |||||||
| chr7:80639435 | A | G | 1 | a0001c0001t0022g0271 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-184+689A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80639435 | |||||||
| chr7:80639570 | T | C | 2 | a0001c0001t0056g0051 a0001c0001t0057g0050 |
2 | HG03041.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-184+824T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80639570 | |||||||
| chr7:80639631 | T | G | 1 | a0001c0001t0007g0052 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-184+885T>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80639631 | |||||||
| chr7:80639661 | G | A | 4 | a0001c0001t0009g0011 a0001c0001t0016g0011 a0001c0001t0016g0054 others(1): Show |
6 | HG02559.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-184+915G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80639661 | |||||||
| chr7:80639730 | T | C | 1 | a0001c0001t0001g0055 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-184+984T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80639730 | |||||||
| chr7:80639769 | T | C | 31 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0065 others(28): Show |
38 | HG00673.hp2 HG01358.hp2 HG01981.hp2 others(35): Show |
intron_variant | MODIFIER | c.-184+1023T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80639769 | |||||||
| chr7:80640135 | C | A | 1 | a0001c0001t0009g0082 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-184+1389C>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80640135 | |||||||
| chr7:80640368 | T | C | 4 | a0001c0001t0009g0011 a0001c0001t0016g0011 a0001c0001t0016g0054 others(1): Show |
6 | HG02559.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-184+1622T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80640368 | |||||||
| chr7:80640692 | G | A | 3 | a0001c0001t0019g0276 a0001c0001t0019g0277 a0002c0002t0007g0278 |
3 | HG02630.hp1 HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-184+1946G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80640692 | |||||||
| chr7:80640760 | G | A | 71 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(68): Show |
99 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.-184+2014G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80640760 | |||||||
| chr7:80640822 | G | A | 276 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(273): Show |
373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.-184+2076G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80640822 | |||||||
| chr7:80640953 | A | G | 281 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(278): Show |
378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.-184+2207A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80640953 | |||||||
| chr7:80641126 | A | G | 281 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(278): Show |
378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.-184+2380A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80641126 | |||||||
| chr7:80641254 | G | T | 1 | a0001c0001t0001g0137 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-184+2508G>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80641254 | |||||||
| chr7:80641506 | A | G | 90 | a0001c0001t0002g0001 a0001c0001t0002g0016 a0001c0001t0002g0017 others(87): Show |
128 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.-184+2760A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80641506 | |||||||
| chr7:80641557 | A | G | 31 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0065 others(28): Show |
38 | HG00673.hp2 HG01358.hp2 HG01981.hp2 others(35): Show |
intron_variant | MODIFIER | c.-184+2811A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80641557 | |||||||
| chr7:80641792 | G | A | 102 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(99): Show |
137 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(134): Show |
intron_variant | MODIFIER | c.-184+3046G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80641792 | |||||||
| chr7:80641808 | T | C | 1 | a0001c0001t0001g0138 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-184+3062T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80641808 | |||||||
| chr7:80641938 | T | C | 1 | a0001c0001t0008g0279 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-184+3192T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80641938 | |||||||
| chr7:80641942 | C | CA | 6 | a0001c0001t0008g0279 a0001c0001t0011g0268 a0001c0001t0019g0267 others(3): Show |
6 | HG01099.hp1 HG02486.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-184+3210dupA | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 80641942 | ||||||
| chr7:80641942 | CA | C | 196 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(193): Show |
269 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.-184+3210delA | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 80641942 | ||||||
| chr7:80641942 | CAA | C | 76 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0033 others(73): Show |
98 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.-184+3209_-184+321 others(6): Show |
CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 80641942 | ||||||
| chr7:80641993 | C | T | 2 | a0001c0001t0003g0265 a0001c0001t0037g0270 |
2 | HG01099.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.-184+3247C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80641993 | |||||||
| chr7:80642011 | T | C | 91 | a0001c0001t0002g0001 a0001c0001t0002g0016 a0001c0001t0002g0017 others(88): Show |
129 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.-184+3265T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80642011 | |||||||
| chr7:80642014 | A | T | 91 | a0001c0001t0002g0001 a0001c0001t0002g0016 a0001c0001t0002g0017 others(88): Show |
129 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.-184+3268A>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80642014 | |||||||
| chr7:80642118 | G | A | 1 | a0001c0001t0003g0142 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-184+3372G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80642118 | |||||||
| chr7:80642218 | C | T | 2 | a0001c0001t0006g0006 a0001c0001t0006g0193 |
7 | HG02027.hp2 NA18957.hp1 NA18984.hp1 others(4): Show |
intron_variant | MODIFIER | c.-184+3472C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80642218 | |||||||
| chr7:80642287 | A | G | 5 | a0001c0001t0003g0081 a0001c0001t0004g0078 a0001c0001t0004g0079 others(2): Show |
5 | NA18953.hp1 NA18956.hp1 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.-184+3541A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80642287 | |||||||
| chr7:80642292 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-184+3546C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80642292 | |||||||
| chr7:80642394 | T | C | 5 | a0001c0001t0011g0268 a0001c0001t0019g0267 a0001c0001t0037g0270 others(2): Show |
5 | HG01099.hp1 HG02486.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.-184+3648T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80642394 | |||||||
| chr7:80642525 | G | A | 9 | a0001c0001t0002g0199 a0001c0001t0008g0196 a0001c0001t0009g0198 others(6): Show |
10 | HG01255.hp1 HG01891.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.-183-3563G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80642525 | |||||||
| chr7:80642667 | C | G | 4 | a0001c0001t0009g0011 a0001c0001t0016g0011 a0001c0001t0016g0054 others(1): Show |
6 | HG02559.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-183-3421C>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80642667 | |||||||
| chr7:80642676 | C | A | 1 | a0001c0001t0017g0083 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-183-3412C>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80642676 | |||||||
| chr7:80642732 | A | T | 1 | a0001c0001t0033g0049 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-183-3356A>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80642732 | |||||||
| chr7:80642864 | A | T | 1 | a0001c0001t0008g0253 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-183-3224A>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80642864 | |||||||
| chr7:80643252 | T | C | 86 | a0001c0001t0002g0001 a0001c0001t0002g0016 a0001c0001t0002g0017 others(83): Show |
122 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.-183-2836T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80643252 | |||||||
| chr7:80643334 | C | A | 1 | a0001c0001t0014g0084 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-183-2754C>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80643334 | |||||||
| chr7:80643469 | A | G | 2 | a0001c0001t0004g0075 a0001c0001t0022g0076 |
2 | NA19002.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.-183-2619A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80643469 | |||||||
| chr7:80643513 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-183-2575T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80643513 | |||||||
| chr7:80643650 | T | C | 3 | a0001c0001t0011g0026 a0001c0001t0027g0027 a0001c0001t0033g0049 |
5 | HG01243.hp1 HG02257.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-183-2438T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80643650 | |||||||
| chr7:80643676 | C | T | 2 | a0001c0001t0056g0051 a0001c0001t0057g0050 |
2 | HG03041.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-183-2412C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80643676 | |||||||
| chr7:80643709 | G | A | 3 | a0001c0001t0026g0256 a0001c0001t0026g0257 a0002c0002t0025g0255 |
3 | HG02818.hp2 HG03486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-183-2379G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80643709 | |||||||
| chr7:80643827 | T | C | 39 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0065 others(36): Show |
46 | HG00673.hp2 HG01099.hp1 HG01358.hp2 others(43): Show |
intron_variant | MODIFIER | c.-183-2261T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80643827 | |||||||
| chr7:80643992 | A | C | 86 | a0001c0001t0002g0001 a0001c0001t0002g0016 a0001c0001t0002g0017 others(83): Show |
122 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.-183-2096A>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80643992 | |||||||
| chr7:80644042 | T | C | 167 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(164): Show |
235 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.-183-2046T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80644042 | |||||||
| chr7:80644043 | G | A | 69 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(66): Show |
95 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.-183-2045G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80644043 | |||||||
| chr7:80644088 | C | A | 1 | a0001c0001t0008g0202 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-183-2000C>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80644088 | |||||||
| chr7:80644117 | T | C | 73 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(70): Show |
101 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.-183-1971T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80644117 | |||||||
| chr7:80644131 | C | T | 1 | a0001c0001t0036g0074 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-183-1957C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80644131 | |||||||
| chr7:80644416 | A | C | 39 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0065 others(36): Show |
46 | HG00673.hp2 HG01099.hp1 HG01358.hp2 others(43): Show |
intron_variant | MODIFIER | c.-183-1672A>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80644416 | |||||||
| chr7:80644750 | A | G | 1 | a0001c0001t0008g0202 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-183-1338A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80644750 | |||||||
| chr7:80645022 | CT | C | 263 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(260): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.-183-1051delT | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 80645022 | ||||||
| chr7:80645030 | T | A | 1 | a0001c0001t0021g0053 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-183-1058T>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80645030 | |||||||
| chr7:80645089 | C | T | 1 | a0001c0001t0005g0252 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-183-999C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80645089 | |||||||
| chr7:80645098 | G | A | 74 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0033 others(71): Show |
96 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.-183-990G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80645098 | |||||||
| chr7:80645109 | C | T | 3 | a0001c0001t0019g0276 a0001c0001t0019g0277 a0002c0002t0007g0278 |
3 | HG02630.hp1 HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-183-979C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80645109 | |||||||
| chr7:80645110 | T | C | 1 | a0001c0001t0021g0141 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-183-978T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80645110 | |||||||
| chr7:80645182 | G | A | 1 | a0001c0001t0020g0203 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-183-906G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80645182 | |||||||
| chr7:80645212 | G | A | 1 | a0001c0001t0001g0086 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-183-876G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80645212 | |||||||
| chr7:80645266 | C | T | 4 | a0001c0001t0002g0047 a0001c0001t0005g0047 a0001c0001t0008g0250 others(1): Show |
4 | HG02040.hp1 HG02129.hp2 NA18941.hp2 others(1): Show |
intron_variant | MODIFIER | c.-183-822C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80645266 | |||||||
| chr7:80645427 | T | A | 6 | a0001c0001t0008g0279 a0001c0001t0011g0268 a0001c0001t0019g0267 others(3): Show |
6 | HG01099.hp1 HG02486.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-183-661T>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80645427 | |||||||
| chr7:80645429 | C | T | 3 | a0001c0001t0014g0190 a0001c0001t0015g0040 a0001c0001t0015g0201 |
4 | HG01255.hp1 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-183-659C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80645429 | |||||||
| chr7:80645486 | A | G | 162 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(159): Show |
224 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.-183-602A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80645486 | |||||||
| chr7:80645581 | G | A | 76 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(73): Show |
102 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.-183-507G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80645581 | |||||||
| chr7:80645594 | T | C | 3 | a0001c0001t0002g0204 a0002c0002t0002g0015 a0002c0002t0002g0205 |
