Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1737 |
| ensemblid | ENSG00000150768.18 |
| hgncid | 2896 |
| symbol | DLAT |
| name | dihydrolipoamide S-acetyltransferase |
| refseq_nuc | NM_001931.5 |
| refseq_prot | NP_001922.2 |
| ensembl_nuc | ENST00000280346.11 |
| ensembl_prot | ENSP00000280346.7 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 112025408 |
| end | 112064404 |
| strand | + |
| ver | v1.2 |
| region | chr11:112025408-112064404 |
| region5000 | chr11:112020408-112069404 |
| regionname0 | DLAT_chr11_112025408_112064404 |
| regionname5000 | DLAT_chr11_112020408_112069404 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 647 | 129 | 11 | 30 | 62 | 8 | 16 | 47 | DLAT_chr11_112020408_112069404 | DLAT | MWRVC others(642): Show |
chr11 | 112020408 | 112069404 |
| a0002 | 0/0 | 647 | 115 | 9 | 23 | 68 | 2 | 13 | 52 | DLAT_chr11_112020408_112069404 | DLAT | MWRVC others(642): Show |
chr11 | 112020408 | 112069404 |
| a0003 | 0/0 | 647 | 52 | 46 | 6 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | MWRVC others(642): Show |
chr11 | 112020408 | 112069404 |
| a0004 | 0/0 | 647 | 15 | 15 | 0 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | MWRVC others(642): Show |
chr11 | 112020408 | 112069404 |
| a0005 | 0/0 | 647 | 12 | 11 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | MWRVC others(642): Show |
chr11 | 112020408 | 112069404 |
| a0006 | 0/0 | 647 | 5 | 0 | 0 | 5 | 0 | 0 | 4 | DLAT_chr11_112020408_112069404 | DLAT | MWRVC others(642): Show |
chr11 | 112020408 | 112069404 |
| a0007 | 0/0 | 647 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | MWRVC others(642): Show |
chr11 | 112020408 | 112069404 |
| a0008 | 0/0 | 647 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | MWRVC others(642): Show |
chr11 | 112020408 | 112069404 |
| a0009 | 0/0 | 647 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | MWRVC others(642): Show |
chr11 | 112020408 | 112069404 |
| a0010 | 0/0 | 647 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | MWRVC others(642): Show |
chr11 | 112020408 | 112069404 |
| a0011 | 0/0 | 647 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DLAT_chr11_112020408_112069404 | DLAT | MWRVC others(642): Show |
chr11 | 112020408 | 112069404 |
| a0012 | 0/0 | 647 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | DLAT_chr11_112020408_112069404 | DLAT | MWRVC others(642): Show |
chr11 | 112020408 | 112069404 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1941 | 129 | 11 | 30 | 62 | 8 | 16 | DLAT_chr11_112020408_112069404 | DLAT | ATGTG others(1936): Show |
chr11 | 112020408 | 112069404 | ||
| a0002c0002 | 0/0 | 1941 | 114 | 9 | 23 | 67 | 2 | 13 | DLAT_chr11_112020408_112069404 | DLAT | ATGTG others(1936): Show |
chr11 | 112020408 | 112069404 | ||
| a0002c0014 | 0/0 | 1941 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | ATGTG others(1936): Show |
chr11 | 112020408 | 112069404 | ||
| a0003c0003 | 0/0 | 1941 | 52 | 46 | 6 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | ATGTG others(1936): Show |
chr11 | 112020408 | 112069404 | ||
| a0004c0004 | 0/0 | 1941 | 15 | 15 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | ATGTG others(1936): Show |
chr11 | 112020408 | 112069404 | ||
| a0005c0005 | 0/0 | 1941 | 11 | 10 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | ATGTG others(1936): Show |
chr11 | 112020408 | 112069404 | ||
| a0005c0013 | 0/0 | 1941 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | ATGTG others(1936): Show |
chr11 | 112020408 | 112069404 | ||
| a0006c0006 | 0/0 | 1941 | 5 | 0 | 0 | 5 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | ATGTG others(1936): Show |
chr11 | 112020408 | 112069404 | ||
| a0007c0007 | 0/0 | 1941 | 2 | 0 | 2 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | ATGTG others(1936): Show |
chr11 | 112020408 | 112069404 | ||
| a0008c0008 | 0/0 | 1941 | 2 | 2 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | ATGTG others(1936): Show |
chr11 | 112020408 | 112069404 | ||
| a0009c0009 | 0/0 | 1941 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | ATGTG others(1936): Show |
chr11 | 112020408 | 112069404 | ||
| a0010c0011 | 0/0 | 1941 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | ATGTG others(1936): Show |
chr11 | 112020408 | 112069404 | ||
| a0011c0012 | 0/0 | 1941 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | ATGTG others(1936): Show |
chr11 | 112020408 | 112069404 | ||
| a0012c0010 | 0/0 | 1941 | 1 | 0 | 0 | 0 | 0 | 1 | DLAT_chr11_112020408_112069404 | DLAT | ATGTG others(1936): Show |
chr11 | 112020408 | 112069404 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3878 | 117 | 11 | 26 | 54 | 8 | 16 | DLAT_chr11_112020408_112069404 | DLAT | GCTGC others(3873): Show |
chr11 | 112020408 | 112069404 |
| a0001c0001t0007 | 0/0 | 3878 | 3 | 0 | 3 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | GCTGC others(3873): Show |
chr11 | 112020408 | 112069404 |
| a0001c0001t0008 | 0/0 | 3878 | 6 | 0 | 0 | 6 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | GCTGC others(3873): Show |
chr11 | 112020408 | 112069404 |
| a0001c0001t0012 | 0/0 | 3878 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | GCTGC others(3873): Show |
chr11 | 112020408 | 112069404 |
| a0001c0001t0013 | 0/0 | 3878 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | GCTGC others(3873): Show |
chr11 | 112020408 | 112069404 |
| a0001c0001t0019 | 0/0 | 3878 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | GCTGC others(3873): Show |
chr11 | 112020408 | 112069404 |
| a0002c0002t0002 | 0/0 | 3878 | 111 | 8 | 22 | 66 | 2 | 13 | DLAT_chr11_112020408_112069404 | DLAT | GCTGC others(3873): Show |
chr11 | 112020408 | 112069404 |
| a0002c0002t0011 | 0/0 | 3878 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | GCTGC others(3873): Show |
chr11 | 112020408 | 112069404 |
| a0002c0002t0015 | 0/0 | 3878 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | GCTGC others(3873): Show |
chr11 | 112020408 | 112069404 |
| a0002c0002t0017 | 0/0 | 3878 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | GCTGC others(3873): Show |
chr11 | 112020408 | 112069404 |
| a0002c0014t0002 | 0/0 | 3878 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | GCTGC others(3873): Show |
chr11 | 112020408 | 112069404 |
| a0003c0003t0003 | 0/0 | 3882 | 5 | 5 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | GCTGC others(3877): Show |
chr11 | 112020408 | 112069404 |
| a0003c0003t0004 | 0/0 | 3878 | 21 | 16 | 5 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | GCTGC others(3873): Show |
chr11 | 112020408 | 112069404 |
| a0003c0003t0006 | 0/0 | 3878 | 12 | 12 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | GCTGC others(3873): Show |
chr11 | 112020408 | 112069404 |
| a0003c0003t0007 | 0/0 | 3878 | 8 | 8 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | GCTGC others(3873): Show |
chr11 | 112020408 | 112069404 |
| a0003c0003t0009 | 0/0 | 3882 | 3 | 2 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | GCTGC others(3877): Show |
chr11 | 112020408 | 112069404 |
| a0003c0003t0014 | 0/0 | 3882 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | GCTGC others(3877): Show |
chr11 | 112020408 | 112069404 |
| a0003c0003t0016 | 0/0 | 3878 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | GCTGC others(3873): Show |
chr11 | 112020408 | 112069404 |
| a0003c0003t0018 | 0/0 | 3882 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | GCTGC others(3877): Show |
chr11 | 112020408 | 112069404 |
| a0004c0004t0003 | 0/0 | 3882 | 13 | 13 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | GCTGC others(3877): Show |
chr11 | 112020408 | 112069404 |
| a0004c0004t0010 | 0/0 | 3882 | 2 | 2 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | GCTGC others(3877): Show |
chr11 | 112020408 | 112069404 |
| a0005c0005t0005 | 0/0 | 3882 | 11 | 10 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | GCTGC others(3877): Show |
chr11 | 112020408 | 112069404 |
| a0005c0013t0005 | 0/0 | 3882 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | GCTGC others(3877): Show |
chr11 | 112020408 | 112069404 |
| a0006c0006t0001 | 0/0 | 3878 | 5 | 0 | 0 | 5 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | GCTGC others(3873): Show |
chr11 | 112020408 | 112069404 |
| a0007c0007t0003 | 0/0 | 3882 | 2 | 0 | 2 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | GCTGC others(3877): Show |
chr11 | 112020408 | 112069404 |
| a0008c0008t0003 | 0/0 | 3882 | 2 | 2 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | GCTGC others(3877): Show |
chr11 | 112020408 | 112069404 |
| a0009c0009t0001 | 0/0 | 3878 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | GCTGC others(3873): Show |
chr11 | 112020408 | 112069404 |
| a0010c0011t0001 | 0/0 | 3878 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | GCTGC others(3873): Show |
chr11 | 112020408 | 112069404 |
| a0011c0012t0002 | 0/0 | 3878 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | GCTGC others(3873): Show |
chr11 | 112020408 | 112069404 |
| a0012c0010t0001 | 0/0 | 3878 | 1 | 0 | 0 | 0 | 0 | 1 | DLAT_chr11_112020408_112069404 | DLAT | GCTGC others(3873): Show |
chr11 | 112020408 | 112069404 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0003 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0145 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0165 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0007g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0007g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0007g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0008g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0008g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0008g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0008g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0008g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0008g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0012g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0013g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0001c0001t0019g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0005 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0011g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0015g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0002t0017g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0002c0014t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0003c0003t0003g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0003c0003t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0003c0003t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0003c0003t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0003c0003t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0003c0003t0004g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0003c0003t0004g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0003c0003t0004g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0003c0003t0004g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0003c0003t0004g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0003c0003t0004g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0003c0003t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0003c0003t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0003c0003t0004g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0003c0003t0004g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0003c0003t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0003c0003t0004g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0003c0003t0004g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0003c0003t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0003c0003t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0003c0003t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0003c0003t0004g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0003c0003t0004g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0003c0003t0004g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0003c0003t0004g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0003c0003t0004g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0003c0003t0006g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0003c0003t0006g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0003c0003t0006g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0003c0003t0006g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0003c0003t0006g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0003c0003t0006g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0003c0003t0006g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0003c0003t0006g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0003c0003t0006g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0003c0003t0006g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0003c0003t0007g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0003c0003t0007g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0003c0003t0007g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0003c0003t0007g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0003c0003t0007g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0003c0003t0007g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0003c0003t0007g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0003c0003t0007g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0003c0003t0009g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0003c0003t0009g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0003c0003t0009g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0003c0003t0014g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0003c0003t0016g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0003c0003t0018g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0004c0004t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0004c0004t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0004c0004t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0004c0004t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0004c0004t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0004c0004t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0004c0004t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0004c0004t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0004c0004t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0004c0004t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0004c0004t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0004c0004t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0004c0004t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0004c0004t0010g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0004c0004t0010g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0005c0005t0005g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0005c0005t0005g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0005c0005t0005g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0005c0005t0005g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0005c0005t0005g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0005c0005t0005g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0005c0005t0005g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0005c0005t0005g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0005c0005t0005g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0005c0005t0005g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0005c0005t0005g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0005c0013t0005g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0006c0006t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0006c0006t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0006c0006t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0006c0006t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0006c0006t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0007c0007t0003g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0007c0007t0003g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0008c0008t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0008c0008t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0009c0009t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0010c0011t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0011c0012t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| a0012c0010t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0103 | EUR | GBR | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0164 | EUR | GBR | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0129 | EUR | GBR | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG00140 | hp2 | a0002 | c0002 | t0002 | g0300 | EUR | GBR | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG00408 | hp2 | a0002 | c0002 | t0002 | g0216 | EAS | CHS | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG00544 | hp2 | a0002 | c0002 | t0002 | g0236 | EAS | CHS | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG00558 | hp2 | a0002 | c0002 | t0017 | g0229 | EAS | CHS | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG00597 | hp1 | a0002 | c0002 | t0002 | g0254 | EAS | CHS | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG00597 | hp2 | a0006 | c0006 | t0001 | g0078 | EAS | CHS | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG00609 | hp1 | a0002 | c0002 | t0002 | g0262 | EAS | CHS | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG00609 | hp2 | a0002 | c0002 | t0002 | g0228 | EAS | CHS | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG00621 | hp1 | a0002 | c0002 | t0002 | g0288 | EAS | CHS | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | CHS | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG00733 | hp1 | a0002 | c0002 | t0002 | g0311 | AMR | PUR | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG00733 | hp2 | a0007 | c0007 | t0003 | g0203 | AMR | PUR | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG00735 | hp1 | a0002 | c0002 | t0002 | g0293 | AMR | PUR | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG00738 | hp1 | a0003 | c0003 | t0004 | g0023 | AMR | PUR | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG00741 | hp1 | a0009 | c0009 | t0001 | g0108 | AMR | PUR | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG00741 | hp2 | a0002 | c0002 | t0002 | g0279 | AMR | PUR | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG01069 | hp2 | a0001 | c0001 | t0007 | g0089 | AMR | PUR | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG01070 | hp1 | a0002 | c0002 | t0002 | g0255 | AMR | PUR | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG01070 | hp2 | a0001 | c0001 | t0007 | g0134 | AMR | PUR | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG01071 | hp2 | a0001 | c0001 | t0007 | g0135 | AMR | PUR | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG01081 | hp1 | a0001 | c0001 | t0013 | g0049 | AMR | PUR | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG01099 | hp1 | a0007 | c0007 | t0003 | g0204 | AMR | PUR | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG01099 | hp2 | a0003 | c0003 | t0004 | g0022 | AMR | PUR | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG01106 | hp2 | a0010 | c0011 | t0001 | g0046 | AMR | PUR | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG01109 | hp1 | a0003 | c0003 | t0004 | g0314 | AMR | PUR | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG01109 | hp2 | a0002 | c0002 | t0002 | g0060 | AMR | PUR | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG01167 | hp1 | a0002 | c0002 | t0002 | g0058 | AMR | PUR | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG01192 | hp1 | a0002 | c0002 | t0002 | g0320 | AMR | PUR | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG01192 | hp2 | a0002 | c0002 | t0015 | g0243 | AMR | PUR | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG01243 | hp1 | a0005 | c0005 | t0005 | g0008 | AMR | PUR | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG01243 | hp2 | a0003 | c0003 | t0004 | g0019 | AMR | PUR | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG01257 | hp2 | a0002 | c0002 | t0002 | g0301 | AMR | CLM | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG01258 | hp1 | a0002 | c0002 | t0002 | g0290 | AMR | CLM | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG01261 | hp2 | a0002 | c0002 | t0002 | g0280 | AMR | CLM | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG01346 | hp2 | a0002 | c0002 | t0002 | g0260 | AMR | CLM | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG01358 | hp1 | a0002 | c0002 | t0002 | g0297 | AMR | CLM | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0132 | EUR | IBS | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG01884 | hp2 | a0004 | c0004 | t0003 | g0194 | AFR | ACB | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG01891 | hp1 | a0005 | c0005 | t0005 | g0212 | AFR | ACB | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG01891 | hp2 | a0004 | c0004 | t0003 | g0038 | AFR | ACB | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG01952 | hp2 | a0003 | c0003 | t0009 | g0201 | AMR | PEL | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG01975 | hp2 | a0002 | c0002 | t0002 | g0242 | AMR | PEL | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG01978 | hp2 | a0002 | c0002 | t0002 | g0220 | AMR | PEL | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG01981 | hp1 | a0002 | c0002 | t0002 | g0286 | AMR | PEL | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG01981 | hp2 | a0002 | c0002 | t0002 | g0285 | AMR | PEL | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG01993 | hp1 | a0002 | c0002 | t0002 | g0218 | AMR | PEL | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PEL | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02004 | hp2 | a0002 | c0002 | t0002 | g0244 | AMR | PEL | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02027 | hp2 | a0002 | c0002 | t0002 | g0224 | EAS | KHV | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02055 | hp1 | a0004 | c0004 | t0003 | g0037 | AFR | ACB | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02056 | hp2 | a0002 | c0002 | t0002 | g0256 | EAS | KHV | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02071 | hp1 | a0002 | c0002 | t0002 | g0219 | EAS | KHV | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02129 | hp2 | a0002 | c0002 | t0002 | g0237 | EAS | KHV | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02135 | hp1 | a0002 | c0002 | t0002 | g0281 | EAS | KHV | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02145 | hp1 | a0004 | c0004 | t0010 | g0189 | AFR | ACB | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02145 | hp2 | a0005 | c0005 | t0005 | g0205 | AFR | ACB | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02148 | hp1 | a0002 | c0002 | t0002 | g0308 | AMR | PEL | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02148 | hp2 | a0002 | c0002 | t0002 | g0217 | AMR | PEL | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | CDX | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02155 | hp2 | a0002 | c0002 | t0002 | g0261 | EAS | CDX | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02165 | hp1 | a0002 | c0002 | t0002 | g0235 | EAS | CDX | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | CDX | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02257 | hp1 | a0002 | c0002 | t0002 | g0239 | AFR | ACB | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02257 | hp2 | a0003 | c0003 | t0007 | g0040 | AFR | ACB | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02258 | hp2 | a0003 | c0003 | t0007 | g0042 | AFR | ACB | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02273 | hp1 | a0002 | c0002 | t0002 | g0221 | AMR | PEL | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02280 | hp1 | a0003 | c0003 | t0004 | g0012 | AFR | ACB | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02280 | hp2 | a0004 | c0004 | t0003 | g0197 | AFR | ACB | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02300 | hp1 | a0002 | c0002 | t0002 | g0245 | AMR | PEL | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02451 | hp1 | a0002 | c0002 | t0002 | g0266 | AFR | ACB | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02451 | hp2 | a0003 | c0003 | t0004 | g0015 | AFR | ACB | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02523 | hp2 | a0002 | c0002 | t0002 | g0310 | EAS | KHV | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02572 | hp1 | a0003 | c0003 | t0003 | g0053 | AFR | GWD | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02572 | hp2 | a0003 | c0003 | t0007 | g0048 | AFR | GWD | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02602 | hp2 | a0002 | c0002 | t0002 | g0265 | SAS | PJL | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02615 | hp1 | a0004 | c0004 | t0003 | g0033 | AFR | GWD | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02630 | hp1 | a0004 | c0004 | t0010 | g0193 | AFR | GWD | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02630 | hp2 | a0003 | c0003 | t0004 | g0026 | AFR | GWD | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02647 | hp1 | a0002 | c0002 | t0002 | g0241 | AFR | GWD | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02647 | hp2 | a0003 | c0003 | t0004 | g0021 | AFR | GWD | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02698 | hp2 | a0002 | c0002 | t0002 | g0007 | SAS | PJL | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02717 | hp1 | a0003 | c0003 | t0004 | g0317 | AFR | GWD | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02717 | hp2 | a0003 | c0003 | t0004 | g0016 | AFR | GWD | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02723 | hp1 | a0003 | c0003 | t0006 | g0002 | AFR | GWD | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02723 | hp2 | a0003 | c0003 | t0007 | g0041 | AFR | GWD | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02735 | hp1 | a0002 | c0002 | t0002 | g0230 | SAS | PJL | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02809 | hp1 | a0003 | c0003 | t0006 | g0181 | AFR | GWD | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02809 | hp2 | a0003 | c0003 | t0004 | g0011 | AFR | GWD | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02818 | hp1 | a0003 | c0003 | t0004 | g0313 | AFR | GWD | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02818 | hp2 | a0004 | c0004 | t0003 | g0034 | AFR | GWD | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02886 | hp1 | a0002 | c0002 | t0002 | g0226 | AFR | GWD | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02886 | hp2 | a0005 | c0005 | t0005 | g0056 | AFR | GWD | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02895 | hp1 | a0003 | c0003 | t0004 | g0316 | AFR | GWD | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02895 | hp2 | a0003 | c0003 | t0006 | g0182 | AFR | GWD | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02896 | hp1 | a0003 | c0003 | t0003 | g0062 | AFR | GWD | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02896 | hp2 | a0002 | c0002 | t0002 | g0234 | AFR | GWD | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02897 | hp1 | a0003 | c0003 | t0006 | g0180 | AFR | GWD | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02897 | hp2 | a0003 | c0003 | t0003 | g0063 | AFR | GWD | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02922 | hp1 | a0003 | c0003 | t0004 | g0017 | AFR | ESN | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02922 | hp2 | a0008 | c0008 | t0003 | g0190 | AFR | ESN | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02970 | hp1 | a0003 | c0003 | t0006 | g0184 | AFR | ESN | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02970 | hp2 | a0003 | c0003 | t0009 | g0199 | AFR | ESN | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02976 | hp1 | a0004 | c0004 | t0003 | g0195 | AFR | ESN | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02976 | hp2 | a0008 | c0008 | t0003 | g0191 | AFR | ESN | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG03017 | hp2 | a0002 | c0002 | t0002 | g0269 | SAS | PJL | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG03041 | hp1 | a0003 | c0003 | t0006 | g0050 | AFR | GWD | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG03041 | hp2 | a0003 | c0003 | t0018 | g0202 | AFR | GWD | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | MSL | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG03098 | hp2 | a0003 | c0003 | t0006 | g0002 | AFR | MSL | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG03130 | hp1 | a0003 | c0003 | t0007 | g0052 | AFR | ESN | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG03130 | hp2 | a0003 | c0003 | t0004 | g0018 | AFR | ESN | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG03139 | hp1 | a0005 | c0005 | t0005 | g0208 | AFR | ESN | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG03195 | hp1 | a0005 | c0005 | t0005 | g0324 | AFR | ESN | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG03195 | hp2 | a0003 | c0003 | t0006 | g0002 | AFR | ESN | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG03209 | hp1 | a0003 | c0003 | t0004 | g0014 | AFR | MSL | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG03209 | hp2 | a0002 | c0002 | t0011 | g0227 | AFR | MSL | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG03225 | hp1 | a0003 | c0003 | t0006 | g0072 | AFR | MSL | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG03225 | hp2 | a0003 | c0003 | t0004 | g0013 | AFR | MSL | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG03453 | hp1 | a0003 | c0003 | t0006 | g0183 | AFR | MSL | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG03453 | hp2 | a0003 | c0003 | t0003 | g0009 | AFR | MSL | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG03490 | hp1 | a0002 | c0002 | t0002 | g0059 | SAS | PJL | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG03516 | hp1 | a0005 | c0005 | t0005 | g0211 | AFR | ESN | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG03516 | hp2 | a0003 | c0003 | t0009 | g0200 | AFR | ESN | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG03540 | hp2 | a0005 | c0005 | t0005 | g0055 | AFR | GWD | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG03579 | hp1 | a0003 | c0003 | t0006 | g0325 | AFR | MSL | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG03579 | hp2 | a0003 | c0003 | t0007 | g0073 | AFR | MSL | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG03654 | hp1 | a0002 | c0002 | t0002 | g0294 | SAS | PJL | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG03669 | hp2 | a0002 | c0002 | t0002 | g0309 | SAS | PJL | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG03704 | hp1 | a0002 | c0002 | t0002 | g0295 | SAS | PJL | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG03710 | hp2 | a0002 | c0002 | t0002 | g0248 | SAS | PJL | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG03831 | hp1 | a0002 | c0002 | t0002 | g0306 | SAS | BEB | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG03831 | hp2 | a0002 | c0002 | t0002 | g0312 | SAS | BEB | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | BEB | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG03834 | hp2 | a0002 | c0002 | t0002 | g0277 | SAS | BEB | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG04204 | hp1 | a0002 | c0002 | t0002 | g0007 | SAS | STU | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | STU | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA18522 | hp1 | a0003 | c0003 | t0004 | g0024 | AFR | YRI | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA18522 | hp2 | a0003 | c0003 | t0006 | g0179 | AFR | YRI | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA18612 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | CHB | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | CHB | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA18906 | hp1 | a0003 | c0003 | t0014 | g0187 | AFR | YRI | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA18906 | hp2 | a0005 | c0013 | t0005 | g0210 | AFR | YRI | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA18939 | hp1 | a0002 | c0002 | t0002 | g0231 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA18941 | hp2 | a0002 | c0002 | t0002 | g0222 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA18942 | hp2 | a0002 | c0002 | t0002 | g0232 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA18947 | hp1 | a0002 | c0002 | t0002 | g0287 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA18950 | hp1 | a0002 | c0002 | t0002 | g0258 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA18950 | hp2 | a0002 | c0002 | t0002 | g0283 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA18956 | hp2 | a0002 | c0002 | t0002 | g0268 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA18957 | hp1 | a0002 | c0002 | t0002 | g0251 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA18961 | hp2 | a0002 | c0014 | t0002 | g0215 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA18964 | hp2 | a0011 | c0012 | t0002 | g0270 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA18965 | hp2 | a0002 | c0002 | t0002 | g0303 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA18968 | hp2 | a0002 | c0002 | t0002 | g0278 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA18969 | hp1 | a0002 | c0002 | t0002 | g0267 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA18974 | hp2 | a0002 | c0002 | t0002 | g0298 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA18977 | hp1 | a0001 | c0001 | t0008 | g0028 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA18977 | hp2 | a0006 | c0006 | t0001 | g0077 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA18978 | hp1 | a0002 | c0002 | t0002 | g0323 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA18979 | hp1 | a0002 | c0002 | t0002 | g0247 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA18982 | hp2 | a0002 | c0002 | t0002 | g0299 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA18983 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA18985 | hp2 | a0002 | c0002 | t0002 | g0305 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA18988 | hp2 | a0002 | c0002 | t0002 | g0276 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA18989 | hp2 | a0002 | c0002 | t0002 | g0302 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA18991 | hp1 | a0001 | c0001 | t0008 | g0030 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA18991 | hp2 | a0002 | c0002 | t0002 | g0274 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA18994 | hp2 | a0002 | c0002 | t0002 | g0225 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA18997 | hp1 | a0002 | c0002 | t0002 | g0214 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA18999 | hp2 | a0002 | c0002 | t0002 | g0322 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA19000 | hp1 | a0002 | c0002 | t0002 | g0321 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA19001 | hp2 | a0002 | c0002 | t0002 | g0304 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA19002 | hp2 | a0002 | c0002 | t0002 | g0271 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA19005 | hp1 | a0001 | c0001 | t0012 | g0075 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA19005 | hp2 | a0002 | c0002 | t0002 | g0296 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA19007 | hp1 | a0002 | c0002 | t0002 | g0257 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA19007 | hp2 | a0001 | c0001 | t0008 | g0031 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA19010 | hp2 | a0002 | c0002 | t0002 | g0275 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA19011 | hp1 | a0002 | c0002 | t0002 | g0252 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA19011 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA19012 | hp1 | a0002 | c0002 | t0002 | g0307 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA19030 | hp1 | a0004 | c0004 | t0003 | g0035 | AFR | LWK | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA19030 | hp2 | a0003 | c0003 | t0004 | g0315 | AFR | LWK | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA19043 | hp1 | a0003 | c0003 | t0007 | g0043 | AFR | LWK | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA19043 | hp2 | a0003 | c0003 | t0007 | g0319 | AFR | LWK | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA19054 | hp1 | a0002 | c0002 | t0002 | g0292 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA19054 | hp2 | a0006 | c0006 | t0001 | g0091 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA19055 | hp2 | a0002 | c0002 | t0002 | g0061 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA19058 | hp1 | a0002 | c0002 | t0002 | g0249 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA19058 | hp2 | a0001 | c0001 | t0008 | g0027 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA19062 | hp2 | a0002 | c0002 | t0002 | g0273 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA19063 | hp1 | a0002 | c0002 | t0002 | g0284 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA19063 | hp2 | a0001 | c0001 | t0019 | g0173 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA19064 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA19066 | hp1 | a0002 | c0002 | t0002 | g0289 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA19066 | hp2 | a0002 | c0002 | t0002 | g0213 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA19068 | hp2 | a0002 | c0002 | t0002 | g0272 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA19076 | hp1 | a0001 | c0001 | t0008 | g0029 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA19076 | hp2 | a0002 | c0002 | t0002 | g0246 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA19077 | hp2 | a0002 | c0002 | t0002 | g0263 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA19081 | hp1 | a0006 | c0006 | t0001 | g0076 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA19081 | hp2 | a0002 | c0002 | t0002 | g0057 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA19084 | hp2 | a0002 | c0002 | t0002 | g0253 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA19086 | hp1 | a0002 | c0002 | t0002 | g0250 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA19086 | hp2 | a0006 | c0006 | t0001 | g0083 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA19088 | hp1 | a0002 | c0002 | t0002 | g0238 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA19088 | hp2 | a0002 | c0002 | t0002 | g0282 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA19089 | hp2 | a0002 | c0002 | t0002 | g0264 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA19090 | hp1 | a0001 | c0001 | t0008 | g0032 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA19090 | hp2 | a0002 | c0002 | t0002 | g0291 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA19240 | hp1 | a0004 | c0004 | t0003 | g0196 | AFR | YRI | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA19240 | hp2 | a0005 | c0005 | t0005 | g0209 | AFR | YRI | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA20129 | hp1 | a0002 | c0002 | t0002 | g0005 | AFR | ASW | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ASW | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0102 | EUR | TSI | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0130 | EUR | TSI | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0097 | EUR | TSI | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA20805 | hp2 | a0002 | c0002 | t0002 | g0259 | EUR | TSI | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | GIH | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA20905 | hp2 | a0012 | c0010 | t0001 | g0001 | SAS | GIH | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG01123 | hp2 | a0003 | c0003 | t0004 | g0020 | AMR | CLM | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02109 | hp1 | a0004 | c0004 | t0003 | g0036 | AFR | ACB | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02109 | hp2 | a0002 | c0002 | t0002 | g0233 | AFR | ACB | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02486 | hp1 | a0004 | c0004 | t0003 | g0192 | AFR | ACB | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02486 | hp2 | a0004 | c0004 | t0003 | g0039 | AFR | ACB | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG02559 | hp2 | a0005 | c0005 | t0005 | g0207 | AFR | ACB | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG03471 | hp1 | a0003 | c0003 | t0003 | g0054 | AFR | MSL | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | MSL | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | USA | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| HG06807 | hp2 | a0004 | c0004 | t0003 | g0198 | AFR | USA | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA18955 | hp2 | a0002 | c0002 | t0002 | g0223 | EAS | JPT | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA20300 | hp1 | a0003 | c0003 | t0004 | g0025 | AFR | USA | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA20300 | hp2 | a0003 | c0003 | t0016 | g0047 | AFR | USA | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA21309 | hp1 | a0002 | c0002 | t0002 | g0240 | AFR | LWK | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| NA21309 | hp2 | a0005 | c0005 | t0005 | g0206 | AFR | LWK | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0145 | REF | REF | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0165 | REF | REF | DLAT_chr11_112020408_112069404 | DLAT | chr11 | 112020408 | 112069404 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:112025518 | G | A | 1 | a0006 | 5 | HG00597.hp2 NA18977.hp2 NA19054.hp2 others(2): Show |
missense_variant | MODERATE | c.46G>A | p.Ala16Thr | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 1/14 | 111/3878 | 46/1944 | 16/647 | chr11 | 112025518 | |||
| chr11:112025527 | G | C | 1 | a0007 | 2 | HG00733.hp2 HG01099.hp1 |
missense_variant | MODERATE | c.55G>C | p.Glu19Gln | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 1/14 | 120/3878 | 55/1944 | 19/647 | chr11 | 112025527 | |||
| chr11:112025600 | C | T | 3 | a0002 a0005 a0011 |
128 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(125): Show |
missense_variant | MODERATE | c.128C>T | p.Ala43Val | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 1/14 | 193/3878 | 128/1944 | 43/647 | chr11 | 112025600 | |||
| chr11:112028911 | A | G | 3 | a0004 a0007 a0008 |
19 | HG00733.hp2 HG01099.hp1 HG01884.hp2 others(16): Show |
missense_variant | MODERATE | c.626A>G | p.Gln209Arg | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 4/14 | 691/3878 | 626/1944 | 209/647 | chr11 | 112028911 | |||
| chr11:112037353 | C | G | 1 | a0010 | 1 | HG01106.hp2 | missense_variant | MODERATE | c.868C>G | p.Leu290Val | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 6/14 | 933/3878 | 868/1944 | 290/647 | chr11 | 112037353 | |||
| chr11:112037413 | G | A | 1 | a0008 | 2 | HG02922.hp2 HG02976.hp2 |
missense_variant | MODERATE | c.928G>A | p.Glu310Lys | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 6/14 | 993/3878 | 928/1944 | 310/647 | chr11 | 112037413 | |||
| chr11:112037438 | T | C | 7 | a0002 a0003 a0004 others(4): Show |
199 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(196): Show |
missense_variant | MODERATE | c.953T>C | p.Val318Ala | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 6/14 | 1018/3878 | 953/1944 | 318/647 | chr11 | 112037438 | |||
| chr11:112045169 | C | G | 1 | a0011 | 1 | NA18964.hp2 | missense_variant | MODERATE | c.1229C>G | p.Pro410Arg | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 9/14 | 1294/3878 | 1229/1944 | 410/647 | chr11 | 112045169 | |||
| chr11:112045923 | G | A | 2 | a0002 a0011 |
116 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(113): Show |
