Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 219988 |
| ensemblid | ENSG00000166889.14 |
| hgncid | 26721 |
| symbol | PATL1 |
| name | PAT1 homolog 1, processing body mRNA decay factor |
| refseq_nuc | NM_152716.3 |
| refseq_prot | NP_689929.2 |
| ensembl_nuc | ENST00000300146.10 |
| ensembl_prot | ENSP00000300146.9 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 59636716 |
| end | 59669037 |
| strand | - |
| ver | v1.2 |
| region | chr11:59636716-59669037 |
| region5000 | chr11:59631716-59674037 |
| regionname0 | PATL1_chr11_59636716_59669037 |
| regionname5000 | PATL1_chr11_59631716_59674037 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 770 | 271 | 75 | 58 | 122 | 0 | 14 | 88 | PATL1_chr11_59631716_59674037 | PATL1 | MFRYE others(765): Show |
chr11 | 59631716 | 59674037 |
| a0002 | 0/0 | 770 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | MFRYE others(765): Show |
chr11 | 59631716 | 59674037 |
| a0003 | 0/0 | 770 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | MFRYE others(765): Show |
chr11 | 59631716 | 59674037 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2310 | 259 | 69 | 53 | 121 | 0 | 14 | PATL1_chr11_59631716_59674037 | PATL1 | ATGTT others(2305): Show |
chr11 | 59631716 | 59674037 | ||
| a0001c0002 | 0/0 | 2310 | 4 | 3 | 1 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | ATGTT others(2305): Show |
chr11 | 59631716 | 59674037 | ||
| a0001c0004 | 0/0 | 2310 | 3 | 0 | 2 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | ATGTT others(2305): Show |
chr11 | 59631716 | 59674037 | ||
| a0001c0006 | 0/0 | 2310 | 1 | 0 | 1 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | ATGTT others(2305): Show |
chr11 | 59631716 | 59674037 | ||
| a0001c0007 | 0/0 | 2310 | 1 | 0 | 1 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | ATGTT others(2305): Show |
chr11 | 59631716 | 59674037 | ||
| a0001c0008 | 0/0 | 2310 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | ATGTT others(2305): Show |
chr11 | 59631716 | 59674037 | ||
| a0001c0009 | 0/0 | 2310 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | ATGTT others(2305): Show |
chr11 | 59631716 | 59674037 | ||
| a0001c0010 | 0/0 | 2310 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | ATGTT others(2305): Show |
chr11 | 59631716 | 59674037 | ||
| a0002c0003 | 0/0 | 2310 | 3 | 3 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | ATGTT others(2305): Show |
chr11 | 59631716 | 59674037 | ||
| a0003c0005 | 0/0 | 2310 | 2 | 2 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | ATGTT others(2305): Show |
chr11 | 59631716 | 59674037 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 4129 | 203 | 60 | 49 | 83 | 0 | 9 | PATL1_chr11_59631716_59674037 | PATL1 | CGTCC others(4124): Show |
chr11 | 59631716 | 59674037 |
| a0001c0001t0002 | 0/0 | 4129 | 28 | 0 | 2 | 22 | 0 | 4 | PATL1_chr11_59631716_59674037 | PATL1 | CGTCC others(4124): Show |
chr11 | 59631716 | 59674037 |
| a0001c0001t0003 | 0/0 | 4129 | 10 | 0 | 0 | 10 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | CGTCC others(4124): Show |
chr11 | 59631716 | 59674037 |
| a0001c0001t0004 | 0/0 | 4129 | 9 | 3 | 2 | 3 | 0 | 1 | PATL1_chr11_59631716_59674037 | PATL1 | CGTCC others(4124): Show |
chr11 | 59631716 | 59674037 |
| a0001c0001t0005 | 0/0 | 4129 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | CGTCC others(4124): Show |
chr11 | 59631716 | 59674037 |
| a0001c0001t0006 | 0/0 | 4129 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | CGTCC others(4124): Show |
chr11 | 59631716 | 59674037 |
| a0001c0001t0007 | 0/0 | 4129 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | CGTCC others(4124): Show |
chr11 | 59631716 | 59674037 |
| a0001c0001t0008 | 0/0 | 4129 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | CGTCC others(4124): Show |
chr11 | 59631716 | 59674037 |
| a0001c0001t0009 | 0/0 | 4129 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | CGTCC others(4124): Show |
chr11 | 59631716 | 59674037 |
| a0001c0001t0010 | 0/0 | 4129 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | CGTCC others(4124): Show |
chr11 | 59631716 | 59674037 |
| a0001c0001t0011 | 0/0 | 4129 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | CGTCC others(4124): Show |
chr11 | 59631716 | 59674037 |
| a0001c0001t0012 | 0/0 | 4129 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | CGTCC others(4124): Show |
chr11 | 59631716 | 59674037 |
| a0001c0001t0013 | 0/0 | 4129 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | CGTCC others(4124): Show |
chr11 | 59631716 | 59674037 |
| a0001c0002t0005 | 0/0 | 4129 | 4 | 3 | 1 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | CGTCC others(4124): Show |
chr11 | 59631716 | 59674037 |
| a0001c0004t0001 | 0/0 | 4129 | 3 | 0 | 2 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | CGTCC others(4124): Show |
chr11 | 59631716 | 59674037 |
| a0001c0006t0001 | 0/0 | 4129 | 1 | 0 | 1 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | CGTCC others(4124): Show |
chr11 | 59631716 | 59674037 |
| a0001c0007t0001 | 0/0 | 4129 | 1 | 0 | 1 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | CGTCC others(4124): Show |
chr11 | 59631716 | 59674037 |
| a0001c0008t0002 | 0/0 | 4129 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | CGTCC others(4124): Show |
chr11 | 59631716 | 59674037 |
| a0001c0009t0001 | 0/0 | 4129 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | CGTCC others(4124): Show |
chr11 | 59631716 | 59674037 |
| a0001c0010t0014 | 0/0 | 4129 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | CGTCC others(4124): Show |
chr11 | 59631716 | 59674037 |
| a0002c0003t0005 | 0/0 | 4129 | 3 | 3 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | CGTCC others(4124): Show |
chr11 | 59631716 | 59674037 |
| a0003c0005t0001 | 0/0 | 4129 | 2 | 2 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | CGTCC others(4124): Show |
chr11 | 59631716 | 59674037 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/1 | 16 | 1 | 1 | 12 | 0 | 1 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0002 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0007 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0008 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0009 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0010 | 0/0 | 3 | 2 | 0 | 0 | 0 | 1 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0143 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0002g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0002g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0003g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0004g0012 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0004g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0004g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0004g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0004g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0004g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0005g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0006g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0007g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0008g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0009g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0010g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0011g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0012g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0001t0013g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0002t0005g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0002t0005g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0002t0005g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0004t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0004t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0004t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0006t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0007t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0008t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0009t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0001c0010t0014g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0002c0003t0005g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0002c0003t0005g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0003c0005t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| a0003c0005t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | CHS | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0114 | EAS | CHS | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | CHS | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG00642 | hp2 | a0001 | c0001 | t0004 | g0195 | AMR | PUR | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | CHS | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | CHS | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG00733 | hp2 | a0001 | c0004 | t0001 | g0092 | AMR | PUR | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG01109 | hp2 | a0001 | c0002 | t0005 | g0038 | AMR | PUR | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG01261 | hp2 | a0001 | c0006 | t0001 | g0155 | AMR | CLM | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | CLM | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0053 | AMR | CLM | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG01884 | hp1 | a0003 | c0005 | t0001 | g0044 | AFR | ACB | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG01891 | hp1 | a0001 | c0001 | t0007 | g0176 | AFR | ACB | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PEL | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG01975 | hp2 | a0001 | c0004 | t0001 | g0091 | AMR | PEL | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0052 | AMR | PEL | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02056 | hp1 | a0001 | c0001 | t0004 | g0012 | EAS | KHV | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02129 | hp2 | a0001 | c0004 | t0001 | g0090 | EAS | KHV | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02145 | hp2 | a0001 | c0002 | t0005 | g0014 | AFR | ACB | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0113 | EAS | CDX | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02258 | hp2 | a0001 | c0001 | t0006 | g0032 | AFR | ACB | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | ACB | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | ACB | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02293 | hp2 | a0001 | c0007 | t0001 | g0104 | AMR | PEL | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0037 | AFR | GWD | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02615 | hp2 | a0001 | c0001 | t0010 | g0047 | AFR | GWD | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0076 | SAS | PJL | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02717 | hp2 | a0003 | c0005 | t0001 | g0045 | AFR | GWD | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02735 | hp2 | a0001 | c0001 | t0004 | g0012 | SAS | PJL | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02818 | hp1 | a0001 | c0010 | t0014 | g0209 | AFR | GWD | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0196 | AFR | GWD | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | ESN | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ESN | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ESN | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ESN | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | ESN | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0168 | AFR | ESN | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ESN | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG03041 | hp1 | a0001 | c0001 | t0013 | g0067 | AFR | GWD | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | ESN | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG03209 | hp1 | a0001 | c0002 | t0005 | g0014 | AFR | MSL | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | MSL | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG03225 | hp1 | a0001 | c0001 | t0008 | g0068 | AFR | MSL | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG03225 | hp2 | a0001 | c0009 | t0001 | g0162 | AFR | MSL | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG03453 | hp1 | a0001 | c0002 | t0005 | g0039 | AFR | MSL | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0075 | SAS | PJL | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ESN | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG03516 | hp2 | a0002 | c0003 | t0005 | g0040 | AFR | ESN | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | STU | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0077 | SAS | STU | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0061 | SAS | BEB | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | BEB | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | YRI | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA18906 | hp2 | a0002 | c0003 | t0005 | g0015 | AFR | YRI | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA18948 | hp1 | a0001 | c0001 | t0004 | g0198 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA18962 | hp2 | a0001 | c0001 | t0009 | g0099 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA18966 | hp1 | a0001 | c0001 | t0012 | g0093 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA18975 | hp2 | a0001 | c0001 | t0011 | g0157 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA18995 | hp1 | a0001 | c0001 | t0004 | g0199 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | LWK | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | LWK | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | LWK | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | LWK | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0160 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA19075 | hp2 | a0001 | c0001 | t0003 | g0159 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | YRI | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA20129 | hp1 | a0001 | c0008 | t0002 | g0139 | AFR | ASW | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | ASW | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | GIH | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | GIH | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG01123 | hp1 | a0001 | c0001 | t0004 | g0012 | AMR | CLM | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0197 | AFR | ACB | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG02559 | hp2 | a0002 | c0003 | t0005 | g0015 | AFR | ACB | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | MSL | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | USA | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | USA | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | USA | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0001 | REF | REF | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0143 | REF | REF | PATL1_chr11_59631716_59674037 | PATL1 | chr11 | 59631716 | 59674037 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:59642995 | T | C | 1 | a0002 | 3 | HG02559.hp2 HG03516.hp2 NA18906.hp2 |
missense_variant | MODERATE | c.1934A>G | p.Tyr645Cys | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 16/19 | 2076/4129 | 1934/2313 | 645/770 | chr11 | 59642995 | |||
| chr11:59654059 | T | C | 1 | a0003 | 2 | HG01884.hp1 HG02717.hp2 |
missense_variant | MODERATE | c.1045A>G | p.Met349Val | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 9/19 | 1187/4129 | 1045/2313 | 349/770 | chr11 | 59654059 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:59643006 | A | T | 1 | a0001c0008 | 1 | NA20129.hp1 | synonymous_variant | LOW | c.1923T>A | p.Ser641Ser | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 16/19 | 2065/4129 | 1923/2313 | 641/770 | chr11 | 59643006 | |||
| chr11:59643024 | G | A | 1 | a0001c0009 | 1 | HG03225.hp2 | synonymous_variant | LOW | c.1905C>T | p.Cys635Cys | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 16/19 | 2047/4129 | 1905/2313 | 635/770 | chr11 | 59643024 | |||
| chr11:59651610 | G | A | 1 | a0001c0010 | 1 | HG02818.hp1 | synonymous_variant | LOW | c.1458C>T | p.Thr486Thr | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 12/19 | 1600/4129 | 1458/2313 | 486/770 | chr11 | 59651610 | |||
| chr11:59652907 | A | G | 1 | a0001c0007 | 1 | HG02293.hp2 | synonymous_variant | LOW | c.1233T>C | p.Asp411Asp | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 10/19 | 1375/4129 | 1233/2313 | 411/770 | chr11 | 59652907 | |||
| chr11:59655570 | A | G | 1 | a0001c0004 | 3 | HG00733.hp2 HG01975.hp2 HG02129.hp2 |
synonymous_variant | LOW | c.984T>C | p.Pro328Pro | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 8/19 | 1126/4129 | 984/2313 | 328/770 | chr11 | 59655570 | |||
| chr11:59655644 | G | T | 2 | a0001c0002 a0002c0003 |
7 | HG01109.hp2 HG02145.hp2 HG02559.hp2 others(4): Show |
synonymous_variant | LOW | c.910C>A | p.Arg304Arg | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 8/19 | 1052/4129 | 910/2313 | 304/770 | chr11 | 59655644 | |||
| chr11:59656547 | A | G | 1 | a0001c0006 | 1 | HG01261.hp2 | synonymous_variant | LOW | c.675T>C | p.Pro225Pro | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 6/19 | 817/4129 | 675/2313 | 225/770 | chr11 | 59656547 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:59636820 | G | A | 1 | a0001c0001t0010 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1570C>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 19/19 | 1570 | chr11 | 59636820 | ||||||
| chr11:59636914 | G | A | 2 | a0001c0001t0002 a0001c0008t0002 |
29 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1476C>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 19/19 | 1476 | chr11 | 59636914 | ||||||
| chr11:59636957 | A | G | 2 | a0001c0001t0009 a0001c0001t0012 |
2 | NA18962.hp2 NA18966.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1433T>C | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 19/19 | 1433 | chr11 | 59636957 | ||||||
| chr11:59637108 | C | T | 1 | a0001c0001t0008 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1282G>A | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 19/19 | 1282 | chr11 | 59637108 | ||||||
| chr11:59637193 | G | C | 1 | a0001c0001t0011 | 1 | NA18975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1197C>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 19/19 | 1197 | chr11 | 59637193 | ||||||
| chr11:59637206 | T | C | 2 | a0001c0001t0004 a0001c0010t0014 |
10 | HG00642.hp2 HG01123.hp1 HG02056.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1184A>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 19/19 | 1184 | chr11 | 59637206 | ||||||
| chr11:59637356 | G | A | 1 | a0001c0001t0012 | 1 | NA18966.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1034C>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 19/19 | 1034 | chr11 | 59637356 | ||||||
| chr11:59637684 | G | C | 1 | a0001c0001t0013 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*706C>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 19/19 | 706 | chr11 | 59637684 | ||||||
| chr11:59637777 | T | G | 3 | a0001c0001t0005 a0001c0002t0005 a0002c0003t0005 |
8 | HG01109.hp2 HG02145.hp2 HG02559.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*613A>C | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 19/19 | 613 | chr11 | 59637777 | ||||||
| chr11:59638203 | A | T | 1 | a0001c0001t0007 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*187T>A | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 19/19 | 187 | chr11 | 59638203 | ||||||
| chr11:59638360 | A | G | 1 | a0001c0001t0003 | 10 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*30T>C | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 19/19 | 30 | chr11 | 59638360 | ||||||
| chr11:59638364 | A | T | 1 | a0001c0001t0003 | 10 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*26T>A | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 19/19 | 26 | chr11 | 59638364 | ||||||
| chr11:59668989 | G | A | 1 | a0001c0010t0014 | 1 | HG02818.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-94C>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 1/19 | chr11 | 59668989 | |||||||
| chr11:59668991 | C | T | 1 | a0001c0001t0006 | 1 | HG02258.hp2 | 5_prime_UTR_variant | MODIFIER | c.-96G>A | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 1/19 | 96 | chr11 | 59668991 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:59638682 | TTTTA | T | 27 | a0001c0001t0001g0011 a0001c0001t0001g0030 a0001c0001t0001g0031 others(24): Show |
31 | HG00639.hp2 HG00733.hp1 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.2292-275_2292-272d others(6): Show |
PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 18/18 | chr11 | 59638682 | |||||||
| chr11:59638792 | T | A | 1 | a0001c0001t0003g0159 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2291+256A>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 18/18 | chr11 | 59638792 | |||||||
| chr11:59638979 | A | T | 1 | a0001c0001t0003g0159 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2291+69T>A | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 18/18 | chr11 | 59638979 | |||||||
| chr11:59639022 | G | A | 1 | a0001c0001t0001g0095 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2291+26C>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 18/18 | chr11 | 59639022 | |||||||
| chr11:59639421 | T | C | 8 | a0001c0001t0004g0012 a0001c0001t0004g0168 a0001c0001t0004g0195 others(5): Show |
10 | HG00642.hp2 HG01123.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.2050-38A>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 16/18 | chr11 | 59639421 | |||||||
| chr11:59639739 | A | G | 6 | a0001c0001t0005g0037 a0001c0002t0005g0014 a0001c0002t0005g0038 others(3): Show |
8 | HG01109.hp2 HG02145.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.2050-356T>C | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 16/18 | chr11 | 59639739 | |||||||
| chr11:59639857 | A | T | 1 | a0001c0001t0001g0095 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2050-474T>A | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 16/18 | chr11 | 59639857 | |||||||
| chr11:59639902 | C | T | 69 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0018 others(66): Show |
79 | HG00639.hp2 HG00642.hp2 HG00733.hp1 others(76): Show |
intron_variant | MODIFIER | c.2050-519G>A | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 16/18 | chr11 | 59639902 | |||||||
| chr11:59640012 | A | G | 2 | a0001c0001t0001g0071 a0001c0001t0001g0072 |
2 | HG03041.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2050-629T>C | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 16/18 | chr11 | 59640012 | |||||||
| chr11:59640039 | G | C | 27 | a0001c0001t0001g0011 a0001c0001t0001g0030 a0001c0001t0001g0031 others(24): Show |
31 | HG00639.hp2 HG00733.hp1 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.2050-656C>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 16/18 | chr11 | 59640039 | |||||||
| chr11:59640072 | T | C | 1 | a0001c0004t0001g0091 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2050-689A>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 16/18 | chr11 | 59640072 | |||||||
| chr11:59640099 | T | C | 1 | a0001c0001t0001g0167 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2050-716A>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 16/18 | chr11 | 59640099 | |||||||
| chr11:59640171 | G | A | 2 | a0001c0001t0001g0041 a0001c0001t0001g0064 |
2 | NA18955.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.2050-788C>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 16/18 | chr11 | 59640171 | |||||||
| chr11:59640204 | G | A | 6 | a0001c0001t0005g0037 a0001c0002t0005g0014 a0001c0002t0005g0038 others(3): Show |
8 | HG01109.hp2 HG02145.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.2050-821C>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 16/18 | chr11 | 59640204 | |||||||
| chr11:59640204 | G | T | 40 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0030 others(37): Show |
45 | HG00639.hp2 HG00733.hp1 HG01106.hp1 others(42): Show |
intron_variant | MODIFIER | c.2050-821C>A | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 16/18 | chr11 | 59640204 | |||||||