6 | HG01891.hp2 HG02922.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-183-494T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80645594 | |||||||
| chr7:80645620 | A | C | 1 | a0001c0001t0008g0249 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-183-468A>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80645620 | |||||||
| chr7:80645863 | G | C | 5 | a0001c0001t0011g0268 a0001c0001t0019g0267 a0001c0001t0037g0270 others(2): Show |
5 | HG01099.hp1 HG02486.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.-183-225G>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80645863 | |||||||
| chr7:80645877 | A | G | 289 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(286): Show |
387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.-183-211A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80645877 | |||||||
| chr7:80645952 | A | G | 1 | a0002c0002t0002g0205 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-183-136A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | chr7 | 80645952 | |||||||
| chr7:80646049 | A | AT | 276 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(273): Show |
371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.-183-32dupT | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 80646049 | ||||||
| chr7:80646203 | T | C | 2 | a0001c0001t0002g0023 a0001c0001t0030g0208 |
4 | NA18956.hp2 NA18966.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.-90+22T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 2/14 | chr7 | 80646203 | |||||||
| chr7:80646236 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-90+55C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 2/14 | chr7 | 80646236 | |||||||
| chr7:80646260 | G | T | 5 | a0001c0001t0011g0268 a0001c0001t0019g0267 a0001c0001t0037g0270 others(2): Show |
5 | HG01099.hp1 HG02486.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.-90+79G>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 2/14 | chr7 | 80646260 | |||||||
| chr7:80646420 | AAGG | A | 3 | a0001c0001t0001g0033 a0001c0001t0001g0143 a0001c0001t0042g0033 |
3 | HG00140.hp2 HG02615.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-89-227_-89-225del others(3): Show |
CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr7 | 80646420 | ||||||
| chr7:80646554 | C | T | 2 | a0001c0001t0006g0188 a0001c0001t0007g0189 |
2 | HG01261.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-89-98C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 2/14 | chr7 | 80646554 | |||||||
| chr7:80647015 | C | T | 281 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(278): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.120+155C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80647015 | |||||||
| chr7:80647167 | C | T | 1 | a0001c0001t0007g0052 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.120+307C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80647167 | |||||||
| chr7:80647175 | T | C | 5 | a0001c0001t0011g0268 a0001c0001t0019g0267 a0001c0001t0037g0270 others(2): Show |
5 | HG01099.hp1 HG02486.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.120+315T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80647175 | |||||||
| chr7:80647178 | G | A | 278 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(275): Show |
373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.120+318G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80647178 | |||||||
| chr7:80647258 | C | CTG | 84 | a0001c0001t0002g0001 a0001c0001t0002g0016 a0001c0001t0002g0017 others(81): Show |
120 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.120+422_120+423dup others(2): Show |
CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr7 | 80647258 | ||||||
| chr7:80647258 | C | CTGTG | 7 | a0001c0001t0005g0245 a0001c0001t0008g0247 a0001c0001t0021g0141 others(4): Show |
9 | HG00738.hp1 HG01175.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.120+420_120+423dup others(4): Show |
CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr7 | 80647258 | ||||||
| chr7:80647258 | C | CTGTGTG | 3 | a0001c0001t0001g0087 a0001c0001t0007g0088 a0001c0001t0009g0140 |
3 | HG02040.hp2 HG02572.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.120+418_120+423dup others(6): Show |
CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr7 | 80647258 | ||||||
| chr7:80647258 | C | CTGTGTGT others(1): Show |
65 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(62): Show |
95 | HG00544.hp1 HG00558.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.120+416_120+423dup others(8): Show |
CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr7 | 80647258 | ||||||
| chr7:80647258 | C | CTGTGTGT others(3): Show |
7 | a0001c0001t0001g0130 a0001c0001t0003g0128 a0001c0001t0003g0129 others(4): Show |
7 | HG01099.hp1 HG01361.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.120+414_120+423dup others(10): Show |
CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr7 | 80647258 | ||||||
| chr7:80647258 | C | CTGTGTGT others(5): Show |
3 | a0001c0001t0001g0131 a0001c0001t0040g0133 a0001c0001t0047g0132 |
3 | HG02723.hp1 HG03041.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.120+412_120+423dup others(12): Show |
CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr7 | 80647258 | ||||||
| chr7:80647258 | C | CTGTGTGT others(7): Show |
2 | a0001c0001t0003g0134 a0001c0001t0043g0135 |
2 | HG00438.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.120+410_120+423dup others(14): Show |
CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr7 | 80647258 | ||||||
| chr7:80647258 | CTG | C | 35 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0065 others(32): Show |
42 | HG00673.hp2 HG01358.hp2 HG01981.hp2 others(39): Show |
intron_variant | MODIFIER | c.120+422_120+423del others(2): Show |
CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr7 | 80647258 | ||||||
| chr7:80647701 | T | G | 7 | a0001c0001t0009g0011 a0001c0001t0016g0011 a0001c0001t0016g0054 others(4): Show |
9 | HG02559.hp1 HG02622.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.120+841T>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80647701 | |||||||
| chr7:80647829 | C | A | 1 | a0001c0001t0008g0279 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.120+969C>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80647829 | |||||||
| chr7:80648002 | T | C | 5 | a0001c0001t0011g0268 a0001c0001t0019g0267 a0001c0001t0037g0270 others(2): Show |
5 | HG01099.hp1 HG02486.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.120+1142T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80648002 | |||||||
| chr7:80648219 | T | C | 1 | a0001c0001t0016g0054 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.120+1359T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80648219 | |||||||
| chr7:80648246 | A | G | 3 | a0001c0001t0021g0206 a0001c0001t0056g0051 a0001c0001t0057g0050 |
3 | HG03041.hp1 HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.120+1386A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80648246 | |||||||
| chr7:80648316 | A | G | 5 | a0001c0001t0011g0268 a0001c0001t0019g0267 a0001c0001t0037g0270 others(2): Show |
5 | HG01099.hp1 HG02486.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.120+1456A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80648316 | |||||||
| chr7:80648321 | AT | A | 31 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0065 others(28): Show |
38 | HG00673.hp2 HG01358.hp2 HG01981.hp2 others(35): Show |
intron_variant | MODIFIER | c.120+1464delT | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr7 | 80648321 | ||||||
| chr7:80648372 | G | A | 2 | a0001c0001t0005g0245 a0001c0001t0058g0139 |
2 | HG00738.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.120+1512G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80648372 | |||||||
| chr7:80648427 | T | G | 3 | a0001c0001t0002g0204 a0002c0002t0002g0015 a0002c0002t0002g0205 |
6 | HG01891.hp2 HG02922.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.120+1567T>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80648427 | |||||||
| chr7:80648452 | C | A | 1 | a0001c0001t0062g0209 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.120+1592C>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80648452 | |||||||
| chr7:80648460 | A | G | 3 | a0001c0001t0011g0268 a0001c0001t0052g0266 a0008c0011t0053g0269 |
3 | HG02486.hp2 HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.120+1600A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80648460 | |||||||
| chr7:80648540 | C | CT | 71 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(68): Show |
99 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.120+1682dupT | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr7 | 80648540 | ||||||
| chr7:80648674 | G | A | 109 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0033 others(106): Show |
138 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.120+1814G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80648674 | |||||||
| chr7:80648766 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.120+1906A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80648766 | |||||||
| chr7:80648791 | T | G | 61 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(58): Show |
84 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.120+1931T>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80648791 | |||||||
| chr7:80649149 | A | C | 162 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(159): Show |
224 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.120+2289A>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80649149 | |||||||
| chr7:80649232 | C | G | 1 | a0001c0001t0021g0141 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.120+2372C>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80649232 | |||||||
| chr7:80649247 | A | G | 86 | a0001c0001t0002g0001 a0001c0001t0002g0016 a0001c0001t0002g0017 others(83): Show |
122 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.120+2387A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80649247 | |||||||
| chr7:80649310 | A | G | 164 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(161): Show |
228 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.120+2450A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80649310 | |||||||
| chr7:80649457 | C | G | 2 | a0001c0004t0001g0039 a0001c0004t0001g0187 |
3 | HG01257.hp1 HG01258.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.120+2597C>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80649457 | |||||||
| chr7:80649493 | GA | G | 278 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(275): Show |
373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.120+2643delA | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr7 | 80649493 | ||||||
| chr7:80649516 | A | T | 31 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0065 others(28): Show |
38 | HG00673.hp2 HG01358.hp2 HG01981.hp2 others(35): Show |
intron_variant | MODIFIER | c.120+2656A>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80649516 | |||||||
| chr7:80649565 | C | T | 5 | a0001c0001t0011g0268 a0001c0001t0019g0267 a0001c0001t0037g0270 others(2): Show |
5 | HG01099.hp1 HG02486.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.120+2705C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80649565 | |||||||
| chr7:80649615 | C | T | 1 | a0001c0001t0002g0244 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.120+2755C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80649615 | |||||||
| chr7:80649844 | G | A | 2 | a0001c0001t0008g0041 a0001c0001t0008g0210 |
3 | HG00140.hp1 HG03239.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.120+2984G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80649844 | |||||||
| chr7:80649865 | CAA | C | 3 | a0002c0002t0007g0048 a0002c0002t0007g0263 a0002c0002t0007g0264 |
4 | HG02970.hp1 HG03195.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.120+3007_120+3008d others(4): Show |
CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr7 | 80649865 | ||||||
| chr7:80649944 | A | T | 1 | a0001c0001t0005g0243 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.120+3084A>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80649944 | |||||||
| chr7:80649973 | A | G | 1 | a0001c0001t0005g0242 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.120+3113A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80649973 | |||||||
| chr7:80650020 | G | C | 30 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0065 others(27): Show |
37 | HG00673.hp2 HG01358.hp2 HG01981.hp2 others(34): Show |
intron_variant | MODIFIER | c.120+3160G>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80650020 | |||||||
| chr7:80650144 | A | C | 75 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0033 others(72): Show |
97 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.120+3284A>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80650144 | |||||||
| chr7:80650166 | C | A | 1 | a0001c0001t0008g0211 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.120+3306C>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80650166 | |||||||
| chr7:80650235 | T | C | 1 | a0001c0001t0027g0027 | 2 | HG01243.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.120+3375T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80650235 | |||||||
| chr7:80650286 | T | G | 1 | a0001c0001t0021g0206 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.120+3426T>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80650286 | |||||||
| chr7:80650287 | T | G | 70 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(67): Show |
96 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.120+3427T>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80650287 | |||||||
| chr7:80650299 | A | G | 1 | a0001c0001t0003g0186 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.120+3439A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80650299 | |||||||
| chr7:80650366 | T | C | 1 | a0001c0001t0008g0212 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.120+3506T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80650366 | |||||||
| chr7:80650402 | C | T | 61 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(58): Show |
84 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.120+3542C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80650402 | |||||||
| chr7:80650437 | T | C | 30 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0065 others(27): Show |
37 | HG00673.hp2 HG01358.hp2 HG01981.hp2 others(34): Show |
intron_variant | MODIFIER | c.120+3577T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80650437 | |||||||
