Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 50619 |
| ensemblid | ENSG00000023892.12 |
| hgncid | 2760 |
| symbol | DEF6 |
| name | DEF6 guanine nucleotide exchange factor |
| refseq_nuc | NM_022047.4 |
| refseq_prot | NP_071330.3 |
| ensembl_nuc | ENST00000316637.7 |
| ensembl_prot | ENSP00000319831.5 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 35297818 |
| end | 35321771 |
| strand | + |
| ver | v1.2 |
| region | chr6:35297818-35321771 |
| region5000 | chr6:35292818-35326771 |
| regionname0 | DEF6_chr6_35297818_35321771 |
| regionname5000 | DEF6_chr6_35292818_35326771 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 631 | 275 | 57 | 41 | 140 | 8 | 29 | 113 | DEF6_chr6_35292818_35326771 | DEF6 | MALRK others(626): Show |
chr6 | 35292818 | 35326771 |
| a0002 | 1/1 | 631 | 32 | 12 | 12 | 0 | 2 | 4 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | MALRK others(626): Show |
chr6 | 35292818 | 35326771 |
| a0003 | 0/0 | 631 | 11 | 11 | 0 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | MALRK others(626): Show |
chr6 | 35292818 | 35326771 |
| a0004 | 0/0 | 631 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | MALRK others(626): Show |
chr6 | 35292818 | 35326771 |
| a0005 | 0/0 | 631 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | MALRK others(626): Show |
chr6 | 35292818 | 35326771 |
| a0006 | 0/0 | 631 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | MALRK others(626): Show |
chr6 | 35292818 | 35326771 |
| a0007 | 0/0 | 631 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | MALRK others(626): Show |
chr6 | 35292818 | 35326771 |
| a0008 | 0/0 | 631 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DEF6_chr6_35292818_35326771 | DEF6 | MALRK others(626): Show |
chr6 | 35292818 | 35326771 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1893 | 247 | 37 | 36 | 138 | 7 | 29 | DEF6_chr6_35292818_35326771 | DEF6 | ATGGC others(1888): Show |
chr6 | 35292818 | 35326771 | ||
| a0001c0004 | 0/0 | 1893 | 8 | 7 | 1 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | ATGGC others(1888): Show |
chr6 | 35292818 | 35326771 | ||
| a0001c0005 | 0/0 | 1893 | 7 | 5 | 0 | 2 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | ATGGC others(1888): Show |
chr6 | 35292818 | 35326771 | ||
| a0001c0006 | 0/0 | 1893 | 6 | 5 | 1 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | ATGGC others(1888): Show |
chr6 | 35292818 | 35326771 | ||
| a0001c0008 | 0/0 | 1893 | 3 | 1 | 2 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | ATGGC others(1888): Show |
chr6 | 35292818 | 35326771 | ||
| a0001c0009 | 0/0 | 1893 | 2 | 0 | 1 | 0 | 1 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | ATGGC others(1888): Show |
chr6 | 35292818 | 35326771 | ||
| a0001c0013 | 0/0 | 1893 | 1 | 1 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | ATGGC others(1888): Show |
chr6 | 35292818 | 35326771 | ||
| a0001c0014 | 0/0 | 1893 | 1 | 1 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | ATGGC others(1888): Show |
chr6 | 35292818 | 35326771 | ||
| a0002c0002 | 1/1 | 1893 | 31 | 12 | 11 | 0 | 2 | 4 | DEF6_chr6_35292818_35326771 | DEF6 | ATGGC others(1888): Show |
chr6 | 35292818 | 35326771 | ||
| a0002c0015 | 0/0 | 1893 | 1 | 0 | 1 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | ATGGC others(1888): Show |
chr6 | 35292818 | 35326771 | ||
| a0003c0003 | 0/0 | 1893 | 11 | 11 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | ATGGC others(1888): Show |
chr6 | 35292818 | 35326771 | ||
| a0004c0007 | 0/0 | 1893 | 4 | 4 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | ATGGC others(1888): Show |
chr6 | 35292818 | 35326771 | ||
| a0005c0011 | 0/0 | 1893 | 1 | 0 | 0 | 1 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | ATGGC others(1888): Show |
chr6 | 35292818 | 35326771 | ||
| a0006c0016 | 0/0 | 1893 | 1 | 0 | 1 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | ATGGC others(1888): Show |
chr6 | 35292818 | 35326771 | ||
| a0007c0012 | 0/0 | 1893 | 1 | 0 | 0 | 0 | 0 | 1 | DEF6_chr6_35292818_35326771 | DEF6 | ATGGC others(1888): Show |
chr6 | 35292818 | 35326771 | ||
| a0008c0010 | 0/0 | 1893 | 1 | 0 | 0 | 1 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | ATGGC others(1888): Show |
chr6 | 35292818 | 35326771 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2296 | 239 | 36 | 36 | 132 | 6 | 29 | DEF6_chr6_35292818_35326771 | DEF6 | AGTGT others(2291): Show |
chr6 | 35292818 | 35326771 |
| a0001c0001t0002 | 0/0 | 2296 | 6 | 0 | 0 | 6 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | AGTGT others(2291): Show |
chr6 | 35292818 | 35326771 |
| a0001c0001t0003 | 0/0 | 2296 | 1 | 0 | 0 | 0 | 1 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | AGTGT others(2291): Show |
chr6 | 35292818 | 35326771 |
| a0001c0001t0005 | 0/0 | 2296 | 1 | 1 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | AGTGT others(2291): Show |
chr6 | 35292818 | 35326771 |
| a0001c0004t0001 | 0/0 | 2296 | 8 | 7 | 1 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | AGTGT others(2291): Show |
chr6 | 35292818 | 35326771 |
| a0001c0005t0001 | 0/0 | 2296 | 7 | 5 | 0 | 2 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | AGTGT others(2291): Show |
chr6 | 35292818 | 35326771 |
| a0001c0006t0001 | 0/0 | 2296 | 6 | 5 | 1 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | AGTGT others(2291): Show |
chr6 | 35292818 | 35326771 |
| a0001c0008t0001 | 0/0 | 2296 | 2 | 1 | 1 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | AGTGT others(2291): Show |
chr6 | 35292818 | 35326771 |
| a0001c0008t0004 | 0/0 | 2279 | 1 | 0 | 1 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | AGTGT others(2274): Show |
chr6 | 35292818 | 35326771 |
| a0001c0009t0002 | 0/0 | 2296 | 2 | 0 | 1 | 0 | 1 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | AGTGT others(2291): Show |
chr6 | 35292818 | 35326771 |
| a0001c0013t0001 | 0/0 | 2296 | 1 | 1 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | AGTGT others(2291): Show |
chr6 | 35292818 | 35326771 |
| a0001c0014t0001 | 0/0 | 2296 | 1 | 1 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | AGTGT others(2291): Show |
chr6 | 35292818 | 35326771 |
| a0002c0002t0001 | 0/0 | 2296 | 12 | 6 | 2 | 0 | 1 | 3 | DEF6_chr6_35292818_35326771 | DEF6 | AGTGT others(2291): Show |
chr6 | 35292818 | 35326771 |
| a0002c0002t0002 | 1/1 | 2296 | 19 | 6 | 9 | 0 | 1 | 1 | DEF6_chr6_35292818_35326771 | DEF6 | AGTGT others(2291): Show |
chr6 | 35292818 | 35326771 |
| a0002c0015t0002 | 0/0 | 2296 | 1 | 0 | 1 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | AGTGT others(2291): Show |
chr6 | 35292818 | 35326771 |
| a0003c0003t0001 | 0/0 | 2296 | 11 | 11 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | AGTGT others(2291): Show |
chr6 | 35292818 | 35326771 |
| a0004c0007t0002 | 0/0 | 2296 | 4 | 4 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | AGTGT others(2291): Show |
chr6 | 35292818 | 35326771 |
| a0005c0011t0001 | 0/0 | 2296 | 1 | 0 | 0 | 1 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | AGTGT others(2291): Show |
chr6 | 35292818 | 35326771 |
| a0006c0016t0001 | 0/0 | 2296 | 1 | 0 | 1 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | AGTGT others(2291): Show |
chr6 | 35292818 | 35326771 |
| a0007c0012t0001 | 0/0 | 2296 | 1 | 0 | 0 | 0 | 0 | 1 | DEF6_chr6_35292818_35326771 | DEF6 | AGTGT others(2291): Show |
chr6 | 35292818 | 35326771 |
| a0008c0010t0001 | 0/0 | 2296 | 1 | 0 | 0 | 1 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | AGTGT others(2291): Show |
chr6 | 35292818 | 35326771 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 42 | 5 | 4 | 22 | 2 | 9 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0002 | 0/0 | 17 | 0 | 3 | 13 | 1 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0003 | 0/0 | 9 | 2 | 2 | 5 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0004 | 0/0 | 8 | 3 | 0 | 3 | 0 | 2 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0006 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0012 | 0/0 | 4 | 1 | 2 | 1 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0023 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0002g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0001t0005g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0004t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0004t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0004t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0004t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0004t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0004t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0005t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0005t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0005t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0005t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0005t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0005t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0006t0001g0015 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0006t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0006t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0008t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0008t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0008t0004g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0009t0002g0033 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0013t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0001c0014t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0002c0002t0001g0008 | 0/0 | 5 | 2 | 2 | 0 | 0 | 1 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0002c0002t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0002c0002t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0002c0002t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0002c0002t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0002c0002t0002g0009 | 1/0 | 5 | 0 | 4 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0002c0002t0002g0022 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0002c0002t0002g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0002c0002t0002g0035 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0002c0002t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0002c0002t0002g0126 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0002c0002t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0002c0002t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0002c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0002c0002t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0002c0002t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0002c0015t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0003c0003t0001g0005 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0003c0003t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0003c0003t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0003c0003t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0003c0003t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0003c0003t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0004c0007t0002g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0004c0007t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0004c0007t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0005c0011t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0006c0016t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0007c0012t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| a0008c0010t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0088 | EUR | GBR | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0061 | EUR | GBR | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | FIN | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG00323 | hp2 | a0001 | c0009 | t0002 | g0033 | EUR | FIN | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | CHS | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG00558 | hp2 | a0005 | c0011 | t0001 | g0058 | EAS | CHS | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | CHS | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG00639 | hp1 | a0002 | c0002 | t0002 | g0009 | AMR | PUR | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG00642 | hp2 | a0006 | c0016 | t0001 | g0103 | AMR | PUR | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG00733 | hp2 | a0002 | c0002 | t0001 | g0008 | AMR | PUR | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG00738 | hp2 | a0001 | c0004 | t0001 | g0140 | AMR | PUR | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG01069 | hp2 | a0001 | c0006 | t0001 | g0015 | AMR | PUR | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG01081 | hp1 | a0002 | c0002 | t0002 | g0009 | AMR | PUR | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG01106 | hp2 | a0002 | c0002 | t0002 | g0127 | AMR | PUR | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG01109 | hp2 | a0002 | c0002 | t0002 | g0175 | AMR | PUR | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG01167 | hp1 | a0002 | c0002 | t0002 | g0035 | AMR | PUR | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG01168 | hp2 | a0002 | c0002 | t0002 | g0009 | AMR | PUR | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG01175 | hp2 | a0001 | c0008 | t0004 | g0026 | AMR | PUR | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG01192 | hp2 | a0002 | c0002 | t0001 | g0008 | AMR | PUR | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG01255 | hp1 | a0002 | c0015 | t0002 | g0125 | AMR | CLM | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG01255 | hp2 | a0001 | c0008 | t0001 | g0026 | AMR | CLM | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG01256 | hp2 | a0002 | c0002 | t0002 | g0133 | AMR | CLM | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG01361 | hp1 | a0002 | c0002 | t0002 | g0022 | AMR | CLM | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG01496 | hp2 | a0002 | c0002 | t0002 | g0009 | AMR | CLM | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0008 | AFR | ACB | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG01891 | hp1 | a0001 | c0014 | t0001 | g0123 | AFR | ACB | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG01934 | hp1 | a0001 | c0009 | t0002 | g0033 | AMR | PEL | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02055 | hp1 | a0002 | c0002 | t0002 | g0034 | AFR | ACB | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02055 | hp2 | a0003 | c0003 | t0001 | g0105 | AFR | ACB | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02080 | hp2 | a0001 | c0005 | t0001 | g0144 | EAS | KHV | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | CDX | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CDX | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | CDX | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02257 | hp2 | a0001 | c0004 | t0001 | g0141 | AFR | ACB | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02451 | hp1 | a0001 | c0005 | t0001 | g0115 | AFR | ACB | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02572 | hp1 | a0001 | c0004 | t0001 | g0038 | AFR | GWD | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02572 | hp2 | a0002 | c0002 | t0001 | g0131 | AFR | GWD | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02622 | hp1 | a0002 | c0002 | t0001 | g0118 | AFR | GWD | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02630 | hp1 | a0002 | c0002 | t0001 | g0008 | AFR | GWD | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02647 | hp1 | a0002 | c0002 | t0002 | g0129 | AFR | GWD | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02647 | hp2 | a0003 | c0003 | t0001 | g0005 | AFR | GWD | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02698 | hp2 | a0002 | c0002 | t0001 | g0143 | SAS | PJL | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02717 | hp1 | a0001 | c0005 | t0001 | g0032 | AFR | GWD | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02723 | hp1 | a0001 | c0006 | t0001 | g0015 | AFR | GWD | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0135 | SAS | PJL | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02818 | hp1 | a0002 | c0002 | t0001 | g0128 | AFR | GWD | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02895 | hp1 | a0003 | c0003 | t0001 | g0005 | AFR | GWD | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02896 | hp2 | a0001 | c0006 | t0001 | g0015 | AFR | GWD | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02922 | hp2 | a0003 | c0003 | t0001 | g0005 | AFR | ESN | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02965 | hp1 | a0001 | c0004 | t0001 | g0139 | AFR | ESN | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02965 | hp2 | a0001 | c0006 | t0001 | g0110 | AFR | ESN | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG03041 | hp2 | a0003 | c0003 | t0001 | g0104 | AFR | GWD | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ESN | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG03130 | hp2 | a0002 | c0002 | t0002 | g0022 | AFR | ESN | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ESN | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG03195 | hp1 | a0004 | c0007 | t0002 | g0138 | AFR | ESN | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG03195 | hp2 | a0001 | c0005 | t0001 | g0145 | AFR | ESN | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG03209 | hp1 | a0001 | c0004 | t0001 | g0037 | AFR | MSL | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG03209 | hp2 | a0001 | c0005 | t0001 | g0117 | AFR | MSL | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG03225 | hp2 | a0004 | c0007 | t0002 | g0036 | AFR | MSL | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG03453 | hp1 | a0003 | c0003 | t0001 | g0005 | AFR | MSL | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG03453 | hp2 | a0004 | c0007 | t0002 | g0036 | AFR | MSL | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG03516 | hp1 | a0004 | c0007 | t0002 | g0137 | AFR | ESN | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG03516 | hp2 | a0001 | c0004 | t0001 | g0038 | AFR | ESN | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG03579 | hp1 | a0001 | c0013 | t0001 | g0112 | AFR | MSL | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG03579 | hp2 | a0002 | c0002 | t0002 | g0022 | AFR | MSL | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG03688 | hp1 | a0007 | c0012 | t0001 | g0001 | SAS | STU | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG03834 | hp1 | a0002 | c0002 | t0002 | g0035 | SAS | BEB | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | BEB | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0008 | SAS | BEB | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | BEB | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | STU | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | STU | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | STU | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | YRI | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18522 | hp2 | a0003 | c0003 | t0001 | g0108 | AFR | YRI | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHB | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHB | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18906 | hp1 | a0002 | c0002 | t0002 | g0034 | AFR | YRI | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18906 | hp2 | a0002 | c0002 | t0002 | g0124 | AFR | YRI | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18977 | hp2 | a0008 | c0010 | t0001 | g0147 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA19030 | hp1 | a0001 | c0001 | t0005 | g0150 | AFR | LWK | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA19030 | hp2 | a0001 | c0004 | t0001 | g0037 | AFR | LWK | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA19043 | hp2 | a0003 | c0003 | t0001 | g0106 | AFR | LWK | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA19066 | hp1 | a0001 | c0005 | t0001 | g0116 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA19240 | hp1 | a0001 | c0004 | t0001 | g0136 | AFR | YRI | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA19240 | hp2 | a0001 | c0005 | t0001 | g0032 | AFR | YRI | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0130 | AFR | ASW | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0084 | EUR | TSI | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0134 | EUR | TSI | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA20805 | hp2 | a0002 | c0002 | t0002 | g0132 | EUR | TSI | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02486 | hp1 | a0001 | c0006 | t0001 | g0046 | AFR | ACB | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02486 | hp2 | a0003 | c0003 | t0001 | g0107 | AFR | ACB | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG02559 | hp2 | a0003 | c0003 | t0001 | g0005 | AFR | ACB | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG03471 | hp1 | a0001 | c0006 | t0001 | g0015 | AFR | MSL | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG03471 | hp2 | a0003 | c0003 | t0001 | g0005 | AFR | MSL | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | USA | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | USA | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA20300 | hp1 | a0001 | c0008 | t0001 | g0063 | AFR | USA | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | USA | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | LWK | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | LWK | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0002 | g0126 | REF | REF | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0002 | g0009 | REF | REF | DEF6_chr6_35292818_35326771 | DEF6 | chr6 | 35292818 | 35326771 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:35312747 | C | T | 1 | a0007 | 1 | HG03688.hp1 | missense_variant | MODERATE | c.782C>T | p.Pro261Leu | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 5/11 | 821/2296 | 782/1896 | 261/631 | chr6 | 35312747 | |||
| chr6:35317942 | A | C | 1 | a0001 | 2 | HG00323.hp2 HG01934.hp1 |
missense_variant | MODERATE | c.859A>C | p.Asn287His | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 6/11 | 898/2296 | 859/1896 | 287/631 | chr6 | 35317942 | |||
| chr6:35317943 | A | C | 6 | a0001 a0003 a0005 others(3): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
missense_variant | MODERATE | c.860A>C | p.Asn287Thr | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 6/11 | 899/2296 | 860/1896 | 287/631 | chr6 | 35317943 | |||
| chr6:35318332 | G | A | 1 | a0006 | 1 | HG00642.hp2 | missense_variant | MODERATE | c.1076G>A | p.Arg359Gln | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 7/11 | 1115/2296 | 1076/1896 | 359/631 | chr6 | 35318332 | |||
| chr6:35319637 | A | T | 1 | a0005 | 1 | HG00558.hp2 | missense_variant | MODERATE | c.1329A>T | p.Gln443His | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 8/11 | 1368/2296 | 1329/1896 | 443/631 | chr6 | 35319637 | |||
| chr6:35321208 | G | A | 1 | a0008 | 1 | NA18977.hp2 | missense_variant | MODERATE | c.1694G>A | p.Ser565Asn | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 11/11 | 1733/2296 | 1694/1896 | 565/631 | chr6 | 35321208 | |||
| chr6:35321247 | G | A | 1 | a0003 | 11 | HG02055.hp2 HG02486.hp2 HG02559.hp2 others(8): Show |
missense_variant | MODERATE | c.1733G>A | p.Arg578His | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 11/11 | 1772/2296 | 1733/1896 | 578/631 | chr6 | 35321247 | |||
| chr6:35321376 | A | C | 1 | a0004 | 4 | HG03195.hp1 HG03225.hp2 HG03453.hp2 others(1): Show |
missense_variant | MODERATE | c.1862A>C | p.Gln621Pro | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 11/11 | 1901/2296 | 1862/1896 | 621/631 | chr6 | 35321376 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:35297934 | C | T | 3 | a0001c0006 a0003c0003 a0006c0016 |
18 | HG00642.hp2 HG01069.hp2 HG02055.hp2 others(15): Show |
synonymous_variant | LOW | c.78C>T | p.Val26Val | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/11 | 117/2296 | 78/1896 | 26/631 | chr6 | 35297934 | |||
| chr6:35310578 | C | T | 1 | a0002c0015 | 1 | HG01255.hp1 | synonymous_variant | LOW | c.357C>T | p.Phe119Phe | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 3/11 | 396/2296 | 357/1896 | 119/631 | chr6 | 35310578 | |||
| chr6:35312406 | C | T | 2 | a0001c0013 a0001c0014 |
2 | HG01891.hp1 HG03579.hp1 |
synonymous_variant | LOW | c.528C>T | p.Thr176Thr | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 4/11 | 567/2296 | 528/1896 | 176/631 | chr6 | 35312406 | |||
| chr6:35318298 | C | T | 2 | a0001c0004 a0001c0014 |
9 | HG00738.hp2 HG01891.hp1 HG02257.hp2 others(6): Show |
synonymous_variant | LOW | c.1042C>T | p.Leu348Leu | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 7/11 | 1081/2296 | 1042/1896 | 348/631 | chr6 | 35318298 | |||
| chr6:35319978 | G | A | 1 | a0001c0005 | 7 | HG02080.hp2 HG02451.hp1 HG02717.hp1 others(4): Show |
synonymous_variant | LOW | c.1542G>A | p.Glu514Glu | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 9/11 | 1581/2296 | 1542/1896 | 514/631 | chr6 | 35319978 | |||
| chr6:35320919 | C | T | 1 | a0001c0005 | 7 | HG02080.hp2 HG02451.hp1 HG02717.hp1 others(4): Show |
synonymous_variant | LOW | c.1617C>T | p.Asn539Asn | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 10/11 | 1656/2296 | 1617/1896 | 539/631 | chr6 | 35320919 | |||
| chr6:35321398 | A | C | 1 | a0001c0008 | 3 | HG01175.hp2 HG01255.hp2 NA20300.hp1 |
synonymous_variant | LOW | c.1884A>C | p.Ala628Ala | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 11/11 | 1923/2296 | 1884/1896 | 628/631 | chr6 | 35321398 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:35297834 | C | G | 1 | a0001c0001t0005 | 1 | NA19030.hp1 | 5_prime_UTR_variant | MODIFIER | c.-23C>G | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/11 | 23 | chr6 | 35297834 | ||||||
| chr6:35321597 | G | A | 1 | a0001c0001t0003 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*187G>A | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 11/11 | 187 | chr6 | 35321597 | ||||||
| chr6:35321669 | T | C | 16 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(13): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
3_prime_UTR_variant | MODIFIER | c.*259T>C | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 11/11 | 259 | chr6 | 35321669 | ||||||
| chr6:35321691 | AGCAAGCC others(10): Show |
A | 1 | a0001c0008t0004 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*284_*300delAAGCCG others(11): Show |
DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 11/11 | 284 | INFO_REALIGN_3_PRIME | chr6 | 35321691 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:35297965 | C | T | 1 | a0002c0002t0002g0175 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.96+13C>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35297965 | |||||||
| chr6:35298010 | G | A | 4 | a0001c0001t0002g0017 a0001c0001t0002g0043 a0001c0001t0002g0044 others(1): Show |
6 | NA18948.hp2 NA18960.hp2 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.96+58G>A | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35298010 | |||||||
| chr6:35298064 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.96+112C>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35298064 | |||||||
| chr6:35298195 | C | T | 39 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0010 others(36): Show |
77 | HG00438.hp2 HG00558.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.96+243C>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35298195 | |||||||
| chr6:35298454 | G | C | 106 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(103): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.96+502G>C | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35298454 | |||||||
| chr6:35298456 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.96+504C>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35298456 | |||||||
| chr6:35298541 | T | C | 1 | a0001c0006t0001g0046 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.96+589T>C | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35298541 | |||||||
| chr6:35298775 | T | C | 1 | a0001c0001t0001g0047 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.96+823T>C | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35298775 | |||||||
| chr6:35298920 | C | A | 1 | a0001c0014t0001g0123 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.96+968C>A | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35298920 | |||||||
| chr6:35299029 | C | G | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 |
3 | HG02895.hp2 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.96+1077C>G | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35299029 | |||||||
| chr6:35299085 | A | T | 1 | a0001c0001t0001g0119 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.96+1133A>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35299085 | |||||||
| chr6:35299107 | T | C | 1 | a0001c0001t0001g0048 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.96+1155T>C | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35299107 | |||||||
| chr6:35299134 | A | G | 1 | a0001c0001t0001g0174 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.96+1182A>G | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35299134 | |||||||
| chr6:35299195 | C | T | 11 | a0001c0001t0001g0111 a0001c0001t0001g0113 a0001c0001t0001g0114 others(8): Show |
12 | HG02080.hp2 HG02109.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.96+1243C>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35299195 | |||||||
| chr6:35299230 | A | C | 1 | a0001c0001t0001g0173 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.96+1278A>C | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35299230 | |||||||
