Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9941 |
| ensemblid | ENSG00000157036.13 |
| hgncid | 3347 |
| symbol | EXOG |
| name | exo/endonuclease G |
| refseq_nuc | NM_005107.4 |
| refseq_prot | NP_005098.2 |
| ensembl_nuc | ENST00000287675.10 |
| ensembl_prot | ENSP00000287675.5 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 38496340 |
| end | 38526303 |
| strand | + |
| ver | v1.2 |
| region | chr3:38496340-38526303 |
| region5000 | chr3:38491340-38531303 |
| regionname0 | EXOG_chr3_38496340_38526303 |
| regionname5000 | EXOG_chr3_38491340_38531303 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 368 | 408 | 92 | 74 | 190 | 10 | 40 | 155 | EXOG_chr3_38491340_38531303 | EXOG | MAIKS others(363): Show |
chr3 | 38491340 | 38531303 |
| a0002 | 0/0 | 368 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | MAIKS others(363): Show |
chr3 | 38491340 | 38531303 |
| a0003 | 0/0 | 368 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EXOG_chr3_38491340_38531303 | EXOG | MAIKS others(363): Show |
chr3 | 38491340 | 38531303 |
| a0004 | 0/0 | 368 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EXOG_chr3_38491340_38531303 | EXOG | MAIKS others(363): Show |
chr3 | 38491340 | 38531303 |
| a0005 | 0/0 | 92 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EXOG_chr3_38491340_38531303 | EXOG | MAIKS others(87): Show |
chr3 | 38491340 | 38531303 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1104 | 406 | 90 | 74 | 190 | 10 | 40 | EXOG_chr3_38491340_38531303 | EXOG | ATGGC others(1099): Show |
chr3 | 38491340 | 38531303 | ||
| a0001c0002 | 0/0 | 1104 | 2 | 2 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | ATGGC others(1099): Show |
chr3 | 38491340 | 38531303 | ||
| a0002c0005 | 0/0 | 1104 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | ATGGC others(1099): Show |
chr3 | 38491340 | 38531303 | ||
| a0003c0006 | 0/0 | 1104 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | ATGGC others(1099): Show |
chr3 | 38491340 | 38531303 | ||
| a0004c0004 | 0/0 | 1104 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | ATGGC others(1099): Show |
chr3 | 38491340 | 38531303 | ||
| a0005c0003 | 0/0 | 1104 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | ATGGC others(1099): Show |
chr3 | 38491340 | 38531303 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3076 | 189 | 42 | 42 | 84 | 5 | 16 | EXOG_chr3_38491340_38531303 | EXOG | GTGGT others(3071): Show |
chr3 | 38491340 | 38531303 |
| a0001c0001t0002 | 1/1 | 3076 | 110 | 11 | 15 | 61 | 5 | 16 | EXOG_chr3_38491340_38531303 | EXOG | GTGGT others(3071): Show |
chr3 | 38491340 | 38531303 |
| a0001c0001t0003 | 0/0 | 3076 | 42 | 8 | 7 | 20 | 0 | 7 | EXOG_chr3_38491340_38531303 | EXOG | GTGGT others(3071): Show |
chr3 | 38491340 | 38531303 |
| a0001c0001t0004 | 0/0 | 3076 | 23 | 0 | 0 | 22 | 0 | 1 | EXOG_chr3_38491340_38531303 | EXOG | GTGGT others(3071): Show |
chr3 | 38491340 | 38531303 |
| a0001c0001t0005 | 0/0 | 3076 | 11 | 11 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | GTGGT others(3071): Show |
chr3 | 38491340 | 38531303 |
| a0001c0001t0006 | 0/0 | 3076 | 8 | 7 | 1 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | GTGGT others(3071): Show |
chr3 | 38491340 | 38531303 |
| a0001c0001t0007 | 0/0 | 3076 | 4 | 0 | 4 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | GTGGT others(3071): Show |
chr3 | 38491340 | 38531303 |
| a0001c0001t0008 | 0/0 | 3076 | 4 | 2 | 2 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | GTGGT others(3071): Show |
chr3 | 38491340 | 38531303 |
| a0001c0001t0009 | 0/0 | 3076 | 3 | 3 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | GTGGT others(3071): Show |
chr3 | 38491340 | 38531303 |
| a0001c0001t0010 | 0/0 | 3076 | 3 | 3 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | GTGGT others(3071): Show |
chr3 | 38491340 | 38531303 |
| a0001c0001t0011 | 0/0 | 3076 | 2 | 0 | 2 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | GTGGT others(3071): Show |
chr3 | 38491340 | 38531303 |
| a0001c0001t0012 | 0/0 | 3076 | 2 | 1 | 1 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | GTGGT others(3071): Show |
chr3 | 38491340 | 38531303 |
| a0001c0001t0013 | 0/0 | 3076 | 1 | 1 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | GTGGT others(3071): Show |
chr3 | 38491340 | 38531303 |
| a0001c0001t0014 | 0/0 | 3076 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | GTGGT others(3071): Show |
chr3 | 38491340 | 38531303 |
| a0001c0001t0015 | 0/0 | 3076 | 1 | 1 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | GTGGT others(3071): Show |
chr3 | 38491340 | 38531303 |
| a0001c0001t0016 | 0/0 | 3076 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | GTGGT others(3071): Show |
chr3 | 38491340 | 38531303 |
| a0001c0001t0017 | 0/0 | 3076 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | GTGGT others(3071): Show |
chr3 | 38491340 | 38531303 |
| a0001c0002t0001 | 0/0 | 3076 | 2 | 2 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | GTGGT others(3071): Show |
chr3 | 38491340 | 38531303 |
| a0002c0005t0003 | 0/0 | 3076 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | GTGGT others(3071): Show |
chr3 | 38491340 | 38531303 |
| a0003c0006t0003 | 0/0 | 3076 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | GTGGT others(3071): Show |
chr3 | 38491340 | 38531303 |
| a0004c0004t0002 | 0/0 | 3076 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | GTGGT others(3071): Show |
chr3 | 38491340 | 38531303 |
| a0005c0003t0003 | 0/0 | 3076 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | GTGGT others(3071): Show |
chr3 | 38491340 | 38531303 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 10 | 2 | 0 | 7 | 1 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0004 | 0/0 | 13 | 0 | 3 | 9 | 0 | 1 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0005 | 0/0 | 9 | 2 | 6 | 0 | 0 | 1 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0008 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0009 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 0 | 0 | 0 | 4 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0014 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0015 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0017 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0018 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 1 | 1 | 1 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0031 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0050 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0053 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0054 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0055 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0057 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0058 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0002g0001 | 1/0 | 42 | 1 | 9 | 22 | 1 | 8 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0002g0006 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0002g0007 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0002g0011 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0002g0023 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0002g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0002g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0002g0076 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0003g0003 | 0/0 | 13 | 0 | 0 | 9 | 0 | 4 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0003g0019 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0003g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0003g0029 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0003g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0003g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0004g0002 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0004g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0004g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0004g0030 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0004g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0004g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0004g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0004g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0004g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0004g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0004g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0005g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0005g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0005g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0005g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0005g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0005g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0006g0012 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0006g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0006g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0006g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0007g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0007g0051 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0008g0020 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0009g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0009g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0010g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0011g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0011g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0012g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0013g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0014g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0015g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0016g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0001t0017g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0001c0002t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0002c0005t0003g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0003c0006t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0004c0004t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| a0005c0003t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | GBR | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | CHS | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0124 | EAS | CHS | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG00438 | hp1 | a0001 | c0001 | t0004 | g0031 | EAS | CHS | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | CHS | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0126 | EAS | CHS | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | CHS | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0028 | EAS | CHS | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | CHS | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | CHS | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG00621 | hp1 | a0001 | c0001 | t0004 | g0153 | EAS | CHS | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | CHS | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0066 | AMR | PUR | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01069 | hp2 | a0001 | c0001 | t0007 | g0021 | AMR | PUR | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0127 | AMR | PUR | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01071 | hp2 | a0001 | c0001 | t0007 | g0021 | AMR | PUR | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01074 | hp1 | a0001 | c0001 | t0012 | g0027 | AMR | PUR | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0064 | AMR | PUR | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01109 | hp2 | a0001 | c0001 | t0007 | g0051 | AMR | PUR | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0023 | AMR | PUR | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01167 | hp2 | a0001 | c0001 | t0008 | g0020 | AMR | PUR | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01169 | hp2 | a0001 | c0001 | t0008 | g0020 | AMR | PUR | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01243 | hp1 | a0001 | c0001 | t0006 | g0012 | AMR | PUR | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01361 | hp1 | a0001 | c0001 | t0011 | g0082 | AMR | CLM | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01433 | hp1 | a0001 | c0001 | t0011 | g0001 | AMR | CLM | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0067 | AMR | CLM | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | CLM | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0128 | AMR | CLM | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0035 | EUR | IBS | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0053 | EUR | IBS | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0054 | EUR | IBS | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0023 | EUR | IBS | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0035 | EUR | IBS | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0054 | EUR | IBS | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01884 | hp1 | a0001 | c0001 | t0006 | g0012 | AFR | ACB | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0005 | AFR | ACB | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0019 | AMR | PEL | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0019 | AMR | PEL | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0062 | AMR | PEL | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02040 | hp2 | a0002 | c0005 | t0003 | g0003 | EAS | KHV | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0073 | AFR | ACB | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | KHV | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0077 | AFR | ACB | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0019 | AMR | PEL | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02148 | hp2 | a0001 | c0001 | t0007 | g0051 | AMR | PEL | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CDX | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | CDX | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0121 | AFR | ACB | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0019 | AMR | PEL | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | ACB | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02280 | hp2 | a0001 | c0001 | t0005 | g0016 | AFR | ACB | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | KHV | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0044 | AFR | GWD | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0085 | SAS | PJL | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02615 | hp1 | a0001 | c0001 | t0009 | g0037 | AFR | GWD | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02622 | hp1 | a0001 | c0001 | t0008 | g0020 | AFR | GWD | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0088 | AFR | GWD | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0123 | AFR | GWD | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0087 | AFR | GWD | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0068 | SAS | PJL | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0192 | SAS | PJL | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02818 | hp1 | a0001 | c0001 | t0009 | g0092 | AFR | GWD | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0005 | AFR | GWD | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02886 | hp1 | a0001 | c0001 | t0009 | g0037 | AFR | GWD | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02895 | hp1 | a0001 | c0001 | t0010 | g0025 | AFR | GWD | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02895 | hp2 | a0001 | c0001 | t0005 | g0046 | AFR | GWD | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0042 | AFR | GWD | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02896 | hp2 | a0001 | c0001 | t0005 | g0046 | AFR | GWD | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02897 | hp1 | a0001 | c0001 | t0010 | g0025 | AFR | GWD | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0042 | AFR | GWD | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02922 | hp1 | a0001 | c0001 | t0006 | g0012 | AFR | ESN | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0033 | AFR | ESN | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ESN | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02970 | hp1 | a0001 | c0001 | t0005 | g0140 | AFR | ESN | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0131 | AFR | ESN | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0016 | AFR | ESN | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02976 | hp2 | a0001 | c0001 | t0006 | g0178 | AFR | ESN | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG03041 | hp1 | a0001 | c0001 | t0008 | g0020 | AFR | GWD | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG03098 | hp1 | a0001 | c0001 | t0005 | g0142 | AFR | MSL | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG03098 | hp2 | a0001 | c0001 | t0015 | g0177 | AFR | MSL | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG03130 | hp1 | a0001 | c0001 | t0005 | g0044 | AFR | ESN | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ESN | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG03139 | hp2 | a0001 | c0001 | t0013 | g0016 | AFR | ESN | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ESN | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG03195 | hp2 | a0001 | c0001 | t0006 | g0012 | AFR | ESN | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG03209 | hp1 | a0001 | c0001 | t0010 | g0025 | AFR | MSL | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0071 | AFR | MSL | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG03225 | hp2 | a0001 | c0001 | t0006 | g0012 | AFR | MSL | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | MSL | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | MSL | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG03486 | hp1 | a0001 | c0001 | t0005 | g0016 | AFR | MSL | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0090 | AFR | MSL | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | ESN | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG03516 | hp2 | a0001 | c0001 | t0006 | g0099 | AFR | ESN | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | MSL | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0029 | AFR | MSL | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0086 | SAS | PJL | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | STU | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | STU | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0080 | SAS | PJL | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0065 | SAS | PJL | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0094 | SAS | BEB | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0129 | SAS | BEB | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | BEB | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0011 | SAS | BEB | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | BEB | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | BEB | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0084 | SAS | STU | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG04115 | hp2 | a0001 | c0001 | t0004 | g0030 | SAS | STU | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0075 | SAS | STU | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | STU | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | STU | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | STU | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | YRI | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | YRI | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18747 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | CHB | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | CHB | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18906 | hp1 | a0001 | c0001 | t0006 | g0098 | AFR | YRI | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18906 | hp2 | a0001 | c0001 | t0012 | g0027 | AFR | YRI | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18945 | hp1 | a0001 | c0001 | t0004 | g0161 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18947 | hp2 | a0001 | c0001 | t0017 | g0056 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18952 | hp2 | a0001 | c0001 | t0014 | g0007 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18961 | hp1 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18963 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18964 | hp2 | a0003 | c0006 | t0003 | g0125 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0132 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18973 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18975 | hp1 | a0004 | c0004 | t0002 | g0001 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18975 | hp2 | a0001 | c0001 | t0004 | g0150 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18985 | hp2 | a0001 | c0001 | t0003 | g0120 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18988 | hp2 | a0001 | c0001 | t0004 | g0022 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18992 | hp1 | a0001 | c0001 | t0004 | g0176 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18998 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18999 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19005 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19010 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0130 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19012 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | LWK | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0122 | AFR | LWK | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | LWK | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | LWK | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19055 | hp2 | a0001 | c0001 | t0004 | g0030 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19057 | hp2 | a0001 | c0001 | t0016 | g0174 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19060 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19062 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19063 | hp2 | a0001 | c0001 | t0004 | g0162 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19070 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19080 | hp1 | a0001 | c0001 | t0004 | g0117 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19080 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19081 | hp2 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19082 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19083 | hp2 | a0005 | c0003 | t0003 | g0043 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0023 | EUR | TSI | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0022 | EUR | TSI | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0016 | AFR | ACB | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | ACB | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02486 | hp1 | a0001 | c0001 | t0005 | g0145 | AFR | ACB | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | MSL | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0089 | AFR | MSL | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | USA | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | USA | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18955 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0091 | AFR | USA | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0113 | AFR | USA | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | LWK | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0076 | REF | REF | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0001 | REF | REF | EXOG_chr3_38491340_38531303 | EXOG | chr3 | 38491340 | 38531303 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:38497743 | G | A | 1 | a0005 | 1 | NA19083.hp2 | stop_gained | HIGH | c.278G>A | p.Trp93* | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 2/6 | 306/3076 | 278/1107 | 93/368 | chr3 | 38497743 | |||
| chr3:38524013 | A | G | 1 | a0003 | 1 | NA18964.hp2 | missense_variant | MODERATE | c.758A>G | p.Asn253Ser | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 6/6 | 786/3076 | 758/1107 | 253/368 | chr3 | 38524013 | |||
| chr3:38524127 | G | A | 1 | a0004 | 1 | NA18975.hp1 | missense_variant | MODERATE | c.872G>A | p.Arg291Gln | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 6/6 | 900/3076 | 872/1107 | 291/368 | chr3 | 38524127 | |||
| chr3:38524214 | G | A | 1 | a0002 | 1 | HG02040.hp2 | missense_variant | MODERATE | c.959G>A | p.Arg320Gln | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 6/6 | 987/3076 | 959/1107 | 320/368 | chr3 | 38524214 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:38497690 | G | A | 1 | a0001c0002 | 2 | HG01884.hp2 HG02818.hp2 |
synonymous_variant | LOW | c.225G>A | p.Arg75Arg | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 2/6 | 253/3076 | 225/1107 | 75/368 | chr3 | 38497690 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:38524412 | T | A | 2 | a0001c0001t0005 a0001c0001t0013 |
12 | HG02109.hp1 HG02280.hp2 HG02486.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*50T>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 6/6 | 50 | chr3 | 38524412 | ||||||
| chr3:38524490 | G | A | 1 | a0001c0001t0011 | 2 | HG01361.hp1 HG01433.hp1 |
3_prime_UTR_variant | MODIFIER | c.*128G>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 6/6 | 128 | chr3 | 38524490 | ||||||
| chr3:38524504 | G | C | 1 | a0001c0001t0012 | 2 | HG01074.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*142G>C | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 6/6 | 142 | chr3 | 38524504 | ||||||
| chr3:38524592 | A | T | 1 | a0001c0001t0004 | 23 | HG00438.hp1 HG00621.hp1 HG04115.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*230A>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 6/6 | 230 | chr3 | 38524592 | ||||||
| chr3:38524700 | A | G | 1 | a0001c0001t0008 | 4 | HG01167.hp2 HG01169.hp2 HG02622.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*338A>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 6/6 | 338 | chr3 | 38524700 | ||||||
| chr3:38524744 | G | T | 11 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(8): Show |
238 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(235): Show |
3_prime_UTR_variant | MODIFIER | c.*382G>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 6/6 | 382 | chr3 | 38524744 | ||||||
| chr3:38524786 | A | T | 1 | a0001c0001t0017 | 1 | NA18947.hp2 | 3_prime_UTR_variant | MODIFIER | c.*424A>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 6/6 | 424 | chr3 | 38524786 | ||||||
| chr3:38524989 | G | A | 17 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(14): Show |
295 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(292): Show |
3_prime_UTR_variant | MODIFIER | c.*627G>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 6/6 | 627 | chr3 | 38524989 | ||||||
| chr3:38525028 | T | C | 12 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(9): Show |
246 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(243): Show |
3_prime_UTR_variant | MODIFIER | c.*666T>C | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 6/6 | 666 | chr3 | 38525028 | ||||||
| chr3:38525072 | G | A | 1 | a0001c0001t0008 | 4 | HG01167.hp2 HG01169.hp2 HG02622.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*710G>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 6/6 | 710 | chr3 | 38525072 | ||||||
| chr3:38525231 | T | C | 12 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(9): Show |
246 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(243): Show |
3_prime_UTR_variant | MODIFIER | c.*869T>C | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 6/6 | 869 | chr3 | 38525231 | ||||||
| chr3:38525232 | G | A | 1 | a0001c0001t0007 | 4 | HG01069.hp2 HG01071.hp2 HG01109.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*870G>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 6/6 | 870 | chr3 | 38525232 | ||||||
| chr3:38525363 | T | C | 1 | a0001c0001t0013 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1001T>C | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 6/6 | 1001 | chr3 | 38525363 | ||||||
| chr3:38525405 | G | A | 1 | a0001c0001t0015 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1043G>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 6/6 | 1043 | chr3 | 38525405 | ||||||
| chr3:38525411 | G | T | 2 | a0001c0001t0010 a0001c0001t0015 |
4 | HG02895.hp1 HG02897.hp1 HG03098.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1049G>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 6/6 | 1049 | chr3 | 38525411 | ||||||
| chr3:38525514 | C | T | 2 | a0001c0001t0010 a0001c0001t0015 |
4 | HG02895.hp1 HG02897.hp1 HG03098.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1152C>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 6/6 | 1152 | chr3 | 38525514 | ||||||
| chr3:38525525 | T | C | 1 | a0001c0001t0016 | 1 | NA19057.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1163T>C | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 6/6 | 1163 | chr3 | 38525525 | ||||||
| chr3:38525576 | T | G | 1 | a0001c0001t0006 | 8 | HG01243.hp1 HG01884.hp1 HG02922.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1214T>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 6/6 | 1214 | chr3 | 38525576 | ||||||
| chr3:38525866 | C | G | 1 | a0001c0001t0014 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1504C>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 6/6 | 1504 | chr3 | 38525866 | ||||||
| chr3:38526234 | A | T | 4 | a0001c0001t0003 a0002c0005t0003 a0003c0006t0003 others(1): Show |
45 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*1872A>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 6/6 | 1872 | chr3 | 38526234 | ||||||
| chr3:38526280 | C | A | 18 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(15): Show |
298 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(295): Show |
3_prime_UTR_variant | MODIFIER | c.*1918C>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 6/6 | 1918 | chr3 | 38526280 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:38496642 | C | G | 1 | a0001c0001t0002g0193 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.163+112C>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 1/5 | chr3 | 38496642 | |||||||
| chr3:38496773 | C | T | 1 | a0001c0001t0003g0192 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.163+243C>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 1/5 | chr3 | 38496773 | |||||||
| chr3:38496794 | A | C | 1 | a0001c0001t0001g0191 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.163+264A>C | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 1/5 | chr3 | 38496794 | |||||||
| chr3:38496807 | G | A | 2 | a0001c0001t0002g0059 a0001c0001t0002g0060 |
2 | NA19086.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.163+277G>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 1/5 | chr3 | 38496807 | |||||||
| chr3:38496888 | A | G | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG02004.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.163+358A>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 1/5 | chr3 | 38496888 | |||||||
| chr3:38496937 | T | C | 1 | a0001c0001t0001g0061 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.163+407T>C | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 1/5 | chr3 | 38496937 | |||||||
| chr3:38496975 | G | C | 2 | a0001c0001t0003g0019 a0001c0001t0003g0062 |
5 | HG01952.hp1 HG01975.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.163+445G>C | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 1/5 | chr3 | 38496975 | |||||||
| chr3:38496975 | G | T | 158 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(155): Show |
287 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(284): Show |
intron_variant | MODIFIER | c.163+445G>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 1/5 | chr3 | 38496975 | |||||||
| chr3:38497015 | T | C | 1 | a0001c0001t0003g0094 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.163+485T>C | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 1/5 | chr3 | 38497015 | |||||||
| chr3:38497035 | T | C | 1 | a0001c0001t0010g0025 | 3 | HG02895.hp1 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.163+505T>C | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 1/5 | chr3 | 38497035 | |||||||
| chr3:38497055 | A | T | 2 | a0001c0001t0002g0006 a0001c0001t0002g0093 |
10 | HG00408.hp2 HG00673.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.163+525A>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 1/5 | chr3 | 38497055 | |||||||
| chr3:38497075 | C | CA | 81 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(78): Show |
156 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.164-538dupA | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 38497075 | ||||||
| chr3:38497075 | C | CAA | 63 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0014 others(60): Show |
111 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.164-539_164-538dup others(2): Show |
EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 38497075 | ||||||