| chr11:59640240 | C | T | 1 | a0001c0001t0001g0175 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2050-857G>A | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 16/18 | chr11 | 59640240 | |||||||
| chr11:59640325 | G | A | 3 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 |
3 | HG03041.hp2 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2050-942C>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 16/18 | chr11 | 59640325 | |||||||
| chr11:59640342 | C | CA | 26 | a0001c0001t0001g0018 a0001c0001t0001g0069 a0001c0001t0001g0070 others(23): Show |
31 | HG00642.hp2 HG01109.hp2 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.2050-960dupT | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 16/18 | chr11 | 59640342 | |||||||
| chr11:59640342 | CA | C | 7 | a0001c0001t0002g0110 a0001c0001t0003g0003 a0001c0001t0003g0113 others(4): Show |
11 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(8): Show |
intron_variant | MODIFIER | c.2050-960delT | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 16/18 | chr11 | 59640342 | |||||||
| chr11:59640501 | A | G | 1 | a0001c0001t0001g0122 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2050-1118T>C | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 16/18 | chr11 | 59640501 | |||||||
| chr11:59640516 | G | A | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.2050-1133C>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 16/18 | chr11 | 59640516 | |||||||
| chr11:59640610 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2050-1227G>A | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 16/18 | chr11 | 59640610 | |||||||
| chr11:59640724 | G | GA | 8 | a0001c0001t0004g0012 a0001c0001t0004g0168 a0001c0001t0004g0195 others(5): Show |
10 | HG00642.hp2 HG01123.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.2050-1342dupT | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 16/18 | chr11 | 59640724 | |||||||
| chr11:59640778 | A | G | 69 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0018 others(66): Show |
79 | HG00639.hp2 HG00642.hp2 HG00733.hp1 others(76): Show |
intron_variant | MODIFIER | c.2050-1395T>C | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 16/18 | chr11 | 59640778 | |||||||
| chr11:59640847 | T | C | 1 | a0001c0001t0001g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2050-1464A>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 16/18 | chr11 | 59640847 | |||||||
| chr11:59640954 | G | A | 10 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(7): Show |
11 | HG01884.hp1 HG02572.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.2050-1571C>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 16/18 | chr11 | 59640954 | |||||||
| chr11:59641013 | A | C | 1 | a0001c0001t0002g0110 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2050-1630T>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 16/18 | chr11 | 59641013 | |||||||
| chr11:59641023 | T | A | 1 | a0001c0001t0002g0110 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2050-1640A>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 16/18 | chr11 | 59641023 | |||||||
| chr11:59641041 | G | A | 2 | a0001c0001t0001g0080 a0001c0006t0001g0155 |
2 | HG01261.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2050-1658C>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 16/18 | chr11 | 59641041 | |||||||
| chr11:59641180 | AAAG | A | 15 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(12): Show |
16 | HG01884.hp1 HG02280.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.2049+1697_2049+169 others(7): Show |
PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 16/18 | chr11 | 59641180 | |||||||
| chr11:59641226 | G | A | 3 | a0001c0001t0001g0023 a0001c0001t0001g0135 a0001c0001t0001g0153 |
4 | HG00642.hp1 HG00741.hp1 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.2049+1654C>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 16/18 | chr11 | 59641226 | |||||||
| chr11:59641531 | T | C | 1 | a0001c0001t0001g0095 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2049+1349A>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 16/18 | chr11 | 59641531 | |||||||
| chr11:59641598 | C | T | 22 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0028 others(19): Show |
29 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.2049+1282G>A | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 16/18 | chr11 | 59641598 | |||||||
| chr11:59642103 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2049+777A>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 16/18 | chr11 | 59642103 | |||||||
| chr11:59642470 | A | T | 29 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(26): Show |
34 | HG00642.hp2 HG01109.hp2 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.2049+410T>A | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 16/18 | chr11 | 59642470 | |||||||
| chr11:59642644 | TG | T | 10 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(7): Show |
11 | HG01884.hp1 HG02572.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.2049+235delC | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 16/18 | chr11 | 59642644 | |||||||
| chr11:59642740 | G | T | 69 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0018 others(66): Show |
79 | HG00639.hp2 HG00642.hp2 HG00733.hp1 others(76): Show |
intron_variant | MODIFIER | c.2049+140C>A | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 16/18 | chr11 | 59642740 | |||||||
| chr11:59643499 | A | G | 8 | a0001c0001t0001g0018 a0001c0001t0001g0069 a0001c0001t0001g0163 others(5): Show |
9 | HG02145.hp1 HG02486.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1894-464T>C | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59643499 | |||||||
| chr11:59643587 | T | C | 3 | a0001c0001t0001g0026 a0001c0001t0001g0136 a0001c0001t0001g0149 |
4 | HG02486.hp2 HG02809.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1894-552A>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59643587 | |||||||
| chr11:59643861 | A | G | 3 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 |
3 | HG03041.hp2 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1894-826T>C | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59643861 | |||||||
| chr11:59643915 | C | G | 1 | a0001c0001t0001g0167 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1894-880G>C | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59643915 | |||||||
| chr11:59644006 | A | G | 1 | a0001c0001t0001g0167 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1894-971T>C | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59644006 | |||||||
| chr11:59644323 | T | C | 27 | a0001c0001t0001g0011 a0001c0001t0001g0030 a0001c0001t0001g0031 others(24): Show |
31 | HG00639.hp2 HG00733.hp1 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.1894-1288A>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59644323 | |||||||
| chr11:59644343 | GGAAA | G | 6 | a0001c0001t0005g0037 a0001c0002t0005g0014 a0001c0002t0005g0038 others(3): Show |
8 | HG01109.hp2 HG02145.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1894-1312_1894-130 others(8): Show |
PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59644343 | |||||||
| chr11:59644348 | G | T | 1 | a0001c0001t0002g0171 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1894-1313C>A | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59644348 | |||||||
| chr11:59644456 | T | C | 2 | a0001c0001t0001g0029 a0001c0001t0001g0124 |
3 | HG00597.hp2 HG02027.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.1894-1421A>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59644456 | |||||||
| chr11:59644508 | ATC | A | 4 | a0001c0001t0001g0018 a0001c0001t0001g0069 a0001c0001t0008g0068 others(1): Show |
5 | HG02145.hp1 HG02486.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1894-1475_1894-147 others(6): Show |
PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59644508 | |||||||
| chr11:59644612 | T | C | 2 | a0001c0001t0001g0086 a0001c0001t0001g0087 |
2 | HG01243.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1894-1577A>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59644612 | |||||||
| chr11:59644739 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1894-1704C>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59644739 | |||||||
| chr11:59644765 | G | T | 6 | a0001c0001t0004g0012 a0001c0001t0004g0195 a0001c0001t0004g0196 others(3): Show |
8 | HG00642.hp2 HG01123.hp1 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.1894-1730C>A | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59644765 | |||||||
| chr11:59644873 | T | G | 6 | a0001c0001t0005g0037 a0001c0002t0005g0014 a0001c0002t0005g0038 others(3): Show |
8 | HG01109.hp2 HG02145.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1894-1838A>C | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59644873 | |||||||
| chr11:59644890 | C | CT | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(116): Show |
172 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.1894-1856dupA | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59644890 | |||||||
| chr11:59644890 | C | CTT | 7 | a0001c0001t0001g0085 a0001c0001t0005g0037 a0001c0002t0005g0014 others(4): Show |
9 | HG01109.hp2 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1894-1857_1894-185 others(6): Show |
PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59644890 | |||||||
| chr11:59644890 | CT | C | 5 | a0001c0001t0001g0071 a0001c0001t0001g0164 a0001c0001t0004g0196 others(2): Show |
5 | HG02615.hp2 HG02723.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1894-1856delA | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59644890 | |||||||
| chr11:59644909 | T | A | 20 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0042 others(17): Show |
22 | HG01884.hp1 HG01993.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.1894-1874A>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59644909 | |||||||
| chr11:59644909 | T | TA | 34 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0046 others(31): Show |
39 | HG00639.hp2 HG00642.hp2 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.1894-1875dupT | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59644909 | |||||||
| chr11:59644909 | T | TTA | 4 | a0001c0001t0001g0009 a0001c0001t0001g0123 a0001c0001t0001g0146 others(1): Show |
6 | HG01192.hp1 HG01192.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1894-1875_1894-187 others(6): Show |
PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59644909 | |||||||
| chr11:59644910 | A | T | 16 | a0001c0001t0001g0022 a0001c0001t0001g0059 a0001c0001t0001g0088 others(13): Show |
19 | HG00558.hp1 HG00558.hp2 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.1894-1875T>A | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59644910 | |||||||
| chr11:59645024 | CT | C | 70 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0018 others(67): Show |
80 | HG00639.hp2 HG00642.hp2 HG00733.hp1 others(77): Show |
intron_variant | MODIFIER | c.1894-1990delA | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59645024 | |||||||
| chr11:59645040 | T | A | 15 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(12): Show |
16 | HG01884.hp1 HG02280.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.1894-2005A>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59645040 | |||||||
| chr11:59645074 | T | G | 1 | a0001c0001t0001g0066 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1894-2039A>C | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59645074 | |||||||
| chr11:59645276 | G | A | 1 | a0001c0001t0007g0176 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1894-2241C>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59645276 | |||||||
| chr11:59645321 | A | AGGGCAGA others(378): Show |
8 | a0001c0001t0004g0012 a0001c0001t0004g0168 a0001c0001t0004g0195 others(5): Show |
10 | HG00642.hp2 HG01123.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.1894-2287_1894-228 others(389): Show |
PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59645321 | |||||||
| chr11:59645321 | A | AGGGCAGA others(378): Show |
21 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0028 others(18): Show |
28 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.1894-2287_1894-228 others(389): Show |
PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59645321 | |||||||
| chr11:59645321 | A | AGGGCAGA others(379): Show |
1 | a0001c0001t0002g0061 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1894-2287_1894-228 others(390): Show |
PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59645321 | |||||||
| chr11:59645321 | A | AGGGCAGA others(378): Show |
131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(128): Show |
181 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(178): Show |
intron_variant | MODIFIER | c.1894-2287_1894-228 others(389): Show |
PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59645321 | |||||||
| chr11:59645321 | A | AGGGCAGA others(378): Show |
1 | a0001c0009t0001g0162 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1894-2287_1894-228 others(389): Show |
PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59645321 | |||||||
| chr11:59645321 | A | AGGGCAGA others(378): Show |
1 | a0001c0001t0001g0056 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1894-2287_1894-228 others(389): Show |
PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59645321 | |||||||
| chr11:59645321 | A | AGGGCAGA others(378): Show |
1 | a0001c0001t0001g0008 | 3 | HG01071.hp2 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1894-2287_1894-228 others(389): Show |
PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59645321 | |||||||
| chr11:59645321 | A | AGGGCAGA others(378): Show |
3 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0166 |
3 | HG00741.hp2 HG02615.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.1894-2287_1894-228 others(389): Show |
PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59645321 | |||||||
| chr11:59645321 | A | AGGGCAGA others(378): Show |
22 | a0001c0001t0001g0011 a0001c0001t0001g0030 a0001c0001t0001g0031 others(19): Show |
26 | HG00639.hp2 HG00733.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.1894-2287_1894-228 others(389): Show |
PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59645321 | |||||||
| chr11:59645321 | A | AGGGCAGA others(379): Show |
1 | a0001c0001t0001g0153 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1894-2287_1894-228 others(390): Show |
PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59645321 | |||||||
| chr11:59645321 | A | AGGGCAGA others(382): Show |
2 | a0001c0001t0001g0205 a0001c0001t0001g0206 |
2 | HG02897.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1894-2287_1894-228 others(393): Show |
PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59645321 | |||||||
| chr11:59645321 | A | AGGGCAGA others(381): Show |
2 | a0001c0001t0001g0207 a0001c0001t0001g0208 |
2 | HG02280.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1894-2287_1894-228 others(392): Show |
PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59645321 | |||||||
| chr11:59645321 | A | AGGGCAGA others(383): Show |
1 | a0001c0001t0001g0048 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1894-2287_1894-228 others(394): Show |
PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59645321 | |||||||
| chr11:59645321 | A | AGGGCAGA others(384): Show |
2 | a0001c0001t0001g0046 a0001c0001t0010g0047 |
2 | HG02572.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1894-2287_1894-228 others(395): Show |
PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59645321 | |||||||
| chr11:59645321 | A | AGGGCAGA others(383): Show |
5 | a0001c0001t0001g0016 a0001c0001t0001g0049 a0001c0001t0001g0050 others(2): Show |
6 | HG01884.hp1 HG02717.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1894-2287_1894-228 others(394): Show |
PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59645321 | |||||||
| chr11:59645321 | A | AGGGCAGA others(385): Show |
2 | a0001c0001t0001g0042 a0001c0001t0001g0043 |
2 | HG02622.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1894-2287_1894-228 others(396): Show |
PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59645321 | |||||||
| chr11:59645321 | A | AGGGCAGA others(379): Show |
1 | a0001c0007t0001g0104 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1894-2287_1894-228 others(390): Show |
PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59645321 | |||||||
| chr11:59645321 | A | AGGGCAGA others(378): Show |
1 | a0001c0001t0001g0203 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1894-2287_1894-228 others(389): Show |
PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59645321 | |||||||
| chr11:59645322 | G | GGGCAGAG others(378): Show |
2 | a0001c0001t0001g0201 a0001c0001t0001g0202 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1894-2288_1894-228 others(389): Show |
PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59645322 | |||||||
| chr11:59645372 | C | T | 3 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 |
3 | HG02723.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1894-2337G>A | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59645372 | |||||||
| chr11:59646087 | T | A | 1 | a0001c0001t0002g0053 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1893+1667A>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59646087 | |||||||
| chr11:59646089 | G | A | 1 | a0001c0001t0002g0053 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1893+1665C>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59646089 | |||||||
| chr11:59646165 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1893+1589C>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59646165 | |||||||
| chr11:59646230 | A | T | 1 | a0001c0001t0001g0206 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1893+1524T>A | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59646230 | |||||||
| chr11:59646278 | A | AT | 29 | a0001c0001t0001g0033 a0001c0001t0001g0066 a0001c0001t0001g0080 others(26): Show |
36 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(33): Show |
intron_variant | MODIFIER | c.1893+1475dupA | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59646278 | |||||||
| chr11:59646278 | AT | A | 62 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0018 others(59): Show |
71 | HG00597.hp2 HG00639.hp2 HG00733.hp1 others(68): Show |
intron_variant | MODIFIER | c.1893+1475delA | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59646278 | |||||||
| chr11:59646278 | ATTTT | A | 6 | a0001c0001t0004g0012 a0001c0001t0004g0195 a0001c0001t0004g0196 others(3): Show |
8 | HG00642.hp2 HG01123.hp1 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.1893+1472_1893+147 others(8): Show |
PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59646278 | |||||||
| chr11:59646368 | T | C | 2 | a0001c0001t0001g0071 a0001c0001t0001g0072 |
2 | HG03041.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1893+1386A>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59646368 | |||||||
| chr11:59646423 | C | T | 1 | a0001c0001t0002g0108 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1893+1331G>A | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59646423 | |||||||
| chr11:59646597 | T | C | 14 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(11): Show |
15 | HG01884.hp1 HG02280.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.1893+1157A>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59646597 | |||||||
| chr11:59646720 | T | C | 27 | a0001c0001t0001g0011 a0001c0001t0001g0030 a0001c0001t0001g0031 others(24): Show |
31 | HG00639.hp2 HG00733.hp1 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.1893+1034A>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59646720 | |||||||
| chr11:59646928 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1893+826C>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59646928 | |||||||
| chr11:59647061 | G | A | 3 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 |
3 | HG03041.hp2 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1893+693C>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59647061 | |||||||
| chr11:59647172 | G | A | 4 | a0001c0001t0001g0018 a0001c0001t0001g0069 a0001c0001t0008g0068 others(1): Show |
5 | HG02145.hp1 HG02486.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1893+582C>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59647172 | |||||||
| chr11:59647222 | C | CA | 41 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0033 others(38): Show |
46 | HG00408.hp2 HG00733.hp2 HG01070.hp1 others(43): Show |
intron_variant | MODIFIER | c.1893+531dupT | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59647222 | |||||||
| chr11:59647222 | C | CAA | 16 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0043 others(13): Show |
18 | HG01884.hp1 HG02145.hp1 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.1893+530_1893+531d others(4): Show |
PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59647222 | |||||||
| chr11:59647222 | C | CAAA | 6 | a0001c0001t0001g0042 a0001c0001t0001g0071 a0001c0001t0001g0205 others(3): Show |
7 | HG01109.hp2 HG02145.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1893+529_1893+531d others(5): Show |
PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59647222 | |||||||
| chr11:59647222 | C | CAAAA | 5 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 others(2): Show |
6 | HG02280.hp1 HG02559.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1893+528_1893+531d others(6): Show |
PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59647222 | |||||||
| chr11:59647235 | A | AC | 27 | a0001c0001t0001g0011 a0001c0001t0001g0030 a0001c0001t0001g0031 others(24): Show |
31 | HG00639.hp2 HG00733.hp1 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.1893+518_1893+519i others(3): Show |
PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59647235 | |||||||
| chr11:59647330 | A | G | 1 | a0001c0001t0001g0149 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1893+424T>C | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59647330 | |||||||
| chr11:59647542 | TCTCATGT others(4): Show |
T | 1 | a0001c0001t0001g0124 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1893+201_1893+211d others(13): Show |
PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59647542 | |||||||
| chr11:59647565 | G | C | 1 | a0001c0001t0001g0124 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1893+189C>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59647565 | |||||||
| chr11:59647566 | T | G | 1 | a0001c0001t0001g0124 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1893+188A>C | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59647566 | |||||||
| chr11:59647599 | G | C | 1 | a0001c0001t0001g0124 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1893+155C>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59647599 | |||||||
| chr11:59647609 | A | C | 1 | a0001c0001t0001g0124 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1893+145T>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59647609 | |||||||
| chr11:59647610 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1893+144C>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59647610 | |||||||
| chr11:59647611 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1893+143C>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59647611 | |||||||
| chr11:59647614 | T | A | 1 | a0001c0001t0001g0124 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1893+140A>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59647614 | |||||||
| chr11:59647615 | T | A | 1 | a0001c0001t0001g0124 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1893+139A>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59647615 | |||||||
| chr11:59647617 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1893+137A>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59647617 | |||||||
| chr11:59647618 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1893+136A>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59647618 | |||||||