| chr6:35299339 | C | T | 1 | a0002c0002t0001g0118 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.96+1387C>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35299339 | |||||||
| chr6:35299445 | C | A | 1 | a0001c0001t0001g0049 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.96+1493C>A | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35299445 | |||||||
| chr6:35299575 | C | A | 1 | a0001c0001t0001g0050 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.96+1623C>A | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35299575 | |||||||
| chr6:35299771 | G | A | 78 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(75): Show |
160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.96+1819G>A | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35299771 | |||||||
| chr6:35299803 | C | T | 3 | a0001c0006t0001g0015 a0001c0006t0001g0046 a0001c0006t0001g0110 |
6 | HG01069.hp2 HG02486.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.96+1851C>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35299803 | |||||||
| chr6:35299879 | C | T | 2 | a0001c0001t0001g0172 a0001c0005t0001g0145 |
2 | HG01433.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.96+1927C>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35299879 | |||||||
| chr6:35299934 | G | A | 1 | a0001c0009t0002g0033 | 2 | HG00323.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.96+1982G>A | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35299934 | |||||||
| chr6:35299938 | C | T | 82 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(79): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.96+1986C>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35299938 | |||||||
| chr6:35299942 | CGAG | C | 3 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0102 |
5 | HG01074.hp2 HG01884.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.96+1991_96+1993del others(3): Show |
DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35299942 | |||||||
| chr6:35300096 | A | T | 1 | a0002c0002t0001g0143 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.96+2144A>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35300096 | |||||||
| chr6:35300125 | G | C | 1 | a0001c0001t0001g0111 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.96+2173G>C | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35300125 | |||||||
| chr6:35300345 | T | A | 1 | a0002c0002t0001g0118 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.96+2393T>A | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35300345 | |||||||
| chr6:35300402 | A | T | 1 | a0001c0001t0001g0031 | 2 | HG03669.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.96+2450A>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35300402 | |||||||
| chr6:35300488 | A | T | 6 | a0001c0005t0001g0032 a0001c0005t0001g0115 a0001c0005t0001g0116 others(3): Show |
7 | HG02080.hp2 HG02451.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.96+2536A>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35300488 | |||||||
| chr6:35300547 | T | G | 2 | a0001c0001t0001g0051 a0001c0001t0001g0052 |
2 | HG02630.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.96+2595T>G | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35300547 | |||||||
| chr6:35300569 | G | T | 6 | a0001c0001t0001g0142 a0001c0004t0001g0037 a0001c0004t0001g0038 others(3): Show |
8 | HG00738.hp2 HG02257.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.96+2617G>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35300569 | |||||||
| chr6:35300583 | C | A | 1 | a0002c0002t0001g0118 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.96+2631C>A | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35300583 | |||||||
| chr6:35300625 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.96+2673A>G | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35300625 | |||||||
| chr6:35300633 | A | G | 108 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(105): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.96+2681A>G | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35300633 | |||||||
| chr6:35300655 | G | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0053 |
3 | HG02735.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.96+2703G>A | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35300655 | |||||||
| chr6:35300756 | G | A | 82 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(79): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.96+2804G>A | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35300756 | |||||||
| chr6:35300874 | T | C | 6 | a0001c0005t0001g0032 a0001c0005t0001g0115 a0001c0005t0001g0116 others(3): Show |
7 | HG02080.hp2 HG02451.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.96+2922T>C | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35300874 | |||||||
| chr6:35300932 | C | G | 1 | a0003c0003t0001g0108 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.96+2980C>G | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35300932 | |||||||
| chr6:35300977 | G | T | 1 | a0001c0006t0001g0110 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.96+3025G>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35300977 | |||||||
| chr6:35301192 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.96+3240T>C | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35301192 | |||||||
| chr6:35301362 | C | T | 1 | a0001c0001t0001g0101 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.96+3410C>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35301362 | |||||||
| chr6:35301376 | C | T | 6 | a0003c0003t0001g0005 a0003c0003t0001g0104 a0003c0003t0001g0105 others(3): Show |
11 | HG02055.hp2 HG02486.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.96+3424C>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35301376 | |||||||
| chr6:35301377 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.96+3425G>A | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35301377 | |||||||
| chr6:35301412 | A | C | 1 | a0001c0001t0001g0174 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.96+3460A>C | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35301412 | |||||||
| chr6:35301608 | G | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0171 |
5 | NA18747.hp2 NA18943.hp1 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.96+3656G>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35301608 | |||||||
| chr6:35301727 | C | CT | 44 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0010 others(41): Show |
84 | HG00438.hp2 HG00558.hp1 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.96+3792dupT | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 35301727 | ||||||
| chr6:35301727 | C | CTTT | 16 | a0001c0001t0001g0018 a0001c0001t0001g0048 a0001c0001t0001g0059 others(13): Show |
23 | HG00558.hp2 HG02055.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.96+3790_96+3792dup others(3): Show |
DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 35301727 | ||||||
| chr6:35301727 | C | CTTTT | 83 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(80): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.96+3789_96+3792dup others(4): Show |
DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 35301727 | ||||||
| chr6:35301794 | T | A | 2 | a0001c0001t0001g0040 a0001c0001t0001g0146 |
3 | NA18951.hp2 NA18953.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.96+3842T>A | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35301794 | |||||||
| chr6:35302167 | G | T | 1 | a0002c0002t0001g0118 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.96+4215G>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35302167 | |||||||
| chr6:35302228 | T | C | 1 | a0002c0002t0002g0124 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.96+4276T>C | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35302228 | |||||||
| chr6:35302273 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.96+4321C>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35302273 | |||||||
| chr6:35302436 | G | A | 1 | a0001c0001t0001g0025 | 2 | HG04199.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.96+4484G>A | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35302436 | |||||||
| chr6:35302493 | C | A | 1 | a0001c0001t0001g0061 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.96+4541C>A | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35302493 | |||||||
| chr6:35302522 | C | A | 3 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0102 |
5 | HG01074.hp2 HG01884.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.96+4570C>A | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35302522 | |||||||
| chr6:35302605 | G | A | 1 | a0001c0013t0001g0112 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.96+4653G>A | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35302605 | |||||||
| chr6:35302770 | G | A | 1 | a0002c0015t0002g0125 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.96+4818G>A | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35302770 | |||||||
| chr6:35302802 | T | C | 107 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(104): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.96+4850T>C | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35302802 | |||||||
| chr6:35302954 | CTGAGGAC others(3): Show |
C | 1 | a0001c0001t0001g0099 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.96+5005_96+5014del others(10): Show |
DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 35302954 | ||||||
| chr6:35303010 | C | T | 1 | a0001c0001t0001g0170 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.96+5058C>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35303010 | |||||||
| chr6:35303019 | T | G | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 |
