Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 50852 |
| ensemblid | ENSG00000163519.14 |
| hgncid | 30698 |
| symbol | TRAT1 |
| name | T cell receptor associated transmembrane adaptor 1 |
| refseq_nuc | NM_016388.4 |
| refseq_prot | NP_057472.2 |
| ensembl_nuc | ENST00000295756.11 |
| ensembl_prot | ENSP00000295756.6 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 108822786 |
| end | 108855005 |
| strand | + |
| ver | v1.2 |
| region | chr3:108822786-108855005 |
| region5000 | chr3:108817786-108860005 |
| regionname0 | TRAT1_chr3_108822786_108855005 |
| regionname5000 | TRAT1_chr3_108817786_108860005 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 186 | 314 | 80 | 72 | 100 | 14 | 46 | 75 | TRAT1_chr3_108817786_108860005 | TRAT1 | MSGIS others(181): Show |
chr3 | 108817786 | 108860005 |
| a0002 | 0/0 | 186 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | MSGIS others(181): Show |
chr3 | 108817786 | 108860005 |
| a0003 | 0/0 | 186 | 5 | 0 | 0 | 5 | 0 | 0 | 4 | TRAT1_chr3_108817786_108860005 | TRAT1 | MSGIS others(181): Show |
chr3 | 108817786 | 108860005 |
| a0004 | 0/0 | 186 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | MSGIS others(181): Show |
chr3 | 108817786 | 108860005 |
| a0005 | 0/0 | 186 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | MSGIS others(181): Show |
chr3 | 108817786 | 108860005 |
| a0006 | 0/0 | 186 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | TRAT1_chr3_108817786_108860005 | TRAT1 | MSGIS others(181): Show |
chr3 | 108817786 | 108860005 |
| a0007 | 0/0 | 186 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | MSGIS others(181): Show |
chr3 | 108817786 | 108860005 |
| a0008 | 0/0 | 186 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | MSGIS others(181): Show |
chr3 | 108817786 | 108860005 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 558 | 314 | 80 | 72 | 100 | 14 | 46 | TRAT1_chr3_108817786_108860005 | TRAT1 | ATGTC others(553): Show |
chr3 | 108817786 | 108860005 | ||
| a0002c0002 | 0/0 | 558 | 9 | 9 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | ATGTC others(553): Show |
chr3 | 108817786 | 108860005 | ||
| a0003c0003 | 0/0 | 558 | 5 | 0 | 0 | 5 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | ATGTC others(553): Show |
chr3 | 108817786 | 108860005 | ||
| a0004c0004 | 0/0 | 558 | 4 | 4 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | ATGTC others(553): Show |
chr3 | 108817786 | 108860005 | ||
| a0005c0005 | 0/0 | 558 | 3 | 3 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | ATGTC others(553): Show |
chr3 | 108817786 | 108860005 | ||
| a0006c0006 | 0/0 | 558 | 3 | 0 | 0 | 3 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | ATGTC others(553): Show |
chr3 | 108817786 | 108860005 | ||
| a0007c0008 | 0/0 | 558 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | ATGTC others(553): Show |
chr3 | 108817786 | 108860005 | ||
| a0008c0007 | 0/0 | 558 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | ATGTC others(553): Show |
chr3 | 108817786 | 108860005 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1831 | 139 | 15 | 28 | 72 | 5 | 19 | TRAT1_chr3_108817786_108860005 | TRAT1 | GGCAC others(1826): Show |
chr3 | 108817786 | 108860005 |
| a0001c0001t0002 | 1/0 | 1831 | 86 | 25 | 23 | 23 | 6 | 8 | TRAT1_chr3_108817786_108860005 | TRAT1 | GGCAC others(1826): Show |
chr3 | 108817786 | 108860005 |
| a0001c0001t0003 | 0/0 | 1831 | 34 | 0 | 13 | 5 | 1 | 15 | TRAT1_chr3_108817786_108860005 | TRAT1 | GGCAC others(1826): Show |
chr3 | 108817786 | 108860005 |
| a0001c0001t0004 | 0/0 | 1831 | 23 | 19 | 4 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | GGCAC others(1826): Show |
chr3 | 108817786 | 108860005 |
| a0001c0001t0005 | 0/1 | 1831 | 14 | 6 | 3 | 0 | 2 | 2 | TRAT1_chr3_108817786_108860005 | TRAT1 | GGCAC others(1826): Show |
chr3 | 108817786 | 108860005 |
| a0001c0001t0006 | 0/0 | 1828 | 6 | 6 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | GGCAC others(1823): Show |
chr3 | 108817786 | 108860005 |
| a0001c0001t0007 | 0/0 | 1828 | 6 | 5 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | GGCAC others(1823): Show |
chr3 | 108817786 | 108860005 |
| a0001c0001t0009 | 0/0 | 1831 | 2 | 2 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | GGCAC others(1826): Show |
chr3 | 108817786 | 108860005 |
| a0001c0001t0010 | 0/0 | 1831 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | GGCAC others(1826): Show |
chr3 | 108817786 | 108860005 |
| a0001c0001t0011 | 0/0 | 1831 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | GGCAC others(1826): Show |
chr3 | 108817786 | 108860005 |
| a0001c0001t0012 | 0/0 | 1831 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | GGCAC others(1826): Show |
chr3 | 108817786 | 108860005 |
| a0001c0001t0013 | 0/0 | 1831 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | GGCAC others(1826): Show |
chr3 | 108817786 | 108860005 |
| a0002c0002t0002 | 0/0 | 1831 | 9 | 9 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | GGCAC others(1826): Show |
chr3 | 108817786 | 108860005 |
| a0003c0003t0001 | 0/0 | 1831 | 5 | 0 | 0 | 5 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | GGCAC others(1826): Show |
chr3 | 108817786 | 108860005 |
| a0004c0004t0008 | 0/0 | 1831 | 4 | 4 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | GGCAC others(1826): Show |
chr3 | 108817786 | 108860005 |
| a0005c0005t0002 | 0/0 | 1831 | 3 | 3 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | GGCAC others(1826): Show |
chr3 | 108817786 | 108860005 |
| a0006c0006t0002 | 0/0 | 1831 | 3 | 0 | 0 | 3 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | GGCAC others(1826): Show |
chr3 | 108817786 | 108860005 |
| a0007c0008t0001 | 0/0 | 1831 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | GGCAC others(1826): Show |
chr3 | 108817786 | 108860005 |
| a0008c0007t0001 | 0/0 | 1831 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | GGCAC others(1826): Show |
chr3 | 108817786 | 108860005 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 11 | 0 | 1 | 8 | 0 | 2 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0004 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0011 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0030 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0031 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0049 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0003g0002 | 0/0 | 7 | 0 | 1 | 2 | 0 | 4 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0003g0012 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0003g0033 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0003g0041 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0003g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0003g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0003g0044 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0003g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0004g0009 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0004g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0004g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0004g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0004g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0004g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0004g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0004g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0004g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0004g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0004g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0004g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0004g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0005g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0005g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0005g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0005g0241 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0005g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0005g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0005g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0005g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0005g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0005g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0005g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0005g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0005g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0006g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0006g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0006g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0006g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0006g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0007g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0007g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0007g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0007g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0007g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0007g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0009g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0009g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0010g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0011g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0012g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0001c0001t0013g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0002c0002t0002g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0002c0002t0002g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0002c0002t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0002c0002t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0002c0002t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0002c0002t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0002c0002t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0003c0003t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0003c0003t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0003c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0004c0004t0008g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0004c0004t0008g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0004c0004t0008g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0004c0004t0008g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0005c0005t0002g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0006c0006t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0006c0006t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0006c0006t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0007c0008t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| a0008c0007t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0005 | g0255 | EUR | GBR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0167 | EUR | GBR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0024 | EUR | FIN | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0029 | EUR | FIN | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | CHS | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG00408 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | CHS | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | CHS | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0247 | EAS | CHS | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | CHS | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0250 | EAS | CHS | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | CHS | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0144 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG00735 | hp1 | a0001 | c0001 | t0004 | g0009 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0023 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG00738 | hp2 | a0001 | c0001 | t0005 | g0263 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0161 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0170 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG01069 | hp2 | a0001 | c0001 | t0004 | g0066 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0145 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0043 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG01071 | hp1 | a0001 | c0001 | t0004 | g0014 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0043 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG01074 | hp2 | a0001 | c0001 | t0005 | g0248 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0072 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG01081 | hp2 | a0001 | c0001 | t0004 | g0048 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0025 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG01106 | hp2 | a0001 | c0001 | t0007 | g0203 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0184 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0165 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0169 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0234 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0147 | AMR | CLM | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0042 | AMR | CLM | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0172 | AMR | CLM | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0252 | AMR | CLM | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0253 | AMR | CLM | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0042 | AMR | CLM | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0205 | AMR | CLM | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0032 | AMR | CLM | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0073 | AMR | CLM | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0031 | AMR | CLM | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0074 | EUR | IBS | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0031 | EUR | IBS | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0028 | EUR | IBS | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG01516 | hp2 | a0001 | c0001 | t0005 | g0261 | EUR | IBS | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0028 | EUR | IBS | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0175 | EUR | IBS | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0109 | AFR | ACB | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0196 | AFR | ACB | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG01891 | hp2 | a0001 | c0001 | t0007 | g0204 | AFR | ACB | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0193 | AMR | PEL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PEL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0012 | AMR | PEL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0227 | AMR | PEL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0033 | AMR | PEL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0171 | AMR | PEL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0139 | AMR | PEL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG01993 | hp1 | a0001 | c0001 | t0005 | g0256 | AMR | PEL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0194 | AMR | PEL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0174 | AMR | PEL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02055 | hp1 | a0002 | c0002 | t0002 | g0237 | AFR | ACB | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02055 | hp2 | a0004 | c0004 | t0008 | g0052 | AFR | ACB | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | KHV | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | ACB | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | CDX | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | CDX | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CDX | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | CDX | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02257 | hp1 | a0004 | c0004 | t0008 | g0051 | AFR | ACB | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02257 | hp2 | a0002 | c0002 | t0002 | g0117 | AFR | ACB | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02258 | hp1 | a0005 | c0005 | t0002 | g0010 | AFR | ACB | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0128 | AFR | ACB | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0240 | AFR | ACB | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0012 | AMR | PEL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0106 | AMR | PEL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0151 | AFR | ACB | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02451 | hp2 | a0005 | c0005 | t0002 | g0010 | AFR | ACB | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0124 | AFR | GWD | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0131 | AFR | GWD | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0133 | SAS | PJL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0110 | AFR | GWD | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0119 | AFR | GWD | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0045 | AFR | GWD | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0233 | AFR | GWD | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0107 | AFR | GWD | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0009 | AFR | GWD | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0242 | SAS | PJL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0071 | SAS | PJL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02717 | hp1 | a0001 | c0001 | t0006 | g0157 | AFR | GWD | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0009 | AFR | GWD | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0140 | AFR | GWD | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02723 | hp2 | a0001 | c0001 | t0012 | g0070 | AFR | GWD | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02738 | hp1 | a0001 | c0001 | t0005 | g0192 | SAS | PJL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02809 | hp1 | a0001 | c0001 | t0007 | g0199 | AFR | GWD | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0118 | AFR | GWD | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0121 | AFR | GWD | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0115 | AFR | GWD | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02886 | hp2 | a0001 | c0001 | t0006 | g0027 | AFR | GWD | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02895 | hp1 | a0001 | c0001 | t0005 | g0257 | AFR | GWD | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0111 | AFR | GWD | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02897 | hp1 | a0001 | c0001 | t0005 | g0238 | AFR | GWD | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02922 | hp1 | a0002 | c0002 | t0002 | g0040 | AFR | ESN | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0050 | AFR | ESN | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02965 | hp2 | a0002 | c0002 | t0002 | g0123 | AFR | ESN | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02970 | hp1 | a0002 | c0002 | t0002 | g0022 | AFR | ESN | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ESN | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02976 | hp1 | a0001 | c0001 | t0009 | g0047 | AFR | ESN | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0236 | AFR | ESN | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0044 | SAS | PJL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0260 | AFR | GWD | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG03041 | hp2 | a0001 | c0001 | t0007 | g0239 | AFR | GWD | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0153 | AFR | MSL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | MSL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG03130 | hp1 | a0001 | c0001 | t0006 | g0158 | AFR | ESN | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0126 | AFR | ESN | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG03139 | hp1 | a0002 | c0002 | t0002 | g0040 | AFR | ESN | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0232 | AFR | ESN | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG03195 | hp1 | a0001 | c0001 | t0006 | g0027 | AFR | ESN | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0045 | AFR | ESN | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | MSL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0150 | AFR | MSL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0055 | AFR | MSL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0130 | AFR | MSL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0030 | SAS | PJL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0122 | AFR | MSL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG03453 | hp2 | a0001 | c0001 | t0006 | g0156 | AFR | MSL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0014 | AFR | MSL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG03486 | hp2 | a0001 | c0001 | t0007 | g0198 | AFR | MSL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0138 | SAS | PJL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0012 | SAS | PJL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0054 | AFR | ESN | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | ESN | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0197 | AFR | MSL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0152 | AFR | MSL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0243 | SAS | PJL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0258 | SAS | PJL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0041 | SAS | PJL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | STU | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0173 | SAS | STU | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0104 | SAS | PJL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0244 | SAS | PJL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG03710 | hp1 | a0001 | c0001 | t0005 | g0262 | SAS | PJL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG03834 | hp1 | a0001 | c0001 | t0011 | g0195 | SAS | BEB | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | BEB | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0041 | SAS | BEB | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0254 | SAS | BEB | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | BEB | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0141 | SAS | BEB | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | STU | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | STU | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG04184 | hp1 | a0001 | c0001 | t0010 | g0249 | SAS | BEB | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0033 | SAS | BEB | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | STU | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0137 | SAS | STU | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0246 | SAS | STU | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | STU | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0222 | AFR | YRI | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0200 | AFR | YRI | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0259 | AFR | YRI | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | YRI | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA18948 | hp1 | a0003 | c0003 | t0001 | g0008 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA18964 | hp2 | a0007 | c0008 | t0001 | g0037 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA18966 | hp1 | a0006 | c0006 | t0002 | g0217 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA18969 | hp2 | a0003 | c0003 | t0001 | g0080 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA18999 | hp1 | a0003 | c0003 | t0001 | g0008 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA19004 | hp1 | a0003 | c0003 | t0001 | g0008 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA19011 | hp1 | a0006 | c0006 | t0002 | g0089 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0245 | AFR | LWK | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | LWK | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0116 | AFR | LWK | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0154 | AFR | LWK | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA19062 | hp1 | a0008 | c0007 | t0001 | g0095 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA19091 | hp2 | a0006 | c0006 | t0002 | g0225 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA19240 | hp1 | a0005 | c0005 | t0002 | g0010 | AFR | YRI | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA19240 | hp2 | a0004 | c0004 | t0008 | g0065 | AFR | YRI | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | ASW | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA20129 | hp2 | a0001 | c0001 | t0013 | g0120 | AFR | ASW | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0251 | EUR | TSI | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0025 | EUR | TSI | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0030 | EUR | TSI | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0024 | EUR | TSI | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | GIH | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | GIH | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0166 | AMR | CLM | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02109 | hp2 | a0001 | c0001 | t0007 | g0202 | AFR | ACB | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02486 | hp1 | a0002 | c0002 | t0002 | g0022 | AFR | ACB | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0143 | AFR | ACB | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02559 | hp1 | a0001 | c0001 | t0009 | g0046 | AFR | ACB | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG02559 | hp2 | a0004 | c0004 | t0008 | g0160 | AFR | ACB | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0159 | AFR | MSL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0177 | AFR | USA | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| HG06807 | hp2 | a0002 | c0002 | t0002 | g0226 | AFR | USA | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA20300 | hp1 | a0002 | c0002 | t0002 | g0127 | AFR | USA | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0129 | AFR | USA | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA21309 | hp1 | a0001 | c0001 | t0006 | g0125 | AFR | LWK | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0155 | AFR | LWK | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0005 | g0241 | REF | REF | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0049 | REF | REF | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:108830780 | G | A | 1 | a0008 | 1 | NA19062.hp1 | missense_variant&splice_region_variant | MODERATE | c.118G>A | p.Asp40Asn | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/6 | 260/1831 | 118/561 | 40/186 | chr3 | 108830780 | |||
| chr3:108849207 | C | T | 2 | a0003 a0008 |
6 | HG00408.hp2 NA18948.hp1 NA18969.hp2 others(3): Show |
missense_variant | MODERATE | c.256C>T | p.Pro86Ser | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/6 | 398/1831 | 256/561 | 86/186 | chr3 | 108849207 | |||
| chr3:108853677 | C | A | 1 | a0007 | 1 | NA18964.hp2 | missense_variant | MODERATE | c.361C>A | p.Arg121Ser | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 6/6 | 503/1831 | 361/561 | 121/186 | chr3 | 108853677 | |||
| chr3:108853686 | C | A | 1 | a0002 | 9 | HG02055.hp1 HG02257.hp2 HG02486.hp1 others(6): Show |
missense_variant | MODERATE | c.370C>A | p.Pro124Thr | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 6/6 | 512/1831 | 370/561 | 124/186 | chr3 | 108853686 | |||
| chr3:108853726 | A | G | 1 | a0004 | 4 | HG02055.hp2 HG02257.hp1 HG02559.hp2 others(1): Show |
missense_variant | MODERATE | c.410A>G | p.Asp137Gly | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 6/6 | 552/1831 | 410/561 | 137/186 | chr3 | 108853726 | |||
| chr3:108853758 | T | C | 1 | a0005 | 3 | HG02258.hp1 HG02451.hp2 NA19240.hp1 |
missense_variant | MODERATE | c.442T>C | p.Ser148Pro | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 6/6 | 584/1831 | 442/561 | 148/186 | chr3 | 108853758 | |||
| chr3:108853852 | G | T | 1 | a0006 | 3 | NA18966.hp1 NA19011.hp1 NA19091.hp2 |
missense_variant | MODERATE | c.536G>T | p.Arg179Leu | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 6/6 | 678/1831 | 536/561 | 179/186 | chr3 | 108853852 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:108822914 | T | C | 4 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0010 others(1): Show |
49 | HG00099.hp1 HG00544.hp2 HG00597.hp2 others(46): Show |
5_prime_UTR_variant | MODIFIER | c.-14T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/6 | 14 | chr3 | 108822914 | ||||||
| chr3:108853941 | G | A | 1 | a0001c0001t0010 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*64G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 6/6 | 64 | chr3 | 108853941 | ||||||
| chr3:108853943 | A | G | 1 | a0001c0001t0013 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*66A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 6/6 | 66 | chr3 | 108853943 | ||||||
| chr3:108854291 | T | A | 1 | a0001c0001t0009 | 2 | HG02559.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*414T>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 6/6 | 414 | chr3 | 108854291 | ||||||
| chr3:108854500 | TCTA | T | 1 | a0001c0001t0007 | 6 | HG01106.hp2 HG01891.hp2 HG02109.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*627_*629delCTA | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 6/6 | 627 | INFO_REALIGN_3_PRIME | chr3 | 108854500 | |||||
| chr3:108854565 | A | C | 1 | a0001c0001t0011 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*688A>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 6/6 | 688 | chr3 | 108854565 | ||||||
| chr3:108854787 | T | A | 1 | a0001c0001t0012 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*910T>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 6/6 | 910 | chr3 | 108854787 | ||||||
| chr3:108854800 | T | A | 2 | a0001c0001t0004 a0001c0001t0013 |
24 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*923T>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 6/6 | 923 | chr3 | 108854800 | ||||||
| chr3:108854802 | T | C | 1 | a0004c0004t0008 | 4 | HG02055.hp2 HG02257.hp1 HG02559.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*925T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 6/6 | 925 | chr3 | 108854802 | ||||||
| chr3:108854936 | C | T | 8 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(5): Show |
191 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(188): Show |
3_prime_UTR_variant | MODIFIER | c.*1059C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 6/6 | 1059 | chr3 | 108854936 | ||||||
| chr3:108854947 | ATTG | A | 1 | a0001c0001t0006 | 6 | HG02717.hp1 HG02886.hp2 HG03130.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1073_*1075delGTT | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 6/6 | 1073 | INFO_REALIGN_3_PRIME | chr3 | 108854947 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:108823084 | CAT | C | 124 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0028 others(121): Show |
161 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.7+151_7+152delAT | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108823084 | |||||||
| chr3:108823147 | C | T | 257 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(254): Show |
332 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(329): Show |
intron_variant | MODIFIER | c.7+213C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108823147 | |||||||
| chr3:108823270 | A | T | 1 | a0001c0001t0001g0163 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.7+336A>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108823270 | |||||||
| chr3:108823337 | A | G | 1 | a0001c0001t0001g0162 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.7+403A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108823337 | |||||||
