Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55763 |
| ensemblid | ENSG00000090989.18 |
| hgncid | 30380 |
| symbol | EXOC1 |
| name | exocyst complex component 1 |
| refseq_nuc | NM_001024924.2 |
| refseq_prot | NP_001020095.1 |
| ensembl_nuc | ENST00000381295.7 |
| ensembl_prot | ENSP00000370695.2 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 55853648 |
| end | 55905086 |
| strand | + |
| ver | v1.2 |
| region | chr4:55853648-55905086 |
| region5000 | chr4:55848648-55910086 |
| regionname0 | EXOC1_chr4_55853648_55905086 |
| regionname5000 | EXOC1_chr4_55848648_55910086 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 894 | 370 | 86 | 71 | 163 | 10 | 38 | 135 | EXOC1_chr4_55848648_55910086 | EXOC1 | MTAIK others(889): Show |
chr4 | 55848648 | 55910086 |
| a0002 | 0/0 | 894 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | MTAIK others(889): Show |
chr4 | 55848648 | 55910086 |
| a0003 | 0/0 | 894 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | MTAIK others(889): Show |
chr4 | 55848648 | 55910086 |
| a0004 | 0/0 | 894 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | MTAIK others(889): Show |
chr4 | 55848648 | 55910086 |
| a0005 | 0/0 | 894 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EXOC1_chr4_55848648_55910086 | EXOC1 | MTAIK others(889): Show |
chr4 | 55848648 | 55910086 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2682 | 255 | 68 | 48 | 99 | 8 | 30 | EXOC1_chr4_55848648_55910086 | EXOC1 | ATGAC others(2677): Show |
chr4 | 55848648 | 55910086 | ||
| a0001c0002 | 0/0 | 2682 | 106 | 18 | 15 | 63 | 2 | 8 | EXOC1_chr4_55848648_55910086 | EXOC1 | ATGAC others(2677): Show |
chr4 | 55848648 | 55910086 | ||
| a0001c0003 | 0/0 | 2682 | 7 | 0 | 7 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | ATGAC others(2677): Show |
chr4 | 55848648 | 55910086 | ||
| a0001c0006 | 0/0 | 2682 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | ATGAC others(2677): Show |
chr4 | 55848648 | 55910086 | ||
| a0001c0007 | 0/0 | 2682 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | ATGAC others(2677): Show |
chr4 | 55848648 | 55910086 | ||
| a0002c0004 | 0/0 | 2682 | 2 | 2 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | ATGAC others(2677): Show |
chr4 | 55848648 | 55910086 | ||
| a0003c0005 | 0/0 | 2682 | 2 | 0 | 0 | 0 | 0 | 2 | EXOC1_chr4_55848648_55910086 | EXOC1 | ATGAC others(2677): Show |
chr4 | 55848648 | 55910086 | ||
| a0004c0009 | 0/0 | 2682 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | ATGAC others(2677): Show |
chr4 | 55848648 | 55910086 | ||
| a0005c0008 | 0/0 | 2682 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | ATGAC others(2677): Show |
chr4 | 55848648 | 55910086 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3592 | 220 | 59 | 33 | 89 | 8 | 29 | EXOC1_chr4_55848648_55910086 | EXOC1 | GAGTT others(3587): Show |
chr4 | 55848648 | 55910086 |
| a0001c0001t0003 | 0/0 | 3592 | 30 | 6 | 13 | 10 | 0 | 1 | EXOC1_chr4_55848648_55910086 | EXOC1 | GAGTT others(3587): Show |
chr4 | 55848648 | 55910086 |
| a0001c0001t0005 | 0/0 | 3592 | 3 | 3 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | GAGTT others(3587): Show |
chr4 | 55848648 | 55910086 |
| a0001c0001t0006 | 0/0 | 3592 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | GAGTT others(3587): Show |
chr4 | 55848648 | 55910086 |
| a0001c0001t0007 | 0/0 | 3592 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | GAGTT others(3587): Show |
chr4 | 55848648 | 55910086 |
| a0001c0002t0001 | 0/0 | 3592 | 8 | 4 | 3 | 0 | 1 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | GAGTT others(3587): Show |
chr4 | 55848648 | 55910086 |
| a0001c0002t0002 | 0/0 | 3592 | 87 | 7 | 10 | 62 | 1 | 7 | EXOC1_chr4_55848648_55910086 | EXOC1 | GAGTT others(3587): Show |
chr4 | 55848648 | 55910086 |
| a0001c0002t0004 | 0/0 | 3592 | 10 | 6 | 2 | 1 | 0 | 1 | EXOC1_chr4_55848648_55910086 | EXOC1 | GAGTT others(3587): Show |
chr4 | 55848648 | 55910086 |
| a0001c0002t0008 | 0/0 | 3592 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | GAGTT others(3587): Show |
chr4 | 55848648 | 55910086 |
| a0001c0003t0001 | 0/0 | 3592 | 7 | 0 | 7 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | GAGTT others(3587): Show |
chr4 | 55848648 | 55910086 |
| a0001c0006t0002 | 0/0 | 3592 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | GAGTT others(3587): Show |
chr4 | 55848648 | 55910086 |
| a0001c0007t0006 | 0/0 | 3592 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | GAGTT others(3587): Show |
chr4 | 55848648 | 55910086 |
| a0002c0004t0004 | 0/0 | 3592 | 2 | 2 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | GAGTT others(3587): Show |
chr4 | 55848648 | 55910086 |
| a0003c0005t0001 | 0/0 | 3592 | 2 | 0 | 0 | 0 | 0 | 2 | EXOC1_chr4_55848648_55910086 | EXOC1 | GAGTT others(3587): Show |
chr4 | 55848648 | 55910086 |
| a0004c0009t0001 | 0/0 | 3592 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | GAGTT others(3587): Show |
chr4 | 55848648 | 55910086 |
| a0005c0008t0001 | 0/0 | 3592 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | GAGTT others(3587): Show |
chr4 | 55848648 | 55910086 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 7 | 2 | 1 | 2 | 1 | 1 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0004 | 0/0 | 6 | 0 | 0 | 5 | 1 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0006 | 0/0 | 6 | 0 | 0 | 4 | 0 | 2 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0007 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0008 | 0/0 | 5 | 1 | 4 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0009 | 0/0 | 4 | 2 | 1 | 0 | 0 | 1 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0012 | 0/0 | 4 | 2 | 0 | 1 | 0 | 1 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0057 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0059 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0003g0001 | 0/0 | 9 | 1 | 6 | 2 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0003g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0003g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0003g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0005g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0005g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0005g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0006g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0001t0007g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0001g0021 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0002 | 0/0 | 9 | 1 | 0 | 6 | 0 | 2 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0005 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0034 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0004g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0004g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0004g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0004g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0004g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0004g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0004g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0004g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0004g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0002t0008g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0003t0001g0011 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0003t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0003t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0003t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0006t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0001c0007t0006g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0002c0004t0004g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0003c0005t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0003c0005t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0004c0009t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| a0005c0008t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0063 | EUR | GBR | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0062 | EUR | FIN | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0021 | EUR | FIN | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG00438 | hp1 | a0001 | c0002 | t0002 | g0172 | EAS | CHS | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG00438 | hp2 | a0001 | c0002 | t0002 | g0183 | EAS | CHS | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG00558 | hp1 | a0001 | c0002 | t0004 | g0156 | EAS | CHS | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG00621 | hp1 | a0001 | c0002 | t0002 | g0210 | EAS | CHS | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | CHS | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG00639 | hp1 | a0004 | c0009 | t0001 | g0003 | AMR | PUR | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0021 | AMR | PUR | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG00673 | hp2 | a0001 | c0002 | t0002 | g0254 | EAS | CHS | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0081 | AMR | PUR | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG00735 | hp2 | a0001 | c0001 | t0007 | g0060 | AMR | PUR | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0072 | AMR | PUR | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG01069 | hp1 | a0001 | c0002 | t0002 | g0162 | AMR | PUR | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG01070 | hp1 | a0001 | c0001 | t0006 | g0004 | AMR | PUR | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG01074 | hp1 | a0001 | c0002 | t0002 | g0196 | AMR | PUR | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG01081 | hp1 | a0001 | c0002 | t0004 | g0154 | AMR | PUR | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0048 | AMR | PUR | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG01109 | hp2 | a0001 | c0002 | t0002 | g0194 | AMR | PUR | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG01168 | hp2 | a0001 | c0002 | t0002 | g0179 | AMR | PUR | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0022 | AMR | PUR | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG01255 | hp1 | a0001 | c0007 | t0006 | g0004 | AMR | CLM | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | CLM | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG01261 | hp2 | a0001 | c0002 | t0004 | g0088 | AMR | CLM | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0079 | AMR | CLM | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG01346 | hp2 | a0001 | c0003 | t0001 | g0011 | AMR | CLM | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG01433 | hp2 | a0001 | c0003 | t0001 | g0133 | AMR | CLM | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0264 | EUR | IBS | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0111 | EUR | IBS | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0263 | EUR | IBS | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG01884 | hp2 | a0002 | c0004 | t0004 | g0029 | AFR | ACB | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | ACB | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0080 | AMR | PEL | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0078 | AMR | PEL | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0049 | AMR | PEL | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG01978 | hp1 | a0001 | c0002 | t0002 | g0173 | AMR | PEL | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG01978 | hp2 | a0001 | c0003 | t0001 | g0011 | AMR | PEL | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG01981 | hp1 | a0001 | c0003 | t0001 | g0095 | AMR | PEL | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG01981 | hp2 | a0001 | c0002 | t0002 | g0201 | AMR | PEL | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PEL | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02004 | hp1 | a0001 | c0003 | t0001 | g0011 | AMR | PEL | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02015 | hp1 | a0001 | c0002 | t0002 | g0189 | EAS | KHV | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02040 | hp2 | a0001 | c0002 | t0002 | g0035 | EAS | KHV | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | ACB | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02080 | hp1 | a0001 | c0002 | t0002 | g0171 | EAS | KHV | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02129 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | KHV | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02132 | hp2 | a0001 | c0002 | t0002 | g0178 | EAS | KHV | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | ACB | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0022 | AMR | PEL | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02148 | hp2 | a0001 | c0002 | t0002 | g0200 | AMR | PEL | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | CDX | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0077 | EAS | CDX | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0051 | AFR | ACB | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | ACB | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02258 | hp2 | a0001 | c0002 | t0004 | g0020 | AFR | ACB | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02273 | hp1 | a0001 | c0002 | t0002 | g0005 | AMR | PEL | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02273 | hp2 | a0001 | c0003 | t0001 | g0011 | AMR | PEL | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | ACB | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | ACB | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02293 | hp1 | a0001 | c0002 | t0002 | g0212 | AMR | PEL | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02293 | hp2 | a0001 | c0003 | t0001 | g0096 | AMR | PEL | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02300 | hp1 | a0001 | c0002 | t0002 | g0034 | AMR | PEL | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PEL | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0001 | AFR | ACB | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | KHV | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02523 | hp2 | a0001 | c0002 | t0002 | g0035 | EAS | KHV | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02572 | hp1 | a0001 | c0002 | t0004 | g0070 | AFR | GWD | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | GWD | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02602 | hp1 | a0001 | c0002 | t0002 | g0193 | SAS | PJL | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02630 | hp2 | a0001 | c0002 | t0002 | g0202 | AFR | GWD | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02647 | hp2 | a0001 | c0002 | t0004 | g0216 | AFR | GWD | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02698 | hp2 | a0001 | c0002 | t0002 | g0203 | SAS | PJL | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | GWD | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02818 | hp1 | a0001 | c0002 | t0002 | g0181 | AFR | GWD | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0047 | AFR | GWD | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02895 | hp2 | a0001 | c0002 | t0002 | g0002 | AFR | GWD | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02896 | hp1 | a0001 | c0002 | t0002 | g0038 | AFR | GWD | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | ESN | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02965 | hp2 | a0001 | c0002 | t0002 | g0036 | AFR | ESN | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | ESN | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ESN | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | ESN | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG03017 | hp1 | a0001 | c0002 | t0004 | g0155 | SAS | PJL | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG03041 | hp1 | a0001 | c0002 | t0004 | g0215 | AFR | GWD | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG03098 | hp1 | a0001 | c0001 | t0005 | g0046 | AFR | MSL | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | MSL | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG03139 | hp1 | a0001 | c0002 | t0008 | g0020 | AFR | ESN | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG03139 | hp2 | a0001 | c0002 | t0002 | g0038 | AFR | ESN | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0052 | AFR | ESN | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0044 | AFR | MSL | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG03225 | hp2 | a0001 | c0002 | t0004 | g0159 | AFR | MSL | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0258 | SAS | PJL | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | MSL | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | MSL | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG03490 | hp2 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0050 | AFR | ESN | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | ESN | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG03540 | hp2 | a0002 | c0004 | t0004 | g0029 | AFR | GWD | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | MSL | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | MSL | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG03669 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0075 | SAS | PJL | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG03704 | hp2 | a0001 | c0002 | t0002 | g0187 | SAS | PJL | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | BEB | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG03834 | hp1 | a0001 | c0002 | t0002 | g0169 | SAS | BEB | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0259 | SAS | BEB | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0267 | SAS | BEB | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | BEB | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | BEB | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG04115 | hp1 | a0003 | c0005 | t0001 | g0089 | SAS | STU | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | STU | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | BEB | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | BEB | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG04199 | hp1 | a0001 | c0002 | t0002 | g0195 | SAS | STU | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | STU | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0269 | SAS | STU | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG04204 | hp2 | a0003 | c0005 | t0001 | g0090 | SAS | STU | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | STU | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | STU | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18612 | hp1 | a0001 | c0002 | t0002 | g0188 | EAS | CHB | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | CHB | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | YRI | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | YRI | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18940 | hp2 | a0001 | c0002 | t0002 | g0165 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18942 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18945 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18946 | hp2 | a0001 | c0002 | t0002 | g0184 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18947 | hp2 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18949 | hp1 | a0001 | c0002 | t0002 | g0168 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18952 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18953 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18954 | hp1 | a0001 | c0002 | t0002 | g0192 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18956 | hp2 | a0001 | c0002 | t0002 | g0207 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18957 | hp1 | a0001 | c0002 | t0002 | g0034 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18960 | hp1 | a0001 | c0002 | t0002 | g0037 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18960 | hp2 | a0001 | c0002 | t0002 | g0170 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18966 | hp1 | a0001 | c0002 | t0002 | g0205 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18966 | hp2 | a0001 | c0002 | t0002 | g0214 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18968 | hp2 | a0001 | c0002 | t0002 | g0160 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18970 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18972 | hp1 | a0001 | c0002 | t0002 | g0166 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18974 | hp2 | a0005 | c0008 | t0001 | g0027 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18975 | hp2 | a0001 | c0002 | t0002 | g0148 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18977 | hp1 | a0001 | c0002 | t0002 | g0191 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18981 | hp2 | a0001 | c0002 | t0002 | g0177 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18985 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18989 | hp2 | a0001 | c0002 | t0002 | g0208 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18991 | hp2 | a0001 | c0002 | t0002 | g0163 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18992 | hp1 | a0001 | c0002 | t0002 | g0182 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18993 | hp2 | a0001 | c0002 | t0002 | g0209 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18995 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18999 | hp1 | a0001 | c0002 | t0002 | g0150 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19000 | hp2 | a0001 | c0006 | t0002 | g0213 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19003 | hp1 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19006 | hp1 | a0001 | c0002 | t0002 | g0206 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19007 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19009 | hp1 | a0001 | c0002 | t0002 | g0204 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19011 | hp2 | a0001 | c0002 | t0002 | g0198 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | LWK | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | LWK | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19043 | hp1 | a0001 | c0002 | t0004 | g0020 | AFR | LWK | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | LWK | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19057 | hp2 | a0001 | c0002 | t0002 | g0037 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19058 | hp1 | a0001 | c0002 | t0002 | g0175 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19060 | hp1 | a0001 | c0002 | t0002 | g0190 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19060 | hp2 | a0001 | c0002 | t0002 | g0176 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19065 | hp2 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19068 | hp2 | a0001 | c0002 | t0002 | g0167 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19070 | hp1 | a0001 | c0002 | t0002 | g0186 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19072 | hp2 | a0001 | c0002 | t0002 | g0199 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19074 | hp1 | a0001 | c0002 | t0002 | g0161 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19076 | hp1 | a0001 | c0002 | t0002 | g0180 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19077 | hp2 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19082 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19083 | hp1 | a0001 | c0002 | t0002 | g0211 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19084 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19087 | hp2 | a0001 | c0002 | t0002 | g0174 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19088 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19091 | hp1 | a0001 | c0002 | t0002 | g0164 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | YRI | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA20752 | hp1 | a0001 | c0002 | t0002 | g0197 | EUR | TSI | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0262 | EUR | TSI | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | GIH | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | GIH | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | ACB | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | ACB | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG03471 | hp1 | a0001 | c0001 | t0005 | g0045 | AFR | MSL | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | MSL | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | USA | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | USA | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA18955 | hp2 | a0001 | c0002 | t0002 | g0185 | EAS | JPT | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0074 | AFR | USA | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA20300 | hp2 | a0001 | c0002 | t0002 | g0036 | AFR | USA | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | LWK | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | LWK | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0057 | REF | REF | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0059 | REF | REF | EXOC1_chr4_55848648_55910086 | EXOC1 | chr4 | 55848648 | 55910086 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:55858409 | C | G | 1 | a0003 | 2 | HG04115.hp1 HG04204.hp2 |
missense_variant | MODERATE | c.86C>G | p.Ala29Gly | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 2/19 | 402/3592 | 86/2685 | 29/894 | chr4 | 55858409 | |||
| chr4:55858444 | A | C | 1 | a0004 | 1 | HG00639.hp1 | missense_variant | MODERATE | c.121A>C | p.Thr41Pro | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 2/19 | 437/3592 | 121/2685 | 41/894 | chr4 | 55858444 | |||
| chr4:55864230 | A | T | 1 | a0005 | 1 | NA18974.hp2 | missense_variant | MODERATE | c.259A>T | p.Asn87Tyr | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 4/19 | 575/3592 | 259/2685 | 87/894 | chr4 | 55864230 | |||
| chr4:55868368 | A | G | 1 | a0002 | 2 | HG01884.hp2 HG03540.hp2 |
missense_variant | MODERATE | c.448A>G | p.Thr150Ala | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 5/19 | 764/3592 | 448/2685 | 150/894 | chr4 | 55868368 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:55890365 | T | C | 3 | a0001c0002 a0001c0006 a0002c0004 |
109 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(106): Show |
synonymous_variant | LOW | c.1518T>C | p.Ala506Ala | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 12/19 | 1834/3592 | 1518/2685 | 506/894 | chr4 | 55890365 | |||
| chr4:55899827 | A | G | 1 | a0001c0006 | 1 | NA19000.hp2 | synonymous_variant | LOW | c.2280A>G | p.Thr760Thr | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 17/19 | 2596/3592 | 2280/2685 | 760/894 | chr4 | 55899827 | |||
| chr4:55899884 | T | C | 1 | a0001c0003 | 7 | HG01346.hp2 HG01433.hp2 HG01978.hp2 others(4): Show |
splice_region_variant&synonymous_variant | LOW | c.2337T>C | p.Asn779Asn | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 17/19 | 2653/3592 | 2337/2685 | 779/894 | chr4 | 55899884 | |||
| chr4:55902487 | C | T | 1 | a0001c0007 | 1 | HG01255.hp1 | synonymous_variant | LOW | c.2481C>T | p.Asn827Asn | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 18/19 | 2797/3592 | 2481/2685 | 827/894 | chr4 | 55902487 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:55853684 | G | T | 1 | a0001c0002t0008 | 1 | HG03139.hp1 | 5_prime_UTR_variant | MODIFIER | c.-280G>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 1/19 | 4640 | chr4 | 55853684 | ||||||
| chr4:55853705 | A | T | 1 | a0001c0001t0007 | 1 | HG00735.hp2 | 5_prime_UTR_variant | MODIFIER | c.-259A>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 1/19 | 4619 | chr4 | 55853705 | ||||||
| chr4:55904542 | A | C | 3 | a0001c0002t0004 a0001c0002t0008 a0002c0004t0004 |
13 | HG00558.hp1 HG01081.hp1 HG01261.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*47A>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 19/19 | 47 | chr4 | 55904542 | ||||||
| chr4:55904750 | A | G | 1 | a0001c0001t0003 | 30 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*255A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 19/19 | 255 | chr4 | 55904750 | ||||||
| chr4:55904884 | T | A | 1 | a0001c0001t0005 | 3 | HG03098.hp1 HG03225.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*389T>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 19/19 | 389 | chr4 | 55904884 | ||||||
| chr4:55904923 | G | A | 2 | a0001c0002t0002 a0001c0006t0002 |
88 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*428G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 19/19 | 428 | chr4 | 55904923 | ||||||
| chr4:55905010 | A | T | 2 | a0001c0001t0006 a0001c0007t0006 |
2 | HG01070.hp1 HG01255.hp1 |
3_prime_UTR_variant | MODIFIER | c.*515A>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 19/19 | 515 | chr4 | 55905010 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:55854138 | G | A | 3 | a0001c0001t0005g0044 a0001c0001t0005g0045 a0001c0001t0005g0046 |
3 | HG03098.hp1 HG03225.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-11+185G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 1/18 | chr4 | 55854138 | |||||||
| chr4:55854455 | G | T | 19 | a0001c0001t0001g0014 a0001c0001t0001g0043 a0001c0001t0001g0258 others(16): Show |
23 | HG00738.hp2 HG00741.hp1 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.-11+502G>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 1/18 | chr4 | 55854455 | |||||||
| chr4:55854461 | C | T | 2 | a0001c0002t0004g0020 a0001c0002t0008g0020 |
3 | HG02258.hp2 HG03139.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-11+508C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 1/18 | chr4 | 55854461 | |||||||
| chr4:55854493 | A | T | 1 | a0001c0001t0001g0257 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-11+540A>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 1/18 | chr4 | 55854493 | |||||||
| chr4:55854523 | C | T | 3 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0274 |
3 | HG03098.hp2 HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-11+570C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 1/18 | chr4 | 55854523 | |||||||
| chr4:55854544 | A | G | 1 | a0001c0001t0001g0256 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-11+591A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 1/18 | chr4 | 55854544 | |||||||
| chr4:55854698 | G | A | 2 | a0001c0002t0004g0020 a0001c0002t0008g0020 |
3 | HG02258.hp2 HG03139.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-11+745G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 1/18 | chr4 | 55854698 | |||||||
| chr4:55855015 | C | T | 1 | a0001c0001t0001g0255 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-11+1062C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 1/18 | chr4 | 55855015 | |||||||
| chr4:55855144 | A | T | 2 | a0001c0002t0004g0020 a0001c0002t0008g0020 |
3 | HG02258.hp2 HG03139.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-11+1191A>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 1/18 | chr4 | 55855144 | |||||||
| chr4:55855155 | A | T | 1 | a0001c0002t0002g0254 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-11+1202A>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 1/18 | chr4 | 55855155 | |||||||
| chr4:55855237 | G | A | 7 | a0001c0002t0001g0021 a0001c0002t0001g0047 a0001c0002t0001g0048 others(4): Show |
8 | HG00323.hp2 HG00642.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-11+1284G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 1/18 | chr4 | 55855237 | |||||||
| chr4:55855294 | A | G | 242 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(239): Show |
330 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(327): Show |
intron_variant | MODIFIER | c.-11+1341A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 1/18 | chr4 | 55855294 | |||||||
| chr4:55855327 | G | T | 1 | a0001c0001t0001g0253 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-11+1374G>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 1/18 | chr4 | 55855327 | |||||||
| chr4:55855366 | G | T | 8 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(5): Show |
8 | HG01167.hp2 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.-11+1413G>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 1/18 | chr4 | 55855366 | |||||||
| chr4:55855401 | T | C | 2 | a0001c0001t0001g0246 a0001c0001t0001g0257 |
2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-11+1448T>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 1/18 | chr4 | 55855401 | |||||||
| chr4:55855441 | G | A | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | NA18940.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.-11+1488G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 1/18 | chr4 | 55855441 | |||||||
| chr4:55855589 | G | A | 1 | a0001c0002t0004g0070 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-11+1636G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 1/18 | chr4 | 55855589 | |||||||
| chr4:55855851 | T | C | 18 | a0001c0001t0001g0071 a0001c0001t0001g0082 a0001c0001t0003g0001 others(15): Show |
32 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.-11+1898T>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 1/18 | chr4 | 55855851 | |||||||
| chr4:55855891 | AAAG | A | 3 | a0001c0001t0003g0016 a0001c0001t0003g0083 a0001c0001t0003g0084 |
5 | NA18961.hp1 NA18977.hp2 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+1939_-11+1941d others(5): Show |
EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 1/18 | chr4 | 55855891 | |||||||
| chr4:55856007 | C | A | 203 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(200): Show |
278 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(275): Show |
intron_variant | MODIFIER | c.-11+2054C>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 1/18 | chr4 | 55856007 | |||||||
| chr4:55856151 | G | T | 1 | a0001c0001t0001g0067 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-10-2163G>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 1/18 | chr4 | 55856151 | |||||||
| chr4:55856202 | A | G | 3 | a0001c0002t0004g0070 a0001c0002t0004g0215 a0001c0002t0004g0216 |
3 | HG02572.hp1 HG02647.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-10-2112A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 1/18 | chr4 | 55856202 | |||||||
| chr4:55856295 | G | A | 3 | a0001c0001t0005g0044 a0001c0001t0005g0045 a0001c0001t0005g0046 |
3 | HG03098.hp1 HG03225.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-10-2019G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 1/18 | chr4 | 55856295 | |||||||
| chr4:55856323 | G | A | 2 | a0001c0002t0004g0020 a0001c0002t0008g0020 |
3 | HG02258.hp2 HG03139.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-10-1991G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 1/18 | chr4 | 55856323 | |||||||
| chr4:55856582 | CATG | C | 64 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(61): Show |
86 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.-10-1729_-10-1727d others(5): Show |
EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 55856582 | ||||||
| chr4:55856705 | A | G | 1 | a0001c0002t0004g0159 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-10-1609A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 1/18 | chr4 | 55856705 | |||||||
| chr4:55856866 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-10-1448A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 1/18 | chr4 | 55856866 | |||||||
| chr4:55857065 | C | G | 2 | a0001c0001t0001g0273 a0001c0001t0001g0274 |
2 | HG03098.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-10-1249C>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 1/18 | chr4 | 55857065 | |||||||
| chr4:55857075 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-10-1239G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 1/18 | chr4 | 55857075 | |||||||
| chr4:55857168 | C | CT | 27 | a0001c0001t0001g0065 a0001c0001t0001g0158 a0001c0001t0001g0267 others(24): Show |
28 | HG00621.hp1 HG00741.hp1 HG01981.hp2 others(25): Show |
intron_variant | MODIFIER | c.-10-1119dupT | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 55857168 | ||||||
| chr4:55857168 | CT | C | 121 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(118): Show |
175 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.-10-1119delT | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 55857168 | ||||||
| chr4:55857168 | CTT | C | 12 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0217 others(9): Show |
15 | HG00738.hp1 HG02258.hp2 HG02300.hp2 others(12): Show |
intron_variant | MODIFIER | c.-10-1120_-10-1119d others(4): Show |
EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 55857168 | ||||||
| chr4:55857168 | CTTTTTTT others(4): Show |
C | 1 | a0001c0002t0004g0088 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-10-1129_-10-1119d others(13): Show |
EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 55857168 | ||||||
| chr4:55857177 | T | G | 4 | a0001c0001t0001g0023 a0001c0001t0001g0085 a0001c0001t0001g0086 others(1): Show |
