Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 137964 |
| ensemblid | ENSG00000158669.11 |
| hgncid | 20880 |
| symbol | GPAT4 |
| name | glycerol-3-phosphate acyltransferase 4 |
| refseq_nuc | NM_178819.4 |
| refseq_prot | NP_848934.1 |
| ensembl_nuc | ENST00000396987.7 |
| ensembl_prot | ENSP00000380184.3 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 41578200 |
| end | 41625001 |
| strand | + |
| ver | v1.2 |
| region | chr8:41578200-41625001 |
| region5000 | chr8:41573200-41630001 |
| regionname0 | GPAT4_chr8_41578200_41625001 |
| regionname5000 | GPAT4_chr8_41573200_41630001 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 456 | 408 | 86 | 64 | 196 | 12 | 48 | 152 | GPAT4_chr8_41573200_41630001 | GPAT4 | MFLLL others(451): Show |
chr8 | 41573200 | 41630001 |
| a0002 | 0/0 | 456 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | MFLLL others(451): Show |
chr8 | 41573200 | 41630001 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1368 | 405 | 86 | 62 | 196 | 12 | 47 | GPAT4_chr8_41573200_41630001 | GPAT4 | ATGTT others(1363): Show |
chr8 | 41573200 | 41630001 | ||
| a0001c0003 | 0/0 | 1368 | 2 | 0 | 2 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | ATGTT others(1363): Show |
chr8 | 41573200 | 41630001 | ||
| a0001c0004 | 0/0 | 1368 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | ATGTT others(1363): Show |
chr8 | 41573200 | 41630001 | ||
| a0002c0002 | 0/0 | 1368 | 2 | 2 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | ATGTT others(1363): Show |
chr8 | 41573200 | 41630001 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 6298 | 150 | 23 | 24 | 74 | 5 | 23 | GPAT4_chr8_41573200_41630001 | GPAT4 | GCAGC others(6293): Show |
chr8 | 41573200 | 41630001 |
| a0001c0001t0002 | 0/1 | 6307 | 55 | 1 | 11 | 32 | 3 | 7 | GPAT4_chr8_41573200_41630001 | GPAT4 | GCAGC others(6302): Show |
chr8 | 41573200 | 41630001 |
| a0001c0001t0003 | 0/0 | 6306 | 50 | 4 | 11 | 29 | 1 | 5 | GPAT4_chr8_41573200_41630001 | GPAT4 | GCAGC others(6301): Show |
chr8 | 41573200 | 41630001 |
| a0001c0001t0004 | 0/0 | 6307 | 32 | 12 | 1 | 19 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | GCAGC others(6302): Show |
chr8 | 41573200 | 41630001 |
| a0001c0001t0005 | 0/0 | 6306 | 28 | 11 | 1 | 12 | 1 | 3 | GPAT4_chr8_41573200_41630001 | GPAT4 | GCAGC others(6301): Show |
chr8 | 41573200 | 41630001 |
| a0001c0001t0006 | 0/0 | 6307 | 13 | 6 | 5 | 0 | 0 | 2 | GPAT4_chr8_41573200_41630001 | GPAT4 | GCAGC others(6302): Show |
chr8 | 41573200 | 41630001 |
| a0001c0001t0007 | 0/0 | 6309 | 11 | 5 | 5 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | GCAGC others(6304): Show |
chr8 | 41573200 | 41630001 |
| a0001c0001t0008 | 0/0 | 6307 | 8 | 8 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | GCAGC others(6302): Show |
chr8 | 41573200 | 41630001 |
| a0001c0001t0009 | 0/0 | 6307 | 5 | 0 | 0 | 5 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | GCAGC others(6302): Show |
chr8 | 41573200 | 41630001 |
| a0001c0001t0010 | 0/0 | 6306 | 3 | 3 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | GCAGC others(6301): Show |
chr8 | 41573200 | 41630001 |
| a0001c0001t0011 | 0/0 | 6298 | 3 | 0 | 0 | 3 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | GCAGC others(6293): Show |
chr8 | 41573200 | 41630001 |
| a0001c0001t0012 | 0/0 | 6307 | 2 | 2 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | GCAGC others(6302): Show |
chr8 | 41573200 | 41630001 |
| a0001c0001t0013 | 0/0 | 6306 | 2 | 0 | 0 | 2 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | GCAGC others(6301): Show |
chr8 | 41573200 | 41630001 |
| a0001c0001t0015 | 0/0 | 6307 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | GCAGC others(6302): Show |
chr8 | 41573200 | 41630001 |
| a0001c0001t0016 | 0/0 | 6306 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | GCAGC others(6301): Show |
chr8 | 41573200 | 41630001 |
| a0001c0001t0017 | 0/0 | 6300 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | GCAGC others(6295): Show |
chr8 | 41573200 | 41630001 |
| a0001c0001t0018 | 0/0 | 6307 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | GCAGC others(6302): Show |
chr8 | 41573200 | 41630001 |
| a0001c0001t0019 | 0/0 | 6307 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | GCAGC others(6302): Show |
chr8 | 41573200 | 41630001 |
| a0001c0001t0020 | 0/0 | 6309 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | GCAGC others(6304): Show |
chr8 | 41573200 | 41630001 |
| a0001c0001t0021 | 0/0 | 6306 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | GCAGC others(6301): Show |
chr8 | 41573200 | 41630001 |
| a0001c0001t0022 | 0/0 | 6306 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | GCAGC others(6301): Show |
chr8 | 41573200 | 41630001 |
| a0001c0001t0023 | 0/0 | 6307 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | GCAGC others(6302): Show |
chr8 | 41573200 | 41630001 |
| a0001c0001t0024 | 0/0 | 6307 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | GCAGC others(6302): Show |
chr8 | 41573200 | 41630001 |
| a0001c0001t0025 | 0/0 | 6307 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | GCAGC others(6302): Show |
chr8 | 41573200 | 41630001 |
| a0001c0001t0026 | 0/0 | 6307 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | GCAGC others(6302): Show |
chr8 | 41573200 | 41630001 |
| a0001c0001t0027 | 0/0 | 6307 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | GCAGC others(6302): Show |
chr8 | 41573200 | 41630001 |
| a0001c0001t0028 | 0/0 | 6306 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | GCAGC others(6301): Show |
chr8 | 41573200 | 41630001 |
| a0001c0001t0029 | 0/0 | 6307 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | GCAGC others(6302): Show |
chr8 | 41573200 | 41630001 |
| a0001c0001t0030 | 0/0 | 6307 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | GCAGC others(6302): Show |
chr8 | 41573200 | 41630001 |
| a0001c0001t0031 | 0/0 | 6307 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | GCAGC others(6302): Show |
chr8 | 41573200 | 41630001 |
| a0001c0001t0032 | 0/0 | 6298 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | GCAGC others(6293): Show |
chr8 | 41573200 | 41630001 |
| a0001c0001t0033 | 0/0 | 6298 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | GCAGC others(6293): Show |
chr8 | 41573200 | 41630001 |
| a0001c0001t0034 | 0/0 | 6298 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | GCAGC others(6293): Show |
chr8 | 41573200 | 41630001 |
| a0001c0001t0035 | 0/0 | 6298 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | GCAGC others(6293): Show |
chr8 | 41573200 | 41630001 |
| a0001c0001t0036 | 0/0 | 6298 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | GCAGC others(6293): Show |
chr8 | 41573200 | 41630001 |
| a0001c0001t0037 | 0/0 | 6298 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | GCAGC others(6293): Show |
chr8 | 41573200 | 41630001 |
| a0001c0001t0038 | 0/0 | 6298 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | GCAGC others(6293): Show |
chr8 | 41573200 | 41630001 |
| a0001c0001t0039 | 0/0 | 6307 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | GCAGC others(6302): Show |
chr8 | 41573200 | 41630001 |
| a0001c0001t0040 | 0/0 | 6302 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | GCAGC others(6297): Show |
chr8 | 41573200 | 41630001 |
| a0001c0001t0041 | 0/0 | 6298 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | GCAGC others(6293): Show |
chr8 | 41573200 | 41630001 |
| a0001c0001t0042 | 0/0 | 6297 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | GCAGC others(6292): Show |
chr8 | 41573200 | 41630001 |
| a0001c0001t0043 | 0/0 | 6298 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | GCAGC others(6293): Show |
chr8 | 41573200 | 41630001 |
| a0001c0001t0044 | 0/0 | 6298 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | GCAGC others(6293): Show |
chr8 | 41573200 | 41630001 |
| a0001c0001t0045 | 0/0 | 6298 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | GCAGC others(6293): Show |
chr8 | 41573200 | 41630001 |
| a0001c0001t0046 | 0/0 | 6298 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | GCAGC others(6293): Show |
chr8 | 41573200 | 41630001 |
| a0001c0001t0047 | 0/0 | 6298 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | GCAGC others(6293): Show |
chr8 | 41573200 | 41630001 |
| a0001c0001t0048 | 0/0 | 6298 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | GCAGC others(6293): Show |
chr8 | 41573200 | 41630001 |
| a0001c0001t0049 | 0/0 | 6298 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | GCAGC others(6293): Show |
chr8 | 41573200 | 41630001 |
| a0001c0001t0050 | 0/0 | 6298 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | GCAGC others(6293): Show |
chr8 | 41573200 | 41630001 |
| a0001c0001t0052 | 0/0 | 6309 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | GCAGC others(6304): Show |
chr8 | 41573200 | 41630001 |
| a0001c0001t0053 | 0/0 | 6309 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | GCAGC others(6304): Show |
chr8 | 41573200 | 41630001 |
| a0001c0001t0054 | 0/0 | 6298 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | GCAGC others(6293): Show |
chr8 | 41573200 | 41630001 |
| a0001c0001t0055 | 0/0 | 6298 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | GCAGC others(6293): Show |
chr8 | 41573200 | 41630001 |
| a0001c0001t0056 | 0/0 | 6302 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | GCAGC others(6297): Show |
chr8 | 41573200 | 41630001 |
| a0001c0001t0057 | 0/0 | 6302 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | GCAGC others(6297): Show |
chr8 | 41573200 | 41630001 |
| a0001c0001t0058 | 0/0 | 6298 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | GCAGC others(6293): Show |
chr8 | 41573200 | 41630001 |
| a0001c0003t0007 | 0/0 | 6309 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | GCAGC others(6304): Show |
chr8 | 41573200 | 41630001 |
| a0001c0003t0051 | 0/0 | 6305 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | GCAGC others(6300): Show |
chr8 | 41573200 | 41630001 |
| a0001c0004t0003 | 0/0 | 6306 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | GCAGC others(6301): Show |
chr8 | 41573200 | 41630001 |
| a0002c0002t0014 | 0/0 | 6307 | 2 | 2 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | GCAGC others(6302): Show |
chr8 | 41573200 | 41630001 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0006 | 1/0 | 4 | 3 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0031 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0002g0001 | 0/0 | 9 | 0 | 3 | 3 | 0 | 3 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0002g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0002g0033 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0002g0342 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0003g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0003g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0003g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0003g0020 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0003g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0003g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0003g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0004g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0004g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0004g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0004g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0004g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0004g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0004g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0004g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0004g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0004g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0004g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0004g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0004g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0004g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0004g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0004g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0004g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0004g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0004g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0004g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0004g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0004g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0004g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0004g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0005g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0005g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0005g0023 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0005g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0005g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0005g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0005g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0005g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0005g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0005g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0005g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0005g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0005g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0005g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0005g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0005g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0005g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0005g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0005g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0005g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0005g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0005g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0005g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0006g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0006g0014 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0006g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0006g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0006g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0006g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0006g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0006g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0006g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0006g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0007g0002 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0007g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0007g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0007g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0007g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0007g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0007g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0007g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0008g0004 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0008g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0008g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0008g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0008g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0009g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0009g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0009g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0010g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0010g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0010g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0011g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0011g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0011g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0012g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0012g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0013g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0013g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0015g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0016g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0017g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0018g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0019g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0020g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0021g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0022g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0023g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0024g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0025g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0026g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0027g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0028g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0029g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0030g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0031g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0032g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0033g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0034g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0035g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0036g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0037g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0038g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0039g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0040g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0041g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0042g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0043g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0044g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0045g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0046g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0047g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0048g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0049g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0050g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0052g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0053g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0054g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0055g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0056g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0057g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0001t0058g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0003t0007g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0003t0051g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0001c0004t0003g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0002c0002t0014g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| a0002c0002t0014g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0152 | EUR | GBR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0258 | EUR | GBR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0157 | EUR | FIN | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0280 | EUR | FIN | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0335 | EAS | CHS | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | CHS | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | CHS | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG00438 | hp1 | a0001 | c0001 | t0004 | g0333 | EAS | CHS | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | CHS | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG00544 | hp1 | a0001 | c0001 | t0004 | g0309 | EAS | CHS | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0077 | EAS | CHS | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG00597 | hp1 | a0001 | c0001 | t0004 | g0015 | EAS | CHS | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0076 | EAS | CHS | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | CHS | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | CHS | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | CHS | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG00621 | hp2 | a0001 | c0001 | t0011 | g0187 | EAS | CHS | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0055 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0315 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG00673 | hp1 | a0001 | c0001 | t0004 | g0287 | EAS | CHS | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0293 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG00738 | hp1 | a0001 | c0001 | t0007 | g0002 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0282 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0319 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG00741 | hp2 | a0001 | c0001 | t0024 | g0036 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG01069 | hp1 | a0001 | c0003 | t0007 | g0002 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG01069 | hp2 | a0001 | c0001 | t0006 | g0014 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG01070 | hp1 | a0001 | c0001 | t0007 | g0045 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0022 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG01071 | hp1 | a0001 | c0001 | t0006 | g0013 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0022 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG01074 | hp1 | a0001 | c0003 | t0051 | g0047 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG01081 | hp2 | a0001 | c0001 | t0007 | g0046 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0073 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG01106 | hp1 | a0001 | c0001 | t0004 | g0290 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG01106 | hp2 | a0001 | c0001 | t0007 | g0043 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0070 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0294 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0056 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0298 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG01192 | hp1 | a0001 | c0001 | t0006 | g0274 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0057 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG01243 | hp2 | a0001 | c0001 | t0007 | g0344 | AMR | PUR | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | CLM | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0088 | AMR | CLM | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG01261 | hp2 | a0001 | c0001 | t0023 | g0289 | AMR | CLM | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0054 | AMR | CLM | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG01346 | hp2 | a0001 | c0001 | t0006 | g0013 | AMR | CLM | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG01361 | hp1 | a0001 | c0001 | t0006 | g0275 | AMR | CLM | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG01361 | hp2 | a0001 | c0001 | t0057 | g0048 | AMR | CLM | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0081 | AMR | CLM | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG01496 | hp1 | a0001 | c0001 | t0033 | g0208 | AMR | CLM | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0034 | EUR | IBS | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG01516 | hp2 | a0001 | c0001 | t0028 | g0086 | EUR | IBS | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0320 | EUR | IBS | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0028 | EUR | IBS | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG01884 | hp1 | a0001 | c0001 | t0007 | g0337 | AFR | ACB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG01884 | hp2 | a0001 | c0001 | t0006 | g0104 | AFR | ACB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0052 | AFR | ACB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0089 | AFR | ACB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PEL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0063 | AMR | PEL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | PEL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02004 | hp2 | a0001 | c0001 | t0005 | g0119 | AMR | PEL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02015 | hp2 | a0001 | c0001 | t0004 | g0015 | EAS | KHV | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02027 | hp1 | a0001 | c0001 | t0004 | g0313 | EAS | KHV | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02027 | hp2 | a0001 | c0001 | t0041 | g0256 | EAS | KHV | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0300 | EAS | KHV | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02055 | hp1 | a0001 | c0001 | t0008 | g0096 | AFR | ACB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02055 | hp2 | a0001 | c0001 | t0005 | g0038 | AFR | ACB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02074 | hp2 | a0001 | c0001 | t0005 | g0107 | EAS | KHV | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02080 | hp1 | a0001 | c0001 | t0004 | g0008 | EAS | KHV | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0018 | EAS | KHV | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | KHV | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02083 | hp2 | a0001 | c0001 | t0039 | g0195 | EAS | KHV | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0336 | EAS | KHV | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | KHV | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02132 | hp1 | a0001 | c0001 | t0005 | g0024 | EAS | KHV | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02135 | hp1 | a0001 | c0001 | t0004 | g0312 | EAS | KHV | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0083 | AFR | ACB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | ACB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02165 | hp1 | a0001 | c0001 | t0005 | g0012 | EAS | CDX | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | CDX | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0090 | AFR | ACB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02258 | hp1 | a0001 | c0001 | t0007 | g0009 | AFR | ACB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PEL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02280 | hp1 | a0001 | c0001 | t0008 | g0099 | AFR | ACB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | ACB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | ACB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0110 | AFR | ACB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02523 | hp1 | a0001 | c0001 | t0049 | g0126 | EAS | KHV | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0051 | AFR | GWD | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0117 | AFR | GWD | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0019 | SAS | PJL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0311 | AFR | GWD | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02630 | hp1 | a0002 | c0002 | t0014 | g0095 | AFR | GWD | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0115 | AFR | GWD | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02647 | hp1 | a0001 | c0001 | t0008 | g0097 | AFR | GWD | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02647 | hp2 | a0001 | c0001 | t0006 | g0273 | AFR | GWD | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0343 | SAS | PJL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0085 | SAS | PJL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02698 | hp1 | a0001 | c0004 | t0003 | g0019 | SAS | PJL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0325 | SAS | PJL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02723 | hp1 | a0001 | c0001 | t0053 | g0041 | AFR | GWD | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02723 | hp2 | a0001 | c0001 | t0047 | g0215 | AFR | GWD | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0257 | SAS | PJL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0039 | AFR | GWD | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02809 | hp2 | a0001 | c0001 | t0012 | g0270 | AFR | GWD | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02818 | hp1 | a0001 | c0001 | t0006 | g0105 | AFR | GWD | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02818 | hp2 | a0001 | c0001 | t0056 | g0049 | AFR | GWD | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0316 | AFR | GWD | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | GWD | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02895 | hp1 | a0001 | c0001 | t0006 | g0269 | AFR | GWD | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02895 | hp2 | a0001 | c0001 | t0005 | g0106 | AFR | GWD | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02896 | hp1 | a0001 | c0001 | t0005 | g0122 | AFR | GWD | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02897 | hp2 | a0001 | c0001 | t0022 | g0272 | AFR | GWD | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02922 | hp2 | a0001 | c0001 | t0006 | g0053 | AFR | ESN | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02965 | hp1 | a0001 | c0001 | t0019 | g0103 | AFR | ESN | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | ESN | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02970 | hp2 | a0001 | c0001 | t0010 | g0093 | AFR | ESN | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG03017 | hp2 | a0001 | c0001 | t0043 | g0144 | SAS | PJL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG03041 | hp1 | a0001 | c0001 | t0008 | g0004 | AFR | GWD | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG03041 | hp2 | a0001 | c0001 | t0005 | g0116 | AFR | GWD | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG03098 | hp1 | a0001 | c0001 | t0015 | g0288 | AFR | MSL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG03098 | hp2 | a0001 | c0001 | t0006 | g0276 | AFR | MSL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0010 | AFR | ESN | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG03139 | hp1 | a0001 | c0001 | t0040 | g0268 | AFR | ESN | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0324 | AFR | ESN | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG03195 | hp1 | a0001 | c0001 | t0010 | g0091 | AFR | ESN | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0037 | AFR | ESN | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG03239 | hp1 | a0001 | c0001 | t0007 | g0002 | SAS | PJL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG03239 | hp2 | a0001 | c0001 | t0026 | g0123 | SAS | PJL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG03453 | hp1 | a0001 | c0001 | t0008 | g0004 | AFR | MSL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0340 | AFR | MSL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0040 | AFR | MSL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG03486 | hp2 | a0001 | c0001 | t0008 | g0004 | AFR | MSL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG03490 | hp1 | a0001 | c0001 | t0006 | g0014 | SAS | PJL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG03490 | hp2 | a0001 | c0001 | t0005 | g0023 | SAS | PJL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG03492 | hp1 | a0001 | c0001 | t0006 | g0014 | SAS | PJL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG03516 | hp1 | a0001 | c0001 | t0029 | g0102 | AFR | ESN | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | ESN | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG03540 | hp1 | a0001 | c0001 | t0007 | g0009 | AFR | GWD | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0010 | AFR | MSL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG03579 | hp2 | a0002 | c0002 | t0014 | g0094 | AFR | MSL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0255 | SAS | PJL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG03654 | hp2 | a0001 | c0001 | t0048 | g0167 | SAS | PJL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG03669 | hp1 | a0001 | c0001 | t0005 | g0120 | SAS | PJL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0281 | SAS | STU | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0262 | SAS | STU | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG03710 | hp1 | a0001 | c0001 | t0050 | g0209 | SAS | PJL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0254 | SAS | BEB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0252 | SAS | BEB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG03834 | hp1 | a0001 | c0001 | t0005 | g0109 | SAS | BEB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0065 | SAS | BEB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | BEB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0314 | SAS | BEB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | BEB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0318 | SAS | BEB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | STU | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG04115 | hp2 | a0001 | c0001 | t0034 | g0193 | SAS | STU | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | BEB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | BEB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | STU | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | STU | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | STU | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | STU | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | STU | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0020 | SAS | STU | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | YRI | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18522 | hp2 | a0001 | c0001 | t0054 | g0339 | AFR | YRI | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | CHB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | CHB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | CHB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0018 | EAS | CHB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | YRI | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18906 | hp2 | a0001 | c0001 | t0010 | g0092 | AFR | YRI | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18942 | hp1 | a0001 | c0001 | t0032 | g0249 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18942 | hp2 | a0001 | c0001 | t0027 | g0299 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18944 | hp1 | a0001 | c0001 | t0004 | g0310 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18944 | hp2 | a0001 | c0001 | t0058 | g0220 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0078 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18946 | hp2 | a0001 | c0001 | t0005 | g0114 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18950 | hp2 | a0001 | c0001 | t0005 | g0111 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18951 | hp2 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18963 | hp2 | a0001 | c0001 | t0009 | g0341 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18966 | hp2 | a0001 | c0001 | t0013 | g0059 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18967 | hp1 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18967 | hp2 | a0001 | c0001 | t0030 | g0278 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18969 | hp1 | a0001 | c0001 | t0038 | g0229 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18969 | hp2 | a0001 | c0001 | t0044 | g0183 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18970 | hp1 | a0001 | c0001 | t0035 | g0238 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18970 | hp2 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18972 | hp1 | a0001 | c0001 | t0046 | g0171 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18972 | hp2 | a0001 | c0001 | t0009 | g0016 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18973 | hp2 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18975 | hp1 | a0001 | c0001 | t0011 | g0186 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18978 | hp1 | a0001 | c0001 | t0004 | g0334 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18979 | hp1 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0326 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18980 | hp1 | a0001 | c0001 | t0005 | g0121 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18980 | hp2 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0327 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18982 | hp1 | a0001 | c0001 | t0042 | g0176 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18982 | hp2 | a0001 | c0001 | t0004 | g0332 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18984 | hp1 | a0001 | c0001 | t0021 | g0302 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18985 | hp2 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18986 | hp1 | a0001 | c0001 | t0045 | g0146 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18986 | hp2 | a0001 | c0001 | t0009 | g0016 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18987 | hp1 | a0001 | c0001 | t0009 | g0292 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18987 | hp2 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18992 | hp2 | a0001 | c0001 | t0004 | g0329 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0321 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18993 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0323 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18999 | hp2 | a0001 | c0001 | t0009 | g0016 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19001 | hp1 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19001 | hp2 | a0001 | c0001 | t0005 | g0113 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19011 | hp1 | a0001 | c0001 | t0013 | g0060 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19012 | hp1 | a0001 | c0001 | t0004 | g0015 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19012 | hp2 | a0001 | c0001 | t0005 | g0112 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19043 | hp1 | a0001 | c0001 | t0031 | g0042 | AFR | LWK | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19043 | hp2 | a0001 | c0001 | t0007 | g0044 | AFR | LWK | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19055 | hp1 | a0001 | c0001 | t0004 | g0331 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19058 | hp1 | a0001 | c0001 | t0005 | g0108 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19060 | hp1 | a0001 | c0001 | t0011 | g0160 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19060 | hp2 | a0001 | c0001 | t0055 | g0151 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0345 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0328 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19074 | hp1 | a0001 | c0001 | t0005 | g0024 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19077 | hp1 | a0001 | c0001 | t0017 | g0286 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19078 | hp2 | a0001 | c0001 | t0016 | g0066 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19080 | hp2 | a0001 | c0001 | t0037 | g0184 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19081 | hp2 | a0001 | c0001 | t0018 | g0296 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19082 | hp2 | a0001 | c0001 | t0004 | g0284 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0322 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19085 | hp1 | a0001 | c0001 | t0036 | g0253 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19088 | hp2 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19090 | hp1 | a0001 | c0001 | t0004 | g0285 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0017 | AFR | YRI | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0338 | AFR | YRI | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ASW | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | ASW | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0068 | EUR | TSI | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA20752 | hp2 | a0001 | c0001 | t0005 | g0023 | EUR | TSI | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA20805 | hp1 | a0001 | c0001 | t0052 | g0002 | EUR | TSI | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0198 | EUR | TSI | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA20905 | hp1 | a0001 | c0001 | t0020 | g0013 | SAS | GIH | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0069 | SAS | GIH | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | ACB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0010 | AFR | ACB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02486 | hp2 | a0001 | c0001 | t0005 | g0118 | AFR | ACB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02559 | hp1 | a0001 | c0001 | t0005 | g0017 | AFR | ACB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0317 | AFR | ACB | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG03471 | hp1 | a0001 | c0001 | t0025 | g0330 | AFR | MSL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG03471 | hp2 | a0001 | c0001 | t0012 | g0271 | AFR | MSL | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0283 | AFR | USA | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0050 | AFR | USA | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA20300 | hp1 | a0001 | c0001 | t0008 | g0004 | AFR | USA | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0087 | AFR | USA | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA21309 | hp1 | a0001 | c0001 | t0007 | g0009 | AFR | LWK | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| NA21309 | hp2 | a0001 | c0001 | t0008 | g0098 | AFR | LWK | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0342 | REF | REF | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0006 | REF | REF | GPAT4_chr8_41573200_41630001 | GPAT4 | chr8 | 41573200 | 41630001 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:41578276 | T | G | 1 | a0001 | 206 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(203): Show |
splice_region_variant | LOW | c.-851T>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/13 | chr8 | 41578276 | |||||||
| chr8:41620928 | C | G | 1 | a0002 | 2 | HG02630.hp1 HG03579.hp2 |
missense_variant | MODERATE | c.1298C>G | p.Thr433Arg | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 2225/6298 | 1298/1371 | 433/456 | chr8 | 41620928 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:41609665 | A | G | 1 | a0001c0003 | 2 | HG01069.hp1 HG01074.hp1 |
synonymous_variant | LOW | c.246A>G | p.Ala82Ala | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 4/13 | 1173/6298 | 246/1371 | 82/456 | chr8 | 41609665 | |||
| chr8:41609839 | G | A | 1 | a0001c0004 | 1 | HG02698.hp1 | synonymous_variant | LOW | c.420G>A | p.Leu140Leu | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 4/13 | 1347/6298 | 420/1371 | 140/456 | chr8 | 41609839 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:41598337 | G | T | 1 | a0001c0001t0058 | 1 | NA18944.hp2 | 5_prime_UTR_variant | MODIFIER | c.-803G>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/13 | 803 | chr8 | 41598337 | ||||||
| chr8:41598365 | G | C | 1 | a0001c0001t0031 | 1 | NA19043.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-775G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/13 | chr8 | 41598365 | |||||||
| chr8:41598557 | C | A | 1 | a0001c0001t0032 | 1 | NA18942.hp1 | 5_prime_UTR_variant | MODIFIER | c.-583C>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/13 | 583 | chr8 | 41598557 | ||||||
| chr8:41598607 | C | T | 2 | a0001c0001t0056 a0001c0001t0057 |
2 | HG01361.hp2 HG02818.hp2 |
5_prime_UTR_variant | MODIFIER | c.-533C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/13 | 533 | chr8 | 41598607 | ||||||
| chr8:41598633 | G | A | 1 | a0001c0001t0015 | 1 | HG03098.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-507G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/13 | chr8 | 41598633 | |||||||
| chr8:41598717 | A | C | 1 | a0001c0001t0013 | 2 | NA18966.hp2 NA19011.hp1 |
5_prime_UTR_variant | MODIFIER | c.-423A>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/13 | 423 | chr8 | 41598717 | ||||||
| chr8:41598753 | G | A | 1 | a0001c0001t0033 | 1 | HG01496.hp1 | 5_prime_UTR_variant | MODIFIER | c.-387G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/13 | 387 | chr8 | 41598753 | ||||||
| chr8:41598791 | A | T | 1 | a0001c0001t0055 | 1 | NA19060.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-349A>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/13 | chr8 | 41598791 | |||||||
| chr8:41598819 | G | A | 1 | a0001c0001t0034 | 1 | HG04115.hp2 | 5_prime_UTR_variant | MODIFIER | c.-321G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/13 | 321 | chr8 | 41598819 | ||||||
| chr8:41621050 | A | G | 6 | a0001c0001t0007 a0001c0001t0052 a0001c0001t0053 others(3): Show |
16 | HG00738.hp1 HG01069.hp1 HG01070.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*49A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 49 | chr8 | 41621050 | ||||||
| chr8:41621068 | G | A | 2 | a0001c0001t0056 a0001c0001t0057 |
2 | HG01361.hp2 HG02818.hp2 |
3_prime_UTR_variant | MODIFIER | c.*67G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 67 | chr8 | 41621068 | ||||||