| chr3:108823514 | T | C | 1 | a0001c0001t0001g0053 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.7+580T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108823514 | |||||||
| chr3:108823650 | T | G | 97 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(94): Show |
128 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.7+716T>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108823650 | |||||||
| chr3:108823656 | C | T | 19 | a0001c0001t0002g0118 a0001c0001t0002g0122 a0001c0001t0002g0126 others(16): Show |
22 | HG00735.hp1 HG02257.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.7+722C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108823656 | |||||||
| chr3:108823723 | A | G | 3 | a0001c0001t0002g0021 a0001c0001t0002g0113 a0001c0001t0002g0114 |
4 | NA18939.hp2 NA18961.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+789A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108823723 | |||||||
| chr3:108823809 | A | G | 1 | a0001c0001t0002g0161 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.7+875A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108823809 | |||||||
| chr3:108823895 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.7+961C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108823895 | |||||||
| chr3:108824018 | C | T | 1 | a0004c0004t0008g0160 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.7+1084C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108824018 | |||||||
| chr3:108824113 | G | A | 41 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0164 others(38): Show |
56 | HG00099.hp2 HG00323.hp2 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.7+1179G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108824113 | |||||||
| chr3:108824149 | C | T | 9 | a0001c0001t0002g0126 a0001c0001t0002g0130 a0001c0001t0002g0131 others(6): Show |
10 | HG02258.hp2 HG02486.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.7+1215C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108824149 | |||||||
| chr3:108824152 | G | A | 9 | a0001c0001t0001g0201 a0001c0001t0002g0197 a0001c0001t0002g0200 others(6): Show |
9 | HG01106.hp2 HG01891.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.7+1218G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108824152 | |||||||
| chr3:108824303 | A | T | 3 | a0001c0001t0004g0109 a0001c0001t0004g0110 a0001c0001t0004g0111 |
3 | HG01884.hp2 HG02615.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.7+1369A>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108824303 | |||||||
| chr3:108824398 | A | T | 66 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(63): Show |
90 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.7+1464A>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108824398 | |||||||
| chr3:108824483 | A | C | 1 | a0001c0001t0002g0159 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.7+1549A>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108824483 | |||||||
| chr3:108824528 | G | T | 257 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(254): Show |
332 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(329): Show |
intron_variant | MODIFIER | c.7+1594G>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108824528 | |||||||
| chr3:108825124 | TA | T | 125 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0020 others(122): Show |
163 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.7+2191delA | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108825124 | |||||||
| chr3:108825128 | T | C | 1 | a0001c0001t0002g0034 | 2 | HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.7+2194T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108825128 | |||||||
| chr3:108825278 | C | T | 4 | a0001c0001t0006g0027 a0001c0001t0006g0156 a0001c0001t0006g0157 others(1): Show |
5 | HG02717.hp1 HG02886.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.7+2344C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108825278 | |||||||
| chr3:108825300 | T | G | 3 | a0001c0001t0004g0014 a0001c0001t0004g0066 a0004c0004t0008g0065 |
4 | HG01069.hp2 HG01071.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+2366T>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108825300 | |||||||
| chr3:108825407 | T | C | 1 | a0001c0001t0001g0006 | 3 | NA18943.hp2 NA18948.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.7+2473T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108825407 | |||||||
| chr3:108825427 | A | T | 78 | a0001c0001t0001g0026 a0001c0001t0001g0132 a0001c0001t0001g0134 others(75): Show |
99 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.7+2493A>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108825427 | |||||||
| chr3:108825428 | A | T | 1 | a0001c0001t0005g0238 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.7+2494A>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108825428 | |||||||
| chr3:108825504 | C | T | 64 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(61): Show |
87 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.7+2570C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108825504 | |||||||
| chr3:108825719 | A | T | 1 | a0001c0001t0005g0263 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.7+2785A>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108825719 | |||||||
| chr3:108825877 | G | A | 2 | a0001c0001t0002g0240 a0001c0001t0007g0239 |
2 | HG02280.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.7+2943G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108825877 | |||||||
| chr3:108825889 | G | T | 2 | a0004c0004t0008g0051 a0004c0004t0008g0052 |
2 | HG02055.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.7+2955G>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108825889 | |||||||
| chr3:108826005 | A | G | 1 | a0001c0001t0002g0240 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.7+3071A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108826005 | |||||||
| chr3:108826227 | T | TCAGTGAT others(11): Show |
220 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(217): Show |
288 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(285): Show |
intron_variant | MODIFIER | c.7+3296_7+3297insTG others(16): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 108826227 | ||||||
| chr3:108826340 | C | T | 7 | a0001c0001t0001g0235 a0001c0001t0002g0232 a0001c0001t0002g0233 others(4): Show |
8 | HG01192.hp1 HG02055.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.7+3406C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108826340 | |||||||
| chr3:108826421 | T | C | 36 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0020 others(33): Show |
46 | HG00408.hp1 HG00597.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.7+3487T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108826421 | |||||||
| chr3:108826515 | G | A | 1 | a0001c0001t0004g0115 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.7+3581G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108826515 | |||||||
| chr3:108826531 | G | A | 18 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0164 others(15): Show |
22 | HG00099.hp2 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.7+3597G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108826531 | |||||||
| chr3:108826598 | C | T | 2 | a0001c0001t0002g0154 a0001c0001t0002g0155 |
2 | NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.7+3664C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108826598 | |||||||
| chr3:108826762 | A | T | 12 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0057 others(9): Show |
16 | HG01243.hp2 HG01884.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.7+3828A>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108826762 | |||||||
| chr3:108826816 | G | A | 36 | a0001c0001t0001g0026 a0001c0001t0001g0132 a0001c0001t0001g0134 others(33): Show |
43 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.8-3854G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108826816 | |||||||
| chr3:108826916 | A | C | 7 | a0001c0001t0002g0197 a0001c0001t0002g0200 a0001c0001t0007g0198 others(4): Show |
7 | HG01106.hp2 HG01891.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.8-3754A>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108826916 | |||||||
| chr3:108827009 | G | A | 7 | a0001c0001t0003g0012 a0001c0001t0003g0033 a0001c0001t0003g0193 others(4): Show |
10 | HG01361.hp1 HG01934.hp1 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.8-3661G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108827009 | |||||||
| chr3:108827115 | T | G | 200 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(197): Show |
253 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.8-3555T>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108827115 | |||||||
| chr3:108827116 | T | C | 200 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(197): Show |
253 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.8-3554T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108827116 | |||||||
| chr3:108827214 | G | T | 31 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0035 others(28): Show |
41 | HG00597.hp1 HG00639.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.8-3456G>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108827214 | |||||||
| chr3:108827268 | G | A | 27 | a0001c0001t0001g0026 a0001c0001t0001g0132 a0001c0001t0001g0134 others(24): Show |
34 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.8-3402G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108827268 | |||||||
| chr3:108827373 | AGTATGT | A | 3 | a0001c0001t0002g0232 a0001c0001t0002g0233 a0001c0001t0002g0234 |
3 | HG01192.hp1 HG02630.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.8-3294_8-3289delAT others(4): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 108827373 | ||||||
| chr3:108827374 | GTA | G | 6 | a0001c0001t0002g0126 a0001c0001t0004g0116 a0001c0001t0006g0125 others(3): Show |
8 | HG02055.hp1 HG02486.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.8-3294_8-3293delAT | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 108827374 | ||||||
| chr3:108827375 | T | A | 1 | a0002c0002t0002g0127 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.8-3295T>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108827375 | |||||||
| chr3:108827376 | A | G | 1 | a0002c0002t0002g0127 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.8-3294A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108827376 | |||||||
| chr3:108827377 | T | A | 6 | a0001c0001t0002g0126 a0001c0001t0004g0116 a0001c0001t0006g0125 others(3): Show |
