Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55726 |
| ensemblid | ENSG00000064102.15 |
| hgncid | 20174 |
| symbol | INTS13 |
| name | integrator complex subunit 13 |
| refseq_nuc | NM_018164.3 |
| refseq_prot | NP_060634.2 |
| ensembl_nuc | ENST00000261191.12 |
| ensembl_prot | ENSP00000261191.7 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 26905181 |
| end | 26937981 |
| strand | - |
| ver | v1.2 |
| region | chr12:26905181-26937981 |
| region5000 | chr12:26900181-26942981 |
| regionname0 | INTS13_chr12_26905181_26937981 |
| regionname5000 | INTS13_chr12_26900181_26942981 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 706 | 384 | 91 | 68 | 164 | 16 | 45 | 122 | INTS13_chr12_26900181_26942981 | INTS13 | MKIFS others(701): Show |
chr12 | 26900181 | 26942981 |
| a0002 | 0/0 | 706 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | MKIFS others(701): Show |
chr12 | 26900181 | 26942981 |
| a0003 | 0/0 | 706 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | MKIFS others(701): Show |
chr12 | 26900181 | 26942981 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2118 | 239 | 52 | 32 | 116 | 10 | 29 | INTS13_chr12_26900181_26942981 | INTS13 | ATGAA others(2113): Show |
chr12 | 26900181 | 26942981 | ||
| a0001c0002 | 0/0 | 2118 | 142 | 37 | 36 | 47 | 6 | 16 | INTS13_chr12_26900181_26942981 | INTS13 | ATGAA others(2113): Show |
chr12 | 26900181 | 26942981 | ||
| a0001c0004 | 0/0 | 2118 | 1 | 1 | 0 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | ATGAA others(2113): Show |
chr12 | 26900181 | 26942981 | ||
| a0001c0005 | 0/0 | 2118 | 1 | 0 | 0 | 1 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | ATGAA others(2113): Show |
chr12 | 26900181 | 26942981 | ||
| a0001c0007 | 0/0 | 2118 | 1 | 1 | 0 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | ATGAA others(2113): Show |
chr12 | 26900181 | 26942981 | ||
| a0002c0003 | 0/0 | 2118 | 1 | 1 | 0 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | ATGAA others(2113): Show |
chr12 | 26900181 | 26942981 | ||
| a0003c0006 | 0/0 | 2118 | 1 | 0 | 0 | 0 | 0 | 1 | INTS13_chr12_26900181_26942981 | INTS13 | ATGAA others(2113): Show |
chr12 | 26900181 | 26942981 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2634 | 233 | 49 | 32 | 116 | 10 | 26 | INTS13_chr12_26900181_26942981 | INTS13 | CCTGC others(2629): Show |
chr12 | 26900181 | 26942981 |
| a0001c0001t0004 | 0/0 | 2634 | 3 | 0 | 0 | 0 | 0 | 3 | INTS13_chr12_26900181_26942981 | INTS13 | CCTGC others(2629): Show |
chr12 | 26900181 | 26942981 |
| a0001c0001t0006 | 0/0 | 2634 | 2 | 2 | 0 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | CCTGC others(2629): Show |
chr12 | 26900181 | 26942981 |
| a0001c0001t0008 | 0/0 | 2634 | 1 | 1 | 0 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | CCTGC others(2629): Show |
chr12 | 26900181 | 26942981 |
| a0001c0002t0001 | 0/0 | 2634 | 131 | 27 | 35 | 47 | 6 | 16 | INTS13_chr12_26900181_26942981 | INTS13 | CCTGC others(2629): Show |
chr12 | 26900181 | 26942981 |
| a0001c0002t0002 | 0/0 | 2634 | 5 | 5 | 0 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | CCTGC others(2629): Show |
chr12 | 26900181 | 26942981 |
| a0001c0002t0003 | 0/0 | 2634 | 3 | 3 | 0 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | CCTGC others(2629): Show |
chr12 | 26900181 | 26942981 |
| a0001c0002t0005 | 0/0 | 2634 | 2 | 2 | 0 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | CCTGC others(2629): Show |
chr12 | 26900181 | 26942981 |
| a0001c0002t0007 | 0/0 | 2634 | 1 | 0 | 1 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | CCTGC others(2629): Show |
chr12 | 26900181 | 26942981 |
| a0001c0004t0001 | 0/0 | 2634 | 1 | 1 | 0 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | CCTGC others(2629): Show |
chr12 | 26900181 | 26942981 |
| a0001c0005t0001 | 0/0 | 2634 | 1 | 0 | 0 | 1 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | CCTGC others(2629): Show |
chr12 | 26900181 | 26942981 |
| a0001c0007t0001 | 0/0 | 2634 | 1 | 1 | 0 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | CCTGC others(2629): Show |
chr12 | 26900181 | 26942981 |
| a0002c0003t0001 | 0/0 | 2634 | 1 | 1 | 0 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | CCTGC others(2629): Show |
chr12 | 26900181 | 26942981 |
| a0003c0006t0001 | 0/0 | 2634 | 1 | 0 | 0 | 0 | 0 | 1 | INTS13_chr12_26900181_26942981 | INTS13 | CCTGC others(2629): Show |
chr12 | 26900181 | 26942981 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 24 | 11 | 1 | 12 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0003 | 0/0 | 19 | 0 | 2 | 14 | 0 | 3 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0005 | 0/0 | 19 | 5 | 2 | 10 | 1 | 1 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0007 | 0/0 | 13 | 1 | 3 | 6 | 1 | 2 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0014 | 0/0 | 4 | 1 | 0 | 3 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0022 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0038 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0004g0020 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0006g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0006g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0001t0008g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0002t0001g0001 | 0/0 | 27 | 0 | 10 | 13 | 1 | 3 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0002t0001g0004 | 0/0 | 19 | 0 | 5 | 11 | 2 | 1 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0002t0001g0006 | 0/0 | 12 | 2 | 7 | 0 | 0 | 3 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0002t0001g0008 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0002t0001g0009 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0002t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0002t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0002t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0002t0001g0029 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0002t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0002t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0002t0001g0035 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0002t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0002t0001g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0002t0001g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0002t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0002t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0002t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0002t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0002t0002g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0002t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0002t0003g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0002t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0002t0005g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0002t0005g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0002t0007g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0004t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0005t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0001c0007t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0002c0003t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| a0003c0006t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | GBR | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0172 | EUR | GBR | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0004 | EUR | GBR | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0165 | EUR | GBR | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0025 | EUR | FIN | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0060 | EUR | FIN | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG00408 | hp1 | a0001 | c0005 | t0001 | g0081 | EAS | CHS | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | CHS | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0094 | EAS | CHS | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | CHS | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0065 | AMR | PUR | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0009 | AMR | PUR | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG00738 | hp2 | a0001 | c0002 | t0007 | g0090 | AMR | PUR | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0098 | AMR | PUR | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | PUR | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | PUR | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0061 | AMR | PUR | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | PUR | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0173 | AMR | PUR | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0179 | AMR | CLM | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0029 | AMR | CLM | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | CLM | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0004 | AMR | CLM | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | CLM | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | CLM | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | CLM | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0164 | EUR | IBS | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0001 | EUR | IBS | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0166 | EUR | IBS | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0129 | EUR | IBS | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0167 | EUR | IBS | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0034 | AFR | ACB | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0054 | AMR | PEL | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0028 | AMR | PEL | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0004 | AMR | PEL | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0095 | AMR | PEL | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0180 | EAS | KHV | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | KHV | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | KHV | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0097 | EAS | KHV | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0102 | EAS | KHV | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | CDX | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CDX | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CDX | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02257 | hp1 | a0001 | c0001 | t0006 | g0182 | AFR | ACB | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0009 | AFR | ACB | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0176 | AFR | ACB | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02280 | hp2 | a0001 | c0002 | t0001 | g0177 | AFR | ACB | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0028 | AMR | PEL | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0096 | AMR | PEL | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0055 | AMR | PEL | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0057 | AFR | ACB | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02572 | hp1 | a0001 | c0002 | t0002 | g0106 | AFR | GWD | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02602 | hp1 | a0001 | c0001 | t0004 | g0020 | SAS | PJL | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0103 | SAS | PJL | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02630 | hp1 | a0001 | c0002 | t0002 | g0012 | AFR | GWD | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02647 | hp1 | a0001 | c0004 | t0001 | g0117 | AFR | GWD | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02647 | hp2 | a0002 | c0003 | t0001 | g0101 | AFR | GWD | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0058 | SAS | PJL | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0052 | SAS | PJL | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02723 | hp1 | a0001 | c0002 | t0002 | g0012 | AFR | GWD | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02723 | hp2 | a0001 | c0002 | t0003 | g0027 | AFR | GWD | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0059 | SAS | PJL | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02809 | hp1 | a0001 | c0002 | t0002 | g0012 | AFR | GWD | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0056 | AFR | GWD | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0175 | AFR | GWD | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0006 | AFR | GWD | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0036 | AFR | GWD | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0036 | AFR | GWD | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02922 | hp2 | a0001 | c0001 | t0008 | g0145 | AFR | ESN | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0009 | AFR | ESN | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0049 | AFR | ESN | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0017 | AFR | ESN | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ESN | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0035 | AFR | GWD | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG03041 | hp2 | a0001 | c0002 | t0003 | g0027 | AFR | GWD | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG03139 | hp1 | a0001 | c0001 | t0006 | g0183 | AFR | ESN | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0181 | AFR | ESN | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG03195 | hp2 | a0001 | c0002 | t0005 | g0092 | AFR | ESN | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0017 | AFR | MSL | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | MSL | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0174 | AFR | MSL | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG03453 | hp1 | a0001 | c0002 | t0003 | g0051 | AFR | MSL | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0050 | AFR | MSL | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | MSL | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG03486 | hp2 | a0001 | c0002 | t0002 | g0012 | AFR | MSL | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0006 | SAS | PJL | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0020 | SAS | PJL | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0034 | AFR | ESN | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | ESN | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG03540 | hp1 | a0001 | c0007 | t0001 | g0148 | AFR | GWD | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG03654 | hp2 | a0001 | c0001 | t0004 | g0020 | SAS | PJL | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0006 | SAS | PJL | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | STU | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | STU | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0053 | SAS | PJL | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | BEB | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0105 | SAS | BEB | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0006 | SAS | BEB | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0004 | SAS | BEB | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | BEB | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0029 | SAS | STU | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG04115 | hp2 | a0003 | c0006 | t0001 | g0121 | SAS | STU | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | BEB | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | BEB | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | STU | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0062 | SAS | STU | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | STU | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | STU | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | STU | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | STU | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | YRI | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | CHB | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHB | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | CHB | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | YRI | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0017 | AFR | YRI | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18939 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18941 | hp2 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18952 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18953 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18956 | hp1 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18959 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18968 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18972 | hp1 | a0001 | c0002 | t0001 | g0171 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18974 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18978 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18989 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18993 | hp1 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA19001 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | LWK | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | LWK | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0049 | AFR | LWK | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA19064 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA19075 | hp1 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA19076 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA19082 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | YRI | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ASW | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA20129 | hp2 | a0001 | c0002 | t0005 | g0091 | AFR | ASW | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | TSI | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0111 | EUR | TSI | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0063 | EUR | TSI | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0004 | EUR | TSI | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | GIH | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0035 | SAS | GIH | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0006 | AFR | ACB | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0050 | AFR | MSL | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | MSL | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | USA | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0104 | AFR | USA | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0009 | AFR | USA | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | USA | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | INTS13_chr12_26900181_26942981 | INTS13 | chr12 | 26900181 | 26942981 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:26913597 | T | A | 1 | a0002 | 1 | HG02647.hp2 | missense_variant | MODERATE | c.1665A>T | p.Glu555Asp | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 14/17 | 1862/2634 | 1665/2121 | 555/706 | chr12 | 26913597 | |||
| chr12:26924476 | G | A | 1 | a0003 | 1 | HG04115.hp2 | missense_variant | MODERATE | c.683C>T | p.Pro228Leu | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 7/17 | 880/2634 | 683/2121 | 228/706 | chr12 | 26924476 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:26911299 | C | T | 5 | a0001c0001 a0001c0004 a0001c0005 others(2): Show |
244 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
synonymous_variant | LOW | c.1824G>A | p.Glu608Glu | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 15/17 | 2021/2634 | 1824/2121 | 608/706 | chr12 | 26911299 | |||
| chr12:26914417 | G | A | 1 | a0001c0004 | 1 | HG02647.hp1 | synonymous_variant | LOW | c.1410C>T | p.Asn470Asn | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 12/17 | 1607/2634 | 1410/2121 | 470/706 | chr12 | 26914417 | |||
| chr12:26922680 | T | C | 1 | a0001c0005 | 1 | HG00408.hp1 | synonymous_variant | LOW | c.825A>G | p.Thr275Thr | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 8/17 | 1022/2634 | 825/2121 | 275/706 | chr12 | 26922680 | |||
| chr12:26925809 | G | A | 1 | a0001c0007 | 1 | HG03540.hp1 | synonymous_variant | LOW | c.627C>T | p.Thr209Thr | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 6/17 | 824/2634 | 627/2121 | 209/706 | chr12 | 26925809 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:26905240 | T | A | 2 | a0001c0002t0003 a0001c0002t0005 |
5 | HG02723.hp2 HG03041.hp2 HG03195.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*257A>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 17/17 | 257 | chr12 | 26905240 | ||||||
| chr12:26905306 | C | A | 1 | a0001c0001t0008 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*191G>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 17/17 | 191 | chr12 | 26905306 | ||||||
| chr12:26905440 | C | T | 1 | a0001c0002t0007 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*57G>A | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 17/17 | 57 | chr12 | 26905440 | ||||||
| chr12:26905443 | A | G | 1 | a0001c0001t0004 | 3 | HG02602.hp1 HG03492.hp1 HG03654.hp2 |
3_prime_UTR_variant | MODIFIER | c.*54T>C | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 17/17 | 54 | chr12 | 26905443 | ||||||
| chr12:26905463 | G | C | 1 | a0001c0002t0002 | 5 | HG02572.hp1 HG02630.hp1 HG02723.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*34C>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 17/17 | 34 | chr12 | 26905463 | ||||||
| chr12:26937864 | T | C | 1 | a0001c0001t0006 | 2 | HG02257.hp1 HG03139.hp1 |
5_prime_UTR_variant | MODIFIER | c.-80A>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 1/17 | 1061 | chr12 | 26937864 | ||||||
| chr12:26937976 | A | C | 1 | a0001c0002t0003 | 3 | HG02723.hp2 HG03041.hp2 HG03453.hp1 |
5_prime_UTR_variant | MODIFIER | c.-192T>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 1/17 | 1173 | chr12 | 26937976 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:26905603 | C | T | 2 | a0001c0001t0001g0022 a0001c0001t0001g0140 |
4 | HG01167.hp2 HG01192.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.2082-67G>A | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 16/16 | chr12 | 26905603 | |||||||
| chr12:26905630 | A | G | 18 | a0001c0002t0001g0001 a0001c0002t0001g0009 a0001c0002t0001g0017 others(15): Show |
53 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.2082-94T>C | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 16/16 | chr12 | 26905630 | |||||||
| chr12:26905975 | T | C | 1 | a0001c0001t0001g0039 | 2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2081+327A>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 16/16 | chr12 | 26905975 | |||||||
| chr12:26906058 | G | A | 175 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(172): Show |