missense_variant | MODERATE | c.1351G>A | p.Asp451Asn | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 10/14 | 1416/3878 | 1351/1944 | 451/647 | chr11 | 112045923 | |||
| chr11:112059929 | C | T | 1 | a0012 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.1541C>T | p.Ala514Val | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 12/14 | 1606/3878 | 1541/1944 | 514/647 | chr11 | 112059929 | |||
| chr11:112060024 | A | G | 1 | a0009 | 1 | HG00741.hp1 | missense_variant | MODERATE | c.1636A>G | p.Thr546Ala | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 12/14 | 1701/3878 | 1636/1944 | 546/647 | chr11 | 112060024 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:112025514 | A | G | 1 | a0002c0014 | 1 | NA18961.hp2 | synonymous_variant | LOW | c.42A>G | p.Pro14Pro | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 1/14 | 107/3878 | 42/1944 | 14/647 | chr11 | 112025514 | |||
| chr11:112033436 | C | T | 2 | a0005c0005 a0005c0013 |
12 | HG01243.hp1 HG01891.hp1 HG02145.hp2 others(9): Show |
synonymous_variant | LOW | c.693C>T | p.Thr231Thr | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/14 | 758/3878 | 693/1944 | 231/647 | chr11 | 112033436 | |||
| chr11:112037355 | C | T | 1 | a0005c0013 | 1 | NA18906.hp2 | synonymous_variant | LOW | c.870C>T | p.Leu290Leu | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 6/14 | 935/3878 | 870/1944 | 290/647 | chr11 | 112037355 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:112025450 | G | T | 1 | a0001c0001t0019 | 1 | NA19063.hp2 | 5_prime_UTR_variant | MODIFIER | c.-23G>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 1/14 | 23 | chr11 | 112025450 | ||||||
| chr11:112025458 | G | A | 1 | a0002c0002t0011 | 1 | HG03209.hp2 | 5_prime_UTR_variant | MODIFIER | c.-15G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 1/14 | 15 | chr11 | 112025458 | ||||||
| chr11:112062631 | C | A | 1 | a0003c0003t0004 | 21 | HG00738.hp1 HG01099.hp2 HG01109.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*96C>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 14/14 | 96 | chr11 | 112062631 | ||||||
| chr11:112062702 | C | T | 1 | a0001c0001t0008 | 6 | NA18977.hp1 NA18991.hp1 NA19007.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*167C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 14/14 | 167 | chr11 | 112062702 | ||||||
| chr11:112062703 | G | A | 1 | a0001c0001t0012 | 1 | NA19005.hp1 | 3_prime_UTR_variant | MODIFIER | c.*168G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 14/14 | 168 | chr11 | 112062703 | ||||||
| chr11:112062954 | A | G | 21 | a0001c0001t0007 a0002c0002t0002 a0002c0002t0011 others(18): Show |
202 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(199): Show |
3_prime_UTR_variant | MODIFIER | c.*419A>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 14/14 | 419 | chr11 | 112062954 | ||||||
| chr11:112063037 | A | C | 1 | a0003c0003t0018 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*502A>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 14/14 | 502 | chr11 | 112063037 | ||||||
| chr11:112063408 | T | C | 2 | a0005c0005t0005 a0005c0013t0005 |
12 | HG01243.hp1 HG01891.hp1 HG02145.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*873T>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 14/14 | 873 | chr11 | 112063408 | ||||||
| chr11:112063553 | A | T | 1 | a0002c0002t0017 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1018A>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 14/14 | 1018 | chr11 | 112063553 | ||||||
| chr11:112063580 | C | G | 1 | a0002c0002t0017 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1045C>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 14/14 | 1045 | chr11 | 112063580 | ||||||
| chr11:112063588 | A | T | 1 | a0002c0002t0017 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1053A>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 14/14 | 1053 | chr11 | 112063588 | ||||||
| chr11:112063589 | A | T | 1 | a0002c0002t0017 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1054A>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 14/14 | 1054 | chr11 | 112063589 | ||||||
| chr11:112063592 | A | T | 1 | a0002c0002t0017 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1057A>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 14/14 | 1057 | chr11 | 112063592 | ||||||
| chr11:112063593 | A | T | 1 | a0002c0002t0017 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1058A>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 14/14 | 1058 | chr11 | 112063593 | ||||||
| chr11:112063594 | A | T | 1 | a0002c0002t0017 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1059A>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 14/14 | 1059 | chr11 | 112063594 | ||||||
| chr11:112063595 | A | G | 1 | a0002c0002t0017 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1060A>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 14/14 | 1060 | chr11 | 112063595 | ||||||
| chr11:112063596 | A | G | 1 | a0002c0002t0017 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1061A>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 14/14 | 1061 | chr11 | 112063596 | ||||||
| chr11:112063597 | A | G | 1 | a0002c0002t0017 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1062A>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 14/14 | 1062 | chr11 | 112063597 | ||||||
| chr11:112063601 | A | T | 1 | a0002c0002t0017 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1066A>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 14/14 | 1066 | chr11 | 112063601 | ||||||
| chr11:112063602 | A | T | 1 | a0002c0002t0017 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1067A>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 14/14 | 1067 | chr11 | 112063602 | ||||||
| chr11:112063603 | A | T | 1 | a0002c0002t0017 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1068A>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 14/14 | 1068 | chr11 | 112063603 | ||||||
| chr11:112063606 | T | G | 1 | a0002c0002t0017 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1071T>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 14/14 | 1071 | chr11 | 112063606 | ||||||
| chr11:112063608 | T | G | 1 | a0002c0002t0017 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1073T>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 14/14 | 1073 | chr11 | 112063608 | ||||||
| chr11:112063611 | A | G | 1 | a0002c0002t0017 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1076A>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 14/14 | 1076 | chr11 | 112063611 | ||||||
| chr11:112063618 | T | G | 1 | a0002c0002t0017 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1083T>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 14/14 | 1083 | chr11 | 112063618 | ||||||
| chr11:112063644 | C | T | 1 | a0003c0003t0006 | 12 | HG02723.hp1 HG02809.hp1 HG02895.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1109C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 14/14 | 1109 | chr11 | 112063644 | ||||||
| chr11:112063759 | T | TGGAA | 10 | a0003c0003t0003 a0003c0003t0009 a0003c0003t0014 others(7): Show |
41 | HG00733.hp2 HG01099.hp1 HG01243.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*1232_*1235dupAGGA | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 14/14 | 1236 | INFO_REALIGN_3_PRIME | chr11 | 112063759 | |||||
| chr11:112063783 | G | C | 6 | a0002c0002t0002 a0002c0002t0011 a0002c0002t0015 others(3): Show |
116 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*1248G>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 14/14 | 1248 | chr11 | 112063783 | ||||||
| chr11:112064029 | T | C | 1 | a0002c0002t0015 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1494T>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 14/14 | 1494 | chr11 | 112064029 | ||||||
| chr11:112064130 | G | A | 1 | a0001c0001t0013 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1595G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 14/14 | 1595 | chr11 | 112064130 | ||||||
| chr11:112064155 | C | T | 1 | a0003c0003t0014 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1620C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 14/14 | 1620 | chr11 | 112064155 | ||||||
| chr11:112064242 | G | C | 1 | a0003c0003t0016 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1707G>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 14/14 | 1707 | chr11 | 112064242 | ||||||
| chr11:112064289 | A | C | 3 | a0003c0003t0009 a0003c0003t0014 a0003c0003t0018 |
5 | HG01952.hp2 HG02970.hp2 HG03041.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1754A>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 14/14 | 1754 | chr11 | 112064289 | ||||||
| chr11:112064342 | G | A | 2 | a0005c0005t0005 a0005c0013t0005 |
12 | HG01243.hp1 HG01891.hp1 HG02145.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1807G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 14/14 | 1807 | chr11 | 112064342 | ||||||
| chr11:112064345 | T | A | 1 | a0004c0004t0010 | 2 | HG02145.hp1 HG02630.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1810T>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 14/14 | 1810 | chr11 | 112064345 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:112025764 | C | A | 1 | a0005c0005t0005g0008 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.279+13C>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 1/13 | chr11 | 112025764 | |||||||
| chr11:112025790 | T | C | 1 | a0003c0003t0003g0009 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.279+39T>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 1/13 | chr11 | 112025790 | |||||||
| chr11:112025800 | A | G | 1 | a0003c0003t0006g0325 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.279+49A>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 1/13 | chr11 | 112025800 | |||||||
| chr11:112025807 | G | A | 1 | a0003c0003t0003g0009 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.279+56G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 1/13 | chr11 | 112025807 | |||||||
| chr11:112025925 | A | G | 1 | a0005c0005t0005g0324 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.279+174A>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 1/13 | chr11 | 112025925 | |||||||
| chr11:112026030 | G | A | 1 | a0002c0002t0002g0010 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.280-168G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 1/13 | chr11 | 112026030 | |||||||
| chr11:112026077 | T | C | 16 | a0003c0003t0004g0011 a0003c0003t0004g0012 a0003c0003t0004g0013 others(13): Show |
16 | HG00738.hp1 HG01099.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.280-121T>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 1/13 | chr11 | 112026077 | |||||||
| chr11:112026304 | G | GT | 26 | a0001c0001t0001g0318 a0002c0002t0002g0320 a0002c0002t0002g0321 others(23): Show |
26 | HG00738.hp1 HG01099.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.381+22dupT | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 112026304 | ||||||
| chr11:112026304 | GT | G | 24 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0051 others(21): Show |
24 | HG01081.hp1 HG01081.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.381+22delT | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 112026304 | ||||||
| chr11:112026321 | T | A | 13 | a0001c0001t0008g0027 a0001c0001t0008g0028 a0001c0001t0008g0029 others(10): Show |
13 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.381+22T>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 2/13 | chr11 | 112026321 | |||||||
| chr11:112026326 | A | T | 155 | a0001c0001t0001g0188 a0002c0002t0002g0005 a0002c0002t0002g0006 others(152): Show |
158 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(155): Show |
intron_variant | MODIFIER | c.381+27A>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 2/13 | chr11 | 112026326 | |||||||
| chr11:112026330 | T | A | 10 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(7): Show |
10 | HG01123.hp1 HG01358.hp2 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.381+31T>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 2/13 | chr11 | 112026330 | |||||||
| chr11:112026378 | A | T | 2 | a0003c0003t0003g0062 a0003c0003t0003g0063 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.381+79A>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 2/13 | chr11 | 112026378 | |||||||
| chr11:112026769 | C | G | 2 | a0003c0003t0007g0052 a0003c0003t0007g0073 |
2 | HG03130.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.381+470C>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 2/13 | chr11 | 112026769 | |||||||
| chr11:112026771 | C | G | 1 | a0002c0002t0002g0312 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.381+472C>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 2/13 | chr11 | 112026771 | |||||||
| chr11:112026777 | T | A | 1 | a0001c0001t0001g0064 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.381+478T>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 2/13 | chr11 | 112026777 | |||||||
| chr11:112026793 | C | T | 4 | a0002c0002t0002g0308 a0002c0002t0002g0309 a0002c0002t0002g0310 others(1): Show |
4 | HG00733.hp1 HG02148.hp1 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.381+494C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 2/13 | chr11 | 112026793 | |||||||
| chr11:112026841 | G | C | 1 | a0001c0001t0001g0074 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.381+542G>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 2/13 | chr11 | 112026841 | |||||||
| chr11:112026844 | A | C | 1 | a0002c0002t0002g0307 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.381+545A>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 2/13 | chr11 | 112026844 | |||||||
| chr11:112026855 | CGGGCAGA others(30): Show |
C | 1 | a0003c0003t0014g0187 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.381+566_381+602del others(37): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 112026855 | ||||||
| chr11:112026892 | T | C | 1 | a0003c0003t0007g0319 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.381+593T>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 2/13 | chr11 | 112026892 | |||||||
| chr11:112026934 | A | G | 157 | a0001c0001t0001g0051 a0002c0002t0002g0005 a0002c0002t0002g0006 others(154): Show |
160 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(157): Show |
intron_variant | MODIFIER | c.381+635A>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 2/13 | chr11 | 112026934 | |||||||
| chr11:112027017 | C | T | 113 | a0002c0002t0002g0005 a0002c0002t0002g0006 a0002c0002t0002g0007 others(110): Show |
116 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.381+718C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 2/13 | chr11 | 112027017 | |||||||
| chr11:112027035 | G | A | 4 | a0002c0002t0002g0213 a0002c0002t0002g0214 a0002c0002t0002g0216 others(1): Show |
4 | HG00408.hp2 NA18961.hp2 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.381+736G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 2/13 | chr11 | 112027035 | |||||||
| chr11:112027143 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.381+844C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 2/13 | chr11 | 112027143 | |||||||
| chr11:112027156 | G | A | 5 | a0004c0004t0003g0192 a0004c0004t0010g0189 a0004c0004t0010g0193 others(2): Show |
5 | HG02145.hp1 HG02486.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.381+857G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 2/13 | chr11 | 112027156 | |||||||
| chr11:112027196 | A | G | 1 | a0005c0005t0005g0212 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.381+897A>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 2/13 | chr11 | 112027196 | |||||||
| chr11:112027217 | C | T | 125 | a0002c0002t0002g0005 a0002c0002t0002g0006 a0002c0002t0002g0007 others(122): Show |
128 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.381+918C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 2/13 | chr11 | 112027217 | |||||||
| chr11:112027228 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.381+929C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 2/13 | chr11 | 112027228 | |||||||
| chr11:112027268 | C | T | 5 | a0004c0004t0003g0192 a0004c0004t0010g0189 a0004c0004t0010g0193 others(2): Show |
5 | HG02145.hp1 HG02486.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.381+969C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 2/13 | chr11 | 112027268 | |||||||
| chr11:112027276 | TAGAGGCG others(30): Show |
T | 25 | a0003c0003t0004g0011 a0003c0003t0004g0012 a0003c0003t0004g0013 others(22): Show |
25 | HG00738.hp1 HG01099.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.381+989_381+1025de others(38): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 112027276 | ||||||
| chr11:112027283 | G | A | 127 | a0002c0002t0002g0005 a0002c0002t0002g0006 a0002c0002t0002g0007 others(124): Show |
130 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(127): Show |
intron_variant | MODIFIER | c.381+984G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 2/13 | chr11 | 112027283 | |||||||
| chr11:112027292 | ATCCCAGA others(185): Show |
A | 1 | a0001c0001t0001g0154 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.381+1006_382-1019d others(2): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 112027292 | ||||||
| chr11:112027306 | G | A | 6 | a0003c0003t0003g0009 a0003c0003t0009g0199 a0003c0003t0009g0200 others(3): Show |
6 | HG01952.hp2 HG02970.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.381+1007G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 2/13 | chr11 | 112027306 | |||||||
| chr11:112027475 | G | T | 10 | a0003c0003t0006g0002 a0003c0003t0006g0050 a0003c0003t0006g0072 others(7): Show |
12 | HG02723.hp1 HG02809.hp1 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.382-1040G>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 2/13 | chr11 | 112027475 | |||||||
| chr11:112027479 | C | T | 115 | a0002c0002t0002g0005 a0002c0002t0002g0006 a0002c0002t0002g0007 others(112): Show |
118 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.382-1036C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 2/13 | chr11 | 112027479 | |||||||
| chr11:112027490 | G | C | 1 | a0002c0002t0002g0308 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.382-1025G>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 2/13 | chr11 | 112027490 | |||||||
| chr11:112027491 | A | T | 1 | a0002c0002t0002g0306 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.382-1024A>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 2/13 | chr11 | 112027491 | |||||||
| chr11:112027500 | C | T | 115 | a0002c0002t0002g0005 a0002c0002t0002g0006 a0002c0002t0002g0007 others(112): Show |
118 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.382-1015C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 2/13 | chr11 | 112027500 | |||||||
| chr11:112027501 | A | G | 156 | a0002c0002t0002g0005 a0002c0002t0002g0006 a0002c0002t0002g0007 others(153): Show |
159 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(156): Show |
intron_variant | MODIFIER | c.382-1014A>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 2/13 | chr11 | 112027501 | |||||||
| chr11:112027584 | C | T | 2 | a0004c0004t0003g0038 a0004c0004t0003g0039 |
2 | HG01891.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.382-931C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 2/13 | chr11 | 112027584 | |||||||
| chr11:112027655 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.382-860C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 2/13 | chr11 | 112027655 | |||||||
| chr11:112027718 | C | T | 1 | a0002c0002t0002g0007 | 2 | HG02698.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.382-797C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 2/13 | chr11 | 112027718 | |||||||
| chr11:112027773 | G | A | 2 | a0003c0003t0003g0053 a0003c0003t0003g0054 |
2 | HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.382-742G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 2/13 | chr11 | 112027773 | |||||||
| chr11:112027838 | G | A | 29 | a0003c0003t0003g0009 a0003c0003t0003g0053 a0003c0003t0003g0054 others(26): Show |
29 | HG00733.hp2 HG01099.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.382-677G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 2/13 | chr11 | 112027838 | |||||||
| chr11:112027893 | A | AGAGAGG | 156 | a0002c0002t0002g0005 a0002c0002t0002g0006 a0002c0002t0002g0007 others(153): Show |
159 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(156): Show |
intron_variant | MODIFIER | c.382-611_382-606dup others(6): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 112027893 | ||||||
| chr11:112027893 | AGAGAGGG others(16): Show |
A | 2 | a0001c0001t0013g0049 a0003c0003t0004g0026 |
2 | HG01081.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.382-604_382-582del others(23): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 112027893 | ||||||
| chr11:112027952 | G | A | 1 | a0003c0003t0006g0179 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.382-563G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 2/13 | chr11 | 112027952 | |||||||
| chr11:112028008 | G | C | 1 | a0001c0001t0001g0065 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.382-507G>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 2/13 | chr11 | 112028008 | |||||||
| chr11:112028140 | C | T | 2 | a0001c0001t0001g0176 a0001c0001t0001g0177 |
2 | NA18951.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.382-375C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 2/13 | chr11 | 112028140 | |||||||
| chr11:112028153 | A | G | 2 | a0007c0007t0003g0203 a0007c0007t0003g0204 |