| chr11:59647620 | T | A | 1 | a0001c0001t0001g0124 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1893+134A>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59647620 | |||||||
| chr11:59647623 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1893+131T>C | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 15/18 | chr11 | 59647623 | |||||||
| chr11:59648185 | C | CT | 14 | a0001c0001t0001g0018 a0001c0001t0001g0048 a0001c0001t0001g0050 others(11): Show |
15 | HG02027.hp2 HG02145.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.1734-273dupA | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 14/18 | chr11 | 59648185 | |||||||
| chr11:59648185 | C | CTT | 8 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(5): Show |
9 | HG01884.hp1 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1734-274_1734-273d others(4): Show |
PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 14/18 | chr11 | 59648185 | |||||||
| chr11:59648190 | T | C | 22 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0028 others(19): Show |
29 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.1734-277A>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 14/18 | chr11 | 59648190 | |||||||
| chr11:59648247 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1734-334C>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 14/18 | chr11 | 59648247 | |||||||
| chr11:59648315 | A | G | 3 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0036 |
6 | HG02080.hp2 NA18949.hp1 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.1734-402T>C | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 14/18 | chr11 | 59648315 | |||||||
| chr11:59648316 | G | A | 3 | a0001c0001t0001g0182 a0001c0001t0001g0185 a0001c0001t0006g0032 |
3 | HG02258.hp2 HG02970.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1734-403C>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 14/18 | chr11 | 59648316 | |||||||
| chr11:59648318 | C | T | 2 | a0001c0001t0001g0013 a0001c0001t0001g0036 |
3 | NA18973.hp1 NA19067.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1734-405G>A | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 14/18 | chr11 | 59648318 | |||||||
| chr11:59648376 | G | T | 3 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 |
3 | HG03041.hp2 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1734-463C>A | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 14/18 | chr11 | 59648376 | |||||||
| chr11:59648381 | C | CA | 14 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(11): Show |
15 | HG01884.hp1 HG02280.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.1734-469dupT | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 14/18 | chr11 | 59648381 | |||||||
| chr11:59648515 | T | TA | 17 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(14): Show |
18 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.1734-603dupT | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 14/18 | chr11 | 59648515 | |||||||
| chr11:59648870 | A | C | 7 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0094 others(4): Show |
7 | HG00733.hp2 HG01070.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1733+592T>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 14/18 | chr11 | 59648870 | |||||||
| chr11:59648903 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1733+559C>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 14/18 | chr11 | 59648903 | |||||||
| chr11:59648930 | A | G | 1 | a0001c0001t0002g0170 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1733+532T>C | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 14/18 | chr11 | 59648930 | |||||||
| chr11:59648952 | A | G | 8 | a0001c0001t0004g0012 a0001c0001t0004g0168 a0001c0001t0004g0195 others(5): Show |
10 | HG00642.hp2 HG01123.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.1733+510T>C | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 14/18 | chr11 | 59648952 | |||||||
| chr11:59649062 | C | T | 29 | a0001c0001t0001g0011 a0001c0001t0001g0030 a0001c0001t0001g0031 others(26): Show |
33 | HG00639.hp2 HG00733.hp1 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.1733+400G>A | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 14/18 | chr11 | 59649062 | |||||||
| chr11:59649698 | T | G | 8 | a0001c0001t0004g0012 a0001c0001t0004g0168 a0001c0001t0004g0195 others(5): Show |
10 | HG00642.hp2 HG01123.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.1585-88A>C | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 13/18 | chr11 | 59649698 | |||||||
| chr11:59649728 | AT | A | 72 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0018 others(69): Show |
82 | HG00639.hp2 HG00642.hp2 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.1585-119delA | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 13/18 | chr11 | 59649728 | |||||||
| chr11:59649753 | C | A | 2 | a0001c0001t0001g0027 a0001c0001t0011g0157 |
3 | NA18975.hp2 NA19002.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.1585-143G>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 13/18 | chr11 | 59649753 | |||||||
| chr11:59649878 | T | C | 1 | a0001c0001t0004g0197 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1585-268A>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 13/18 | chr11 | 59649878 | |||||||
| chr11:59650039 | T | C | 2 | a0001c0001t0004g0198 a0001c0001t0004g0199 |
2 | NA18948.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.1585-429A>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 13/18 | chr11 | 59650039 | |||||||
| chr11:59650127 | G | GA | 20 | a0001c0001t0001g0060 a0001c0001t0001g0116 a0001c0001t0001g0133 others(17): Show |
23 | HG00597.hp1 HG00673.hp2 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.1585-518dupT | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 13/18 | chr11 | 59650127 | |||||||
| chr11:59650127 | GAA | G | 7 | a0001c0001t0001g0018 a0001c0001t0001g0069 a0001c0001t0001g0163 others(4): Show |
8 | HG02145.hp1 HG02486.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1585-519_1585-518d others(4): Show |
PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 13/18 | chr11 | 59650127 | |||||||
| chr11:59650496 | G | C | 1 | a0001c0001t0001g0186 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1584+258C>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 13/18 | chr11 | 59650496 | |||||||
| chr11:59650507 | A | C | 1 | a0001c0001t0001g0186 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1584+247T>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 13/18 | chr11 | 59650507 | |||||||
| chr11:59650661 | T | C | 9 | a0001c0001t0001g0167 a0001c0001t0004g0012 a0001c0001t0004g0168 others(6): Show |
11 | HG00642.hp2 HG01123.hp1 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.1584+93A>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 13/18 | chr11 | 59650661 | |||||||
| chr11:59650721 | G | A | 2 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
2 | HG00738.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.1584+33C>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 13/18 | chr11 | 59650721 | |||||||
| chr11:59651218 | A | G | 1 | a0001c0001t0001g0080 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1524+326T>C | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 12/18 | chr11 | 59651218 | |||||||
| chr11:59651264 | G | T | 1 | a0001c0001t0001g0144 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1524+280C>A | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 12/18 | chr11 | 59651264 | |||||||
| chr11:59651651 | C | CA | 41 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0030 others(38): Show |
49 | HG00639.hp2 HG00642.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.1427-11dupT | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 11/18 | chr11 | 59651651 | |||||||
| chr11:59651740 | C | T | 1 | a0001c0001t0012g0093 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1427-99G>A | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 11/18 | chr11 | 59651740 | |||||||
| chr11:59651870 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1427-229C>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 11/18 | chr11 | 59651870 | |||||||
| chr11:59651947 | C | A | 1 | a0001c0001t0001g0074 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1427-306G>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 11/18 | chr11 | 59651947 | |||||||
| chr11:59652064 | C | CAAAA | 23 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0094 others(20): Show |
39 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(36): Show |
intron_variant | MODIFIER | c.1426+396_1426+399d others(6): Show |
PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 11/18 | chr11 | 59652064 | |||||||
| chr11:59652064 | C | CAAAAA | 12 | a0001c0001t0001g0019 a0001c0001t0001g0088 a0001c0001t0001g0089 others(9): Show |
13 | HG00544.hp1 HG00733.hp2 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.1426+395_1426+399d others(7): Show |
PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 11/18 | chr11 | 59652064 | |||||||
| chr11:59652064 | C | CAAAAAAA others(3): Show |
1 | a0001c0002t0005g0014 | 2 | HG02145.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1426+390_1426+399d others(12): Show |
PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 11/18 | chr11 | 59652064 | |||||||
| chr11:59652064 | C | CAAAAAAA others(4): Show |
9 | a0001c0001t0001g0030 a0001c0001t0001g0071 a0001c0001t0001g0167 others(6): Show |
10 | HG01891.hp1 HG02273.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.1426+389_1426+399d others(13): Show |
PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 11/18 | chr11 | 59652064 | |||||||
| chr11:59652064 | C | CAAAAAAA others(5): Show |
7 | a0001c0001t0001g0072 a0001c0001t0001g0172 a0001c0001t0001g0177 others(4): Show |
8 | HG01243.hp1 HG01978.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1426+388_1426+399d others(14): Show |
PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 11/18 | chr11 | 59652064 | |||||||
| chr11:59652064 | C | CAAAAAAA others(6): Show |
6 | a0001c0001t0001g0011 a0001c0001t0001g0080 a0001c0001t0001g0178 others(3): Show |
8 | HG00639.hp2 HG00733.hp1 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.1426+387_1426+399d others(15): Show |
PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 11/18 | chr11 | 59652064 | |||||||
| chr11:59652064 | C | CAAAAAAA others(7): Show |
8 | a0001c0001t0001g0031 a0001c0001t0001g0054 a0001c0001t0001g0180 others(5): Show |
9 | HG01106.hp1 HG01934.hp1 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.1426+386_1426+399d others(16): Show |
PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 11/18 | chr11 | 59652064 | |||||||
| chr11:59652064 | C | CAAAAAAA others(8): Show |
4 | a0001c0001t0001g0173 a0001c0001t0001g0183 a0001c0001t0001g0184 others(1): Show |
4 | HG01361.hp2 HG02970.hp2 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.1426+385_1426+399d others(17): Show |
PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 11/18 | chr11 | 59652064 | |||||||
| chr11:59652064 | C | CAAAAAAA others(9): Show |
2 | a0001c0001t0001g0186 a0001c0001t0001g0190 |
2 | NA18949.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.1426+384_1426+399d others(18): Show |
PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 11/18 | chr11 | 59652064 | |||||||
| chr11:59652064 | C | CAAAAAAA others(17): Show |
1 | a0001c0001t0001g0085 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1426+376_1426+399d others(26): Show |
PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 11/18 | chr11 | 59652064 | |||||||
| chr11:59652064 | C | CAAAAAAA others(20): Show |
1 | a0001c0001t0001g0150 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1426+373_1426+399d others(29): Show |
PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 11/18 | chr11 | 59652064 | |||||||
| chr11:59652064 | C | CAAAAAAA others(21): Show |
1 | a0001c0001t0001g0025 | 2 | HG00639.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.1426+372_1426+399d others(30): Show |
PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 11/18 | chr11 | 59652064 | |||||||
| chr11:59652064 | CA | C | 14 | a0001c0001t0001g0026 a0001c0001t0001g0056 a0001c0001t0001g0079 others(11): Show |
15 | HG00741.hp1 HG00741.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.1426+399delT | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 11/18 | chr11 | 59652064 | |||||||
| chr11:59652064 | CAA | C | 15 | a0001c0001t0001g0041 a0001c0001t0001g0057 a0001c0001t0001g0059 others(12): Show |
15 | HG00558.hp1 HG01123.hp2 HG02027.hp1 others(12): Show |
intron_variant | MODIFIER | c.1426+398_1426+399d others(4): Show |
PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 11/18 | chr11 | 59652064 | |||||||
| chr11:59652064 | CAAA | C | 36 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0017 others(33): Show |
64 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.1426+397_1426+399d others(5): Show |
PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 11/18 | chr11 | 59652064 | |||||||
| chr11:59652064 | CAAAAA | C | 6 | a0001c0001t0001g0070 a0001c0001t0001g0129 a0001c0001t0001g0206 others(3): Show |
6 | HG02280.hp1 HG02717.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1426+395_1426+399d others(7): Show |
PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 11/18 | chr11 | 59652064 | |||||||
| chr11:59652064 | CAAAAAA | C | 9 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(6): Show |
10 | HG01884.hp1 HG02572.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1426+394_1426+399d others(8): Show |
PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 11/18 | chr11 | 59652064 | |||||||
| chr11:59652064 | CAAAAAAA others(5): Show |
C | 7 | a0001c0001t0001g0018 a0001c0001t0001g0069 a0001c0001t0001g0163 others(4): Show |
8 | HG02145.hp1 HG02486.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1426+388_1426+399d others(14): Show |
PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 11/18 | chr11 | 59652064 | |||||||
| chr11:59652064 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0013g0067 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1426+387_1426+399d others(15): Show |
PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 11/18 | chr11 | 59652064 | |||||||
| chr11:59652064 | CAAAAAAA others(10): Show |
C | 8 | a0001c0001t0004g0012 a0001c0001t0004g0168 a0001c0001t0004g0195 others(5): Show |
10 | HG00642.hp2 HG01123.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.1426+383_1426+399d others(19): Show |
PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 11/18 | chr11 | 59652064 | |||||||
| chr11:59652150 | C | CTT | 204 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(201): Show |
270 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(267): Show |
intron_variant | MODIFIER | c.1426+313_1426+314i others(4): Show |
PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 11/18 | chr11 | 59652150 | |||||||
| chr11:59652329 | A | G | 10 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(7): Show |
11 | HG01884.hp1 HG02572.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1426+135T>C | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 11/18 | chr11 | 59652329 | |||||||
| chr11:59652428 | C | A | 4 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(1): Show |
4 | HG02280.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1426+36G>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 11/18 | chr11 | 59652428 | |||||||
| chr11:59652610 | G | A | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG01109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1303-23C>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 10/18 | chr11 | 59652610 | |||||||
| chr11:59652613 | G | T | 1 | a0001c0002t0005g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1303-26C>A | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 10/18 | chr11 | 59652613 | |||||||
| chr11:59652644 | A | G | 6 | a0001c0001t0005g0037 a0001c0002t0005g0014 a0001c0002t0005g0038 others(3): Show |
8 | HG01109.hp2 HG02145.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1303-57T>C | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 10/18 | chr11 | 59652644 | |||||||
| chr11:59652815 | C | G | 1 | a0001c0001t0001g0167 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1302+23G>C | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 10/18 | chr11 | 59652815 | |||||||
| chr11:59653086 | A | G | 7 | a0001c0001t0001g0029 a0001c0001t0001g0124 a0001c0001t0001g0125 others(4): Show |
8 | HG00597.hp2 HG02027.hp2 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.1122-68T>C | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 9/18 | chr11 | 59653086 | |||||||
| chr11:59653097 | G | GT | 3 | a0001c0001t0001g0009 a0001c0001t0001g0123 a0001c0001t0001g0156 |
5 | HG01192.hp2 HG02970.hp1 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1122-80dupA | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 9/18 | chr11 | 59653097 | |||||||
| chr11:59653097 | GT | G | 7 | a0001c0001t0001g0035 a0001c0001t0001g0080 a0001c0001t0001g0086 others(4): Show |
7 | HG01243.hp2 HG02897.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1122-80delA | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 9/18 | chr11 | 59653097 | |||||||
| chr11:59653101 | T | TG | 4 | a0001c0001t0001g0018 a0001c0001t0001g0069 a0001c0001t0008g0068 others(1): Show |
5 | HG02145.hp1 HG02486.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1122-84_1122-83ins others(1): Show |
PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 9/18 | chr11 | 59653101 | |||||||
| chr11:59653114 | T | A | 6 | a0001c0001t0001g0018 a0001c0001t0001g0069 a0001c0001t0001g0164 others(3): Show |
7 | HG02145.hp1 HG02486.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1122-96A>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 9/18 | chr11 | 59653114 | |||||||
| chr11:59653702 | G | C | 20 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0074 others(17): Show |
30 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(27): Show |
intron_variant | MODIFIER | c.1121+281C>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 9/18 | chr11 | 59653702 | |||||||
| chr11:59653905 | A | T | 5 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(2): Show |
5 | HG01175.hp1 HG01192.hp1 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.1121+78T>A | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 9/18 | chr11 | 59653905 | |||||||
| chr11:59654204 | C | T | 2 | a0001c0001t0001g0167 a0001c0001t0001g0189 |
2 | HG02280.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1032-132G>A | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 8/18 | chr11 | 59654204 | |||||||
| chr11:59654226 | T | C | 71 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0018 others(68): Show |
81 | HG00639.hp2 HG00642.hp2 HG00733.hp1 others(78): Show |
intron_variant | MODIFIER | c.1032-154A>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 8/18 | chr11 | 59654226 | |||||||
| chr11:59654275 | G | A | 8 | a0001c0001t0004g0012 a0001c0001t0004g0168 a0001c0001t0004g0195 others(5): Show |
10 | HG00642.hp2 HG01123.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.1032-203C>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 8/18 | chr11 | 59654275 | |||||||
| chr11:59654489 | T | TA | 47 | a0001c0001t0001g0011 a0001c0001t0001g0026 a0001c0001t0001g0030 others(44): Show |
54 | HG00639.hp2 HG00642.hp2 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.1032-418dupT | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 8/18 | chr11 | 59654489 | |||||||
| chr11:59654489 | TA | T | 6 | a0001c0001t0001g0021 a0001c0001t0001g0080 a0001c0001t0001g0115 others(3): Show |
7 | HG00738.hp1 HG01070.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.1032-418delT | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 8/18 | chr11 | 59654489 | |||||||
| chr11:59654510 | A | C | 1 | a0001c0001t0001g0194 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1032-438T>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 8/18 | chr11 | 59654510 | |||||||
| chr11:59654543 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1032-471C>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 8/18 | chr11 | 59654543 | |||||||
| chr11:59654545 | T | A | 1 | a0001c0001t0001g0056 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1032-473A>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 8/18 | chr11 | 59654545 | |||||||
| chr11:59654568 | T | C | 1 | a0001c0001t0001g0080 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1032-496A>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 8/18 | chr11 | 59654568 | |||||||
| chr11:59654629 | A | G | 1 | a0001c0001t0001g0121 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1032-557T>C | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 8/18 | chr11 | 59654629 | |||||||
| chr11:59654796 | G | A | 2 | a0001c0002t0005g0014 a0001c0002t0005g0038 |
3 | HG01109.hp2 HG02145.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1032-724C>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 8/18 | chr11 | 59654796 | |||||||
| chr11:59654934 | T | A | 1 | a0001c0001t0001g0051 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1031+589A>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 8/18 | chr11 | 59654934 | |||||||
| chr11:59655398 | A | G | 1 | a0001c0001t0001g0057 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1031+125T>C | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 8/18 | chr11 | 59655398 | |||||||
| chr11:59655795 | T | G | 1 | a0001c0001t0004g0198 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.814-55A>C | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 7/18 | chr11 | 59655795 | |||||||
| chr11:59655816 | G | A | 8 | a0001c0001t0001g0018 a0001c0001t0001g0069 a0001c0001t0001g0163 others(5): Show |
9 | HG02145.hp1 HG02486.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.814-76C>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 7/18 | chr11 | 59655816 | |||||||
| chr11:59656052 | T | TA | 29 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0051 others(26): Show |
33 | HG00642.hp2 HG01123.hp1 HG01175.hp1 others(30): Show |
splice_region_variant&intron_variant | LOW | c.724-8dupT | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 6/18 | chr11 | 59656052 | |||||||
| chr11:59656052 | T | TAA | 6 | a0001c0001t0004g0199 a0001c0002t0005g0014 a0001c0002t0005g0038 others(3): Show |
8 | HG01109.hp2 HG02145.hp2 HG02559.hp2 others(5): Show |
splice_region_variant&intron_variant | LOW | c.724-9_724-8dupTT | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 6/18 | chr11 | 59656052 | |||||||
| chr11:59656052 | TA | T | 29 | a0001c0001t0001g0011 a0001c0001t0001g0030 a0001c0001t0001g0031 others(26): Show |
33 | HG00639.hp2 HG00733.hp1 HG01106.hp1 others(30): Show |
splice_region_variant&intron_variant | LOW | c.724-8delT | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 6/18 | chr11 | 59656052 | |||||||
| chr11:59656405 | G | A | 1 | a0001c0006t0001g0155 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.723+94C>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 6/18 | chr11 | 59656405 | |||||||
| chr11:59656446 | T | C | 1 | a0001c0001t0001g0064 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.723+53A>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 6/18 | chr11 | 59656446 | |||||||
| chr11:59656782 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.622-182T>C | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 5/18 | chr11 | 59656782 | |||||||
| chr11:59657215 | C | A | 15 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(12): Show |
16 | HG01884.hp1 HG02280.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.621+315G>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 5/18 | chr11 | 59657215 | |||||||
| chr11:59657331 | G | T | 20 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0074 others(17): Show |
30 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(27): Show |