| chr3:38497584 | T | G | 1 | a0001c0001t0001g0134 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.164-45T>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 1/5 | chr3 | 38497584 | |||||||
| chr3:38497604 | CTT | C | 140 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(137): Show |
248 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(245): Show |
intron_variant | MODIFIER | c.164-11_164-10delTT | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 38497604 | ||||||
| chr3:38497604 | CTTT | C | 18 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0014 others(15): Show |
40 | HG00621.hp2 HG01070.hp2 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.164-12_164-10delTT others(1): Show |
EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 38497604 | ||||||
| chr3:38497607 | T | C | 20 | a0001c0001t0001g0005 a0001c0001t0001g0045 a0001c0001t0001g0096 others(17): Show |
35 | HG00639.hp2 HG00741.hp2 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.164-22T>C | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 1/5 | chr3 | 38497607 | |||||||
| chr3:38497608 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.164-21T>C | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 1/5 | chr3 | 38497608 | |||||||
| chr3:38498029 | C | T | 1 | a0001c0001t0004g0176 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.313+251C>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 2/5 | chr3 | 38498029 | |||||||
| chr3:38498510 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.313+732G>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 2/5 | chr3 | 38498510 | |||||||
| chr3:38498555 | A | C | 2 | a0001c0001t0002g0001 a0001c0001t0002g0011 |
6 | NA18956.hp1 NA19007.hp1 NA19057.hp1 others(3): Show |
intron_variant | MODIFIER | c.313+777A>C | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 2/5 | chr3 | 38498555 | |||||||
| chr3:38498773 | A | T | 40 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0018 others(37): Show |
73 | HG00423.hp2 HG00558.hp2 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.313+995A>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 2/5 | chr3 | 38498773 | |||||||
| chr3:38498829 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.313+1051G>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 2/5 | chr3 | 38498829 | |||||||
| chr3:38499050 | A | G | 158 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(155): Show |
288 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(285): Show |
intron_variant | MODIFIER | c.313+1272A>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 2/5 | chr3 | 38499050 | |||||||
| chr3:38499143 | G | A | 15 | a0001c0001t0001g0015 a0001c0001t0001g0027 a0001c0001t0001g0041 others(12): Show |
21 | HG00639.hp1 HG01074.hp1 HG01981.hp2 others(18): Show |
intron_variant | MODIFIER | c.313+1365G>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 2/5 | chr3 | 38499143 | |||||||
| chr3:38499318 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.313+1540C>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 2/5 | chr3 | 38499318 | |||||||
| chr3:38499502 | G | A | 1 | a0001c0001t0001g0167 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.313+1724G>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 2/5 | chr3 | 38499502 | |||||||
| chr3:38499670 | A | C | 42 | a0001c0001t0001g0015 a0001c0001t0001g0027 a0001c0001t0001g0041 others(39): Show |
68 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.314-1685A>C | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 2/5 | chr3 | 38499670 | |||||||
| chr3:38499713 | T | G | 1 | a0001c0001t0002g0064 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.314-1642T>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 2/5 | chr3 | 38499713 | |||||||
| chr3:38499754 | G | A | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.314-1601G>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 2/5 | chr3 | 38499754 | |||||||
| chr3:38499827 | C | A | 118 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(115): Show |
224 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(221): Show |
intron_variant | MODIFIER | c.314-1528C>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 2/5 | chr3 | 38499827 | |||||||
| chr3:38499961 | A | G | 168 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(165): Show |
304 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(301): Show |
intron_variant | MODIFIER | c.314-1394A>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 2/5 | chr3 | 38499961 | |||||||
| chr3:38500143 | T | TAAAAAGT others(339): Show |
1 | a0001c0001t0002g0086 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.314-1196_314-1195i others(348): Show |
EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 38500143 | ||||||
| chr3:38500249 | A | G | 3 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0188 |
3 | HG01081.hp2 HG01106.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.314-1106A>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 2/5 | chr3 | 38500249 | |||||||
| chr3:38500256 | A | C | 1 | a0001c0001t0001g0115 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.314-1099A>C | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 2/5 | chr3 | 38500256 | |||||||
| chr3:38500324 | A | G | 2 | a0001c0001t0010g0025 a0001c0001t0015g0177 |
4 | HG02895.hp1 HG02897.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.314-1031A>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 2/5 | chr3 | 38500324 | |||||||
| chr3:38500674 | G | C | 2 | a0001c0001t0001g0105 a0001c0001t0002g0065 |
2 | HG03710.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.314-681G>C | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 2/5 | chr3 | 38500674 | |||||||
| chr3:38500962 | C | G | 7 | a0001c0001t0001g0018 a0001c0001t0001g0057 a0001c0001t0001g0133 others(4): Show |
12 | HG00558.hp2 HG02809.hp2 NA18944.hp1 others(9): Show |
intron_variant | MODIFIER | c.314-393C>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 2/5 | chr3 | 38500962 | |||||||
| chr3:38501279 | C | T | 1 | a0001c0001t0001g0163 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.314-76C>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 2/5 | chr3 | 38501279 | |||||||
| chr3:38501308 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.314-47G>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 2/5 | chr3 | 38501308 | |||||||
| chr3:38501570 | C | A | 1 | a0001c0001t0001g0047 | 2 | NA18982.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.453+76C>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 3/5 | chr3 | 38501570 | |||||||
| chr3:38501714 | A | C | 1 | a0001c0001t0005g0145 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.453+220A>C | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 3/5 | chr3 | 38501714 | |||||||
| chr3:38501818 | G | A | 3 | a0001c0001t0002g0033 a0001c0001t0002g0066 a0001c0001t0002g0067 |
4 | HG00738.hp1 HG01433.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.453+324G>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 3/5 | chr3 | 38501818 | |||||||
| chr3:38501894 | C | T | 2 | a0001c0001t0002g0084 a0001c0001t0002g0085 |
2 | HG02602.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.453+400C>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 3/5 | chr3 | 38501894 | |||||||
| chr3:38501953 | C | CA | 2 | a0001c0001t0001g0057 a0001c0001t0001g0134 |
3 | HG00558.hp2 NA18954.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.453+459_453+460ins others(1): Show |
EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 3/5 | chr3 | 38501953 | |||||||
| chr3:38502064 | A | G | 1 | a0001c0001t0002g0083 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.453+570A>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 3/5 | chr3 | 38502064 | |||||||
| chr3:38502200 | C | T | 1 | a0001c0001t0004g0162 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.453+706C>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 3/5 | chr3 | 38502200 | |||||||
| chr3:38502252 | CAG | C | 42 | a0001c0001t0001g0015 a0001c0001t0001g0027 a0001c0001t0001g0041 others(39): Show |
68 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.453+761_453+762del others(2): Show |
EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 38502252 | ||||||
| chr3:38502354 | C | T | 4 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0143 others(1): Show |
4 | HG01255.hp1 HG02055.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.453+860C>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 3/5 | chr3 | 38502354 | |||||||
| chr3:38502385 | ATGCC | A | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
4 | HG01346.hp2 HG01515.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.453+894_453+897del others(4): Show |
EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 38502385 | ||||||
| chr3:38502393 | C | G | 1 | a0001c0001t0001g0114 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.453+899C>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 3/5 | chr3 | 38502393 | |||||||
| chr3:38502404 | T | A | 2 | a0001c0001t0001g0048 a0001c0001t0002g0087 |
3 | HG01928.hp1 HG02723.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.453+910T>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 3/5 | chr3 | 38502404 | |||||||
| chr3:38502623 | G | C | 1 | a0001c0001t0001g0105 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.454-992G>C | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 3/5 | chr3 | 38502623 | |||||||
| chr3:38502679 | A | T | 1 | a0001c0001t0011g0082 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.454-936A>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 3/5 | chr3 | 38502679 | |||||||
| chr3:38502847 | T | C | 1 | a0001c0001t0001g0135 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.454-768T>C | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 3/5 | chr3 | 38502847 | |||||||
| chr3:38502852 | A | G | 1 | a0001c0001t0002g0081 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.454-763A>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 3/5 | chr3 | 38502852 | |||||||
| chr3:38502858 | G | A | 118 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(115): Show |
224 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(221): Show |
intron_variant | MODIFIER | c.454-757G>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 3/5 | chr3 | 38502858 | |||||||
| chr3:38502928 | G | C | 42 | a0001c0001t0001g0015 a0001c0001t0001g0027 a0001c0001t0001g0041 others(39): Show |
68 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.454-687G>C | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 3/5 | chr3 | 38502928 | |||||||
| chr3:38502999 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.454-616G>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 3/5 | chr3 | 38502999 | |||||||
| chr3:38503367 | G | A | 3 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0114 |