| chr8:41621071 | G | A | 1 | a0001c0001t0035 | 1 | NA18970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*70G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 70 | chr8 | 41621071 | ||||||
| chr8:41621154 | G | A | 1 | a0001c0001t0031 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*153G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 153 | chr8 | 41621154 | ||||||
| chr8:41621165 | G | A | 1 | a0001c0001t0036 | 1 | NA19085.hp1 | 3_prime_UTR_variant | MODIFIER | c.*164G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 164 | chr8 | 41621165 | ||||||
| chr8:41621183 | A | C | 1 | a0001c0001t0010 | 3 | HG02970.hp2 HG03195.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*182A>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 182 | chr8 | 41621183 | ||||||
| chr8:41621201 | G | A | 1 | a0001c0001t0016 | 1 | NA19078.hp2 | 3_prime_UTR_variant | MODIFIER | c.*200G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 200 | chr8 | 41621201 | ||||||
| chr8:41621220 | G | A | 1 | a0001c0001t0017 | 1 | NA19077.hp1 | 3_prime_UTR_variant | MODIFIER | c.*219G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 219 | chr8 | 41621220 | ||||||
| chr8:41621307 | G | A | 1 | a0001c0001t0031 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*306G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 306 | chr8 | 41621307 | ||||||
| chr8:41621373 | T | G | 1 | a0001c0001t0018 | 1 | NA19081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*372T>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 372 | chr8 | 41621373 | ||||||
| chr8:41621467 | C | T | 1 | a0001c0001t0030 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*466C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 466 | chr8 | 41621467 | ||||||
| chr8:41621774 | T | C | 5 | a0001c0001t0007 a0001c0001t0052 a0001c0001t0053 others(2): Show |
15 | HG00738.hp1 HG01069.hp1 HG01070.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*773T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 773 | chr8 | 41621774 | ||||||
| chr8:41621797 | A | G | 1 | a0001c0001t0053 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*796A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 796 | chr8 | 41621797 | ||||||
| chr8:41621837 | G | A | 1 | a0001c0001t0037 | 1 | NA19080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*836G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 836 | chr8 | 41621837 | ||||||
| chr8:41621862 | C | T | 1 | a0001c0001t0029 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*861C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 861 | chr8 | 41621862 | ||||||
| chr8:41621887 | G | A | 3 | a0001c0001t0009 a0001c0001t0017 a0001c0001t0038 |
7 | NA18963.hp2 NA18969.hp1 NA18972.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*886G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 886 | chr8 | 41621887 | ||||||
| chr8:41621918 | G | A | 2 | a0001c0001t0019 a0001c0001t0029 |
2 | HG02965.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*917G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 917 | chr8 | 41621918 | ||||||
| chr8:41621922 | A | G | 1 | a0001c0001t0050 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*921A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 921 | chr8 | 41621922 | ||||||
| chr8:41622175 | A | G | 6 | a0001c0001t0003 a0001c0001t0010 a0001c0001t0013 others(3): Show |
58 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*1174A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 1174 | chr8 | 41622175 | ||||||
| chr8:41622286 | A | AGGAACAG | 34 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(31): Show |
232 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(229): Show |
3_prime_UTR_variant | MODIFIER | c.*1287_*1288insAACA others(3): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 1288 | INFO_REALIGN_3_PRIME | chr8 | 41622286 | |||||
| chr8:41622387 | C | T | 1 | a0001c0001t0052 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1386C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 1386 | chr8 | 41622387 | ||||||
| chr8:41622396 | G | T | 1 | a0001c0001t0049 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1395G>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 1395 | chr8 | 41622396 | ||||||
| chr8:41622579 | C | T | 1 | a0001c0001t0005 | 28 | HG02004.hp2 HG02055.hp2 HG02074.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1578C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 1578 | chr8 | 41622579 | ||||||
| chr8:41622810 | TA | T | 6 | a0001c0001t0003 a0001c0001t0010 a0001c0001t0013 others(3): Show |
58 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*1812delA | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 1812 | INFO_REALIGN_3_PRIME | chr8 | 41622810 | |||||
| chr8:41622861 | C | T | 1 | a0001c0001t0048 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1860C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 1860 | chr8 | 41622861 | ||||||
| chr8:41622943 | C | T | 1 | a0001c0001t0027 | 1 | NA18942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1942C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 1942 | chr8 | 41622943 | ||||||
| chr8:41622990 | G | A | 30 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(27): Show |
218 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(215): Show |
3_prime_UTR_variant | MODIFIER | c.*1989G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 1989 | chr8 | 41622990 | ||||||
| chr8:41623027 | TAC | T | 29 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(26): Show |
217 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(214): Show |
3_prime_UTR_variant | MODIFIER | c.*2038_*2039delCA | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 2038 | INFO_REALIGN_3_PRIME | chr8 | 41623027 | |||||
| chr8:41623067 | A | C | 2 | a0001c0001t0008 a0002c0002t0014 |
10 | HG02055.hp1 HG02280.hp1 HG02630.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2066A>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 2066 | chr8 | 41623067 | ||||||
| chr8:41623153 | C | T | 2 | a0001c0001t0008 a0002c0002t0014 |
10 | HG02055.hp1 HG02280.hp1 HG02630.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2152C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 2152 | chr8 | 41623153 | ||||||
| chr8:41623317 | C | T | 1 | a0001c0001t0047 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2316C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 2316 | chr8 | 41623317 | ||||||
| chr8:41623517 | A | T | 16 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0007 others(13): Show |
105 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*2516A>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 2516 | chr8 | 41623517 | ||||||
| chr8:41623518 | G | T | 16 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0007 others(13): Show |
105 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*2517G>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 2517 | chr8 | 41623518 | ||||||
| chr8:41623577 | G | A | 35 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(32): Show |
233 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(230): Show |
3_prime_UTR_variant | MODIFIER | c.*2576G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 2576 | chr8 | 41623577 | ||||||
| chr8:41623705 | G | A | 17 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(14): Show |
118 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*2704G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 2704 | chr8 | 41623705 | ||||||
| chr8:41623785 | T | TCAGA | 37 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(34): Show |
235 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(232): Show |
3_prime_UTR_variant | MODIFIER | c.*2788_*2791dupACAG | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 2792 | INFO_REALIGN_3_PRIME | chr8 | 41623785 | |||||
| chr8:41623819 | C | A | 1 | a0001c0001t0041 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2818C>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 2818 | chr8 | 41623819 | ||||||
| chr8:41623838 | CT | C | 4 | a0001c0001t0005 a0001c0001t0021 a0001c0001t0022 others(1): Show |
31 | HG02004.hp2 HG02055.hp2 HG02074.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*2852delT | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 2852 | INFO_REALIGN_3_PRIME | chr8 | 41623838 | |||||
| chr8:41623859 | C | T | 1 | a0001c0001t0046 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2858C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 2858 | chr8 | 41623859 | ||||||
| chr8:41623879 | C | T | 1 | a0001c0001t0019 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2878C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 2878 | chr8 | 41623879 | ||||||
| chr8:41623887 | G | T | 1 | a0001c0001t0025 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2886G>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 2886 | chr8 | 41623887 | ||||||
| chr8:41623931 | C | T | 1 | a0001c0001t0040 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2930C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 2930 | chr8 | 41623931 | ||||||
| chr8:41623983 | A | G | 1 | a0001c0001t0045 | 1 | NA18986.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2982A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 2982 | chr8 | 41623983 | ||||||
| chr8:41624117 | G | A | 1 | a0001c0001t0008 | 8 | HG02055.hp1 HG02280.hp1 HG02647.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3116G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 3116 | chr8 | 41624117 | ||||||
| chr8:41624121 | G | C | 1 | a0001c0001t0056 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3120G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 3120 | chr8 | 41624121 | ||||||
| chr8:41624266 | G | A | 1 | a0001c0001t0023 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3265G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 3265 | chr8 | 41624266 | ||||||
| chr8:41624433 | C | G | 1 | a0001c0001t0044 | 1 | NA18969.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3432C>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 3432 | chr8 | 41624433 | ||||||
| chr8:41624529 | C | T | 1 | a0001c0001t0029 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3528C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 3528 | chr8 | 41624529 | ||||||
| chr8:41624561 | T | C | 1 | a0001c0001t0028 | 1 | HG01516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3560T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 3560 | chr8 | 41624561 | ||||||
| chr8:41624582 | G | A | 2 | a0001c0001t0026 a0001c0001t0043 |
2 | HG03017.hp2 HG03239.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3581G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 3581 | chr8 | 41624582 | ||||||
| chr8:41624717 | A | T | 1 | a0001c0001t0012 | 2 | HG02809.hp2 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3716A>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 3716 | chr8 | 41624717 | ||||||
| chr8:41624749 | C | T | 4 | a0001c0001t0006 a0001c0001t0012 a0001c0001t0020 others(1): Show |
17 | HG01069.hp2 HG01071.hp1 HG01192.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*3748C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 3748 | chr8 | 41624749 | ||||||
| chr8:41624802 | G | A | 1 | a0001c0001t0024 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3801G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 3801 | chr8 | 41624802 | ||||||
| chr8:41624835 | G | A | 1 | a0001c0001t0011 | 3 | HG00621.hp2 NA18975.hp1 NA19060.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3834G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 3834 | chr8 | 41624835 | ||||||
| chr8:41624842 | G | C | 10 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0017 others(7): Show |
67 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*3841G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 13/13 | 3841 | chr8 | 41624842 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:41578330 | G | C | 3 | a0001c0001t0005g0017 a0001c0001t0005g0037 a0001c0001t0005g0038 |
4 | HG02055.hp2 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-849+52G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41578330 | |||||||
| chr8:41578350 | G | A | 1 | a0001c0001t0004g0039 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-849+72G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41578350 | |||||||
| chr8:41578350 | G | C | 1 | a0001c0001t0004g0040 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-849+72G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41578350 | |||||||
| chr8:41578388 | A | G | 1 | a0001c0001t0003g0345 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-849+110A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41578388 | |||||||
| chr8:41578530 | C | T | 1 | a0001c0001t0007g0344 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-849+252C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41578530 | |||||||
| chr8:41578566 | T | A | 14 | a0001c0001t0007g0002 a0001c0001t0007g0009 a0001c0001t0007g0043 others(11): Show |
17 | HG00738.hp1 HG01069.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.-849+288T>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41578566 | |||||||
| chr8:41578595 | C | T | 2 | a0001c0001t0056g0049 a0001c0001t0057g0048 |
2 | HG01361.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-849+317C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41578595 | |||||||
| chr8:41578612 | G | A | 5 | a0001c0001t0004g0010 a0001c0001t0004g0039 a0001c0001t0004g0050 others(2): Show |
7 | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.-849+334G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41578612 | |||||||
| chr8:41578659 | C | T | 1 | a0001c0001t0001g0343 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-849+381C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41578659 | |||||||
| chr8:41578930 | G | C | 1 | a0001c0001t0006g0053 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-849+652G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41578930 | |||||||
| chr8:41579016 | G | A | 49 | a0001c0001t0003g0003 a0001c0001t0003g0011 a0001c0001t0003g0018 others(46): Show |
58 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.-849+738G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41579016 | |||||||
| chr8:41579223 | T | C | 7 | a0001c0001t0008g0004 a0001c0001t0008g0096 a0001c0001t0008g0097 others(4): Show |
10 | HG02055.hp1 HG02280.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.-849+945T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41579223 | |||||||
| chr8:41579320 | T | C | 1 | a0001c0001t0001g0100 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-849+1042T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41579320 | |||||||
| chr8:41579360 | G | C | 1 | a0001c0001t0001g0101 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-849+1082G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41579360 | |||||||
| chr8:41579503 | G | A | 2 | a0001c0001t0019g0103 a0001c0001t0029g0102 |
2 | HG02965.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-849+1225G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41579503 | |||||||
| chr8:41579557 | G | T | 1 | a0001c0001t0009g0341 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-849+1279G>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41579557 | |||||||
| chr8:41579576 | G | GC | 40 | a0001c0001t0003g0003 a0001c0001t0003g0011 a0001c0001t0003g0018 others(37): Show |
48 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.-849+1300dupC | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41579576 | ||||||
| chr8:41579657 | G | A | 2 | a0001c0001t0006g0104 a0001c0001t0006g0105 |
2 | HG01884.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-849+1379G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41579657 | |||||||
| chr8:41579665 | C | T | 4 | a0001c0001t0001g0338 a0001c0001t0001g0340 a0001c0001t0007g0337 others(1): Show |
4 | HG01884.hp1 HG03453.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-849+1387C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41579665 | |||||||
| chr8:41579694 | C | T | 2 | a0001c0001t0002g0335 a0001c0001t0002g0336 |
2 | HG00408.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.-849+1416C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41579694 | |||||||
| chr8:41579720 | C | G | 40 | a0001c0001t0003g0003 a0001c0001t0003g0011 a0001c0001t0003g0018 others(37): Show |
48 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.-849+1442C>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41579720 | |||||||
| chr8:41579794 | C | G | 91 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(88): Show |
117 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.-849+1516C>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41579794 | |||||||
| chr8:41579798 | G | A | 173 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(170): Show |
216 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(213): Show |
intron_variant | MODIFIER | c.-849+1520G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41579798 | |||||||
| chr8:41579831 | C | T | 2 | a0001c0001t0002g0036 a0001c0001t0024g0036 |
2 | HG00741.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.-849+1553C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41579831 | |||||||
| chr8:41579836 | C | CA | 14 | a0001c0001t0006g0013 a0001c0001t0006g0014 a0001c0001t0006g0053 others(11): Show |
17 | HG01069.hp2 HG01071.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.-849+1569dupA | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41579836 | ||||||
| chr8:41579858 | A | G | 4 | a0001c0001t0004g0331 a0001c0001t0004g0332 a0001c0001t0004g0333 others(1): Show |
4 | HG00438.hp1 NA18978.hp1 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.-849+1580A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41579858 | |||||||
| chr8:41579963 | C | G | 1 | a0001c0001t0006g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-849+1685C>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41579963 | |||||||
| chr8:41580001 | G | C | 187 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(184): Show |
233 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(230): Show |
intron_variant | MODIFIER | c.-849+1723G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41580001 | |||||||
| chr8:41580054 | G | A | 2 | a0001c0001t0002g0277 a0001c0001t0030g0278 |
2 | NA18967.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.-849+1776G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41580054 | |||||||
| chr8:41580124 | C | A | 2 | a0002c0002t0014g0094 a0002c0002t0014g0095 |
2 | HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-849+1846C>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41580124 | |||||||
| chr8:41580185 | G | A | 1 | a0001c0001t0004g0040 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-849+1907G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41580185 | |||||||
| chr8:41580209 | G | A | 91 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(88): Show |
117 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.-849+1931G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41580209 | |||||||
| chr8:41580226 | C | T | 2 | a0001c0001t0006g0104 a0001c0001t0006g0105 |
2 | HG01884.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-849+1948C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41580226 | |||||||
| chr8:41580264 | C | T | 1 | a0002c0002t0014g0095 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-849+1986C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41580264 | |||||||
| chr8:41580385 | A | C | 1 | a0001c0001t0003g0085 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-849+2107A>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41580385 | |||||||
| chr8:41580403 | T | C | 1 | a0001c0001t0053g0041 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-849+2125T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41580403 | |||||||
| chr8:41580805 | G | A | 4 | a0001c0001t0001g0025 a0001c0001t0001g0124 a0001c0001t0001g0125 others(1): Show |
5 | HG02135.hp2 HG02523.hp1 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.-849+2527G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41580805 | |||||||
| chr8:41580850 | T | G | 1 | a0001c0001t0002g0279 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-849+2572T>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41580850 | |||||||
| chr8:41580859 | T | C | 187 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(184): Show |
233 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(230): Show |
intron_variant | MODIFIER | c.-849+2581T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41580859 | |||||||
| chr8:41580879 | G | C | 4 | a0001c0001t0001g0025 a0001c0001t0001g0124 a0001c0001t0001g0125 others(1): Show |
5 | HG02135.hp2 HG02523.hp1 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.-849+2601G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41580879 | |||||||
| chr8:41580948 | C | T | 1 | a0001c0001t0004g0052 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-849+2670C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41580948 | |||||||
| chr8:41581051 | A | G | 1 | a0001c0001t0025g0330 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-849+2773A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41581051 | |||||||
| chr8:41581105 | A | C | 166 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(163): Show |
206 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(203): Show |
intron_variant | MODIFIER | c.-849+2827A>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41581105 | |||||||
| chr8:41581109 | A | G | 188 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(185): Show |
234 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(231): Show |
intron_variant | MODIFIER | c.-849+2831A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41581109 | |||||||
| chr8:41581111 | A | G | 1 | a0001c0001t0001g0267 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-849+2833A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41581111 | |||||||
| chr8:41581160 | A | G | 1 | a0001c0001t0001g0266 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-849+2882A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41581160 | |||||||