8 | HG02055.hp1 HG02486.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.8-3293T>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108827377 | |||||||
| chr3:108827381 | T | A | 3 | a0001c0001t0002g0232 a0001c0001t0002g0233 a0001c0001t0002g0234 |
3 | HG01192.hp1 HG02630.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.8-3289T>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108827381 | |||||||
| chr3:108827384 | A | ATG | 14 | a0001c0001t0001g0180 a0001c0001t0002g0153 a0001c0001t0002g0170 others(11): Show |
16 | HG00735.hp1 HG00741.hp2 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.8-3250_8-3249dupGT | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 108827384 | ||||||
| chr3:108827384 | A | ATGTG | 3 | a0001c0001t0002g0240 a0001c0001t0004g0245 a0001c0001t0007g0239 |
3 | HG02280.hp2 HG03041.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.8-3252_8-3249dupGT others(2): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 108827384 | ||||||
| chr3:108827384 | A | G | 10 | a0001c0001t0002g0126 a0001c0001t0002g0232 a0001c0001t0002g0233 others(7): Show |
12 | HG01192.hp1 HG02055.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.8-3286A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108827384 | |||||||
| chr3:108827384 | ATG | A | 20 | a0001c0001t0001g0018 a0001c0001t0001g0061 a0001c0001t0001g0062 others(17): Show |
23 | HG01106.hp2 HG01109.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.8-3250_8-3249delGT | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 108827384 | ||||||
| chr3:108827384 | ATGTG | A | 97 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(94): Show |
129 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.8-3252_8-3249delGT others(2): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 108827384 | ||||||
| chr3:108827384 | ATGTGTG | A | 33 | a0001c0001t0001g0001 a0001c0001t0001g0026 a0001c0001t0001g0132 others(30): Show |
40 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.8-3254_8-3249delGT others(4): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 108827384 | ||||||
| chr3:108827384 | ATGTGTGT others(1): Show |
A | 4 | a0001c0001t0001g0037 a0001c0001t0002g0114 a0001c0001t0003g0012 others(1): Show |
4 | HG01952.hp2 HG02976.hp1 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.8-3256_8-3249delGT others(6): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 108827384 | ||||||
| chr3:108827384 | ATGTGTGT others(3): Show |
A | 31 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0035 others(28): Show |
42 | HG00597.hp1 HG00639.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.8-3258_8-3249delGT others(8): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 108827384 | ||||||
| chr3:108827413 | T | A | 1 | a0001c0001t0001g0235 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.8-3257T>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108827413 | |||||||
| chr3:108827482 | C | G | 6 | a0001c0001t0002g0200 a0001c0001t0007g0198 a0001c0001t0007g0199 others(3): Show |
6 | HG01106.hp2 HG01891.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.8-3188C>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108827482 | |||||||
| chr3:108827498 | C | T | 1 | a0001c0001t0002g0177 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.8-3172C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108827498 | |||||||
| chr3:108827662 | C | T | 7 | a0001c0001t0001g0201 a0001c0001t0002g0131 a0001c0001t0004g0048 others(4): Show |
7 | HG01081.hp2 HG01891.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.8-3008C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108827662 | |||||||
| chr3:108827823 | T | C | 147 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(144): Show |
195 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(192): Show |
intron_variant | MODIFIER | c.8-2847T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108827823 | |||||||
| chr3:108827912 | T | C | 3 | a0001c0001t0002g0232 a0001c0001t0002g0233 a0001c0001t0002g0234 |
3 | HG01192.hp1 HG02630.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.8-2758T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108827912 | |||||||
| chr3:108827971 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.8-2699T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108827971 | |||||||
| chr3:108828100 | A | T | 10 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(7): Show |
10 | HG01243.hp2 HG02818.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.8-2570A>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108828100 | |||||||
| chr3:108828284 | C | G | 261 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(258): Show |
336 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(333): Show |
intron_variant | MODIFIER | c.8-2386C>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108828284 | |||||||
| chr3:108828707 | C | A | 5 | a0001c0001t0006g0027 a0001c0001t0006g0125 a0001c0001t0006g0156 others(2): Show |
6 | HG02717.hp1 HG02886.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.8-1963C>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108828707 | |||||||
| chr3:108828827 | T | C | 4 | a0001c0001t0002g0131 a0001c0001t0004g0048 a0001c0001t0004g0107 others(1): Show |
4 | HG01081.hp2 HG02559.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.8-1843T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108828827 | |||||||
| chr3:108828871 | TTGAAAAC others(5): Show |
T | 14 | a0001c0001t0001g0026 a0001c0001t0001g0105 a0001c0001t0001g0149 others(11): Show |
21 | HG00597.hp2 HG00642.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.8-1796_8-1785delAA others(10): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 108828871 | ||||||
| chr3:108828995 | C | T | 12 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0201 others(9): Show |
16 | HG01069.hp2 HG01071.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.8-1675C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108828995 | |||||||
| chr3:108829031 | G | T | 3 | a0001c0001t0001g0176 a0001c0001t0005g0261 a0001c0001t0005g0262 |
3 | HG01192.hp2 HG01516.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.8-1639G>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108829031 | |||||||
| chr3:108829563 | G | A | 1 | a0001c0001t0001g0069 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.8-1107G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108829563 | |||||||
| chr3:108829586 | A | AAC | 1 | a0005c0005t0002g0010 | 3 | HG02258.hp1 HG02451.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.8-1054_8-1053dupCA | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 108829586 | ||||||
| chr3:108829586 | A | AACAC | 9 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0057 others(6): Show |
13 | HG01884.hp1 HG02109.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.8-1056_8-1053dupCA others(2): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 108829586 | ||||||
| chr3:108829586 | A | AACACAC | 19 | a0001c0001t0001g0060 a0001c0001t0001g0068 a0001c0001t0001g0074 others(16): Show |
20 | HG01081.hp1 HG01109.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.8-1058_8-1053dupCA others(4): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 108829586 | ||||||
| chr3:108829586 | A | AACACACA others(1): Show |
29 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0035 others(26): Show |
40 | HG00099.hp1 HG00597.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.8-1060_8-1053dupCA others(6): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 108829586 | ||||||
| chr3:108829586 | A | AACACACA others(3): Show |
99 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(96): Show |
133 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.8-1062_8-1053dupCA others(8): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 108829586 | ||||||
| chr3:108829586 | A | AACACACA others(5): Show |
25 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0097 others(22): Show |
30 | HG00099.hp2 HG00609.hp1 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.8-1064_8-1053dupCA others(10): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 108829586 | ||||||
| chr3:108829586 | A | AACACACA others(7): Show |
14 | a0001c0001t0001g0019 a0001c0001t0001g0028 a0001c0001t0001g0039 others(11): Show |
18 | HG00323.hp1 HG00639.hp2 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.8-1066_8-1053dupCA others(12): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 108829586 | ||||||
| chr3:108829586 | A | AACACACA others(9): Show |
33 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0102 others(30): Show |
41 | HG00558.hp1 HG00639.hp1 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.8-1068_8-1053dupCA others(14): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 108829586 | ||||||
| chr3:108829586 | A | AACACACA others(11): Show |
9 | a0001c0001t0001g0029 a0001c0001t0001g0064 a0001c0001t0002g0030 others(6): Show |
12 | HG00323.hp2 HG00741.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.8-1070_8-1053dupCA others(16): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 108829586 | ||||||
| chr3:108829586 | A | AACACACA others(13): Show |
3 | a0001c0001t0002g0173 a0001c0001t0002g0177 a0004c0004t0008g0051 |
3 | HG02257.hp1 HG03688.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.8-1072_8-1053dupCA others(18): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 108829586 | ||||||
| chr3:108829586 | A | AACACACA others(15): Show |
1 | a0001c0001t0002g0174 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.8-1074_8-1053dupCA others(20): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 108829586 | ||||||
| chr3:108829586 | A | AACACACA others(19): Show |
1 | a0004c0004t0008g0052 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.8-1078_8-1053dupCA others(24): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 108829586 | ||||||
| chr3:108829586 | A | ACACACAC others(4): Show |
2 | a0001c0001t0001g0103 a0006c0006t0002g0225 |
2 | HG02273.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.8-1084_8-1083insCA others(9): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108829586 | |||||||
| chr3:108829586 | A | ACACACAC others(12): Show |
1 | a0001c0001t0002g0175 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.8-1084_8-1083insCA others(17): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108829586 | |||||||
| chr3:108829604 | C | CACACAG | 4 | a0001c0001t0002g0130 a0001c0001t0002g0153 a0001c0001t0004g0009 others(1): Show |