| chr7:80650519 | A | T | 78 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0033 others(75): Show |
100 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.120+3659A>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80650519 | |||||||
| chr7:80650524 | G | C | 2 | a0001c0001t0004g0018 a0001c0001t0004g0056 |
4 | NA18945.hp2 NA18955.hp2 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.120+3664G>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80650524 | |||||||
| chr7:80650529 | T | G | 1 | a0001c0001t0001g0089 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.120+3669T>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80650529 | |||||||
| chr7:80650801 | A | C | 172 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(169): Show |
240 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.120+3941A>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80650801 | |||||||
| chr7:80650829 | A | G | 1 | a0001c0001t0021g0206 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.120+3969A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80650829 | |||||||
| chr7:80650905 | C | A | 2 | a0001c0001t0020g0194 a0007c0006t0020g0195 |
2 | HG03098.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.120+4045C>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80650905 | |||||||
| chr7:80650927 | C | CA | 161 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0033 others(158): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.120+4083dupA | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr7 | 80650927 | ||||||
| chr7:80650927 | C | CAA | 13 | a0001c0001t0002g0019 a0001c0001t0002g0199 a0001c0001t0005g0213 others(10): Show |
15 | HG02055.hp2 HG02486.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.120+4082_120+4083d others(4): Show |
CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr7 | 80650927 | ||||||
| chr7:80650927 | C | CAGAA | 28 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0065 others(25): Show |
35 | HG00673.hp2 HG01358.hp2 HG01981.hp2 others(32): Show |
intron_variant | MODIFIER | c.120+4068_120+4069i others(6): Show |
CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr7 | 80650927 | ||||||
| chr7:80651005 | G | T | 1 | a0001c0001t0001g0089 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.120+4145G>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80651005 | |||||||
| chr7:80651143 | C | T | 67 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(64): Show |
93 | HG00544.hp1 HG00558.hp1 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.120+4283C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80651143 | |||||||
| chr7:80651146 | G | A | 193 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(190): Show |
254 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.120+4286G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80651146 | |||||||
| chr7:80651259 | G | A | 2 | a0001c0001t0001g0138 a0001c0001t0001g0146 |
2 | NA18977.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.120+4399G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80651259 | |||||||
| chr7:80651394 | G | C | 2 | a0001c0001t0002g0019 a0001c0001t0009g0140 |
4 | HG02572.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.120+4534G>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80651394 | |||||||
| chr7:80651449 | C | A | 31 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0065 others(28): Show |
38 | HG00673.hp2 HG01358.hp2 HG01981.hp2 others(35): Show |
intron_variant | MODIFIER | c.120+4589C>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80651449 | |||||||
| chr7:80651550 | G | T | 31 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0065 others(28): Show |
38 | HG00673.hp2 HG01358.hp2 HG01981.hp2 others(35): Show |
intron_variant | MODIFIER | c.120+4690G>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80651550 | |||||||
| chr7:80651621 | T | C | 5 | a0001c0001t0003g0081 a0001c0001t0004g0078 a0001c0001t0004g0079 others(2): Show |
5 | NA18953.hp1 NA18956.hp1 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.120+4761T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80651621 | |||||||
| chr7:80651832 | C | T | 1 | a0001c0007t0024g0183 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.121-4708C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80651832 | |||||||
| chr7:80651866 | G | A | 1 | a0001c0001t0015g0201 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.121-4674G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80651866 | |||||||
| chr7:80651984 | T | C | 30 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0065 others(27): Show |
37 | HG00673.hp2 HG01358.hp2 HG01981.hp2 others(34): Show |
intron_variant | MODIFIER | c.121-4556T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80651984 | |||||||
| chr7:80652160 | C | T | 2 | a0001c0001t0002g0019 a0001c0001t0009g0140 |
4 | HG02572.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.121-4380C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80652160 | |||||||
| chr7:80652661 | T | A | 1 | a0001c0001t0004g0070 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.121-3879T>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80652661 | |||||||
| chr7:80652775 | AG | A | 31 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0065 others(28): Show |
38 | HG00673.hp2 HG01358.hp2 HG01981.hp2 others(35): Show |
intron_variant | MODIFIER | c.121-3764delG | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80652775 | |||||||
| chr7:80652778 | A | T | 31 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0065 others(28): Show |
38 | HG00673.hp2 HG01358.hp2 HG01981.hp2 others(35): Show |
intron_variant | MODIFIER | c.121-3762A>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80652778 | |||||||
| chr7:80652791 | G | T | 1 | a0001c0001t0021g0141 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.121-3749G>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80652791 | |||||||
| chr7:80653030 | G | A | 2 | a0001c0001t0003g0262 a0001c0001t0003g0265 |
2 | HG02258.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.121-3510G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80653030 | |||||||
| chr7:80653062 | A | G | 1 | a0001c0001t0009g0140 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.121-3478A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80653062 | |||||||
| chr7:80653198 | C | T | 6 | a0001c0001t0003g0081 a0001c0001t0004g0078 a0001c0001t0004g0079 others(3): Show |
6 | NA18953.hp1 NA18956.hp1 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.121-3342C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80653198 | |||||||
| chr7:80653299 | A | G | 2 | a0001c0001t0056g0051 a0001c0001t0057g0050 |
2 | HG03041.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.121-3241A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80653299 | |||||||
| chr7:80653320 | G | A | 142 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(139): Show |
190 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.121-3220G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80653320 | |||||||
| chr7:80653328 | A | G | 3 | a0001c0001t0019g0276 a0001c0001t0019g0277 a0002c0002t0007g0278 |
3 | HG02630.hp1 HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.121-3212A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80653328 | |||||||
| chr7:80653354 | T | C | 31 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0065 others(28): Show |
38 | HG00673.hp2 HG01358.hp2 HG01981.hp2 others(35): Show |
intron_variant | MODIFIER | c.121-3186T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80653354 | |||||||
| chr7:80653418 | G | T | 3 | a0001c0001t0019g0276 a0001c0001t0019g0277 a0002c0002t0007g0278 |
3 | HG02630.hp1 HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.121-3122G>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80653418 | |||||||
| chr7:80653459 | G | A | 3 | a0001c0001t0007g0147 a0001c0001t0007g0148 a0001c0007t0024g0183 |
3 | HG03669.hp2 HG03704.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.121-3081G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80653459 | |||||||
| chr7:80653504 | T | A | 1 | a0001c0001t0021g0206 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.121-3036T>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80653504 | |||||||
| chr7:80653583 | C | A | 36 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0065 others(33): Show |
43 | HG00673.hp2 HG01099.hp1 HG01358.hp2 others(40): Show |
intron_variant | MODIFIER | c.121-2957C>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80653583 | |||||||
| chr7:80653639 | C | A | 3 | a0001c0001t0019g0276 a0001c0001t0019g0277 a0002c0002t0007g0278 |
3 | HG02630.hp1 HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.121-2901C>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80653639 | |||||||
| chr7:80653816 | C | T | 5 | a0001c0001t0003g0125 a0001c0001t0003g0126 a0001c0001t0012g0014 others(2): Show |
8 | HG01433.hp2 HG02559.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.121-2724C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80653816 | |||||||
| chr7:80653853 | T | C | 4 | a0001c0001t0007g0149 a0003c0003t0001g0150 a0003c0003t0006g0034 others(1): Show |
5 | HG00609.hp1 NA18969.hp1 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.121-2687T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80653853 | |||||||
| chr7:80653887 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.121-2653C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80653887 | |||||||
| chr7:80654007 | A | G | 186 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(183): Show |
243 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.121-2533A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80654007 | |||||||
| chr7:80654100 | G | A | 7 | a0001c0001t0009g0011 a0001c0001t0011g0026 a0001c0001t0016g0011 others(4): Show |
11 | HG01243.hp1 HG02257.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.121-2440G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80654100 | |||||||
| chr7:80654141 | A | C | 66 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(63): Show |
92 | HG00544.hp1 HG00558.hp1 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.121-2399A>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80654141 | |||||||
| chr7:80654161 | C | A | 1 | a0001c0001t0019g0267 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.121-2379C>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80654161 | |||||||
| chr7:80654305 | A | G | 289 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(286): Show |
387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.121-2235A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80654305 | |||||||
| chr7:80654345 | C | T | 1 | a0001c0001t0014g0119 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.121-2195C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80654345 | |||||||
| chr7:80654462 | G | A | 1 | a0001c0001t0059g0215 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.121-2078G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80654462 | |||||||
| chr7:80654606 | G | A | 1 | a0001c0001t0009g0140 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.121-1934G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80654606 | |||||||
| chr7:80654714 | C | A | 1 | a0001c0001t0008g0216 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.121-1826C>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80654714 | |||||||
| chr7:80654736 | C | T | 5 | a0001c0001t0003g0125 a0001c0001t0003g0126 a0001c0001t0012g0014 others(2): Show |
8 | HG01433.hp2 HG02559.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.121-1804C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80654736 | |||||||
| chr7:80654748 | A | T | 278 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(275): Show |
373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.121-1792A>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80654748 | |||||||
| chr7:80654759 | T | C | 31 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0065 others(28): Show |
38 | HG00673.hp2 HG01358.hp2 HG01981.hp2 others(35): Show |
intron_variant | MODIFIER | c.121-1781T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80654759 | |||||||
| chr7:80654767 | T | C | 1 | a0001c0001t0001g0274 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.121-1773T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80654767 | |||||||
| chr7:80654880 | GAA | G | 200 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(197): Show |
273 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(270): Show |
intron_variant | MODIFIER | c.121-1645_121-1644d others(4): Show |
CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr7 | 80654880 | ||||||
| chr7:80654949 | A | G | 4 | a0001c0001t0009g0011 a0001c0001t0016g0011 a0001c0001t0016g0054 others(1): Show |
6 | HG02559.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.121-1591A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80654949 | |||||||
| chr7:80655026 | A | G | 3 | a0001c0001t0007g0088 a0001c0001t0007g0118 a0001c0001t0014g0119 |
3 | HG02717.hp1 HG02886.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.121-1514A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80655026 | |||||||
| chr7:80655198 | T | A | 1 | a0001c0001t0021g0141 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.121-1342T>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80655198 | |||||||
| chr7:80655251 | C | T | 3 | a0001c0001t0001g0085 a0001c0001t0001g0117 a0001c0001t0003g0116 |
3 | HG01934.hp1 HG02015.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.121-1289C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80655251 | |||||||
| chr7:80655270 | T | G | 1 | a0001c0001t0014g0084 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.121-1270T>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80655270 | |||||||
| chr7:80655304 | TC | T | 8 | a0001c0001t0003g0125 a0001c0001t0003g0126 a0001c0001t0007g0123 others(5): Show |
11 | HG01433.hp2 HG02145.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.121-1235delC | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80655304 | |||||||
| chr7:80655626 | T | C | 119 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0065 others(116): Show |
162 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.121-914T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80655626 | |||||||
| chr7:80655627 | G | A | 4 | a0001c0001t0009g0011 a0001c0001t0016g0011 a0001c0001t0016g0054 others(1): Show |
6 | HG02559.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.121-913G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80655627 | |||||||