5 | HG02809.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10-1137T>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 1/18 | chr4 | 55857177 | |||||||
| chr4:55857192 | T | G | 2 | a0003c0005t0001g0089 a0003c0005t0001g0090 |
2 | HG04115.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-10-1122T>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 1/18 | chr4 | 55857192 | |||||||
| chr4:55857339 | C | G | 1 | a0001c0001t0001g0064 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-10-975C>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 1/18 | chr4 | 55857339 | |||||||
| chr4:55857389 | C | T | 4 | a0001c0002t0004g0070 a0001c0002t0004g0159 a0001c0002t0004g0215 others(1): Show |
4 | HG02572.hp1 HG02647.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10-925C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 1/18 | chr4 | 55857389 | |||||||
| chr4:55857400 | C | A | 1 | a0001c0002t0002g0197 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-10-914C>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 1/18 | chr4 | 55857400 | |||||||
| chr4:55857436 | G | A | 4 | a0001c0002t0004g0070 a0001c0002t0004g0159 a0001c0002t0004g0215 others(1): Show |
4 | HG02572.hp1 HG02647.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10-878G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 1/18 | chr4 | 55857436 | |||||||
| chr4:55857619 | T | C | 1 | a0001c0001t0001g0131 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-10-695T>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 1/18 | chr4 | 55857619 | |||||||
| chr4:55857642 | T | TG | 11 | a0001c0001t0001g0157 a0001c0002t0004g0020 a0001c0002t0004g0070 others(8): Show |
12 | HG00558.hp1 HG01081.hp1 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.-10-670dupG | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | 55857642 | ||||||
| chr4:55857736 | C | A | 1 | a0001c0001t0001g0091 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-10-578C>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 1/18 | chr4 | 55857736 | |||||||
| chr4:55857945 | A | G | 3 | a0001c0002t0004g0070 a0001c0002t0004g0215 a0001c0002t0004g0216 |
3 | HG02572.hp1 HG02647.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-10-369A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 1/18 | chr4 | 55857945 | |||||||
| chr4:55857972 | A | C | 2 | a0001c0001t0001g0265 a0001c0001t0001g0266 |
2 | HG02109.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-10-342A>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 1/18 | chr4 | 55857972 | |||||||
| chr4:55858109 | A | G | 1 | a0002c0004t0004g0029 | 2 | HG01884.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-10-205A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 1/18 | chr4 | 55858109 | |||||||
| chr4:55858307 | T | C | 1 | a0001c0001t0001g0253 | 1 | NA18906.hp1 | splice_region_variant&intron_variant | LOW | c.-10-7T>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 1/18 | chr4 | 55858307 | |||||||
| chr4:55858559 | G | T | 2 | a0001c0001t0001g0265 a0001c0001t0001g0266 |
2 | HG02109.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.124+112G>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 2/18 | chr4 | 55858559 | |||||||
| chr4:55858760 | G | T | 1 | a0001c0001t0001g0240 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.124+313G>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 2/18 | chr4 | 55858760 | |||||||
| chr4:55858879 | G | T | 157 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(154): Show |
215 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(212): Show |
intron_variant | MODIFIER | c.124+432G>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 2/18 | chr4 | 55858879 | |||||||
| chr4:55859483 | A | G | 1 | a0001c0001t0001g0245 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.125-928A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 2/18 | chr4 | 55859483 | |||||||
| chr4:55859531 | T | C | 1 | a0001c0001t0001g0250 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.125-880T>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 2/18 | chr4 | 55859531 | |||||||
| chr4:55859787 | A | G | 1 | a0001c0001t0003g0010 | 4 | HG02280.hp1 HG03471.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.125-624A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 2/18 | chr4 | 55859787 | |||||||
| chr4:55859888 | G | A | 5 | a0001c0001t0001g0157 a0001c0002t0004g0088 a0001c0002t0004g0154 others(2): Show |
5 | HG00558.hp1 HG01081.hp1 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.125-523G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 2/18 | chr4 | 55859888 | |||||||
| chr4:55860075 | C | G | 5 | a0001c0001t0001g0157 a0001c0002t0004g0088 a0001c0002t0004g0154 others(2): Show |
5 | HG00558.hp1 HG01081.hp1 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.125-336C>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 2/18 | chr4 | 55860075 | |||||||
| chr4:55860101 | A | T | 1 | a0001c0001t0001g0153 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.125-310A>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 2/18 | chr4 | 55860101 | |||||||
| chr4:55860121 | T | C | 1 | a0001c0001t0001g0092 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.125-290T>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 2/18 | chr4 | 55860121 | |||||||
| chr4:55860217 | C | T | 8 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0219 others(5): Show |
10 | HG01255.hp2 HG01891.hp2 HG02300.hp2 others(7): Show |
intron_variant | MODIFIER | c.125-194C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 2/18 | chr4 | 55860217 | |||||||
| chr4:55860237 | T | G | 5 | a0001c0001t0001g0157 a0001c0002t0004g0088 a0001c0002t0004g0154 others(2): Show |
5 | HG00558.hp1 HG01081.hp1 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.125-174T>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 2/18 | chr4 | 55860237 | |||||||
| chr4:55860673 | T | A | 5 | a0001c0001t0001g0157 a0001c0002t0004g0088 a0001c0002t0004g0154 others(2): Show |
5 | HG00558.hp1 HG01081.hp1 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.255+132T>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 3/18 | chr4 | 55860673 | |||||||
| chr4:55860679 | A | C | 1 | a0001c0001t0001g0274 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.255+138A>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 3/18 | chr4 | 55860679 | |||||||
| chr4:55860697 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.255+156A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 3/18 | chr4 | 55860697 | |||||||
| chr4:55860725 | TTGAC | T | 11 | a0001c0001t0001g0017 a0001c0001t0001g0028 a0001c0001t0001g0151 others(8): Show |
15 | HG00323.hp2 HG00642.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.255+187_255+190del others(4): Show |
EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 55860725 | ||||||
| chr4:55860854 | A | G | 16 | a0001c0001t0003g0001 a0001c0001t0003g0010 a0001c0001t0003g0016 others(13): Show |
30 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.255+313A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 3/18 | chr4 | 55860854 | |||||||
| chr4:55860938 | T | G | 36 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0017 others(33): Show |
53 | HG00408.hp1 HG00558.hp2 HG01346.hp2 others(50): Show |
intron_variant | MODIFIER | c.255+397T>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 3/18 | chr4 | 55860938 | |||||||
| chr4:55860958 | C | CA | 9 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0219 others(6): Show |
11 | HG01255.hp2 HG01891.hp2 HG02300.hp2 others(8): Show |
intron_variant | MODIFIER | c.255+432dupA | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 55860958 | ||||||
| chr4:55861165 | A | T | 1 | a0001c0001t0001g0130 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.255+624A>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 3/18 | chr4 | 55861165 | |||||||
| chr4:55861282 | G | A | 4 | a0001c0002t0004g0070 a0001c0002t0004g0159 a0001c0002t0004g0215 others(1): Show |
4 | HG02572.hp1 HG02647.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.255+741G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 3/18 | chr4 | 55861282 | |||||||
| chr4:55861322 | G | A | 7 | a0001c0002t0001g0021 a0001c0002t0001g0047 a0001c0002t0001g0048 others(4): Show |
8 | HG00323.hp2 HG00642.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.255+781G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 3/18 | chr4 | 55861322 | |||||||
| chr4:55861385 | A | T | 11 | a0001c0001t0001g0157 a0001c0002t0004g0020 a0001c0002t0004g0070 others(8): Show |
12 | HG00558.hp1 HG01081.hp1 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.255+844A>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 3/18 | chr4 | 55861385 | |||||||
| chr4:55861525 | G | A | 1 | a0001c0001t0001g0141 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.255+984G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 3/18 | chr4 | 55861525 | |||||||
| chr4:55861589 | G | T | 5 | a0001c0001t0001g0157 a0001c0002t0004g0088 a0001c0002t0004g0154 others(2): Show |
5 | HG00558.hp1 HG01081.hp1 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.255+1048G>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 3/18 | chr4 | 55861589 | |||||||
| chr4:55861710 | C | T | 8 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(5): Show |
8 | HG01167.hp2 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.255+1169C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 3/18 | chr4 | 55861710 | |||||||
| chr4:55861912 | G | A | 4 | a0001c0001t0001g0023 a0001c0001t0001g0085 a0001c0001t0001g0086 others(1): Show |
5 | HG02809.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.255+1371G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 3/18 | chr4 | 55861912 | |||||||
| chr4:55861962 | G | C | 2 | a0001c0002t0004g0020 a0001c0002t0008g0020 |
3 | HG02258.hp2 HG03139.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.255+1421G>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 3/18 | chr4 | 55861962 | |||||||
| chr4:55861992 | T | TGCAGTGA others(12): Show |
5 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0249 others(2): Show |
5 | HG01167.hp2 HG02258.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.255+1452_255+1470d others(21): Show |
EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 55861992 | ||||||
| chr4:55862043 | G | A | 4 | a0001c0002t0002g0034 a0001c0002t0002g0164 a0001c0002t0002g0165 others(1): Show |
5 | HG02300.hp1 NA18940.hp2 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.255+1502G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 3/18 | chr4 | 55862043 | |||||||
| chr4:55862056 | C | CA | 19 | a0001c0001t0003g0001 a0001c0001t0003g0010 a0001c0001t0003g0016 others(16): Show |
33 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.255+1524dupA | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 55862056 | ||||||
| chr4:55862204 | T | A | 1 | a0001c0001t0001g0107 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.255+1663T>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 3/18 | chr4 | 55862204 | |||||||
| chr4:55862316 | A | AT | 43 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0017 others(40): Show |
61 | HG00408.hp1 HG00558.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.255+1787dupT | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 55862316 | ||||||
| chr4:55862316 | AT | A | 7 | a0001c0002t0001g0021 a0001c0002t0001g0047 a0001c0002t0001g0048 others(4): Show |
8 | HG00323.hp2 HG00642.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.255+1787delT | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 55862316 | ||||||
| chr4:55862462 | T | G | 1 | a0001c0001t0001g0217 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.256-1765T>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 3/18 | chr4 | 55862462 | |||||||
| chr4:55862553 | T | G | 5 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0249 others(2): Show |
5 | HG01167.hp2 HG02258.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.256-1674T>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 3/18 | chr4 | 55862553 | |||||||
| chr4:55862609 | G | A | 1 | a0001c0001t0005g0044 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.256-1618G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 3/18 | chr4 | 55862609 | |||||||
| chr4:55862615 | A | G | 1 | a0001c0002t0002g0195 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.256-1612A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 3/18 | chr4 | 55862615 | |||||||
| chr4:55862756 | A | G | 1 | a0001c0001t0001g0250 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.256-1471A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 3/18 | chr4 | 55862756 | |||||||
| chr4:55862885 | A | G | 2 | a0001c0001t0001g0071 a0001c0001t0001g0082 |
2 | HG01884.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.256-1342A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 3/18 | chr4 | 55862885 | |||||||
| chr4:55862956 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.256-1271G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 3/18 | chr4 | 55862956 | |||||||
| chr4:55862999 | C | T | 1 | a0001c0001t0001g0106 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.256-1228C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 3/18 | chr4 | 55862999 | |||||||
| chr4:55863176 | A | T | 1 | a0001c0002t0002g0197 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.256-1051A>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 3/18 | chr4 | 55863176 | |||||||
| chr4:55863301 | C | T | 3 | a0001c0002t0002g0162 a0001c0002t0002g0193 a0001c0002t0002g0194 |
3 | HG01069.hp1 HG01109.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.256-926C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 3/18 | chr4 | 55863301 | |||||||
| chr4:55863403 | C | T | 30 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(27): Show |
41 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.256-824C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 3/18 | chr4 | 55863403 | |||||||
| chr4:55863721 | C | T | 1 | a0002c0004t0004g0029 | 2 | HG01884.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.256-506C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 3/18 | chr4 | 55863721 | |||||||
| chr4:55863813 | G | A | 1 | a0001c0002t0002g0169 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.256-414G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 3/18 | chr4 | 55863813 | |||||||
| chr4:55863953 | A | G | 2 | a0001c0002t0004g0020 a0001c0002t0008g0020 |
3 | HG02258.hp2 HG03139.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.256-274A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 3/18 | chr4 | 55863953 | |||||||
| chr4:55863982 | T | G | 1 | a0001c0002t0002g0170 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.256-245T>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 3/18 | chr4 | 55863982 | |||||||
| chr4:55864138 | A | G | 66 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(63): Show |
88 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.256-89A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 3/18 | chr4 | 55864138 | |||||||
| chr4:55864442 | T | C | 1 | a0001c0002t0004g0159 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.415+56T>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 4/18 | chr4 | 55864442 | |||||||
| chr4:55864477 | ATTATC | A | 4 | a0001c0001t0001g0023 a0001c0001t0001g0085 a0001c0001t0001g0086 others(1): Show |
5 | HG02809.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.415+97_415+101delT others(4): Show |
EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr4 | 55864477 | ||||||
| chr4:55864487 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.415+101C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 4/18 | chr4 | 55864487 | |||||||
| chr4:55864553 | T | G | 16 | a0001c0001t0003g0001 a0001c0001t0003g0010 a0001c0001t0003g0016 others(13): Show |
30 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.415+167T>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 4/18 | chr4 | 55864553 | |||||||
| chr4:55864983 | C | G | 1 | a0001c0002t0004g0216 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.415+597C>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 4/18 | chr4 | 55864983 | |||||||
| chr4:55864997 | C | G | 1 | a0001c0001t0001g0250 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.415+611C>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 4/18 | chr4 | 55864997 | |||||||
| chr4:55865006 | T | G | 1 | a0001c0001t0001g0158 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.415+620T>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 4/18 | chr4 | 55865006 | |||||||
| chr4:55865061 | G | T | 1 | a0001c0002t0004g0216 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.415+675G>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 4/18 | chr4 | 55865061 | |||||||
| chr4:55865276 | T | C | 1 | a0002c0004t0004g0029 | 2 | HG01884.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.415+890T>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 4/18 | chr4 | 55865276 | |||||||
| chr4:55865493 | G | A | 2 | a0001c0001t0003g0072 a0001c0001t0003g0081 |
2 | HG00735.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.415+1107G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 4/18 | chr4 | 55865493 | |||||||
| chr4:55865565 | C | T | 1 | a0001c0001t0003g0080 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.415+1179C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 4/18 | chr4 | 55865565 | |||||||
| chr4:55865593 | C | A | 3 | a0001c0001t0005g0044 a0001c0001t0005g0045 a0001c0001t0005g0046 |
3 | HG03098.hp1 HG03225.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.415+1207C>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 4/18 | chr4 | 55865593 | |||||||
| chr4:55865673 | G | A | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG01243.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.415+1287G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 4/18 | chr4 | 55865673 | |||||||
| chr4:55865677 | T | G | 36 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0017 others(33): Show |
53 | HG00408.hp1 HG00558.hp2 HG01346.hp2 others(50): Show |