6 | HG00735.hp1 HG02647.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.8-1061_8-1060insGA others(4): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 108829604 | ||||||
| chr3:108829785 | C | T | 261 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(258): Show |
336 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(333): Show |
intron_variant | MODIFIER | c.8-885C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108829785 | |||||||
| chr3:108829961 | G | A | 3 | a0001c0001t0002g0021 a0001c0001t0002g0113 a0001c0001t0002g0114 |
4 | NA18939.hp2 NA18961.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.8-709G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108829961 | |||||||
| chr3:108830144 | A | G | 84 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(81): Show |
115 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.8-526A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108830144 | |||||||
| chr3:108830175 | T | G | 68 | a0001c0001t0001g0029 a0001c0001t0001g0142 a0001c0001t0001g0146 others(65): Show |
85 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.8-495T>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108830175 | |||||||
| chr3:108830202 | T | C | 2 | a0001c0001t0003g0252 a0001c0001t0003g0253 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.8-468T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108830202 | |||||||
| chr3:108830283 | G | A | 5 | a0001c0001t0001g0016 a0001c0001t0001g0077 a0001c0001t0001g0097 others(2): Show |
6 | HG00408.hp1 HG00558.hp2 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.8-387G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108830283 | |||||||
| chr3:108830427 | G | A | 1 | a0001c0001t0001g0178 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.8-243G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108830427 | |||||||
| chr3:108830815 | C | A | 1 | a0001c0001t0002g0148 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.118+35C>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108830815 | |||||||
| chr3:108830852 | G | A | 3 | a0001c0001t0002g0021 a0001c0001t0002g0113 a0001c0001t0002g0114 |
4 | NA18939.hp2 NA18961.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.118+72G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108830852 | |||||||
| chr3:108830873 | T | G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(100): Show |
143 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.118+93T>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108830873 | |||||||
| chr3:108830927 | G | A | 9 | a0001c0001t0001g0078 a0001c0001t0001g0201 a0001c0001t0002g0130 others(6): Show |
11 | HG00735.hp1 HG01192.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.118+147G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108830927 | |||||||
| chr3:108831040 | A | G | 1 | a0001c0001t0001g0059 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.118+260A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108831040 | |||||||
| chr3:108831195 | C | A | 5 | a0001c0001t0007g0198 a0001c0001t0007g0199 a0001c0001t0007g0202 others(2): Show |
5 | HG01106.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.118+415C>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108831195 | |||||||
| chr3:108831290 | G | C | 2 | a0006c0006t0002g0217 a0006c0006t0002g0225 |
2 | NA18966.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.118+510G>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108831290 | |||||||
| chr3:108831297 | A | G | 14 | a0001c0001t0001g0026 a0001c0001t0001g0105 a0001c0001t0001g0149 others(11): Show |
21 | HG00597.hp2 HG00642.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.118+517A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108831297 | |||||||
| chr3:108831538 | C | CT | 14 | a0001c0001t0001g0136 a0001c0001t0001g0168 a0001c0001t0001g0201 others(11): Show |
17 | HG01106.hp1 HG01106.hp2 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.118+777dupT | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 108831538 | ||||||
| chr3:108831538 | CT | C | 40 | a0001c0001t0001g0029 a0001c0001t0001g0061 a0001c0001t0001g0062 others(37): Show |
44 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.118+777delT | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 108831538 | ||||||
| chr3:108831586 | C | A | 4 | a0001c0001t0001g0201 a0001c0001t0002g0233 a0001c0001t0002g0234 others(1): Show |
4 | HG01192.hp1 HG01891.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.118+806C>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108831586 | |||||||
| chr3:108831596 | G | A | 2 | a0004c0004t0008g0051 a0004c0004t0008g0052 |
2 | HG02055.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.118+816G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108831596 | |||||||
| chr3:108831703 | C | CT | 1 | a0001c0001t0001g0006 | 3 | NA18943.hp2 NA18948.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.118+924dupT | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 108831703 | ||||||
| chr3:108831835 | G | A | 4 | a0001c0001t0002g0131 a0001c0001t0004g0048 a0001c0001t0004g0107 others(1): Show |
4 | HG01081.hp2 HG02559.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.118+1055G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108831835 | |||||||
| chr3:108831850 | T | C | 5 | a0001c0001t0006g0027 a0001c0001t0006g0125 a0001c0001t0006g0156 others(2): Show |
6 | HG02717.hp1 HG02886.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.118+1070T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108831850 | |||||||
| chr3:108831926 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.118+1146C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108831926 | |||||||
| chr3:108832182 | T | C | 102 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(99): Show |
142 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.118+1402T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108832182 | |||||||
| chr3:108832334 | G | C | 118 | a0001c0001t0001g0013 a0001c0001t0001g0028 a0001c0001t0001g0029 others(115): Show |
144 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.118+1554G>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108832334 | |||||||
| chr3:108832447 | C | T | 2 | a0001c0001t0004g0014 a0001c0001t0004g0066 |
3 | HG01069.hp2 HG01071.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.118+1667C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108832447 | |||||||
| chr3:108832652 | G | C | 83 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(80): Show |
113 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.118+1872G>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108832652 | |||||||
| chr3:108832654 | C | A | 6 | a0001c0001t0001g0201 a0001c0001t0002g0233 a0001c0001t0002g0234 others(3): Show |
7 | HG01069.hp2 HG01071.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.118+1874C>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108832654 | |||||||
| chr3:108832690 | T | G | 1 | a0001c0001t0001g0039 | 2 | HG00639.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.118+1910T>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108832690 | |||||||
| chr3:108832826 | A | G | 2 | a0003c0003t0001g0008 a0003c0003t0001g0080 |
4 | NA18948.hp1 NA18969.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.118+2046A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108832826 | |||||||
| chr3:108833104 | A | G | 5 | a0001c0001t0006g0027 a0001c0001t0006g0125 a0001c0001t0006g0156 others(2): Show |
6 | HG02717.hp1 HG02886.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.118+2324A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108833104 | |||||||
| chr3:108833145 | A | T | 1 | a0001c0001t0001g0018 | 2 | NA18974.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.118+2365A>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108833145 | |||||||
| chr3:108833171 | G | T | 1 | a0001c0001t0004g0048 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.118+2391G>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108833171 | |||||||
| chr3:108833248 | T | A | 1 | a0001c0001t0001g0081 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.118+2468T>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108833248 | |||||||
| chr3:108833286 | C | T | 2 | a0001c0001t0004g0014 a0001c0001t0004g0066 |
3 | HG01069.hp2 HG01071.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.118+2506C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108833286 | |||||||
| chr3:108833308 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.118+2528C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108833308 | |||||||
| chr3:108833310 | C | T | 3 | a0001c0001t0007g0202 a0001c0001t0007g0203 a0001c0001t0007g0204 |
3 | HG01106.hp2 HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.118+2530C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108833310 | |||||||
| chr3:108833445 | G | A | 4 | a0001c0001t0002g0130 a0001c0001t0002g0153 a0001c0001t0004g0009 others(1): Show |
6 | HG00735.hp1 HG02647.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.118+2665G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108833445 | |||||||
| chr3:108833525 | G | A | 14 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(11): Show |
14 | HG01081.hp2 HG01243.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.118+2745G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108833525 | |||||||
| chr3:108833580 | C | T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0103 |
5 | HG01123.hp1 HG01433.hp1 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.118+2800C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108833580 | |||||||
| chr3:108833649 | C | T | 2 | a0001c0001t0009g0046 a0001c0001t0009g0047 |
2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.118+2869C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108833649 | |||||||
| chr3:108833783 | G | A | 1 | a0001c0001t0002g0197 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.118+3003G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108833783 | |||||||
| chr3:108833799 | T | TAC | 32 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0028 others(29): Show |
40 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.118+3051_118+3052d others(4): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 108833799 | ||||||
| chr3:108833799 | T | TACAC | 20 | a0001c0001t0001g0020 a0001c0001t0001g0035 a0001c0001t0001g0036 others(17): Show |
24 | HG02080.hp1 HG02647.hp1 HG02735.hp2 others(21): Show |