| chr7:80655658 | T | A | 4 | a0001c0001t0009g0011 a0001c0001t0016g0011 a0001c0001t0016g0054 others(1): Show |
6 | HG02559.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.121-882T>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80655658 | |||||||
| chr7:80655687 | C | T | 141 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(138): Show |
189 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.121-853C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80655687 | |||||||
| chr7:80655753 | G | A | 202 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0033 others(199): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.121-787G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80655753 | |||||||
| chr7:80655816 | G | A | 2 | a0001c0001t0002g0218 a0001c0001t0005g0217 |
2 | HG01074.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.121-724G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80655816 | |||||||
| chr7:80655852 | T | C | 1 | a0001c0001t0008g0279 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.121-688T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80655852 | |||||||
| chr7:80655920 | C | CA | 8 | a0001c0001t0001g0154 a0001c0001t0003g0035 a0001c0001t0003g0152 others(5): Show |
11 | HG02056.hp2 HG02559.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.121-606dupA | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr7 | 80655920 | ||||||
| chr7:80655935 | G | A | 66 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(63): Show |
92 | HG00544.hp1 HG00558.hp1 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.121-605G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80655935 | |||||||
| chr7:80655935 | GAAAAGA | G | 15 | a0001c0001t0002g0023 a0001c0001t0002g0025 a0001c0001t0002g0204 others(12): Show |
23 | HG00438.hp2 HG00621.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.121-593_121-588del others(6): Show |
CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr7 | 80655935 | ||||||
| chr7:80655936 | A | AG | 3 | a0001c0001t0007g0123 a0001c0001t0046g0124 a0001c0008t0007g0122 |
3 | HG02145.hp2 HG02622.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.121-604_121-603ins others(1): Show |
CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80655936 | |||||||
| chr7:80655936 | A | G | 63 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(60): Show |
89 | HG00544.hp1 HG00558.hp1 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.121-604A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80655936 | |||||||
| chr7:80656072 | A | C | 1 | a0001c0001t0029g0241 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.121-468A>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80656072 | |||||||
| chr7:80656098 | C | T | 1 | a0001c0001t0014g0115 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.121-442C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80656098 | |||||||
| chr7:80656198 | C | T | 1 | a0001c0001t0014g0084 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.121-342C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80656198 | |||||||
| chr7:80656256 | T | C | 1 | a0001c0001t0021g0206 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.121-284T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80656256 | |||||||
| chr7:80656495 | T | C | 1 | a0001c0001t0008g0279 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.121-45T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80656495 | |||||||
| chr7:80656534 | T | C | 98 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(95): Show |
131 | HG00544.hp1 HG00558.hp1 HG00609.hp2 others(128): Show |
splice_region_variant&intron_variant | LOW | c.121-6T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 3/14 | chr7 | 80656534 | |||||||
| chr7:80656765 | A | G | 1 | a0001c0001t0005g0236 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.281+65A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 4/14 | chr7 | 80656765 | |||||||
| chr7:80656954 | C | G | 31 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0065 others(28): Show |
38 | HG00673.hp2 HG01358.hp2 HG01981.hp2 others(35): Show |
intron_variant | MODIFIER | c.281+254C>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 4/14 | chr7 | 80656954 | |||||||
| chr7:80657026 | G | A | 1 | a0001c0001t0008g0279 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.281+326G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 4/14 | chr7 | 80657026 | |||||||
| chr7:80657028 | A | G | 14 | a0001c0001t0002g0023 a0001c0001t0002g0025 a0001c0001t0002g0204 others(11): Show |
22 | HG00438.hp2 HG00621.hp2 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.281+328A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 4/14 | chr7 | 80657028 | |||||||
| chr7:80657127 | G | A | 5 | a0001c0001t0003g0262 a0001c0001t0003g0265 a0001c0001t0026g0256 others(2): Show |
5 | HG02258.hp2 HG02280.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.281+427G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 4/14 | chr7 | 80657127 | |||||||
| chr7:80657274 | A | G | 1 | a0001c0001t0002g0019 | 3 | HG02895.hp1 HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.281+574A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 4/14 | chr7 | 80657274 | |||||||
| chr7:80657288 | AG | A | 8 | a0001c0001t0003g0125 a0001c0001t0003g0126 a0001c0001t0007g0123 others(5): Show |
11 | HG01433.hp2 HG02145.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.281+589delG | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 4/14 | chr7 | 80657288 | |||||||
| chr7:80657307 | C | T | 3 | a0001c0001t0019g0276 a0001c0001t0019g0277 a0002c0002t0007g0278 |
3 | HG02630.hp1 HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.281+607C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 4/14 | chr7 | 80657307 | |||||||
| chr7:80657490 | T | C | 1 | a0001c0001t0001g0144 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.281+790T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 4/14 | chr7 | 80657490 | |||||||
| chr7:80657592 | T | C | 2 | a0001c0001t0001g0020 a0001c0001t0001g0184 |
4 | HG00733.hp2 HG01069.hp1 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.281+892T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 4/14 | chr7 | 80657592 | |||||||
| chr7:80657624 | C | A | 73 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(70): Show |
101 | HG00544.hp1 HG00558.hp1 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.281+924C>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 4/14 | chr7 | 80657624 | |||||||
| chr7:80657706 | T | C | 98 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(95): Show |
131 | HG00544.hp1 HG00558.hp1 HG00609.hp2 others(128): Show |
intron_variant | MODIFIER | c.281+1006T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 4/14 | chr7 | 80657706 | |||||||
| chr7:80657792 | G | A | 2 | a0001c0001t0019g0267 a0001c0001t0037g0270 |
2 | HG01099.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.281+1092G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 4/14 | chr7 | 80657792 | |||||||
| chr7:80657809 | T | G | 1 | a0001c0001t0013g0093 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.281+1109T>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 4/14 | chr7 | 80657809 | |||||||
| chr7:80657836 | T | A | 55 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(52): Show |
75 | HG00558.hp1 HG00609.hp2 HG01109.hp1 others(72): Show |
intron_variant | MODIFIER | c.281+1136T>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 4/14 | chr7 | 80657836 | |||||||
| chr7:80657893 | C | T | 138 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(135): Show |
184 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.281+1193C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 4/14 | chr7 | 80657893 | |||||||
| chr7:80658012 | G | C | 1 | a0001c0001t0018g0057 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.281+1312G>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 4/14 | chr7 | 80658012 | |||||||
| chr7:80658042 | A | G | 70 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0033 others(67): Show |
92 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.281+1342A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 4/14 | chr7 | 80658042 | |||||||
| chr7:80658050 | C | T | 1 | a0002c0002t0007g0264 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.281+1350C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 4/14 | chr7 | 80658050 | |||||||
| chr7:80658095 | C | T | 1 | a0001c0001t0014g0084 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.281+1395C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 4/14 | chr7 | 80658095 | |||||||
| chr7:80658276 | T | C | 3 | a0001c0001t0019g0276 a0001c0001t0019g0277 a0002c0002t0007g0278 |
3 | HG02630.hp1 HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.281+1576T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 4/14 | chr7 | 80658276 | |||||||
| chr7:80658276 | T | TAC | 73 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0033 others(70): Show |
95 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.281+1582_281+1583d others(4): Show |
CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr7 | 80658276 | ||||||
| chr7:80658282 | C | CAT | 14 | a0001c0001t0002g0042 a0001c0001t0002g0047 a0001c0001t0003g0029 others(11): Show |
15 | HG00642.hp2 HG02040.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.281+1593_281+1594d others(4): Show |
CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr7 | 80658282 | ||||||
| chr7:80658295 | G | A | 55 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(52): Show |
75 | HG00558.hp1 HG00609.hp2 HG01109.hp1 others(72): Show |
intron_variant | MODIFIER | c.281+1595G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 4/14 | chr7 | 80658295 | |||||||
| chr7:80658418 | AGTT | A | 75 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0033 others(72): Show |
97 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.281+1722_281+1724d others(5): Show |
CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr7 | 80658418 | ||||||
| chr7:80658553 | C | G | 55 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(52): Show |
75 | HG00558.hp1 HG00609.hp2 HG01109.hp1 others(72): Show |
intron_variant | MODIFIER | c.281+1853C>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 4/14 | chr7 | 80658553 | |||||||
| chr7:80658759 | G | C | 3 | a0001c0001t0011g0026 a0001c0001t0027g0027 a0001c0001t0033g0049 |
5 | HG01243.hp1 HG02257.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.281+2059G>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 4/14 | chr7 | 80658759 | |||||||
| chr7:80658925 | A | G | 2 | a0001c0001t0005g0045 a0001c0001t0008g0044 |
4 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.282-2138A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 4/14 | chr7 | 80658925 | |||||||
| chr7:80658926 | A | G | 1 | a0001c0001t0001g0181 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.282-2137A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 4/14 | chr7 | 80658926 | |||||||
| chr7:80658942 | A | T | 3 | a0001c0001t0003g0179 a0001c0001t0003g0185 a0001c0001t0050g0180 |
3 | NA18944.hp2 NA18946.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.282-2121A>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 4/14 | chr7 | 80658942 | |||||||
| chr7:80659032 | C | G | 1 | a0001c0001t0060g0235 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.282-2031C>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 4/14 | chr7 | 80659032 | |||||||
| chr7:80659069 | G | A | 179 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(176): Show |
232 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.282-1994G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 4/14 | chr7 | 80659069 | |||||||
| chr7:80659148 | C | A | 5 | a0001c0001t0011g0268 a0001c0001t0019g0267 a0001c0001t0037g0270 others(2): Show |
5 | HG01099.hp1 HG02486.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.282-1915C>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 4/14 | chr7 | 80659148 | |||||||
| chr7:80659206 | C | T | 31 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0065 others(28): Show |
38 | HG00673.hp2 HG01358.hp2 HG01981.hp2 others(35): Show |
intron_variant | MODIFIER | c.282-1857C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 4/14 | chr7 | 80659206 | |||||||
| chr7:80659244 | T | A | 15 | a0001c0001t0002g0023 a0001c0001t0002g0025 a0001c0001t0002g0204 others(12): Show |
23 | HG00438.hp2 HG00621.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.282-1819T>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 4/14 | chr7 | 80659244 | |||||||
| chr7:80659496 | T | C | 2 | a0002c0002t0002g0015 a0002c0002t0002g0205 |
5 | HG01891.hp2 HG02922.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.282-1567T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 4/14 | chr7 | 80659496 | |||||||
| chr7:80659538 | A | G | 15 | a0001c0001t0002g0023 a0001c0001t0002g0025 a0001c0001t0002g0204 others(12): Show |
23 | HG00438.hp2 HG00621.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.282-1525A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 4/14 | chr7 | 80659538 | |||||||
| chr7:80659629 | C | G | 1 | a0001c0001t0008g0211 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.282-1434C>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 4/14 | chr7 | 80659629 | |||||||
| chr7:80659674 | ATGT | A | 75 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0033 others(72): Show |
97 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.282-1385_282-1383d others(5): Show |
CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr7 | 80659674 | ||||||
| chr7:80659727 | A | T | 176 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0020 others(173): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.282-1336A>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 4/14 | chr7 | 80659727 | |||||||
| chr7:80659836 | TTGTG | T | 3 | a0001c0001t0021g0206 a0001c0001t0056g0051 a0001c0001t0057g0050 |
3 | HG03041.hp1 HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.282-1223_282-1220d others(6): Show |
CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr7 | 80659836 | ||||||
| chr7:80659908 | T | C | 5 | a0001c0001t0011g0268 a0001c0001t0019g0267 a0001c0001t0037g0270 others(2): Show |
5 | HG01099.hp1 HG02486.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.282-1155T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 4/14 | chr7 | 80659908 | |||||||
| chr7:80659949 | A | G | 3 | a0001c0001t0021g0206 a0001c0001t0056g0051 a0001c0001t0057g0050 |
3 | HG03041.hp1 HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.282-1114A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 4/14 | chr7 | 80659949 | |||||||