3 | HG02622.hp2 HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.454-248G>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 3/5 | chr3 | 38503367 | |||||||
| chr3:38503374 | G | T | 1 | a0001c0001t0001g0175 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.454-241G>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 3/5 | chr3 | 38503374 | |||||||
| chr3:38503410 | T | C | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.454-205T>C | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 3/5 | chr3 | 38503410 | |||||||
| chr3:38503422 | C | A | 1 | a0001c0001t0001g0055 | 2 | HG01243.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.454-193C>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 3/5 | chr3 | 38503422 | |||||||
| chr3:38503425 | C | T | 42 | a0001c0001t0001g0015 a0001c0001t0001g0027 a0001c0001t0001g0041 others(39): Show |
68 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.454-190C>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 3/5 | chr3 | 38503425 | |||||||
| chr3:38503604 | T | C | 2 | a0001c0001t0010g0025 a0001c0001t0015g0177 |
4 | HG02895.hp1 HG02897.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.454-11T>C | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 3/5 | chr3 | 38503604 | |||||||
| chr3:38503858 | C | T | 163 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(160): Show |
299 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(296): Show |
intron_variant | MODIFIER | c.530+167C>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 4/5 | chr3 | 38503858 | |||||||
| chr3:38503902 | A | T | 1 | a0001c0001t0002g0067 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.530+211A>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 4/5 | chr3 | 38503902 | |||||||
| chr3:38504078 | G | A | 1 | a0001c0001t0006g0098 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.530+387G>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 4/5 | chr3 | 38504078 | |||||||
| chr3:38504112 | A | G | 1 | a0001c0001t0005g0046 | 2 | HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.530+421A>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 4/5 | chr3 | 38504112 | |||||||
| chr3:38504213 | A | G | 1 | a0001c0001t0009g0037 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.530+522A>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 4/5 | chr3 | 38504213 | |||||||
| chr3:38504365 | C | CA | 164 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(161): Show |
300 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(297): Show |
intron_variant | MODIFIER | c.530+684dupA | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 38504365 | ||||||
| chr3:38504699 | G | A | 1 | a0001c0001t0015g0177 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.530+1008G>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 4/5 | chr3 | 38504699 | |||||||
| chr3:38504868 | C | T | 1 | a0001c0001t0001g0036 | 2 | NA18950.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.530+1177C>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 4/5 | chr3 | 38504868 | |||||||
| chr3:38505235 | G | A | 119 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(116): Show |
226 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(223): Show |
intron_variant | MODIFIER | c.530+1544G>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 4/5 | chr3 | 38505235 | |||||||
| chr3:38505440 | C | CAT | 12 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0014 others(9): Show |
28 | HG00621.hp2 HG01070.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.531-1406_531-1405d others(4): Show |
EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 38505440 | ||||||
| chr3:38505452 | C | A | 2 | a0001c0001t0001g0038 a0001c0001t0001g0039 |
4 | HG01943.hp2 HG01952.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.531-1402C>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 4/5 | chr3 | 38505452 | |||||||
| chr3:38505567 | G | A | 1 | a0001c0001t0008g0020 | 4 | HG01167.hp2 HG01169.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.531-1287G>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 4/5 | chr3 | 38505567 | |||||||
| chr3:38505676 | C | T | 1 | a0001c0001t0004g0161 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.531-1178C>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 4/5 | chr3 | 38505676 | |||||||
| chr3:38505820 | G | T | 1 | a0001c0001t0001g0165 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.531-1034G>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 4/5 | chr3 | 38505820 | |||||||
| chr3:38505876 | G | A | 1 | a0001c0001t0002g0088 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.531-978G>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 4/5 | chr3 | 38505876 | |||||||
| chr3:38505890 | C | T | 1 | a0001c0001t0002g0080 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.531-964C>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 4/5 | chr3 | 38505890 | |||||||
| chr3:38505954 | GA | G | 6 | a0001c0001t0001g0052 a0001c0001t0001g0187 a0001c0001t0006g0012 others(3): Show |
11 | HG01243.hp1 HG01884.hp1 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.531-886delA | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 38505954 | ||||||
| chr3:38506094 | G | A | 1 | a0001c0001t0004g0150 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.531-760G>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 4/5 | chr3 | 38506094 | |||||||
| chr3:38506123 | T | G | 1 | a0001c0001t0002g0068 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.531-731T>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 4/5 | chr3 | 38506123 | |||||||
| chr3:38506238 | A | G | 1 | a0001c0001t0002g0068 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.531-616A>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 4/5 | chr3 | 38506238 | |||||||
| chr3:38506315 | T | G | 1 | a0001c0001t0001g0179 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.531-539T>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 4/5 | chr3 | 38506315 | |||||||
| chr3:38506530 | T | C | 129 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(126): Show |
238 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(235): Show |
intron_variant | MODIFIER | c.531-324T>C | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 4/5 | chr3 | 38506530 | |||||||
| chr3:38506560 | A | G | 1 | a0001c0001t0008g0020 | 4 | HG01167.hp2 HG01169.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.531-294A>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 4/5 | chr3 | 38506560 | |||||||
| chr3:38506583 | T | G | 1 | a0001c0001t0001g0148 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.531-271T>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 4/5 | chr3 | 38506583 | |||||||
| chr3:38507167 | A | G | 5 | a0001c0001t0001g0021 a0001c0001t0001g0050 a0001c0001t0001g0160 others(2): Show |
9 | HG00738.hp2 HG01069.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.645+199A>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38507167 | |||||||
| chr3:38507379 | A | G | 1 | a0001c0001t0001g0163 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.645+411A>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38507379 | |||||||
| chr3:38507386 | A | C | 1 | a0001c0001t0016g0174 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.645+418A>C | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38507386 | |||||||
| chr3:38507589 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.645+621G>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38507589 | |||||||
| chr3:38507631 | T | C | 2 | a0001c0001t0001g0096 a0001c0001t0001g0097 |
2 | HG02145.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.645+663T>C | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38507631 | |||||||
| chr3:38507797 | A | G | 1 | a0001c0001t0003g0132 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.645+829A>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38507797 | |||||||
| chr3:38507869 | C | T | 1 | a0001c0001t0002g0079 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.645+901C>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38507869 | |||||||
| chr3:38507909 | G | A | 1 | a0001c0001t0001g0058 | 2 | HG03710.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.645+941G>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38507909 | |||||||
| chr3:38508133 | A | G | 1 | a0001c0001t0002g0088 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.645+1165A>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38508133 | |||||||
| chr3:38508250 | G | A | 1 | a0001c0001t0001g0169 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.645+1282G>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38508250 | |||||||
| chr3:38508648 | T | C | 1 | a0001c0001t0006g0178 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.645+1680T>C | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38508648 | |||||||
| chr3:38508680 | T | G | 1 | a0001c0001t0001g0108 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.645+1712T>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38508680 | |||||||
| chr3:38508711 | A | AC | 100 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(97): Show |
200 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(197): Show |
intron_variant | MODIFIER | c.645+1753dupC | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 38508711 | ||||||
| chr3:38508711 | A | ACC | 33 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0015 others(30): Show |
53 | HG00438.hp1 HG00639.hp1 HG01070.hp2 others(50): Show |
intron_variant | MODIFIER | c.645+1752_645+1753d others(4): Show |
EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 38508711 | ||||||
| chr3:38508711 | A | C | 1 | a0001c0001t0008g0020 | 4 | HG01167.hp2 HG01169.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.645+1743A>C | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38508711 | |||||||
| chr3:38508722 | A | C | 8 | a0001c0001t0001g0049 a0001c0001t0001g0108 a0001c0001t0001g0159 others(5): Show |
13 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.645+1754A>C | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38508722 | |||||||
| chr3:38508750 | T | C | 3 | a0001c0001t0002g0033 a0001c0001t0002g0066 a0001c0001t0002g0067 |
4 | HG00738.hp1 HG01433.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.645+1782T>C | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38508750 | |||||||
| chr3:38508796 | T | G | 1 | a0001c0001t0002g0032 | 2 | HG01168.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.645+1828T>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38508796 | |||||||
| chr3:38508810 | A | G | 2 | a0001c0001t0003g0127 a0001c0001t0003g0128 |
2 | HG01070.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.645+1842A>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38508810 | |||||||