intron_variant | MODIFIER | c.415+1291T>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 4/18 | chr4 | 55865677 | |||||||
| chr4:55865769 | A | G | 2 | a0001c0001t0001g0235 a0001c0001t0001g0236 |
2 | NA18959.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.415+1383A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 4/18 | chr4 | 55865769 | |||||||
| chr4:55865797 | T | G | 71 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(68): Show |
104 | HG00408.hp2 HG00639.hp1 HG00639.hp2 others(101): Show |
intron_variant | MODIFIER | c.415+1411T>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 4/18 | chr4 | 55865797 | |||||||
| chr4:55865820 | C | A | 5 | a0001c0001t0001g0157 a0001c0002t0004g0088 a0001c0002t0004g0154 others(2): Show |
5 | HG00558.hp1 HG01081.hp1 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.415+1434C>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 4/18 | chr4 | 55865820 | |||||||
| chr4:55865975 | G | A | 2 | a0001c0001t0001g0055 a0001c0001t0001g0056 |
2 | NA19002.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.415+1589G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 4/18 | chr4 | 55865975 | |||||||
| chr4:55866055 | A | T | 1 | a0001c0001t0001g0253 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.415+1669A>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 4/18 | chr4 | 55866055 | |||||||
| chr4:55866171 | A | G | 2 | a0001c0001t0001g0008 a0001c0001t0001g0128 |
6 | HG01070.hp2 HG01071.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.415+1785A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 4/18 | chr4 | 55866171 | |||||||
| chr4:55866627 | G | A | 1 | a0001c0002t0004g0216 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.416-1709G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 4/18 | chr4 | 55866627 | |||||||
| chr4:55866689 | G | A | 5 | a0001c0001t0001g0157 a0001c0002t0004g0088 a0001c0002t0004g0154 others(2): Show |
5 | HG00558.hp1 HG01081.hp1 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.416-1647G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 4/18 | chr4 | 55866689 | |||||||
| chr4:55866714 | T | G | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | NA19240.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.416-1622T>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 4/18 | chr4 | 55866714 | |||||||
| chr4:55866729 | G | C | 1 | a0001c0002t0001g0048 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.416-1607G>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 4/18 | chr4 | 55866729 | |||||||
| chr4:55866731 | T | C | 2 | a0001c0001t0001g0071 a0001c0001t0001g0082 |
2 | HG01884.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.416-1605T>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 4/18 | chr4 | 55866731 | |||||||
| chr4:55867008 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.416-1328C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 4/18 | chr4 | 55867008 | |||||||
| chr4:55867028 | TG | T | 4 | a0001c0003t0001g0011 a0001c0003t0001g0095 a0001c0003t0001g0096 others(1): Show |
7 | HG01346.hp2 HG01433.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.416-1307delG | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 4/18 | chr4 | 55867028 | |||||||
| chr4:55867209 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.416-1127C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 4/18 | chr4 | 55867209 | |||||||
| chr4:55867230 | G | A | 4 | a0001c0001t0001g0023 a0001c0001t0001g0085 a0001c0001t0001g0086 others(1): Show |
5 | HG02809.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.416-1106G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 4/18 | chr4 | 55867230 | |||||||
| chr4:55867239 | A | T | 2 | a0001c0001t0001g0071 a0001c0001t0001g0082 |
2 | HG01884.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.416-1097A>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 4/18 | chr4 | 55867239 | |||||||
| chr4:55867541 | G | A | 4 | a0001c0002t0002g0169 a0001c0002t0002g0171 a0001c0002t0002g0172 others(1): Show |
4 | HG00438.hp1 HG02080.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.416-795G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 4/18 | chr4 | 55867541 | |||||||
| chr4:55867561 | C | A | 20 | a0001c0001t0001g0023 a0001c0001t0001g0085 a0001c0001t0001g0086 others(17): Show |
35 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.416-775C>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 4/18 | chr4 | 55867561 | |||||||
| chr4:55867564 | C | CA | 50 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(47): Show |
69 | HG00408.hp2 HG00639.hp1 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.416-756dupA | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr4 | 55867564 | ||||||
| chr4:55867564 | CA | C | 9 | a0001c0001t0001g0071 a0001c0001t0001g0082 a0001c0001t0001g0085 others(6): Show |
9 | HG01884.hp1 HG01891.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.416-756delA | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr4 | 55867564 | ||||||
| chr4:55867661 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.416-675A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 4/18 | chr4 | 55867661 | |||||||
| chr4:55867727 | T | C | 3 | a0001c0002t0002g0173 a0001c0002t0002g0200 a0001c0002t0002g0201 |
3 | HG01978.hp1 HG01981.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.416-609T>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 4/18 | chr4 | 55867727 | |||||||
| chr4:55867736 | T | C | 1 | a0001c0001t0001g0142 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.416-600T>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 4/18 | chr4 | 55867736 | |||||||
| chr4:55867893 | A | G | 5 | a0001c0001t0001g0157 a0001c0002t0004g0088 a0001c0002t0004g0154 others(2): Show |
5 | HG00558.hp1 HG01081.hp1 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.416-443A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 4/18 | chr4 | 55867893 | |||||||
| chr4:55867995 | C | T | 3 | a0001c0001t0003g0079 a0001c0002t0004g0020 a0001c0002t0008g0020 |
4 | HG01346.hp1 HG02258.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.416-341C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 4/18 | chr4 | 55867995 | |||||||
| chr4:55868097 | T | G | 2 | a0001c0001t0001g0071 a0001c0001t0001g0082 |
2 | HG01884.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.416-239T>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 4/18 | chr4 | 55868097 | |||||||
| chr4:55868307 | A | G | 1 | a0001c0001t0003g0084 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.416-29A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 4/18 | chr4 | 55868307 | |||||||
| chr4:55868309 | T | G | 4 | a0001c0002t0004g0070 a0001c0002t0004g0159 a0001c0002t0004g0215 others(1): Show |
4 | HG02572.hp1 HG02647.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.416-27T>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 4/18 | chr4 | 55868309 | |||||||
| chr4:55868535 | C | T | 156 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(153): Show |
213 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(210): Show |
intron_variant | MODIFIER | c.603+12C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 5/18 | chr4 | 55868535 | |||||||
| chr4:55868620 | A | G | 1 | a0001c0001t0003g0078 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.603+97A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 5/18 | chr4 | 55868620 | |||||||
| chr4:55868624 | T | G | 1 | a0003c0005t0001g0089 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.603+101T>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 5/18 | chr4 | 55868624 | |||||||
| chr4:55868634 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.603+111A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 5/18 | chr4 | 55868634 | |||||||
| chr4:55868667 | C | G | 2 | a0001c0001t0001g0071 a0001c0001t0001g0082 |
2 | HG01884.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.603+144C>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 5/18 | chr4 | 55868667 | |||||||
| chr4:55868679 | G | C | 1 | a0001c0002t0004g0159 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.603+156G>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 5/18 | chr4 | 55868679 | |||||||
| chr4:55868707 | G | A | 1 | a0001c0001t0001g0259 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.603+184G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 5/18 | chr4 | 55868707 | |||||||
| chr4:55868781 | A | C | 3 | a0001c0001t0005g0044 a0001c0001t0005g0045 a0001c0001t0005g0046 |
3 | HG03098.hp1 HG03225.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.603+258A>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 5/18 | chr4 | 55868781 | |||||||
| chr4:55869019 | A | G | 1 | a0002c0004t0004g0029 | 2 | HG01884.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.603+496A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 5/18 | chr4 | 55869019 | |||||||
| chr4:55869123 | T | C | 3 | a0001c0001t0001g0023 a0001c0001t0001g0086 a0001c0001t0001g0087 |
4 | HG02809.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.603+600T>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 5/18 | chr4 | 55869123 | |||||||
| chr4:55869182 | A | G | 73 | a0001c0002t0001g0021 a0001c0002t0001g0047 a0001c0002t0001g0048 others(70): Show |
96 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.603+659A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 5/18 | chr4 | 55869182 | |||||||
| chr4:55869246 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.603+723G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 5/18 | chr4 | 55869246 | |||||||
| chr4:55869320 | C | T | 1 | a0001c0002t0002g0192 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.603+797C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 5/18 | chr4 | 55869320 | |||||||
| chr4:55869666 | G | A | 48 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(45): Show |
66 | HG00408.hp2 HG00639.hp1 HG01070.hp2 others(63): Show |
intron_variant | MODIFIER | c.604-1012G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 5/18 | chr4 | 55869666 | |||||||
| chr4:55869863 | T | C | 2 | a0001c0001t0001g0031 a0001c0001t0001g0127 |
3 | NA18953.hp1 NA18959.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.604-815T>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 5/18 | chr4 | 55869863 | |||||||
| chr4:55870020 | A | T | 1 | a0001c0001t0001g0217 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.604-658A>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 5/18 | chr4 | 55870020 | |||||||
| chr4:55870028 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.604-650A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 5/18 | chr4 | 55870028 | |||||||
| chr4:55870073 | T | C | 2 | a0001c0002t0002g0035 a0001c0002t0002g0174 |
3 | HG02040.hp2 HG02523.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.604-605T>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 5/18 | chr4 | 55870073 | |||||||
| chr4:55870126 | C | T | 69 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(66): Show |
102 | HG00408.hp2 HG00639.hp1 HG00639.hp2 others(99): Show |
intron_variant | MODIFIER | c.604-552C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 5/18 | chr4 | 55870126 | |||||||
| chr4:55870155 | T | A | 5 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0249 others(2): Show |
5 | HG01167.hp2 HG02258.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.604-523T>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 5/18 | chr4 | 55870155 | |||||||
| chr4:55870175 | A | G | 15 | a0001c0001t0003g0001 a0001c0001t0003g0016 a0001c0001t0003g0022 others(12): Show |
26 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.604-503A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 5/18 | chr4 | 55870175 | |||||||
| chr4:55870261 | A | G | 2 | a0001c0002t0002g0191 a0001c0002t0002g0214 |
2 | NA18966.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.604-417A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 5/18 | chr4 | 55870261 | |||||||
| chr4:55870454 | A | G | 9 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0217 others(6): Show |
11 | HG01255.hp2 HG01891.hp2 HG02300.hp2 others(8): Show |
intron_variant | MODIFIER | c.604-224A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 5/18 | chr4 | 55870454 | |||||||
| chr4:55870533 | G | A | 53 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(50): Show |
72 | HG00408.hp2 HG00639.hp1 HG01070.hp2 others(69): Show |
intron_variant | MODIFIER | c.604-145G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 5/18 | chr4 | 55870533 | |||||||
| chr4:55870607 | C | T | 5 | a0001c0001t0001g0157 a0001c0002t0004g0088 a0001c0002t0004g0154 others(2): Show |
5 | HG00558.hp1 HG01081.hp1 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.604-71C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 5/18 | chr4 | 55870607 | |||||||
| chr4:55870628 | T | TTTTG | 111 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(108): Show |
151 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.604-22_604-19dupGT others(2): Show |
EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr4 | 55870628 | ||||||
| chr4:55870628 | T | TTTTGTTT others(1): Show |
2 | a0001c0001t0001g0026 a0001c0001t0001g0108 |
3 | HG01099.hp1 HG01106.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.604-26_604-19dupGT others(6): Show |
EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr4 | 55870628 | ||||||
| chr4:55870628 | TTTTG | T | 4 | a0001c0001t0001g0054 a0001c0001t0005g0044 a0001c0001t0005g0045 others(1): Show |
4 | HG02886.hp1 HG03098.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.604-22_604-19delGT others(2): Show |
EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr4 | 55870628 | ||||||
| chr4:55871323 | G | A | 66 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(63): Show |
88 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.964+90G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 7/18 | chr4 | 55871323 | |||||||
| chr4:55871404 | T | C | 2 | a0001c0001t0001g0031 a0001c0001t0001g0127 |
3 | NA18953.hp1 NA18959.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.964+171T>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 7/18 | chr4 | 55871404 | |||||||
| chr4:55871437 | A | G | 9 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0217 others(6): Show |
11 | HG01255.hp2 HG01891.hp2 HG02300.hp2 others(8): Show |
intron_variant | MODIFIER | c.964+204A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 7/18 | chr4 | 55871437 | |||||||
| chr4:55871464 | A | C | 3 | a0001c0001t0001g0023 a0001c0001t0001g0086 a0001c0001t0001g0087 |
4 | HG02809.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.964+231A>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 7/18 | chr4 | 55871464 | |||||||
| chr4:55871514 | G | C | 11 | a0001c0001t0001g0157 a0001c0002t0004g0020 a0001c0002t0004g0070 others(8): Show |
12 | HG00558.hp1 HG01081.hp1 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.964+281G>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 7/18 | chr4 | 55871514 | |||||||
| chr4:55871543 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.965-306C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 7/18 | chr4 | 55871543 | |||||||
| chr4:55871544 | G | A | 4 | a0001c0001t0001g0023 a0001c0001t0001g0085 a0001c0001t0001g0086 others(1): Show |
5 | HG02809.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.965-305G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 7/18 | chr4 | 55871544 | |||||||
| chr4:55871591 | A | G | 1 | a0001c0002t0002g0190 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.965-258A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 7/18 | chr4 | 55871591 | |||||||
| chr4:55871592 | G | C | 1 | a0001c0001t0001g0219 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.965-257G>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 7/18 | chr4 | 55871592 | |||||||
| chr4:55871734 | T | C | 5 | a0001c0001t0001g0157 a0001c0002t0004g0088 a0001c0002t0004g0154 others(2): Show |
5 | HG00558.hp1 HG01081.hp1 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.965-115T>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 7/18 | chr4 | 55871734 | |||||||
| chr4:55871978 | A | T | 2 | a0001c0002t0004g0020 a0001c0002t0008g0020 |
3 | HG02258.hp2 HG03139.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1074+20A>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 8/18 | chr4 | 55871978 | |||||||
| chr4:55871982 | C | T | 2 | a0001c0001t0001g0124 a0001c0001t0001g0146 |
2 | NA18975.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.1074+24C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 8/18 | chr4 | 55871982 | |||||||
| chr4:55872107 | C | T | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG00140.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.1074+149C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 8/18 | chr4 | 55872107 | |||||||
| chr4:55872154 | C | T | 1 | a0001c0001t0001g0123 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1074+196C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 8/18 | chr4 | 55872154 | |||||||
| chr4:55872246 | T | TA | 11 | a0001c0001t0001g0157 a0001c0002t0004g0020 a0001c0002t0004g0070 others(8): Show |
12 | HG00558.hp1 HG01081.hp1 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.1074+291dupA | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr4 | 55872246 | ||||||
| chr4:55872260 | A | G | 2 | a0001c0001t0001g0219 a0001c0001t0001g0220 |
2 | HG02300.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1074+302A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 8/18 | chr4 | 55872260 | |||||||
| chr4:55872323 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1074+365C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 8/18 | chr4 | 55872323 | |||||||
| chr4:55872357 | A | G | 5 | a0001c0001t0001g0157 a0001c0002t0004g0088 a0001c0002t0004g0154 others(2): Show |
5 | HG00558.hp1 HG01081.hp1 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.1074+399A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 8/18 | chr4 | 55872357 | |||||||
| chr4:55872394 | C | CTG | 167 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(164): Show |
225 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(222): Show |
intron_variant | MODIFIER | c.1074+437_1074+438i others(4): Show |
EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr4 | 55872394 | ||||||
| chr4:55872646 | A | G | 11 | a0001c0001t0001g0157 a0001c0002t0004g0020 a0001c0002t0004g0070 others(8): Show |
12 | HG00558.hp1 HG01081.hp1 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.1074+688A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 8/18 | chr4 | 55872646 | |||||||
| chr4:55872721 | A | T | 15 | a0001c0001t0001g0008 a0001c0001t0001g0027 a0001c0001t0001g0031 others(12): Show |
20 | HG01070.hp2 HG01071.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.1074+763A>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 8/18 | chr4 | 55872721 | |||||||
| chr4:55872847 | GT | G | 16 | a0001c0001t0003g0001 a0001c0001t0003g0010 a0001c0001t0003g0016 others(13): Show |
30 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.1074+900delT | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr4 | 55872847 | ||||||
| chr4:55872858 | T | C | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | NA19240.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1074+900T>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 8/18 | chr4 | 55872858 | |||||||
| chr4:55872967 | A | G | 1 | a0001c0002t0004g0159 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1074+1009A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 8/18 | chr4 | 55872967 | |||||||
| chr4:55873064 | C | T | 4 | a0001c0002t0004g0070 a0001c0002t0004g0159 a0001c0002t0004g0215 others(1): Show |
4 | HG02572.hp1 HG02647.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1074+1106C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 8/18 | chr4 | 55873064 | |||||||
| chr4:55873118 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1074+1160G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 8/18 | chr4 | 55873118 | |||||||
| chr4:55873222 | C | T | 1 | a0002c0004t0004g0029 | 2 | HG01884.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1074+1264C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 8/18 | chr4 | 55873222 | |||||||
| chr4:55873800 | G | T | 11 | a0001c0001t0001g0157 a0001c0002t0004g0020 a0001c0002t0004g0070 others(8): Show |
12 | HG00558.hp1 HG01081.hp1 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.1074+1842G>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 8/18 | chr4 | 55873800 | |||||||
| chr4:55874175 | G | A | 1 | a0001c0001t0001g0271 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1074+2217G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 8/18 | chr4 | 55874175 | |||||||
| chr4:55874320 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1074+2362C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 8/18 | chr4 | 55874320 | |||||||
| chr4:55874384 | A | G | 1 | a0001c0002t0002g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1074+2426A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 8/18 | chr4 | 55874384 | |||||||
| chr4:55874433 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1074+2475A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 8/18 | chr4 | 55874433 | |||||||
| chr4:55874609 | G | A | 1 | a0001c0002t0002g0202 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1074+2651G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 8/18 | chr4 | 55874609 | |||||||
| chr4:55874682 | T | G | 1 | a0001c0002t0002g0175 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1074+2724T>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 8/18 | chr4 | 55874682 | |||||||
| chr4:55874931 | T | A | 1 | a0001c0001t0001g0109 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1074+2973T>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 8/18 | chr4 | 55874931 | |||||||
| chr4:55875012 | A | G | 1 | a0001c0001t0001g0062 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1075-2905A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 8/18 | chr4 | 55875012 | |||||||
| chr4:55875075 | A | G | 2 | a0001c0001t0001g0157 a0001c0002t0004g0156 |
2 | HG00558.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.1075-2842A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 8/18 | chr4 | 55875075 | |||||||
| chr4:55875117 | A | G | 5 | a0001c0001t0001g0157 a0001c0002t0004g0088 a0001c0002t0004g0154 others(2): Show |
5 | HG00558.hp1 HG01081.hp1 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.1075-2800A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 8/18 | chr4 | 55875117 | |||||||
| chr4:55875151 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1075-2766G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 8/18 | chr4 | 55875151 | |||||||
| chr4:55875161 | T | G | 1 | a0001c0002t0004g0216 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1075-2756T>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 8/18 | chr4 | 55875161 | |||||||
| chr4:55875182 | C | T | 2 | a0001c0001t0001g0265 a0001c0001t0001g0266 |
2 | HG02109.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1075-2735C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 8/18 | chr4 | 55875182 | |||||||
| chr4:55875195 | T | C | 16 | a0001c0001t0003g0001 a0001c0001t0003g0010 a0001c0001t0003g0016 others(13): Show |
30 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.1075-2722T>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 8/18 | chr4 | 55875195 | |||||||
| chr4:55875448 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1075-2469A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 8/18 | chr4 | 55875448 | |||||||
| chr4:55875566 | A | C | 3 | a0001c0001t0005g0044 a0001c0001t0005g0045 a0001c0001t0005g0046 |
3 | HG03098.hp1 HG03225.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1075-2351A>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 8/18 | chr4 | 55875566 | |||||||
| chr4:55875857 | G | A | 1 | a0002c0004t0004g0029 | 2 | HG01884.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1075-2060G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 8/18 | chr4 | 55875857 | |||||||
| chr4:55875945 | A | G | 16 | a0001c0001t0003g0001 a0001c0001t0003g0010 a0001c0001t0003g0016 others(13): Show |
30 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.1075-1972A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 8/18 | chr4 | 55875945 | |||||||
| chr4:55876004 | G | C | 3 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 |
3 | HG01515.hp2 HG04115.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1075-1913G>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 8/18 | chr4 | 55876004 | |||||||
| chr4:55876039 | G | A | 202 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(199): Show |
277 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(274): Show |
intron_variant | MODIFIER | c.1075-1878G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 8/18 | chr4 | 55876039 | |||||||
| chr4:55876095 | A | G | 1 | a0001c0001t0001g0250 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1075-1822A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 8/18 | chr4 | 55876095 | |||||||
| chr4:55876179 | T | C | 1 | a0001c0001t0001g0272 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1075-1738T>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 8/18 | chr4 | 55876179 | |||||||
| chr4:55876318 | C | T | 3 | a0001c0002t0002g0171 a0001c0002t0002g0172 a0001c0002t0002g0199 |
3 | HG00438.hp1 HG02080.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.1075-1599C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 8/18 | chr4 | 55876318 | |||||||
| chr4:55876592 | A | G | 3 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0140 |
3 | NA18985.hp1 NA18991.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.1075-1325A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 8/18 | chr4 | 55876592 | |||||||
| chr4:55876636 | G | T | 2 | a0001c0002t0004g0020 a0001c0002t0008g0020 |
3 | HG02258.hp2 HG03139.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1075-1281G>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 8/18 | chr4 | 55876636 | |||||||
| chr4:55876637 | C | T | 2 | a0001c0002t0004g0020 a0001c0002t0008g0020 |
3 | HG02258.hp2 HG03139.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1075-1280C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 8/18 | chr4 | 55876637 | |||||||
| chr4:55876874 | A | G | 4 | a0001c0001t0001g0040 a0001c0001t0001g0237 a0001c0001t0001g0238 others(1): Show |
5 | HG01255.hp2 HG01891.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1075-1043A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 8/18 | chr4 | 55876874 | |||||||
| chr4:55877110 | C | T | 53 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(50): Show |
72 | HG00408.hp2 HG00639.hp1 HG01070.hp2 others(69): Show |
intron_variant | MODIFIER | c.1075-807C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 8/18 | chr4 | 55877110 | |||||||
| chr4:55877156 | T | C | 1 | a0001c0001t0001g0141 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1075-761T>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 8/18 | chr4 | 55877156 | |||||||
| chr4:55877239 | A | G | 1 | a0001c0001t0001g0217 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1075-678A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 8/18 | chr4 | 55877239 | |||||||
| chr4:55877506 | A | T | 4 | a0001c0002t0004g0088 a0001c0002t0004g0154 a0001c0002t0004g0155 others(1): Show |
4 | HG00558.hp1 HG01081.hp1 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.1075-411A>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 8/18 | chr4 | 55877506 | |||||||
| chr4:55877713 | TATG | T | 3 | a0001c0001t0005g0044 a0001c0001t0005g0045 a0001c0001t0005g0046 |
3 | HG03098.hp1 HG03225.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1075-203_1075-201d others(5): Show |
EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 8/18 | chr4 | 55877713 | |||||||
| chr4:55877867 | G | A | 2 | a0001c0002t0004g0070 a0001c0002t0004g0215 |
2 | HG02572.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1075-50G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 8/18 | chr4 | 55877867 | |||||||
| chr4:55878080 | G | A | 3 | a0001c0001t0005g0044 a0001c0001t0005g0045 a0001c0001t0005g0046 |
3 | HG03098.hp1 HG03225.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1224+14G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 9/18 | chr4 | 55878080 | |||||||
| chr4:55878635 | A | C | 1 | a0001c0001t0001g0264 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1224+569A>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 9/18 | chr4 | 55878635 | |||||||
| chr4:55878756 | A | C | 1 | a0001c0001t0001g0065 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1224+690A>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 9/18 | chr4 | 55878756 | |||||||
| chr4:55878934 | C | T | 1 | a0001c0001t0001g0234 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1224+868C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 9/18 | chr4 | 55878934 | |||||||
| chr4:55879064 | A | G | 36 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0017 others(33): Show |
53 | HG00408.hp1 HG00558.hp2 HG01346.hp2 others(50): Show |
intron_variant | MODIFIER | c.1224+998A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 9/18 | chr4 | 55879064 | |||||||
| chr4:55879151 | A | T | 1 | a0001c0001t0001g0152 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1224+1085A>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 9/18 | chr4 | 55879151 | |||||||
| chr4:55879153 | G | A | 1 | a0002c0004t0004g0029 | 2 | HG01884.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1224+1087G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 9/18 | chr4 | 55879153 | |||||||
| chr4:55879476 | AG | A | 9 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0217 others(6): Show |
11 | HG01255.hp2 HG01891.hp2 HG02300.hp2 others(8): Show |
intron_variant | MODIFIER | c.1224+1413delG | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr4 | 55879476 | ||||||
| chr4:55879632 | A | C | 1 | a0001c0001t0001g0152 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1224+1566A>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 9/18 | chr4 | 55879632 | |||||||
| chr4:55880019 | A | G | 3 | a0001c0001t0005g0044 a0001c0001t0005g0045 a0001c0001t0005g0046 |
3 | HG03098.hp1 HG03225.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1224+1953A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 9/18 | chr4 | 55880019 | |||||||
| chr4:55880168 | A | G | 1 | a0001c0001t0003g0077 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1224+2102A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 9/18 | chr4 | 55880168 | |||||||
| chr4:55880364 | A | G | 66 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(63): Show |
88 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.1224+2298A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 9/18 | chr4 | 55880364 | |||||||
| chr4:55880576 | A | G | 1 | a0001c0002t0001g0048 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1224+2510A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 9/18 | chr4 | 55880576 | |||||||
| chr4:55880843 | C | T | 1 | a0001c0002t0002g0188 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1224+2777C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 9/18 | chr4 | 55880843 | |||||||
| chr4:55880862 | C | A | 1 | a0002c0004t0004g0029 | 2 | HG01884.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1224+2796C>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 9/18 | chr4 | 55880862 | |||||||
| chr4:55881027 | T | C | 4 | a0001c0002t0004g0088 a0001c0002t0004g0154 a0001c0002t0004g0155 others(1): Show |
4 | HG00558.hp1 HG01081.hp1 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.1225-2796T>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 9/18 | chr4 | 55881027 | |||||||
| chr4:55881161 | T | C | 1 | a0001c0001t0001g0267 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1225-2662T>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 9/18 | chr4 | 55881161 | |||||||
| chr4:55881359 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1225-2464C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 9/18 | chr4 | 55881359 | |||||||
| chr4:55881501 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1225-2322C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 9/18 | chr4 | 55881501 | |||||||
| chr4:55881563 | C | T | 1 | a0001c0002t0004g0155 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1225-2260C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 9/18 | chr4 | 55881563 | |||||||
| chr4:55881622 | A | T | 1 | a0001c0002t0002g0187 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1225-2201A>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 9/18 | chr4 | 55881622 | |||||||
| chr4:55881713 | C | T | 1 | a0001c0002t0002g0201 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1225-2110C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 9/18 | chr4 | 55881713 | |||||||
| chr4:55881738 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1225-2085C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 9/18 | chr4 | 55881738 | |||||||
| chr4:55881850 | GAT | G | 36 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0017 others(33): Show |
53 | HG00408.hp1 HG00558.hp2 HG01346.hp2 others(50): Show |
intron_variant | MODIFIER | c.1225-1972_1225-197 others(6): Show |
EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 9/18 | chr4 | 55881850 | |||||||
| chr4:55881855 | AT | A | 36 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0017 others(33): Show |
53 | HG00408.hp1 HG00558.hp2 HG01346.hp2 others(50): Show |
intron_variant | MODIFIER | c.1225-1964delT | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr4 | 55881855 | ||||||
| chr4:55881879 | A | G | 10 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0158 others(7): Show |
12 | HG01255.hp2 HG01891.hp2 HG02300.hp2 others(9): Show |
intron_variant | MODIFIER | c.1225-1944A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 9/18 | chr4 | 55881879 | |||||||
| chr4:55881907 | G | A | 3 | a0001c0001t0005g0044 a0001c0001t0005g0045 a0001c0001t0005g0046 |
3 | HG03098.hp1 HG03225.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1225-1916G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 9/18 | chr4 | 55881907 | |||||||
| chr4:55881935 | A | G | 3 | a0001c0002t0002g0170 a0001c0002t0002g0186 a0001c0006t0002g0213 |
3 | NA18960.hp2 NA19000.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1225-1888A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 9/18 | chr4 | 55881935 | |||||||
| chr4:55882034 | G | A | 4 | a0001c0001t0001g0040 a0001c0001t0001g0237 a0001c0001t0001g0238 others(1): Show |
5 | HG01255.hp2 HG01891.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1225-1789G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 9/18 | chr4 | 55882034 | |||||||
| chr4:55882069 | A | G | 1 | a0001c0001t0001g0244 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1225-1754A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 9/18 | chr4 | 55882069 | |||||||
| chr4:55882099 | T | TTTGTTG | 210 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(207): Show |
287 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(284): Show |
intron_variant | MODIFIER | c.1225-1710_1225-170 others(10): Show |
EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr4 | 55882099 | ||||||
| chr4:55882139 | T | C | 3 | a0001c0001t0005g0044 a0001c0001t0005g0045 a0001c0001t0005g0046 |
3 | HG03098.hp1 HG03225.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1225-1684T>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 9/18 | chr4 | 55882139 | |||||||
| chr4:55882295 | C | T | 2 | a0001c0001t0001g0071 a0001c0001t0001g0082 |
2 | HG01884.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.1225-1528C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 9/18 | chr4 | 55882295 | |||||||
| chr4:55882349 | A | T | 1 | a0001c0001t0001g0250 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1225-1474A>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 9/18 | chr4 | 55882349 | |||||||
| chr4:55882367 | T | C | 3 | a0001c0001t0005g0044 a0001c0001t0005g0045 a0001c0001t0005g0046 |
3 | HG03098.hp1 HG03225.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1225-1456T>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 9/18 | chr4 | 55882367 | |||||||
| chr4:55882769 | A | G | 2 | a0001c0001t0001g0071 a0001c0001t0001g0082 |