2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.382-362A>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 2/13 | chr11 | 112028153 | |||||||
| chr11:112028270 | T | C | 6 | a0002c0002t0002g0217 a0002c0002t0002g0218 a0002c0002t0002g0219 others(3): Show |
6 | HG01192.hp1 HG01978.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.382-245T>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 2/13 | chr11 | 112028270 | |||||||
| chr11:112028367 | C | T | 1 | a0002c0002t0002g0305 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.382-148C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 2/13 | chr11 | 112028367 | |||||||
| chr11:112028420 | C | CA | 14 | a0001c0001t0001g0064 a0001c0001t0001g0079 a0001c0001t0001g0080 others(11): Show |
14 | HG00558.hp1 HG00597.hp2 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.382-70dupA | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 112028420 | ||||||
| chr11:112028420 | CA | C | 26 | a0001c0001t0001g0071 a0001c0001t0001g0170 a0001c0001t0001g0171 others(23): Show |
26 | HG00408.hp1 HG01884.hp2 HG01943.hp1 others(23): Show |
intron_variant | MODIFIER | c.382-70delA | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 112028420 | ||||||
| chr11:112028420 | CAA | C | 101 | a0002c0002t0002g0005 a0002c0002t0002g0006 a0002c0002t0002g0007 others(98): Show |
104 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.382-71_382-70delAA | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 112028420 | ||||||
| chr11:112028420 | CAAA | C | 29 | a0002c0002t0002g0061 a0002c0002t0002g0299 a0002c0002t0002g0300 others(26): Show |
31 | HG00140.hp2 HG01257.hp2 HG01952.hp2 others(28): Show |
intron_variant | MODIFIER | c.382-72_382-70delAA others(1): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 112028420 | ||||||
| chr11:112028420 | CAAAA | C | 7 | a0004c0004t0003g0033 a0004c0004t0003g0034 a0004c0004t0003g0035 others(4): Show |
7 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.382-73_382-70delAA others(2): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 112028420 | ||||||
| chr11:112028443 | AAAT | A | 11 | a0005c0005t0005g0055 a0005c0005t0005g0056 a0005c0005t0005g0205 others(8): Show |
11 | HG01891.hp1 HG02145.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.382-71_382-69delAA others(1): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 2/13 | chr11 | 112028443 | |||||||
| chr11:112029028 | A | C | 1 | a0001c0001t0001g0169 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.660+83A>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 4/13 | chr11 | 112029028 | |||||||
| chr11:112029164 | G | A | 3 | a0003c0003t0009g0199 a0003c0003t0009g0200 a0003c0003t0009g0201 |
3 | HG01952.hp2 HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.660+219G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 4/13 | chr11 | 112029164 | |||||||
| chr11:112029255 | T | A | 1 | a0001c0001t0001g0082 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.660+310T>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 4/13 | chr11 | 112029255 | |||||||
| chr11:112029282 | T | A | 1 | a0006c0006t0001g0083 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.660+337T>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 4/13 | chr11 | 112029282 | |||||||
| chr11:112029314 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.660+369C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 4/13 | chr11 | 112029314 | |||||||
| chr11:112029328 | T | A | 1 | a0006c0006t0001g0083 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.660+383T>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 4/13 | chr11 | 112029328 | |||||||
| chr11:112029645 | C | CT | 30 | a0003c0003t0003g0054 a0004c0004t0003g0033 a0004c0004t0003g0034 others(27): Show |
30 | HG00733.hp2 HG01099.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.660+713dupT | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 112029645 | ||||||
| chr11:112029821 | A | T | 2 | a0003c0003t0004g0024 a0003c0003t0004g0025 |
2 | NA18522.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.660+876A>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 4/13 | chr11 | 112029821 | |||||||
| chr11:112029835 | C | T | 1 | a0002c0002t0002g0306 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.660+890C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 4/13 | chr11 | 112029835 | |||||||
| chr11:112029846 | C | T | 1 | a0002c0002t0002g0298 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.660+901C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 4/13 | chr11 | 112029846 | |||||||
| chr11:112030129 | A | C | 6 | a0003c0003t0003g0009 a0003c0003t0009g0199 a0003c0003t0009g0200 others(3): Show |
6 | HG01952.hp2 HG02970.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.660+1184A>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 4/13 | chr11 | 112030129 | |||||||
| chr11:112030141 | C | A | 1 | a0001c0001t0001g0051 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.660+1196C>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 4/13 | chr11 | 112030141 | |||||||
| chr11:112030391 | C | CA | 194 | a0002c0002t0002g0005 a0002c0002t0002g0006 a0002c0002t0002g0007 others(191): Show |
199 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(196): Show |
intron_variant | MODIFIER | c.660+1446_660+1447i others(3): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 4/13 | chr11 | 112030391 | |||||||
| chr11:112030557 | A | C | 1 | a0003c0003t0003g0009 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.660+1612A>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 4/13 | chr11 | 112030557 | |||||||
| chr11:112030563 | C | T | 25 | a0003c0003t0004g0011 a0003c0003t0004g0012 a0003c0003t0004g0013 others(22): Show |
25 | HG00738.hp1 HG01099.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.660+1618C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 4/13 | chr11 | 112030563 | |||||||
| chr11:112030644 | T | G | 2 | a0002c0002t0002g0213 a0002c0002t0002g0214 |
2 | NA18997.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.660+1699T>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 4/13 | chr11 | 112030644 | |||||||
| chr11:112030786 | C | T | 6 | a0003c0003t0003g0009 a0003c0003t0009g0199 a0003c0003t0009g0200 others(3): Show |
6 | HG01952.hp2 HG02970.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.660+1841C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 4/13 | chr11 | 112030786 | |||||||
| chr11:112030856 | C | T | 1 | a0002c0002t0002g0297 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.660+1911C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 4/13 | chr11 | 112030856 | |||||||
| chr11:112030895 | A | G | 8 | a0003c0003t0003g0009 a0003c0003t0003g0053 a0003c0003t0003g0054 others(5): Show |
8 | HG01952.hp2 HG02572.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.660+1950A>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 4/13 | chr11 | 112030895 | |||||||
| chr11:112030959 | A | G | 4 | a0001c0001t0001g0064 a0001c0001t0001g0081 a0001c0001t0001g0166 others(1): Show |
4 | HG00673.hp1 NA18969.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.660+2014A>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 4/13 | chr11 | 112030959 | |||||||
| chr11:112031226 | C | T | 2 | a0003c0003t0003g0053 a0003c0003t0003g0054 |
2 | HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.661-2178C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 4/13 | chr11 | 112031226 | |||||||
| chr11:112031390 | G | A | 2 | a0002c0002t0002g0226 a0002c0002t0011g0227 |
2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.661-2014G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 4/13 | chr11 | 112031390 | |||||||
| chr11:112031407 | G | A | 2 | a0003c0003t0003g0053 a0003c0003t0003g0054 |
2 | HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.661-1997G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 4/13 | chr11 | 112031407 | |||||||
| chr11:112031478 | A | G | 156 | a0002c0002t0002g0005 a0002c0002t0002g0006 a0002c0002t0002g0007 others(153): Show |
159 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(156): Show |
intron_variant | MODIFIER | c.661-1926A>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 4/13 | chr11 | 112031478 | |||||||
| chr11:112031541 | C | T | 8 | a0003c0003t0003g0009 a0003c0003t0003g0053 a0003c0003t0003g0054 others(5): Show |
8 | HG01952.hp2 HG02572.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.661-1863C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 4/13 | chr11 | 112031541 | |||||||
| chr11:112031542 | G | A | 1 | a0002c0002t0002g0228 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.661-1862G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 4/13 | chr11 | 112031542 | |||||||
| chr11:112031720 | C | T | 12 | a0003c0003t0006g0002 a0003c0003t0006g0050 a0003c0003t0006g0072 others(9): Show |
14 | HG02572.hp2 HG02723.hp1 HG02809.hp1 others(11): Show |
intron_variant | MODIFIER | c.661-1684C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 4/13 | chr11 | 112031720 | |||||||
| chr11:112031740 | AT | A | 30 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(27): Show |
30 | HG00558.hp1 HG00733.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.661-1643delT | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 112031740 | ||||||
| chr11:112031740 | ATT | A | 135 | a0002c0002t0002g0005 a0002c0002t0002g0006 a0002c0002t0002g0007 others(132): Show |
138 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(135): Show |
intron_variant | MODIFIER | c.661-1644_661-1643d others(4): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 112031740 | ||||||
| chr11:112031740 | ATTT | A | 10 | a0002c0002t0002g0061 a0002c0002t0002g0222 a0002c0002t0002g0230 others(7): Show |
10 | HG00140.hp2 HG00558.hp2 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.661-1645_661-1643d others(5): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 112031740 | ||||||
| chr11:112031871 | T | G | 1 | a0007c0007t0003g0203 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.661-1533T>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 4/13 | chr11 | 112031871 | |||||||
| chr11:112031885 | GT | G | 13 | a0001c0001t0001g0065 a0001c0001t0001g0068 a0001c0001t0001g0069 others(10): Show |
13 | HG00099.hp2 HG01109.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.661-1489delT | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 112031885 | ||||||
| chr11:112031885 | GTT | G | 77 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0064 others(74): Show |
78 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.661-1490_661-1489d others(4): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 112031885 | ||||||
| chr11:112031885 | GTTT | G | 194 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0044 others(191): Show |
203 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.661-1491_661-1489d others(5): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 112031885 | ||||||
| chr11:112031885 | GTTTT | G | 11 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0093 others(8): Show |
11 | HG00558.hp2 HG01167.hp2 HG01943.hp2 others(8): Show |
intron_variant | MODIFIER | c.661-1492_661-1489d others(6): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 112031885 | ||||||
| chr11:112031885 | GTTTTT | G | 9 | a0003c0003t0003g0062 a0003c0003t0003g0063 a0003c0003t0009g0199 others(6): Show |
9 | HG01884.hp2 HG01952.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.661-1493_661-1489d others(7): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 112031885 | ||||||
| chr11:112031885 | GTTTTTTT others(5): Show |
G | 4 | a0003c0003t0004g0012 a0003c0003t0004g0013 a0003c0003t0004g0014 others(1): Show |
4 | HG02280.hp1 HG02630.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.661-1500_661-1489d others(14): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 112031885 | ||||||
| chr11:112031885 | GTTTTTTT others(6): Show |
G | 1 | a0002c0002t0002g0233 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.661-1501_661-1489d others(15): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 112031885 | ||||||
| chr11:112031900 | T | G | 1 | a0001c0001t0001g0092 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.661-1504T>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 4/13 | chr11 | 112031900 | |||||||
| chr11:112031939 | T | C | 2 | a0002c0002t0002g0226 a0002c0002t0011g0227 |
2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.661-1465T>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 4/13 | chr11 | 112031939 | |||||||
| chr11:112032053 | G | T | 1 | a0007c0007t0003g0203 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.661-1351G>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 4/13 | chr11 | 112032053 | |||||||
| chr11:112032074 | G | A | 3 | a0003c0003t0004g0313 a0003c0003t0004g0314 a0003c0003t0004g0315 |
3 | HG01109.hp1 HG02818.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.661-1330G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 4/13 | chr11 | 112032074 | |||||||
| chr11:112032235 | C | T | 1 | a0002c0002t0002g0294 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.661-1169C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 4/13 | chr11 | 112032235 | |||||||
| chr11:112032287 | ATAAAATT others(5): Show |
A | 3 | a0003c0003t0009g0199 a0003c0003t0009g0200 a0003c0003t0009g0201 |
3 | HG01952.hp2 HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.661-1113_661-1102d others(14): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 112032287 | ||||||
| chr11:112032326 | TACA | T | 16 | a0003c0003t0004g0011 a0003c0003t0004g0012 a0003c0003t0004g0013 others(13): Show |
16 | HG00738.hp1 HG01099.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.661-1073_661-1071d others(5): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 112032326 | ||||||
| chr11:112032336 | T | C | 1 | a0003c0003t0004g0317 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.661-1068T>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 4/13 | chr11 | 112032336 | |||||||
| chr11:112032408 | A | T | 1 | a0001c0001t0008g0030 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.661-996A>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 4/13 | chr11 | 112032408 | |||||||
| chr11:112032535 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.661-869C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 4/13 | chr11 | 112032535 | |||||||
| chr11:112032618 | C | T | 1 | a0001c0001t0001g0177 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.661-786C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 4/13 | chr11 | 112032618 | |||||||
| chr11:112032705 | G | A | 2 | a0003c0003t0003g0062 a0003c0003t0003g0063 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.661-699G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 4/13 | chr11 | 112032705 | |||||||
| chr11:112032868 | A | G | 2 | a0003c0003t0003g0062 a0003c0003t0003g0063 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.661-536A>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 4/13 | chr11 | 112032868 | |||||||
| chr11:112032937 | C | T | 2 | a0003c0003t0003g0062 a0003c0003t0003g0063 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.661-467C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 4/13 | chr11 | 112032937 | |||||||
| chr11:112033021 | G | A | 12 | a0005c0005t0005g0008 a0005c0005t0005g0055 a0005c0005t0005g0056 others(9): Show |
12 | HG01243.hp1 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.661-383G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 4/13 | chr11 | 112033021 | |||||||
| chr11:112033119 | G | A | 7 | a0004c0004t0003g0033 a0004c0004t0003g0034 a0004c0004t0003g0035 others(4): Show |
7 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.661-285G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 4/13 | chr11 | 112033119 | |||||||
| chr11:112033135 | G | C | 1 | a0001c0001t0001g0094 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.661-269G>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 4/13 | chr11 | 112033135 | |||||||
| chr11:112033271 | T | C | 194 | a0002c0002t0002g0005 a0002c0002t0002g0006 a0002c0002t0002g0007 others(191): Show |
199 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(196): Show |
intron_variant | MODIFIER | c.661-133T>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 4/13 | chr11 | 112033271 | |||||||
| chr11:112033348 | T | C | 41 | a0003c0003t0003g0009 a0003c0003t0003g0053 a0003c0003t0003g0054 others(38): Show |
41 | HG00733.hp2 HG01099.hp1 HG01243.hp1 others(38): Show |
intron_variant | MODIFIER | c.661-56T>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 4/13 | chr11 | 112033348 | |||||||
| chr11:112033772 | C | T | 1 | a0002c0002t0002g0283 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.787+242C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112033772 | |||||||
| chr11:112033789 | C | T | 1 | a0003c0003t0003g0009 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.787+259C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112033789 | |||||||
| chr11:112033802 | T | C | 194 | a0002c0002t0002g0005 a0002c0002t0002g0006 a0002c0002t0002g0007 others(191): Show |
199 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(196): Show |
intron_variant | MODIFIER | c.787+272T>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112033802 | |||||||
| chr11:112033896 | T | A | 29 | a0003c0003t0003g0009 a0003c0003t0003g0053 a0003c0003t0003g0054 others(26): Show |
29 | HG00733.hp2 HG01099.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.787+366T>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112033896 | |||||||
| chr11:112033916 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.787+386G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112033916 | |||||||
| chr11:112033941 | T | A | 1 | a0003c0003t0018g0202 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.787+411T>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112033941 | |||||||
| chr11:112034446 | A | T | 4 | a0001c0001t0001g0144 a0003c0003t0004g0022 a0003c0003t0004g0023 others(1): Show |
4 | HG00621.hp2 HG00738.hp1 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.787+916A>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112034446 | |||||||
| chr11:112034449 | T | A | 35 | a0001c0001t0001g0079 a0001c0001t0013g0049 a0002c0002t0002g0235 others(32): Show |
35 | HG00544.hp2 HG00733.hp2 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.787+919T>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112034449 | |||||||
| chr11:112034460 | TGAGAC | T | 6 | a0005c0005t0005g0055 a0005c0005t0005g0056 a0005c0005t0005g0206 others(3): Show |
6 | HG02886.hp2 HG03139.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.787+932_787+936del others(5): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr11 | 112034460 | ||||||
| chr11:112034626 | T | G | 1 | a0003c0003t0007g0319 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.787+1096T>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112034626 | |||||||
| chr11:112034737 | T | C | 2 | a0001c0001t0001g0044 a0010c0011t0001g0046 |
2 | HG01081.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.787+1207T>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112034737 | |||||||
| chr11:112034744 | A | G | 127 | a0002c0002t0002g0005 a0002c0002t0002g0006 a0002c0002t0002g0007 others(124): Show |
130 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(127): Show |
intron_variant | MODIFIER | c.787+1214A>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112034744 | |||||||
| chr11:112034836 | C | T | 2 | a0001c0001t0001g0090 a0001c0001t0001g0163 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.787+1306C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112034836 | |||||||
| chr11:112034899 | G | A | 3 | a0001c0001t0001g0066 a0001c0001t0001g0068 a0001c0001t0001g0071 |
3 | NA18939.hp2 NA18959.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.787+1369G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112034899 | |||||||
| chr11:112034943 | T | G | 1 | a0002c0002t0002g0238 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.787+1413T>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112034943 | |||||||
| chr11:112034995 | G | A | 1 | a0005c0005t0005g0206 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.787+1465G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112034995 | |||||||
| chr11:112035124 | A | G | 17 | a0004c0004t0003g0033 a0004c0004t0003g0034 a0004c0004t0003g0035 others(14): Show |
17 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.787+1594A>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112035124 | |||||||
| chr11:112035217 | A | T | 1 | a0002c0002t0002g0297 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.787+1687A>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112035217 | |||||||
| chr11:112035491 | C | CT | 10 | a0001c0001t0001g0079 a0001c0001t0008g0029 a0002c0002t0002g0235 others(7): Show |
10 | HG00544.hp2 HG01884.hp2 HG02129.hp2 others(7): Show |
intron_variant | MODIFIER | c.788-1768dupT | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr11 | 112035491 | ||||||
| chr11:112035506 | G | T | 323 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(320): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.788-1767G>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112035506 | |||||||
| chr11:112035667 | T | G | 7 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(4): Show |
7 | HG01123.hp1 HG01358.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.788-1606T>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112035667 | |||||||
| chr11:112035722 | C | T | 1 | a0002c0002t0002g0282 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.788-1551C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112035722 | |||||||