364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.2081+244C>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 16/16 | chr12 | 26906058 | |||||||
| chr12:26906140 | G | C | 172 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(169): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.2081+162C>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 16/16 | chr12 | 26906140 | |||||||
| chr12:26906196 | A | T | 1 | a0002c0003t0001g0101 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2081+106T>A | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 16/16 | chr12 | 26906196 | |||||||
| chr12:26906216 | C | T | 145 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(142): Show |
295 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.2081+86G>A | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 16/16 | chr12 | 26906216 | |||||||
| chr12:26906257 | T | TA | 1 | a0001c0001t0001g0013 | 4 | NA18948.hp2 NA18953.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.2081+44dupT | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 16/16 | chr12 | 26906257 | |||||||
| chr12:26906261 | G | C | 3 | a0001c0001t0001g0026 a0001c0001t0001g0047 a0001c0002t0001g0036 |
7 | HG02145.hp1 HG02615.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.2081+41C>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 16/16 | chr12 | 26906261 | |||||||
| chr12:26906291 | G | A | 175 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(172): Show |
364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.2081+11C>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 16/16 | chr12 | 26906291 | |||||||
| chr12:26906489 | T | C | 145 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(142): Show |
295 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.1946-52A>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 15/16 | chr12 | 26906489 | |||||||
| chr12:26906579 | G | A | 127 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(124): Show |
249 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.1946-142C>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 15/16 | chr12 | 26906579 | |||||||
| chr12:26906710 | A | T | 1 | a0001c0001t0001g0130 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1946-273T>A | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 15/16 | chr12 | 26906710 | |||||||
| chr12:26906872 | T | G | 1 | a0001c0001t0008g0145 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1946-435A>C | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 15/16 | chr12 | 26906872 | |||||||
| chr12:26907069 | A | C | 4 | a0001c0002t0001g0174 a0001c0002t0001g0175 a0001c0002t0001g0176 others(1): Show |
4 | HG02258.hp2 HG02280.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1946-632T>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 15/16 | chr12 | 26907069 | |||||||
| chr12:26907180 | C | G | 1 | a0001c0002t0001g0057 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1946-743G>C | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 15/16 | chr12 | 26907180 | |||||||
| chr12:26907303 | A | AC | 175 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(172): Show |
364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.1946-867_1946-866i others(3): Show |
INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 15/16 | chr12 | 26907303 | |||||||
| chr12:26907455 | C | A | 4 | a0001c0002t0001g0034 a0001c0002t0001g0052 a0001c0002t0001g0053 others(1): Show |
5 | HG00738.hp2 HG01884.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.1946-1018G>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 15/16 | chr12 | 26907455 | |||||||
| chr12:26907543 | A | G | 4 | a0001c0002t0001g0174 a0001c0002t0001g0175 a0001c0002t0001g0176 others(1): Show |
4 | HG02258.hp2 HG02280.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1946-1106T>C | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 15/16 | chr12 | 26907543 | |||||||
| chr12:26907620 | T | A | 4 | a0001c0002t0001g0034 a0001c0002t0001g0052 a0001c0002t0001g0053 others(1): Show |
5 | HG00738.hp2 HG01884.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.1946-1183A>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 15/16 | chr12 | 26907620 | |||||||
| chr12:26907649 | C | G | 175 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(172): Show |
364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.1946-1212G>C | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 15/16 | chr12 | 26907649 | |||||||
| chr12:26907844 | T | C | 1 | a0001c0001t0001g0154 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1946-1407A>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 15/16 | chr12 | 26907844 | |||||||
| chr12:26907951 | A | G | 1 | a0001c0001t0001g0075 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1946-1514T>C | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 15/16 | chr12 | 26907951 | |||||||
| chr12:26907964 | A | G | 1 | a0001c0002t0003g0051 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1946-1527T>C | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 15/16 | chr12 | 26907964 | |||||||
| chr12:26908137 | C | T | 1 | a0001c0002t0001g0030 | 2 | NA18941.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1946-1700G>A | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 15/16 | chr12 | 26908137 | |||||||
| chr12:26908511 | A | G | 2 | a0001c0001t0001g0044 a0001c0001t0001g0137 |
3 | HG00735.hp1 HG04204.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1946-2074T>C | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 15/16 | chr12 | 26908511 | |||||||
| chr12:26908537 | G | GT | 6 | a0001c0001t0001g0067 a0001c0001t0001g0112 a0001c0001t0001g0114 others(3): Show |
6 | HG01517.hp1 HG01517.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.1946-2101dupA | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 15/16 | chr12 | 26908537 | |||||||
| chr12:26908539 | T | G | 1 | a0001c0002t0001g0060 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1946-2102A>C | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 15/16 | chr12 | 26908539 | |||||||
| chr12:26908556 | G | A | 1 | a0001c0002t0005g0092 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1946-2119C>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 15/16 | chr12 | 26908556 | |||||||
| chr12:26908562 | T | A | 1 | a0001c0001t0001g0155 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1946-2125A>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 15/16 | chr12 | 26908562 | |||||||
| chr12:26908573 | T | C | 1 | a0001c0001t0001g0115 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1946-2136A>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 15/16 | chr12 | 26908573 | |||||||
| chr12:26908837 | A | G | 172 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(169): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.1945+2341T>C | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 15/16 | chr12 | 26908837 | |||||||
| chr12:26909051 | T | C | 1 | a0001c0002t0001g0093 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1945+2127A>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 15/16 | chr12 | 26909051 | |||||||
| chr12:26909098 | T | C | 1 | a0001c0002t0007g0090 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1945+2080A>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 15/16 | chr12 | 26909098 | |||||||
| chr12:26909187 | C | T | 1 | a0001c0002t0001g0179 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1945+1991G>A | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 15/16 | chr12 | 26909187 | |||||||
| chr12:26909253 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1945+1925G>A | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 15/16 | chr12 | 26909253 | |||||||
| chr12:26909355 | C | T | 1 | a0001c0002t0001g0059 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1945+1823G>A | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 15/16 | chr12 | 26909355 | |||||||
| chr12:26909458 | G | A | 1 | a0001c0001t0001g0131 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1945+1720C>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 15/16 | chr12 | 26909458 | |||||||
| chr12:26909472 | C | CT | 44 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0022 others(41): Show |
77 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.1945+1705dupA | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 15/16 | chr12 | 26909472 | |||||||
| chr12:26909472 | CT | C | 16 | a0001c0001t0001g0033 a0001c0001t0001g0079 a0001c0001t0001g0144 others(13): Show |
18 | HG01069.hp2 HG01169.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.1945+1705delA | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 15/16 | chr12 | 26909472 | |||||||
| chr12:26909472 | CTT | C | 19 | a0001c0001t0001g0132 a0001c0002t0001g0001 a0001c0002t0001g0009 others(16): Show |
54 | HG00280.hp2 HG00438.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.1945+1704_1945+170 others(6): Show |
INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 15/16 | chr12 | 26909472 | |||||||
| chr12:26909475 | T | C | 17 | a0001c0002t0001g0001 a0001c0002t0001g0009 a0001c0002t0001g0017 others(14): Show |
52 | HG00280.hp2 HG00438.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.1945+1703A>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 15/16 | chr12 | 26909475 | |||||||
| chr12:26909493 | T | C | 1 | a0001c0001t0001g0042 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1945+1685A>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 15/16 | chr12 | 26909493 | |||||||
| chr12:26909516 | G | A | 3 | a0001c0002t0001g0049 a0001c0002t0001g0050 a0001c0002t0001g0181 |
5 | HG02970.hp2 HG03139.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1945+1662C>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 15/16 | chr12 | 26909516 | |||||||
| chr12:26909694 | T | C | 1 | a0001c0001t0001g0133 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1945+1484A>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 15/16 | chr12 | 26909694 | |||||||
| chr12:26909869 | C | T | 1 | a0001c0002t0001g0097 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1945+1309G>A | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 15/16 | chr12 | 26909869 | |||||||
| chr12:26909926 | G | A | 17 | a0001c0002t0001g0001 a0001c0002t0001g0009 a0001c0002t0001g0017 others(14): Show |
52 | HG00280.hp2 HG00438.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.1945+1252C>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 15/16 | chr12 | 26909926 | |||||||
| chr12:26910024 | C | T | 138 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(135): Show |
286 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.1945+1154G>A | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 15/16 | chr12 | 26910024 | |||||||
| chr12:26910311 | A | T | 4 | a0001c0002t0001g0174 a0001c0002t0001g0175 a0001c0002t0001g0176 others(1): Show |
4 | HG02258.hp2 HG02280.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1945+867T>A | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 15/16 | chr12 | 26910311 | |||||||
| chr12:26910356 | A | C | 1 | a0001c0002t0001g0036 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1945+822T>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 15/16 | chr12 | 26910356 | |||||||