| chr3:38508862 | C | T | 1 | a0001c0001t0001g0157 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.645+1894C>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38508862 | |||||||
| chr3:38508947 | A | G | 2 | a0001c0001t0003g0122 a0001c0001t0003g0131 |
2 | HG02970.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.645+1979A>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38508947 | |||||||
| chr3:38509634 | A | G | 22 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0050 others(19): Show |
36 | HG00609.hp1 HG00738.hp2 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.645+2666A>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38509634 | |||||||
| chr3:38509672 | A | G | 2 | a0001c0001t0003g0126 a0003c0006t0003g0125 |
2 | HG00544.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.645+2704A>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38509672 | |||||||
| chr3:38509677 | G | C | 4 | a0001c0001t0006g0012 a0001c0001t0006g0098 a0001c0001t0006g0099 others(1): Show |
8 | HG01243.hp1 HG01884.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.645+2709G>C | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38509677 | |||||||
| chr3:38509904 | C | G | 27 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0014 others(24): Show |
49 | HG00621.hp2 HG00639.hp1 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.645+2936C>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38509904 | |||||||
| chr3:38509986 | C | T | 1 | a0001c0001t0001g0104 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.645+3018C>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38509986 | |||||||
| chr3:38510036 | A | G | 6 | a0001c0001t0001g0015 a0001c0001t0001g0106 a0001c0001t0001g0107 others(3): Show |
10 | HG00639.hp1 HG02257.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.645+3068A>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38510036 | |||||||
| chr3:38510114 | C | T | 1 | a0001c0001t0008g0020 | 4 | HG01167.hp2 HG01169.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.645+3146C>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38510114 | |||||||
| chr3:38510127 | G | C | 2 | a0001c0001t0001g0057 a0001c0001t0001g0134 |
3 | HG00558.hp2 NA18954.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.645+3159G>C | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38510127 | |||||||
| chr3:38510186 | A | T | 1 | a0001c0001t0002g0080 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.645+3218A>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38510186 | |||||||
| chr3:38510699 | A | T | 1 | a0001c0001t0003g0042 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.645+3731A>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38510699 | |||||||
| chr3:38510721 | G | T | 1 | a0001c0001t0002g0093 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.645+3753G>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38510721 | |||||||
| chr3:38510759 | A | G | 167 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(164): Show |
304 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(301): Show |
intron_variant | MODIFIER | c.645+3791A>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38510759 | |||||||
| chr3:38510789 | A | G | 2 | a0001c0001t0001g0017 a0001c0001t0001g0179 |
6 | HG02132.hp2 NA18948.hp1 NA18949.hp2 others(3): Show |
intron_variant | MODIFIER | c.645+3821A>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38510789 | |||||||
| chr3:38510812 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.645+3844A>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38510812 | |||||||
| chr3:38510830 | A | G | 1 | a0001c0001t0002g0074 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.645+3862A>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38510830 | |||||||
| chr3:38510887 | A | G | 2 | a0001c0001t0001g0045 a0001c0001t0001g0141 |
3 | HG02965.hp2 HG03130.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.645+3919A>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38510887 | |||||||
| chr3:38511477 | A | T | 1 | a0001c0001t0001g0141 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.645+4509A>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38511477 | |||||||
| chr3:38511924 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.645+4956C>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38511924 | |||||||
| chr3:38512003 | T | A | 3 | a0001c0001t0001g0041 a0001c0001t0001g0108 a0001c0001t0001g0111 |
4 | HG02647.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.645+5035T>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38512003 | |||||||
| chr3:38512120 | T | C | 1 | a0001c0001t0001g0170 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.645+5152T>C | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38512120 | |||||||
| chr3:38512148 | C | T | 159 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(156): Show |
295 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(292): Show |
intron_variant | MODIFIER | c.645+5180C>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38512148 | |||||||
| chr3:38512473 | G | A | 12 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0014 others(9): Show |
28 | HG00621.hp2 HG01070.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.645+5505G>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38512473 | |||||||
| chr3:38512474 | C | T | 129 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(126): Show |
238 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(235): Show |
intron_variant | MODIFIER | c.645+5506C>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38512474 | |||||||
| chr3:38512518 | G | T | 2 | a0001c0001t0001g0048 a0001c0001t0001g0149 |
3 | HG01928.hp1 HG02647.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.645+5550G>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38512518 | |||||||
| chr3:38512797 | A | T | 1 | a0001c0001t0001g0054 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.645+5829A>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38512797 | |||||||
| chr3:38512868 | C | T | 12 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0014 others(9): Show |
28 | HG00621.hp2 HG01070.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.645+5900C>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38512868 | |||||||
| chr3:38513093 | C | T | 1 | a0001c0001t0002g0068 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.645+6125C>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38513093 | |||||||
| chr3:38513410 | T | C | 133 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(130): Show |
246 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(243): Show |
intron_variant | MODIFIER | c.645+6442T>C | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38513410 | |||||||
| chr3:38513513 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.645+6545G>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38513513 | |||||||
| chr3:38513555 | A | ATGGAATA others(5): Show |
1 | a0001c0001t0008g0020 | 4 | HG01167.hp2 HG01169.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.645+6587_645+6588i others(14): Show |
EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38513555 | |||||||
| chr3:38513556 | A | ATGGAATA others(6): Show |
160 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(157): Show |
294 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(291): Show |
intron_variant | MODIFIER | c.645+6589_645+6590i others(15): Show |
EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 38513556 | ||||||
| chr3:38513556 | A | T | 1 | a0001c0001t0008g0020 | 4 | HG01167.hp2 HG01169.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.645+6588A>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38513556 | |||||||
| chr3:38513687 | G | A | 119 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(116): Show |
226 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(223): Show |
intron_variant | MODIFIER | c.645+6719G>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38513687 | |||||||
| chr3:38513983 | G | A | 55 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0010 others(52): Show |
104 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.645+7015G>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38513983 | |||||||
| chr3:38513984 | C | A | 13 | a0001c0001t0001g0015 a0001c0001t0001g0027 a0001c0001t0001g0041 others(10): Show |
19 | HG00639.hp1 HG01074.hp1 HG01981.hp2 others(16): Show |
intron_variant | MODIFIER | c.645+7016C>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38513984 | |||||||
| chr3:38514068 | A | G | 1 | a0001c0001t0003g0042 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.645+7100A>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38514068 | |||||||
| chr3:38514078 | G | C | 13 | a0001c0001t0001g0015 a0001c0001t0001g0027 a0001c0001t0001g0041 others(10): Show |
19 | HG00639.hp1 HG01074.hp1 HG01981.hp2 others(16): Show |
intron_variant | MODIFIER | c.645+7110G>C | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38514078 | |||||||
| chr3:38514324 | A | G | 58 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0010 others(55): Show |
108 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.645+7356A>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38514324 | |||||||
| chr3:38514507 | G | A | 7 | a0001c0001t0001g0027 a0001c0001t0001g0041 a0001c0001t0001g0108 others(4): Show |
9 | HG01074.hp1 HG01981.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.645+7539G>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38514507 | |||||||
| chr3:38514634 | A | G | 1 | a0001c0001t0002g0073 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.645+7666A>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38514634 | |||||||
| chr3:38514761 | T | TC | 41 | a0001c0001t0001g0030 a0001c0001t0001g0102 a0001c0001t0001g0106 others(38): Show |
67 | HG00423.hp1 HG00558.hp1 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.645+7801dupC | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 38514761 | ||||||
| chr3:38514768 | C | A | 1 | a0001c0001t0002g0088 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.645+7800C>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38514768 | |||||||
| chr3:38514769 | CT | C | 6 | a0001c0001t0001g0014 a0001c0001t0001g0038 a0001c0001t0001g0040 others(3): Show |
12 | HG01070.hp2 HG01943.hp2 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.645+7802delT | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38514769 | |||||||
| chr3:38514770 | T | C | 10 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0039 others(7): Show |
20 | HG00621.hp2 HG01071.hp1 HG01952.hp2 others(17): Show |
intron_variant | MODIFIER | c.645+7802T>C | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38514770 | |||||||
| chr3:38514775 | C | G | 1 | a0001c0001t0005g0140 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.645+7807C>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38514775 | |||||||