2 | HG01884.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.1225-1054A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 9/18 | chr4 | 55882769 | |||||||
| chr4:55882832 | T | C | 7 | a0001c0002t0001g0021 a0001c0002t0001g0047 a0001c0002t0001g0048 others(4): Show |
8 | HG00323.hp2 HG00642.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1225-991T>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 9/18 | chr4 | 55882832 | |||||||
| chr4:55882967 | A | G | 2 | a0001c0001t0001g0263 a0001c0001t0001g0270 |
2 | HG00741.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.1225-856A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 9/18 | chr4 | 55882967 | |||||||
| chr4:55883238 | C | A | 1 | a0001c0001t0001g0222 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1225-585C>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 9/18 | chr4 | 55883238 | |||||||
| chr4:55883401 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1225-422A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 9/18 | chr4 | 55883401 | |||||||
| chr4:55883408 | G | A | 4 | a0001c0002t0004g0088 a0001c0002t0004g0154 a0001c0002t0004g0155 others(1): Show |
4 | HG00558.hp1 HG01081.hp1 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.1225-415G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 9/18 | chr4 | 55883408 | |||||||
| chr4:55883438 | A | T | 4 | a0001c0002t0004g0088 a0001c0002t0004g0154 a0001c0002t0004g0155 others(1): Show |
4 | HG00558.hp1 HG01081.hp1 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.1225-385A>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 9/18 | chr4 | 55883438 | |||||||
| chr4:55883584 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1225-239G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 9/18 | chr4 | 55883584 | |||||||
| chr4:55884094 | T | C | 7 | a0001c0002t0001g0021 a0001c0002t0001g0047 a0001c0002t0001g0048 others(4): Show |
8 | HG00323.hp2 HG00642.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1330+166T>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 10/18 | chr4 | 55884094 | |||||||
| chr4:55884600 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1330+672G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 10/18 | chr4 | 55884600 | |||||||
| chr4:55884629 | A | G | 1 | a0002c0004t0004g0029 | 2 | HG01884.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1330+701A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 10/18 | chr4 | 55884629 | |||||||
| chr4:55884870 | G | T | 2 | a0001c0002t0001g0050 a0001c0002t0001g0052 |
2 | HG03195.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1330+942G>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 10/18 | chr4 | 55884870 | |||||||
| chr4:55884933 | G | C | 10 | a0001c0002t0004g0020 a0001c0002t0004g0070 a0001c0002t0004g0088 others(7): Show |
11 | HG00558.hp1 HG01081.hp1 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.1330+1005G>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 10/18 | chr4 | 55884933 | |||||||
| chr4:55885019 | C | T | 8 | a0001c0001t0001g0085 a0001c0002t0001g0021 a0001c0002t0001g0047 others(5): Show |
9 | HG00323.hp2 HG00642.hp2 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1330+1091C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 10/18 | chr4 | 55885019 | |||||||
| chr4:55885245 | G | A | 1 | a0001c0002t0002g0176 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1330+1317G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 10/18 | chr4 | 55885245 | |||||||
| chr4:55885494 | T | C | 3 | a0001c0001t0003g0016 a0001c0001t0003g0083 a0001c0001t0003g0084 |
5 | NA18961.hp1 NA18977.hp2 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.1330+1566T>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 10/18 | chr4 | 55885494 | |||||||
| chr4:55885574 | C | T | 48 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(45): Show |
66 | HG00408.hp2 HG00639.hp1 HG01070.hp2 others(63): Show |
intron_variant | MODIFIER | c.1330+1646C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 10/18 | chr4 | 55885574 | |||||||
| chr4:55885689 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1330+1761G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 10/18 | chr4 | 55885689 | |||||||
| chr4:55885911 | T | C | 3 | a0001c0001t0001g0042 a0001c0001t0001g0223 a0001c0001t0001g0241 |
4 | HG00621.hp2 HG02015.hp2 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.1330+1983T>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 10/18 | chr4 | 55885911 | |||||||
| chr4:55885941 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1330+2013A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 10/18 | chr4 | 55885941 | |||||||
| chr4:55885947 | C | T | 1 | a0002c0004t0004g0029 | 2 | HG01884.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1330+2019C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 10/18 | chr4 | 55885947 | |||||||
| chr4:55885987 | A | T | 66 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(63): Show |
88 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.1330+2059A>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 10/18 | chr4 | 55885987 | |||||||
| chr4:55886022 | A | G | 1 | a0002c0004t0004g0029 | 2 | HG01884.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1330+2094A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 10/18 | chr4 | 55886022 | |||||||
| chr4:55886163 | A | G | 3 | a0001c0001t0005g0044 a0001c0001t0005g0045 a0001c0001t0005g0046 |
3 | HG03098.hp1 HG03225.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1330+2235A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 10/18 | chr4 | 55886163 | |||||||
| chr4:55886171 | G | A | 1 | a0001c0002t0002g0164 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1330+2243G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 10/18 | chr4 | 55886171 | |||||||
| chr4:55886333 | A | T | 1 | a0002c0004t0004g0029 | 2 | HG01884.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1330+2405A>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 10/18 | chr4 | 55886333 | |||||||
| chr4:55886339 | G | A | 1 | a0002c0004t0004g0029 | 2 | HG01884.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1330+2411G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 10/18 | chr4 | 55886339 | |||||||
| chr4:55886463 | G | A | 2 | a0001c0001t0001g0121 a0001c0001t0001g0144 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1331-2425G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 10/18 | chr4 | 55886463 | |||||||
| chr4:55886476 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1331-2412C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 10/18 | chr4 | 55886476 | |||||||
| chr4:55886552 | C | CAAAAAAC others(1): Show |
20 | a0001c0002t0002g0005 a0001c0002t0002g0037 a0001c0002t0002g0148 others(17): Show |
27 | HG00621.hp1 HG01069.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.1331-2313_1331-230 others(12): Show |
EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr4 | 55886552 | ||||||
| chr4:55886582 | A | C | 36 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0017 others(33): Show |
53 | HG00408.hp1 HG00558.hp2 HG01346.hp2 others(50): Show |
intron_variant | MODIFIER | c.1331-2306A>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 10/18 | chr4 | 55886582 | |||||||
| chr4:55887063 | G | A | 1 | a0001c0002t0004g0159 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1331-1825G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 10/18 | chr4 | 55887063 | |||||||
| chr4:55887180 | A | ATTTGTAT others(6): Show |
77 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(74): Show |
101 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.1331-1706_1331-170 others(17): Show |
EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr4 | 55887180 | ||||||
| chr4:55887261 | T | C | 4 | a0001c0001t0001g0028 a0001c0001t0001g0113 a0001c0001t0001g0151 others(1): Show |
5 | NA18961.hp2 NA18995.hp1 NA19001.hp2 others(2): Show |
intron_variant | MODIFIER | c.1331-1627T>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 10/18 | chr4 | 55887261 | |||||||
| chr4:55887481 | T | C | 1 | a0001c0001t0001g0224 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1331-1407T>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 10/18 | chr4 | 55887481 | |||||||
| chr4:55887540 | C | A | 3 | a0001c0002t0004g0070 a0001c0002t0004g0215 a0001c0002t0004g0216 |
3 | HG02572.hp1 HG02647.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1331-1348C>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 10/18 | chr4 | 55887540 | |||||||
| chr4:55887616 | G | C | 4 | a0001c0002t0004g0088 a0001c0002t0004g0154 a0001c0002t0004g0155 others(1): Show |
4 | HG00558.hp1 HG01081.hp1 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.1331-1272G>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 10/18 | chr4 | 55887616 | |||||||
| chr4:55887725 | C | CA | 6 | a0001c0001t0001g0132 a0001c0001t0005g0044 a0001c0001t0005g0045 others(3): Show |
7 | HG01884.hp2 HG03098.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.1331-1147dupA | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr4 | 55887725 | ||||||
| chr4:55887725 | CA | C | 8 | a0001c0001t0001g0094 a0001c0001t0001g0111 a0001c0001t0001g0118 others(5): Show |
8 | HG00438.hp1 HG00438.hp2 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.1331-1147delA | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr4 | 55887725 | ||||||
| chr4:55887920 | G | GA | 30 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(27): Show |
41 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.1331-968_1331-967i others(3): Show |
EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 10/18 | chr4 | 55887920 | |||||||
| chr4:55887921 | G | T | 30 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(27): Show |
41 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.1331-967G>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 10/18 | chr4 | 55887921 | |||||||
| chr4:55887922 | C | A | 30 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(27): Show |
41 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.1331-966C>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 10/18 | chr4 | 55887922 | |||||||
| chr4:55887924 | A | ATCC | 30 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(27): Show |
41 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.1331-964_1331-963i others(5): Show |
EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 10/18 | chr4 | 55887924 | |||||||
| chr4:55887925 | G | C | 30 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(27): Show |
41 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.1331-963G>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 10/18 | chr4 | 55887925 | |||||||
| chr4:55887933 | T | C | 16 | a0001c0001t0003g0001 a0001c0001t0003g0010 a0001c0001t0003g0016 others(13): Show |
30 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.1331-955T>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 10/18 | chr4 | 55887933 | |||||||
| chr4:55887933 | T | G | 66 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(63): Show |
88 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.1331-955T>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 10/18 | chr4 | 55887933 | |||||||
| chr4:55888348 | T | C | 1 | a0001c0002t0002g0214 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1331-540T>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 10/18 | chr4 | 55888348 | |||||||
| chr4:55888349 | T | A | 1 | a0001c0002t0002g0214 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1331-539T>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 10/18 | chr4 | 55888349 | |||||||
| chr4:55888600 | TA | T | 19 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0217 others(16): Show |
21 | HG01255.hp2 HG01891.hp2 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.1331-276delA | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr4 | 55888600 | ||||||
| chr4:55888965 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1375+33C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 11/18 | chr4 | 55888965 | |||||||
| chr4:55889253 | A | G | 4 | a0001c0002t0004g0070 a0001c0002t0004g0159 a0001c0002t0004g0215 others(1): Show |
4 | HG02572.hp1 HG02647.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1375+321A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 11/18 | chr4 | 55889253 | |||||||
| chr4:55889326 | TGA | T | 4 | a0001c0002t0004g0088 a0001c0002t0004g0154 a0001c0002t0004g0155 others(1): Show |
4 | HG00558.hp1 HG01081.hp1 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.1375+399_1375+400d others(4): Show |
EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr4 | 55889326 | ||||||
| chr4:55889629 | T | C | 1 | a0001c0001t0001g0058 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1376-594T>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 11/18 | chr4 | 55889629 | |||||||
| chr4:55889717 | A | G | 2 | a0001c0001t0001g0071 a0001c0001t0001g0082 |
2 | HG01884.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.1376-506A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 11/18 | chr4 | 55889717 | |||||||
| chr4:55889942 | A | G | 1 | a0001c0001t0001g0255 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1376-281A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 11/18 | chr4 | 55889942 | |||||||
| chr4:55889954 | T | C | 3 | a0001c0002t0004g0070 a0001c0002t0004g0215 a0001c0002t0004g0216 |
3 | HG02572.hp1 HG02647.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1376-269T>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 11/18 | chr4 | 55889954 | |||||||
| chr4:55890011 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1376-212C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 11/18 | chr4 | 55890011 | |||||||
| chr4:55890012 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1376-211G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 11/18 | chr4 | 55890012 | |||||||
| chr4:55890035 | A | G | 85 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(82): Show |
120 | HG00408.hp2 HG00558.hp1 HG00639.hp1 others(117): Show |
intron_variant | MODIFIER | c.1376-188A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 11/18 | chr4 | 55890035 | |||||||
| chr4:55890117 | G | A | 1 | a0002c0004t0004g0029 | 2 | HG01884.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1376-106G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 11/18 | chr4 | 55890117 | |||||||
| chr4:55890158 | C | T | 1 | a0001c0002t0004g0159 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1376-65C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 11/18 | chr4 | 55890158 | |||||||
| chr4:55890162 | T | A | 1 | a0003c0005t0001g0090 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1376-61T>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 11/18 | chr4 | 55890162 | |||||||
| chr4:55890523 | G | A | 1 | a0002c0004t0004g0029 | 2 | HG01884.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1539+137G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 12/18 | chr4 | 55890523 | |||||||
| chr4:55890531 | G | GA | 48 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(45): Show |
66 | HG00408.hp2 HG00639.hp1 HG01070.hp2 others(63): Show |
intron_variant | MODIFIER | c.1539+162dupA | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr4 | 55890531 | ||||||
| chr4:55890531 | GA | G | 79 | a0001c0001t0001g0023 a0001c0001t0001g0086 a0001c0001t0001g0087 others(76): Show |
103 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.1539+162delA | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr4 | 55890531 | ||||||
| chr4:55890532 | A | G | 2 | a0001c0001t0001g0055 a0001c0001t0001g0056 |
2 | NA19002.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.1539+146A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 12/18 | chr4 | 55890532 | |||||||
| chr4:55890542 | A | C | 36 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0017 others(33): Show |
53 | HG00408.hp1 HG00558.hp2 HG01346.hp2 others(50): Show |
intron_variant | MODIFIER | c.1539+156A>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 12/18 | chr4 | 55890542 | |||||||
| chr4:55890617 | T | C | 2 | a0001c0001t0001g0071 a0001c0001t0001g0082 |
2 | HG01884.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.1539+231T>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 12/18 | chr4 | 55890617 | |||||||
| chr4:55890892 | T | G | 4 | a0001c0001t0001g0023 a0001c0001t0001g0085 a0001c0001t0001g0086 others(1): Show |
5 | HG02809.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1540-423T>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 12/18 | chr4 | 55890892 | |||||||
| chr4:55891297 | C | T | 2 | a0001c0002t0004g0020 a0001c0002t0008g0020 |
3 | HG02258.hp2 HG03139.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1540-18C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 12/18 | chr4 | 55891297 | |||||||
| chr4:55891451 | A | G | 1 | a0001c0001t0001g0250 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1647+29A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 13/18 | chr4 | 55891451 | |||||||
| chr4:55891677 | T | C | 1 | a0001c0001t0001g0138 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1647+255T>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 13/18 | chr4 | 55891677 | |||||||
| chr4:55891678 | G | T | 1 | a0001c0001t0001g0138 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1647+256G>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 13/18 | chr4 | 55891678 | |||||||
| chr4:55891757 | AAATAT | A | 7 | a0001c0002t0004g0020 a0001c0002t0004g0070 a0001c0002t0004g0159 others(4): Show |
9 | HG01884.hp2 HG02258.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1647+339_1647+343d others(7): Show |
EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr4 | 55891757 | ||||||
| chr4:55891776 | G | T | 2 | a0001c0001t0001g0265 a0001c0001t0001g0266 |
2 | HG02109.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1647+354G>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 13/18 | chr4 | 55891776 | |||||||
| chr4:55891783 | G | A | 2 | a0001c0002t0004g0020 a0001c0002t0008g0020 |
3 | HG02258.hp2 HG03139.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1647+361G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 13/18 | chr4 | 55891783 | |||||||