| chr12:26910684 | T | G | 3 | a0001c0002t0001g0049 a0001c0002t0001g0050 a0001c0002t0001g0181 |
5 | HG02970.hp2 HG03139.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1945+494A>C | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 15/16 | chr12 | 26910684 | |||||||
| chr12:26910768 | T | A | 1 | a0001c0001t0008g0145 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1945+410A>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 15/16 | chr12 | 26910768 | |||||||
| chr12:26911089 | C | T | 4 | a0001c0002t0003g0027 a0001c0002t0003g0051 a0001c0002t0005g0091 others(1): Show |
5 | HG02723.hp2 HG03041.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1945+89G>A | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 15/16 | chr12 | 26911089 | |||||||
| chr12:26911143 | T | C | 4 | a0001c0002t0003g0027 a0001c0002t0003g0051 a0001c0002t0005g0091 others(1): Show |
5 | HG02723.hp2 HG03041.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1945+35A>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 15/16 | chr12 | 26911143 | |||||||
| chr12:26911549 | G | A | 1 | a0001c0002t0001g0094 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1806-232C>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 14/16 | chr12 | 26911549 | |||||||
| chr12:26911557 | T | C | 2 | a0001c0001t0001g0076 a0001c0001t0001g0086 |
2 | NA18955.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.1806-240A>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 14/16 | chr12 | 26911557 | |||||||
| chr12:26911565 | A | G | 3 | a0001c0002t0001g0049 a0001c0002t0001g0050 a0001c0002t0001g0181 |
5 | HG02970.hp2 HG03139.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1806-248T>C | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 14/16 | chr12 | 26911565 | |||||||
| chr12:26911647 | T | C | 2 | a0001c0001t0001g0149 a0001c0001t0001g0156 |
2 | HG03669.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1806-330A>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 14/16 | chr12 | 26911647 | |||||||
| chr12:26911852 | A | C | 3 | a0001c0001t0001g0025 a0001c0001t0001g0153 a0001c0001t0001g0157 |
5 | HG00280.hp1 HG01175.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1806-535T>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 14/16 | chr12 | 26911852 | |||||||
| chr12:26911857 | T | C | 1 | a0001c0002t0007g0090 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1806-540A>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 14/16 | chr12 | 26911857 | |||||||
| chr12:26911872 | G | T | 1 | a0001c0002t0001g0029 | 2 | HG01255.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1806-555C>A | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 14/16 | chr12 | 26911872 | |||||||
| chr12:26912090 | A | G | 18 | a0001c0002t0001g0001 a0001c0002t0001g0009 a0001c0002t0001g0017 others(15): Show |
53 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.1806-773T>C | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 14/16 | chr12 | 26912090 | |||||||
| chr12:26912154 | G | A | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(122): Show |
245 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.1806-837C>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 14/16 | chr12 | 26912154 | |||||||
| chr12:26912167 | G | C | 1 | a0001c0001t0001g0147 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1806-850C>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 14/16 | chr12 | 26912167 | |||||||
| chr12:26912174 | C | T | 14 | a0001c0002t0001g0004 a0001c0002t0001g0008 a0001c0002t0001g0011 others(11): Show |
42 | HG00140.hp1 HG00438.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.1806-857G>A | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 14/16 | chr12 | 26912174 | |||||||
| chr12:26912292 | C | T | 1 | a0001c0002t0001g0062 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1806-975G>A | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 14/16 | chr12 | 26912292 | |||||||
| chr12:26912395 | C | A | 1 | a0001c0001t0001g0088 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1805+1062G>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 14/16 | chr12 | 26912395 | |||||||
| chr12:26912409 | C | A | 1 | a0001c0001t0001g0045 | 2 | NA18954.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.1805+1048G>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 14/16 | chr12 | 26912409 | |||||||
| chr12:26912508 | TAGAGGAT others(6): Show |
T | 1 | a0001c0002t0001g0096 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1805+936_1805+948d others(15): Show |
INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 14/16 | chr12 | 26912508 | |||||||
| chr12:26912510 | G | C | 1 | a0001c0001t0001g0116 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1805+947C>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 14/16 | chr12 | 26912510 | |||||||
| chr12:26912553 | T | G | 1 | a0001c0002t0001g0061 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1805+904A>C | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 14/16 | chr12 | 26912553 | |||||||
| chr12:26912581 | G | A | 1 | a0001c0002t0001g0104 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1805+876C>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 14/16 | chr12 | 26912581 | |||||||
| chr12:26912649 | G | T | 14 | a0001c0002t0001g0004 a0001c0002t0001g0008 a0001c0002t0001g0011 others(11): Show |
42 | HG00140.hp1 HG00438.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.1805+808C>A | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 14/16 | chr12 | 26912649 | |||||||
| chr12:26912693 | A | G | 1 | a0001c0001t0001g0024 | 3 | HG02083.hp1 NA18747.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.1805+764T>C | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 14/16 | chr12 | 26912693 | |||||||
| chr12:26912731 | CT | C | 154 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(151): Show |
312 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.1805+725delA | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 14/16 | chr12 | 26912731 | |||||||
| chr12:26912763 | T | C | 1 | a0001c0001t0001g0077 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1805+694A>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 14/16 | chr12 | 26912763 | |||||||
| chr12:26912828 | C | G | 3 | a0001c0002t0001g0049 a0001c0002t0001g0050 a0001c0002t0001g0181 |
5 | HG02970.hp2 HG03139.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1805+629G>C | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 14/16 | chr12 | 26912828 | |||||||
| chr12:26912862 | A | C | 1 | a0001c0001t0001g0178 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1805+595T>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 14/16 | chr12 | 26912862 | |||||||
| chr12:26913000 | G | A | 2 | a0001c0002t0002g0012 a0001c0002t0002g0106 |
5 | HG02572.hp1 HG02630.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1805+457C>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 14/16 | chr12 | 26913000 | |||||||
| chr12:26913106 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1805+351C>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 14/16 | chr12 | 26913106 | |||||||
| chr12:26913152 | A | G | 3 | a0001c0002t0001g0049 a0001c0002t0001g0050 a0001c0002t0001g0181 |
5 | HG02970.hp2 HG03139.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1805+305T>C | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 14/16 | chr12 | 26913152 | |||||||
| chr12:26913417 | C | T | 124 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(121): Show |
244 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.1805+40G>A | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 14/16 | chr12 | 26913417 | |||||||
| chr12:26914194 | C | A | 4 | a0001c0002t0003g0027 a0001c0002t0003g0051 a0001c0002t0005g0091 others(1): Show |
5 | HG02723.hp2 HG03041.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1420-66G>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 12/16 | chr12 | 26914194 | |||||||
| chr12:26914280 | T | C | 1 | a0001c0001t0001g0019 | 3 | NA18950.hp2 NA18951.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.1419+128A>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 12/16 | chr12 | 26914280 | |||||||
| chr12:26914325 | T | C | 4 | a0001c0002t0003g0027 a0001c0002t0003g0051 a0001c0002t0005g0091 others(1): Show |
5 | HG02723.hp2 HG03041.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1419+83A>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 12/16 | chr12 | 26914325 | |||||||
| chr12:26914378 | T | C | 3 | a0001c0002t0001g0049 a0001c0002t0001g0050 a0001c0002t0001g0181 |
5 | HG02970.hp2 HG03139.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1419+30A>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 12/16 | chr12 | 26914378 | |||||||
| chr12:26914698 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1249-120G>A | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 11/16 | chr12 | 26914698 | |||||||
| chr12:26914729 | T | C | 5 | a0001c0002t0001g0008 a0001c0002t0001g0093 a0001c0002t0001g0094 others(2): Show |
12 | HG00438.hp2 HG00597.hp2 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.1249-151A>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 11/16 | chr12 | 26914729 | |||||||
| chr12:26914843 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1249-265G>A | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 11/16 | chr12 | 26914843 | |||||||
| chr12:26914955 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1249-377C>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 11/16 | chr12 | 26914955 | |||||||
| chr12:26915045 | G | A | 124 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(121): Show |
244 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.1249-467C>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 11/16 | chr12 | 26915045 | |||||||
| chr12:26915099 | G | A | 124 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(121): Show |
244 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.1249-521C>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 11/16 | chr12 | 26915099 | |||||||
| chr12:26915323 | G | A | 4 | a0001c0002t0001g0174 a0001c0002t0001g0175 a0001c0002t0001g0176 others(1): Show |
4 | HG02258.hp2 HG02280.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1248+679C>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 11/16 | chr12 | 26915323 | |||||||
| chr12:26915374 | T | C | 4 | a0001c0002t0001g0174 a0001c0002t0001g0175 a0001c0002t0001g0176 others(1): Show |
4 | HG02258.hp2 HG02280.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1248+628A>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 11/16 | chr12 | 26915374 | |||||||
| chr12:26915384 | T | G | 25 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0021 others(22): Show |
46 | HG00544.hp1 HG00642.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.1248+618A>C | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 11/16 | chr12 | 26915384 | |||||||
| chr12:26915411 | T | A | 6 | a0001c0002t0001g0028 a0001c0002t0001g0034 a0001c0002t0001g0052 others(3): Show |
8 | HG00738.hp2 HG01884.hp2 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.1248+591A>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 11/16 | chr12 | 26915411 | |||||||