| chr3:38514776 | T | C | 1 | a0001c0001t0005g0140 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.645+7808T>C | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38514776 | |||||||
| chr3:38514777 | G | T | 1 | a0001c0001t0005g0140 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.645+7809G>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38514777 | |||||||
| chr3:38514778 | C | CTT | 129 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(126): Show |
241 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(238): Show |
intron_variant | MODIFIER | c.645+7819_645+7820d others(4): Show |
EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 38514778 | ||||||
| chr3:38514778 | C | T | 1 | a0001c0001t0005g0140 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.645+7810C>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38514778 | |||||||
| chr3:38514791 | G | A | 1 | a0001c0001t0002g0069 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.645+7823G>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38514791 | |||||||
| chr3:38515165 | T | C | 1 | a0001c0001t0001g0115 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.645+8197T>C | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38515165 | |||||||
| chr3:38515202 | G | A | 1 | a0001c0001t0015g0177 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.645+8234G>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38515202 | |||||||
| chr3:38515311 | G | A | 19 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0026 others(16): Show |
39 | HG00423.hp2 HG00558.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.645+8343G>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38515311 | |||||||
| chr3:38515348 | A | C | 1 | a0001c0001t0001g0118 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.645+8380A>C | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38515348 | |||||||
| chr3:38515504 | G | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0171 |
4 | HG02071.hp1 NA18944.hp2 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.646-8397G>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38515504 | |||||||
| chr3:38515516 | G | C | 2 | a0001c0001t0002g0088 a0001c0001t0002g0089 |
2 | HG02630.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.646-8385G>C | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38515516 | |||||||
| chr3:38515559 | G | T | 2 | a0001c0001t0009g0037 a0001c0001t0009g0092 |
3 | HG02615.hp1 HG02818.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.646-8342G>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38515559 | |||||||
| chr3:38515670 | T | C | 166 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(163): Show |
303 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(300): Show |
intron_variant | MODIFIER | c.646-8231T>C | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38515670 | |||||||
| chr3:38515687 | C | T | 2 | a0001c0001t0002g0006 a0001c0001t0002g0093 |
10 | HG00408.hp2 HG00673.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.646-8214C>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38515687 | |||||||
| chr3:38515698 | T | C | 1 | a0001c0001t0002g0035 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.646-8203T>C | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38515698 | |||||||
| chr3:38515778 | C | G | 2 | a0001c0001t0002g0034 a0001c0001t0002g0072 |
3 | HG02523.hp1 NA18955.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.646-8123C>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38515778 | |||||||
| chr3:38515904 | G | T | 1 | a0001c0001t0001g0172 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.646-7997G>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38515904 | |||||||
| chr3:38515909 | T | C | 1 | a0001c0001t0001g0050 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.646-7992T>C | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38515909 | |||||||
| chr3:38515913 | G | A | 1 | a0001c0001t0003g0129 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.646-7988G>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38515913 | |||||||
| chr3:38516202 | A | T | 1 | a0001c0001t0003g0121 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.646-7699A>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38516202 | |||||||
| chr3:38516411 | A | G | 1 | a0001c0001t0001g0118 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.646-7490A>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38516411 | |||||||
| chr3:38516430 | T | C | 159 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(156): Show |
295 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(292): Show |
intron_variant | MODIFIER | c.646-7471T>C | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38516430 | |||||||
| chr3:38516469 | T | G | 1 | a0001c0001t0001g0175 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.646-7432T>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38516469 | |||||||
| chr3:38516489 | C | A | 2 | a0001c0001t0001g0045 a0001c0001t0001g0141 |
3 | HG02965.hp2 HG03130.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.646-7412C>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38516489 | |||||||
| chr3:38516548 | A | C | 1 | a0001c0001t0003g0124 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.646-7353A>C | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38516548 | |||||||
| chr3:38516613 | A | C | 133 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(130): Show |
246 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(243): Show |
intron_variant | MODIFIER | c.646-7288A>C | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38516613 | |||||||
| chr3:38516688 | G | GT | 5 | a0001c0001t0001g0146 a0001c0001t0006g0012 a0001c0001t0006g0098 others(2): Show |
9 | HG01243.hp1 HG01884.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.646-7203dupT | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 38516688 | ||||||
| chr3:38516706 | A | G | 159 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(156): Show |
295 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(292): Show |
intron_variant | MODIFIER | c.646-7195A>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38516706 | |||||||
| chr3:38516719 | G | A | 41 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0018 others(38): Show |
76 | HG00423.hp2 HG00558.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.646-7182G>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38516719 | |||||||
| chr3:38516825 | C | T | 133 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(130): Show |
246 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(243): Show |
intron_variant | MODIFIER | c.646-7076C>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38516825 | |||||||
| chr3:38516947 | G | A | 25 | a0001c0001t0003g0003 a0001c0001t0003g0019 a0001c0001t0003g0028 others(22): Show |
45 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.646-6954G>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38516947 | |||||||
| chr3:38517037 | C | T | 2 | a0001c0001t0009g0037 a0001c0001t0009g0092 |
3 | HG02615.hp1 HG02818.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.646-6864C>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38517037 | |||||||
| chr3:38517052 | A | T | 1 | a0001c0001t0001g0107 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.646-6849A>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38517052 | |||||||
| chr3:38517339 | A | G | 133 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(130): Show |
246 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(243): Show |
intron_variant | MODIFIER | c.646-6562A>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38517339 | |||||||
| chr3:38517415 | T | C | 159 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(156): Show |
295 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(292): Show |
intron_variant | MODIFIER | c.646-6486T>C | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38517415 | |||||||
| chr3:38517420 | G | A | 1 | a0001c0001t0001g0152 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.646-6481G>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38517420 | |||||||
| chr3:38517462 | A | C | 1 | a0001c0001t0002g0090 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.646-6439A>C | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38517462 | |||||||
| chr3:38517724 | A | G | 58 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0010 others(55): Show |
108 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.646-6177A>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38517724 | |||||||
| chr3:38517727 | G | C | 1 | a0001c0001t0001g0104 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.646-6174G>C | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38517727 | |||||||
| chr3:38517779 | A | T | 12 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0014 others(9): Show |
28 | HG00621.hp2 HG01070.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.646-6122A>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38517779 | |||||||
| chr3:38517797 | C | T | 1 | a0001c0001t0003g0113 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.646-6104C>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38517797 | |||||||
| chr3:38517816 | G | A | 133 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(130): Show |
246 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(243): Show |
intron_variant | MODIFIER | c.646-6085G>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38517816 | |||||||
| chr3:38518037 | T | C | 1 | a0001c0001t0002g0069 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.646-5864T>C | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38518037 | |||||||
| chr3:38518258 | A | G | 56 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0010 others(53): Show |
105 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.646-5643A>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38518258 | |||||||
| chr3:38518623 | T | G | 2 | a0001c0001t0001g0057 a0001c0001t0001g0134 |
3 | HG00558.hp2 NA18954.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.646-5278T>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38518623 | |||||||
| chr3:38518763 | A | G | 133 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(130): Show |
246 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(243): Show |
intron_variant | MODIFIER | c.646-5138A>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38518763 | |||||||
| chr3:38518778 | A | C | 1 | a0001c0001t0001g0115 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.646-5123A>C | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38518778 | |||||||
| chr3:38518812 | C | A | 99 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(96): Show |
184 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.646-5089C>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38518812 | |||||||
| chr3:38518854 | A | G | 159 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(156): Show |