| chr11:112035757 | G | A | 1 | a0003c0003t0007g0052 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.788-1516G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112035757 | |||||||
| chr11:112035790 | C | CT | 47 | a0001c0001t0001g0070 a0001c0001t0001g0136 a0001c0001t0001g0137 others(44): Show |
47 | HG00597.hp2 HG00621.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.788-1465dupT | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr11 | 112035790 | ||||||
| chr11:112035829 | C | T | 2 | a0005c0005t0005g0209 a0005c0005t0005g0211 |
2 | HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.788-1444C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112035829 | |||||||
| chr11:112035857 | C | T | 3 | a0001c0001t0007g0089 a0001c0001t0007g0134 a0001c0001t0007g0135 |
3 | HG01069.hp2 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.788-1416C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112035857 | |||||||
| chr11:112035933 | G | A | 29 | a0003c0003t0003g0009 a0003c0003t0003g0053 a0003c0003t0003g0054 others(26): Show |
29 | HG00733.hp2 HG01099.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.788-1340G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112035933 | |||||||
| chr11:112035965 | A | G | 1 | a0003c0003t0018g0202 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.788-1308A>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112035965 | |||||||
| chr11:112036094 | A | AAC | 12 | a0005c0005t0005g0008 a0005c0005t0005g0055 a0005c0005t0005g0056 others(9): Show |
12 | HG01243.hp1 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.788-1177_788-1176d others(4): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr11 | 112036094 | ||||||
| chr11:112036096 | C | CAT | 115 | a0002c0002t0002g0005 a0002c0002t0002g0006 a0002c0002t0002g0007 others(112): Show |
118 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.788-1164_788-1163d others(4): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr11 | 112036096 | ||||||
| chr11:112036109 | A | C | 1 | a0001c0001t0001g0133 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.788-1164A>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112036109 | |||||||
| chr11:112036141 | G | GTA | 4 | a0003c0003t0007g0040 a0003c0003t0007g0041 a0003c0003t0007g0042 others(1): Show |
4 | HG02257.hp2 HG02258.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.788-1120_788-1119d others(4): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr11 | 112036141 | ||||||
| chr11:112036143 | A | G | 8 | a0003c0003t0003g0009 a0003c0003t0003g0053 a0003c0003t0003g0054 others(5): Show |
8 | HG01952.hp2 HG02572.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.788-1130A>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112036143 | |||||||
| chr11:112036151 | ATATGTGT others(17): Show |
A | 1 | a0007c0007t0003g0203 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.788-1120_788-1097d others(26): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr11 | 112036151 | ||||||
| chr11:112036153 | A | G | 1 | a0007c0007t0003g0204 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.788-1120A>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112036153 | |||||||
| chr11:112036155 | GTGTGTGT others(5): Show |
G | 3 | a0001c0001t0001g0066 a0001c0001t0001g0068 a0001c0001t0001g0071 |
3 | NA18939.hp2 NA18959.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.788-1110_788-1099d others(14): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr11 | 112036155 | ||||||
| chr11:112036157 | GTGTGTAT others(3): Show |
G | 4 | a0001c0001t0001g0065 a0001c0001t0001g0067 a0001c0001t0001g0069 others(1): Show |
4 | HG01123.hp1 HG01358.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.788-1110_788-1101d others(12): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr11 | 112036157 | ||||||
| chr11:112036163 | A | G | 2 | a0001c0001t0001g0074 a0001c0001t0001g0103 |
2 | HG00099.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.788-1110A>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112036163 | |||||||
| chr11:112036165 | A | ATGTG | 3 | a0004c0004t0003g0195 a0004c0004t0003g0196 a0004c0004t0003g0198 |
3 | HG02976.hp1 HG06807.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.788-1107_788-1106i others(6): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr11 | 112036165 | ||||||
| chr11:112036165 | A | ATGTGTGT others(5): Show |
2 | a0004c0004t0003g0033 a0004c0004t0003g0038 |
2 | HG01891.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.788-1107_788-1106i others(14): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr11 | 112036165 | ||||||
| chr11:112036165 | A | ATGTGTGT others(7): Show |
1 | a0004c0004t0003g0039 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.788-1107_788-1106i others(16): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr11 | 112036165 | ||||||
| chr11:112036167 | A | ATG | 5 | a0001c0001t0001g0151 a0003c0003t0004g0011 a0006c0006t0001g0076 others(2): Show |
5 | HG02809.hp2 NA18942.hp1 NA19054.hp2 others(2): Show |
intron_variant | MODIFIER | c.788-1072_788-1071d others(4): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr11 | 112036167 | ||||||
| chr11:112036167 | A | G | 28 | a0001c0001t0001g0003 a0003c0003t0003g0009 a0003c0003t0003g0053 others(25): Show |
28 | HG01515.hp1 HG01884.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.788-1106A>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112036167 | |||||||
| chr11:112036167 | ATGTGTG | A | 8 | a0003c0003t0006g0002 a0003c0003t0006g0050 a0003c0003t0006g0072 others(5): Show |
9 | HG02723.hp1 HG02809.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.788-1076_788-1071d others(8): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr11 | 112036167 | ||||||
| chr11:112036169 | G | A | 3 | a0001c0001t0001g0074 a0001c0001t0001g0103 a0002c0002t0002g0221 |
3 | HG00099.hp1 HG02273.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.788-1104G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112036169 | |||||||
| chr11:112036185 | GTGTGTGT others(21): Show |
G | 1 | a0007c0007t0003g0204 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.788-1086_788-1059d others(30): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr11 | 112036185 | ||||||
| chr11:112036189 | GTGTGTGT others(14): Show |
G | 2 | a0002c0002t0002g0236 a0002c0002t0002g0237 |
2 | HG00544.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.788-1082_788-1062d others(23): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr11 | 112036189 | ||||||
| chr11:112036194 | TGTGTG | T | 3 | a0003c0003t0006g0002 a0003c0003t0006g0180 a0003c0003t0006g0184 |
3 | HG02897.hp1 HG02970.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.788-1078_788-1074d others(7): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112036194 | |||||||
| chr11:112036195 | GTGTGTGT others(3): Show |
G | 2 | a0004c0004t0003g0192 a0004c0004t0010g0193 |
2 | HG02486.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.788-1076_788-1067d others(12): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr11 | 112036195 | ||||||
| chr11:112036197 | G | T | 5 | a0003c0003t0007g0040 a0003c0003t0007g0041 a0003c0003t0007g0042 others(2): Show |
5 | HG02257.hp2 HG02258.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.788-1076G>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112036197 | |||||||
| chr11:112036199 | G | GT | 18 | a0001c0001t0001g0003 a0001c0001t0001g0082 a0001c0001t0001g0087 others(15): Show |
18 | HG00408.hp1 HG00741.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.788-1073dupT | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr11 | 112036199 | ||||||
| chr11:112036199 | G | GTT | 17 | a0001c0001t0001g0001 a0001c0001t0001g0101 a0001c0001t0001g0105 others(14): Show |
19 | HG00558.hp1 HG00621.hp2 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.788-1073_788-1072i others(4): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr11 | 112036199 | ||||||
| chr11:112036199 | G | GTTT | 8 | a0001c0001t0001g0045 a0001c0001t0001g0099 a0001c0001t0001g0146 others(5): Show |
8 | HG01943.hp2 HG01993.hp2 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.788-1073_788-1072i others(5): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr11 | 112036199 | ||||||
| chr11:112036199 | G | T | 4 | a0001c0001t0001g0003 a0001c0001t0001g0065 a0001c0001t0001g0067 others(1): Show |
4 | HG01496.hp2 HG01515.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.788-1074G>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112036199 | |||||||
| chr11:112036199 | GTGTTTTT others(4): Show |
G | 9 | a0002c0002t0002g0005 a0002c0002t0002g0059 a0002c0002t0002g0060 others(6): Show |
9 | HG01109.hp2 HG01257.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.788-1072_788-1062d others(13): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr11 | 112036199 | ||||||
| chr11:112036199 | GTGTTTTT others(5): Show |
G | 1 | a0002c0002t0002g0322 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.788-1072_788-1061d others(14): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr11 | 112036199 | ||||||
| chr11:112036199 | GTGTTTTT others(6): Show |
G | 4 | a0002c0002t0002g0010 a0002c0002t0002g0246 a0002c0002t0002g0256 others(1): Show |
4 | HG02056.hp2 HG02155.hp2 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.788-1072_788-1060d others(15): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr11 | 112036199 | ||||||
| chr11:112036201 | G | GTGTGTGT others(3): Show |
2 | a0001c0001t0001g0140 a0001c0001t0001g0163 |
2 | HG01071.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.788-1071_788-1070i others(12): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr11 | 112036201 | ||||||
| chr11:112036201 | G | GTGTT | 9 | a0001c0001t0001g0064 a0001c0001t0001g0081 a0001c0001t0001g0085 others(6): Show |
9 | HG00673.hp1 HG00673.hp2 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.788-1071_788-1070i others(6): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr11 | 112036201 | ||||||
| chr11:112036201 | G | GTGTTTT | 7 | a0001c0001t0001g0102 a0001c0001t0001g0116 a0001c0001t0001g0122 others(4): Show |
7 | HG00140.hp1 HG00544.hp1 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.788-1071_788-1070i others(8): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr11 | 112036201 | ||||||
| chr11:112036201 | G | GTT | 15 | a0001c0001t0001g0004 a0001c0001t0001g0110 a0001c0001t0001g0113 others(12): Show |
15 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.788-1044_788-1043d others(4): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr11 | 112036201 | ||||||
| chr11:112036201 | G | GTTT | 13 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0051 others(10): Show |
13 | HG01258.hp2 HG01934.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.788-1045_788-1043d others(5): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr11 | 112036201 | ||||||
| chr11:112036201 | G | GTTTT | 6 | a0001c0001t0001g0074 a0001c0001t0001g0130 a0001c0001t0001g0131 others(3): Show |
6 | HG02257.hp2 HG02602.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.788-1046_788-1043d others(6): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr11 | 112036201 | ||||||
| chr11:112036201 | G | GTTTTTTG others(9): Show |
1 | a0003c0003t0003g0054 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.788-1066_788-1065i others(18): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr11 | 112036201 | ||||||
| chr11:112036201 | G | GTTTTTTG others(11): Show |
1 | a0003c0003t0003g0053 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.788-1066_788-1065i others(20): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr11 | 112036201 | ||||||
| chr11:112036201 | G | T | 66 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0045 others(63): Show |
71 | HG00408.hp1 HG00558.hp1 HG00621.hp2 others(68): Show |
intron_variant | MODIFIER | c.788-1072G>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112036201 | |||||||
| chr11:112036201 | GTTTTTTT | G | 14 | a0002c0002t0002g0221 a0002c0002t0002g0223 a0002c0002t0002g0231 others(11): Show |
14 | HG01261.hp2 HG02135.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.788-1049_788-1043d others(9): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr11 | 112036201 | ||||||
| chr11:112036201 | GTTTTTTT others(1): Show |
G | 8 | a0002c0002t0002g0005 a0002c0002t0002g0232 a0002c0002t0002g0257 others(5): Show |
8 | HG01243.hp1 HG02723.hp2 NA18942.hp2 others(5): Show |
intron_variant | MODIFIER | c.788-1050_788-1043d others(10): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr11 | 112036201 | ||||||
| chr11:112036201 | GTTTTTTT others(2): Show |
G | 72 | a0002c0002t0002g0006 a0002c0002t0002g0007 a0002c0002t0002g0058 others(69): Show |
74 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.788-1051_788-1043d others(11): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr11 | 112036201 | ||||||
| chr11:112036201 | GTTTTTTT others(3): Show |
G | 4 | a0002c0002t0002g0213 a0002c0002t0002g0289 a0002c0002t0002g0308 others(1): Show |
4 | HG00733.hp2 HG02148.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.788-1052_788-1043d others(12): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr11 | 112036201 | ||||||
| chr11:112036201 | GTTTTTTT others(4): Show |
G | 13 | a0002c0002t0002g0057 a0002c0002t0002g0214 a0002c0002t0002g0225 others(10): Show |
13 | HG02109.hp2 HG02257.hp1 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.788-1053_788-1043d others(13): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr11 | 112036201 | ||||||
| chr11:112036201 | GTTTTTTT others(6): Show |
G | 2 | a0005c0005t0005g0055 a0005c0005t0005g0056 |
2 | HG02886.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.788-1055_788-1043d others(15): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr11 | 112036201 | ||||||
| chr11:112036202 | T | TGTG | 10 | a0003c0003t0003g0062 a0003c0003t0004g0014 a0003c0003t0004g0015 others(7): Show |
10 | HG02451.hp2 HG02630.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.788-1071_788-1070i others(5): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112036202 | |||||||
| chr11:112036202 | T | TGTGTGTG others(4): Show |
3 | a0004c0004t0003g0034 a0004c0004t0003g0035 a0004c0004t0003g0036 |
3 | HG02109.hp1 HG02818.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.788-1071_788-1070i others(13): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112036202 | |||||||
| chr11:112036202 | T | TGTGTGTG others(6): Show |
1 | a0004c0004t0003g0037 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.788-1071_788-1070i others(15): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112036202 | |||||||
| chr11:112036203 | T | G | 10 | a0003c0003t0003g0009 a0003c0003t0003g0062 a0003c0003t0004g0011 others(7): Show |
10 | HG01884.hp2 HG01952.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.788-1070T>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112036203 | |||||||
| chr11:112036204 | T | G | 3 | a0003c0003t0007g0319 a0003c0003t0014g0187 a0004c0004t0003g0197 |
3 | HG02280.hp2 NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.788-1069T>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112036204 | |||||||
| chr11:112036205 | T | G | 7 | a0003c0003t0009g0199 a0003c0003t0009g0200 a0003c0003t0009g0201 others(4): Show |
7 | HG01884.hp2 HG01952.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.788-1068T>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112036205 | |||||||
| chr11:112036206 | T | G | 1 | a0003c0003t0007g0319 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.788-1067T>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112036206 | |||||||
| chr11:112036207 | T | G | 1 | a0003c0003t0018g0202 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.788-1066T>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112036207 | |||||||
| chr11:112036209 | T | G | 1 | a0003c0003t0018g0202 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.788-1064T>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112036209 | |||||||
| chr11:112036210 | T | G | 14 | a0002c0002t0002g0221 a0002c0002t0002g0223 a0002c0002t0002g0231 others(11): Show |
14 | HG01261.hp2 HG02135.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.788-1063T>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112036210 | |||||||
| chr11:112036211 | T | G | 4 | a0002c0002t0002g0232 a0002c0002t0002g0264 a0003c0003t0018g0202 others(1): Show |
4 | HG01243.hp1 HG03041.hp2 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.788-1062T>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112036211 | |||||||
| chr11:112036212 | T | G | 32 | a0002c0002t0002g0216 a0002c0002t0002g0223 a0002c0002t0002g0231 others(29): Show |
32 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.788-1061T>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112036212 | |||||||
| chr11:112036213 | T | G | 2 | a0003c0003t0018g0202 a0005c0005t0005g0008 |
2 | HG01243.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.788-1060T>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112036213 | |||||||
| chr11:112036214 | T | G | 16 | a0002c0002t0002g0233 a0002c0002t0002g0234 a0002c0002t0002g0239 others(13): Show |
16 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.788-1059T>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112036214 | |||||||
| chr11:112036215 | T | G | 2 | a0003c0003t0018g0202 a0005c0005t0005g0008 |
2 | HG01243.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.788-1058T>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112036215 | |||||||
| chr11:112036216 | T | G | 14 | a0002c0002t0002g0233 a0002c0002t0002g0239 a0003c0003t0007g0052 others(11): Show |
14 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.788-1057T>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112036216 | |||||||
| chr11:112036217 | T | G | 1 | a0003c0003t0018g0202 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.788-1056T>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112036217 | |||||||
| chr11:112036218 | T | G | 1 | a0003c0003t0007g0052 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.788-1055T>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112036218 | |||||||
| chr11:112036219 | T | G | 1 | a0003c0003t0018g0202 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.788-1054T>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112036219 | |||||||
| chr11:112036229 | T | G | 2 | a0003c0003t0003g0062 a0003c0003t0003g0063 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.788-1044T>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112036229 | |||||||
| chr11:112036243 | C | T | 2 | a0007c0007t0003g0203 a0007c0007t0003g0204 |
2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.788-1030C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112036243 | |||||||
| chr11:112036282 | C | T | 1 | a0003c0003t0007g0048 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.788-991C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112036282 | |||||||
| chr11:112036341 | G | T | 1 | a0001c0001t0001g0170 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.788-932G>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112036341 | |||||||
| chr11:112036467 | T | C | 19 | a0004c0004t0003g0033 a0004c0004t0003g0034 a0004c0004t0003g0035 others(16): Show |
19 | HG00733.hp2 HG01099.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.788-806T>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112036467 | |||||||
| chr11:112036706 | A | G | 2 | a0003c0003t0009g0200 a0003c0003t0009g0201 |
2 | HG01952.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.788-567A>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112036706 | |||||||
| chr11:112037027 | T | G | 2 | a0007c0007t0003g0203 a0007c0007t0003g0204 |
2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.788-246T>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112037027 | |||||||
| chr11:112037065 | C | T | 1 | a0003c0003t0016g0047 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.788-208C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112037065 | |||||||
| chr11:112037078 | A | G | 2 | a0003c0003t0003g0062 a0003c0003t0003g0063 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.788-195A>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112037078 | |||||||
| chr11:112037165 | A | G | 1 | a0001c0001t0001g0051 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.788-108A>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 5/13 | chr11 | 112037165 | |||||||
| chr11:112037472 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.975+12T>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 6/13 | chr11 | 112037472 | |||||||
| chr11:112037476 | G | T | 25 | a0003c0003t0004g0011 a0003c0003t0004g0012 a0003c0003t0004g0013 others(22): Show |
25 | HG00738.hp1 HG01099.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.975+16G>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 6/13 | chr11 | 112037476 | |||||||
| chr11:112037763 | C | T | 2 | a0003c0003t0003g0062 a0003c0003t0003g0063 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.975+303C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 6/13 | chr11 | 112037763 | |||||||
| chr11:112037778 | C | CT | 241 | a0001c0001t0001g0044 a0001c0001t0001g0051 a0001c0001t0001g0064 others(238): Show |
246 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.975+333dupT | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr11 | 112037778 | ||||||
| chr11:112037778 | CT | C | 8 | a0001c0001t0001g0176 a0004c0004t0003g0033 a0004c0004t0003g0034 others(5): Show |
8 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.975+333delT | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr11 | 112037778 | ||||||