| chr12:26915455 | T | G | 1 | a0001c0001t0001g0119 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1248+547A>C | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 11/16 | chr12 | 26915455 | |||||||
| chr12:26915488 | C | G | 1 | a0001c0001t0001g0072 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1248+514G>C | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 11/16 | chr12 | 26915488 | |||||||
| chr12:26915744 | A | G | 1 | a0001c0002t0001g0057 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1248+258T>C | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 11/16 | chr12 | 26915744 | |||||||
| chr12:26916241 | T | C | 2 | a0001c0001t0001g0031 a0001c0001t0001g0067 |
3 | HG01243.hp2 HG01258.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1070-61A>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 10/16 | chr12 | 26916241 | |||||||
| chr12:26916466 | T | C | 1 | a0001c0001t0001g0134 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1070-286A>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 10/16 | chr12 | 26916466 | |||||||
| chr12:26916702 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1070-522A>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 10/16 | chr12 | 26916702 | |||||||
| chr12:26916915 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1069+437A>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 10/16 | chr12 | 26916915 | |||||||
| chr12:26916952 | A | G | 1 | a0001c0002t0001g0104 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1069+400T>C | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 10/16 | chr12 | 26916952 | |||||||
| chr12:26916973 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1069+379T>C | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 10/16 | chr12 | 26916973 | |||||||
| chr12:26917078 | TCA | T | 4 | a0001c0002t0003g0027 a0001c0002t0003g0051 a0001c0002t0005g0091 others(1): Show |
5 | HG02723.hp2 HG03041.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1069+272_1069+273d others(4): Show |
INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 10/16 | chr12 | 26917078 | |||||||
| chr12:26917185 | A | G | 1 | a0001c0002t0001g0058 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1069+167T>C | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 10/16 | chr12 | 26917185 | |||||||
| chr12:26917186 | T | C | 1 | a0001c0001t0001g0079 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1069+166A>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 10/16 | chr12 | 26917186 | |||||||
| chr12:26917481 | A | G | 3 | a0001c0002t0001g0049 a0001c0002t0001g0050 a0001c0002t0001g0181 |
5 | HG02970.hp2 HG03139.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.980-40T>C | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 9/16 | chr12 | 26917481 | |||||||
| chr12:26917607 | T | C | 1 | a0001c0001t0001g0135 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.979+37A>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 9/16 | chr12 | 26917607 | |||||||
| chr12:26917844 | C | T | 2 | a0001c0001t0001g0123 a0001c0001t0001g0141 |
2 | HG02055.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.890-111G>A | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 8/16 | chr12 | 26917844 | |||||||
| chr12:26917872 | C | T | 2 | a0001c0002t0001g0034 a0001c0002t0007g0090 |
3 | HG00738.hp2 HG01884.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.890-139G>A | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 8/16 | chr12 | 26917872 | |||||||
| chr12:26918015 | G | A | 4 | a0001c0002t0001g0174 a0001c0002t0001g0175 a0001c0002t0001g0176 others(1): Show |
4 | HG02258.hp2 HG02280.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.890-282C>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 8/16 | chr12 | 26918015 | |||||||
| chr12:26918036 | C | T | 1 | a0001c0001t0001g0023 | 3 | HG03688.hp2 NA19082.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.890-303G>A | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 8/16 | chr12 | 26918036 | |||||||
| chr12:26918063 | G | A | 1 | a0001c0002t0001g0175 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.890-330C>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 8/16 | chr12 | 26918063 | |||||||
| chr12:26918072 | C | A | 4 | a0001c0002t0001g0174 a0001c0002t0001g0175 a0001c0002t0001g0176 others(1): Show |
4 | HG02258.hp2 HG02280.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.890-339G>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 8/16 | chr12 | 26918072 | |||||||
| chr12:26918403 | C | T | 7 | a0001c0001t0001g0040 a0001c0001t0001g0108 a0001c0001t0001g0112 others(4): Show |
8 | HG02015.hp1 HG02132.hp2 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.890-670G>A | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 8/16 | chr12 | 26918403 | |||||||
| chr12:26918679 | A | G | 2 | a0001c0001t0001g0022 a0001c0001t0001g0140 |
4 | HG01167.hp2 HG01192.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.890-946T>C | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 8/16 | chr12 | 26918679 | |||||||
| chr12:26918783 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.890-1050A>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 8/16 | chr12 | 26918783 | |||||||
| chr12:26918790 | A | C | 1 | a0001c0002t0001g0065 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.890-1057T>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 8/16 | chr12 | 26918790 | |||||||
| chr12:26918991 | C | A | 1 | a0002c0003t0001g0101 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.890-1258G>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 8/16 | chr12 | 26918991 | |||||||
| chr12:26919091 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.890-1358G>A | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 8/16 | chr12 | 26919091 | |||||||
| chr12:26919196 | A | G | 127 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(124): Show |
249 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.890-1463T>C | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 8/16 | chr12 | 26919196 | |||||||
| chr12:26919219 | A | T | 69 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0013 others(66): Show |
123 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.890-1486T>A | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 8/16 | chr12 | 26919219 | |||||||
| chr12:26919354 | C | A | 1 | a0001c0002t0005g0091 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.890-1621G>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 8/16 | chr12 | 26919354 | |||||||
| chr12:26919418 | A | G | 131 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(128): Show |
253 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.890-1685T>C | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 8/16 | chr12 | 26919418 | |||||||
| chr12:26919654 | AT | A | 14 | a0001c0002t0001g0004 a0001c0002t0001g0008 a0001c0002t0001g0011 others(11): Show |
42 | HG00140.hp1 HG00438.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.890-1922delA | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 8/16 | chr12 | 26919654 | |||||||
| chr12:26919774 | GT | G | 60 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0013 others(57): Show |
112 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.890-2042delA | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 8/16 | chr12 | 26919774 | |||||||
| chr12:26919792 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.890-2059C>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 8/16 | chr12 | 26919792 | |||||||
| chr12:26919910 | C | T | 2 | a0001c0001t0001g0015 a0001c0001t0001g0124 |
5 | NA18950.hp1 NA18956.hp2 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.890-2177G>A | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 8/16 | chr12 | 26919910 | |||||||
| chr12:26919944 | C | G | 1 | a0001c0001t0001g0021 | 3 | NA18979.hp2 NA19000.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.890-2211G>C | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 8/16 | chr12 | 26919944 | |||||||
| chr12:26919962 | A | G | 2 | a0001c0001t0006g0182 a0001c0001t0006g0183 |
2 | HG02257.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.890-2229T>C | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 8/16 | chr12 | 26919962 | |||||||
| chr12:26919979 | T | G | 1 | a0001c0001t0001g0047 | 2 | HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.890-2246A>C | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 8/16 | chr12 | 26919979 | |||||||
| chr12:26920020 | C | T | 1 | a0001c0001t0001g0126 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.890-2287G>A | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 8/16 | chr12 | 26920020 | |||||||
| chr12:26920082 | C | T | 1 | a0001c0002t0007g0090 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.890-2349G>A | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 8/16 | chr12 | 26920082 | |||||||
| chr12:26920115 | G | A | 2 | a0001c0002t0003g0027 a0001c0002t0003g0051 |
3 | HG02723.hp2 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.890-2382C>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 8/16 | chr12 | 26920115 | |||||||
| chr12:26920127 | C | CA | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(122): Show |
247 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.890-2395dupT | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 8/16 | chr12 | 26920127 | |||||||
| chr12:26920267 | G | A | 14 | a0001c0002t0001g0004 a0001c0002t0001g0008 a0001c0002t0001g0011 others(11): Show |
42 | HG00140.hp1 HG00438.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.889+2349C>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 8/16 | chr12 | 26920267 | |||||||
| chr12:26920403 | CT | C | 126 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(123): Show |
247 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.889+2212delA | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 8/16 | chr12 | 26920403 | |||||||
| chr12:26920423 | A | T | 14 | a0001c0002t0001g0004 a0001c0002t0001g0008 a0001c0002t0001g0011 others(11): Show |
42 | HG00140.hp1 HG00438.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.889+2193T>A | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 8/16 | chr12 | 26920423 | |||||||
| chr12:26920475 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.889+2141A>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 8/16 | chr12 | 26920475 | |||||||
| chr12:26920589 | C | T | 4 | a0001c0002t0001g0174 a0001c0002t0001g0175 a0001c0002t0001g0176 others(1): Show |
4 | HG02258.hp2 HG02280.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.889+2027G>A | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 8/16 | chr12 | 26920589 | |||||||
| chr12:26920591 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.889+2025C>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 8/16 | chr12 | 26920591 | |||||||
| chr12:26920615 | A | G | 131 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(128): Show |
253 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.889+2001T>C | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 8/16 | chr12 | 26920615 | |||||||