| chr7:80659959 | T | C | 1 | a0001c0001t0057g0050 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.282-1104T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 4/14 | chr7 | 80659959 | |||||||
| chr7:80660086 | C | T | 131 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(128): Show |
175 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.282-977C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 4/14 | chr7 | 80660086 | |||||||
| chr7:80660116 | T | A | 1 | a0001c0001t0003g0134 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.282-947T>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 4/14 | chr7 | 80660116 | |||||||
| chr7:80660123 | G | A | 74 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0033 others(71): Show |
96 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.282-940G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 4/14 | chr7 | 80660123 | |||||||
| chr7:80660227 | C | T | 1 | a0001c0001t0060g0235 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.282-836C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 4/14 | chr7 | 80660227 | |||||||
| chr7:80660229 | T | C | 2 | a0001c0001t0004g0018 a0001c0001t0004g0056 |
4 | NA18945.hp2 NA18955.hp2 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.282-834T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 4/14 | chr7 | 80660229 | |||||||
| chr7:80660231 | C | A | 5 | a0001c0001t0011g0268 a0001c0001t0019g0267 a0001c0001t0037g0270 others(2): Show |
5 | HG01099.hp1 HG02486.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.282-832C>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 4/14 | chr7 | 80660231 | |||||||
| chr7:80660340 | T | C | 3 | a0001c0001t0019g0276 a0001c0001t0019g0277 a0002c0002t0007g0278 |
3 | HG02630.hp1 HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.282-723T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 4/14 | chr7 | 80660340 | |||||||
| chr7:80660449 | A | G | 69 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(66): Show |
95 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.282-614A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 4/14 | chr7 | 80660449 | |||||||
| chr7:80660605 | A | T | 75 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0033 others(72): Show |
97 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.282-458A>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 4/14 | chr7 | 80660605 | |||||||
| chr7:80660755 | A | T | 1 | a0001c0001t0001g0089 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.282-308A>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 4/14 | chr7 | 80660755 | |||||||
| chr7:80660757 | C | A | 1 | a0001c0001t0001g0089 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.282-306C>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 4/14 | chr7 | 80660757 | |||||||
| chr7:80660963 | T | A | 1 | a0001c0001t0001g0089 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.282-100T>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 4/14 | chr7 | 80660963 | |||||||
| chr7:80661032 | T | C | 5 | a0001c0001t0011g0268 a0001c0001t0019g0267 a0001c0001t0037g0270 others(2): Show |
5 | HG01099.hp1 HG02486.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.282-31T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 4/14 | chr7 | 80661032 | |||||||
| chr7:80661053 | A | G | 274 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(271): Show |
371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.282-10A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 4/14 | chr7 | 80661053 | |||||||
| chr7:80661431 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.429+221C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 5/14 | chr7 | 80661431 | |||||||
| chr7:80661555 | A | G | 1 | a0001c0001t0008g0279 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.429+345A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 5/14 | chr7 | 80661555 | |||||||
| chr7:80661575 | G | A | 1 | a0001c0001t0014g0084 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.429+365G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 5/14 | chr7 | 80661575 | |||||||
| chr7:80661684 | AAAAC | A | 15 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0086 others(12): Show |
23 | HG00609.hp2 HG00621.hp2 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.429+494_429+497del others(4): Show |
CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr7 | 80661684 | ||||||
| chr7:80661826 | A | G | 1 | a0008c0011t0053g0269 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.429+616A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 5/14 | chr7 | 80661826 | |||||||
| chr7:80661944 | G | T | 1 | a0001c0001t0007g0148 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.429+734G>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 5/14 | chr7 | 80661944 | |||||||
| chr7:80661954 | G | A | 1 | a0001c0001t0004g0158 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.429+744G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 5/14 | chr7 | 80661954 | |||||||
| chr7:80661983 | C | A | 1 | a0001c0001t0001g0108 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.429+773C>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 5/14 | chr7 | 80661983 | |||||||
| chr7:80661983 | C | T | 3 | a0001c0001t0005g0043 a0001c0001t0005g0245 a0001c0001t0058g0139 |
4 | HG00738.hp1 HG01928.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.429+773C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 5/14 | chr7 | 80661983 | |||||||
| chr7:80662082 | G | A | 64 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(61): Show |
88 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(85): Show |
intron_variant | MODIFIER | c.429+872G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 5/14 | chr7 | 80662082 | |||||||
| chr7:80662125 | A | G | 5 | a0001c0001t0011g0268 a0001c0001t0019g0267 a0001c0001t0037g0270 others(2): Show |
5 | HG01099.hp1 HG02486.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.430-865A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 5/14 | chr7 | 80662125 | |||||||
| chr7:80662190 | G | T | 2 | a0001c0001t0003g0107 a0001c0001t0011g0032 |
3 | HG02109.hp2 HG02647.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.430-800G>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 5/14 | chr7 | 80662190 | |||||||
| chr7:80662313 | G | A | 3 | a0001c0001t0021g0206 a0001c0001t0056g0051 a0001c0001t0057g0050 |
3 | HG03041.hp1 HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.430-677G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 5/14 | chr7 | 80662313 | |||||||
| chr7:80662348 | C | T | 2 | a0001c0001t0002g0017 a0001c0001t0005g0017 |
4 | HG01256.hp1 HG01258.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.430-642C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 5/14 | chr7 | 80662348 | |||||||
| chr7:80662377 | G | T | 1 | a0003c0003t0006g0151 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.430-613G>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 5/14 | chr7 | 80662377 | |||||||
| chr7:80662445 | C | T | 3 | a0001c0001t0007g0123 a0001c0001t0046g0124 a0001c0008t0007g0122 |
3 | HG02145.hp2 HG02622.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.430-545C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 5/14 | chr7 | 80662445 | |||||||
| chr7:80662535 | C | T | 2 | a0001c0001t0007g0147 a0001c0001t0007g0148 |
2 | HG03669.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.430-455C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 5/14 | chr7 | 80662535 | |||||||
| chr7:80662585 | CT | C | 80 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0033 others(77): Show |
103 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.430-392delT | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr7 | 80662585 | ||||||
| chr7:80662623 | T | C | 27 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0065 others(24): Show |
34 | HG00673.hp2 HG01358.hp2 HG01928.hp2 others(31): Show |
intron_variant | MODIFIER | c.430-367T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 5/14 | chr7 | 80662623 | |||||||
| chr7:80662715 | T | G | 1 | a0001c0001t0011g0258 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.430-275T>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 5/14 | chr7 | 80662715 | |||||||
| chr7:80662718 | A | G | 8 | a0001c0001t0008g0196 a0001c0001t0019g0276 a0001c0001t0019g0277 others(5): Show |
8 | HG02630.hp1 HG02886.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.430-272A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 5/14 | chr7 | 80662718 | |||||||
| chr7:80662764 | G | A | 1 | a0001c0001t0003g0152 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.430-226G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 5/14 | chr7 | 80662764 | |||||||
| chr7:80662783 | G | A | 2 | a0001c0001t0004g0071 a0001c0001t0004g0097 |
2 | NA18960.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.430-207G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 5/14 | chr7 | 80662783 | |||||||
| chr7:80662788 | C | T | 26 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0065 others(23): Show |
33 | HG00673.hp2 HG01358.hp2 HG01981.hp2 others(30): Show |
intron_variant | MODIFIER | c.430-202C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 5/14 | chr7 | 80662788 | |||||||
| chr7:80662891 | A | G | 2 | a0001c0001t0019g0267 a0001c0001t0037g0270 |
2 | HG01099.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.430-99A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 5/14 | chr7 | 80662891 | |||||||
| chr7:80663243 | T | A | 4 | a0001c0001t0009g0140 a0001c0001t0011g0268 a0001c0001t0031g0197 others(1): Show |
4 | HG02055.hp2 HG02486.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.609+74T>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 6/14 | chr7 | 80663243 | |||||||
| chr7:80663290 | T | A | 1 | a0001c0008t0007g0122 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.609+121T>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 6/14 | chr7 | 80663290 | |||||||
| chr7:80663429 | T | G | 1 | a0001c0001t0001g0101 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.609+260T>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 6/14 | chr7 | 80663429 | |||||||
| chr7:80663432 | T | A | 4 | a0001c0001t0009g0140 a0001c0001t0011g0268 a0001c0001t0031g0197 others(1): Show |
4 | HG02055.hp2 HG02486.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.609+263T>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 6/14 | chr7 | 80663432 | |||||||
| chr7:80663442 | G | A | 1 | a0001c0001t0055g0221 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.609+273G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 6/14 | chr7 | 80663442 | |||||||
| chr7:80663481 | T | TTTTA | 3 | a0001c0001t0001g0161 a0001c0001t0003g0159 a0001c0001t0034g0160 |
3 | HG02683.hp1 HG03834.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.609+316_609+319dup others(4): Show |
CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr7 | 80663481 | ||||||
| chr7:80663545 | T | A | 13 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0065 others(10): Show |
18 | HG01358.hp2 HG01978.hp1 HG01981.hp2 others(15): Show |
intron_variant | MODIFIER | c.609+376T>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 6/14 | chr7 | 80663545 | |||||||
| chr7:80663567 | CTTACAAT others(6): Show |
C | 7 | a0001c0001t0003g0029 a0001c0001t0003g0125 a0001c0001t0003g0126 others(4): Show |
10 | HG01433.hp2 HG02055.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.609+402_609+414del others(13): Show |
CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr7 | 80663567 | ||||||
| chr7:80663587 | T | G | 1 | a0001c0001t0054g0222 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.609+418T>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 6/14 | chr7 | 80663587 | |||||||
| chr7:80663610 | A | AT | 6 | a0001c0001t0002g0204 a0001c0001t0009g0140 a0001c0001t0011g0026 others(3): Show |
7 | HG02055.hp2 HG02486.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.609+442dupT | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr7 | 80663610 | ||||||
| chr7:80663725 | G | C | 27 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0065 others(24): Show |
34 | HG00673.hp2 HG01358.hp2 HG01978.hp1 others(31): Show |
intron_variant | MODIFIER | c.609+556G>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 6/14 | chr7 | 80663725 | |||||||
| chr7:80663782 | C | A | 1 | a0001c0001t0001g0061 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.609+613C>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 6/14 | chr7 | 80663782 | |||||||
| chr7:80663790 | G | A | 1 | a0001c0001t0003g0186 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.610-616G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 6/14 | chr7 | 80663790 | |||||||
| chr7:80663873 | A | C | 26 | a0001c0001t0001g0138 a0001c0001t0001g0146 a0001c0001t0001g0154 others(23): Show |
36 | HG00609.hp1 HG00673.hp1 HG02027.hp2 others(33): Show |
intron_variant | MODIFIER | c.610-533A>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 6/14 | chr7 | 80663873 | |||||||
| chr7:80663892 | A | G | 11 | a0001c0001t0003g0262 a0001c0001t0003g0265 a0001c0001t0006g0156 others(8): Show |
12 | HG01243.hp1 HG01243.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.610-514A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 6/14 | chr7 | 80663892 | |||||||
| chr7:80663897 | A | G | 26 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0065 others(23): Show |
33 | HG00673.hp2 HG01358.hp2 HG01978.hp1 others(30): Show |
intron_variant | MODIFIER | c.610-509A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 6/14 | chr7 | 80663897 | |||||||
| chr7:80663948 | A | ATACTCAT | 9 | a0001c0001t0008g0279 a0001c0001t0019g0276 a0001c0001t0019g0277 others(6): Show |
13 | HG01891.hp2 HG02486.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.610-457_610-451dup others(7): Show |
CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr7 | 80663948 | ||||||
| chr7:80663999 | TTTATCAT others(15): Show |
T | 1 | a0001c0001t0004g0162 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.610-381_610-360del others(22): Show |
CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr7 | 80663999 | ||||||
| chr7:80664084 | T | C | 2 | a0001c0001t0003g0262 a0001c0001t0003g0265 |
2 | HG02258.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.610-322T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 6/14 | chr7 | 80664084 | |||||||
| chr7:80664271 | T | TA | 18 | a0001c0001t0003g0262 a0001c0001t0003g0265 a0001c0001t0008g0196 others(15): Show |
23 | HG01243.hp1 HG01891.hp2 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.610-128dupA | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr7 | 80664271 | ||||||