| chr8:41581163 | G | A | 1 | a0001c0001t0001g0127 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-849+2885G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41581163 | |||||||
| chr8:41581170 | A | G | 1 | a0001c0001t0001g0266 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-849+2892A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41581170 | |||||||
| chr8:41581367 | C | T | 1 | a0001c0001t0004g0040 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-849+3089C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41581367 | |||||||
| chr8:41581555 | G | A | 187 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(184): Show |
233 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(230): Show |
intron_variant | MODIFIER | c.-849+3277G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41581555 | |||||||
| chr8:41581584 | C | T | 49 | a0001c0001t0003g0003 a0001c0001t0003g0011 a0001c0001t0003g0018 others(46): Show |
58 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.-849+3306C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41581584 | |||||||
| chr8:41581625 | C | CT | 25 | a0001c0001t0001g0248 a0001c0001t0001g0250 a0001c0001t0001g0251 others(22): Show |
25 | HG00099.hp2 HG00438.hp2 HG00609.hp2 others(22): Show |
intron_variant | MODIFIER | c.-849+3368dupT | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41581625 | ||||||
| chr8:41581625 | CT | C | 11 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0003g0345 others(8): Show |
11 | HG01243.hp2 HG01361.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.-849+3368delT | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41581625 | ||||||
| chr8:41581626 | T | C | 4 | a0001c0001t0003g0054 a0001c0001t0003g0055 a0001c0001t0003g0056 others(1): Show |
4 | HG00639.hp2 HG01175.hp1 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.-849+3348T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41581626 | |||||||
| chr8:41581774 | G | A | 12 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 others(9): Show |
12 | HG02071.hp1 NA18954.hp2 NA18955.hp1 others(9): Show |
intron_variant | MODIFIER | c.-849+3496G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41581774 | |||||||
| chr8:41581817 | T | C | 1 | a0001c0001t0029g0102 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-849+3539T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41581817 | |||||||
| chr8:41581855 | G | A | 80 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0026 others(77): Show |
88 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.-849+3577G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41581855 | |||||||
| chr8:41581939 | T | C | 1 | a0001c0001t0002g0280 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-849+3661T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41581939 | |||||||
| chr8:41581945 | T | C | 1 | a0001c0001t0002g0281 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-849+3667T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41581945 | |||||||
| chr8:41581946 | T | TAA | 47 | a0001c0001t0003g0003 a0001c0001t0003g0011 a0001c0001t0003g0018 others(44): Show |
56 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.-849+3679_-849+368 others(6): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41581946 | ||||||
| chr8:41581989 | A | T | 1 | a0001c0001t0001g0199 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-849+3711A>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41581989 | |||||||
| chr8:41581993 | A | AT | 87 | a0001c0001t0001g0025 a0001c0001t0001g0029 a0001c0001t0001g0125 others(84): Show |
95 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.-849+3747dupT | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41581993 | ||||||
| chr8:41581993 | A | ATT | 24 | a0001c0001t0001g0005 a0001c0001t0001g0031 a0001c0001t0001g0140 others(21): Show |
29 | HG00735.hp2 HG01070.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.-849+3746_-849+374 others(6): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41581993 | ||||||
| chr8:41581993 | A | ATTT | 9 | a0001c0001t0001g0129 a0001c0001t0001g0196 a0001c0001t0001g0197 others(6): Show |
9 | HG01243.hp1 HG02145.hp1 HG02165.hp2 others(6): Show |
intron_variant | MODIFIER | c.-849+3745_-849+374 others(7): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41581993 | ||||||
| chr8:41581993 | A | ATTTT | 6 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0242 others(3): Show |
6 | HG01099.hp1 HG02015.hp1 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.-849+3744_-849+374 others(8): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41581993 | ||||||
| chr8:41581993 | A | ATTTTT | 5 | a0001c0001t0001g0032 a0001c0001t0001g0198 a0001c0001t0001g0245 others(2): Show |
6 | HG01358.hp1 HG01952.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.-849+3743_-849+374 others(9): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41581993 | ||||||
| chr8:41581993 | ATTTTTT | A | 5 | a0001c0001t0002g0325 a0001c0001t0004g0010 a0001c0001t0004g0324 others(2): Show |
7 | HG02109.hp2 HG02630.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.-849+3742_-849+374 others(10): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41581993 | ||||||
| chr8:41581993 | ATTTTTTT | A | 32 | a0001c0001t0002g0034 a0001c0001t0002g0035 a0001c0001t0002g0277 others(29): Show |
34 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.-849+3741_-849+374 others(11): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41581993 | ||||||
| chr8:41581993 | ATTTTTTT others(1): Show |
A | 62 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(59): Show |
84 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.-849+3740_-849+374 others(12): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41581993 | ||||||
| chr8:41581993 | ATTTTTTT others(2): Show |
A | 17 | a0001c0001t0005g0012 a0001c0001t0005g0017 a0001c0001t0005g0023 others(14): Show |
22 | HG02074.hp2 HG02132.hp1 HG02165.hp1 others(19): Show |
intron_variant | MODIFIER | c.-849+3739_-849+374 others(13): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41581993 | ||||||
| chr8:41581993 | ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0001g0257 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-849+3736_-849+374 others(16): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41581993 | ||||||
| chr8:41581993 | ATTTTTTT others(6): Show |
A | 4 | a0001c0001t0001g0200 a0001c0001t0002g0283 a0001c0001t0056g0049 others(1): Show |
4 | HG01361.hp2 HG02040.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.-849+3735_-849+374 others(17): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41581993 | ||||||
| chr8:41581993 | ATTTTTTT others(7): Show |
A | 12 | a0001c0001t0002g0282 a0001c0001t0007g0002 a0001c0001t0007g0009 others(9): Show |
15 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.-849+3734_-849+374 others(18): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41581993 | ||||||
| chr8:41581993 | ATTTTTTT others(8): Show |
A | 1 | a0001c0001t0031g0042 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-849+3733_-849+374 others(19): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41581993 | ||||||
| chr8:41582005 | T | A | 4 | a0001c0001t0001g0338 a0001c0001t0001g0340 a0001c0001t0007g0337 others(1): Show |
4 | HG01884.hp1 HG03453.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-849+3727T>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41582005 | |||||||
| chr8:41582018 | T | A | 4 | a0001c0001t0001g0338 a0001c0001t0001g0340 a0001c0001t0007g0337 others(1): Show |
4 | HG01884.hp1 HG03453.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-849+3740T>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41582018 | |||||||
| chr8:41582122 | A | G | 2 | a0001c0001t0003g0021 a0001c0001t0003g0079 |
3 | HG00621.hp1 HG02083.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.-849+3844A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41582122 | |||||||
| chr8:41582154 | C | G | 1 | a0001c0001t0001g0265 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-849+3876C>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41582154 | |||||||
| chr8:41582241 | T | G | 1 | a0001c0001t0041g0256 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-849+3963T>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41582241 | |||||||
| chr8:41582304 | G | A | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG04184.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.-849+4026G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41582304 | |||||||
| chr8:41582337 | T | C | 1 | a0001c0001t0001g0201 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-849+4059T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41582337 | |||||||
| chr8:41582358 | A | G | 1 | a0001c0001t0038g0229 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-849+4080A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41582358 | |||||||
| chr8:41582444 | T | TAC | 28 | a0001c0001t0001g0143 a0001c0001t0001g0145 a0001c0001t0001g0147 others(25): Show |
31 | HG00642.hp2 HG01081.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.-849+4198_-849+419 others(6): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41582444 | ||||||
| chr8:41582444 | T | TACAC | 63 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0189 others(60): Show |
83 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.-849+4196_-849+419 others(8): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41582444 | ||||||
| chr8:41582444 | T | TACACAC | 15 | a0001c0001t0001g0163 a0001c0001t0002g0282 a0001c0001t0002g0314 others(12): Show |
16 | HG00642.hp1 HG00738.hp1 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.-849+4194_-849+419 others(10): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41582444 | ||||||
| chr8:41582444 | T | TACACACA others(1): Show |
13 | a0001c0001t0004g0015 a0001c0001t0004g0284 a0001c0001t0004g0285 others(10): Show |
15 | HG00438.hp1 HG00597.hp1 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.-849+4192_-849+419 others(12): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41582444 | ||||||
| chr8:41582444 | T | TACACACA others(3): Show |
4 | a0001c0001t0004g0309 a0001c0001t0004g0310 a0001c0001t0004g0329 others(1): Show |
4 | HG00544.hp1 NA18944.hp1 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.-849+4190_-849+419 others(14): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41582444 | ||||||
| chr8:41582444 | TACAC | T | 3 | a0001c0001t0040g0268 a0002c0002t0014g0094 a0002c0002t0014g0095 |
3 | HG02630.hp1 HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-849+4196_-849+419 others(8): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41582444 | ||||||
| chr8:41582472 | CACACAT | C | 48 | a0001c0001t0003g0003 a0001c0001t0003g0011 a0001c0001t0003g0018 others(45): Show |
57 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.-849+4195_-849+420 others(10): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41582472 | |||||||
| chr8:41582474 | CACAT | C | 21 | a0001c0001t0003g0058 a0001c0001t0004g0008 a0001c0001t0005g0012 others(18): Show |
25 | HG02004.hp2 HG02055.hp2 HG02132.hp1 others(22): Show |
intron_variant | MODIFIER | c.-849+4197_-849+420 others(8): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41582474 | |||||||
| chr8:41582476 | CAT | C | 4 | a0001c0001t0005g0107 a0001c0001t0005g0109 a0001c0001t0005g0116 others(1): Show |
4 | HG02074.hp2 HG02572.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-849+4199_-849+420 others(6): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41582476 | |||||||
| chr8:41582478 | T | C | 95 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(92): Show |
120 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.-849+4200T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41582478 | |||||||
| chr8:41582674 | A | AGT | 9 | a0001c0001t0006g0013 a0001c0001t0006g0014 a0001c0001t0006g0053 others(6): Show |
12 | HG01069.hp2 HG01071.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.-849+4416_-849+441 others(6): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41582674 | ||||||
| chr8:41582674 | A | AGTGT | 11 | a0001c0001t0007g0002 a0001c0001t0007g0009 a0001c0001t0007g0043 others(8): Show |
14 | HG00738.hp1 HG01069.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.-849+4414_-849+441 others(8): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41582674 | ||||||
| chr8:41582674 | A | AGTGTGT | 49 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(46): Show |
67 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.-849+4412_-849+441 others(10): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41582674 | ||||||
| chr8:41582674 | A | AGTGTGTG others(1): Show |
31 | a0001c0001t0002g0306 a0001c0001t0002g0307 a0001c0001t0002g0308 others(28): Show |
36 | HG00408.hp2 HG02004.hp2 HG02055.hp2 others(33): Show |
intron_variant | MODIFIER | c.-849+4410_-849+441 others(12): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41582674 | ||||||
| chr8:41582674 | A | AGTGTGTG others(3): Show |
1 | a0001c0001t0029g0102 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-849+4408_-849+441 others(14): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41582674 | ||||||
| chr8:41582674 | A | T | 3 | a0001c0001t0001g0237 a0001c0001t0001g0239 a0001c0001t0001g0266 |
3 | NA18984.hp2 NA18988.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.-849+4396A>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41582674 | |||||||
| chr8:41582676 | T | A | 2 | a0002c0002t0014g0094 a0002c0002t0014g0095 |
2 | HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-849+4398T>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41582676 | |||||||
| chr8:41582684 | T | TGTGTGTG others(8): Show |
1 | a0001c0001t0026g0123 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-849+4417_-849+441 others(19): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41582684 | ||||||
| chr8:41582688 | T | TGTGTGG | 49 | a0001c0001t0003g0003 a0001c0001t0003g0011 a0001c0001t0003g0018 others(46): Show |
58 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.-849+4415_-849+441 others(10): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41582688 | ||||||
| chr8:41582694 | T | TGTGTGG | 4 | a0001c0001t0004g0290 a0001c0001t0004g0311 a0001c0001t0015g0288 others(1): Show |
4 | HG01106.hp1 HG02622.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-849+4417_-849+441 others(10): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41582694 | ||||||
| chr8:41582694 | T | TGTGTGTG others(1): Show |
13 | a0001c0001t0004g0008 a0001c0001t0004g0015 a0001c0001t0004g0284 others(10): Show |
18 | HG00438.hp1 HG00544.hp1 HG00597.hp1 others(15): Show |
intron_variant | MODIFIER | c.-849+4417_-849+441 others(12): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41582694 | ||||||
| chr8:41582694 | T | TGTGTGTG others(3): Show |
1 | a0001c0001t0004g0287 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-849+4417_-849+441 others(14): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41582694 | ||||||
| chr8:41582696 | G | C | 1 | a0001c0001t0029g0102 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-849+4418G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41582696 | |||||||
| chr8:41582696 | G | T | 1 | a0001c0001t0001g0214 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-849+4418G>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41582696 | |||||||
| chr8:41582814 | T | G | 3 | a0001c0001t0001g0149 a0001c0001t0001g0168 a0001c0001t0048g0167 |
3 | HG01109.hp2 HG01496.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.-849+4536T>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41582814 | |||||||
| chr8:41582948 | C | T | 166 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(163): Show |
206 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(203): Show |
intron_variant | MODIFIER | c.-849+4670C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41582948 | |||||||
| chr8:41583044 | G | A | 5 | a0001c0001t0008g0004 a0001c0001t0008g0096 a0001c0001t0008g0097 others(2): Show |
8 | HG02055.hp1 HG02280.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.-849+4766G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41583044 | |||||||
| chr8:41583087 | G | A | 18 | a0001c0001t0005g0012 a0001c0001t0005g0017 a0001c0001t0005g0023 others(15): Show |
23 | HG02004.hp2 HG02055.hp2 HG02074.hp2 others(20): Show |
intron_variant | MODIFIER | c.-849+4809G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41583087 | |||||||
| chr8:41583232 | AT | A | 5 | a0001c0001t0008g0004 a0001c0001t0008g0096 a0001c0001t0008g0097 others(2): Show |
8 | HG02055.hp1 HG02280.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.-849+4955delT | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41583232 | |||||||
| chr8:41583330 | A | C | 2 | a0001c0001t0003g0081 a0001c0001t0003g0083 |
2 | HG01433.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.-849+5052A>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41583330 | |||||||
| chr8:41583341 | A | G | 1 | a0001c0001t0001g0255 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-849+5063A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41583341 | |||||||
| chr8:41583456 | T | A | 186 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(183): Show |
232 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(229): Show |
intron_variant | MODIFIER | c.-849+5178T>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41583456 | |||||||
| chr8:41583561 | A | G | 1 | a0001c0003t0051g0047 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-849+5283A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41583561 | |||||||
| chr8:41583985 | C | T | 8 | a0001c0001t0006g0013 a0001c0001t0006g0014 a0001c0001t0006g0053 others(5): Show |
11 | HG01069.hp2 HG01071.hp1 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.-849+5707C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41583985 | |||||||
| chr8:41584022 | A | G | 2 | a0001c0001t0005g0114 a0001c0001t0005g0121 |
2 | NA18946.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.-849+5744A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41584022 | |||||||
| chr8:41584160 | A | G | 188 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(185): Show |
234 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(231): Show |
intron_variant | MODIFIER | c.-849+5882A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41584160 | |||||||
| chr8:41584189 | G | A | 4 | a0001c0001t0001g0191 a0001c0001t0007g0009 a0001c0001t0007g0344 others(1): Show |
6 | HG00735.hp2 HG01243.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-849+5911G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41584189 | |||||||
| chr8:41584507 | G | A | 1 | a0001c0001t0026g0123 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-849+6229G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41584507 | |||||||
| chr8:41584647 | G | A | 4 | a0001c0001t0003g0018 a0001c0001t0003g0084 a0001c0001t0013g0059 others(1): Show |
5 | HG02080.hp2 NA18747.hp2 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.-849+6369G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41584647 | |||||||
| chr8:41584670 | G | A | 1 | a0001c0001t0007g0043 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-849+6392G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41584670 | |||||||
| chr8:41584688 | G | T | 1 | a0001c0001t0003g0055 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-849+6410G>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41584688 | |||||||
| chr8:41584794 | C | CT | 7 | a0001c0001t0008g0004 a0001c0001t0008g0096 a0001c0001t0008g0097 others(4): Show |
10 | HG02055.hp1 HG02280.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.-849+6519dupT | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41584794 | ||||||
| chr8:41584920 | G | T | 7 | a0001c0001t0008g0004 a0001c0001t0008g0096 a0001c0001t0008g0097 others(4): Show |
10 | HG02055.hp1 HG02280.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.-849+6642G>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41584920 | |||||||
| chr8:41584938 | G | A | 14 | a0001c0001t0007g0002 a0001c0001t0007g0009 a0001c0001t0007g0043 others(11): Show |
17 | HG00738.hp1 HG01069.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.-849+6660G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41584938 | |||||||
| chr8:41585209 | T | G | 7 | a0001c0001t0001g0026 a0001c0001t0001g0150 a0001c0001t0001g0169 others(4): Show |
8 | HG00408.hp1 HG02523.hp2 NA18942.hp1 others(5): Show |
intron_variant | MODIFIER | c.-849+6931T>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41585209 | |||||||
| chr8:41585285 | C | T | 2 | a0001c0001t0005g0024 a0001c0001t0005g0113 |
3 | HG02132.hp1 NA19001.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.-849+7007C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41585285 | |||||||
| chr8:41585333 | G | A | 1 | a0001c0001t0001g0246 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-849+7055G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41585333 | |||||||
| chr8:41585362 | T | C | 1 | a0001c0001t0004g0040 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-849+7084T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41585362 | |||||||
| chr8:41585376 | G | A | 7 | a0001c0001t0008g0004 a0001c0001t0008g0096 a0001c0001t0008g0097 others(4): Show |
10 | HG02055.hp1 HG02280.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.-849+7098G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41585376 | |||||||
| chr8:41585381 | TCCGTA | T | 23 | a0001c0001t0005g0012 a0001c0001t0005g0017 a0001c0001t0005g0023 others(20): Show |
28 | HG02004.hp2 HG02055.hp2 HG02074.hp2 others(25): Show |
intron_variant | MODIFIER | c.-849+7104_-849+710 others(9): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41585381 | |||||||
| chr8:41585412 | C | T | 7 | a0001c0001t0008g0004 a0001c0001t0008g0096 a0001c0001t0008g0097 others(4): Show |
10 | HG02055.hp1 HG02280.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.-849+7134C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41585412 | |||||||
| chr8:41585457 | A | G | 50 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(47): Show |