3 | HG02895.hp2 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.96+5067T>G | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35303019 | |||||||
| chr6:35303065 | C | A | 1 | a0001c0001t0001g0062 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.96+5113C>A | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35303065 | |||||||
| chr6:35303071 | C | T | 4 | a0001c0001t0002g0017 a0001c0001t0002g0043 a0001c0001t0002g0044 others(1): Show |
6 | NA18948.hp2 NA18960.hp2 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.96+5119C>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35303071 | |||||||
| chr6:35303107 | G | A | 3 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0102 |
5 | HG01074.hp2 HG01884.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.96+5155G>A | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35303107 | |||||||
| chr6:35303168 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.96+5216A>G | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35303168 | |||||||
| chr6:35303537 | C | T | 2 | a0001c0001t0001g0109 a0001c0001t0001g0174 |
2 | HG00741.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.96+5585C>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35303537 | |||||||
| chr6:35303538 | G | A | 4 | a0001c0001t0002g0017 a0001c0001t0002g0043 a0001c0001t0002g0044 others(1): Show |
6 | NA18948.hp2 NA18960.hp2 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.96+5586G>A | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35303538 | |||||||
| chr6:35303642 | A | G | 2 | a0001c0001t0001g0096 a0001c0001t0001g0097 |
2 | NA19068.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.96+5690A>G | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35303642 | |||||||
| chr6:35303899 | G | A | 4 | a0001c0001t0002g0017 a0001c0001t0002g0043 a0001c0001t0002g0044 others(1): Show |
6 | NA18948.hp2 NA18960.hp2 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.97-5771G>A | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35303899 | |||||||
| chr6:35304057 | C | T | 11 | a0001c0001t0001g0111 a0001c0001t0001g0113 a0001c0001t0001g0114 others(8): Show |
12 | HG02080.hp2 HG02109.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.97-5613C>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35304057 | |||||||
| chr6:35304159 | A | G | 3 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0102 |
5 | HG01074.hp2 HG01884.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.97-5511A>G | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35304159 | |||||||
| chr6:35304200 | A | G | 5 | a0001c0001t0001g0007 a0001c0001t0001g0057 a0001c0001t0001g0094 others(2): Show |
9 | HG02074.hp1 NA18939.hp2 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.97-5470A>G | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35304200 | |||||||
| chr6:35304340 | G | T | 1 | a0001c0001t0001g0169 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.97-5330G>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35304340 | |||||||
| chr6:35304497 | C | T | 71 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(68): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.97-5173C>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35304497 | |||||||
| chr6:35304759 | A | G | 1 | a0001c0001t0001g0174 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.97-4911A>G | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35304759 | |||||||
| chr6:35304826 | A | G | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 |
3 | HG02895.hp2 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.97-4844A>G | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35304826 | |||||||
| chr6:35305146 | A | AT | 7 | a0001c0001t0001g0049 a0001c0001t0001g0092 a0001c0001t0001g0093 others(4): Show |
7 | HG00741.hp2 HG01261.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.97-4508dupT | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 35305146 | ||||||
| chr6:35305162 | T | C | 1 | a0002c0002t0002g0127 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.97-4508T>C | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35305162 | |||||||
| chr6:35305182 | G | A | 11 | a0001c0001t0001g0111 a0001c0001t0001g0113 a0001c0001t0001g0114 others(8): Show |
12 | HG02080.hp2 HG02109.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.97-4488G>A | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35305182 | |||||||
| chr6:35305297 | C | T | 3 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0102 |
5 | HG01074.hp2 HG01884.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.97-4373C>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35305297 | |||||||
| chr6:35305484 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.97-4186C>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35305484 | |||||||
| chr6:35305559 | T | C | 1 | a0001c0001t0001g0027 | 2 | HG00741.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.97-4111T>C | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35305559 | |||||||
| chr6:35305565 | G | T | 1 | a0001c0005t0001g0117 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.97-4105G>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35305565 | |||||||
| chr6:35305696 | C | T | 1 | a0001c0001t0001g0090 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.97-3974C>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35305696 | |||||||
| chr6:35305767 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.97-3903T>C | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35305767 | |||||||
| chr6:35305784 | G | A | 1 | a0002c0002t0002g0034 | 2 | HG02055.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.97-3886G>A | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35305784 | |||||||
| chr6:35306022 | A | G | 77 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(74): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.97-3648A>G | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35306022 | |||||||
| chr6:35306232 | C | T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0167 |
7 | HG00558.hp1 HG00673.hp1 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.97-3438C>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35306232 | |||||||
| chr6:35306233 | G | C | 4 | a0001c0001t0002g0017 a0001c0001t0002g0043 a0001c0001t0002g0044 others(1): Show |
6 | NA18948.hp2 NA18960.hp2 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.97-3437G>C | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35306233 | |||||||
| chr6:35306248 | T | C | 48 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0010 others(45): Show |
89 | HG00438.hp2 HG00558.hp1 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.97-3422T>C | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35306248 | |||||||
| chr6:35306468 | G | A | 3 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0102 |
5 | HG01074.hp2 HG01884.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.97-3202G>A | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35306468 | |||||||
| chr6:35306483 | C | T | 2 | a0002c0002t0001g0134 a0002c0002t0001g0135 |
2 | HG02735.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.97-3187C>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35306483 | |||||||
| chr6:35306511 | TA | T | 6 | a0001c0001t0001g0056 a0001c0001t0001g0089 a0001c0001t0001g0091 others(3): Show |
6 | HG01256.hp2 HG02257.hp1 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.97-3145delA | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 35306511 | ||||||
| chr6:35306653 | C | T | 6 | a0003c0003t0001g0005 a0003c0003t0001g0104 a0003c0003t0001g0105 others(3): Show |
11 | HG02055.hp2 HG02486.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.97-3017C>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35306653 | |||||||
| chr6:35306822 | C | T | 10 | a0001c0006t0001g0015 a0001c0006t0001g0046 a0001c0006t0001g0110 others(7): Show |
18 | HG00642.hp2 HG01069.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.97-2848C>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35306822 | |||||||
| chr6:35306830 | A | G | 1 | a0001c0005t0001g0145 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.97-2840A>G | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35306830 | |||||||
| chr6:35307050 | C | T | 1 | a0001c0001t0001g0090 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.97-2620C>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35307050 | |||||||
| chr6:35307124 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.97-2546G>A | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35307124 | |||||||
| chr6:35307329 | G | A | 1 | a0001c0001t0001g0041 | 2 | HG02155.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.97-2341G>A | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35307329 | |||||||
| chr6:35307354 | G | T | 1 | a0001c0001t0001g0165 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.97-2316G>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35307354 | |||||||
| chr6:35307367 | C | G | 1 | a0004c0007t0002g0138 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.97-2303C>G | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35307367 | |||||||
| chr6:35307390 | A | C | 107 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(104): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.97-2280A>C | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35307390 | |||||||
| chr6:35307392 | G | A | 1 | a0001c0001t0001g0064 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.97-2278G>A | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35307392 | |||||||
| chr6:35307393 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.97-2277C>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35307393 | |||||||
| chr6:35307455 | A | G | 2 | a0001c0001t0001g0011 a0001c0001t0001g0164 |
6 | NA18969.hp1 NA18985.hp1 NA19002.hp1 others(3): Show |