| chr4:55891977 | A | G | 1 | a0001c0001t0001g0259 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1647+555A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 13/18 | chr4 | 55891977 | |||||||
| chr4:55892167 | G | A | 1 | a0001c0002t0002g0178 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1648-468G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 13/18 | chr4 | 55892167 | |||||||
| chr4:55892202 | AT | A | 16 | a0001c0001t0003g0001 a0001c0001t0003g0010 a0001c0001t0003g0016 others(13): Show |
30 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.1648-427delT | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr4 | 55892202 | ||||||
| chr4:55892305 | T | G | 2 | a0001c0001t0001g0071 a0001c0001t0001g0082 |
2 | HG01884.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.1648-330T>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 13/18 | chr4 | 55892305 | |||||||
| chr4:55892367 | A | G | 15 | a0001c0001t0003g0001 a0001c0001t0003g0016 a0001c0001t0003g0022 others(12): Show |
26 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.1648-268A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 13/18 | chr4 | 55892367 | |||||||
| chr4:55892377 | T | G | 1 | a0001c0001t0001g0158 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1648-258T>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 13/18 | chr4 | 55892377 | |||||||
| chr4:55892564 | G | A | 4 | a0001c0002t0004g0070 a0001c0002t0004g0159 a0001c0002t0004g0215 others(1): Show |
4 | HG02572.hp1 HG02647.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1648-71G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 13/18 | chr4 | 55892564 | |||||||
| chr4:55892631 | G | T | 1 | a0001c0002t0001g0048 | 1 | HG01109.hp1 | splice_region_variant&intron_variant | LOW | c.1648-4G>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 13/18 | chr4 | 55892631 | |||||||
| chr4:55892827 | A | G | 34 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0017 others(31): Show |
51 | HG00408.hp1 HG00558.hp2 HG01346.hp2 others(48): Show |
intron_variant | MODIFIER | c.1724+116A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 14/18 | chr4 | 55892827 | |||||||
| chr4:55892854 | C | T | 1 | a0001c0001t0003g0075 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1724+143C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 14/18 | chr4 | 55892854 | |||||||
| chr4:55892890 | T | C | 2 | a0001c0001t0001g0225 a0001c0001t0001g0226 |
2 | HG02523.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.1724+179T>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 14/18 | chr4 | 55892890 | |||||||
| chr4:55892914 | A | C | 2 | a0001c0002t0002g0013 a0001c0002t0002g0205 |
5 | NA18947.hp2 NA18966.hp1 NA19003.hp1 others(2): Show |
intron_variant | MODIFIER | c.1724+203A>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 14/18 | chr4 | 55892914 | |||||||
| chr4:55893115 | TTTG | T | 4 | a0001c0002t0004g0070 a0001c0002t0004g0159 a0001c0002t0004g0215 others(1): Show |
4 | HG02572.hp1 HG02647.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1724+416_1724+418d others(5): Show |
EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr4 | 55893115 | ||||||
| chr4:55893306 | G | C | 55 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(52): Show |
74 | HG00408.hp2 HG00639.hp1 HG01070.hp2 others(71): Show |
intron_variant | MODIFIER | c.1725-246G>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 14/18 | chr4 | 55893306 | |||||||
| chr4:55893312 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1725-240G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 14/18 | chr4 | 55893312 | |||||||
| chr4:55893379 | C | G | 1 | a0001c0001t0001g0101 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1725-173C>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 14/18 | chr4 | 55893379 | |||||||
| chr4:55893411 | C | T | 4 | a0001c0002t0004g0070 a0001c0002t0004g0159 a0001c0002t0004g0215 others(1): Show |
4 | HG02572.hp1 HG02647.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1725-141C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 14/18 | chr4 | 55893411 | |||||||
| chr4:55893418 | C | T | 2 | a0001c0001t0001g0071 a0001c0001t0001g0082 |
2 | HG01884.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.1725-134C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 14/18 | chr4 | 55893418 | |||||||
| chr4:55893854 | G | T | 1 | a0001c0003t0001g0096 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1953+74G>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 15/18 | chr4 | 55893854 | |||||||
| chr4:55893863 | C | A | 1 | a0001c0001t0001g0142 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1953+83C>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 15/18 | chr4 | 55893863 | |||||||
| chr4:55894000 | G | C | 75 | a0001c0002t0001g0021 a0001c0002t0001g0047 a0001c0002t0001g0048 others(72): Show |
99 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.1953+220G>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 15/18 | chr4 | 55894000 | |||||||
| chr4:55894050 | C | T | 1 | a0001c0001t0001g0131 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1953+270C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 15/18 | chr4 | 55894050 | |||||||
| chr4:55894122 | C | T | 36 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0017 others(33): Show |
53 | HG00408.hp1 HG00558.hp2 HG01346.hp2 others(50): Show |
intron_variant | MODIFIER | c.1953+342C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 15/18 | chr4 | 55894122 | |||||||
| chr4:55894162 | C | T | 11 | a0001c0002t0004g0020 a0001c0002t0004g0070 a0001c0002t0004g0088 others(8): Show |
13 | HG00558.hp1 HG01081.hp1 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.1953+382C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 15/18 | chr4 | 55894162 | |||||||
| chr4:55894204 | A | G | 4 | a0001c0001t0001g0040 a0001c0001t0001g0237 a0001c0001t0001g0238 others(1): Show |
5 | HG01255.hp2 HG01891.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1953+424A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 15/18 | chr4 | 55894204 | |||||||
| chr4:55894207 | T | C | 202 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(199): Show |
277 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(274): Show |
intron_variant | MODIFIER | c.1953+427T>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 15/18 | chr4 | 55894207 | |||||||
| chr4:55894324 | C | CA | 18 | a0001c0001t0001g0082 a0001c0001t0001g0114 a0001c0001t0001g0127 others(15): Show |
19 | HG01169.hp1 HG01175.hp1 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.1953+563dupA | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr4 | 55894324 | ||||||
| chr4:55894324 | CA | C | 22 | a0001c0001t0001g0085 a0001c0001t0001g0116 a0001c0002t0002g0005 others(19): Show |
29 | HG00621.hp1 HG01069.hp1 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.1953+563delA | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr4 | 55894324 | ||||||
| chr4:55894350 | G | A | 4 | a0001c0002t0004g0070 a0001c0002t0004g0159 a0001c0002t0004g0215 others(1): Show |
4 | HG02572.hp1 HG02647.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1953+570G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 15/18 | chr4 | 55894350 | |||||||
| chr4:55894379 | A | G | 4 | a0001c0002t0004g0070 a0001c0002t0004g0159 a0001c0002t0004g0215 others(1): Show |
4 | HG02572.hp1 HG02647.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1953+599A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 15/18 | chr4 | 55894379 | |||||||
| chr4:55894410 | A | T | 211 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(208): Show |
288 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(285): Show |
intron_variant | MODIFIER | c.1953+630A>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 15/18 | chr4 | 55894410 | |||||||
| chr4:55894614 | C | CT | 36 | a0001c0001t0001g0033 a0001c0001t0001g0071 a0001c0001t0001g0082 others(33): Show |
50 | HG00408.hp2 HG00639.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.1953+859dupT | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr4 | 55894614 | ||||||
| chr4:55894614 | C | CTT | 88 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(85): Show |
121 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1953+858_1953+859d others(4): Show |
EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr4 | 55894614 | ||||||
| chr4:55894614 | C | CTTT | 28 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0030 others(25): Show |
36 | HG00408.hp1 HG00673.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.1953+857_1953+859d others(5): Show |
EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr4 | 55894614 | ||||||
| chr4:55894614 | CT | C | 55 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(52): Show |
77 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.1953+859delT | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr4 | 55894614 | ||||||
| chr4:55894614 | CTTTTTTT others(6): Show |
C | 3 | a0001c0001t0005g0044 a0001c0001t0005g0045 a0001c0001t0005g0046 |
3 | HG03098.hp1 HG03225.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1953+847_1953+859d others(15): Show |
EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr4 | 55894614 | ||||||
| chr4:55894648 | G | A | 3 | a0001c0001t0005g0044 a0001c0001t0005g0045 a0001c0001t0005g0046 |
3 | HG03098.hp1 HG03225.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1953+868G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 15/18 | chr4 | 55894648 | |||||||
| chr4:55894705 | C | T | 66 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(63): Show |
88 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.1953+925C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 15/18 | chr4 | 55894705 | |||||||
| chr4:55895382 | A | G | 55 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(52): Show |
74 | HG00408.hp2 HG00639.hp1 HG01070.hp2 others(71): Show |
intron_variant | MODIFIER | c.1954-1335A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 15/18 | chr4 | 55895382 | |||||||
| chr4:55895494 | A | G | 4 | a0001c0002t0004g0088 a0001c0002t0004g0154 a0001c0002t0004g0155 others(1): Show |
4 | HG00558.hp1 HG01081.hp1 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.1954-1223A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 15/18 | chr4 | 55895494 | |||||||
| chr4:55895552 | AT | A | 7 | a0001c0002t0001g0021 a0001c0002t0001g0047 a0001c0002t0001g0048 others(4): Show |
8 | HG00323.hp2 HG00642.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1954-1160delT | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr4 | 55895552 | ||||||
| chr4:55895575 | T | A | 66 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(63): Show |
88 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.1954-1142T>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 15/18 | chr4 | 55895575 | |||||||
| chr4:55895610 | A | G | 2 | a0001c0002t0004g0020 a0001c0002t0008g0020 |
3 | HG02258.hp2 HG03139.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1954-1107A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 15/18 | chr4 | 55895610 | |||||||
| chr4:55895621 | G | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0099 |
3 | HG00558.hp2 NA18950.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.1954-1096G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 15/18 | chr4 | 55895621 | |||||||
| chr4:55895765 | C | T | 66 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(63): Show |
88 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.1954-952C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 15/18 | chr4 | 55895765 | |||||||
| chr4:55895799 | G | A | 4 | a0001c0002t0004g0088 a0001c0002t0004g0154 a0001c0002t0004g0155 others(1): Show |
4 | HG00558.hp1 HG01081.hp1 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.1954-918G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 15/18 | chr4 | 55895799 | |||||||
| chr4:55895809 | TAA | T | 77 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(74): Show |
101 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.1954-907_1954-906d others(4): Show |
EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 15/18 | chr4 | 55895809 | |||||||
| chr4:55895852 | A | C | 1 | a0001c0001t0001g0158 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1954-865A>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 15/18 | chr4 | 55895852 | |||||||
| chr4:55895862 | G | A | 1 | a0001c0002t0002g0199 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1954-855G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 15/18 | chr4 | 55895862 | |||||||
| chr4:55895932 | T | G | 1 | a0001c0002t0002g0174 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1954-785T>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 15/18 | chr4 | 55895932 | |||||||
| chr4:55895935 | C | T | 77 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(74): Show |
101 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.1954-782C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 15/18 | chr4 | 55895935 | |||||||
| chr4:55895941 | T | C | 2 | a0001c0001t0001g0032 a0001c0001t0001g0114 |
3 | HG02129.hp2 NA18952.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.1954-776T>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 15/18 | chr4 | 55895941 | |||||||
| chr4:55895998 | G | A | 11 | a0001c0002t0004g0020 a0001c0002t0004g0070 a0001c0002t0004g0088 others(8): Show |
13 | HG00558.hp1 HG01081.hp1 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.1954-719G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 15/18 | chr4 | 55895998 | |||||||
| chr4:55896006 | C | T | 1 | a0001c0001t0001g0258 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1954-711C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 15/18 | chr4 | 55896006 | |||||||
| chr4:55896042 | A | C | 67 | a0001c0001t0001g0087 a0001c0002t0002g0002 a0001c0002t0002g0005 others(64): Show |
89 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.1954-675A>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 15/18 | chr4 | 55896042 | |||||||
| chr4:55896101 | T | C | 16 | a0001c0001t0003g0001 a0001c0001t0003g0010 a0001c0001t0003g0016 others(13): Show |
30 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.1954-616T>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 15/18 | chr4 | 55896101 | |||||||
| chr4:55896203 | G | A | 8 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(5): Show |
8 | HG01167.hp2 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1954-514G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 15/18 | chr4 | 55896203 | |||||||
| chr4:55896210 | C | T | 1 | a0001c0001t0001g0106 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1954-507C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 15/18 | chr4 | 55896210 | |||||||
| chr4:55896252 | C | A | 5 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0249 others(2): Show |
5 | HG01167.hp2 HG02258.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1954-465C>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 15/18 | chr4 | 55896252 | |||||||
| chr4:55896422 | G | A | 16 | a0001c0001t0003g0001 a0001c0001t0003g0010 a0001c0001t0003g0016 others(13): Show |
30 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.1954-295G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 15/18 | chr4 | 55896422 | |||||||
| chr4:55896604 | C | T | 1 | a0001c0002t0002g0167 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1954-113C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 15/18 | chr4 | 55896604 | |||||||
| chr4:55896641 | A | T | 4 | a0001c0001t0003g0016 a0001c0001t0003g0076 a0001c0001t0003g0083 others(1): Show |
6 | NA18961.hp1 NA18977.hp2 NA19005.hp2 others(3): Show |
intron_variant | MODIFIER | c.1954-76A>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 15/18 | chr4 | 55896641 | |||||||
| chr4:55896979 | G | A | 1 | a0001c0002t0004g0159 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2137+79G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 16/18 | chr4 | 55896979 | |||||||
| chr4:55896996 | A | C | 1 | a0002c0004t0004g0029 | 2 | HG01884.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2137+96A>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 16/18 | chr4 | 55896996 | |||||||
| chr4:55897004 | A | G | 241 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(238): Show |
329 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(326): Show |
intron_variant | MODIFIER | c.2137+104A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 16/18 | chr4 | 55897004 | |||||||
| chr4:55897129 | CT | C | 21 | a0001c0001t0001g0062 a0001c0001t0001g0124 a0001c0001t0001g0140 others(18): Show |
35 | HG00323.hp1 HG00639.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.2137+245delT | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr4 | 55897129 | ||||||
| chr4:55897181 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2137+281C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 16/18 | chr4 | 55897181 | |||||||
| chr4:55897182 | G | A | 1 | a0001c0001t0001g0106 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2137+282G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 16/18 | chr4 | 55897182 | |||||||
| chr4:55897229 | A | C | 158 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(155): Show |
216 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(213): Show |
intron_variant | MODIFIER | c.2137+329A>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 16/18 | chr4 | 55897229 | |||||||
| chr4:55897230 | G | A | 16 | a0001c0001t0003g0001 a0001c0001t0003g0010 a0001c0001t0003g0016 others(13): Show |
30 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.2137+330G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 16/18 | chr4 | 55897230 | |||||||
| chr4:55897420 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2137+520C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 16/18 | chr4 | 55897420 | |||||||
| chr4:55897478 | A | G | 1 | a0001c0001t0001g0244 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.2137+578A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 16/18 | chr4 | 55897478 | |||||||
| chr4:55897651 | TGTTGCCC others(8): Show |
T | 1 | a0001c0001t0001g0097 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2137+754_2137+768d others(17): Show |
EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr4 | 55897651 | ||||||