intron_variant | MODIFIER | c.621+199C>A | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 5/18 | chr11 | 59657331 | |||||||
| chr11:59657508 | T | C | 1 | a0001c0001t0002g0112 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.621+22A>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 5/18 | chr11 | 59657508 | |||||||
| chr11:59657813 | A | AT | 69 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0018 others(66): Show |
79 | HG00639.hp2 HG00642.hp2 HG00733.hp1 others(76): Show |
intron_variant | MODIFIER | c.427-90dupA | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 4/18 | chr11 | 59657813 | |||||||
| chr11:59658011 | A | G | 39 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0030 others(36): Show |
44 | HG00639.hp2 HG00733.hp1 HG01106.hp1 others(41): Show |
intron_variant | MODIFIER | c.427-287T>C | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 4/18 | chr11 | 59658011 | |||||||
| chr11:59658174 | A | AAAAG | 65 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0018 others(62): Show |
75 | HG00639.hp2 HG00642.hp2 HG00733.hp1 others(72): Show |
intron_variant | MODIFIER | c.427-454_427-451dup others(4): Show |
PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 4/18 | chr11 | 59658174 | |||||||
| chr11:59658184 | A | G | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.427-460T>C | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 4/18 | chr11 | 59658184 | |||||||
| chr11:59658321 | G | GT | 7 | a0001c0001t0001g0008 a0001c0001t0001g0054 a0001c0001t0001g0070 others(4): Show |
9 | HG01071.hp2 HG01257.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.426+544dupA | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 4/18 | chr11 | 59658321 | |||||||
| chr11:59658336 | G | C | 1 | a0001c0001t0001g0189 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.426+530C>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 4/18 | chr11 | 59658336 | |||||||
| chr11:59658479 | C | T | 2 | a0001c0001t0001g0020 a0001c0001t0001g0172 |
3 | HG01978.hp2 NA18961.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.426+387G>A | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 4/18 | chr11 | 59658479 | |||||||
| chr11:59658563 | T | C | 1 | a0001c0001t0001g0167 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.426+303A>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 4/18 | chr11 | 59658563 | |||||||
| chr11:59658957 | A | C | 2 | a0001c0001t0001g0086 a0001c0001t0001g0087 |
2 | HG01243.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.346-11T>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 3/18 | chr11 | 59658957 | |||||||
| chr11:59658990 | T | A | 1 | a0001c0001t0006g0032 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.346-44A>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 3/18 | chr11 | 59658990 | |||||||
| chr11:59659083 | T | C | 8 | a0001c0001t0001g0018 a0001c0001t0001g0069 a0001c0001t0001g0163 others(5): Show |
9 | HG02145.hp1 HG02486.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.346-137A>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 3/18 | chr11 | 59659083 | |||||||
| chr11:59659127 | T | A | 1 | a0001c0001t0001g0190 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.345+125A>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 3/18 | chr11 | 59659127 | |||||||
| chr11:59659222 | A | G | 39 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0030 others(36): Show |
44 | HG00639.hp2 HG00733.hp1 HG01106.hp1 others(41): Show |
intron_variant | MODIFIER | c.345+30T>C | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 3/18 | chr11 | 59659222 | |||||||
| chr11:59659237 | C | T | 8 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(5): Show |
9 | HG01884.hp1 HG02572.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.345+15G>A | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 3/18 | chr11 | 59659237 | |||||||
| chr11:59659571 | G | A | 28 | a0001c0001t0001g0011 a0001c0001t0001g0030 a0001c0001t0001g0031 others(25): Show |
32 | HG00639.hp2 HG00733.hp1 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.128-102C>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59659571 | |||||||
| chr11:59659593 | G | A | 8 | a0001c0001t0004g0012 a0001c0001t0004g0168 a0001c0001t0004g0195 others(5): Show |
10 | HG00642.hp2 HG01123.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.128-124C>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59659593 | |||||||
| chr11:59659601 | G | A | 1 | a0001c0001t0004g0199 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.128-132C>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59659601 | |||||||
| chr11:59660130 | C | T | 6 | a0001c0001t0003g0003 a0001c0001t0003g0113 a0001c0001t0003g0114 others(3): Show |
10 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(7): Show |
intron_variant | MODIFIER | c.128-661G>A | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59660130 | |||||||
| chr11:59660155 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.128-686C>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59660155 | |||||||
| chr11:59660172 | C | T | 30 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(27): Show |
35 | HG00642.hp2 HG01109.hp2 HG01123.hp1 others(32): Show |
intron_variant | MODIFIER | c.128-703G>A | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59660172 | |||||||
| chr11:59660277 | C | T | 1 | a0001c0006t0001g0155 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.128-808G>A | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59660277 | |||||||
| chr11:59660376 | T | C | 1 | a0001c0001t0001g0051 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.128-907A>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59660376 | |||||||
| chr11:59660472 | T | C | 3 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 |
3 | HG02723.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.128-1003A>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59660472 | |||||||
| chr11:59660513 | G | A | 1 | a0001c0001t0001g0065 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.128-1044C>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59660513 | |||||||
| chr11:59660516 | T | C | 2 | a0001c0001t0004g0198 a0001c0001t0004g0199 |
2 | NA18948.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.128-1047A>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59660516 | |||||||
| chr11:59660758 | T | C | 1 | a0001c0001t0001g0152 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.128-1289A>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59660758 | |||||||
| chr11:59661124 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.128-1655G>A | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59661124 | |||||||
| chr11:59661361 | C | T | 3 | a0001c0002t0005g0039 a0002c0003t0005g0015 a0002c0003t0005g0040 |
4 | HG02559.hp2 HG03453.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.128-1892G>A | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59661361 | |||||||
| chr11:59661378 | C | A | 69 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0018 others(66): Show |
79 | HG00639.hp2 HG00642.hp2 HG00733.hp1 others(76): Show |
intron_variant | MODIFIER | c.128-1909G>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59661378 | |||||||
| chr11:59661417 | TTCC | T | 124 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(121): Show |
156 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.128-1951_128-1949d others(5): Show |
PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59661417 | |||||||
| chr11:59661466 | C | A | 6 | a0001c0001t0004g0012 a0001c0001t0004g0195 a0001c0001t0004g0196 others(3): Show |
8 | HG00642.hp2 HG01123.hp1 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.128-1997G>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59661466 | |||||||
| chr11:59661470 | C | T | 15 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(12): Show |
16 | HG01884.hp1 HG02280.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.128-2001G>A | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59661470 | |||||||
| chr11:59661648 | A | C | 3 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 |
3 | HG01496.hp2 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.128-2179T>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59661648 | |||||||
| chr11:59661734 | A | G | 2 | a0001c0002t0005g0014 a0001c0002t0005g0038 |
3 | HG01109.hp2 HG02145.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.128-2265T>C | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59661734 | |||||||
| chr11:59661840 | T | C | 2 | a0001c0001t0001g0191 a0001c0001t0001g0192 |
2 | HG00639.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.128-2371A>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59661840 | |||||||
| chr11:59661859 | A | G | 1 | a0001c0001t0001g0080 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.128-2390T>C | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59661859 | |||||||
| chr11:59662142 | T | C | 1 | a0001c0001t0001g0193 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.128-2673A>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59662142 | |||||||
| chr11:59662181 | T | C | 71 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0018 others(68): Show |
81 | HG00639.hp2 HG00642.hp2 HG00733.hp1 others(78): Show |
intron_variant | MODIFIER | c.128-2712A>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59662181 | |||||||
| chr11:59662211 | C | T | 1 | a0001c0001t0002g0081 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.128-2742G>A | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59662211 | |||||||
| chr11:59662697 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.128-3228A>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59662697 | |||||||
| chr11:59662752 | C | T | 27 | a0001c0001t0001g0011 a0001c0001t0001g0030 a0001c0001t0001g0031 others(24): Show |
31 | HG00639.hp2 HG00733.hp1 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.128-3283G>A | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59662752 | |||||||
| chr11:59662836 | A | G | 2 | a0001c0001t0001g0080 a0001c0006t0001g0155 |
2 | HG01261.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.128-3367T>C | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59662836 | |||||||
| chr11:59662963 | T | C | 1 | a0001c0001t0001g0153 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.128-3494A>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59662963 | |||||||
| chr11:59663045 | T | C | 1 | a0001c0001t0001g0154 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.128-3576A>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59663045 | |||||||
| chr11:59663232 | T | TA | 6 | a0001c0001t0005g0037 a0001c0002t0005g0014 a0001c0002t0005g0038 others(3): Show |
8 | HG01109.hp2 HG02145.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.127+3620dupT | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59663232 | |||||||
| chr11:59663234 | C | T | 2 | a0001c0001t0001g0033 a0001c0001t0001g0034 |
2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.127+3619G>A | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59663234 | |||||||
| chr11:59663436 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.127+3417C>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59663436 | |||||||
| chr11:59663503 | A | G | 1 | a0001c0001t0001g0167 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.127+3350T>C | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59663503 | |||||||
| chr11:59663523 | T | TC | 8 | a0001c0001t0004g0012 a0001c0001t0004g0168 a0001c0001t0004g0195 others(5): Show |
10 | HG00642.hp2 HG01123.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.127+3329dupG | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59663523 | |||||||
| chr11:59663810 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.127+3043G>A | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59663810 | |||||||