66 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.-849+7179A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41585457 | |||||||
| chr8:41585487 | T | C | 1 | a0001c0001t0007g0009 | 3 | HG02258.hp1 HG03540.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-849+7209T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41585487 | |||||||
| chr8:41585563 | T | G | 2 | a0001c0001t0001g0200 a0001c0001t0001g0257 |
2 | HG02040.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.-849+7285T>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41585563 | |||||||
| chr8:41585634 | G | A | 1 | a0001c0001t0007g0009 | 3 | HG02258.hp1 HG03540.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-849+7356G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41585634 | |||||||
| chr8:41585676 | T | G | 76 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(73): Show |
99 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.-849+7398T>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41585676 | |||||||
| chr8:41585845 | A | G | 1 | a0001c0001t0001g0213 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-849+7567A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41585845 | |||||||
| chr8:41585917 | G | A | 188 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(185): Show |
234 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(231): Show |
intron_variant | MODIFIER | c.-849+7639G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41585917 | |||||||
| chr8:41586007 | G | C | 49 | a0001c0001t0003g0003 a0001c0001t0003g0011 a0001c0001t0003g0018 others(46): Show |
58 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.-849+7729G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41586007 | |||||||
| chr8:41586128 | C | T | 1 | a0001c0001t0005g0120 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-849+7850C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41586128 | |||||||
| chr8:41586206 | G | C | 1 | a0001c0001t0047g0215 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-849+7928G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41586206 | |||||||
| chr8:41586505 | C | G | 251 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0101 others(248): Show |
299 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(296): Show |
intron_variant | MODIFIER | c.-849+8227C>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41586505 | |||||||
| chr8:41586524 | T | G | 1 | a0001c0001t0026g0123 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-849+8246T>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41586524 | |||||||
| chr8:41586736 | C | A | 1 | a0001c0001t0046g0171 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-849+8458C>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41586736 | |||||||
| chr8:41586768 | G | A | 5 | a0001c0001t0005g0106 a0001c0001t0005g0115 a0001c0001t0005g0116 others(2): Show |
5 | HG02572.hp2 HG02630.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-849+8490G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41586768 | |||||||
| chr8:41586868 | C | A | 187 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(184): Show |
233 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(230): Show |
intron_variant | MODIFIER | c.-849+8590C>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41586868 | |||||||
| chr8:41586880 | C | T | 1 | a0001c0001t0055g0151 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-849+8602C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41586880 | |||||||
| chr8:41586891 | G | C | 173 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(170): Show |
216 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(213): Show |
intron_variant | MODIFIER | c.-849+8613G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41586891 | |||||||
| chr8:41587191 | G | C | 1 | a0001c0001t0026g0123 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-849+8913G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41587191 | |||||||
| chr8:41587368 | A | G | 173 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(170): Show |
216 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(213): Show |
intron_variant | MODIFIER | c.-849+9090A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41587368 | |||||||
| chr8:41587382 | TCTC | T | 5 | a0001c0001t0008g0004 a0001c0001t0008g0096 a0001c0001t0008g0097 others(2): Show |
8 | HG02055.hp1 HG02280.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.-849+9107_-849+910 others(7): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41587382 | ||||||
| chr8:41587511 | T | C | 1 | a0001c0001t0004g0309 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-849+9233T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41587511 | |||||||
| chr8:41587518 | T | C | 1 | a0001c0001t0001g0199 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-849+9240T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41587518 | |||||||
| chr8:41587537 | C | T | 8 | a0001c0001t0006g0013 a0001c0001t0006g0014 a0001c0001t0006g0053 others(5): Show |
11 | HG01069.hp2 HG01071.hp1 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.-849+9259C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41587537 | |||||||
| chr8:41587617 | A | C | 1 | a0001c0001t0007g0046 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-849+9339A>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41587617 | |||||||
| chr8:41587737 | C | G | 1 | a0001c0001t0031g0042 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-849+9459C>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41587737 | |||||||
| chr8:41587754 | G | T | 8 | a0001c0001t0002g0007 a0001c0001t0002g0035 a0001c0001t0002g0280 others(5): Show |
12 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(9): Show |
intron_variant | MODIFIER | c.-849+9476G>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41587754 | |||||||
| chr8:41587859 | G | A | 1 | a0001c0001t0008g0096 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-849+9581G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41587859 | |||||||
| chr8:41587990 | A | G | 8 | a0001c0001t0006g0013 a0001c0001t0006g0014 a0001c0001t0006g0053 others(5): Show |
11 | HG01069.hp2 HG01071.hp1 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.-849+9712A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41587990 | |||||||
| chr8:41588339 | G | A | 1 | a0001c0001t0001g0231 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-848-9953G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41588339 | |||||||
| chr8:41588341 | C | T | 1 | a0001c0001t0004g0309 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-848-9951C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41588341 | |||||||
| chr8:41588442 | A | AGTTCT | 164 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(161): Show |
204 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(201): Show |
intron_variant | MODIFIER | c.-848-9834_-848-983 others(9): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41588442 | ||||||
| chr8:41588463 | T | G | 1 | a0001c0001t0002g0335 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-848-9829T>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41588463 | |||||||
| chr8:41588466 | T | C | 1 | a0001c0001t0002g0335 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-848-9826T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41588466 | |||||||
| chr8:41588473 | C | T | 1 | a0001c0001t0002g0335 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-848-9819C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41588473 | |||||||
| chr8:41588756 | G | C | 2 | a0002c0002t0014g0094 a0002c0002t0014g0095 |
2 | HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-848-9536G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41588756 | |||||||
| chr8:41588907 | G | A | 173 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(170): Show |
216 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(213): Show |
intron_variant | MODIFIER | c.-848-9385G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41588907 | |||||||
| chr8:41588912 | C | A | 2 | a0001c0001t0001g0128 a0001c0001t0001g0216 |
2 | HG02257.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.-848-9380C>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41588912 | |||||||
| chr8:41589124 | T | C | 187 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(184): Show |
233 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(230): Show |
intron_variant | MODIFIER | c.-848-9168T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41589124 | |||||||
| chr8:41589206 | C | T | 1 | a0001c0001t0001g0247 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-848-9086C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41589206 | |||||||
| chr8:41589360 | CGGGAT | C | 171 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(168): Show |
214 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(211): Show |
intron_variant | MODIFIER | c.-848-8923_-848-891 others(9): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41589360 | ||||||
| chr8:41589466 | G | T | 1 | a0001c0001t0001g0202 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-848-8826G>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41589466 | |||||||
| chr8:41589751 | C | T | 5 | a0001c0001t0005g0106 a0001c0001t0005g0115 a0001c0001t0005g0116 others(2): Show |
5 | HG02572.hp2 HG02630.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-848-8541C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41589751 | |||||||
| chr8:41589925 | G | C | 1 | a0001c0001t0001g0152 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-848-8367G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41589925 | |||||||
| chr8:41589951 | T | G | 173 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(170): Show |
216 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(213): Show |
intron_variant | MODIFIER | c.-848-8341T>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41589951 | |||||||
| chr8:41590032 | G | A | 1 | a0001c0001t0001g0218 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-848-8260G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41590032 | |||||||
| chr8:41590070 | A | G | 1 | a0001c0001t0003g0078 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-848-8222A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41590070 | |||||||
| chr8:41590142 | A | T | 1 | a0001c0001t0001g0188 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-848-8150A>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41590142 | |||||||
| chr8:41590158 | T | C | 91 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(88): Show |
117 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.-848-8134T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41590158 | |||||||
| chr8:41590227 | C | T | 1 | a0001c0001t0015g0288 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-848-8065C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41590227 | |||||||
| chr8:41590235 | C | T | 166 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(163): Show |
206 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(203): Show |
intron_variant | MODIFIER | c.-848-8057C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41590235 | |||||||
| chr8:41590261 | A | T | 18 | a0001c0001t0004g0008 a0001c0001t0004g0015 a0001c0001t0004g0284 others(15): Show |
23 | HG00438.hp1 HG00544.hp1 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.-848-8031A>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41590261 | |||||||
| chr8:41590618 | T | G | 1 | a0001c0001t0002g0282 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-848-7674T>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41590618 | |||||||
| chr8:41590633 | G | C | 1 | a0001c0001t0002g0282 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-848-7659G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41590633 | |||||||
| chr8:41590664 | A | T | 2 | a0002c0002t0014g0094 a0002c0002t0014g0095 |
2 | HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-848-7628A>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41590664 | |||||||
| chr8:41590706 | G | C | 2 | a0001c0001t0001g0172 a0001c0001t0046g0171 |
2 | HG02071.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.-848-7586G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41590706 | |||||||
| chr8:41590747 | T | G | 2 | a0001c0001t0002g0291 a0001c0001t0002g0326 |
2 | NA18975.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.-848-7545T>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41590747 | |||||||
| chr8:41590803 | A | G | 3 | a0001c0001t0011g0160 a0001c0001t0011g0186 a0001c0001t0011g0187 |
3 | HG00621.hp2 NA18975.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.-848-7489A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41590803 | |||||||
| chr8:41590877 | G | T | 1 | a0001c0001t0001g0212 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-848-7415G>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41590877 | |||||||
| chr8:41590894 | TAAAC | T | 23 | a0001c0001t0005g0012 a0001c0001t0005g0017 a0001c0001t0005g0023 others(20): Show |
28 | HG02004.hp2 HG02055.hp2 HG02074.hp2 others(25): Show |
intron_variant | MODIFIER | c.-848-7393_-848-739 others(8): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41590894 | ||||||
| chr8:41591082 | T | C | 1 | a0001c0001t0031g0042 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-848-7210T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41591082 | |||||||
| chr8:41591103 | C | T | 2 | a0001c0001t0001g0237 a0001c0001t0001g0239 |
2 | NA18988.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.-848-7189C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41591103 | |||||||
| chr8:41591279 | G | A | 90 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(87): Show |
116 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.-848-7013G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41591279 | |||||||
| chr8:41591420 | C | T | 166 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(163): Show |
206 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(203): Show |
intron_variant | MODIFIER | c.-848-6872C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41591420 | |||||||
| chr8:41591596 | G | A | 91 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(88): Show |
117 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.-848-6696G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41591596 | |||||||
| chr8:41591944 | A | G | 173 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(170): Show |
216 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(213): Show |
intron_variant | MODIFIER | c.-848-6348A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41591944 | |||||||
| chr8:41591980 | A | C | 173 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(170): Show |
216 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(213): Show |
intron_variant | MODIFIER | c.-848-6312A>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41591980 | |||||||
| chr8:41592055 | A | G | 1 | a0001c0001t0002g0300 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-848-6237A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41592055 | |||||||
| chr8:41592244 | T | G | 188 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(185): Show |
234 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(231): Show |
intron_variant | MODIFIER | c.-848-6048T>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41592244 | |||||||
| chr8:41592265 | C | T | 4 | a0001c0001t0001g0338 a0001c0001t0001g0340 a0001c0001t0007g0337 others(1): Show |
4 | HG01884.hp1 HG03453.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-848-6027C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41592265 | |||||||
| chr8:41592404 | A | T | 188 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(185): Show |
234 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(231): Show |
intron_variant | MODIFIER | c.-848-5888A>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41592404 | |||||||
| chr8:41592585 | C | G | 1 | a0001c0001t0001g0139 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-848-5707C>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41592585 | |||||||
| chr8:41592640 | A | G | 1 | a0001c0001t0001g0247 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-848-5652A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41592640 | |||||||
| chr8:41592777 | T | C | 173 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(170): Show |
216 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(213): Show |
intron_variant | MODIFIER | c.-848-5515T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41592777 | |||||||
| chr8:41592826 | A | G | 3 | a0001c0001t0001g0159 a0001c0001t0001g0185 a0001c0001t0001g0252 |
3 | HG03669.hp2 HG03710.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.-848-5466A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41592826 | |||||||
| chr8:41592968 | C | T | 1 | a0001c0001t0001g0211 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-848-5324C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41592968 | |||||||
| chr8:41593014 | A | G | 1 | a0001c0001t0004g0285 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-848-5278A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41593014 | |||||||
| chr8:41593052 | A | G | 1 | a0001c0001t0005g0023 | 2 | HG03490.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-848-5240A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41593052 | |||||||
| chr8:41593141 | G | A | 1 | a0001c0001t0004g0008 | 4 | HG02080.hp1 NA18970.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.-848-5151G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41593141 | |||||||
| chr8:41593343 | A | T | 1 | a0001c0001t0001g0254 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-848-4949A>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41593343 | |||||||
| chr8:41593410 | A | C | 173 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(170): Show |
216 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(213): Show |
intron_variant | MODIFIER | c.-848-4882A>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41593410 | |||||||
| chr8:41593512 | G | A | 5 | a0001c0001t0009g0016 a0001c0001t0009g0292 a0001c0001t0009g0341 others(2): Show |
7 | HG03239.hp2 NA18963.hp2 NA18972.hp2 others(4): Show |
intron_variant | MODIFIER | c.-848-4780G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41593512 | |||||||
| chr8:41593593 | G | C | 3 | a0001c0001t0002g0293 a0001c0001t0002g0314 a0001c0001t0002g0318 |
3 | HG00735.hp1 HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-848-4699G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41593593 | |||||||
| chr8:41593649 | A | G | 14 | a0001c0001t0007g0002 a0001c0001t0007g0009 a0001c0001t0007g0043 others(11): Show |
17 | HG00738.hp1 HG01069.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.-848-4643A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41593649 | |||||||
| chr8:41593713 | C | T | 1 | a0001c0001t0001g0139 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-848-4579C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41593713 | |||||||
| chr8:41593908 | A | G | 1 | a0001c0001t0002g0308 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-848-4384A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41593908 | |||||||
| chr8:41594097 | A | G | 3 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0138 |
3 | NA18954.hp2 NA19057.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.-848-4195A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41594097 | |||||||
| chr8:41594110 | C | A | 2 | a0001c0001t0019g0103 a0001c0001t0029g0102 |
2 | HG02965.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-848-4182C>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41594110 | |||||||
| chr8:41594169 | T | C | 2 | a0001c0001t0004g0290 a0001c0001t0004g0311 |
2 | HG01106.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-848-4123T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41594169 | |||||||
| chr8:41594218 | C | G | 1 | a0001c0001t0001g0148 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-848-4074C>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41594218 | |||||||
| chr8:41594262 | A | G | 1 | a0001c0001t0001g0239 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-848-4030A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41594262 | |||||||
| chr8:41594438 | A | G | 1 | a0001c0001t0026g0123 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-848-3854A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41594438 | |||||||
| chr8:41594546 | C | CT | 39 | a0001c0001t0001g0192 a0001c0001t0002g0294 a0001c0001t0004g0329 others(36): Show |
47 | HG00738.hp1 HG01069.hp1 HG01070.hp1 others(44): Show |
intron_variant | MODIFIER | c.-848-3729dupT | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41594546 | ||||||
| chr8:41594546 | C | CTT | 142 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(139): Show |
180 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.-848-3730_-848-372 others(6): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41594546 | ||||||
| chr8:41594546 | C | CTTT | 7 | a0001c0001t0002g0322 a0001c0001t0003g0077 a0001c0001t0003g0079 others(4): Show |
7 | HG00544.hp2 HG02559.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.-848-3731_-848-372 others(7): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41594546 | ||||||
| chr8:41594568 | T | C | 1 | a0001c0001t0001g0232 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-848-3724T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41594568 | |||||||
| chr8:41594600 | C | G | 4 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(1): Show |
4 | NA18954.hp2 NA19057.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.-848-3692C>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41594600 | |||||||
| chr8:41594606 | T | C | 1 | a0001c0001t0001g0232 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-848-3686T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41594606 | |||||||
| chr8:41594607 | C | G | 1 | a0001c0001t0001g0232 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-848-3685C>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41594607 | |||||||