| chr7:80664497 | G | GGTAA | 5 | a0001c0001t0009g0140 a0001c0001t0011g0026 a0001c0001t0011g0268 others(2): Show |
6 | HG02055.hp2 HG02486.hp2 HG02572.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.701+4_701+7dupAGTA | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr7 | 80664497 | ||||||
| chr7:80664600 | C | T | 30 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0030 others(27): Show |
42 | HG00558.hp1 HG00609.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.701+103C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 7/14 | chr7 | 80664600 | |||||||
| chr7:80664664 | G | A | 5 | a0001c0001t0009g0140 a0001c0001t0011g0026 a0001c0001t0011g0268 others(2): Show |
6 | HG02055.hp2 HG02486.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.701+167G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 7/14 | chr7 | 80664664 | |||||||
| chr7:80664799 | T | C | 18 | a0001c0001t0003g0262 a0001c0001t0003g0265 a0001c0001t0008g0196 others(15): Show |
23 | HG01243.hp1 HG01891.hp2 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.701+302T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 7/14 | chr7 | 80664799 | |||||||
| chr7:80664840 | TA | T | 27 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0065 others(24): Show |
34 | HG00673.hp2 HG01358.hp2 HG01978.hp1 others(31): Show |
intron_variant | MODIFIER | c.701+346delA | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr7 | 80664840 | ||||||
| chr7:80664852 | T | TA | 192 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0020 others(189): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.701+369dupA | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr7 | 80664852 | ||||||
| chr7:80664852 | T | TAA | 27 | a0001c0001t0001g0062 a0001c0001t0003g0152 a0001c0001t0003g0163 others(24): Show |
33 | HG00673.hp1 HG01891.hp2 HG02055.hp2 others(30): Show |
intron_variant | MODIFIER | c.701+368_701+369dup others(2): Show |
CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr7 | 80664852 | ||||||
| chr7:80664867 | C | A | 1 | a0001c0001t0001g0121 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.701+370C>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 7/14 | chr7 | 80664867 | |||||||
| chr7:80664921 | C | T | 1 | a0001c0001t0054g0222 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.701+424C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 7/14 | chr7 | 80664921 | |||||||
| chr7:80664922 | G | A | 4 | a0001c0001t0009g0140 a0001c0001t0011g0268 a0001c0001t0031g0197 others(1): Show |
4 | HG02055.hp2 HG02486.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.701+425G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 7/14 | chr7 | 80664922 | |||||||
| chr7:80664931 | G | A | 1 | a0001c0001t0005g0242 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.701+434G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 7/14 | chr7 | 80664931 | |||||||
| chr7:80665048 | T | G | 1 | a0001c0001t0007g0164 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.701+551T>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 7/14 | chr7 | 80665048 | |||||||
| chr7:80665076 | A | C | 1 | a0001c0001t0060g0235 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.701+579A>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 7/14 | chr7 | 80665076 | |||||||
| chr7:80665103 | G | A | 3 | a0001c0001t0008g0196 a0001c0001t0014g0190 a0001c0001t0027g0027 |
4 | HG01243.hp1 HG02257.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.701+606G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 7/14 | chr7 | 80665103 | |||||||
| chr7:80665153 | C | A | 2 | a0001c0001t0003g0262 a0001c0001t0003g0265 |
2 | HG02258.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.701+656C>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 7/14 | chr7 | 80665153 | |||||||
| chr7:80665199 | C | CT | 17 | a0001c0001t0003g0262 a0001c0001t0003g0265 a0001c0001t0008g0196 others(14): Show |
21 | HG01891.hp2 HG02258.hp2 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.701+713dupT | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr7 | 80665199 | ||||||
| chr7:80665199 | CT | C | 5 | a0001c0001t0009g0140 a0001c0001t0011g0026 a0001c0001t0011g0268 others(2): Show |
6 | HG02055.hp2 HG02486.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.701+713delT | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr7 | 80665199 | ||||||
| chr7:80665288 | A | G | 56 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0065 others(53): Show |
69 | HG00673.hp2 HG01099.hp1 HG01243.hp1 others(66): Show |
intron_variant | MODIFIER | c.701+791A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 7/14 | chr7 | 80665288 | |||||||
| chr7:80665293 | C | A | 27 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0065 others(24): Show |
34 | HG00673.hp2 HG01358.hp2 HG01978.hp1 others(31): Show |
intron_variant | MODIFIER | c.701+796C>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 7/14 | chr7 | 80665293 | |||||||
| chr7:80665365 | A | C | 3 | a0001c0001t0008g0041 a0001c0001t0008g0210 a0001c0001t0008g0272 |
4 | HG00140.hp1 HG01081.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.701+868A>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 7/14 | chr7 | 80665365 | |||||||
| chr7:80665369 | C | T | 1 | a0001c0001t0006g0193 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.701+872C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 7/14 | chr7 | 80665369 | |||||||
| chr7:80665413 | C | CTCAAACT others(22): Show |
19 | a0001c0001t0001g0175 a0001c0001t0002g0016 a0001c0001t0002g0024 others(16): Show |
28 | HG00280.hp2 HG00642.hp2 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.701+918_701+946dup others(29): Show |
CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr7 | 80665413 | ||||||
| chr7:80665494 | T | C | 9 | a0001c0001t0008g0279 a0001c0001t0019g0276 a0001c0001t0019g0277 others(6): Show |
13 | HG01891.hp2 HG02486.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.702-949T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 7/14 | chr7 | 80665494 | |||||||
| chr7:80665617 | G | C | 1 | a0001c0001t0022g0271 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.702-826G>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 7/14 | chr7 | 80665617 | |||||||
| chr7:80665781 | A | T | 1 | a0001c0001t0021g0053 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.702-662A>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 7/14 | chr7 | 80665781 | |||||||
| chr7:80665786 | T | G | 19 | a0001c0001t0003g0262 a0001c0001t0003g0265 a0001c0001t0007g0259 others(16): Show |
24 | HG01243.hp1 HG01891.hp2 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.702-657T>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 7/14 | chr7 | 80665786 | |||||||
| chr7:80665878 | T | A | 1 | a0001c0001t0055g0221 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.702-565T>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 7/14 | chr7 | 80665878 | |||||||
| chr7:80665918 | G | A | 23 | a0001c0001t0003g0262 a0001c0001t0003g0265 a0001c0001t0008g0196 others(20): Show |
28 | HG01243.hp1 HG01891.hp2 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.702-525G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 7/14 | chr7 | 80665918 | |||||||
| chr7:80665985 | T | C | 4 | a0001c0001t0009g0140 a0001c0001t0011g0268 a0001c0001t0031g0197 others(1): Show |
4 | HG02055.hp2 HG02486.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.702-458T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 7/14 | chr7 | 80665985 | |||||||
| chr7:80665994 | C | T | 1 | a0001c0001t0003g0186 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.702-449C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 7/14 | chr7 | 80665994 | |||||||
| chr7:80666118 | C | A | 1 | a0001c0001t0002g0223 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.702-325C>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 7/14 | chr7 | 80666118 | |||||||
| chr7:80666125 | GA | G | 12 | a0001c0001t0001g0127 a0001c0001t0006g0092 a0001c0001t0019g0276 others(9): Show |
16 | HG01099.hp1 HG01243.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.702-307delA | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr7 | 80666125 | ||||||
| chr7:80666137 | T | A | 1 | a0001c0001t0059g0215 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.702-306T>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 7/14 | chr7 | 80666137 | |||||||
| chr7:80666204 | C | CTAATTAA others(16): Show |
1 | a0001c0001t0021g0053 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.702-237_702-215dup others(23): Show |
CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr7 | 80666204 | ||||||
| chr7:80666216 | T | G | 2 | a0001c0001t0056g0051 a0001c0001t0057g0050 |
2 | HG03041.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.702-227T>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 7/14 | chr7 | 80666216 | |||||||
| chr7:80666219 | C | A | 1 | a0001c0001t0022g0271 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.702-224C>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 7/14 | chr7 | 80666219 | |||||||
| chr7:80666548 | A | G | 2 | a0001c0001t0007g0052 a0001c0001t0007g0164 |
2 | HG02109.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.748+59A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 8/14 | chr7 | 80666548 | |||||||
| chr7:80666692 | A | T | 1 | a0001c0001t0021g0141 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.748+203A>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 8/14 | chr7 | 80666692 | |||||||
| chr7:80666738 | C | T | 3 | a0001c0001t0001g0020 a0001c0001t0001g0037 a0001c0001t0001g0184 |
6 | HG00733.hp2 HG01069.hp1 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.748+249C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 8/14 | chr7 | 80666738 | |||||||
| chr7:80666752 | T | G | 10 | a0001c0001t0019g0267 a0001c0001t0019g0276 a0001c0001t0019g0277 others(7): Show |
11 | HG01099.hp1 HG01243.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.748+263T>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 8/14 | chr7 | 80666752 | |||||||
| chr7:80667028 | G | A | 1 | a0001c0001t0001g0062 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.748+539G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 8/14 | chr7 | 80667028 | |||||||
| chr7:80667050 | A | C | 1 | a0001c0001t0004g0178 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.748+561A>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 8/14 | chr7 | 80667050 | |||||||
| chr7:80667142 | G | A | 27 | a0001c0001t0001g0273 a0001c0001t0004g0007 a0001c0001t0004g0018 others(24): Show |
34 | HG00673.hp2 HG03834.hp1 HG04184.hp1 others(31): Show |
intron_variant | MODIFIER | c.748+653G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 8/14 | chr7 | 80667142 | |||||||
| chr7:80667219 | G | A | 3 | a0001c0001t0049g0155 a0001c0001t0052g0266 a0001c0001t0062g0209 |
3 | HG02818.hp1 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.748+730G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 8/14 | chr7 | 80667219 | |||||||
| chr7:80667246 | A | G | 288 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(285): Show |
386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.748+757A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 8/14 | chr7 | 80667246 | |||||||
| chr7:80667282 | T | C | 2 | a0001c0001t0052g0266 a0001c0001t0062g0209 |
2 | HG02818.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.748+793T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 8/14 | chr7 | 80667282 | |||||||
| chr7:80667314 | C | T | 1 | a0001c0001t0009g0231 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.748+825C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 8/14 | chr7 | 80667314 | |||||||
| chr7:80667429 | C | CA | 127 | a0001c0001t0001g0065 a0001c0001t0001g0089 a0001c0001t0001g0109 others(124): Show |
178 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.748+962dupA | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr7 | 80667429 | ||||||
| chr7:80667429 | C | CAA | 11 | a0001c0001t0003g0107 a0001c0001t0003g0125 a0001c0001t0005g0234 others(8): Show |
11 | HG00544.hp2 HG00609.hp1 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.748+961_748+962dup others(2): Show |
CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr7 | 80667429 | ||||||
| chr7:80667429 | CA | C | 9 | a0001c0001t0001g0161 a0001c0001t0001g0174 a0001c0001t0005g0220 others(6): Show |
10 | HG01175.hp2 HG01243.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.748+962delA | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr7 | 80667429 | ||||||
| chr7:80667476 | G | C | 3 | a0001c0001t0001g0020 a0001c0001t0001g0037 a0001c0001t0001g0184 |
6 | HG00733.hp2 HG01069.hp1 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.748+987G>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 8/14 | chr7 | 80667476 | |||||||
| chr7:80667491 | A | G | 1 | a0001c0001t0008g0196 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.748+1002A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 8/14 | chr7 | 80667491 | |||||||
| chr7:80667499 | T | C | 1 | a0001c0001t0001g0121 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.748+1010T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 8/14 | chr7 | 80667499 | |||||||
| chr7:80667524 | T | G | 1 | a0001c0001t0027g0027 | 2 | HG01243.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.748+1035T>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 8/14 | chr7 | 80667524 | |||||||
| chr7:80667614 | A | G | 28 | a0001c0001t0001g0273 a0001c0001t0004g0007 a0001c0001t0004g0018 others(25): Show |
35 | HG00673.hp2 HG03834.hp1 HG04184.hp1 others(32): Show |
intron_variant | MODIFIER | c.748+1125A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 8/14 | chr7 | 80667614 | |||||||
| chr7:80667649 | G | GTACTTGA others(1): Show |
136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.748+1162_748+1169d others(10): Show |
CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr7 | 80667649 | ||||||
| chr7:80667701 | AAAAAAAA others(4): Show |
A | 1 | a0001c0001t0027g0027 | 2 | HG01243.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.748+1218_748+1228d others(13): Show |
CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr7 | 80667701 | ||||||
| chr7:80667747 | G | GT | 52 | a0001c0001t0002g0016 a0001c0001t0002g0019 a0001c0001t0002g0023 others(49): Show |
61 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.748+1279dupT | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr7 | 80667747 | ||||||
| chr7:80667747 | G | GTT | 12 | a0001c0001t0002g0025 a0001c0001t0002g0223 a0001c0001t0002g0239 others(9): Show |