| chr11:112037888 | A | G | 8 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(5): Show |
8 | HG00140.hp1 HG00735.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.975+428A>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 6/13 | chr11 | 112037888 | |||||||
| chr11:112038202 | TTTG | T | 12 | a0005c0005t0005g0008 a0005c0005t0005g0055 a0005c0005t0005g0056 others(9): Show |
12 | HG01243.hp1 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.975+755_975+757del others(3): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr11 | 112038202 | ||||||
| chr11:112038241 | C | G | 1 | a0001c0001t0001g0109 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.975+781C>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 6/13 | chr11 | 112038241 | |||||||
| chr11:112038250 | G | A | 2 | a0003c0003t0007g0052 a0003c0003t0007g0073 |
2 | HG03130.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.975+790G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 6/13 | chr11 | 112038250 | |||||||
| chr11:112038666 | G | A | 21 | a0003c0003t0004g0011 a0003c0003t0004g0012 a0003c0003t0004g0013 others(18): Show |
21 | HG00738.hp1 HG01099.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.976-578G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 6/13 | chr11 | 112038666 | |||||||
| chr11:112038777 | C | T | 1 | a0002c0002t0002g0306 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.976-467C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 6/13 | chr11 | 112038777 | |||||||
| chr11:112038855 | GA | G | 22 | a0002c0002t0002g0301 a0003c0003t0003g0062 a0003c0003t0003g0063 others(19): Show |
22 | HG00733.hp2 HG01099.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.976-377delA | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr11 | 112038855 | ||||||
| chr11:112038921 | A | G | 3 | a0001c0001t0001g0085 a0001c0001t0001g0127 a0001c0001t0001g0128 |
3 | HG01167.hp2 HG02004.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.976-323A>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 6/13 | chr11 | 112038921 | |||||||
| chr11:112039067 | T | C | 1 | a0001c0001t0001g0168 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.976-177T>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 6/13 | chr11 | 112039067 | |||||||
| chr11:112039095 | C | A | 154 | a0002c0002t0002g0005 a0002c0002t0002g0006 a0002c0002t0002g0007 others(151): Show |
157 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(154): Show |
intron_variant | MODIFIER | c.976-149C>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 6/13 | chr11 | 112039095 | |||||||
| chr11:112039129 | G | A | 5 | a0004c0004t0003g0192 a0004c0004t0010g0189 a0004c0004t0010g0193 others(2): Show |
5 | HG02145.hp1 HG02486.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.976-115G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 6/13 | chr11 | 112039129 | |||||||
| chr11:112039186 | C | T | 1 | a0001c0001t0001g0188 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.976-58C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 6/13 | chr11 | 112039186 | |||||||
| chr11:112039644 | C | G | 1 | a0002c0002t0002g0007 | 2 | HG02698.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1129+247C>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 7/13 | chr11 | 112039644 | |||||||
| chr11:112039775 | A | G | 5 | a0003c0003t0009g0199 a0003c0003t0009g0200 a0003c0003t0009g0201 others(2): Show |
5 | HG01952.hp2 HG02970.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1129+378A>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 7/13 | chr11 | 112039775 | |||||||
| chr11:112039851 | G | A | 10 | a0002c0002t0002g0217 a0002c0002t0002g0218 a0002c0002t0002g0219 others(7): Show |
10 | HG01192.hp1 HG01192.hp2 HG01975.hp2 others(7): Show |
intron_variant | MODIFIER | c.1129+454G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 7/13 | chr11 | 112039851 | |||||||
| chr11:112039903 | C | A | 1 | a0003c0003t0007g0048 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1129+506C>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 7/13 | chr11 | 112039903 | |||||||
| chr11:112040117 | A | G | 10 | a0004c0004t0003g0192 a0004c0004t0003g0194 a0004c0004t0003g0195 others(7): Show |
10 | HG01884.hp2 HG02145.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1129+720A>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 7/13 | chr11 | 112040117 | |||||||
| chr11:112040300 | T | C | 1 | a0002c0002t0002g0286 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1129+903T>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 7/13 | chr11 | 112040300 | |||||||
| chr11:112040491 | C | T | 2 | a0007c0007t0003g0203 a0007c0007t0003g0204 |
2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1129+1094C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 7/13 | chr11 | 112040491 | |||||||
| chr11:112040556 | A | G | 1 | a0002c0002t0002g0323 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1129+1159A>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 7/13 | chr11 | 112040556 | |||||||
| chr11:112040664 | G | C | 1 | a0001c0001t0001g0096 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1129+1267G>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 7/13 | chr11 | 112040664 | |||||||
| chr11:112040732 | A | G | 5 | a0004c0004t0003g0194 a0004c0004t0003g0195 a0004c0004t0003g0196 others(2): Show |
5 | HG01884.hp2 HG02280.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1129+1335A>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 7/13 | chr11 | 112040732 | |||||||
| chr11:112040825 | C | G | 25 | a0003c0003t0004g0011 a0003c0003t0004g0012 a0003c0003t0004g0013 others(22): Show |
25 | HG00738.hp1 HG01099.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.1129+1428C>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 7/13 | chr11 | 112040825 | |||||||
| chr11:112040923 | T | TA | 39 | a0003c0003t0003g0009 a0003c0003t0003g0062 a0003c0003t0003g0063 others(36): Show |
39 | HG00733.hp2 HG01099.hp1 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.1129+1538dupA | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 112040923 | ||||||
| chr11:112041065 | C | G | 1 | a0001c0001t0001g0143 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1129+1668C>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 7/13 | chr11 | 112041065 | |||||||
| chr11:112041132 | G | A | 5 | a0002c0002t0002g0242 a0002c0002t0002g0244 a0002c0002t0002g0245 others(2): Show |
5 | HG01192.hp2 HG01975.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.1129+1735G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 7/13 | chr11 | 112041132 | |||||||
| chr11:112041359 | A | G | 127 | a0002c0002t0002g0005 a0002c0002t0002g0006 a0002c0002t0002g0007 others(124): Show |
132 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.1129+1962A>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 7/13 | chr11 | 112041359 | |||||||
| chr11:112041472 | A | G | 3 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0126 |
3 | NA18941.hp1 NA18994.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.1130-1994A>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 7/13 | chr11 | 112041472 | |||||||
| chr11:112041618 | C | A | 2 | a0007c0007t0003g0203 a0007c0007t0003g0204 |
2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1130-1848C>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 7/13 | chr11 | 112041618 | |||||||
| chr11:112041708 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1130-1758C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 7/13 | chr11 | 112041708 | |||||||
| chr11:112041775 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1130-1691G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 7/13 | chr11 | 112041775 | |||||||
| chr11:112041798 | C | T | 1 | a0003c0003t0018g0202 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1130-1668C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 7/13 | chr11 | 112041798 | |||||||
| chr11:112041881 | C | T | 5 | a0004c0004t0003g0194 a0004c0004t0003g0195 a0004c0004t0003g0196 others(2): Show |
5 | HG01884.hp2 HG02280.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1130-1585C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 7/13 | chr11 | 112041881 | |||||||
| chr11:112042176 | T | G | 2 | a0007c0007t0003g0203 a0007c0007t0003g0204 |
2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1130-1290T>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 7/13 | chr11 | 112042176 | |||||||
| chr11:112042231 | T | C | 5 | a0004c0004t0003g0192 a0004c0004t0010g0189 a0004c0004t0010g0193 others(2): Show |
5 | HG02145.hp1 HG02486.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1130-1235T>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 7/13 | chr11 | 112042231 | |||||||
| chr11:112042358 | C | T | 16 | a0003c0003t0004g0011 a0003c0003t0004g0012 a0003c0003t0004g0013 others(13): Show |
16 | HG00738.hp1 HG01099.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.1130-1108C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 7/13 | chr11 | 112042358 | |||||||
| chr11:112042379 | G | C | 1 | a0003c0003t0007g0048 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1130-1087G>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 7/13 | chr11 | 112042379 | |||||||
| chr11:112042425 | C | T | 1 | a0003c0003t0007g0048 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1130-1041C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 7/13 | chr11 | 112042425 | |||||||
| chr11:112042520 | A | C | 1 | a0002c0002t0002g0277 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1130-946A>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 7/13 | chr11 | 112042520 | |||||||
| chr11:112042566 | G | A | 41 | a0003c0003t0003g0009 a0003c0003t0003g0053 a0003c0003t0003g0054 others(38): Show |
41 | HG00733.hp2 HG01099.hp1 HG01243.hp1 others(38): Show |
intron_variant | MODIFIER | c.1130-900G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 7/13 | chr11 | 112042566 | |||||||
| chr11:112042640 | G | A | 127 | a0002c0002t0002g0005 a0002c0002t0002g0006 a0002c0002t0002g0007 others(124): Show |
132 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.1130-826G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 7/13 | chr11 | 112042640 | |||||||
| chr11:112042759 | A | G | 8 | a0003c0003t0003g0009 a0003c0003t0003g0053 a0003c0003t0003g0054 others(5): Show |
8 | HG01952.hp2 HG02572.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.1130-707A>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 7/13 | chr11 | 112042759 | |||||||
| chr11:112042809 | C | T | 1 | a0003c0003t0007g0073 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1130-657C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 7/13 | chr11 | 112042809 | |||||||
| chr11:112042820 | A | C | 1 | a0002c0002t0002g0276 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1130-646A>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 7/13 | chr11 | 112042820 | |||||||
| chr11:112042970 | C | A | 6 | a0003c0003t0003g0009 a0003c0003t0009g0199 a0003c0003t0009g0200 others(3): Show |
6 | HG01952.hp2 HG02970.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1130-496C>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 7/13 | chr11 | 112042970 | |||||||
| chr11:112043040 | C | T | 1 | a0002c0002t0002g0320 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1130-426C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 7/13 | chr11 | 112043040 | |||||||
| chr11:112043100 | A | T | 6 | a0003c0003t0003g0009 a0003c0003t0009g0199 a0003c0003t0009g0200 others(3): Show |
6 | HG01952.hp2 HG02970.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1130-366A>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 7/13 | chr11 | 112043100 | |||||||
| chr11:112043114 | C | T | 1 | a0003c0003t0007g0048 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1130-352C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 7/13 | chr11 | 112043114 | |||||||
| chr11:112043125 | T | G | 3 | a0003c0003t0004g0313 a0003c0003t0004g0314 a0003c0003t0004g0315 |
3 | HG01109.hp1 HG02818.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1130-341T>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 7/13 | chr11 | 112043125 | |||||||
| chr11:112043403 | C | T | 2 | a0003c0003t0003g0053 a0003c0003t0003g0054 |
2 | HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1130-63C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 7/13 | chr11 | 112043403 | |||||||
| chr11:112043572 | C | G | 1 | a0003c0003t0007g0319 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1197+39C>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 8/13 | chr11 | 112043572 | |||||||
| chr11:112043725 | G | A | 322 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(319): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1197+192G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 8/13 | chr11 | 112043725 | |||||||
| chr11:112043842 | A | G | 194 | a0002c0002t0002g0005 a0002c0002t0002g0006 a0002c0002t0002g0007 others(191): Show |
199 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(196): Show |
intron_variant | MODIFIER | c.1197+309A>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 8/13 | chr11 | 112043842 | |||||||
| chr11:112044266 | C | T | 1 | a0006c0006t0001g0077 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1197+733C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 8/13 | chr11 | 112044266 | |||||||
| chr11:112044342 | A | G | 3 | a0003c0003t0004g0313 a0003c0003t0004g0314 a0003c0003t0004g0315 |
3 | HG01109.hp1 HG02818.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1198-796A>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 8/13 | chr11 | 112044342 | |||||||
| chr11:112044872 | G | A | 41 | a0003c0003t0003g0009 a0003c0003t0003g0053 a0003c0003t0003g0054 others(38): Show |
41 | HG00733.hp2 HG01099.hp1 HG01243.hp1 others(38): Show |
intron_variant | MODIFIER | c.1198-266G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 8/13 | chr11 | 112044872 | |||||||
| chr11:112044907 | C | G | 1 | a0003c0003t0004g0017 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1198-231C>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 8/13 | chr11 | 112044907 | |||||||
| chr11:112044974 | G | A | 2 | a0003c0003t0003g0062 a0003c0003t0003g0063 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1198-164G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 8/13 | chr11 | 112044974 | |||||||
| chr11:112045041 | C | CAA | 13 | a0001c0001t0001g0110 a0001c0001t0001g0147 a0001c0001t0001g0167 others(10): Show |
13 | HG01884.hp2 HG02280.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1198-86_1198-85dup others(2): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr11 | 112045041 | ||||||
| chr11:112045400 | T | G | 29 | a0003c0003t0003g0009 a0003c0003t0003g0053 a0003c0003t0003g0054 others(26): Show |
29 | HG00733.hp2 HG01099.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1290+170T>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 9/13 | chr11 | 112045400 | |||||||
| chr11:112045413 | C | T | 6 | a0001c0001t0008g0027 a0001c0001t0008g0028 a0001c0001t0008g0029 others(3): Show |
6 | NA18977.hp1 NA18991.hp1 NA19007.hp2 others(3): Show |
intron_variant | MODIFIER | c.1290+183C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 9/13 | chr11 | 112045413 | |||||||
| chr11:112045545 | G | A | 12 | a0005c0005t0005g0008 a0005c0005t0005g0055 a0005c0005t0005g0056 others(9): Show |
12 | HG01243.hp1 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1290+315G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 9/13 | chr11 | 112045545 | |||||||
| chr11:112045618 | A | G | 194 | a0002c0002t0002g0005 a0002c0002t0002g0006 a0002c0002t0002g0007 others(191): Show |
199 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(196): Show |
intron_variant | MODIFIER | c.1291-245A>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 9/13 | chr11 | 112045618 | |||||||
| chr11:112045642 | C | G | 16 | a0002c0002t0002g0223 a0002c0002t0002g0224 a0002c0002t0002g0231 others(13): Show |
16 | HG00558.hp2 HG01981.hp1 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.1291-221C>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 9/13 | chr11 | 112045642 | |||||||
| chr11:112045642 | C | T | 2 | a0007c0007t0003g0203 a0007c0007t0003g0204 |
2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1291-221C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 9/13 | chr11 | 112045642 | |||||||
| chr11:112045835 | T | C | 2 | a0007c0007t0003g0203 a0007c0007t0003g0204 |
2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1291-28T>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 9/13 | chr11 | 112045835 | |||||||
| chr11:112045858 | T | C | 1 | a0002c0002t0002g0285 | 1 | HG01981.hp2 | splice_region_variant&intron_variant | LOW | c.1291-5T>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 9/13 | chr11 | 112045858 | |||||||
| chr11:112046004 | A | G | 1 | a0001c0001t0001g0123 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1398+34A>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 10/13 | chr11 | 112046004 | |||||||
| chr11:112046134 | A | G | 2 | a0003c0003t0003g0053 a0003c0003t0003g0054 |
2 | HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1398+164A>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 10/13 | chr11 | 112046134 | |||||||
| chr11:112046275 | T | C | 2 | a0001c0001t0001g0097 a0001c0001t0001g0170 |
2 | HG01943.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1398+305T>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 10/13 | chr11 | 112046275 | |||||||
| chr11:112046371 | A | G | 1 | a0003c0003t0004g0317 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1398+401A>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 10/13 | chr11 | 112046371 | |||||||
| chr11:112046405 | C | A | 1 | a0002c0002t0002g0271 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1398+435C>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 10/13 | chr11 | 112046405 | |||||||
| chr11:112046509 | A | T | 2 | a0002c0002t0002g0232 a0002c0002t0002g0275 |
2 | NA18942.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.1398+539A>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 10/13 | chr11 | 112046509 | |||||||
| chr11:112046570 | C | A | 2 | a0005c0005t0005g0209 a0005c0005t0005g0211 |
2 | HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1398+600C>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 10/13 | chr11 | 112046570 | |||||||
| chr11:112046801 | CT | C | 27 | a0003c0003t0003g0009 a0003c0003t0003g0053 a0003c0003t0003g0054 others(24): Show |
27 | HG00733.hp2 HG01099.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.1398+839delT | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 112046801 | ||||||
| chr11:112046818 | A | T | 20 | a0003c0003t0004g0011 a0003c0003t0004g0012 a0003c0003t0004g0013 others(17): Show |
20 | HG00738.hp1 HG01099.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.1398+848A>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 10/13 | chr11 | 112046818 | |||||||
| chr11:112046901 | C | A | 2 | a0003c0003t0003g0062 a0003c0003t0003g0063 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1398+931C>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 10/13 | chr11 | 112046901 | |||||||
| chr11:112046951 | T | C | 1 | a0001c0001t0001g0098 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1398+981T>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 10/13 | chr11 | 112046951 | |||||||
| chr11:112047014 | T | C | 1 | a0002c0002t0002g0247 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1398+1044T>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 10/13 | chr11 | 112047014 | |||||||
| chr11:112047178 | ACT | A | 6 | a0003c0003t0003g0009 a0003c0003t0009g0199 a0003c0003t0009g0200 others(3): Show |
6 | HG01952.hp2 HG02970.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1398+1210_1398+121 others(6): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 112047178 | ||||||
| chr11:112047315 | G | GT | 6 | a0003c0003t0003g0009 a0003c0003t0009g0199 a0003c0003t0009g0200 others(3): Show |
6 | HG01952.hp2 HG02970.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1398+1352dupT | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 112047315 | ||||||
| chr11:112047390 | A | G | 4 | a0003c0003t0007g0040 a0003c0003t0007g0041 a0003c0003t0007g0042 others(1): Show |
4 | HG02257.hp2 HG02258.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1398+1420A>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 10/13 | chr11 | 112047390 | |||||||
| chr11:112047454 | A | G | 12 | a0001c0001t0001g0044 a0001c0001t0001g0079 a0001c0001t0001g0090 others(9): Show |
12 | HG00544.hp1 HG00738.hp2 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.1398+1484A>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 10/13 | chr11 | 112047454 | |||||||
| chr11:112047809 | G | C | 7 | a0004c0004t0003g0033 a0004c0004t0003g0034 a0004c0004t0003g0035 others(4): Show |
7 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1398+1839G>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 10/13 | chr11 | 112047809 | |||||||
| chr11:112047889 | C | T | 1 | a0003c0003t0007g0048 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1398+1919C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 10/13 | chr11 | 112047889 | |||||||
| chr11:112047942 | A | C | 1 | a0001c0001t0001g0110 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1398+1972A>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 10/13 | chr11 | 112047942 | |||||||
| chr11:112048224 | A | G | 41 | a0003c0003t0003g0009 a0003c0003t0003g0053 a0003c0003t0003g0054 others(38): Show |