| chr8:41594608 | C | G | 1 | a0001c0001t0001g0232 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-848-3684C>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41594608 | |||||||
| chr8:41594639 | G | A | 2 | a0001c0001t0002g0279 a0001c0001t0002g0322 |
2 | NA18949.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.-848-3653G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41594639 | |||||||
| chr8:41594693 | C | A | 1 | a0001c0001t0005g0107 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-848-3599C>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41594693 | |||||||
| chr8:41594747 | G | T | 69 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(66): Show |
90 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.-848-3545G>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41594747 | |||||||
| chr8:41594796 | C | T | 89 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(86): Show |
115 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.-848-3496C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41594796 | |||||||
| chr8:41594827 | A | G | 88 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(85): Show |
114 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.-848-3465A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41594827 | |||||||
| chr8:41594980 | A | G | 1 | a0001c0001t0009g0341 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-848-3312A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41594980 | |||||||
| chr8:41595077 | C | T | 173 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(170): Show |
216 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(213): Show |
intron_variant | MODIFIER | c.-848-3215C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41595077 | |||||||
| chr8:41595156 | G | GT | 117 | a0001c0001t0001g0129 a0001c0001t0001g0148 a0001c0001t0001g0158 others(114): Show |
143 | HG00438.hp1 HG00544.hp1 HG00544.hp2 others(140): Show |
intron_variant | MODIFIER | c.-848-3117dupT | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41595156 | ||||||
| chr8:41595156 | G | GTT | 17 | a0001c0001t0003g0020 a0001c0001t0003g0076 a0001c0001t0003g0081 others(14): Show |
18 | HG00597.hp2 HG01433.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.-848-3118_-848-311 others(6): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41595156 | ||||||
| chr8:41595325 | C | CT | 29 | a0001c0001t0001g0101 a0001c0001t0001g0125 a0001c0001t0001g0127 others(26): Show |
29 | HG01109.hp1 HG01109.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.-848-2939dupT | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41595325 | ||||||
| chr8:41595325 | CT | C | 14 | a0001c0001t0001g0153 a0001c0001t0001g0204 a0001c0001t0001g0219 others(11): Show |
17 | HG00738.hp1 HG01069.hp1 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.-848-2939delT | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41595325 | ||||||
| chr8:41595325 | CTTTT | C | 32 | a0001c0001t0002g0305 a0001c0001t0003g0057 a0001c0001t0003g0074 others(29): Show |
37 | HG01106.hp1 HG01243.hp1 HG02004.hp2 others(34): Show |
intron_variant | MODIFIER | c.-848-2942_-848-293 others(8): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41595325 | ||||||
| chr8:41595325 | CTTTTT | C | 135 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(132): Show |
173 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(170): Show |
intron_variant | MODIFIER | c.-848-2943_-848-293 others(9): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41595325 | ||||||
| chr8:41595434 | G | A | 8 | a0001c0001t0002g0007 a0001c0001t0002g0035 a0001c0001t0002g0280 others(5): Show |
12 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(9): Show |
intron_variant | MODIFIER | c.-848-2858G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41595434 | |||||||
| chr8:41595573 | G | A | 90 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(87): Show |
116 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.-848-2719G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41595573 | |||||||
| chr8:41595687 | A | G | 2 | a0002c0002t0014g0094 a0002c0002t0014g0095 |
2 | HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-848-2605A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41595687 | |||||||
| chr8:41595691 | CTCTT | C | 3 | a0001c0001t0001g0198 a0001c0001t0011g0160 a0001c0001t0011g0186 |
3 | NA18975.hp1 NA19060.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.-848-2593_-848-259 others(8): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41595691 | ||||||
| chr8:41595811 | TCTCTTTT others(1): Show |
T | 40 | a0001c0001t0003g0003 a0001c0001t0003g0011 a0001c0001t0003g0018 others(37): Show |
48 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.-848-2468_-848-246 others(12): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 41595811 | ||||||
| chr8:41595871 | G | A | 2 | a0002c0002t0014g0094 a0002c0002t0014g0095 |
2 | HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-848-2421G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41595871 | |||||||
| chr8:41595959 | A | G | 12 | a0001c0001t0007g0002 a0001c0001t0007g0009 a0001c0001t0007g0043 others(9): Show |
15 | HG00738.hp1 HG01069.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.-848-2333A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41595959 | |||||||
| chr8:41595974 | G | T | 5 | a0001c0001t0005g0106 a0001c0001t0005g0115 a0001c0001t0005g0116 others(2): Show |
5 | HG02572.hp2 HG02630.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-848-2318G>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41595974 | |||||||
| chr8:41595987 | C | T | 24 | a0001c0001t0002g0294 a0001c0001t0005g0012 a0001c0001t0005g0017 others(21): Show |
29 | HG01169.hp1 HG02004.hp2 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.-848-2305C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41595987 | |||||||
| chr8:41596061 | A | G | 5 | a0001c0001t0008g0004 a0001c0001t0008g0096 a0001c0001t0008g0097 others(2): Show |
8 | HG02055.hp1 HG02280.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.-848-2231A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41596061 | |||||||
| chr8:41596146 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-848-2146C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41596146 | |||||||
| chr8:41596247 | C | T | 1 | a0001c0001t0002g0298 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-848-2045C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41596247 | |||||||
| chr8:41596338 | A | C | 1 | a0001c0001t0001g0267 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-848-1954A>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41596338 | |||||||
| chr8:41596425 | C | G | 187 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(184): Show |
233 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(230): Show |
intron_variant | MODIFIER | c.-848-1867C>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41596425 | |||||||
| chr8:41596614 | A | G | 1 | a0001c0001t0002g0315 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-848-1678A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41596614 | |||||||
| chr8:41596704 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-848-1588C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41596704 | |||||||
| chr8:41596731 | A | C | 8 | a0001c0001t0002g0007 a0001c0001t0002g0035 a0001c0001t0002g0280 others(5): Show |
12 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(9): Show |
intron_variant | MODIFIER | c.-848-1561A>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41596731 | |||||||
| chr8:41596752 | G | A | 2 | a0001c0001t0001g0172 a0001c0001t0046g0171 |
2 | HG02071.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.-848-1540G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41596752 | |||||||
| chr8:41596779 | C | T | 1 | a0001c0001t0003g0022 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-848-1513C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41596779 | |||||||
| chr8:41596787 | A | C | 1 | a0001c0001t0053g0041 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-848-1505A>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41596787 | |||||||
| chr8:41596845 | G | A | 1 | a0001c0001t0058g0220 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-848-1447G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41596845 | |||||||
| chr8:41597013 | G | A | 5 | a0001c0001t0005g0106 a0001c0001t0005g0115 a0001c0001t0005g0116 others(2): Show |
5 | HG02572.hp2 HG02630.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-848-1279G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41597013 | |||||||
| chr8:41597027 | C | T | 12 | a0001c0001t0007g0002 a0001c0001t0007g0009 a0001c0001t0007g0043 others(9): Show |
15 | HG00738.hp1 HG01069.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.-848-1265C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41597027 | |||||||
| chr8:41597028 | G | A | 1 | a0001c0001t0041g0256 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-848-1264G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41597028 | |||||||
| chr8:41597060 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-848-1232G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41597060 | |||||||
| chr8:41597268 | A | G | 1 | a0001c0001t0001g0180 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-848-1024A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41597268 | |||||||
| chr8:41597472 | G | C | 1 | a0001c0001t0040g0268 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-848-820G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41597472 | |||||||
| chr8:41597485 | A | G | 15 | a0001c0001t0004g0040 a0001c0001t0006g0013 a0001c0001t0006g0014 others(12): Show |
18 | HG01069.hp2 HG01071.hp1 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.-848-807A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41597485 | |||||||
| chr8:41597824 | G | A | 7 | a0001c0001t0008g0004 a0001c0001t0008g0096 a0001c0001t0008g0097 others(4): Show |
10 | HG02055.hp1 HG02280.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.-848-468G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41597824 | |||||||
| chr8:41598060 | C | T | 166 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(163): Show |
206 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(203): Show |
intron_variant | MODIFIER | c.-848-232C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41598060 | |||||||
| chr8:41598133 | G | A | 7 | a0001c0001t0008g0004 a0001c0001t0008g0096 a0001c0001t0008g0097 others(4): Show |
10 | HG02055.hp1 HG02280.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.-848-159G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41598133 | |||||||
| chr8:41598136 | C | G | 1 | a0001c0001t0008g0099 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-848-156C>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 1/12 | chr8 | 41598136 | |||||||
| chr8:41599321 | C | A | 1 | a0001c0001t0004g0008 | 4 | HG02080.hp1 NA18970.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.165+17C>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41599321 | |||||||
| chr8:41599353 | G | A | 1 | a0001c0001t0001g0266 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.165+49G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41599353 | |||||||
| chr8:41599575 | C | T | 59 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0101 others(56): Show |
61 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.165+271C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41599575 | |||||||
| chr8:41599620 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.165+316G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41599620 | |||||||
| chr8:41599629 | G | A | 2 | a0001c0001t0003g0021 a0001c0001t0003g0079 |
3 | HG00621.hp1 HG02083.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.165+325G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41599629 | |||||||
| chr8:41599784 | A | G | 2 | a0001c0001t0019g0103 a0001c0001t0029g0102 |
2 | HG02965.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.165+480A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41599784 | |||||||
| chr8:41600036 | C | CT | 14 | a0001c0001t0001g0192 a0001c0001t0007g0002 a0001c0001t0007g0009 others(11): Show |
17 | HG00738.hp1 HG01069.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.165+750dupT | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 41600036 | ||||||
| chr8:41600036 | C | CTTTT | 4 | a0001c0001t0008g0004 a0001c0001t0008g0096 a0001c0001t0008g0098 others(1): Show |
7 | HG02055.hp1 HG02280.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.165+747_165+750dup others(4): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 41600036 | ||||||
| chr8:41600036 | C | CTTTTTT | 71 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0034 others(68): Show |
94 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.165+745_165+750dup others(6): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 41600036 | ||||||
| chr8:41600036 | C | CTTTTTTT | 30 | a0001c0001t0002g0279 a0001c0001t0002g0297 a0001c0001t0002g0307 others(27): Show |
38 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.165+744_165+750dup others(7): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 41600036 | ||||||
| chr8:41600036 | C | CTTTTTTT others(1): Show |
46 | a0001c0001t0003g0003 a0001c0001t0003g0011 a0001c0001t0003g0018 others(43): Show |
54 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.165+743_165+750dup others(8): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 41600036 | ||||||
| chr8:41600036 | C | CTTTTTTT others(2): Show |
11 | a0001c0001t0003g0019 a0001c0001t0003g0058 a0001c0001t0003g0065 others(8): Show |
11 | HG00597.hp2 HG01099.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.165+742_165+750dup others(9): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 41600036 | ||||||
| chr8:41600036 | CT | C | 6 | a0001c0001t0001g0174 a0001c0001t0001g0207 a0001c0001t0001g0222 others(3): Show |
6 | HG01496.hp1 HG02735.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.165+750delT | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 41600036 | ||||||
| chr8:41600054 | TC | T | 3 | a0001c0001t0004g0316 a0001c0001t0004g0317 a0001c0001t0004g0324 |
3 | HG02559.hp2 HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.165+751delC | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41600054 | |||||||
| chr8:41600055 | C | T | 170 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(167): Show |
212 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(209): Show |
intron_variant | MODIFIER | c.165+751C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41600055 | |||||||
| chr8:41600100 | G | T | 2 | a0001c0001t0056g0049 a0001c0001t0057g0048 |
2 | HG01361.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.165+796G>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41600100 | |||||||
| chr8:41600178 | A | G | 14 | a0001c0001t0007g0002 a0001c0001t0007g0009 a0001c0001t0007g0043 others(11): Show |
17 | HG00738.hp1 HG01069.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.165+874A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41600178 | |||||||
| chr8:41600289 | A | T | 1 | a0002c0002t0014g0095 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.165+985A>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41600289 | |||||||
| chr8:41600334 | ACCTGGCC others(10): Show |
A | 1 | a0001c0001t0002g0279 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.165+1032_165+1048d others(19): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 41600334 | ||||||
| chr8:41600476 | A | T | 1 | a0001c0001t0002g0279 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.165+1172A>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41600476 | |||||||
| chr8:41600540 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.165+1236C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41600540 | |||||||
| chr8:41600552 | C | T | 1 | a0001c0001t0001g0156 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.165+1248C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41600552 | |||||||
| chr8:41600553 | T | C | 1 | a0001c0001t0001g0156 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.165+1249T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41600553 | |||||||
| chr8:41600588 | G | GT | 20 | a0001c0001t0001g0129 a0001c0001t0002g0279 a0001c0001t0003g0054 others(17): Show |
23 | HG00639.hp2 HG00738.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.165+1296dupT | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 41600588 | ||||||
| chr8:41600660 | G | C | 1 | a0001c0001t0001g0241 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.165+1356G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41600660 | |||||||
| chr8:41600668 | G | A | 3 | a0001c0001t0011g0160 a0001c0001t0011g0186 a0001c0001t0011g0187 |
3 | HG00621.hp2 NA18975.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.165+1364G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41600668 | |||||||
| chr8:41600688 | G | C | 1 | a0001c0001t0029g0102 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.165+1384G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41600688 | |||||||
| chr8:41600915 | T | G | 12 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0100 others(9): Show |
14 | HG04115.hp2 NA18945.hp2 NA18955.hp2 others(11): Show |
intron_variant | MODIFIER | c.165+1611T>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41600915 | |||||||
| chr8:41601087 | G | A | 187 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(184): Show |
233 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(230): Show |
intron_variant | MODIFIER | c.165+1783G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41601087 | |||||||
| chr8:41601134 | A | G | 1 | a0001c0001t0003g0090 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.165+1830A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41601134 | |||||||
| chr8:41601140 | TA | T | 173 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(170): Show |
216 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(213): Show |
intron_variant | MODIFIER | c.165+1838delA | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 41601140 | ||||||
| chr8:41601167 | C | T | 2 | a0002c0002t0014g0094 a0002c0002t0014g0095 |
2 | HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.165+1863C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41601167 | |||||||
| chr8:41601434 | G | T | 3 | a0001c0001t0001g0165 a0001c0001t0001g0251 a0001c0001t0001g0255 |
3 | HG00642.hp2 HG03540.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.165+2130G>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41601434 | |||||||
| chr8:41601767 | T | C | 7 | a0001c0001t0008g0004 a0001c0001t0008g0096 a0001c0001t0008g0097 others(4): Show |
10 | HG02055.hp1 HG02280.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.165+2463T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41601767 | |||||||
| chr8:41601902 | C | T | 12 | a0001c0001t0007g0002 a0001c0001t0007g0009 a0001c0001t0007g0043 others(9): Show |
15 | HG00738.hp1 HG01069.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.165+2598C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41601902 | |||||||
| chr8:41601954 | C | T | 188 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(185): Show |
234 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(231): Show |
intron_variant | MODIFIER | c.165+2650C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41601954 | |||||||
| chr8:41601955 | C | G | 188 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(185): Show |
234 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(231): Show |
intron_variant | MODIFIER | c.165+2651C>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41601955 | |||||||
| chr8:41601956 | C | T | 188 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(185): Show |
234 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(231): Show |
intron_variant | MODIFIER | c.165+2652C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41601956 | |||||||
| chr8:41601957 | A | ATG | 188 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(185): Show |
234 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(231): Show |
intron_variant | MODIFIER | c.165+2653_165+2654i others(4): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41601957 | |||||||
| chr8:41601958 | A | T | 188 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(185): Show |
234 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(231): Show |
intron_variant | MODIFIER | c.165+2654A>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41601958 | |||||||
| chr8:41602014 | G | A | 2 | a0001c0001t0010g0092 a0001c0001t0010g0093 |
2 | HG02970.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.165+2710G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41602014 | |||||||
| chr8:41602015 | C | T | 2 | a0001c0001t0010g0092 a0001c0001t0010g0093 |
2 | HG02970.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.165+2711C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41602015 | |||||||
| chr8:41602084 | A | AGCTGGGA others(7): Show |
1 | a0001c0001t0002g0279 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.165+2781_165+2794d others(16): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 41602084 | ||||||
| chr8:41602201 | C | T | 1 | a0001c0001t0005g0110 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.165+2897C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41602201 | |||||||
| chr8:41602231 | T | A | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG04184.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.165+2927T>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41602231 | |||||||
| chr8:41602485 | G | T | 12 | a0001c0001t0007g0002 a0001c0001t0007g0009 a0001c0001t0007g0043 others(9): Show |
15 | HG00738.hp1 HG01069.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.165+3181G>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41602485 | |||||||
| chr8:41602495 | T | C | 1 | a0001c0001t0037g0184 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.165+3191T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41602495 | |||||||
| chr8:41602504 | A | C | 187 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(184): Show |