13 | HG00642.hp1 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.748+1278_748+1279d others(4): Show |
CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr7 | 80667747 | ||||||
| chr7:80667747 | G | GTTTTTTT others(5): Show |
1 | a0001c0001t0049g0155 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.748+1268_748+1279d others(14): Show |
CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr7 | 80667747 | ||||||
| chr7:80667747 | G | GTTTTTTT others(9): Show |
1 | a0001c0001t0040g0133 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.748+1264_748+1279d others(18): Show |
CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr7 | 80667747 | ||||||
| chr7:80667747 | G | GTTTTTTT others(11): Show |
1 | a0001c0001t0015g0200 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.748+1262_748+1279d others(20): Show |
CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr7 | 80667747 | ||||||
| chr7:80667747 | G | GTTTTTTT others(14): Show |
1 | a0008c0011t0053g0269 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.748+1259_748+1279d others(23): Show |
CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr7 | 80667747 | ||||||
| chr7:80667747 | G | T | 3 | a0001c0001t0003g0107 a0001c0001t0011g0026 a0001c0001t0011g0032 |
5 | HG02109.hp2 HG02647.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.748+1258G>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 8/14 | chr7 | 80667747 | |||||||
| chr7:80667747 | GTTTTTTT others(5): Show |
G | 1 | a0001c0001t0002g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.748+1268_748+1279d others(14): Show |
CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr7 | 80667747 | ||||||
| chr7:80667750 | T | TTTTTTG | 10 | a0001c0001t0004g0028 a0001c0001t0004g0064 a0001c0001t0004g0079 others(7): Show |
11 | HG01243.hp2 HG04184.hp1 NA18953.hp1 others(8): Show |
intron_variant | MODIFIER | c.748+1266_748+1267i others(8): Show |
CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr7 | 80667750 | ||||||
| chr7:80667751 | T | TTTTTG | 19 | a0001c0001t0001g0273 a0001c0001t0004g0007 a0001c0001t0004g0018 others(16): Show |
25 | HG00673.hp2 HG03834.hp1 NA18940.hp2 others(22): Show |
intron_variant | MODIFIER | c.748+1266_748+1267i others(7): Show |
CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr7 | 80667751 | ||||||
| chr7:80667752 | T | G | 1 | a0001c0001t0005g0225 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.748+1263T>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 8/14 | chr7 | 80667752 | |||||||
| chr7:80667753 | T | TTTTTTTT others(2): Show |
10 | a0001c0001t0001g0091 a0001c0001t0001g0100 a0001c0001t0001g0120 others(7): Show |
10 | HG01109.hp1 HG02074.hp2 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.748+1272_748+1273i others(11): Show |
CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr7 | 80667753 | ||||||
| chr7:80667754 | T | TTTTTTTT others(1): Show |
95 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(92): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.748+1272_748+1273i others(10): Show |
CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr7 | 80667754 | ||||||
| chr7:80667812 | C | T | 4 | a0001c0001t0019g0267 a0001c0001t0019g0276 a0001c0001t0019g0277 others(1): Show |
4 | HG02615.hp2 HG02630.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.748+1323C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 8/14 | chr7 | 80667812 | |||||||
| chr7:80667833 | T | TCTGC | 9 | a0001c0001t0014g0190 a0001c0001t0019g0267 a0001c0001t0019g0276 others(6): Show |
10 | HG01099.hp1 HG01243.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.748+1347_748+1350d others(6): Show |
CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr7 | 80667833 | ||||||
| chr7:80667925 | A | G | 1 | a0001c0001t0013g0170 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.748+1436A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 8/14 | chr7 | 80667925 | |||||||
| chr7:80667958 | A | G | 1 | a0001c0001t0049g0155 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.748+1469A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 8/14 | chr7 | 80667958 | |||||||
| chr7:80667990 | G | A | 1 | a0001c0001t0041g0157 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.748+1501G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 8/14 | chr7 | 80667990 | |||||||
| chr7:80667999 | G | A | 4 | a0001c0001t0015g0040 a0001c0001t0015g0200 a0001c0001t0015g0201 others(1): Show |
5 | HG01255.hp1 HG01891.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.748+1510G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 8/14 | chr7 | 80667999 | |||||||
| chr7:80668035 | C | T | 4 | a0001c0001t0015g0040 a0001c0001t0015g0200 a0001c0001t0015g0201 others(1): Show |
5 | HG01255.hp1 HG01891.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.748+1546C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 8/14 | chr7 | 80668035 | |||||||
| chr7:80668092 | T | C | 1 | a0001c0001t0041g0157 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.748+1603T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 8/14 | chr7 | 80668092 | |||||||
| chr7:80668227 | T | C | 1 | a0001c0001t0058g0139 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.749-1726T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 8/14 | chr7 | 80668227 | |||||||
| chr7:80668404 | C | G | 151 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(148): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.749-1549C>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 8/14 | chr7 | 80668404 | |||||||
| chr7:80668446 | A | G | 4 | a0001c0001t0015g0040 a0001c0001t0015g0200 a0001c0001t0015g0201 others(1): Show |
5 | HG01255.hp1 HG01891.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.749-1507A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 8/14 | chr7 | 80668446 | |||||||
| chr7:80668459 | A | C | 3 | a0001c0001t0020g0194 a0001c0001t0020g0203 a0007c0006t0020g0195 |
3 | HG03098.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.749-1494A>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 8/14 | chr7 | 80668459 | |||||||
| chr7:80668472 | T | C | 1 | a0001c0001t0011g0026 | 2 | HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.749-1481T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 8/14 | chr7 | 80668472 | |||||||
| chr7:80668679 | A | C | 2 | a0001c0001t0001g0031 a0001c0001t0001g0101 |
3 | HG03017.hp2 HG03704.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.749-1274A>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 8/14 | chr7 | 80668679 | |||||||
| chr7:80668857 | C | T | 150 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(147): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.749-1096C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 8/14 | chr7 | 80668857 | |||||||
| chr7:80669116 | G | C | 29 | a0001c0001t0001g0273 a0001c0001t0004g0007 a0001c0001t0004g0018 others(26): Show |
36 | HG00673.hp2 HG03195.hp1 HG03834.hp1 others(33): Show |
intron_variant | MODIFIER | c.749-837G>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 8/14 | chr7 | 80669116 | |||||||
| chr7:80669124 | C | A | 9 | a0001c0001t0001g0273 a0001c0001t0004g0007 a0001c0001t0004g0028 others(6): Show |
14 | NA18940.hp2 NA18967.hp1 NA18971.hp1 others(11): Show |
intron_variant | MODIFIER | c.749-829C>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 8/14 | chr7 | 80669124 | |||||||
| chr7:80669209 | T | A | 1 | a0001c0001t0001g0104 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.749-744T>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 8/14 | chr7 | 80669209 | |||||||
| chr7:80669271 | G | A | 1 | a0001c0001t0002g0223 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.749-682G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 8/14 | chr7 | 80669271 | |||||||
| chr7:80669486 | G | A | 3 | a0001c0001t0006g0022 a0001c0001t0006g0182 a0001c0001t0030g0208 |
5 | HG02155.hp2 NA18612.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.749-467G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 8/14 | chr7 | 80669486 | |||||||
| chr7:80669571 | T | C | 151 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(148): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.749-382T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 8/14 | chr7 | 80669571 | |||||||
| chr7:80669622 | A | G | 2 | a0001c0001t0027g0027 a0001c0001t0049g0155 |
3 | HG01243.hp1 HG02257.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.749-331A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 8/14 | chr7 | 80669622 | |||||||
| chr7:80669641 | G | A | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.749-312G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 8/14 | chr7 | 80669641 | |||||||
| chr7:80669797 | G | A | 151 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(148): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.749-156G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 8/14 | chr7 | 80669797 | |||||||
| chr7:80669888 | G | A | 1 | a0001c0001t0041g0157 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.749-65G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 8/14 | chr7 | 80669888 | |||||||
| chr7:80670118 | T | C | 1 | a0001c0001t0007g0147 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.818+96T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 9/14 | chr7 | 80670118 | |||||||
| chr7:80670139 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.818+117C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 9/14 | chr7 | 80670139 | |||||||
| chr7:80670179 | A | AT | 7 | a0001c0001t0002g0239 a0001c0001t0007g0052 a0001c0001t0007g0164 others(4): Show |
7 | HG02109.hp1 HG03195.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.818+171dupT | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr7 | 80670179 | ||||||
| chr7:80670179 | A | T | 3 | a0001c0001t0001g0121 a0001c0001t0030g0251 a0001c0001t0054g0222 |
3 | HG02040.hp1 HG03540.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.818+157A>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 9/14 | chr7 | 80670179 | |||||||
| chr7:80670179 | AT | A | 9 | a0001c0001t0002g0199 a0001c0001t0002g0237 a0001c0001t0006g0182 others(6): Show |
9 | HG02723.hp2 HG02818.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.818+171delT | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr7 | 80670179 | ||||||
| chr7:80670188 | T | C | 9 | a0001c0001t0019g0267 a0001c0001t0019g0276 a0001c0001t0019g0277 others(6): Show |
10 | HG01099.hp1 HG01243.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.818+166T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 9/14 | chr7 | 80670188 | |||||||
| chr7:80670273 | C | T | 5 | a0001c0001t0015g0040 a0001c0001t0015g0200 a0001c0001t0015g0201 others(2): Show |
6 | HG01243.hp2 HG01255.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.818+251C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 9/14 | chr7 | 80670273 | |||||||
| chr7:80670274 | G | A | 3 | a0001c0001t0007g0052 a0001c0001t0007g0164 a0001c0001t0021g0206 |
3 | HG02109.hp1 HG03471.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.818+252G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 9/14 | chr7 | 80670274 | |||||||
| chr7:80670294 | C | G | 2 | a0001c0001t0052g0266 a0001c0001t0062g0209 |
2 | HG02818.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.818+272C>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 9/14 | chr7 | 80670294 | |||||||
| chr7:80670492 | A | G | 2 | a0001c0001t0004g0058 a0001c0001t0004g0060 |
2 | HG00673.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.818+470A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 9/14 | chr7 | 80670492 | |||||||
| chr7:80670534 | T | A | 122 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(119): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.819-443T>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 9/14 | chr7 | 80670534 | |||||||
| chr7:80670535 | A | T | 6 | a0001c0001t0019g0267 a0001c0001t0019g0276 a0001c0001t0019g0277 others(3): Show |
7 | HG01243.hp1 HG02257.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.819-442A>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 9/14 | chr7 | 80670535 | |||||||
| chr7:80670653 | C | T | 1 | a0001c0001t0007g0259 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.819-324C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 9/14 | chr7 | 80670653 | |||||||
| chr7:80670765 | T | C | 1 | a0001c0001t0041g0157 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.819-212T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 9/14 | chr7 | 80670765 | |||||||
| chr7:80671222 | T | A | 1 | a0001c0001t0059g0215 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1006+58T>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 10/14 | chr7 | 80671222 | |||||||
| chr7:80671353 | G | A | 1 | a0001c0001t0030g0251 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1006+189G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 10/14 | chr7 | 80671353 | |||||||
| chr7:80671384 | T | C | 4 | a0001c0001t0019g0267 a0001c0001t0019g0276 a0001c0001t0019g0277 others(1): Show |
4 | HG02615.hp2 HG02630.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1006+220T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 10/14 | chr7 | 80671384 | |||||||
| chr7:80671413 | C | T | 30 | a0001c0001t0001g0273 a0001c0001t0004g0007 a0001c0001t0004g0018 others(27): Show |
37 | HG00673.hp2 HG03834.hp1 HG04184.hp1 others(34): Show |
intron_variant | MODIFIER | c.1006+249C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 10/14 | chr7 | 80671413 | |||||||
| chr7:80671419 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1006+255G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 10/14 | chr7 | 80671419 | |||||||
| chr7:80671658 | G | A | 6 | a0001c0001t0015g0040 a0001c0001t0015g0200 a0001c0001t0015g0201 others(3): Show |
8 | HG01243.hp1 HG01243.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.1007-264G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 10/14 | chr7 | 80671658 | |||||||
| chr7:80671688 | T | C | 109 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(106): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.1007-234T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 10/14 | chr7 | 80671688 | |||||||
| chr7:80671715 | A | ATATTACT others(32): Show |
3 | a0001c0001t0037g0270 a0001c0001t0056g0051 a0001c0001t0057g0050 |
3 | HG01099.hp1 HG03041.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1007-205_1007-167d others(41): Show |
CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr7 | 80671715 | ||||||
| chr7:80671803 | T | C | 4 | a0001c0001t0019g0267 a0001c0001t0019g0276 a0001c0001t0019g0277 others(1): Show |