41 | HG00733.hp2 HG01099.hp1 HG01243.hp1 others(38): Show |
intron_variant | MODIFIER | c.1398+2254A>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 10/13 | chr11 | 112048224 | |||||||
| chr11:112048277 | A | G | 2 | a0002c0002t0002g0006 a0002c0002t0002g0291 |
3 | NA18612.hp1 NA19011.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1398+2307A>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 10/13 | chr11 | 112048277 | |||||||
| chr11:112048461 | T | C | 1 | a0003c0003t0014g0187 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1398+2491T>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 10/13 | chr11 | 112048461 | |||||||
| chr11:112048638 | A | G | 21 | a0003c0003t0004g0011 a0003c0003t0004g0012 a0003c0003t0004g0013 others(18): Show |
21 | HG00738.hp1 HG01099.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.1399-2596A>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 10/13 | chr11 | 112048638 | |||||||
| chr11:112048734 | A | G | 1 | a0003c0003t0006g0184 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1399-2500A>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 10/13 | chr11 | 112048734 | |||||||
| chr11:112048777 | ACC | A | 3 | a0004c0004t0003g0192 a0008c0008t0003g0190 a0008c0008t0003g0191 |
3 | HG02486.hp1 HG02922.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1399-2455_1399-245 others(6): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 112048777 | ||||||
| chr11:112048782 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1399-2452C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 10/13 | chr11 | 112048782 | |||||||
| chr11:112048878 | T | A | 1 | a0002c0002t0002g0010 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1399-2356T>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 10/13 | chr11 | 112048878 | |||||||
| chr11:112048969 | A | AT | 34 | a0001c0001t0001g0045 a0001c0001t0001g0065 a0001c0001t0001g0066 others(31): Show |
34 | HG00597.hp2 HG00733.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.1399-2238dupT | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 112048969 | ||||||
| chr11:112048969 | AT | A | 124 | a0001c0001t0007g0089 a0001c0001t0007g0134 a0001c0001t0007g0135 others(121): Show |
129 | HG00140.hp2 HG00544.hp2 HG00558.hp2 others(126): Show |
intron_variant | MODIFIER | c.1399-2238delT | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 112048969 | ||||||
| chr11:112048969 | ATT | A | 11 | a0002c0002t0002g0058 a0002c0002t0002g0242 a0002c0002t0002g0248 others(8): Show |
11 | HG01167.hp1 HG01975.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.1399-2239_1399-223 others(6): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 112048969 | ||||||
| chr11:112049140 | C | T | 4 | a0003c0003t0004g0313 a0003c0003t0004g0314 a0003c0003t0004g0315 others(1): Show |
4 | HG01109.hp1 HG02717.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1399-2094C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 10/13 | chr11 | 112049140 | |||||||
| chr11:112049146 | A | AT | 17 | a0004c0004t0003g0033 a0004c0004t0003g0034 a0004c0004t0003g0035 others(14): Show |
17 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1399-2082dupT | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 112049146 | ||||||
| chr11:112049230 | G | C | 1 | a0003c0003t0018g0202 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1399-2004G>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 10/13 | chr11 | 112049230 | |||||||
| chr11:112049247 | C | G | 1 | a0003c0003t0004g0317 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1399-1987C>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 10/13 | chr11 | 112049247 | |||||||
| chr11:112049450 | T | A | 1 | a0001c0001t0001g0111 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1399-1784T>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 10/13 | chr11 | 112049450 | |||||||
| chr11:112049572 | AT | A | 15 | a0002c0002t0002g0248 a0002c0002t0002g0251 a0002c0002t0002g0292 others(12): Show |
15 | HG01884.hp2 HG01952.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1399-1647delT | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 112049572 | ||||||
| chr11:112049741 | T | C | 2 | a0003c0003t0007g0052 a0003c0003t0007g0073 |
2 | HG03130.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1399-1493T>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 10/13 | chr11 | 112049741 | |||||||
| chr11:112049866 | A | T | 1 | a0001c0001t0001g0154 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1399-1368A>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 10/13 | chr11 | 112049866 | |||||||
| chr11:112049967 | C | T | 322 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(319): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1399-1267C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 10/13 | chr11 | 112049967 | |||||||
| chr11:112050017 | A | G | 197 | a0001c0001t0007g0089 a0001c0001t0007g0134 a0001c0001t0007g0135 others(194): Show |
202 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(199): Show |
intron_variant | MODIFIER | c.1399-1217A>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 10/13 | chr11 | 112050017 | |||||||
| chr11:112050025 | G | A | 1 | a0003c0003t0016g0047 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1399-1209G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 10/13 | chr11 | 112050025 | |||||||
| chr11:112050274 | G | A | 3 | a0003c0003t0006g0180 a0003c0003t0006g0181 a0003c0003t0006g0182 |
3 | HG02809.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1399-960G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 10/13 | chr11 | 112050274 | |||||||
| chr11:112050322 | CT | C | 14 | a0001c0001t0007g0089 a0001c0001t0007g0134 a0001c0001t0007g0135 others(11): Show |
14 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.1399-898delT | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 112050322 | ||||||
| chr11:112050377 | G | A | 1 | a0005c0005t0005g0008 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1399-857G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 10/13 | chr11 | 112050377 | |||||||
| chr11:112050384 | C | T | 197 | a0001c0001t0007g0089 a0001c0001t0007g0134 a0001c0001t0007g0135 others(194): Show |
202 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(199): Show |
intron_variant | MODIFIER | c.1399-850C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 10/13 | chr11 | 112050384 | |||||||
| chr11:112050488 | G | A | 2 | a0007c0007t0003g0203 a0007c0007t0003g0204 |
2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1399-746G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 10/13 | chr11 | 112050488 | |||||||
| chr11:112050889 | G | A | 7 | a0004c0004t0003g0033 a0004c0004t0003g0034 a0004c0004t0003g0035 others(4): Show |
7 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1399-345G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 10/13 | chr11 | 112050889 | |||||||
| chr11:112051129 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1399-105G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 10/13 | chr11 | 112051129 | |||||||
| chr11:112051169 | C | T | 2 | a0002c0002t0002g0267 a0002c0002t0002g0268 |
2 | NA18956.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.1399-65C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 10/13 | chr11 | 112051169 | |||||||
| chr11:112051182 | A | C | 2 | a0007c0007t0003g0203 a0007c0007t0003g0204 |
2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1399-52A>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 10/13 | chr11 | 112051182 | |||||||
| chr11:112051568 | T | G | 3 | a0002c0002t0002g0233 a0002c0002t0002g0234 a0002c0002t0002g0239 |
3 | HG02109.hp2 HG02257.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1514+219T>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112051568 | |||||||
| chr11:112051836 | C | T | 1 | a0003c0003t0016g0047 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1514+487C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112051836 | |||||||
| chr11:112052241 | C | A | 1 | a0003c0003t0018g0202 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1514+892C>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112052241 | |||||||
| chr11:112052268 | G | A | 10 | a0004c0004t0003g0192 a0004c0004t0003g0194 a0004c0004t0003g0195 others(7): Show |
10 | HG01884.hp2 HG02145.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1514+919G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112052268 | |||||||
| chr11:112052319 | A | G | 6 | a0003c0003t0003g0009 a0003c0003t0009g0199 a0003c0003t0009g0200 others(3): Show |
6 | HG01952.hp2 HG02970.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1514+970A>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112052319 | |||||||
| chr11:112052377 | T | TG | 12 | a0005c0005t0005g0008 a0005c0005t0005g0055 a0005c0005t0005g0056 others(9): Show |
12 | HG01243.hp1 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1514+1029dupG | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 112052377 | ||||||
| chr11:112052505 | T | C | 1 | a0001c0001t0001g0081 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1514+1156T>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112052505 | |||||||
| chr11:112052589 | G | A | 10 | a0004c0004t0003g0192 a0004c0004t0003g0194 a0004c0004t0003g0195 others(7): Show |
10 | HG01884.hp2 HG02145.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1514+1240G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112052589 | |||||||
| chr11:112052635 | G | A | 1 | a0002c0002t0002g0217 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1514+1286G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112052635 | |||||||
| chr11:112052886 | G | A | 21 | a0003c0003t0003g0062 a0003c0003t0003g0063 a0004c0004t0003g0033 others(18): Show |
21 | HG00733.hp2 HG01099.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.1514+1537G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112052886 | |||||||
| chr11:112052909 | G | A | 7 | a0002c0002t0002g0252 a0002c0002t0002g0253 a0002c0002t0002g0254 others(4): Show |
7 | HG00597.hp1 NA18968.hp2 NA18974.hp2 others(4): Show |
intron_variant | MODIFIER | c.1514+1560G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112052909 | |||||||
| chr11:112052919 | A | C | 6 | a0003c0003t0003g0009 a0003c0003t0009g0199 a0003c0003t0009g0200 others(3): Show |
6 | HG01952.hp2 HG02970.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1514+1570A>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112052919 | |||||||
| chr11:112052955 | G | A | 1 | a0008c0008t0003g0191 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1514+1606G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112052955 | |||||||
| chr11:112052980 | C | A | 2 | a0005c0005t0005g0055 a0005c0005t0005g0056 |
2 | HG02886.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1514+1631C>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112052980 | |||||||
| chr11:112052990 | G | A | 4 | a0003c0003t0007g0040 a0003c0003t0007g0041 a0003c0003t0007g0042 others(1): Show |
4 | HG02257.hp2 HG02258.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1514+1641G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112052990 | |||||||
| chr11:112053111 | C | T | 21 | a0003c0003t0004g0011 a0003c0003t0004g0012 a0003c0003t0004g0013 others(18): Show |
21 | HG00738.hp1 HG01099.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.1514+1762C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112053111 | |||||||
| chr11:112053313 | A | G | 1 | a0003c0003t0004g0315 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1514+1964A>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112053313 | |||||||
| chr11:112053485 | T | C | 41 | a0003c0003t0003g0009 a0003c0003t0003g0053 a0003c0003t0003g0054 others(38): Show |
41 | HG00733.hp2 HG01099.hp1 HG01243.hp1 others(38): Show |
intron_variant | MODIFIER | c.1514+2136T>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112053485 | |||||||
| chr11:112053533 | A | G | 7 | a0004c0004t0003g0033 a0004c0004t0003g0034 a0004c0004t0003g0035 others(4): Show |
7 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1514+2184A>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112053533 | |||||||
| chr11:112053906 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1514+2557C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112053906 | |||||||
| chr11:112053961 | T | A | 2 | a0002c0002t0002g0281 a0002c0002t0017g0229 |
2 | HG00558.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.1514+2612T>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112053961 | |||||||
| chr11:112054033 | G | T | 1 | a0007c0007t0003g0204 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1514+2684G>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112054033 | |||||||
| chr11:112054047 | A | T | 10 | a0003c0003t0006g0002 a0003c0003t0006g0050 a0003c0003t0006g0072 others(7): Show |
12 | HG02723.hp1 HG02809.hp1 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.1514+2698A>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112054047 | |||||||
| chr11:112054088 | C | T | 7 | a0004c0004t0003g0033 a0004c0004t0003g0034 a0004c0004t0003g0035 others(4): Show |
7 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1514+2739C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112054088 | |||||||
| chr11:112054186 | C | T | 1 | a0002c0002t0002g0237 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1514+2837C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112054186 | |||||||
| chr11:112054198 | C | T | 1 | a0002c0002t0002g0280 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1514+2849C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112054198 | |||||||
| chr11:112054248 | G | A | 1 | a0003c0003t0014g0187 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1514+2899G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112054248 | |||||||
| chr11:112054283 | G | C | 1 | a0006c0006t0001g0083 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1514+2934G>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112054283 | |||||||
| chr11:112054284 | C | A | 1 | a0006c0006t0001g0083 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1514+2935C>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112054284 | |||||||
| chr11:112054286 | C | T | 1 | a0006c0006t0001g0083 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1514+2937C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112054286 | |||||||
| chr11:112054287 | T | C | 1 | a0006c0006t0001g0083 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1514+2938T>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112054287 | |||||||
| chr11:112054320 | AAAT | A | 12 | a0003c0003t0006g0002 a0003c0003t0006g0050 a0003c0003t0006g0072 others(9): Show |
14 | HG02572.hp2 HG02723.hp1 HG02809.hp1 others(11): Show |
intron_variant | MODIFIER | c.1514+2986_1514+298 others(7): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 112054320 | ||||||
| chr11:112054525 | G | C | 12 | a0005c0005t0005g0008 a0005c0005t0005g0055 a0005c0005t0005g0056 others(9): Show |
12 | HG01243.hp1 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1514+3176G>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112054525 | |||||||
| chr11:112054734 | T | C | 2 | a0003c0003t0003g0053 a0003c0003t0003g0054 |
2 | HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1514+3385T>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112054734 | |||||||
| chr11:112054958 | T | C | 2 | a0001c0001t0001g0045 a0001c0001t0001g0099 |
2 | NA18947.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.1514+3609T>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112054958 | |||||||
| chr11:112055190 | G | C | 1 | a0008c0008t0003g0190 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1514+3841G>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112055190 | |||||||
| chr11:112055235 | A | AT | 125 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.1514+3912dupT | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 112055235 | ||||||
| chr11:112055235 | A | ATT | 24 | a0001c0001t0001g0071 a0001c0001t0001g0080 a0001c0001t0001g0087 others(21): Show |
24 | HG00597.hp2 HG00621.hp2 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.1514+3911_1514+391 others(6): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 112055235 | ||||||
| chr11:112055235 | AT | A | 37 | a0002c0002t0002g0223 a0002c0002t0002g0255 a0003c0003t0003g0009 others(34): Show |
37 | HG00733.hp2 HG00738.hp1 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.1514+3912delT | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 112055235 | ||||||
| chr11:112055235 | ATT | A | 6 | a0003c0003t0003g0053 a0003c0003t0003g0054 a0003c0003t0003g0062 others(3): Show |
6 | HG02451.hp2 HG02572.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1514+3911_1514+391 others(6): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 112055235 | ||||||
| chr11:112055235 | ATTT | A | 11 | a0005c0005t0005g0008 a0005c0005t0005g0055 a0005c0005t0005g0056 others(8): Show |
11 | HG01243.hp1 HG01891.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1514+3910_1514+391 others(7): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 112055235 | ||||||
| chr11:112055304 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1514+3955C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112055304 | |||||||
| chr11:112055348 | G | C | 113 | a0002c0002t0002g0005 a0002c0002t0002g0006 a0002c0002t0002g0007 others(110): Show |
116 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.1514+3999G>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112055348 | |||||||
| chr11:112055368 | C | T | 2 | a0002c0002t0002g0273 a0002c0002t0002g0292 |
2 | NA19054.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.1514+4019C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112055368 | |||||||
| chr11:112055385 | A | C | 1 | a0002c0002t0002g0250 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1514+4036A>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112055385 | |||||||
| chr11:112055392 | C | T | 12 | a0003c0003t0006g0002 a0003c0003t0006g0050 a0003c0003t0006g0072 others(9): Show |
14 | HG02572.hp2 HG02723.hp1 HG02809.hp1 others(11): Show |
intron_variant | MODIFIER | c.1514+4043C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112055392 | |||||||
| chr11:112055400 | C | T | 1 | a0001c0001t0001g0147 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1514+4051C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112055400 | |||||||
| chr11:112055562 | T | C | 1 | a0001c0001t0001g0148 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1514+4213T>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112055562 | |||||||
| chr11:112055614 | C | G | 9 | a0002c0002t0002g0061 a0002c0002t0002g0238 a0002c0002t0002g0249 others(6): Show |
9 | HG00609.hp1 NA18957.hp1 NA19055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1514+4265C>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112055614 | |||||||
| chr11:112055692 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1515-4211T>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112055692 | |||||||
| chr11:112055804 | T | C | 125 | a0002c0002t0002g0005 a0002c0002t0002g0006 a0002c0002t0002g0007 others(122): Show |
130 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(127): Show |
intron_variant | MODIFIER | c.1515-4099T>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112055804 | |||||||
| chr11:112055848 | C | CT | 49 | a0001c0001t0001g0080 a0001c0001t0001g0084 a0001c0001t0001g0099 others(46): Show |
52 | HG00558.hp2 HG00741.hp2 HG01070.hp1 others(49): Show |
intron_variant | MODIFIER | c.1515-4017dupT | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 112055848 | ||||||
| chr11:112055848 | C | CTT | 46 | a0001c0001t0001g0087 a0001c0001t0001g0107 a0001c0001t0001g0118 others(43): Show |
47 | HG00544.hp2 HG00609.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.1515-4018_1515-401 others(6): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 112055848 | ||||||
| chr11:112055848 | C | CTTT | 26 | a0001c0001t0001g0153 a0002c0002t0002g0007 a0002c0002t0002g0214 others(23): Show |
27 | HG00140.hp2 HG00408.hp2 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.1515-4019_1515-401 others(7): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 112055848 | ||||||
| chr11:112055848 | C | CTTTT | 9 | a0001c0001t0001g0131 a0002c0002t0002g0261 a0002c0002t0002g0308 others(6): Show |
9 | HG00733.hp1 HG01109.hp1 HG02148.hp1 others(6): Show |
intron_variant | MODIFIER | c.1515-4020_1515-401 others(8): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 112055848 | ||||||
| chr11:112055848 | C | CTTTTTTT others(2): Show |
7 | a0002c0002t0002g0254 a0002c0002t0002g0297 a0003c0003t0004g0012 others(4): Show |
7 | HG00597.hp1 HG01358.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1515-4025_1515-401 others(13): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 112055848 | ||||||
| chr11:112055848 | C | CTTTTTTT others(3): Show |
2 | a0003c0003t0004g0017 a0003c0003t0004g0025 |
2 | HG02922.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1515-4026_1515-401 others(14): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 112055848 | ||||||
| chr11:112055848 | C | CTTTTTTT others(4): Show |
3 | a0003c0003t0004g0022 a0003c0003t0004g0023 a0003c0003t0007g0041 |
3 | HG00738.hp1 HG01099.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1515-4027_1515-401 others(15): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 112055848 | ||||||
| chr11:112055848 | C | CTTTTTTT others(6): Show |
2 | a0002c0002t0002g0058 a0003c0003t0004g0016 |