| chr11:59663820 | A | G | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG01109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.127+3033T>C | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59663820 | |||||||
| chr11:59664201 | G | T | 3 | a0001c0001t0002g0075 a0001c0001t0002g0076 a0001c0001t0002g0077 |
3 | HG02698.hp2 HG03492.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.127+2652C>A | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59664201 | |||||||
| chr11:59664237 | A | G | 1 | a0001c0001t0001g0074 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.127+2616T>C | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59664237 | |||||||
| chr11:59664270 | T | C | 1 | a0001c0001t0001g0066 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.127+2583A>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59664270 | |||||||
| chr11:59664364 | T | C | 69 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0018 others(66): Show |
79 | HG00639.hp2 HG00642.hp2 HG00733.hp1 others(76): Show |
intron_variant | MODIFIER | c.127+2489A>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59664364 | |||||||
| chr11:59664413 | T | C | 1 | a0001c0006t0001g0155 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.127+2440A>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59664413 | |||||||
| chr11:59664752 | T | C | 2 | a0001c0001t0001g0049 a0001c0001t0001g0050 |
2 | HG02723.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.127+2101A>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59664752 | |||||||
| chr11:59664792 | A | C | 1 | a0001c0001t0001g0073 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.127+2061T>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59664792 | |||||||
| chr11:59664937 | T | C | 4 | a0001c0001t0001g0027 a0001c0001t0001g0156 a0001c0001t0001g0158 others(1): Show |
5 | HG00597.hp1 NA18965.hp1 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.127+1916A>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59664937 | |||||||
| chr11:59665407 | C | T | 69 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0018 others(66): Show |
79 | HG00639.hp2 HG00642.hp2 HG00733.hp1 others(76): Show |
intron_variant | MODIFIER | c.127+1446G>A | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59665407 | |||||||
| chr11:59665570 | GAGGGA | G | 4 | a0001c0001t0001g0018 a0001c0001t0001g0069 a0001c0001t0008g0068 others(1): Show |
5 | HG02145.hp1 HG02486.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.127+1278_127+1282d others(7): Show |
PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59665570 | |||||||
| chr11:59665578 | ACT | A | 4 | a0001c0001t0001g0018 a0001c0001t0001g0069 a0001c0001t0008g0068 others(1): Show |
5 | HG02145.hp1 HG02486.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.127+1273_127+1274d others(4): Show |
PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59665578 | |||||||
| chr11:59665581 | T | G | 4 | a0001c0001t0001g0018 a0001c0001t0001g0069 a0001c0001t0008g0068 others(1): Show |
5 | HG02145.hp1 HG02486.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.127+1272A>C | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59665581 | |||||||
| chr11:59665585 | G | T | 4 | a0001c0001t0001g0018 a0001c0001t0001g0069 a0001c0001t0008g0068 others(1): Show |
5 | HG02145.hp1 HG02486.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.127+1268C>A | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59665585 | |||||||
| chr11:59665692 | AG | A | 3 | a0001c0001t0003g0159 a0001c0001t0003g0160 a0001c0001t0003g0161 |
3 | NA18943.hp1 NA19064.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.127+1160delC | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59665692 | |||||||
| chr11:59665764 | T | C | 1 | a0001c0009t0001g0162 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.127+1089A>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59665764 | |||||||
| chr11:59665769 | G | A | 6 | a0001c0001t0005g0037 a0001c0002t0005g0014 a0001c0002t0005g0038 others(3): Show |
8 | HG01109.hp2 HG02145.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.127+1084C>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59665769 | |||||||
| chr11:59665800 | T | G | 6 | a0001c0001t0005g0037 a0001c0002t0005g0014 a0001c0002t0005g0038 others(3): Show |
8 | HG01109.hp2 HG02145.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.127+1053A>C | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59665800 | |||||||
| chr11:59665852 | TACACCTG others(9): Show |
T | 12 | a0001c0001t0001g0017 a0001c0001t0001g0041 a0001c0001t0001g0057 others(9): Show |
13 | HG02293.hp1 HG04184.hp1 HG04184.hp2 others(10): Show |
intron_variant | MODIFIER | c.127+985_127+1000de others(17): Show |
PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59665852 | |||||||
| chr11:59665854 | C | T | 1 | a0001c0001t0001g0001 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.127+999G>A | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59665854 | |||||||
| chr11:59665937 | G | A | 3 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 |
3 | HG02723.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.127+916C>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59665937 | |||||||
| chr11:59665948 | C | G | 30 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(27): Show |
35 | HG00642.hp2 HG01109.hp2 HG01123.hp1 others(32): Show |
intron_variant | MODIFIER | c.127+905G>C | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59665948 | |||||||
| chr11:59666015 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.127+838G>A | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59666015 | |||||||
| chr11:59666070 | G | A | 1 | a0001c0001t0001g0166 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.127+783C>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59666070 | |||||||
| chr11:59666126 | A | G | 1 | a0001c0001t0001g0051 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.127+727T>C | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59666126 | |||||||
| chr11:59666201 | G | A | 30 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(27): Show |
35 | HG00642.hp2 HG01109.hp2 HG01123.hp1 others(32): Show |
intron_variant | MODIFIER | c.127+652C>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59666201 | |||||||
| chr11:59666252 | G | GAATA | 28 | a0001c0001t0001g0011 a0001c0001t0001g0030 a0001c0001t0001g0031 others(25): Show |
32 | HG00639.hp2 HG00733.hp1 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.127+597_127+600dup others(4): Show |
PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59666252 | |||||||
| chr11:59666400 | A | C | 1 | a0001c0001t0005g0037 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.127+453T>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59666400 | |||||||
| chr11:59666495 | A | G | 4 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0035 others(1): Show |
7 | HG02080.hp2 NA18949.hp1 NA18952.hp1 others(4): Show |
intron_variant | MODIFIER | c.127+358T>C | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59666495 | |||||||
| chr11:59666827 | T | C | 1 | a0001c0001t0001g0194 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.127+26A>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59666827 | |||||||
| chr11:59666849 | T | C | 4 | a0001c0001t0002g0028 a0001c0001t0002g0169 a0001c0001t0002g0170 others(1): Show |
5 | NA18943.hp2 NA18970.hp2 NA18971.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.127+4A>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 2/18 | chr11 | 59666849 | |||||||
| chr11:59666976 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.16-12C>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 1/18 | chr11 | 59666976 | |||||||
| chr11:59666996 | T | A | 1 | a0001c0001t0001g0029 | 2 | HG00597.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.16-32A>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 1/18 | chr11 | 59666996 | |||||||
| chr11:59667045 | CT | C | 28 | a0001c0001t0001g0011 a0001c0001t0001g0030 a0001c0001t0001g0031 others(25): Show |
32 | HG00639.hp2 HG00733.hp1 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.16-82delA | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 1/18 | chr11 | 59667045 | |||||||
| chr11:59667079 | T | A | 6 | a0001c0001t0005g0037 a0001c0002t0005g0014 a0001c0002t0005g0038 others(3): Show |
8 | HG01109.hp2 HG02145.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.16-115A>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 1/18 | chr11 | 59667079 | |||||||
| chr11:59667080 | T | C | 6 | a0001c0001t0005g0037 a0001c0002t0005g0014 a0001c0002t0005g0038 others(3): Show |
8 | HG01109.hp2 HG02145.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.16-116A>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 1/18 | chr11 | 59667080 | |||||||
| chr11:59667130 | G | T | 1 | a0001c0001t0001g0055 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.16-166C>A | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 1/18 | chr11 | 59667130 | |||||||
| chr11:59667157 | A | T | 1 | a0001c0001t0001g0054 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.16-193T>A | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 1/18 | chr11 | 59667157 | |||||||
| chr11:59667291 | G | T | 2 | a0001c0001t0002g0052 a0001c0001t0002g0053 |
2 | HG01496.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.16-327C>A | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 1/18 | chr11 | 59667291 | |||||||
| chr11:59667307 | C | T | 15 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(12): Show |
16 | HG01884.hp1 HG02280.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.16-343G>A | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 1/18 | chr11 | 59667307 | |||||||
| chr11:59667666 | A | G | 1 | a0001c0001t0001g0041 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.16-702T>C | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 1/18 | chr11 | 59667666 | |||||||
| chr11:59667997 | C | A | 6 | a0001c0001t0004g0012 a0001c0001t0004g0195 a0001c0001t0004g0196 others(3): Show |
8 | HG00642.hp2 HG01123.hp1 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.15+884G>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 1/18 | chr11 | 59667997 | |||||||
| chr11:59668037 | T | C | 1 | a0001c0001t0001g0200 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.15+844A>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 1/18 | chr11 | 59668037 | |||||||
| chr11:59668253 | T | C | 2 | a0001c0001t0001g0201 a0001c0001t0001g0202 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.15+628A>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 1/18 | chr11 | 59668253 | |||||||
| chr11:59668282 | G | C | 1 | a0001c0001t0001g0203 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.15+599C>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 1/18 | chr11 | 59668282 | |||||||
| chr11:59668295 | A | G | 6 | a0001c0001t0005g0037 a0001c0002t0005g0014 a0001c0002t0005g0038 others(3): Show |
8 | HG01109.hp2 HG02145.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.15+586T>C | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 1/18 | chr11 | 59668295 | |||||||
| chr11:59668344 | C | T | 4 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0035 others(1): Show |
7 | HG02080.hp2 NA18949.hp1 NA18952.hp1 others(4): Show |
intron_variant | MODIFIER | c.15+537G>A | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 1/18 | chr11 | 59668344 | |||||||
| chr11:59668381 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.15+500C>T | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 1/18 | chr11 | 59668381 | |||||||
| chr11:59668445 | G | C | 4 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(1): Show |
4 | HG02280.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+436C>G | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 1/18 | chr11 | 59668445 | |||||||
| chr11:59668734 | C | T | 2 | a0001c0001t0001g0033 a0001c0001t0001g0034 |
2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.15+147G>A | PATL1 | ENSG00000166889.14 | transcript | ENST00000300146.10 | protein_coding | 1/18 | chr11 | 59668734 |