intron_variant | MODIFIER | c.118+3049_118+3052d others(6): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 108833799 | ||||||
| chr3:108833799 | T | TACACAC | 12 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(9): Show |
12 | HG01243.hp2 HG02622.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.118+3047_118+3052d others(8): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 108833799 | ||||||
| chr3:108833799 | T | TACACACA others(1): Show |
5 | a0001c0001t0002g0153 a0001c0001t0004g0014 a0001c0001t0004g0054 others(2): Show |
6 | HG01069.hp2 HG01071.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.118+3045_118+3052d others(10): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 108833799 | ||||||
| chr3:108833799 | T | TACACACA others(3): Show |
10 | a0001c0001t0001g0026 a0001c0001t0001g0105 a0001c0001t0001g0149 others(7): Show |
19 | HG00597.hp2 HG00642.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.118+3043_118+3052d others(12): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 108833799 | ||||||
| chr3:108833799 | T | TACACACA others(9): Show |
1 | a0001c0001t0004g0129 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.118+3037_118+3052d others(18): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 108833799 | ||||||
| chr3:108833799 | TAC | T | 14 | a0001c0001t0002g0100 a0001c0001t0002g0161 a0001c0001t0004g0110 others(11): Show |
15 | HG00609.hp1 HG00741.hp1 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.118+3051_118+3052d others(4): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 108833799 | ||||||
| chr3:108833799 | TACAC | T | 80 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(77): Show |
110 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.118+3049_118+3052d others(6): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 108833799 | ||||||
| chr3:108833799 | TACACAC | T | 7 | a0001c0001t0001g0096 a0001c0001t0001g0135 a0001c0001t0001g0136 others(4): Show |
10 | HG01106.hp1 HG01261.hp1 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.118+3047_118+3052d others(8): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 108833799 | ||||||
| chr3:108833879 | G | A | 4 | a0001c0001t0002g0131 a0001c0001t0004g0048 a0001c0001t0004g0107 others(1): Show |
4 | HG01081.hp2 HG02559.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.118+3099G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108833879 | |||||||
| chr3:108833884 | C | T | 4 | a0001c0001t0002g0131 a0001c0001t0004g0048 a0001c0001t0004g0107 others(1): Show |
4 | HG01081.hp2 HG02559.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.118+3104C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108833884 | |||||||
| chr3:108833933 | T | G | 1 | a0001c0001t0001g0082 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.118+3153T>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108833933 | |||||||
| chr3:108834113 | C | T | 240 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(237): Show |
307 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.118+3333C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108834113 | |||||||
| chr3:108834250 | A | G | 2 | a0001c0001t0009g0046 a0001c0001t0009g0047 |
2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.118+3470A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108834250 | |||||||
| chr3:108834255 | C | T | 1 | a0001c0001t0009g0047 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.118+3475C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108834255 | |||||||
| chr3:108834273 | C | G | 4 | a0001c0001t0002g0131 a0001c0001t0004g0048 a0001c0001t0004g0107 others(1): Show |
4 | HG01081.hp2 HG02559.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.118+3493C>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108834273 | |||||||
| chr3:108834930 | A | G | 2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | HG02080.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.119-4004A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108834930 | |||||||
| chr3:108835025 | C | G | 3 | a0001c0001t0004g0110 a0001c0001t0004g0111 a0001c0001t0004g0222 |
3 | HG02615.hp2 HG02895.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.119-3909C>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108835025 | |||||||
| chr3:108835043 | G | A | 6 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0002g0025 others(3): Show |
9 | HG01106.hp1 HG01261.hp1 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.119-3891G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108835043 | |||||||
| chr3:108835346 | C | A | 1 | a0001c0001t0002g0055 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.119-3588C>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108835346 | |||||||
| chr3:108835524 | C | T | 252 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(249): Show |
323 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(320): Show |
intron_variant | MODIFIER | c.119-3410C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108835524 | |||||||
| chr3:108835584 | T | C | 1 | a0001c0001t0011g0195 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.119-3350T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108835584 | |||||||
| chr3:108835629 | C | G | 6 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(3): Show |
6 | HG01243.hp2 HG02818.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.119-3305C>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108835629 | |||||||
| chr3:108835784 | T | C | 6 | a0001c0001t0007g0198 a0001c0001t0007g0199 a0001c0001t0007g0202 others(3): Show |
6 | HG01106.hp2 HG01891.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.119-3150T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108835784 | |||||||
| chr3:108835895 | GTATTTAT others(5): Show |
G | 50 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(47): Show |
56 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(53): Show |
intron_variant | MODIFIER | c.119-3009_119-2998d others(14): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 108835895 | ||||||
| chr3:108835895 | GTATTTAT others(9): Show |
G | 203 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(200): Show |
269 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(266): Show |
intron_variant | MODIFIER | c.119-3013_119-2998d others(18): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 108835895 | ||||||
| chr3:108835895 | GTATTTAT others(13): Show |
G | 1 | a0001c0001t0001g0176 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.119-3017_119-2998d others(22): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 108835895 | ||||||
| chr3:108835983 | G | A | 14 | a0001c0001t0001g0026 a0001c0001t0001g0105 a0001c0001t0001g0149 others(11): Show |
21 | HG00597.hp2 HG00642.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.119-2951G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108835983 | |||||||
| chr3:108836067 | A | C | 2 | a0001c0001t0002g0161 a0001c0001t0002g0165 |
2 | HG00741.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.119-2867A>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108836067 | |||||||
| chr3:108836068 | T | C | 2 | a0001c0001t0002g0161 a0001c0001t0002g0165 |
2 | HG00741.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.119-2866T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108836068 | |||||||
| chr3:108836076 | T | C | 1 | a0001c0001t0001g0224 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.119-2858T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108836076 | |||||||
| chr3:108836108 | T | C | 3 | a0001c0001t0001g0219 a0001c0001t0002g0141 a0001c0001t0005g0192 |
3 | HG01952.hp1 HG02738.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.119-2826T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108836108 | |||||||
| chr3:108836136 | T | C | 1 | a0001c0001t0002g0126 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.119-2798T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108836136 | |||||||
| chr3:108836197 | C | G | 2 | a0001c0001t0004g0110 a0001c0001t0004g0111 |
2 | HG02615.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.119-2737C>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108836197 | |||||||
| chr3:108836317 | A | G | 6 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(3): Show |
6 | HG01243.hp2 HG02818.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.119-2617A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108836317 | |||||||
| chr3:108836368 | T | A | 8 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0057 others(5): Show |
12 | HG01884.hp1 HG02109.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.119-2566T>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108836368 | |||||||
| chr3:108836409 | T | C | 154 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0016 others(151): Show |
187 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.119-2525T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108836409 | |||||||
| chr3:108836415 | A | G | 1 | a0001c0001t0002g0143 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.119-2519A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108836415 | |||||||
| chr3:108836635 | T | C | 1 | a0001c0001t0001g0035 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.119-2299T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108836635 | |||||||
| chr3:108836639 | T | C | 1 | a0001c0001t0002g0153 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.119-2295T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108836639 | |||||||
| chr3:108836666 | C | G | 2 | a0001c0001t0002g0031 a0001c0001t0002g0175 |
3 | HG01496.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.119-2268C>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108836666 | |||||||
| chr3:108836720 | A | C | 1 | a0001c0001t0007g0239 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.119-2214A>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108836720 | |||||||
| chr3:108836928 | C | A | 1 | a0001c0001t0001g0101 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.119-2006C>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108836928 | |||||||
| chr3:108836965 | T | C | 50 | a0001c0001t0001g0142 a0001c0001t0001g0185 a0001c0001t0001g0208 others(47): Show |
62 | HG00323.hp1 HG00609.hp1 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.119-1969T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108836965 | |||||||
| chr3:108837050 | G | T | 260 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(257): Show |