| chr12:26921221 | C | A | 1 | a0001c0001t0001g0048 | 2 | NA18962.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.889+1395G>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 8/16 | chr12 | 26921221 | |||||||
| chr12:26921241 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.889+1375T>C | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 8/16 | chr12 | 26921241 | |||||||
| chr12:26921664 | T | C | 6 | a0001c0002t0001g0028 a0001c0002t0001g0034 a0001c0002t0001g0052 others(3): Show |
8 | HG00738.hp2 HG01884.hp2 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.889+952A>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 8/16 | chr12 | 26921664 | |||||||
| chr12:26921783 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.889+833C>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 8/16 | chr12 | 26921783 | |||||||
| chr12:26922015 | T | C | 1 | a0001c0001t0001g0136 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.889+601A>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 8/16 | chr12 | 26922015 | |||||||
| chr12:26922097 | G | C | 5 | a0001c0001t0001g0019 a0001c0001t0001g0080 a0001c0001t0001g0082 others(2): Show |
7 | HG02071.hp1 HG02165.hp2 NA18947.hp1 others(4): Show |
intron_variant | MODIFIER | c.889+519C>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 8/16 | chr12 | 26922097 | |||||||
| chr12:26922497 | T | A | 1 | a0001c0002t0003g0027 | 2 | HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.889+119A>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 8/16 | chr12 | 26922497 | |||||||
| chr12:26922772 | A | T | 127 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(124): Show |
249 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.805-72T>A | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 7/16 | chr12 | 26922772 | |||||||
| chr12:26922948 | A | G | 1 | a0001c0001t0001g0083 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.805-248T>C | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 7/16 | chr12 | 26922948 | |||||||
| chr12:26922974 | A | AT | 4 | a0001c0002t0003g0027 a0001c0002t0003g0051 a0001c0002t0005g0091 others(1): Show |
5 | HG02723.hp2 HG03041.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.805-275dupA | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 7/16 | chr12 | 26922974 | |||||||
| chr12:26923011 | T | C | 2 | a0001c0001t0006g0182 a0001c0001t0006g0183 |
2 | HG02257.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.805-311A>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 7/16 | chr12 | 26923011 | |||||||
| chr12:26923059 | G | A | 1 | a0001c0001t0001g0039 | 2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.805-359C>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 7/16 | chr12 | 26923059 | |||||||
| chr12:26923135 | T | C | 174 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(171): Show |
363 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(360): Show |
intron_variant | MODIFIER | c.805-435A>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 7/16 | chr12 | 26923135 | |||||||
| chr12:26923452 | T | C | 1 | a0001c0002t0001g0050 | 2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.805-752A>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 7/16 | chr12 | 26923452 | |||||||
| chr12:26923593 | A | G | 1 | a0001c0001t0001g0151 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.804+762T>C | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 7/16 | chr12 | 26923593 | |||||||
| chr12:26923862 | C | A | 1 | a0001c0002t0001g0034 | 2 | HG01884.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.804+493G>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 7/16 | chr12 | 26923862 | |||||||
| chr12:26923893 | A | G | 2 | a0001c0001t0001g0016 a0001c0001t0001g0150 |
5 | HG01169.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.804+462T>C | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 7/16 | chr12 | 26923893 | |||||||
| chr12:26924060 | G | A | 1 | a0001c0002t0001g0062 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.804+295C>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 7/16 | chr12 | 26924060 | |||||||
| chr12:26924261 | G | C | 1 | a0001c0002t0002g0106 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.804+94C>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 7/16 | chr12 | 26924261 | |||||||
| chr12:26924776 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.676-293A>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 6/16 | chr12 | 26924776 | |||||||
| chr12:26924802 | C | T | 2 | a0001c0001t0001g0110 a0001c0001t0001g0111 |
2 | HG01261.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.676-319G>A | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 6/16 | chr12 | 26924802 | |||||||
| chr12:26924993 | C | G | 4 | a0001c0002t0001g0009 a0001c0002t0001g0017 a0001c0002t0001g0056 others(1): Show |
11 | HG00642.hp2 HG02258.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.676-510G>C | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 6/16 | chr12 | 26924993 | |||||||
| chr12:26925025 | G | A | 4 | a0001c0002t0001g0174 a0001c0002t0001g0175 a0001c0002t0001g0176 others(1): Show |
4 | HG02258.hp2 HG02280.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.676-542C>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 6/16 | chr12 | 26925025 | |||||||
| chr12:26925520 | T | C | 2 | a0001c0001t0001g0166 a0001c0001t0001g0167 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.675+241A>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 6/16 | chr12 | 26925520 | |||||||
| chr12:26925582 | A | G | 1 | a0001c0002t0007g0090 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.675+179T>C | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 6/16 | chr12 | 26925582 | |||||||
| chr12:26925858 | GA | G | 4 | a0001c0002t0003g0027 a0001c0002t0003g0051 a0001c0002t0005g0091 others(1): Show |
5 | HG02723.hp2 HG03041.hp2 HG03195.hp2 others(2): Show |
splice_region_variant&intron_variant | LOW | c.585-8delT | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 5/16 | chr12 | 26925858 | |||||||
| chr12:26925921 | C | T | 4 | a0001c0002t0001g0174 a0001c0002t0001g0175 a0001c0002t0001g0176 others(1): Show |
4 | HG02258.hp2 HG02280.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.585-70G>A | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 5/16 | chr12 | 26925921 | |||||||
| chr12:26926032 | C | T | 1 | a0002c0003t0001g0101 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.585-181G>A | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 5/16 | chr12 | 26926032 | |||||||
| chr12:26926130 | T | C | 1 | a0001c0001t0001g0161 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.585-279A>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 5/16 | chr12 | 26926130 | |||||||
| chr12:26926147 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.585-296C>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 5/16 | chr12 | 26926147 | |||||||
| chr12:26926325 | A | G | 1 | a0002c0003t0001g0101 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.585-474T>C | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 5/16 | chr12 | 26926325 | |||||||
| chr12:26926358 | C | G | 1 | a0001c0001t0001g0140 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.585-507G>C | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 5/16 | chr12 | 26926358 | |||||||
| chr12:26926468 | C | A | 4 | a0001c0002t0001g0034 a0001c0002t0001g0052 a0001c0002t0001g0053 others(1): Show |
5 | HG00738.hp2 HG01884.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.585-617G>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 5/16 | chr12 | 26926468 | |||||||
| chr12:26926509 | A | G | 1 | a0001c0002t0001g0105 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.585-658T>C | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 5/16 | chr12 | 26926509 | |||||||
| chr12:26926611 | CA | C | 4 | a0001c0002t0003g0027 a0001c0002t0003g0051 a0001c0002t0005g0091 others(1): Show |
5 | HG02723.hp2 HG03041.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.585-761delT | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 5/16 | chr12 | 26926611 | |||||||
| chr12:26926766 | T | C | 4 | a0001c0002t0001g0174 a0001c0002t0001g0175 a0001c0002t0001g0176 others(1): Show |
4 | HG02258.hp2 HG02280.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.585-915A>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 5/16 | chr12 | 26926766 | |||||||
| chr12:26926808 | G | A | 2 | a0001c0001t0001g0089 a0001c0001t0001g0122 |
2 | HG01109.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.585-957C>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 5/16 | chr12 | 26926808 | |||||||
| chr12:26926879 | A | C | 2 | a0001c0002t0001g0034 a0001c0002t0007g0090 |
3 | HG00738.hp2 HG01884.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.585-1028T>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 5/16 | chr12 | 26926879 | |||||||
| chr12:26926922 | G | A | 1 | a0001c0007t0001g0148 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.585-1071C>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 5/16 | chr12 | 26926922 | |||||||
| chr12:26926966 | T | C | 14 | a0001c0002t0001g0004 a0001c0002t0001g0008 a0001c0002t0001g0011 others(11): Show |
42 | HG00140.hp1 HG00438.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.585-1115A>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 5/16 | chr12 | 26926966 | |||||||
| chr12:26926977 | T | TA | 4 | a0001c0002t0003g0027 a0001c0002t0003g0051 a0001c0002t0005g0091 others(1): Show |
5 | HG02723.hp2 HG03041.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.585-1127dupT | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 5/16 | chr12 | 26926977 | |||||||
| chr12:26927249 | G | A | 1 | a0001c0002t0001g0176 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.584+956C>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 5/16 | chr12 | 26927249 | |||||||
| chr12:26927463 | GA | G | 4 | a0001c0002t0001g0174 a0001c0002t0001g0175 a0001c0002t0001g0176 others(1): Show |
4 | HG02258.hp2 HG02280.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.584+741delT | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 5/16 | chr12 | 26927463 | |||||||
| chr12:26927767 | C | A | 1 | a0001c0002t0001g0063 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.584+438G>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 5/16 | chr12 | 26927767 | |||||||
| chr12:26927769 | C | A | 2 | a0001c0002t0001g0052 a0001c0002t0001g0053 |
2 | HG02683.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.584+436G>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 5/16 | chr12 | 26927769 | |||||||
| chr12:26927782 | AT | A | 25 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0021 others(22): Show |
46 | HG00544.hp1 HG00642.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.584+422delA | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 5/16 | chr12 | 26927782 | |||||||
| chr12:26927911 | C | A | 4 | a0001c0002t0001g0174 a0001c0002t0001g0175 a0001c0002t0001g0176 others(1): Show |
4 | HG02258.hp2 HG02280.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.584+294G>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 5/16 | chr12 | 26927911 | |||||||
| chr12:26927962 | C | T | 2 | a0001c0002t0001g0034 a0001c0002t0007g0090 |