295 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(292): Show |
intron_variant | MODIFIER | c.646-5047A>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38518854 | |||||||
| chr3:38519023 | G | A | 2 | a0001c0001t0002g0059 a0001c0001t0002g0060 |
2 | NA19086.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.646-4878G>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38519023 | |||||||
| chr3:38519193 | G | A | 1 | a0001c0001t0002g0091 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.646-4708G>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38519193 | |||||||
| chr3:38519285 | C | T | 3 | a0001c0001t0002g0024 a0001c0001t0002g0063 a0001c0001t0002g0074 |
5 | HG00438.hp2 HG00544.hp2 HG02071.hp2 others(2): Show |
intron_variant | MODIFIER | c.646-4616C>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38519285 | |||||||
| chr3:38519359 | T | G | 1 | a0001c0001t0008g0020 | 4 | HG01167.hp2 HG01169.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.646-4542T>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38519359 | |||||||
| chr3:38519365 | G | A | 3 | a0001c0001t0006g0012 a0001c0001t0006g0098 a0001c0001t0006g0099 |
7 | HG01243.hp1 HG01884.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.646-4536G>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38519365 | |||||||
| chr3:38519451 | C | G | 12 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0014 others(9): Show |
28 | HG00621.hp2 HG01070.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.646-4450C>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38519451 | |||||||
| chr3:38519551 | AT | A | 3 | a0001c0001t0003g0028 a0001c0001t0003g0126 a0003c0006t0003g0125 |
5 | HG00544.hp1 HG00558.hp1 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.646-4341delT | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 38519551 | ||||||
| chr3:38519588 | G | A | 25 | a0001c0001t0003g0003 a0001c0001t0003g0019 a0001c0001t0003g0028 others(22): Show |
45 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.646-4313G>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38519588 | |||||||
| chr3:38519816 | C | T | 33 | a0001c0001t0002g0087 a0001c0001t0002g0088 a0001c0001t0002g0089 others(30): Show |
57 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.646-4085C>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38519816 | |||||||
| chr3:38519995 | C | T | 1 | a0001c0001t0004g0153 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.646-3906C>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38519995 | |||||||
| chr3:38520090 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.646-3811T>C | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38520090 | |||||||
| chr3:38520238 | G | A | 5 | a0001c0001t0001g0146 a0001c0001t0006g0012 a0001c0001t0006g0098 others(2): Show |
9 | HG01243.hp1 HG01884.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.646-3663G>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38520238 | |||||||
| chr3:38520347 | A | G | 2 | a0001c0001t0002g0023 a0001c0001t0002g0073 |
4 | HG01167.hp1 HG01516.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.646-3554A>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38520347 | |||||||
| chr3:38520391 | T | TTAATAGC others(13): Show |
1 | a0001c0001t0001g0168 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.646-3508_646-3489d others(22): Show |
EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 38520391 | ||||||
| chr3:38520557 | C | T | 25 | a0001c0001t0003g0003 a0001c0001t0003g0019 a0001c0001t0003g0028 others(22): Show |
45 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.646-3344C>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38520557 | |||||||
| chr3:38520599 | G | A | 1 | a0001c0001t0002g0086 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.646-3302G>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38520599 | |||||||
| chr3:38520606 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.646-3295C>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38520606 | |||||||
| chr3:38520797 | C | T | 161 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(158): Show |
298 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(295): Show |
intron_variant | MODIFIER | c.646-3104C>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38520797 | |||||||
| chr3:38520813 | G | A | 1 | a0001c0001t0002g0070 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.646-3088G>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38520813 | |||||||
| chr3:38520849 | G | A | 1 | a0001c0001t0003g0113 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.646-3052G>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38520849 | |||||||
| chr3:38520901 | A | G | 25 | a0001c0001t0003g0003 a0001c0001t0003g0019 a0001c0001t0003g0028 others(22): Show |
45 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.646-3000A>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38520901 | |||||||
| chr3:38521088 | C | T | 161 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(158): Show |
298 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(295): Show |
intron_variant | MODIFIER | c.646-2813C>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38521088 | |||||||
| chr3:38521443 | CT | C | 8 | a0001c0001t0001g0005 a0001c0001t0001g0096 a0001c0001t0001g0097 others(5): Show |
17 | HG00639.hp2 HG00741.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.646-2457delT | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38521443 | |||||||
| chr3:38521758 | T | C | 25 | a0001c0001t0003g0003 a0001c0001t0003g0019 a0001c0001t0003g0028 others(22): Show |
45 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.646-2143T>C | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38521758 | |||||||
| chr3:38521816 | G | T | 1 | a0001c0001t0002g0034 | 2 | HG02523.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.646-2085G>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38521816 | |||||||
| chr3:38521846 | A | G | 2 | a0001c0001t0010g0025 a0001c0001t0015g0177 |
4 | HG02895.hp1 HG02897.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.646-2055A>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38521846 | |||||||
| chr3:38521881 | G | GC | 4 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0143 others(1): Show |
4 | HG01255.hp1 HG02055.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.646-2019dupC | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 38521881 | ||||||
| chr3:38521918 | A | T | 2 | a0001c0001t0001g0101 a0001c0001t0001g0103 |
2 | HG01993.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.646-1983A>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38521918 | |||||||
| chr3:38522175 | A | G | 1 | a0001c0001t0001g0104 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.646-1726A>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38522175 | |||||||
| chr3:38522264 | A | G | 1 | a0001c0001t0001g0104 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.646-1637A>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38522264 | |||||||
| chr3:38522394 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.646-1507G>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38522394 | |||||||
| chr3:38522571 | C | T | 1 | a0001c0001t0003g0123 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.646-1330C>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38522571 | |||||||
| chr3:38522573 | C | T | 4 | a0001c0001t0006g0012 a0001c0001t0006g0098 a0001c0001t0006g0099 others(1): Show |
8 | HG01243.hp1 HG01884.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.646-1328C>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38522573 | |||||||
| chr3:38522597 | C | T | 14 | a0001c0001t0001g0015 a0001c0001t0001g0027 a0001c0001t0001g0041 others(11): Show |
20 | HG00639.hp1 HG01074.hp1 HG01981.hp2 others(17): Show |
intron_variant | MODIFIER | c.646-1304C>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38522597 | |||||||
| chr3:38522632 | G | A | 2 | a0001c0001t0009g0037 a0001c0001t0009g0092 |
3 | HG02615.hp1 HG02818.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.646-1269G>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38522632 | |||||||
| chr3:38522693 | G | A | 27 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0014 others(24): Show |
49 | HG00621.hp2 HG00639.hp1 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.646-1208G>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38522693 | |||||||
| chr3:38522788 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.646-1113G>A | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38522788 | |||||||
| chr3:38522794 | A | G | 1 | a0001c0001t0002g0071 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.646-1107A>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38522794 | |||||||
| chr3:38522795 | C | T | 25 | a0001c0001t0003g0003 a0001c0001t0003g0019 a0001c0001t0003g0028 others(22): Show |
45 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.646-1106C>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38522795 | |||||||
| chr3:38523042 | T | C | 6 | a0001c0001t0001g0018 a0001c0001t0001g0057 a0001c0001t0001g0133 others(3): Show |
11 | HG00558.hp2 NA18944.hp1 NA18949.hp1 others(8): Show |
intron_variant | MODIFIER | c.646-859T>C | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38523042 | |||||||
| chr3:38523133 | T | C | 1 | a0001c0001t0001g0118 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.646-768T>C | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38523133 | |||||||
| chr3:38523223 | C | G | 1 | a0001c0001t0002g0066 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.646-678C>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38523223 | |||||||
| chr3:38523411 | T | G | 2 | a0001c0001t0010g0025 a0001c0001t0015g0177 |
4 | HG02895.hp1 HG02897.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.646-490T>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38523411 | |||||||
| chr3:38523416 | T | C | 8 | a0001c0001t0002g0007 a0001c0001t0002g0069 a0001c0001t0002g0070 others(5): Show |
14 | NA18952.hp2 NA18954.hp1 NA18978.hp2 others(11): Show |
intron_variant | MODIFIER | c.646-485T>C | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38523416 | |||||||
| chr3:38523432 | C | T | 1 | a0001c0001t0001g0049 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.646-469C>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38523432 | |||||||
| chr3:38523648 | A | G | 4 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0185 others(1): Show |
4 | HG01255.hp2 HG01496.hp1 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.646-253A>G | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38523648 | |||||||
| chr3:38523657 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.646-244C>T | EXOG | ENSG00000157036.13 | transcript | ENST00000287675.10 | protein_coding | 5/5 | chr3 | 38523657 |