| chr4:55897668 | T | C | 1 | a0001c0001t0001g0097 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2137+768T>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 16/18 | chr4 | 55897668 | |||||||
| chr4:55897708 | C | T | 2 | a0001c0001t0001g0101 a0001c0002t0002g0190 |
2 | HG04228.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.2137+808C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 16/18 | chr4 | 55897708 | |||||||
| chr4:55897993 | C | T | 1 | a0001c0001t0007g0060 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2137+1093C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 16/18 | chr4 | 55897993 | |||||||
| chr4:55898061 | C | G | 2 | a0001c0001t0001g0231 a0001c0001t0001g0243 |
2 | HG01175.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.2137+1161C>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 16/18 | chr4 | 55898061 | |||||||
| chr4:55898112 | G | T | 4 | a0001c0002t0004g0088 a0001c0002t0004g0154 a0001c0002t0004g0155 others(1): Show |
4 | HG00558.hp1 HG01081.hp1 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.2137+1212G>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 16/18 | chr4 | 55898112 | |||||||
| chr4:55898339 | A | G | 85 | a0001c0001t0001g0104 a0001c0002t0001g0021 a0001c0002t0001g0047 others(82): Show |
110 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.2138-1346A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 16/18 | chr4 | 55898339 | |||||||
| chr4:55898427 | T | C | 48 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(45): Show |
66 | HG00408.hp2 HG00639.hp1 HG01070.hp2 others(63): Show |
intron_variant | MODIFIER | c.2138-1258T>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 16/18 | chr4 | 55898427 | |||||||
| chr4:55898480 | GTTA | G | 48 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(45): Show |
66 | HG00408.hp2 HG00639.hp1 HG01070.hp2 others(63): Show |
intron_variant | MODIFIER | c.2138-1202_2138-120 others(7): Show |
EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr4 | 55898480 | ||||||
| chr4:55898486 | G | T | 48 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(45): Show |
66 | HG00408.hp2 HG00639.hp1 HG01070.hp2 others(63): Show |
intron_variant | MODIFIER | c.2138-1199G>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 16/18 | chr4 | 55898486 | |||||||
| chr4:55898548 | T | C | 2 | a0001c0001t0001g0227 a0001c0001t0001g0260 |
2 | HG00738.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.2138-1137T>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 16/18 | chr4 | 55898548 | |||||||
| chr4:55898579 | T | A | 1 | a0001c0001t0001g0250 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2138-1106T>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 16/18 | chr4 | 55898579 | |||||||
| chr4:55898617 | T | C | 1 | a0001c0001t0001g0055 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.2138-1068T>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 16/18 | chr4 | 55898617 | |||||||
| chr4:55898658 | A | G | 48 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(45): Show |
66 | HG00408.hp2 HG00639.hp1 HG01070.hp2 others(63): Show |
intron_variant | MODIFIER | c.2138-1027A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 16/18 | chr4 | 55898658 | |||||||
| chr4:55898776 | A | G | 4 | a0001c0001t0001g0023 a0001c0001t0001g0085 a0001c0001t0001g0086 others(1): Show |
5 | HG02809.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.2138-909A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 16/18 | chr4 | 55898776 | |||||||
| chr4:55898838 | A | G | 9 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0217 others(6): Show |
11 | HG01255.hp2 HG01891.hp2 HG02300.hp2 others(8): Show |
intron_variant | MODIFIER | c.2138-847A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 16/18 | chr4 | 55898838 | |||||||
| chr4:55898954 | T | C | 1 | a0001c0001t0001g0247 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2138-731T>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 16/18 | chr4 | 55898954 | |||||||
| chr4:55899120 | G | A | 2 | a0001c0002t0004g0020 a0001c0002t0008g0020 |
3 | HG02258.hp2 HG03139.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2138-565G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 16/18 | chr4 | 55899120 | |||||||
| chr4:55899237 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2138-448G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 16/18 | chr4 | 55899237 | |||||||
| chr4:55899482 | A | G | 1 | a0003c0005t0001g0089 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2138-203A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 16/18 | chr4 | 55899482 | |||||||
| chr4:55899530 | G | C | 1 | a0001c0001t0001g0228 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2138-155G>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 16/18 | chr4 | 55899530 | |||||||
| chr4:55899892 | T | C | 7 | a0001c0002t0002g0037 a0001c0002t0002g0175 a0001c0002t0002g0176 others(4): Show |
8 | NA18946.hp2 NA18956.hp2 NA18960.hp1 others(5): Show |
splice_region_variant&intron_variant | LOW | c.2337+8T>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 17/18 | chr4 | 55899892 | |||||||
| chr4:55899904 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2337+20G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 17/18 | chr4 | 55899904 | |||||||
| chr4:55899992 | C | T | 7 | a0001c0002t0001g0021 a0001c0002t0001g0047 a0001c0002t0001g0048 others(4): Show |
8 | HG00323.hp2 HG00642.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.2337+108C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 17/18 | chr4 | 55899992 | |||||||
| chr4:55900004 | A | G | 1 | a0001c0001t0003g0010 | 4 | HG02280.hp1 HG03471.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2337+120A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 17/18 | chr4 | 55900004 | |||||||
| chr4:55900058 | C | A | 3 | a0001c0001t0003g0016 a0001c0001t0003g0083 a0001c0001t0003g0084 |
5 | NA18961.hp1 NA18977.hp2 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.2337+174C>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 17/18 | chr4 | 55900058 | |||||||
| chr4:55900121 | G | T | 1 | a0001c0002t0002g0198 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2337+237G>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 17/18 | chr4 | 55900121 | |||||||
| chr4:55900125 | T | G | 1 | a0001c0002t0002g0198 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2337+241T>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 17/18 | chr4 | 55900125 | |||||||
| chr4:55900219 | A | G | 1 | a0001c0001t0001g0250 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2337+335A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 17/18 | chr4 | 55900219 | |||||||
| chr4:55900265 | G | A | 2 | a0001c0001t0001g0224 a0001c0001t0001g0228 |
2 | HG03942.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.2337+381G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 17/18 | chr4 | 55900265 | |||||||
| chr4:55900275 | T | A | 1 | a0001c0001t0001g0135 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2337+391T>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 17/18 | chr4 | 55900275 | |||||||
| chr4:55900307 | TCTTA | T | 2 | a0001c0001t0001g0015 a0001c0001t0001g0065 |
4 | HG02257.hp1 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2337+427_2337+430d others(6): Show |
EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr4 | 55900307 | ||||||
| chr4:55900402 | G | A | 1 | a0001c0002t0002g0193 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2337+518G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 17/18 | chr4 | 55900402 | |||||||
| chr4:55900496 | G | A | 1 | a0001c0001t0001g0229 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2337+612G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 17/18 | chr4 | 55900496 | |||||||
| chr4:55900843 | G | A | 7 | a0001c0002t0001g0021 a0001c0002t0001g0047 a0001c0002t0001g0048 others(4): Show |
8 | HG00323.hp2 HG00642.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.2337+959G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 17/18 | chr4 | 55900843 | |||||||
| chr4:55901179 | A | T | 2 | a0001c0002t0004g0020 a0001c0002t0008g0020 |
3 | HG02258.hp2 HG03139.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2338-1165A>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 17/18 | chr4 | 55901179 | |||||||
| chr4:55901216 | T | C | 2 | a0001c0001t0001g0025 a0001c0001t0001g0136 |
3 | NA18942.hp1 NA18988.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.2338-1128T>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 17/18 | chr4 | 55901216 | |||||||
| chr4:55901358 | T | TTTAA | 16 | a0001c0001t0003g0001 a0001c0001t0003g0010 a0001c0001t0003g0016 others(13): Show |
30 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.2338-984_2338-981d others(6): Show |
EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr4 | 55901358 | ||||||
| chr4:55901601 | G | A | 1 | a0001c0002t0002g0207 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2338-743G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 17/18 | chr4 | 55901601 | |||||||
| chr4:55901623 | A | G | 1 | a0002c0004t0004g0029 | 2 | HG01884.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2338-721A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 17/18 | chr4 | 55901623 | |||||||
| chr4:55901974 | A | G | 5 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0249 others(2): Show |
5 | HG01167.hp2 HG02258.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2338-370A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 17/18 | chr4 | 55901974 | |||||||
| chr4:55902075 | A | G | 1 | a0001c0002t0002g0160 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2338-269A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 17/18 | chr4 | 55902075 | |||||||
| chr4:55902123 | TCTC | T | 36 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0017 others(33): Show |
53 | HG00408.hp1 HG00558.hp2 HG01346.hp2 others(50): Show |
intron_variant | MODIFIER | c.2338-218_2338-216d others(5): Show |
EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr4 | 55902123 | ||||||
| chr4:55902201 | A | G | 1 | a0001c0001t0001g0100 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2338-143A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 17/18 | chr4 | 55902201 | |||||||
| chr4:55902624 | T | C | 40 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0017 others(37): Show |
57 | HG00408.hp1 HG00558.hp2 HG01346.hp2 others(54): Show |
intron_variant | MODIFIER | c.2532+86T>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 18/18 | chr4 | 55902624 | |||||||
| chr4:55902742 | A | G | 1 | a0001c0002t0002g0170 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2532+204A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 18/18 | chr4 | 55902742 | |||||||
| chr4:55902773 | T | TTTGG | 171 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(168): Show |
237 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(234): Show |
intron_variant | MODIFIER | c.2532+267_2532+270d others(6): Show |
EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr4 | 55902773 | ||||||
| chr4:55902773 | T | TTTGGTTG others(1): Show |
3 | a0001c0001t0001g0105 a0001c0001t0001g0134 a0001c0002t0004g0155 |
3 | HG02145.hp1 HG02809.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.2532+263_2532+270d others(10): Show |
EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr4 | 55902773 | ||||||
| chr4:55902773 | TTTGG | T | 4 | a0001c0002t0004g0020 a0001c0002t0004g0159 a0001c0002t0008g0020 others(1): Show |
6 | HG01884.hp2 HG02258.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.2532+267_2532+270d others(6): Show |
EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr4 | 55902773 | ||||||
| chr4:55902773 | TTTGGTTG others(1): Show |
T | 81 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(78): Show |
110 | HG00140.hp2 HG00408.hp2 HG00621.hp2 others(107): Show |
intron_variant | MODIFIER | c.2532+263_2532+270d others(10): Show |
EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr4 | 55902773 | ||||||
| chr4:55902862 | A | G | 1 | a0001c0002t0001g0049 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2532+324A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 18/18 | chr4 | 55902862 | |||||||
| chr4:55902920 | C | T | 1 | a0001c0002t0002g0163 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2532+382C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 18/18 | chr4 | 55902920 | |||||||
| chr4:55902926 | A | G | 11 | a0001c0002t0004g0020 a0001c0002t0004g0070 a0001c0002t0004g0088 others(8): Show |
13 | HG00558.hp1 HG01081.hp1 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.2532+388A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 18/18 | chr4 | 55902926 | |||||||
| chr4:55903007 | G | C | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | NA19240.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2532+469G>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 18/18 | chr4 | 55903007 | |||||||
| chr4:55903137 | G | A | 24 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(21): Show |
38 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.2532+599G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 18/18 | chr4 | 55903137 | |||||||
| chr4:55903145 | AT | A | 4 | a0001c0002t0004g0070 a0001c0002t0004g0215 a0001c0002t0004g0216 others(1): Show |
5 | HG01884.hp2 HG02572.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.2532+609delT | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr4 | 55903145 | ||||||
| chr4:55903146 | TTA | T | 4 | a0001c0002t0004g0088 a0001c0002t0004g0154 a0001c0002t0004g0155 others(1): Show |
4 | HG00558.hp1 HG01081.hp1 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.2532+609_2532+610d others(4): Show |
EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 18/18 | chr4 | 55903146 | |||||||
| chr4:55903147 | T | A | 3 | a0001c0002t0004g0020 a0001c0002t0004g0159 a0001c0002t0008g0020 |
4 | HG02258.hp2 HG03139.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2532+609T>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 18/18 | chr4 | 55903147 | |||||||
| chr4:55903147 | TA | T | 16 | a0001c0001t0001g0071 a0001c0001t0001g0082 a0001c0001t0001g0230 others(13): Show |
16 | HG01167.hp2 HG01884.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.2532+626delA | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr4 | 55903147 | ||||||
| chr4:55903154 | AAAAAAAA others(12): Show |
A | 3 | a0001c0001t0003g0016 a0001c0001t0003g0083 a0001c0001t0003g0084 |
5 | NA18961.hp1 NA18977.hp2 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.2532+620_2532+638d others(21): Show |
EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr4 | 55903154 | ||||||
| chr4:55903160 | AAAAAG | A | 64 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(61): Show |
94 | HG00408.hp2 HG00639.hp1 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.2532+626_2532+630d others(7): Show |
EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr4 | 55903160 | ||||||
| chr4:55903161 | A | G | 1 | a0001c0001t0001g0234 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2532+623A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 18/18 | chr4 | 55903161 | |||||||
| chr4:55903179 | AAAAG | A | 4 | a0001c0002t0004g0088 a0001c0002t0004g0154 a0001c0002t0004g0155 others(1): Show |
4 | HG00558.hp1 HG01081.hp1 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.2532+651_2532+654d others(6): Show |
EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr4 | 55903179 | ||||||
| chr4:55903271 | A | G | 1 | a0001c0002t0002g0181 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2532+733A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 18/18 | chr4 | 55903271 | |||||||
| chr4:55903358 | A | G | 36 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0017 others(33): Show |
53 | HG00408.hp1 HG00558.hp2 HG01346.hp2 others(50): Show |
intron_variant | MODIFIER | c.2532+820A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 18/18 | chr4 | 55903358 | |||||||
| chr4:55903496 | C | T | 1 | a0001c0002t0002g0196 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2533-847C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 18/18 | chr4 | 55903496 | |||||||
| chr4:55903624 | TA | T | 16 | a0001c0001t0003g0001 a0001c0001t0003g0010 a0001c0001t0003g0016 others(13): Show |
30 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.2533-718delA | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 18/18 | chr4 | 55903624 | |||||||
| chr4:55903785 | G | A | 2 | a0001c0001t0003g0083 a0001c0001t0003g0084 |
2 | NA18961.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.2533-558G>A | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 18/18 | chr4 | 55903785 | |||||||
| chr4:55903802 | A | G | 1 | a0001c0001t0001g0250 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2533-541A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 18/18 | chr4 | 55903802 | |||||||
| chr4:55903898 | C | T | 4 | a0001c0002t0004g0088 a0001c0002t0004g0154 a0001c0002t0004g0155 others(1): Show |
4 | HG00558.hp1 HG01081.hp1 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.2533-445C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 18/18 | chr4 | 55903898 | |||||||
| chr4:55903901 | T | C | 1 | a0001c0002t0002g0174 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2533-442T>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 18/18 | chr4 | 55903901 | |||||||
| chr4:55903970 | T | C | 1 | a0001c0001t0001g0248 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2533-373T>C | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 18/18 | chr4 | 55903970 | |||||||
| chr4:55904016 | T | G | 1 | a0001c0001t0001g0233 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2533-327T>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 18/18 | chr4 | 55904016 | |||||||
| chr4:55904036 | C | T | 3 | a0001c0001t0005g0044 a0001c0001t0005g0045 a0001c0001t0005g0046 |
3 | HG03098.hp1 HG03225.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2533-307C>T | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 18/18 | chr4 | 55904036 | |||||||
| chr4:55904285 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2533-58A>G | EXOC1 | ENSG00000090989.18 | transcript | ENST00000381295.7 | protein_coding | 18/18 | chr4 | 55904285 |