233 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(230): Show |
intron_variant | MODIFIER | c.165+3200A>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41602504 | |||||||
| chr8:41602564 | G | C | 11 | a0001c0001t0007g0002 a0001c0001t0007g0009 a0001c0001t0007g0043 others(8): Show |
14 | HG00738.hp1 HG01069.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.165+3260G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41602564 | |||||||
| chr8:41602668 | C | T | 91 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(88): Show |
117 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.165+3364C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41602668 | |||||||
| chr8:41602756 | T | G | 14 | a0001c0001t0007g0002 a0001c0001t0007g0009 a0001c0001t0007g0043 others(11): Show |
17 | HG00738.hp1 HG01069.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.165+3452T>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41602756 | |||||||
| chr8:41602780 | A | G | 1 | a0001c0001t0029g0102 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.165+3476A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41602780 | |||||||
| chr8:41602868 | T | A | 1 | a0001c0001t0002g0319 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.165+3564T>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41602868 | |||||||
| chr8:41602893 | C | T | 1 | a0001c0001t0026g0123 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.165+3589C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41602893 | |||||||
| chr8:41603075 | G | A | 3 | a0001c0001t0011g0160 a0001c0001t0011g0186 a0001c0001t0011g0187 |
3 | HG00621.hp2 NA18975.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.165+3771G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41603075 | |||||||
| chr8:41603151 | G | C | 1 | a0001c0001t0004g0332 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.165+3847G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41603151 | |||||||
| chr8:41603270 | T | C | 166 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(163): Show |
206 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(203): Show |
intron_variant | MODIFIER | c.165+3966T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41603270 | |||||||
| chr8:41603292 | C | T | 1 | a0001c0001t0001g0134 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.165+3988C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41603292 | |||||||
| chr8:41603525 | CA | C | 152 | a0001c0001t0001g0124 a0001c0001t0001g0133 a0001c0001t0001g0154 others(149): Show |
192 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(189): Show |
intron_variant | MODIFIER | c.165+4242delA | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 41603525 | ||||||
| chr8:41603525 | CAA | C | 12 | a0001c0001t0002g0036 a0001c0001t0003g0064 a0001c0001t0003g0072 others(9): Show |
12 | HG00741.hp2 HG01192.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.165+4241_165+4242d others(4): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 41603525 | ||||||
| chr8:41603525 | CAAAAAAA | C | 5 | a0001c0001t0008g0004 a0001c0001t0008g0096 a0001c0001t0008g0097 others(2): Show |
8 | HG02055.hp1 HG02280.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.165+4236_165+4242d others(9): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 41603525 | ||||||
| chr8:41603539 | A | C | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG04184.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.165+4235A>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41603539 | |||||||
| chr8:41603586 | T | A | 5 | a0001c0001t0008g0004 a0001c0001t0008g0096 a0001c0001t0008g0097 others(2): Show |
8 | HG02055.hp1 HG02280.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.165+4282T>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41603586 | |||||||
| chr8:41603896 | A | AGAAT | 45 | a0001c0001t0001g0032 a0001c0001t0001g0127 a0001c0001t0001g0182 others(42): Show |
52 | HG00423.hp1 HG00438.hp2 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.165+4618_165+4621d others(6): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 41603896 | ||||||
| chr8:41603896 | A | AGAATGAA others(1): Show |
52 | a0001c0001t0001g0031 a0001c0001t0001g0101 a0001c0001t0001g0129 others(49): Show |
53 | HG00099.hp2 HG00673.hp2 HG01109.hp2 others(50): Show |
intron_variant | MODIFIER | c.165+4614_165+4621d others(10): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 41603896 | ||||||
| chr8:41603896 | A | AGAATGAA others(5): Show |
61 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0026 others(58): Show |
69 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.165+4610_165+4621d others(14): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 41603896 | ||||||
| chr8:41603896 | A | AGAATGAA others(9): Show |
15 | a0001c0001t0001g0125 a0001c0001t0001g0156 a0001c0001t0001g0161 others(12): Show |
15 | HG00642.hp2 HG00735.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.165+4606_165+4621d others(18): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 41603896 | ||||||
| chr8:41603896 | A | AGAATGAA others(13): Show |
5 | a0001c0001t0001g0157 a0001c0001t0001g0159 a0001c0001t0001g0214 others(2): Show |
5 | HG00323.hp1 HG02109.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.165+4602_165+4621d others(22): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 41603896 | ||||||
| chr8:41603904 | T | A | 1 | a0002c0002t0014g0095 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.165+4600T>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41603904 | |||||||
| chr8:41604036 | A | AT | 9 | a0001c0001t0001g0155 a0001c0001t0001g0157 a0001c0001t0001g0166 others(6): Show |
9 | HG00323.hp1 HG01952.hp1 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.165+4749dupT | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 41604036 | ||||||
| chr8:41604036 | AT | A | 21 | a0001c0001t0002g0279 a0001c0001t0007g0002 a0001c0001t0007g0009 others(18): Show |
27 | HG00738.hp1 HG01069.hp1 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.165+4749delT | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 41604036 | ||||||
| chr8:41604036 | ATT | A | 142 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(139): Show |
177 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.165+4748_165+4749d others(4): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 41604036 | ||||||
| chr8:41604036 | ATTTT | A | 23 | a0001c0001t0005g0012 a0001c0001t0005g0017 a0001c0001t0005g0023 others(20): Show |
28 | HG02004.hp2 HG02055.hp2 HG02074.hp2 others(25): Show |
intron_variant | MODIFIER | c.165+4746_165+4749d others(6): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 41604036 | ||||||
| chr8:41604284 | C | G | 1 | a0001c0001t0004g0040 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.165+4980C>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41604284 | |||||||
| chr8:41604463 | G | C | 2 | a0001c0001t0004g0290 a0001c0001t0004g0311 |
2 | HG01106.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.166-4953G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41604463 | |||||||
| chr8:41604588 | A | G | 4 | a0001c0001t0001g0030 a0001c0001t0001g0201 a0001c0001t0001g0202 others(1): Show |
5 | HG02886.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.166-4828A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41604588 | |||||||
| chr8:41604655 | T | G | 1 | a0001c0001t0002g0303 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.166-4761T>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41604655 | |||||||
| chr8:41605119 | T | C | 91 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(88): Show |
117 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.166-4297T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41605119 | |||||||
| chr8:41605201 | A | G | 1 | a0001c0001t0001g0230 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.166-4215A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41605201 | |||||||
| chr8:41605206 | C | T | 1 | a0001c0001t0004g0040 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.166-4210C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41605206 | |||||||
| chr8:41605239 | G | T | 2 | a0001c0001t0056g0049 a0001c0001t0057g0048 |
2 | HG01361.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.166-4177G>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41605239 | |||||||
| chr8:41605249 | C | T | 2 | a0001c0001t0056g0049 a0001c0001t0057g0048 |
2 | HG01361.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.166-4167C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41605249 | |||||||
| chr8:41605294 | G | C | 1 | a0001c0001t0001g0199 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.166-4122G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41605294 | |||||||
| chr8:41605379 | A | G | 49 | a0001c0001t0003g0003 a0001c0001t0003g0011 a0001c0001t0003g0018 others(46): Show |
58 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.166-4037A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41605379 | |||||||
| chr8:41605390 | G | A | 1 | a0001c0001t0002g0280 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.166-4026G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41605390 | |||||||
| chr8:41605436 | A | C | 188 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(185): Show |
234 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(231): Show |
intron_variant | MODIFIER | c.166-3980A>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41605436 | |||||||
| chr8:41605454 | A | G | 1 | a0001c0001t0026g0123 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.166-3962A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41605454 | |||||||
| chr8:41605546 | TTTTG | T | 67 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0026 others(64): Show |
75 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.166-3830_166-3827d others(6): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 41605546 | ||||||
| chr8:41605546 | TTTTGTTT others(1): Show |
T | 84 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0101 others(81): Show |
86 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.166-3834_166-3827d others(10): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 41605546 | ||||||
| chr8:41605546 | TTTTGTTT others(5): Show |
T | 51 | a0001c0001t0001g0200 a0001c0001t0001g0235 a0001c0001t0003g0003 others(48): Show |
60 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.166-3838_166-3827d others(14): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 41605546 | ||||||
| chr8:41605546 | TTTTGTTT others(9): Show |
T | 122 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(119): Show |
156 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.166-3842_166-3827d others(18): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 41605546 | ||||||
| chr8:41605546 | TTTTGTTT others(17): Show |
T | 15 | a0001c0001t0007g0002 a0001c0001t0007g0009 a0001c0001t0007g0043 others(12): Show |
18 | HG00738.hp1 HG01069.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.166-3850_166-3827d others(26): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 41605546 | ||||||
| chr8:41605558 | G | T | 6 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(3): Show |
6 | HG02071.hp1 NA18959.hp1 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.166-3858G>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41605558 | |||||||
| chr8:41605697 | C | T | 2 | a0001c0001t0056g0049 a0001c0001t0057g0048 |
2 | HG01361.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.166-3719C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41605697 | |||||||
| chr8:41605698 | G | A | 1 | a0001c0001t0026g0123 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.166-3718G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41605698 | |||||||
| chr8:41605800 | G | A | 1 | a0001c0001t0001g0340 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.166-3616G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41605800 | |||||||
| chr8:41605840 | G | A | 2 | a0001c0001t0001g0125 a0001c0001t0049g0126 |
2 | HG02135.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.166-3576G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41605840 | |||||||
| chr8:41605901 | G | A | 2 | a0001c0001t0005g0114 a0001c0001t0005g0121 |
2 | NA18946.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.166-3515G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41605901 | |||||||
| chr8:41606007 | G | T | 1 | a0001c0001t0003g0088 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.166-3409G>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41606007 | |||||||
| chr8:41606045 | G | A | 1 | a0001c0001t0029g0102 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.166-3371G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41606045 | |||||||
| chr8:41606201 | C | G | 72 | a0001c0001t0003g0003 a0001c0001t0003g0011 a0001c0001t0003g0018 others(69): Show |
86 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.166-3215C>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41606201 | |||||||
| chr8:41606301 | A | G | 5 | a0001c0001t0001g0145 a0001c0001t0001g0148 a0001c0001t0001g0164 others(2): Show |
5 | HG01081.hp1 HG01109.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.166-3115A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41606301 | |||||||
| chr8:41606572 | A | G | 1 | a0001c0001t0001g0134 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.166-2844A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41606572 | |||||||
| chr8:41606580 | C | T | 1 | a0001c0001t0019g0103 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.166-2836C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41606580 | |||||||
| chr8:41606628 | A | G | 1 | a0001c0001t0031g0042 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.166-2788A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41606628 | |||||||
| chr8:41607213 | G | T | 1 | a0001c0001t0001g0149 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.166-2203G>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41607213 | |||||||
| chr8:41607238 | G | T | 1 | a0001c0001t0004g0040 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.166-2178G>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41607238 | |||||||
| chr8:41607284 | G | A | 1 | a0001c0001t0003g0061 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.166-2132G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41607284 | |||||||
| chr8:41607352 | G | A | 72 | a0001c0001t0003g0003 a0001c0001t0003g0011 a0001c0001t0003g0018 others(69): Show |
86 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.166-2064G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41607352 | |||||||
| chr8:41607453 | A | G | 1 | a0001c0001t0005g0106 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.166-1963A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41607453 | |||||||
| chr8:41607461 | G | C | 1 | a0001c0001t0040g0268 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.166-1955G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41607461 | |||||||
| chr8:41607540 | C | CT | 37 | a0001c0001t0001g0030 a0001c0001t0001g0225 a0001c0001t0002g0326 others(34): Show |
46 | HG00423.hp1 HG02004.hp2 HG02055.hp1 others(43): Show |
intron_variant | MODIFIER | c.166-1860dupT | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 41607540 | ||||||
| chr8:41607540 | CT | C | 8 | a0001c0001t0001g0153 a0001c0001t0001g0175 a0001c0001t0001g0244 others(5): Show |
8 | HG00323.hp2 HG01099.hp1 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.166-1860delT | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 41607540 | ||||||
| chr8:41607608 | C | T | 1 | a0001c0001t0026g0123 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.166-1808C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41607608 | |||||||
| chr8:41607658 | A | G | 1 | a0001c0001t0003g0057 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.166-1758A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41607658 | |||||||
| chr8:41607662 | G | A | 1 | a0001c0001t0005g0110 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.166-1754G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41607662 | |||||||
| chr8:41607881 | C | T | 2 | a0001c0001t0003g0081 a0001c0001t0003g0083 |
2 | HG01433.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.166-1535C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41607881 | |||||||
| chr8:41607982 | G | A | 1 | a0001c0001t0023g0289 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.166-1434G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41607982 | |||||||
| chr8:41608046 | C | T | 14 | a0001c0001t0004g0008 a0001c0001t0004g0015 a0001c0001t0004g0284 others(11): Show |
19 | HG00438.hp1 HG00544.hp1 HG00597.hp1 others(16): Show |
intron_variant | MODIFIER | c.166-1370C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41608046 | |||||||
| chr8:41608074 | A | G | 7 | a0001c0001t0008g0004 a0001c0001t0008g0096 a0001c0001t0008g0097 others(4): Show |
10 | HG02055.hp1 HG02280.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.166-1342A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41608074 | |||||||
| chr8:41608200 | G | A | 23 | a0001c0001t0005g0012 a0001c0001t0005g0017 a0001c0001t0005g0023 others(20): Show |
28 | HG02004.hp2 HG02055.hp2 HG02074.hp2 others(25): Show |
intron_variant | MODIFIER | c.166-1216G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41608200 | |||||||
| chr8:41608293 | C | T | 12 | a0001c0001t0007g0002 a0001c0001t0007g0009 a0001c0001t0007g0043 others(9): Show |
15 | HG00738.hp1 HG01069.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.166-1123C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41608293 | |||||||
| chr8:41608819 | GT | G | 189 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(186): Show |
235 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(232): Show |
intron_variant | MODIFIER | c.166-586delT | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 41608819 | ||||||
| chr8:41608879 | C | T | 1 | a0001c0001t0003g0081 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.166-537C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41608879 | |||||||
| chr8:41608955 | G | T | 1 | a0001c0001t0002g0304 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.166-461G>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41608955 | |||||||
| chr8:41609049 | C | T | 8 | a0001c0001t0002g0007 a0001c0001t0002g0035 a0001c0001t0002g0280 others(5): Show |
12 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(9): Show |
intron_variant | MODIFIER | c.166-367C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41609049 | |||||||
| chr8:41609270 | T | C | 173 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(170): Show |
216 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(213): Show |
intron_variant | MODIFIER | c.166-146T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 2/12 | chr8 | 41609270 | |||||||
| chr8:41609560 | C | T | 1 | a0001c0001t0001g0199 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.235+75C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 3/12 | chr8 | 41609560 | |||||||
| chr8:41609610 | G | T | 1 | a0001c0001t0015g0288 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.236-45G>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 3/12 | chr8 | 41609610 | |||||||
| chr8:41610070 | G | A | 1 | a0001c0001t0005g0107 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.536+115G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 4/12 | chr8 | 41610070 | |||||||
| chr8:41610245 | G | A | 1 | a0001c0001t0031g0042 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.536+290G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 4/12 | chr8 | 41610245 | |||||||
| chr8:41610300 | T | C | 5 | a0001c0001t0004g0010 a0001c0001t0004g0039 a0001c0001t0004g0050 others(2): Show |
7 | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.536+345T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 4/12 | chr8 | 41610300 | |||||||
| chr8:41610308 | C | T | 12 | a0001c0001t0007g0002 a0001c0001t0007g0009 a0001c0001t0007g0043 others(9): Show |
15 | HG00738.hp1 HG01069.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.536+353C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 4/12 | chr8 | 41610308 | |||||||
| chr8:41610457 | A | G | 4 | a0001c0001t0001g0128 a0001c0001t0001g0206 a0001c0001t0001g0216 others(1): Show |
4 | HG02257.hp2 HG02258.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.537-279A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 4/12 | chr8 | 41610457 | |||||||
| chr8:41610488 | C | T | 1 | a0001c0001t0001g0267 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.537-248C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 4/12 | chr8 | 41610488 | |||||||
| chr8:41610541 | C | T | 5 | a0001c0001t0001g0145 a0001c0001t0001g0148 a0001c0001t0001g0164 others(2): Show |
5 | HG01081.hp1 HG01109.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.537-195C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 4/12 | chr8 | 41610541 | |||||||
| chr8:41610943 | G | A | 1 | a0001c0001t0003g0067 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.611+133G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 5/12 | chr8 | 41610943 | |||||||
| chr8:41611047 | C | T | 1 | a0001c0001t0003g0070 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.611+237C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 5/12 | chr8 | 41611047 | |||||||
| chr8:41611051 | A | AC | 173 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(170): Show |
216 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(213): Show |
intron_variant | MODIFIER | c.611+243dupC | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 41611051 | ||||||
| chr8:41611087 | A | G | 188 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(185): Show |
234 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(231): Show |
intron_variant | MODIFIER | c.611+277A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 5/12 | chr8 | 41611087 | |||||||
| chr8:41611089 | G | A | 93 | a0001c0001t0001g0194 a0001c0001t0002g0001 a0001c0001t0002g0007 others(90): Show |
119 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.611+279G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 5/12 | chr8 | 41611089 | |||||||