intron_variant | MODIFIER | c.97-2215A>G | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35307455 | |||||||
| chr6:35307605 | G | C | 21 | a0001c0001t0001g0111 a0001c0001t0001g0113 a0001c0001t0001g0114 others(18): Show |
30 | HG00642.hp2 HG01069.hp2 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.97-2065G>C | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35307605 | |||||||
| chr6:35307723 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.97-1947G>A | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35307723 | |||||||
| chr6:35307726 | A | G | 4 | a0001c0001t0002g0017 a0001c0001t0002g0043 a0001c0001t0002g0044 others(1): Show |
6 | NA18948.hp2 NA18960.hp2 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.97-1944A>G | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35307726 | |||||||
| chr6:35307743 | C | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0050 a0001c0001t0001g0087 |
6 | HG01109.hp1 HG01167.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.97-1927C>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35307743 | |||||||
| chr6:35307811 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.97-1859G>A | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35307811 | |||||||
| chr6:35307952 | A | C | 6 | a0003c0003t0001g0005 a0003c0003t0001g0104 a0003c0003t0001g0105 others(3): Show |
11 | HG02055.hp2 HG02486.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.97-1718A>C | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35307952 | |||||||
| chr6:35308186 | C | T | 80 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(77): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.97-1484C>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35308186 | |||||||
| chr6:35308369 | C | CA | 7 | a0001c0001t0001g0099 a0003c0003t0001g0005 a0003c0003t0001g0104 others(4): Show |
12 | HG02055.hp2 HG02486.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.97-1301_97-1300ins others(1): Show |
DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35308369 | |||||||
| chr6:35308370 | G | A | 104 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(101): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.97-1300G>A | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35308370 | |||||||
| chr6:35308395 | G | A | 1 | a0001c0013t0001g0112 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.97-1275G>A | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35308395 | |||||||
| chr6:35308537 | A | T | 1 | a0001c0001t0001g0060 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.97-1133A>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35308537 | |||||||
| chr6:35308672 | C | CAAAAT | 13 | a0001c0001t0001g0028 a0001c0001t0001g0049 a0001c0001t0001g0066 others(10): Show |
15 | HG00738.hp1 HG00741.hp2 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.97-944_97-940dupAT others(3): Show |
DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 35308672 | ||||||
| chr6:35308672 | C | CAAAATAA others(3): Show |
8 | a0001c0005t0001g0032 a0001c0005t0001g0117 a0001c0005t0001g0144 others(5): Show |
14 | HG00733.hp2 HG01192.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.97-949_97-940dupAT others(8): Show |
DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 35308672 | ||||||
| chr6:35308672 | C | CAAAATAA others(8): Show |
1 | a0002c0002t0001g0128 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.97-954_97-940dupAT others(13): Show |
DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 35308672 | ||||||
| chr6:35308672 | C | CAAAATAA others(18): Show |
1 | a0001c0001t0001g0114 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.97-964_97-940dupAT others(23): Show |
DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 35308672 | ||||||
| chr6:35308672 | C | CAAAATAA others(23): Show |
1 | a0001c0001t0001g0113 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.97-969_97-940dupAT others(28): Show |
DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 35308672 | ||||||
| chr6:35308672 | CAAAAT | C | 49 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(46): Show |
95 | HG00438.hp2 HG00558.hp1 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.97-944_97-940delAT others(3): Show |
DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 35308672 | ||||||
| chr6:35308672 | CAAAATAA others(3): Show |
C | 45 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0014 others(42): Show |
105 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.97-949_97-940delAT others(8): Show |
DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 35308672 | ||||||
| chr6:35308672 | CAAAATAA others(8): Show |
C | 13 | a0001c0001t0001g0013 a0001c0001t0001g0021 a0001c0001t0001g0047 others(10): Show |
23 | HG00673.hp2 HG01891.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.97-954_97-940delAT others(13): Show |
DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 35308672 | ||||||
| chr6:35308672 | CAAAATAA others(13): Show |
C | 8 | a0001c0001t0001g0093 a0001c0001t0001g0121 a0001c0001t0001g0122 others(5): Show |
10 | HG02257.hp1 HG02895.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.97-959_97-940delAT others(18): Show |
DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 35308672 | ||||||
| chr6:35308672 | CAAAATAA others(18): Show |
C | 1 | a0003c0003t0001g0106 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.97-964_97-940delAT others(23): Show |
DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 35308672 | ||||||
| chr6:35308678 | A | G | 1 | a0006c0016t0001g0103 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.97-992A>G | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35308678 | |||||||
| chr6:35308731 | T | A | 2 | a0001c0001t0001g0149 a0002c0002t0001g0134 |
2 | NA19064.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.97-939T>A | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35308731 | |||||||
| chr6:35308732 | A | T | 2 | a0001c0001t0001g0149 a0002c0002t0001g0134 |
2 | NA19064.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.97-938A>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35308732 | |||||||
| chr6:35308739 | T | A | 2 | a0001c0001t0001g0149 a0002c0002t0001g0134 |
2 | NA19064.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.97-931T>A | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35308739 | |||||||
| chr6:35308741 | A | T | 2 | a0001c0001t0001g0149 a0002c0002t0001g0134 |
2 | NA19064.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.97-929A>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35308741 | |||||||
| chr6:35308759 | TAAA | T | 40 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0010 others(37): Show |
79 | HG00438.hp2 HG00558.hp1 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.97-907_97-905delAA others(1): Show |
DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 35308759 | ||||||
| chr6:35308803 | G | A | 1 | a0001c0001t0001g0072 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.97-867G>A | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35308803 | |||||||
| chr6:35309048 | G | T | 1 | a0001c0001t0001g0071 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.97-622G>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35309048 | |||||||
| chr6:35309190 | G | C | 1 | a0001c0001t0001g0153 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.97-480G>C | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35309190 | |||||||
| chr6:35309550 | AGT | A | 3 | a0001c0006t0001g0015 a0001c0006t0001g0046 a0001c0006t0001g0110 |
6 | HG01069.hp2 HG02486.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.97-113_97-112delGT | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 35309550 | ||||||
| chr6:35309578 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.97-92G>A | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35309578 | |||||||
| chr6:35309619 | C | T | 6 | a0003c0003t0001g0005 a0003c0003t0001g0104 a0003c0003t0001g0105 others(3): Show |
11 | HG02055.hp2 HG02486.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.97-51C>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 1/10 | chr6 | 35309619 | |||||||
| chr6:35309838 | G | T | 1 | a0001c0001t0001g0085 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.237+28G>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 2/10 | chr6 | 35309838 | |||||||
| chr6:35310012 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.237+202T>C | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 2/10 | chr6 | 35310012 | |||||||
| chr6:35310013 | G | A | 6 | a0001c0005t0001g0032 a0001c0005t0001g0115 a0001c0005t0001g0116 others(3): Show |
7 | HG02080.hp2 HG02451.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.237+203G>A | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 2/10 | chr6 | 35310013 | |||||||
| chr6:35310257 | T | G | 1 | a0001c0001t0001g0170 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.238-202T>G | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 2/10 | chr6 | 35310257 | |||||||
| chr6:35310409 | C | G | 1 | a0001c0001t0001g0162 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.238-50C>G | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 2/10 | chr6 | 35310409 | |||||||
| chr6:35310705 | G | A | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 |
3 | HG02895.hp2 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.423+61G>A | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 3/10 | chr6 | 35310705 | |||||||
| chr6:35310722 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.423+78C>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 3/10 | chr6 | 35310722 | |||||||
| chr6:35311019 | A | C | 73 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(70): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.423+375A>C | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 3/10 | chr6 | 35311019 | |||||||