3 | HG00738.hp2 HG01884.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.584+243G>A | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 5/16 | chr12 | 26927962 | |||||||
| chr12:26928051 | GA | G | 35 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(32): Show |
66 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.584+153delT | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 5/16 | chr12 | 26928051 | |||||||
| chr12:26928089 | A | C | 1 | a0001c0001t0001g0149 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.584+116T>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 5/16 | chr12 | 26928089 | |||||||
| chr12:26928164 | T | C | 6 | a0001c0002t0001g0028 a0001c0002t0001g0034 a0001c0002t0001g0052 others(3): Show |
8 | HG00738.hp2 HG01884.hp2 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.584+41A>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 5/16 | chr12 | 26928164 | |||||||
| chr12:26928449 | C | A | 1 | a0001c0001t0001g0178 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.504-164G>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 4/16 | chr12 | 26928449 | |||||||
| chr12:26928512 | A | G | 1 | a0001c0002t0007g0090 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.503+191T>C | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 4/16 | chr12 | 26928512 | |||||||
| chr12:26928564 | A | G | 1 | a0001c0001t0008g0145 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.503+139T>C | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 4/16 | chr12 | 26928564 | |||||||
| chr12:26928607 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.503+96C>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 4/16 | chr12 | 26928607 | |||||||
| chr12:26928633 | C | G | 173 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(170): Show |
361 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(358): Show |
intron_variant | MODIFIER | c.503+70G>C | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 4/16 | chr12 | 26928633 | |||||||
| chr12:26928676 | A | T | 1 | a0001c0002t0001g0056 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.503+27T>A | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 4/16 | chr12 | 26928676 | |||||||
| chr12:26928940 | G | A | 55 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(52): Show |
121 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.301-35C>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 3/16 | chr12 | 26928940 | |||||||
| chr12:26928948 | A | C | 1 | a0001c0001t0001g0146 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.301-43T>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 3/16 | chr12 | 26928948 | |||||||
| chr12:26929083 | G | A | 2 | a0001c0001t0001g0022 a0001c0001t0001g0140 |
4 | HG01167.hp2 HG01192.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.301-178C>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 3/16 | chr12 | 26929083 | |||||||
| chr12:26929300 | C | T | 1 | a0001c0001t0008g0145 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.301-395G>A | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 3/16 | chr12 | 26929300 | |||||||
| chr12:26929397 | T | C | 1 | a0001c0001t0001g0082 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.301-492A>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 3/16 | chr12 | 26929397 | |||||||
| chr12:26929428 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.301-523T>C | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 3/16 | chr12 | 26929428 | |||||||
| chr12:26929483 | A | G | 1 | a0001c0002t0001g0049 | 2 | HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.301-578T>C | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 3/16 | chr12 | 26929483 | |||||||
| chr12:26929563 | GA | G | 43 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0019 others(40): Show |
96 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.301-659delT | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 3/16 | chr12 | 26929563 | |||||||
| chr12:26929597 | G | T | 1 | a0001c0002t0001g0034 | 2 | HG01884.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.301-692C>A | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 3/16 | chr12 | 26929597 | |||||||
| chr12:26929916 | T | C | 17 | a0001c0002t0001g0001 a0001c0002t0001g0009 a0001c0002t0001g0017 others(14): Show |
52 | HG00280.hp2 HG00438.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.301-1011A>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 3/16 | chr12 | 26929916 | |||||||
| chr12:26929919 | C | T | 1 | a0001c0002t0007g0090 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.301-1014G>A | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 3/16 | chr12 | 26929919 | |||||||
| chr12:26930165 | C | G | 1 | a0001c0002t0007g0090 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.301-1260G>C | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 3/16 | chr12 | 26930165 | |||||||
| chr12:26930195 | G | A | 4 | a0001c0002t0001g0174 a0001c0002t0001g0175 a0001c0002t0001g0176 others(1): Show |
4 | HG02258.hp2 HG02280.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.301-1290C>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 3/16 | chr12 | 26930195 | |||||||
| chr12:26930198 | T | C | 1 | a0001c0001t0001g0160 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.301-1293A>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 3/16 | chr12 | 26930198 | |||||||
| chr12:26930427 | C | T | 60 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(57): Show |
126 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.301-1522G>A | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 3/16 | chr12 | 26930427 | |||||||
| chr12:26930589 | T | C | 124 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(121): Show |
244 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.301-1684A>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 3/16 | chr12 | 26930589 | |||||||
| chr12:26930662 | C | T | 14 | a0001c0002t0001g0004 a0001c0002t0001g0008 a0001c0002t0001g0011 others(11): Show |
42 | HG00140.hp1 HG00438.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.301-1757G>A | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 3/16 | chr12 | 26930662 | |||||||
| chr12:26930892 | G | T | 4 | a0001c0002t0001g0174 a0001c0002t0001g0175 a0001c0002t0001g0176 others(1): Show |
4 | HG02258.hp2 HG02280.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.301-1987C>A | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 3/16 | chr12 | 26930892 | |||||||
| chr12:26931113 | C | T | 1 | a0001c0002t0001g0011 | 4 | HG02040.hp1 HG02155.hp2 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.301-2208G>A | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 3/16 | chr12 | 26931113 | |||||||
| chr12:26931140 | A | T | 1 | a0001c0001t0001g0039 | 2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.301-2235T>A | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 3/16 | chr12 | 26931140 | |||||||
| chr12:26931164 | C | T | 2 | a0001c0001t0001g0010 a0001c0001t0001g0085 |
5 | NA18981.hp2 NA18989.hp2 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.301-2259G>A | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 3/16 | chr12 | 26931164 | |||||||
| chr12:26931190 | C | T | 1 | a0001c0001t0001g0143 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.301-2285G>A | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 3/16 | chr12 | 26931190 | |||||||
| chr12:26931288 | C | T | 1 | a0001c0002t0001g0095 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.301-2383G>A | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 3/16 | chr12 | 26931288 | |||||||
| chr12:26931430 | C | T | 1 | a0001c0002t0001g0181 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.301-2525G>A | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 3/16 | chr12 | 26931430 | |||||||
| chr12:26931452 | T | TAAAAGA | 173 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(170): Show |
361 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(358): Show |
intron_variant | MODIFIER | c.301-2553_301-2548d others(8): Show |
INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 3/16 | chr12 | 26931452 | |||||||
| chr12:26931589 | G | C | 1 | a0001c0002t0005g0092 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.301-2684C>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 3/16 | chr12 | 26931589 | |||||||
| chr12:26931765 | T | A | 21 | a0001c0002t0001g0001 a0001c0002t0001g0009 a0001c0002t0001g0017 others(18): Show |
57 | HG00280.hp2 HG00438.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.300+2791A>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 3/16 | chr12 | 26931765 | |||||||
| chr12:26931797 | T | C | 1 | a0001c0001t0001g0084 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.300+2759A>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 3/16 | chr12 | 26931797 | |||||||
| chr12:26931811 | GC | G | 14 | a0001c0002t0001g0004 a0001c0002t0001g0008 a0001c0002t0001g0011 others(11): Show |
42 | HG00140.hp1 HG00438.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.300+2744delG | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 3/16 | chr12 | 26931811 | |||||||
| chr12:26931856 | G | A | 7 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(4): Show |
7 | HG00140.hp2 HG00733.hp1 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.300+2700C>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 3/16 | chr12 | 26931856 | |||||||
| chr12:26931858 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.300+2698C>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 3/16 | chr12 | 26931858 | |||||||
| chr12:26931873 | C | T | 64 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0013 others(61): Show |
118 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.300+2683G>A | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 3/16 | chr12 | 26931873 | |||||||
| chr12:26932079 | C | A | 1 | a0001c0002t0001g0177 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.300+2477G>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 3/16 | chr12 | 26932079 | |||||||
| chr12:26932087 | C | CA | 60 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(57): Show |
129 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.300+2468dupT | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 3/16 | chr12 | 26932087 | |||||||
| chr12:26932087 | C | CAA | 7 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(4): Show |
7 | HG01928.hp1 HG02572.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.300+2467_300+2468d others(4): Show |
INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 3/16 | chr12 | 26932087 | |||||||
| chr12:26932103 | A | C | 13 | a0001c0002t0001g0004 a0001c0002t0001g0008 a0001c0002t0001g0011 others(10): Show |
41 | HG00140.hp1 HG00438.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.300+2453T>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 3/16 | chr12 | 26932103 | |||||||
| chr12:26932142 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.300+2414C>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 3/16 | chr12 | 26932142 | |||||||
| chr12:26932272 | C | G | 4 | a0001c0002t0001g0174 a0001c0002t0001g0175 a0001c0002t0001g0176 others(1): Show |