| chr8:41611290 | T | A | 160 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(157): Show |
200 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(197): Show |
intron_variant | MODIFIER | c.611+480T>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 5/12 | chr8 | 41611290 | |||||||
| chr8:41611303 | G | C | 1 | a0001c0001t0001g0214 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.611+493G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 5/12 | chr8 | 41611303 | |||||||
| chr8:41611332 | T | C | 1 | a0001c0001t0001g0212 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.611+522T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 5/12 | chr8 | 41611332 | |||||||
| chr8:41611376 | T | G | 2 | a0001c0001t0003g0068 a0001c0001t0003g0073 |
2 | HG01099.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.612-527T>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 5/12 | chr8 | 41611376 | |||||||
| chr8:41611523 | C | T | 15 | a0001c0001t0007g0002 a0001c0001t0007g0009 a0001c0001t0007g0043 others(12): Show |
18 | HG00738.hp1 HG01069.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.612-380C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 5/12 | chr8 | 41611523 | |||||||
| chr8:41612000 | C | T | 2 | a0001c0001t0001g0159 a0001c0001t0001g0252 |
2 | HG03710.hp2 HG03831.hp2 |
splice_region_variant&intron_variant | LOW | c.701+8C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 6/12 | chr8 | 41612000 | |||||||
| chr8:41612001 | G | A | 1 | a0001c0001t0001g0182 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.701+9G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 6/12 | chr8 | 41612001 | |||||||
| chr8:41612028 | C | T | 7 | a0001c0001t0008g0004 a0001c0001t0008g0096 a0001c0001t0008g0097 others(4): Show |
10 | HG02055.hp1 HG02280.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.701+36C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 6/12 | chr8 | 41612028 | |||||||
| chr8:41612061 | C | T | 14 | a0001c0001t0006g0013 a0001c0001t0006g0014 a0001c0001t0006g0053 others(11): Show |
17 | HG01069.hp2 HG01071.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.701+69C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 6/12 | chr8 | 41612061 | |||||||
| chr8:41612284 | T | C | 2 | a0001c0001t0001g0168 a0001c0001t0048g0167 |
2 | HG01109.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.795+11T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 7/12 | chr8 | 41612284 | |||||||
| chr8:41612288 | C | T | 15 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0100 others(12): Show |
17 | HG04115.hp2 NA18945.hp2 NA18955.hp2 others(14): Show |
intron_variant | MODIFIER | c.795+15C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 7/12 | chr8 | 41612288 | |||||||
| chr8:41612984 | C | G | 2 | a0001c0001t0001g0132 a0001c0001t0001g0133 |
2 | NA18959.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.911+24C>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 8/12 | chr8 | 41612984 | |||||||
| chr8:41613080 | A | T | 2 | a0001c0001t0003g0069 a0001c0001t0003g0085 |
2 | HG02683.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.911+120A>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 8/12 | chr8 | 41613080 | |||||||
| chr8:41613172 | G | A | 166 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(163): Show |
206 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(203): Show |
intron_variant | MODIFIER | c.911+212G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 8/12 | chr8 | 41613172 | |||||||
| chr8:41613244 | A | C | 1 | a0001c0001t0007g0009 | 3 | HG02258.hp1 HG03540.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.911+284A>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 8/12 | chr8 | 41613244 | |||||||
| chr8:41613259 | A | G | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG04184.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.911+299A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 8/12 | chr8 | 41613259 | |||||||
| chr8:41613299 | T | C | 5 | a0001c0001t0008g0004 a0001c0001t0008g0096 a0001c0001t0008g0097 others(2): Show |
8 | HG02055.hp1 HG02280.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.911+339T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 8/12 | chr8 | 41613299 | |||||||
| chr8:41613365 | G | A | 62 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0101 others(59): Show |
64 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.911+405G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 8/12 | chr8 | 41613365 | |||||||
| chr8:41613386 | A | G | 1 | a0001c0001t0019g0103 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.911+426A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 8/12 | chr8 | 41613386 | |||||||
| chr8:41613481 | T | C | 166 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(163): Show |
206 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(203): Show |
intron_variant | MODIFIER | c.911+521T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 8/12 | chr8 | 41613481 | |||||||
| chr8:41613647 | G | A | 13 | a0001c0001t0007g0002 a0001c0001t0007g0009 a0001c0001t0007g0043 others(10): Show |
16 | HG00738.hp1 HG01069.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.911+687G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 8/12 | chr8 | 41613647 | |||||||
| chr8:41613730 | C | T | 1 | a0001c0001t0002g0315 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.912-656C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 8/12 | chr8 | 41613730 | |||||||
| chr8:41613802 | G | C | 2 | a0002c0002t0014g0094 a0002c0002t0014g0095 |
2 | HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.912-584G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 8/12 | chr8 | 41613802 | |||||||
| chr8:41613855 | T | G | 173 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(170): Show |
216 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(213): Show |
intron_variant | MODIFIER | c.912-531T>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 8/12 | chr8 | 41613855 | |||||||
| chr8:41613878 | C | T | 2 | a0001c0001t0006g0269 a0001c0001t0022g0272 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.912-508C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 8/12 | chr8 | 41613878 | |||||||
| chr8:41614014 | C | T | 188 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(185): Show |
234 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(231): Show |
intron_variant | MODIFIER | c.912-372C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 8/12 | chr8 | 41614014 | |||||||
| chr8:41614124 | C | T | 1 | a0001c0001t0001g0155 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.912-262C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 8/12 | chr8 | 41614124 | |||||||
| chr8:41614159 | C | T | 1 | a0001c0001t0026g0123 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.912-227C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 8/12 | chr8 | 41614159 | |||||||
| chr8:41614267 | A | G | 73 | a0001c0001t0002g0294 a0001c0001t0003g0003 a0001c0001t0003g0011 others(70): Show |
87 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.912-119A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 8/12 | chr8 | 41614267 | |||||||
| chr8:41614683 | T | C | 1 | a0001c0001t0001g0207 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.967+242T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 9/12 | chr8 | 41614683 | |||||||
| chr8:41614713 | A | G | 8 | a0001c0001t0007g0002 a0001c0001t0007g0043 a0001c0001t0007g0044 others(5): Show |
9 | HG00738.hp1 HG01069.hp1 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.968-250A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 9/12 | chr8 | 41614713 | |||||||
| chr8:41614718 | G | A | 1 | a0001c0001t0037g0184 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.968-245G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 9/12 | chr8 | 41614718 | |||||||
| chr8:41614856 | G | A | 91 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(88): Show |
117 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.968-107G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 9/12 | chr8 | 41614856 | |||||||
| chr8:41615093 | G | A | 1 | a0001c0001t0001g0135 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1053+45G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41615093 | |||||||
| chr8:41615115 | A | C | 1 | a0001c0001t0004g0311 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1053+67A>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41615115 | |||||||
| chr8:41615165 | G | A | 1 | a0001c0001t0002g0291 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1053+117G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41615165 | |||||||
| chr8:41615167 | G | C | 1 | a0001c0001t0046g0171 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1053+119G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41615167 | |||||||
| chr8:41615278 | C | T | 4 | a0001c0001t0002g0307 a0001c0001t0002g0308 a0001c0001t0002g0323 others(1): Show |
4 | NA18943.hp2 NA18981.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.1053+230C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41615278 | |||||||
| chr8:41615326 | C | T | 90 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(87): Show |
116 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.1053+278C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41615326 | |||||||
| chr8:41615363 | G | C | 1 | a0001c0001t0003g0022 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1053+315G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41615363 | |||||||
| chr8:41615389 | T | C | 1 | a0001c0001t0013g0060 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1053+341T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41615389 | |||||||
| chr8:41615449 | AT | A | 140 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(137): Show |
175 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.1053+403delT | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 41615449 | ||||||
| chr8:41615450 | T | TG | 6 | a0001c0001t0006g0013 a0001c0001t0006g0276 a0001c0001t0007g0337 others(3): Show |
6 | HG01243.hp2 HG01346.hp2 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.1053+402_1053+403i others(3): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41615450 | |||||||
| chr8:41615450 | TTG | T | 13 | a0001c0001t0002g0281 a0001c0001t0004g0010 a0001c0001t0004g0039 others(10): Show |
18 | HG01361.hp2 HG01891.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1053+403_1053+404d others(4): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41615450 | |||||||
| chr8:41615451 | T | G | 35 | a0001c0001t0002g0323 a0001c0001t0004g0312 a0001c0001t0006g0013 others(32): Show |
41 | HG00738.hp1 HG01069.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.1053+403T>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41615451 | |||||||
| chr8:41615630 | G | T | 1 | a0001c0001t0005g0119 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1053+582G>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41615630 | |||||||
| chr8:41615768 | G | A | 1 | a0001c0001t0003g0057 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1053+720G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41615768 | |||||||
| chr8:41615898 | G | A | 166 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(163): Show |
206 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(203): Show |
intron_variant | MODIFIER | c.1053+850G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41615898 | |||||||
| chr8:41616265 | T | C | 1 | a0001c0001t0001g0134 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1053+1217T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41616265 | |||||||
| chr8:41616495 | G | T | 2 | a0001c0001t0007g0009 a0001c0001t0053g0041 |
4 | HG02258.hp1 HG02723.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1053+1447G>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41616495 | |||||||
| chr8:41616592 | G | C | 1 | a0001c0001t0031g0042 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1053+1544G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41616592 | |||||||
| chr8:41616710 | C | T | 7 | a0001c0001t0008g0004 a0001c0001t0008g0096 a0001c0001t0008g0097 others(4): Show |
10 | HG02055.hp1 HG02280.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1053+1662C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41616710 | |||||||
| chr8:41616735 | AGTAAAAT others(2): Show |
A | 5 | a0001c0001t0008g0004 a0001c0001t0008g0096 a0001c0001t0008g0097 others(2): Show |
8 | HG02055.hp1 HG02280.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1053+1688_1053+169 others(13): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41616735 | |||||||
| chr8:41616771 | T | C | 189 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(186): Show |
235 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(232): Show |
intron_variant | MODIFIER | c.1053+1723T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41616771 | |||||||
| chr8:41616827 | G | T | 1 | a0001c0001t0003g0089 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1053+1779G>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41616827 | |||||||
| chr8:41616851 | A | T | 1 | a0001c0001t0001g0148 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1053+1803A>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41616851 | |||||||
| chr8:41617095 | T | C | 188 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(185): Show |
234 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(231): Show |
intron_variant | MODIFIER | c.1054-1589T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41617095 | |||||||
| chr8:41617225 | G | A | 1 | a0001c0001t0045g0146 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1054-1459G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41617225 | |||||||
| chr8:41617294 | G | A | 1 | a0001c0001t0002g0298 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1054-1390G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41617294 | |||||||
| chr8:41617338 | T | C | 1 | a0001c0001t0026g0123 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1054-1346T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41617338 | |||||||
| chr8:41617343 | G | A | 5 | a0001c0001t0008g0004 a0001c0001t0008g0096 a0001c0001t0008g0097 others(2): Show |
8 | HG02055.hp1 HG02280.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1054-1341G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41617343 | |||||||
| chr8:41617556 | T | C | 5 | a0001c0001t0004g0010 a0001c0001t0004g0039 a0001c0001t0004g0050 others(2): Show |
7 | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1054-1128T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41617556 | |||||||
| chr8:41617587 | A | T | 188 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(185): Show |
234 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(231): Show |
intron_variant | MODIFIER | c.1054-1097A>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41617587 | |||||||
| chr8:41617674 | G | T | 1 | a0001c0001t0019g0103 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1054-1010G>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41617674 | |||||||
| chr8:41617704 | G | A | 1 | a0001c0001t0043g0144 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1054-980G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41617704 | |||||||
| chr8:41617779 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1054-905C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41617779 | |||||||
| chr8:41618133 | T | G | 1 | a0001c0001t0003g0088 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1054-551T>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41618133 | |||||||
| chr8:41618162 | A | C | 2 | a0001c0001t0001g0258 a0001c0001t0001g0265 |
2 | HG00099.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.1054-522A>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41618162 | |||||||
| chr8:41618169 | T | C | 93 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(90): Show |
120 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.1054-515T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41618169 | |||||||
| chr8:41618231 | T | C | 1 | a0001c0001t0003g0069 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1054-453T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41618231 | |||||||
| chr8:41618370 | T | C | 1 | a0001c0001t0006g0275 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1054-314T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41618370 | |||||||
| chr8:41618443 | G | A | 3 | a0001c0001t0001g0203 a0001c0001t0001g0261 a0001c0001t0001g0263 |
3 | HG00609.hp2 HG02129.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.1054-241G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41618443 | |||||||
| chr8:41618466 | T | C | 5 | a0001c0001t0003g0062 a0001c0001t0003g0065 a0001c0001t0003g0076 others(2): Show |
5 | HG00544.hp2 HG00597.hp2 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.1054-218T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41618466 | |||||||
| chr8:41618484 | G | A | 12 | a0001c0001t0007g0002 a0001c0001t0007g0009 a0001c0001t0007g0043 others(9): Show |
15 | HG00738.hp1 HG01069.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.1054-200G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41618484 | |||||||
| chr8:41618509 | GC | G | 3 | a0001c0001t0004g0316 a0001c0001t0004g0317 a0001c0001t0004g0324 |
3 | HG02559.hp2 HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1054-174delC | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41618509 | |||||||
| chr8:41618538 | G | C | 1 | a0001c0001t0008g0097 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1054-146G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41618538 | |||||||
| chr8:41618630 | G | A | 1 | a0001c0001t0005g0119 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1054-54G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 10/12 | chr8 | 41618630 | |||||||
| chr8:41618864 | G | A | 1 | a0001c0001t0004g0040 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1183-34G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 11/12 | chr8 | 41618864 | |||||||
| chr8:41619025 | T | C | 5 | a0001c0001t0008g0004 a0001c0001t0008g0096 a0001c0001t0008g0097 others(2): Show |
8 | HG02055.hp1 HG02280.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1262+48T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 12/12 | chr8 | 41619025 | |||||||
| chr8:41619152 | GGGAACCT others(15): Show |
G | 1 | a0001c0001t0003g0063 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1262+179_1262+200d others(24): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 41619152 | ||||||
| chr8:41619300 | G | C | 1 | a0001c0001t0006g0104 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1262+323G>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 12/12 | chr8 | 41619300 | |||||||
| chr8:41619472 | A | G | 12 | a0001c0001t0007g0002 a0001c0001t0007g0009 a0001c0001t0007g0043 others(9): Show |
15 | HG00738.hp1 HG01069.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.1262+495A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 12/12 | chr8 | 41619472 | |||||||
| chr8:41619530 | T | C | 2 | a0001c0001t0008g0098 a0001c0001t0008g0099 |
2 | HG02280.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1262+553T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 12/12 | chr8 | 41619530 | |||||||
| chr8:41619572 | A | G | 5 | a0001c0001t0005g0012 a0001c0001t0005g0107 a0001c0001t0005g0108 others(2): Show |
7 | HG02074.hp2 HG02165.hp1 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.1262+595A>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 12/12 | chr8 | 41619572 | |||||||
| chr8:41619919 | C | T | 1 | a0001c0001t0017g0286 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1262+942C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 12/12 | chr8 | 41619919 | |||||||
| chr8:41619921 | C | G | 5 | a0001c0001t0008g0004 a0001c0001t0008g0096 a0001c0001t0008g0097 others(2): Show |
8 | HG02055.hp1 HG02280.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1262+944C>G | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 12/12 | chr8 | 41619921 | |||||||
| chr8:41620161 | G | A | 1 | a0001c0001t0001g0262 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1263-732G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 12/12 | chr8 | 41620161 | |||||||
| chr8:41620165 | C | T | 12 | a0001c0001t0007g0002 a0001c0001t0007g0009 a0001c0001t0007g0043 others(9): Show |
15 | HG00738.hp1 HG01069.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.1263-728C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 12/12 | chr8 | 41620165 | |||||||
| chr8:41620273 | T | C | 337 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0026 others(334): Show |
393 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(390): Show |
intron_variant | MODIFIER | c.1263-620T>C | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 12/12 | chr8 | 41620273 | |||||||
| chr8:41620283 | C | A | 2 | a0001c0001t0001g0241 a0001c0001t0001g0247 |
2 | HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1263-610C>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 12/12 | chr8 | 41620283 | |||||||
| chr8:41620314 | C | CAGGG | 94 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(91): Show |
121 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.1263-575_1263-572d others(6): Show |
GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 41620314 | ||||||
| chr8:41620420 | C | T | 1 | a0001c0001t0023g0289 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1263-473C>T | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 12/12 | chr8 | 41620420 | |||||||
| chr8:41620515 | G | A | 7 | a0001c0001t0008g0004 a0001c0001t0008g0096 a0001c0001t0008g0097 others(4): Show |
10 | HG02055.hp1 HG02280.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1263-378G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 12/12 | chr8 | 41620515 | |||||||
| chr8:41620842 | G | A | 49 | a0001c0001t0003g0003 a0001c0001t0003g0011 a0001c0001t0003g0018 others(46): Show |
58 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.1263-51G>A | GPAT4 | ENSG00000158669.11 | transcript | ENST00000396987.7 | protein_coding | 12/12 | chr8 | 41620842 |