4 | HG02615.hp2 HG02630.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1007-119T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 10/14 | chr7 | 80671803 | |||||||
| chr7:80671871 | T | C | 1 | a0001c0001t0052g0266 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1007-51T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 10/14 | chr7 | 80671871 | |||||||
| chr7:80671902 | C | G | 1 | a0001c0001t0001g0172 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1007-20C>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 10/14 | chr7 | 80671902 | |||||||
| chr7:80672053 | C | A | 39 | a0001c0001t0001g0273 a0001c0001t0004g0007 a0001c0001t0004g0018 others(36): Show |
47 | HG00673.hp2 HG01099.hp1 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.1125+13C>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 11/14 | chr7 | 80672053 | |||||||
| chr7:80672184 | G | A | 38 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(35): Show |
55 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.1125+144G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 11/14 | chr7 | 80672184 | |||||||
| chr7:80672197 | G | T | 9 | a0001c0001t0015g0040 a0001c0001t0015g0200 a0001c0001t0015g0201 others(6): Show |
11 | HG01099.hp1 HG01243.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.1125+157G>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 11/14 | chr7 | 80672197 | |||||||
| chr7:80672266 | T | C | 31 | a0001c0001t0001g0273 a0001c0001t0004g0007 a0001c0001t0004g0018 others(28): Show |
38 | HG00673.hp2 HG03195.hp1 HG03834.hp1 others(35): Show |
intron_variant | MODIFIER | c.1125+226T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 11/14 | chr7 | 80672266 | |||||||
| chr7:80672344 | G | A | 3 | a0001c0001t0008g0216 a0001c0001t0008g0250 a0001c0001t0008g0253 |
3 | HG02129.hp2 NA18964.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.1125+304G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 11/14 | chr7 | 80672344 | |||||||
| chr7:80672370 | T | C | 31 | a0001c0001t0001g0273 a0001c0001t0004g0007 a0001c0001t0004g0018 others(28): Show |
38 | HG00673.hp2 HG03195.hp1 HG03834.hp1 others(35): Show |
intron_variant | MODIFIER | c.1125+330T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 11/14 | chr7 | 80672370 | |||||||
| chr7:80672413 | G | A | 4 | a0001c0001t0015g0040 a0001c0001t0015g0200 a0001c0001t0015g0201 others(1): Show |
5 | HG01255.hp1 HG01891.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1126-357G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 11/14 | chr7 | 80672413 | |||||||
| chr7:80672454 | C | T | 1 | a0001c0001t0033g0049 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1126-316C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 11/14 | chr7 | 80672454 | |||||||
| chr7:80672543 | A | T | 1 | a0001c0001t0003g0126 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1126-227A>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 11/14 | chr7 | 80672543 | |||||||
| chr7:80672592 | G | A | 2 | a0001c0001t0049g0155 a0008c0011t0053g0269 |
2 | HG03195.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1126-178G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 11/14 | chr7 | 80672592 | |||||||
| chr7:80672620 | C | A | 154 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(151): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.1126-150C>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 11/14 | chr7 | 80672620 | |||||||
| chr7:80672711 | T | C | 1 | a0008c0011t0053g0269 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1126-59T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 11/14 | chr7 | 80672711 | |||||||
| chr7:80672880 | G | A | 29 | a0001c0001t0001g0273 a0001c0001t0004g0007 a0001c0001t0004g0018 others(26): Show |
36 | HG00673.hp2 HG03834.hp1 HG04184.hp1 others(33): Show |
intron_variant | MODIFIER | c.1199+37G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 12/14 | chr7 | 80672880 | |||||||
| chr7:80672884 | T | C | 4 | a0001c0001t0015g0040 a0001c0001t0015g0200 a0001c0001t0015g0201 others(1): Show |
5 | HG01255.hp1 HG01891.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1199+41T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 12/14 | chr7 | 80672884 | |||||||
| chr7:80672899 | T | G | 1 | a0002c0002t0007g0263 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1199+56T>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 12/14 | chr7 | 80672899 | |||||||
| chr7:80673006 | C | T | 1 | a0001c0001t0010g0227 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1199+163C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 12/14 | chr7 | 80673006 | |||||||
| chr7:80673018 | A | AATGGTTT others(30): Show |
4 | a0001c0001t0027g0027 a0001c0001t0037g0270 a0001c0001t0056g0051 others(1): Show |
5 | HG01099.hp1 HG01243.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1199+176_1199+212d others(39): Show |
CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr7 | 80673018 | ||||||
| chr7:80673035 | A | G | 2 | a0001c0001t0005g0234 a0001c0001t0033g0049 |
2 | HG00544.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1199+192A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 12/14 | chr7 | 80673035 | |||||||
| chr7:80673056 | T | G | 29 | a0001c0001t0001g0273 a0001c0001t0004g0007 a0001c0001t0004g0018 others(26): Show |
36 | HG00673.hp2 HG03834.hp1 HG04184.hp1 others(33): Show |
intron_variant | MODIFIER | c.1199+213T>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 12/14 | chr7 | 80673056 | |||||||
| chr7:80673074 | C | T | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(109): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.1199+231C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 12/14 | chr7 | 80673074 | |||||||
| chr7:80673482 | G | T | 2 | a0001c0004t0001g0039 a0001c0004t0001g0187 |
3 | HG01257.hp1 HG01258.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1254+73G>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 13/14 | chr7 | 80673482 | |||||||
| chr7:80673489 | T | C | 1 | a0001c0001t0007g0261 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1254+80T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 13/14 | chr7 | 80673489 | |||||||
| chr7:80673705 | A | T | 1 | a0001c0001t0002g0199 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1255-278A>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 13/14 | chr7 | 80673705 | |||||||
| chr7:80673731 | GGAGCAAA others(30): Show |
G | 3 | a0001c0001t0001g0105 a0001c0001t0001g0114 a0001c0001t0008g0233 |
3 | HG00558.hp1 NA18985.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1255-240_1255-204d others(39): Show |
CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr7 | 80673731 | ||||||
| chr7:80673821 | A | ATTGCCTT others(9): Show |
1 | a0001c0001t0001g0275 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1255-161_1255-146d others(18): Show |
CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr7 | 80673821 | ||||||
| chr7:80673889 | T | C | 29 | a0001c0001t0001g0273 a0001c0001t0004g0007 a0001c0001t0004g0018 others(26): Show |
36 | HG00673.hp2 HG03834.hp1 HG04184.hp1 others(33): Show |
intron_variant | MODIFIER | c.1255-94T>C | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 13/14 | chr7 | 80673889 | |||||||
| chr7:80674144 | ATAAG | A | 3 | a0001c0001t0029g0238 a0001c0001t0029g0241 a0001c0001t0033g0049 |
3 | HG01074.hp2 HG02976.hp2 HG03710.hp1 |
splice_region_variant&intron_variant | LOW | c.1419+4_1419+7delAG others(2): Show |
CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr7 | 80674144 | ||||||
| chr7:80674349 | G | T | 1 | a0001c0001t0033g0049 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1419+202G>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 14/14 | chr7 | 80674349 | |||||||
| chr7:80674373 | A | G | 4 | a0001c0001t0019g0267 a0001c0001t0019g0276 a0001c0001t0019g0277 others(1): Show |
4 | HG02615.hp2 HG02630.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1419+226A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 14/14 | chr7 | 80674373 | |||||||
| chr7:80674384 | AGCACAAA others(9): Show |
A | 19 | a0001c0001t0002g0237 a0001c0001t0005g0243 a0001c0001t0009g0010 others(16): Show |
27 | HG00544.hp1 HG00733.hp1 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.1419+238_1419+253d others(18): Show |
CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 14/14 | chr7 | 80674384 | |||||||
| chr7:80674395 | A | T | 2 | a0001c0001t0002g0244 a0001c0001t0003g0125 |
2 | HG01433.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1419+248A>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 14/14 | chr7 | 80674395 | |||||||
| chr7:80674440 | A | ATTATAGA others(17): Show |
1 | a0001c0001t0001g0069 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1419+298_1419+299i others(26): Show |
CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr7 | 80674440 | ||||||
| chr7:80674446 | T | G | 40 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(37): Show |
57 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.1419+299T>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 14/14 | chr7 | 80674446 | |||||||
| chr7:80674483 | G | A | 1 | a0001c0001t0002g0240 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1419+336G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 14/14 | chr7 | 80674483 | |||||||
| chr7:80674536 | G | A | 1 | a0001c0008t0007g0122 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1419+389G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 14/14 | chr7 | 80674536 | |||||||
| chr7:80674580 | A | T | 1 | a0001c0001t0054g0222 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1419+433A>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 14/14 | chr7 | 80674580 | |||||||
| chr7:80674643 | G | T | 2 | a0001c0001t0001g0171 a0001c0001t0001g0174 |
2 | HG00099.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.1419+496G>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 14/14 | chr7 | 80674643 | |||||||
| chr7:80674690 | A | T | 1 | a0001c0001t0027g0027 | 2 | HG01243.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.1419+543A>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 14/14 | chr7 | 80674690 | |||||||
| chr7:80674756 | A | G | 113 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(110): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.1419+609A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 14/14 | chr7 | 80674756 | |||||||
| chr7:80674973 | C | T | 1 | a0001c0001t0049g0155 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1419+826C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 14/14 | chr7 | 80674973 | |||||||
| chr7:80675018 | G | A | 4 | a0001c0001t0027g0027 a0001c0001t0037g0270 a0001c0001t0056g0051 others(1): Show |
5 | HG01099.hp1 HG01243.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1419+871G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 14/14 | chr7 | 80675018 | |||||||
| chr7:80675106 | C | G | 1 | a0001c0001t0003g0177 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1419+959C>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 14/14 | chr7 | 80675106 | |||||||
| chr7:80675153 | G | A | 2 | a0001c0001t0041g0157 a0001c0001t0054g0222 |
2 | HG01243.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1419+1006G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 14/14 | chr7 | 80675153 | |||||||
| chr7:80675240 | C | T | 1 | a0001c0001t0046g0124 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1419+1093C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 14/14 | chr7 | 80675240 | |||||||
| chr7:80675296 | A | G | 109 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(106): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.*1-1088A>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 14/14 | chr7 | 80675296 | |||||||
| chr7:80675323 | A | AAAGTAAA others(45): Show |
2 | a0001c0001t0007g0088 a0001c0001t0014g0119 |
2 | HG02717.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.*1-1058_*1-1007dup others(52): Show |
CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr7 | 80675323 | ||||||
| chr7:80675407 | T | TGTAA | 2 | a0001c0001t0001g0012 a0001c0001t0001g0100 |
5 | HG02074.hp2 NA18941.hp1 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.*1-969_*1-966dupAG others(2): Show |
CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr7 | 80675407 | ||||||
| chr7:80675539 | T | G | 2 | a0003c0003t0006g0034 a0003c0003t0006g0151 |
3 | NA18969.hp1 NA18981.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.*1-845T>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 14/14 | chr7 | 80675539 | |||||||
| chr7:80675777 | C | A | 3 | a0001c0001t0037g0270 a0001c0001t0056g0051 a0001c0001t0057g0050 |
3 | HG01099.hp1 HG03041.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.*1-607C>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 14/14 | chr7 | 80675777 | |||||||
| chr7:80675936 | G | T | 2 | a0001c0001t0004g0071 a0001c0001t0004g0098 |
2 | NA19060.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.*1-448G>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 14/14 | chr7 | 80675936 | |||||||
| chr7:80675962 | T | TGAGGGTT others(2): Show |
123 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(120): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.*1-420_*1-419insGG others(7): Show |
CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr7 | 80675962 | ||||||
| chr7:80676025 | G | A | 2 | a0001c0001t0049g0155 a0008c0011t0053g0269 |
2 | HG03195.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.*1-359G>A | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 14/14 | chr7 | 80676025 | |||||||
| chr7:80676102 | C | G | 27 | a0001c0001t0004g0007 a0001c0001t0004g0018 a0001c0001t0004g0028 others(24): Show |
34 | HG00673.hp2 HG03834.hp1 NA18940.hp2 others(31): Show |
intron_variant | MODIFIER | c.*1-282C>G | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 14/14 | chr7 | 80676102 | |||||||
| chr7:80676256 | C | T | 5 | a0001c0001t0002g0016 a0001c0001t0002g0042 a0001c0001t0002g0218 others(2): Show |
9 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.*1-128C>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 14/14 | chr7 | 80676256 | |||||||
| chr7:80676317 | C | CA | 6 | a0001c0001t0001g0154 a0001c0001t0003g0168 a0001c0001t0008g0216 others(3): Show |
6 | HG02129.hp2 HG03453.hp2 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.*1-58dupA | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr7 | 80676317 | ||||||
| chr7:80676324 | A | T | 1 | a0001c0001t0001g0275 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.*1-60A>T | CD36 | ENSG00000135218.19 | transcript | ENST00000447544.7 | protein_coding | 14/14 | chr7 | 80676324 |