4 | HG02258.hp2 HG02280.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.300+2284G>C | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 3/16 | chr12 | 26932272 | |||||||
| chr12:26932329 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.300+2227T>C | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 3/16 | chr12 | 26932329 | |||||||
| chr12:26932354 | C | T | 124 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(121): Show |
244 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.300+2202G>A | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 3/16 | chr12 | 26932354 | |||||||
| chr12:26932625 | C | T | 1 | a0001c0002t0001g0104 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.300+1931G>A | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 3/16 | chr12 | 26932625 | |||||||
| chr12:26932635 | C | T | 4 | a0001c0002t0001g0174 a0001c0002t0001g0175 a0001c0002t0001g0176 others(1): Show |
4 | HG02258.hp2 HG02280.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.300+1921G>A | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 3/16 | chr12 | 26932635 | |||||||
| chr12:26932762 | A | G | 17 | a0001c0002t0001g0001 a0001c0002t0001g0009 a0001c0002t0001g0017 others(14): Show |
52 | HG00280.hp2 HG00438.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.300+1794T>C | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 3/16 | chr12 | 26932762 | |||||||
| chr12:26932766 | TAGA | T | 14 | a0001c0002t0001g0004 a0001c0002t0001g0008 a0001c0002t0001g0011 others(11): Show |
42 | HG00140.hp1 HG00438.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.300+1787_300+1789d others(5): Show |
INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 3/16 | chr12 | 26932766 | |||||||
| chr12:26932823 | T | C | 126 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(123): Show |
247 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.300+1733A>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 3/16 | chr12 | 26932823 | |||||||
| chr12:26932878 | T | A | 7 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(4): Show |
7 | HG00140.hp2 HG00733.hp1 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.300+1678A>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 3/16 | chr12 | 26932878 | |||||||
| chr12:26932953 | A | G | 4 | a0001c0002t0001g0174 a0001c0002t0001g0175 a0001c0002t0001g0176 others(1): Show |
4 | HG02258.hp2 HG02280.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.300+1603T>C | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 3/16 | chr12 | 26932953 | |||||||
| chr12:26933058 | A | G | 1 | a0001c0001t0001g0038 | 2 | HG00741.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.300+1498T>C | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 3/16 | chr12 | 26933058 | |||||||
| chr12:26933098 | AGAGTAT | A | 4 | a0001c0002t0001g0008 a0001c0002t0001g0093 a0001c0002t0001g0094 others(1): Show |
11 | HG00438.hp2 HG00597.hp2 NA18939.hp1 others(8): Show |
intron_variant | MODIFIER | c.300+1452_300+1457d others(8): Show |
INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 3/16 | chr12 | 26933098 | |||||||
| chr12:26933528 | G | A | 10 | a0001c0002t0001g0004 a0001c0002t0001g0011 a0001c0002t0001g0095 others(7): Show |
31 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.300+1028C>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 3/16 | chr12 | 26933528 | |||||||
| chr12:26933584 | A | G | 1 | a0001c0002t0001g0103 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.300+972T>C | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 3/16 | chr12 | 26933584 | |||||||
| chr12:26933605 | A | G | 1 | a0001c0001t0001g0032 | 2 | HG02165.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.300+951T>C | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 3/16 | chr12 | 26933605 | |||||||
| chr12:26933645 | C | T | 2 | a0001c0001t0001g0037 a0001c0001t0001g0107 |
3 | HG00544.hp1 HG00642.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.300+911G>A | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 3/16 | chr12 | 26933645 | |||||||
| chr12:26933807 | G | A | 1 | a0002c0003t0001g0101 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.300+749C>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 3/16 | chr12 | 26933807 | |||||||
| chr12:26934072 | A | G | 1 | a0001c0001t0001g0069 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.300+484T>C | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 3/16 | chr12 | 26934072 | |||||||
| chr12:26934076 | C | A | 13 | a0001c0002t0001g0001 a0001c0002t0001g0029 a0001c0002t0001g0030 others(10): Show |
41 | HG00280.hp2 HG00438.hp1 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.300+480G>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 3/16 | chr12 | 26934076 | |||||||
| chr12:26934077 | C | A | 13 | a0001c0002t0001g0001 a0001c0002t0001g0029 a0001c0002t0001g0030 others(10): Show |
41 | HG00280.hp2 HG00438.hp1 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.300+479G>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 3/16 | chr12 | 26934077 | |||||||
| chr12:26934416 | G | A | 4 | a0001c0002t0001g0028 a0001c0002t0001g0052 a0001c0002t0001g0053 others(1): Show |
5 | HG01928.hp1 HG01943.hp1 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.300+140C>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 3/16 | chr12 | 26934416 | |||||||
| chr12:26934723 | T | G | 1 | a0001c0001t0001g0048 | 2 | NA18962.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.226-93A>C | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 2/16 | chr12 | 26934723 | |||||||
| chr12:26934770 | T | C | 172 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(169): Show |
360 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(357): Show |
intron_variant | MODIFIER | c.226-140A>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 2/16 | chr12 | 26934770 | |||||||
| chr12:26934800 | C | T | 173 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(170): Show |
361 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(358): Show |
intron_variant | MODIFIER | c.226-170G>A | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 2/16 | chr12 | 26934800 | |||||||
| chr12:26934845 | T | C | 128 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(125): Show |
248 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.226-215A>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 2/16 | chr12 | 26934845 | |||||||
| chr12:26934868 | T | C | 1 | a0001c0001t0001g0169 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.226-238A>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 2/16 | chr12 | 26934868 | |||||||
| chr12:26935000 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.226-370G>A | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 2/16 | chr12 | 26935000 | |||||||
| chr12:26935053 | T | C | 1 | a0001c0002t0001g0065 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.226-423A>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 2/16 | chr12 | 26935053 | |||||||
| chr12:26935062 | T | C | 1 | a0001c0002t0003g0027 | 2 | HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.226-432A>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 2/16 | chr12 | 26935062 | |||||||
| chr12:26935211 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.226-581C>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 2/16 | chr12 | 26935211 | |||||||
| chr12:26935413 | G | A | 1 | a0001c0002t0001g0171 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.226-783C>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 2/16 | chr12 | 26935413 | |||||||
| chr12:26935472 | A | G | 25 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0019 others(22): Show |
50 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.226-842T>C | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 2/16 | chr12 | 26935472 | |||||||
| chr12:26935521 | T | C | 4 | a0001c0002t0001g0028 a0001c0002t0001g0052 a0001c0002t0001g0053 others(1): Show |
5 | HG01928.hp1 HG01943.hp1 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.226-891A>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 2/16 | chr12 | 26935521 | |||||||
| chr12:26935843 | G | A | 2 | a0001c0002t0001g0172 a0001c0002t0001g0173 |
2 | HG00099.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.225+736C>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 2/16 | chr12 | 26935843 | |||||||
| chr12:26936102 | C | G | 2 | a0001c0001t0006g0182 a0001c0001t0006g0183 |
2 | HG02257.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.225+477G>C | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 2/16 | chr12 | 26936102 | |||||||
| chr12:26936165 | G | A | 4 | a0001c0002t0001g0174 a0001c0002t0001g0175 a0001c0002t0001g0176 others(1): Show |
4 | HG02258.hp2 HG02280.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.225+414C>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 2/16 | chr12 | 26936165 | |||||||
| chr12:26936513 | TA | T | 4 | a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0067 others(1): Show |
7 | HG01243.hp1 HG01243.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.225+65delT | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 2/16 | chr12 | 26936513 | |||||||
| chr12:26936551 | C | A | 1 | a0001c0001t0001g0178 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.225+28G>T | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 2/16 | chr12 | 26936551 | |||||||
| chr12:26936853 | T | C | 1 | a0001c0002t0001g0179 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-11-39A>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 1/16 | chr12 | 26936853 | |||||||
| chr12:26936873 | A | C | 1 | a0001c0002t0001g0052 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-11-59T>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 1/16 | chr12 | 26936873 | |||||||
| chr12:26937020 | T | C | 1 | a0001c0002t0001g0180 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-11-206A>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 1/16 | chr12 | 26937020 | |||||||
| chr12:26937215 | C | T | 1 | a0001c0002t0001g0055 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-11-401G>A | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 1/16 | chr12 | 26937215 | |||||||
| chr12:26937358 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-12+438T>C | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 1/16 | chr12 | 26937358 | |||||||
| chr12:26937617 | A | C | 16 | a0001c0002t0001g0001 a0001c0002t0001g0009 a0001c0002t0001g0017 others(13): Show |
51 | HG00280.hp2 HG00438.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.-12+179T>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 1/16 | chr12 | 26937617 | |||||||
| chr12:26937654 | T | C | 3 | a0001c0002t0001g0049 a0001c0002t0001g0050 a0001c0002t0001g0181 |
5 | HG02970.hp2 HG03139.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.-12+142A>G | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 1/16 | chr12 | 26937654 | |||||||
| chr12:26937720 | C | T | 4 | a0001c0002t0001g0028 a0001c0002t0001g0052 a0001c0002t0001g0053 others(1): Show |
5 | HG01928.hp1 HG01943.hp1 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12+76G>A | INTS13 | ENSG00000064102.15 | transcript | ENST00000261191.12 | protein_coding | 1/16 | chr12 | 26937720 |