| chr6:35311147 | C | A | 10 | a0001c0006t0001g0015 a0001c0006t0001g0046 a0001c0006t0001g0110 others(7): Show |
18 | HG00642.hp2 HG01069.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.423+503C>A | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 3/10 | chr6 | 35311147 | |||||||
| chr6:35311187 | C | T | 4 | a0001c0001t0002g0017 a0001c0001t0002g0043 a0001c0001t0002g0044 others(1): Show |
6 | NA18948.hp2 NA18960.hp2 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.423+543C>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 3/10 | chr6 | 35311187 | |||||||
| chr6:35311221 | C | T | 1 | a0001c0004t0001g0141 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.423+577C>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 3/10 | chr6 | 35311221 | |||||||
| chr6:35311256 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.423+612C>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 3/10 | chr6 | 35311256 | |||||||
| chr6:35311325 | T | A | 1 | a0002c0002t0001g0130 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.423+681T>A | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 3/10 | chr6 | 35311325 | |||||||
| chr6:35311399 | A | G | 1 | a0001c0001t0001g0161 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.423+755A>G | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 3/10 | chr6 | 35311399 | |||||||
| chr6:35311517 | A | T | 2 | a0001c0001t0001g0021 a0001c0001t0001g0119 |
4 | HG02602.hp1 HG02738.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.424-785A>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 3/10 | chr6 | 35311517 | |||||||
| chr6:35311797 | C | G | 8 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0102 others(5): Show |
10 | HG01074.hp2 HG01884.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.424-505C>G | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 3/10 | chr6 | 35311797 | |||||||
| chr6:35311826 | A | G | 6 | a0003c0003t0001g0005 a0003c0003t0001g0104 a0003c0003t0001g0105 others(3): Show |
11 | HG02055.hp2 HG02486.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.424-476A>G | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 3/10 | chr6 | 35311826 | |||||||
| chr6:35312085 | G | A | 1 | a0001c0001t0001g0074 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.424-217G>A | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 3/10 | chr6 | 35312085 | |||||||
| chr6:35312166 | G | A | 1 | a0001c0001t0001g0057 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.424-136G>A | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 3/10 | chr6 | 35312166 | |||||||
| chr6:35312176 | C | A | 4 | a0001c0001t0002g0017 a0001c0001t0002g0043 a0001c0001t0002g0044 others(1): Show |
6 | NA18948.hp2 NA18960.hp2 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.424-126C>A | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 3/10 | chr6 | 35312176 | |||||||
| chr6:35312830 | T | C | 3 | a0001c0006t0001g0015 a0001c0006t0001g0046 a0001c0006t0001g0110 |
6 | HG01069.hp2 HG02486.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.807+58T>C | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 5/10 | chr6 | 35312830 | |||||||
| chr6:35312920 | C | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(104): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.807+148C>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 5/10 | chr6 | 35312920 | |||||||
| chr6:35312929 | C | T | 1 | a0001c0001t0003g0084 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.807+157C>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 5/10 | chr6 | 35312929 | |||||||
| chr6:35313008 | A | G | 18 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0102 others(15): Show |
28 | HG00642.hp2 HG01069.hp2 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.807+236A>G | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 5/10 | chr6 | 35313008 | |||||||
| chr6:35313051 | A | C | 2 | a0001c0001t0001g0039 a0001c0001t0001g0152 |
3 | NA18979.hp2 NA18985.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.807+279A>C | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 5/10 | chr6 | 35313051 | |||||||
| chr6:35313081 | A | G | 23 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0102 others(20): Show |
28 | HG00738.hp2 HG00741.hp2 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.807+309A>G | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 5/10 | chr6 | 35313081 | |||||||
| chr6:35313137 | T | TCTCCTTC others(12): Show |
2 | a0001c0001t0001g0030 a0001c0001t0001g0031 |
4 | HG01074.hp2 HG02976.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.807+369_807+387dup others(19): Show |
DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr6 | 35313137 | ||||||
| chr6:35313194 | C | T | 31 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0102 others(28): Show |
45 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.807+422C>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 5/10 | chr6 | 35313194 | |||||||
| chr6:35313414 | C | A | 1 | a0001c0001t0001g0075 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.807+642C>A | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 5/10 | chr6 | 35313414 | |||||||
| chr6:35313425 | A | G | 2 | a0001c0001t0001g0148 a0001c0001t0001g0160 |
2 | NA18978.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.807+653A>G | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 5/10 | chr6 | 35313425 | |||||||
| chr6:35313443 | C | T | 18 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0102 others(15): Show |
22 | HG00738.hp2 HG01074.hp2 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.807+671C>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 5/10 | chr6 | 35313443 | |||||||
| chr6:35313501 | A | G | 4 | a0001c0001t0002g0017 a0001c0001t0002g0043 a0001c0001t0002g0044 others(1): Show |
6 | NA18948.hp2 NA18960.hp2 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.807+729A>G | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 5/10 | chr6 | 35313501 | |||||||
| chr6:35313570 | T | C | 5 | a0001c0001t0001g0111 a0001c0001t0001g0113 a0001c0001t0001g0114 others(2): Show |
5 | HG02109.hp1 HG02145.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.807+798T>C | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 5/10 | chr6 | 35313570 | |||||||
| chr6:35313631 | G | C | 3 | a0001c0001t0001g0073 a0001c0001t0001g0076 a0001c0001t0001g0077 |
3 | HG02145.hp1 HG02717.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.807+859G>C | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 5/10 | chr6 | 35313631 | |||||||
| chr6:35313962 | A | T | 4 | a0001c0001t0002g0017 a0001c0001t0002g0043 a0001c0001t0002g0044 others(1): Show |
6 | NA18948.hp2 NA18960.hp2 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.807+1190A>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 5/10 | chr6 | 35313962 | |||||||
| chr6:35314067 | A | G | 1 | a0001c0001t0001g0016 | 4 | NA18747.hp2 NA18943.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.807+1295A>G | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 5/10 | chr6 | 35314067 | |||||||
| chr6:35314089 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.807+1317G>A | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 5/10 | chr6 | 35314089 | |||||||
| chr6:35314132 | G | T | 1 | a0001c0009t0002g0033 | 2 | HG00323.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.807+1360G>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 5/10 | chr6 | 35314132 | |||||||
| chr6:35314134 | G | A | 40 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0010 others(37): Show |
79 | HG00438.hp2 HG00558.hp1 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.807+1362G>A | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 5/10 | chr6 | 35314134 | |||||||
| chr6:35314313 | C | T | 84 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(81): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.807+1541C>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 5/10 | chr6 | 35314313 | |||||||
| chr6:35314407 | CA | C | 125 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(122): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.807+1655delA | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr6 | 35314407 | ||||||
| chr6:35314523 | T | C | 1 | a0001c0004t0001g0141 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.807+1751T>C | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 5/10 | chr6 | 35314523 | |||||||
| chr6:35314598 | A | G | 83 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(80): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.807+1826A>G | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 5/10 | chr6 | 35314598 | |||||||
| chr6:35314619 | G | T | 6 | a0003c0003t0001g0005 a0003c0003t0001g0104 a0003c0003t0001g0105 others(3): Show |
11 | HG02055.hp2 HG02486.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.807+1847G>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 5/10 | chr6 | 35314619 | |||||||
| chr6:35314686 | C | G | 113 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(110): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.807+1914C>G | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 5/10 | chr6 | 35314686 | |||||||
| chr6:35314827 | C | CA | 88 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(85): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.807+2061dupA | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr6 | 35314827 | ||||||
| chr6:35315216 | A | G | 113 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(110): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.807+2444A>G | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 5/10 | chr6 | 35315216 | |||||||
| chr6:35315274 | C | T | 1 | a0008c0010t0001g0147 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.807+2502C>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 5/10 | chr6 | 35315274 | |||||||