2 | HG01167.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1515-4029_1515-401 others(17): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 112055848 | ||||||
| chr11:112055848 | C | CTTTTTTT others(7): Show |
1 | a0003c0003t0004g0011 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1515-4030_1515-401 others(18): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 112055848 | ||||||
| chr11:112055848 | CT | C | 55 | a0001c0001t0001g0001 a0001c0001t0001g0051 a0001c0001t0001g0064 others(52): Show |
58 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.1515-4017delT | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 112055848 | ||||||
| chr11:112055848 | CTT | C | 11 | a0001c0001t0001g0044 a0001c0001t0001g0079 a0001c0001t0001g0090 others(8): Show |
11 | HG01069.hp1 HG01071.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.1515-4018_1515-401 others(6): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 112055848 | ||||||
| chr11:112055848 | CTTTTTTT others(3): Show |
C | 3 | a0004c0004t0003g0195 a0004c0004t0003g0196 a0004c0004t0003g0197 |
3 | HG02280.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1515-4026_1515-401 others(14): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 112055848 | ||||||
| chr11:112055848 | CTTTTTTT others(4): Show |
C | 3 | a0004c0004t0003g0194 a0005c0005t0005g0205 a0005c0005t0005g0324 |
3 | HG01884.hp2 HG02145.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1515-4027_1515-401 others(15): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 112055848 | ||||||
| chr11:112055848 | CTTTTTTT others(5): Show |
C | 16 | a0003c0003t0006g0072 a0004c0004t0003g0037 a0004c0004t0003g0192 others(13): Show |
16 | HG01243.hp1 HG01891.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.1515-4028_1515-401 others(16): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 112055848 | ||||||
| chr11:112055848 | CTTTTTTT others(6): Show |
C | 10 | a0001c0001t0001g0148 a0003c0003t0004g0316 a0003c0003t0014g0187 others(7): Show |
10 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1515-4029_1515-401 others(17): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 112055848 | ||||||
| chr11:112055848 | CTTTTTTT others(7): Show |
C | 7 | a0002c0002t0002g0256 a0003c0003t0003g0009 a0003c0003t0003g0053 others(4): Show |
7 | HG01952.hp2 HG02056.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1515-4030_1515-401 others(18): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 112055848 | ||||||
| chr11:112055848 | CTTTTTTT others(8): Show |
C | 4 | a0003c0003t0003g0054 a0003c0003t0003g0062 a0003c0003t0003g0063 others(1): Show |
4 | HG02717.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1515-4031_1515-401 others(19): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 112055848 | ||||||
| chr11:112055848 | CTTTTTTT others(10): Show |
C | 2 | a0007c0007t0003g0203 a0007c0007t0003g0204 |
2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1515-4033_1515-401 others(21): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 112055848 | ||||||
| chr11:112055848 | CTTTTTTT others(12): Show |
C | 2 | a0001c0001t0001g0160 a0003c0003t0007g0052 |
2 | HG02738.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1515-4035_1515-401 others(23): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 112055848 | ||||||
| chr11:112055888 | A | T | 1 | a0006c0006t0001g0077 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1515-4015A>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112055888 | |||||||
| chr11:112055949 | C | T | 3 | a0003c0003t0009g0199 a0003c0003t0009g0200 a0003c0003t0009g0201 |
3 | HG01952.hp2 HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1515-3954C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112055949 | |||||||
| chr11:112055954 | G | A | 1 | a0003c0003t0016g0047 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1515-3949G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112055954 | |||||||
| chr11:112055960 | C | T | 2 | a0003c0003t0003g0062 a0003c0003t0003g0063 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1515-3943C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112055960 | |||||||
| chr11:112056060 | A | G | 41 | a0003c0003t0003g0009 a0003c0003t0003g0053 a0003c0003t0003g0054 others(38): Show |
41 | HG00733.hp2 HG01099.hp1 HG01243.hp1 others(38): Show |
intron_variant | MODIFIER | c.1515-3843A>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112056060 | |||||||
| chr11:112056145 | A | G | 2 | a0001c0001t0001g0069 a0001c0001t0001g0070 |
2 | HG01123.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.1515-3758A>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112056145 | |||||||
| chr11:112056392 | C | T | 4 | a0005c0005t0005g0205 a0005c0005t0005g0207 a0005c0005t0005g0212 others(1): Show |
4 | HG01891.hp1 HG02145.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1515-3511C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112056392 | |||||||
| chr11:112056555 | T | G | 2 | a0001c0001t0001g0086 a0001c0001t0001g0171 |
2 | HG02698.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1515-3348T>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112056555 | |||||||
| chr11:112056639 | AT | A | 113 | a0002c0002t0002g0005 a0002c0002t0002g0006 a0002c0002t0002g0007 others(110): Show |
116 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.1515-3263delT | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112056639 | |||||||
| chr11:112056836 | G | T | 1 | a0002c0002t0002g0250 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1515-3067G>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112056836 | |||||||
| chr11:112056996 | G | A | 2 | a0003c0003t0003g0053 a0003c0003t0003g0054 |
2 | HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1515-2907G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112056996 | |||||||
| chr11:112057047 | G | A | 266 | a0001c0001t0001g0044 a0001c0001t0001g0051 a0001c0001t0001g0064 others(263): Show |
271 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.1515-2856G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112057047 | |||||||
| chr11:112057057 | T | C | 1 | a0001c0001t0001g0169 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1515-2846T>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112057057 | |||||||
| chr11:112057291 | A | G | 12 | a0005c0005t0005g0008 a0005c0005t0005g0055 a0005c0005t0005g0056 others(9): Show |
12 | HG01243.hp1 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1515-2612A>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112057291 | |||||||
| chr11:112057329 | C | T | 2 | a0001c0001t0001g0074 a0001c0001t0001g0103 |
2 | HG00099.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.1515-2574C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112057329 | |||||||
| chr11:112057439 | T | C | 2 | a0001c0001t0001g0112 a0001c0001t0001g0148 |
2 | HG02602.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1515-2464T>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112057439 | |||||||
| chr11:112057483 | C | T | 4 | a0003c0003t0007g0040 a0003c0003t0007g0041 a0003c0003t0007g0042 others(1): Show |
4 | HG02257.hp2 HG02258.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1515-2420C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112057483 | |||||||
| chr11:112057502 | T | C | 29 | a0003c0003t0003g0009 a0003c0003t0003g0053 a0003c0003t0003g0054 others(26): Show |
29 | HG00733.hp2 HG01099.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1515-2401T>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112057502 | |||||||
| chr11:112057515 | C | T | 2 | a0003c0003t0003g0053 a0003c0003t0003g0054 |
2 | HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1515-2388C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112057515 | |||||||
| chr11:112057545 | G | A | 2 | a0007c0007t0003g0203 a0007c0007t0003g0204 |
2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1515-2358G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112057545 | |||||||
| chr11:112057630 | T | C | 1 | a0002c0002t0002g0289 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1515-2273T>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112057630 | |||||||
| chr11:112057728 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1515-2175A>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112057728 | |||||||
| chr11:112057782 | G | GATATCCC others(16): Show |
2 | a0002c0002t0002g0226 a0002c0002t0011g0227 |
2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1515-2118_1515-209 others(27): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 112057782 | ||||||
| chr11:112057864 | A | G | 1 | a0003c0003t0007g0048 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1515-2039A>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112057864 | |||||||
| chr11:112057933 | G | A | 7 | a0004c0004t0003g0033 a0004c0004t0003g0034 a0004c0004t0003g0035 others(4): Show |
7 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1515-1970G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112057933 | |||||||
| chr11:112057984 | G | A | 12 | a0005c0005t0005g0008 a0005c0005t0005g0055 a0005c0005t0005g0056 others(9): Show |
12 | HG01243.hp1 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1515-1919G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112057984 | |||||||
| chr11:112058307 | C | G | 1 | a0001c0001t0001g0159 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1515-1596C>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112058307 | |||||||
| chr11:112058391 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1515-1512T>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112058391 | |||||||
| chr11:112058432 | A | C | 1 | a0002c0002t0002g0296 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1515-1471A>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112058432 | |||||||
| chr11:112058515 | C | T | 21 | a0003c0003t0003g0062 a0003c0003t0003g0063 a0004c0004t0003g0033 others(18): Show |
21 | HG00733.hp2 HG01099.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.1515-1388C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112058515 | |||||||
| chr11:112058589 | C | T | 12 | a0005c0005t0005g0008 a0005c0005t0005g0055 a0005c0005t0005g0056 others(9): Show |
12 | HG01243.hp1 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1515-1314C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112058589 | |||||||
| chr11:112058616 | A | AG | 64 | a0001c0001t0001g0044 a0001c0001t0001g0051 a0001c0001t0001g0065 others(61): Show |
66 | HG00140.hp1 HG00408.hp1 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.1515-1279dupG | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 112058616 | ||||||
| chr11:112058616 | A | AGG | 23 | a0001c0001t0001g0071 a0001c0001t0001g0095 a0001c0001t0001g0111 others(20): Show |
23 | HG00099.hp2 HG00735.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.1515-1280_1515-127 others(6): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 112058616 | ||||||
| chr11:112058618 | G | A | 11 | a0001c0001t0001g0098 a0001c0001t0001g0104 a0004c0004t0003g0194 others(8): Show |
11 | HG01884.hp2 HG02145.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1515-1285G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112058618 | |||||||
| chr11:112058623 | G | GGGT | 40 | a0002c0002t0002g0010 a0002c0002t0002g0057 a0002c0002t0002g0058 others(37): Show |
40 | HG00735.hp1 HG00741.hp2 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.1515-1279_1515-127 others(7): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 112058623 | ||||||
| chr11:112058624 | G | GGGT | 27 | a0001c0001t0001g0067 a0001c0001t0001g0079 a0001c0001t0001g0118 others(24): Show |
27 | HG00558.hp2 HG00597.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.1515-1279_1515-127 others(7): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112058624 | |||||||
| chr11:112058624 | G | GGT | 64 | a0001c0001t0001g0070 a0001c0001t0001g0090 a0001c0001t0001g0110 others(61): Show |
67 | HG00609.hp1 HG00609.hp2 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.1515-1279_1515-127 others(6): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112058624 | |||||||
| chr11:112058625 | T | G | 189 | a0001c0001t0001g0064 a0001c0001t0001g0066 a0001c0001t0001g0067 others(186): Show |
192 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(189): Show |
intron_variant | MODIFIER | c.1515-1278T>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112058625 | |||||||
| chr11:112058626 | G | GT | 16 | a0001c0001t0001g0068 a0001c0001t0001g0158 a0003c0003t0003g0009 others(13): Show |
16 | HG00544.hp1 HG01243.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.1515-1277_1515-127 others(5): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112058626 | |||||||
| chr11:112058626 | G | T | 22 | a0001c0001t0001g0064 a0001c0001t0001g0066 a0003c0003t0003g0062 others(19): Show |
22 | HG01884.hp2 HG01952.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1515-1277G>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112058626 | |||||||
| chr11:112058631 | G | C | 1 | a0003c0003t0018g0202 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1515-1272G>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112058631 | |||||||
| chr11:112058635 | G | A | 1 | a0003c0003t0003g0054 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1515-1268G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112058635 | |||||||
| chr11:112058636 | A | G | 1 | a0003c0003t0004g0018 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1515-1267A>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112058636 | |||||||
| chr11:112058642 | CT | C | 30 | a0001c0001t0001g0123 a0003c0003t0003g0009 a0003c0003t0003g0053 others(27): Show |
30 | HG00733.hp2 HG01099.hp1 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.1515-1250delT | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 112058642 | ||||||
| chr11:112059048 | G | A | 1 | a0003c0003t0007g0073 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1515-855G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112059048 | |||||||
| chr11:112059051 | TA | T | 6 | a0001c0001t0001g0112 a0001c0001t0001g0114 a0001c0001t0001g0148 others(3): Show |
6 | HG01884.hp1 HG02602.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1515-838delA | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 112059051 | ||||||
| chr11:112059074 | C | A | 41 | a0003c0003t0003g0009 a0003c0003t0003g0053 a0003c0003t0003g0054 others(38): Show |
41 | HG00733.hp2 HG01099.hp1 HG01243.hp1 others(38): Show |
intron_variant | MODIFIER | c.1515-829C>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112059074 | |||||||
| chr11:112059187 | C | T | 12 | a0005c0005t0005g0008 a0005c0005t0005g0055 a0005c0005t0005g0056 others(9): Show |
12 | HG01243.hp1 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1515-716C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112059187 | |||||||
| chr11:112059229 | T | G | 2 | a0003c0003t0003g0062 a0003c0003t0003g0063 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1515-674T>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112059229 | |||||||
| chr11:112059278 | C | T | 1 | a0003c0003t0003g0009 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1515-625C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112059278 | |||||||
| chr11:112059353 | C | CT | 13 | a0001c0001t0001g0098 a0001c0001t0001g0122 a0001c0001t0001g0156 others(10): Show |
13 | HG00621.hp1 HG01934.hp1 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.1515-532dupT | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 112059353 | ||||||
| chr11:112059424 | G | A | 1 | a0002c0002t0002g0299 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1515-479G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112059424 | |||||||
| chr11:112059594 | T | C | 1 | a0002c0002t0002g0321 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1515-309T>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112059594 | |||||||
| chr11:112059656 | G | A | 1 | a0003c0003t0014g0187 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1515-247G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112059656 | |||||||
| chr11:112059689 | G | A | 27 | a0003c0003t0004g0011 a0003c0003t0004g0012 a0003c0003t0004g0013 others(24): Show |
27 | HG00738.hp1 HG01099.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.1515-214G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112059689 | |||||||
| chr11:112059810 | A | T | 1 | a0001c0001t0001g0154 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1515-93A>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112059810 | |||||||
| chr11:112059852 | C | T | 173 | a0002c0002t0002g0005 a0002c0002t0002g0006 a0002c0002t0002g0007 others(170): Show |
178 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(175): Show |
intron_variant | MODIFIER | c.1515-51C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 11/13 | chr11 | 112059852 | |||||||
| chr11:112060158 | A | AT | 44 | a0001c0001t0001g0044 a0001c0001t0001g0079 a0001c0001t0001g0080 others(41): Show |
44 | HG01081.hp2 HG01106.hp2 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.1677+116dupT | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr11 | 112060158 | ||||||
| chr11:112060158 | AT | A | 17 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0158 others(14): Show |
17 | HG00544.hp1 HG00733.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.1677+116delT | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr11 | 112060158 | ||||||
| chr11:112060158 | ATT | A | 13 | a0003c0003t0003g0009 a0003c0003t0003g0053 a0003c0003t0003g0054 others(10): Show |
13 | HG02280.hp2 HG02486.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.1677+115_1677+116d others(4): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr11 | 112060158 | ||||||
| chr11:112060451 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1677+386C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 12/13 | chr11 | 112060451 | |||||||
| chr11:112060458 | C | T | 12 | a0005c0005t0005g0008 a0005c0005t0005g0055 a0005c0005t0005g0056 others(9): Show |
12 | HG01243.hp1 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1677+393C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 12/13 | chr11 | 112060458 | |||||||
| chr11:112060459 | G | A | 2 | a0003c0003t0003g0053 a0003c0003t0003g0054 |
2 | HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1677+394G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 12/13 | chr11 | 112060459 | |||||||
| chr11:112060782 | T | C | 1 | a0003c0003t0004g0021 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1678-256T>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 12/13 | chr11 | 112060782 | |||||||
| chr11:112060802 | T | C | 1 | a0001c0001t0001g0084 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1678-236T>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 12/13 | chr11 | 112060802 | |||||||
| chr11:112060803 | A | G | 1 | a0002c0002t0002g0233 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1678-235A>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 12/13 | chr11 | 112060803 | |||||||
| chr11:112060899 | C | A | 1 | a0002c0002t0002g0268 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1678-139C>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 12/13 | chr11 | 112060899 | |||||||
| chr11:112061006 | C | CAA | 41 | a0003c0003t0003g0009 a0003c0003t0003g0053 a0003c0003t0003g0054 others(38): Show |
41 | HG00733.hp2 HG01099.hp1 HG01243.hp1 others(38): Show |
intron_variant | MODIFIER | c.1678-32_1678-31ins others(2): Show |
DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 12/13 | chr11 | 112061006 | |||||||
| chr11:112061648 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1814+474G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 13/13 | chr11 | 112061648 | |||||||
| chr11:112061893 | T | G | 11 | a0003c0003t0006g0002 a0003c0003t0006g0050 a0003c0003t0006g0072 others(8): Show |
13 | HG02572.hp2 HG02723.hp1 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.1815-513T>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 13/13 | chr11 | 112061893 | |||||||
| chr11:112061952 | A | T | 1 | a0001c0001t0001g0129 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1815-454A>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 13/13 | chr11 | 112061952 | |||||||
| chr11:112061959 | C | T | 1 | a0002c0002t0002g0320 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1815-447C>T | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 13/13 | chr11 | 112061959 | |||||||
| chr11:112062033 | G | A | 2 | a0002c0002t0002g0266 a0002c0002t0002g0300 |
2 | HG00140.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1815-373G>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 13/13 | chr11 | 112062033 | |||||||
| chr11:112062095 | T | A | 1 | a0002c0002t0002g0271 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1815-311T>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 13/13 | chr11 | 112062095 | |||||||
| chr11:112062218 | C | A | 2 | a0003c0003t0003g0053 a0003c0003t0003g0054 |
2 | HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1815-188C>A | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 13/13 | chr11 | 112062218 | |||||||
| chr11:112062355 | A | C | 1 | a0005c0013t0005g0210 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1815-51A>C | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 13/13 | chr11 | 112062355 | |||||||
| chr11:112062364 | A | G | 118 | a0001c0001t0007g0089 a0001c0001t0007g0134 a0001c0001t0007g0135 others(115): Show |
121 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.1815-42A>G | DLAT | ENSG00000150768.18 | transcript | ENST00000280346.11 | protein_coding | 13/13 | chr11 | 112062364 |