| chr6:35315384 | G | A | 2 | a0001c0001t0001g0019 a0001c0001t0001g0080 |
4 | HG00323.hp1 HG01243.hp2 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.808-2507G>A | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 5/10 | chr6 | 35315384 | |||||||
| chr6:35315463 | A | AT | 108 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(105): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.808-2420dupT | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr6 | 35315463 | ||||||
| chr6:35315564 | A | T | 10 | a0001c0006t0001g0015 a0001c0006t0001g0046 a0001c0006t0001g0110 others(7): Show |
18 | HG00642.hp2 HG01069.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.808-2327A>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 5/10 | chr6 | 35315564 | |||||||
| chr6:35315829 | G | A | 1 | a0002c0015t0002g0125 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.808-2062G>A | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 5/10 | chr6 | 35315829 | |||||||
| chr6:35315847 | C | CT | 22 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0023 others(19): Show |
32 | HG00323.hp1 HG01175.hp1 HG01175.hp2 others(29): Show |
intron_variant | MODIFIER | c.808-2022dupT | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr6 | 35315847 | ||||||
| chr6:35315847 | C | CTT | 7 | a0001c0001t0001g0053 a0001c0001t0001g0109 a0001c0005t0001g0032 others(4): Show |
8 | HG00741.hp2 HG02451.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.808-2023_808-2022d others(4): Show |
DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr6 | 35315847 | ||||||
| chr6:35315847 | C | CTTTT | 6 | a0001c0004t0001g0037 a0001c0004t0001g0038 a0001c0004t0001g0136 others(3): Show |
8 | HG00738.hp2 HG02257.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.808-2025_808-2022d others(6): Show |
DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr6 | 35315847 | ||||||
| chr6:35315847 | CT | C | 8 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0001g0154 others(5): Show |
8 | HG00558.hp1 HG01168.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.808-2022delT | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr6 | 35315847 | ||||||
| chr6:35315879 | G | A | 4 | a0001c0001t0002g0017 a0001c0001t0002g0043 a0001c0001t0002g0044 others(1): Show |
6 | NA18948.hp2 NA18960.hp2 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.808-2012G>A | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 5/10 | chr6 | 35315879 | |||||||
| chr6:35316026 | A | AT | 75 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(72): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.808-1851dupT | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr6 | 35316026 | ||||||
| chr6:35316026 | A | ATT | 6 | a0001c0001t0001g0020 a0001c0001t0001g0052 a0001c0001t0001g0059 others(3): Show |
8 | HG01192.hp1 HG01258.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.808-1852_808-1851d others(4): Show |
DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr6 | 35316026 | ||||||
| chr6:35316069 | G | A | 3 | a0001c0006t0001g0015 a0001c0006t0001g0046 a0001c0006t0001g0110 |
6 | HG01069.hp2 HG02486.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.808-1822G>A | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 5/10 | chr6 | 35316069 | |||||||
| chr6:35316168 | CT | C | 108 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(105): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.808-1709delT | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr6 | 35316168 | ||||||
| chr6:35316181 | T | C | 74 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(71): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.808-1710T>C | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 5/10 | chr6 | 35316181 | |||||||
| chr6:35316196 | G | T | 6 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0067 others(3): Show |
14 | NA18943.hp2 NA18950.hp1 NA18951.hp1 others(11): Show |
intron_variant | MODIFIER | c.808-1695G>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 5/10 | chr6 | 35316196 | |||||||
| chr6:35316289 | G | A | 1 | a0002c0015t0002g0125 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.808-1602G>A | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 5/10 | chr6 | 35316289 | |||||||
| chr6:35316352 | G | A | 1 | a0002c0002t0002g0132 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.808-1539G>A | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 5/10 | chr6 | 35316352 | |||||||
| chr6:35316664 | T | C | 6 | a0001c0005t0001g0032 a0001c0005t0001g0115 a0001c0005t0001g0116 others(3): Show |
7 | HG02080.hp2 HG02451.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.808-1227T>C | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 5/10 | chr6 | 35316664 | |||||||
| chr6:35316885 | C | G | 1 | a0001c0001t0001g0174 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.808-1006C>G | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 5/10 | chr6 | 35316885 | |||||||
| chr6:35317121 | A | AGTT | 116 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(113): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.808-766_808-764dup others(3): Show |
DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr6 | 35317121 | ||||||
| chr6:35317472 | C | T | 7 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0102 others(4): Show |
9 | HG01074.hp2 HG01884.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.808-419C>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 5/10 | chr6 | 35317472 | |||||||
| chr6:35317696 | A | C | 2 | a0001c0001t0001g0042 a0001c0001t0001g0161 |
3 | NA18950.hp2 NA18962.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.808-195A>C | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 5/10 | chr6 | 35317696 | |||||||
| chr6:35317697 | G | A | 2 | a0001c0001t0001g0042 a0001c0001t0001g0161 |
3 | NA18950.hp2 NA18962.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.808-194G>A | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 5/10 | chr6 | 35317697 | |||||||
| chr6:35317761 | C | A | 1 | a0001c0001t0001g0082 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.808-130C>A | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 5/10 | chr6 | 35317761 | |||||||
| chr6:35317766 | G | C | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(121): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.808-125G>C | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 5/10 | chr6 | 35317766 | |||||||
| chr6:35317862 | C | A | 1 | a0001c0001t0001g0102 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.808-29C>A | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 5/10 | chr6 | 35317862 | |||||||
| chr6:35318003 | A | G | 3 | a0001c0001t0001g0111 a0001c0001t0001g0113 a0001c0001t0001g0114 |
3 | HG02109.hp1 HG02145.hp2 HG06807.hp2 |
splice_region_variant&intron_variant | LOW | c.916+4A>G | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 6/10 | chr6 | 35318003 | |||||||
| chr6:35318126 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.917-47C>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 6/10 | chr6 | 35318126 | |||||||
| chr6:35318518 | G | T | 7 | a0001c0004t0001g0037 a0001c0004t0001g0038 a0001c0004t0001g0136 others(4): Show |
9 | HG00738.hp2 HG01891.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1215+47G>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 7/10 | chr6 | 35318518 | |||||||
| chr6:35318556 | A | C | 7 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0102 others(4): Show |
9 | HG01074.hp2 HG01884.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1215+85A>C | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 7/10 | chr6 | 35318556 | |||||||
| chr6:35318559 | G | A | 1 | a0001c0013t0001g0112 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1215+88G>A | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 7/10 | chr6 | 35318559 | |||||||
| chr6:35318725 | G | A | 2 | a0001c0001t0001g0059 a0001c0001t0001g0069 |
2 | NA18960.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1215+254G>A | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 7/10 | chr6 | 35318725 | |||||||
| chr6:35318955 | T | C | 1 | a0001c0014t0001g0123 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1215+484T>C | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 7/10 | chr6 | 35318955 | |||||||
| chr6:35319192 | T | C | 1 | a0001c0008t0001g0063 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1216-332T>C | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 7/10 | chr6 | 35319192 | |||||||
| chr6:35319470 | C | T | 4 | a0001c0001t0002g0017 a0001c0001t0002g0043 a0001c0001t0002g0044 others(1): Show |
6 | NA18948.hp2 NA18960.hp2 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1216-54C>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 7/10 | chr6 | 35319470 | |||||||
| chr6:35319746 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1382+56A>G | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 8/10 | chr6 | 35319746 | |||||||
| chr6:35320034 | G | T | 8 | a0002c0002t0001g0008 a0002c0002t0001g0118 a0002c0002t0001g0128 others(5): Show |
12 | HG00733.hp2 HG01192.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1581+17G>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 9/10 | chr6 | 35320034 | |||||||
| chr6:35320439 | C | T | 1 | a0001c0001t0001g0094 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1581+422C>T | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 9/10 | chr6 | 35320439 | |||||||
| chr6:35321134 | G | A | 4 | a0001c0001t0002g0017 a0001c0001t0002g0043 a0001c0001t0002g0044 others(1): Show |
6 | NA18948.hp2 NA18960.hp2 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1673-53G>A | DEF6 | ENSG00000023892.12 | transcript | ENST00000316637.7 | protein_coding | 10/10 | chr6 | 35321134 |