335 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.119-1884G>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108837050 | |||||||
| chr3:108837174 | T | A | 1 | a0001c0001t0002g0145 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.119-1760T>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108837174 | |||||||
| chr3:108837398 | C | T | 4 | a0001c0001t0004g0115 a0001c0001t0004g0119 a0001c0001t0004g0121 others(1): Show |
4 | HG02622.hp1 HG02818.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.119-1536C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108837398 | |||||||
| chr3:108837446 | G | C | 1 | a0001c0001t0002g0170 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.119-1488G>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108837446 | |||||||
| chr3:108837578 | T | C | 171 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(168): Show |
229 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.119-1356T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108837578 | |||||||
| chr3:108837673 | T | C | 1 | a0001c0001t0001g0201 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.119-1261T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108837673 | |||||||
| chr3:108837712 | A | G | 73 | a0001c0001t0001g0142 a0001c0001t0001g0185 a0001c0001t0001g0208 others(70): Show |
88 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(85): Show |
intron_variant | MODIFIER | c.119-1222A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108837712 | |||||||
| chr3:108837753 | A | T | 4 | a0001c0001t0002g0021 a0001c0001t0002g0100 a0001c0001t0002g0113 others(1): Show |
5 | HG00609.hp1 NA18939.hp2 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.119-1181A>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108837753 | |||||||
| chr3:108837780 | T | C | 2 | a0001c0001t0001g0020 a0001c0001t0002g0209 |
3 | NA18950.hp1 NA18969.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.119-1154T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108837780 | |||||||
| chr3:108837809 | T | C | 1 | a0001c0001t0001g0136 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.119-1125T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108837809 | |||||||
| chr3:108837885 | A | G | 1 | a0001c0001t0001g0214 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.119-1049A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108837885 | |||||||
| chr3:108837941 | A | G | 1 | a0001c0001t0004g0196 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.119-993A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108837941 | |||||||
| chr3:108837985 | G | A | 256 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(253): Show |
331 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(328): Show |
intron_variant | MODIFIER | c.119-949G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108837985 | |||||||
| chr3:108838087 | T | C | 1 | a0001c0001t0001g0087 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.119-847T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108838087 | |||||||
| chr3:108838262 | C | T | 1 | a0001c0001t0002g0147 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.119-672C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108838262 | |||||||
| chr3:108838325 | GATAGATA others(14): Show |
G | 4 | a0001c0001t0007g0202 a0001c0001t0007g0203 a0001c0001t0007g0204 others(1): Show |
4 | HG01106.hp2 HG01891.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.119-598_119-578del others(21): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 108838325 | ||||||
| chr3:108838335 | TAGATGAT others(7): Show |
T | 13 | a0001c0001t0001g0201 a0001c0001t0004g0124 a0001c0001t0004g0196 others(10): Show |
14 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.119-598_119-585del others(14): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108838335 | |||||||
| chr3:108838337 | GATGATAG others(2): Show |
G | 4 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0064 others(1): Show |
4 | HG01243.hp2 HG02818.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.119-594_119-586del others(9): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 108838337 | ||||||
| chr3:108838344 | GATATAGA others(8): Show |
G | 6 | a0001c0001t0002g0126 a0002c0002t0002g0022 a0002c0002t0002g0040 others(3): Show |
8 | HG02055.hp1 HG02486.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.119-588_119-574del others(15): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 108838344 | ||||||
| chr3:108838345 | ATATAGAT others(4): Show |
A | 2 | a0002c0002t0002g0117 a0002c0002t0002g0123 |
2 | HG02257.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.119-588_119-578del others(11): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108838345 | |||||||
| chr3:108838346 | TATAGATA others(4): Show |
T | 37 | a0001c0001t0001g0135 a0001c0001t0001g0208 a0001c0001t0002g0011 others(34): Show |
40 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.119-577_119-567del others(11): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 108838346 | ||||||
| chr3:108838346 | TATAGATA others(8): Show |
T | 48 | a0001c0001t0001g0185 a0001c0001t0002g0003 a0001c0001t0002g0011 others(45): Show |
58 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.119-577_119-563del others(15): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 108838346 | ||||||
| chr3:108838346 | TATAGATA others(12): Show |
T | 7 | a0001c0001t0001g0142 a0001c0001t0002g0023 a0001c0001t0002g0024 others(4): Show |
8 | HG00738.hp1 HG01192.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.119-577_119-559del others(19): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 108838346 | ||||||
| chr3:108838346 | TATAGATA others(20): Show |
T | 1 | a0001c0001t0002g0227 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.119-577_119-551del others(27): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 108838346 | ||||||
| chr3:108838349 | AGATAGAT | A | 6 | a0001c0001t0002g0138 a0001c0001t0002g0148 a0001c0001t0002g0154 others(3): Show |
6 | HG02135.hp2 HG02738.hp1 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.119-577_119-571del others(7): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 108838349 | ||||||
| chr3:108838356 | T | TGATA | 30 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(27): Show |
32 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.119-531_119-528dup others(4): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 108838356 | ||||||
| chr3:108838356 | T | TGATAGAT others(1): Show |
8 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0056 others(5): Show |
8 | HG00558.hp1 HG00621.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.119-535_119-528dup others(8): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 108838356 | ||||||
| chr3:108838356 | TG | T | 6 | a0001c0001t0001g0062 a0001c0001t0004g0196 a0001c0001t0006g0156 others(3): Show |
6 | HG01891.hp1 HG02717.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.119-577delG | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108838356 | |||||||
| chr3:108838356 | TGATA | T | 55 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(52): Show |
69 | HG00323.hp2 HG00544.hp1 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.119-531_119-528del others(4): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 108838356 | ||||||
| chr3:108838356 | TGATAG | T | 8 | a0001c0001t0001g0201 a0001c0001t0004g0124 a0001c0001t0006g0027 others(5): Show |
9 | HG02055.hp2 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.119-577_119-573del others(5): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108838356 | |||||||
| chr3:108838356 | TGATAGAT others(1): Show |
T | 10 | a0001c0001t0001g0060 a0001c0001t0001g0088 a0001c0001t0001g0101 others(7): Show |
13 | HG00408.hp2 HG00609.hp2 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.119-535_119-528del others(8): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 108838356 | ||||||
| chr3:108838361 | G | GAT | 4 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0064 others(1): Show |
4 | HG01243.hp2 HG02818.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.119-571_119-570dup others(2): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 108838361 | ||||||
| chr3:108838363 | TAG | T | 4 | a0001c0001t0007g0202 a0001c0001t0007g0203 a0001c0001t0007g0204 others(1): Show |
4 | HG01106.hp2 HG01891.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.119-569_119-568del others(2): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 108838363 | ||||||
| chr3:108838419 | A | G | 136 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(133): Show |
189 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.119-515A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108838419 | |||||||
| chr3:108838443 | G | A | 121 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(118): Show |
165 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.119-491G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108838443 | |||||||
| chr3:108838520 | T | C | 1 | a0001c0001t0001g0056 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.119-414T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108838520 | |||||||
| chr3:108838654 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.119-280G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108838654 | |||||||
| chr3:108838973 | T | C | 122 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(119): Show |
166 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(163): Show |
splice_region_variant&intron_variant | LOW | c.152+6T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108838973 | |||||||
| chr3:108838980 | T | G | 1 | a0004c0004t0008g0160 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.152+13T>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108838980 | |||||||
| chr3:108839197 | T | G | 8 | a0001c0001t0002g0126 a0002c0002t0002g0022 a0002c0002t0002g0040 others(5): Show |
10 | HG02055.hp1 HG02257.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.152+230T>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108839197 | |||||||
| chr3:108839205 | T | C | 1 | a0001c0001t0004g0115 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.152+238T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108839205 | |||||||
| chr3:108839243 | T | C | 261 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(258): Show |
336 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(333): Show |
intron_variant | MODIFIER | c.152+276T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108839243 | |||||||
| chr3:108839382 | C | T | 6 | a0001c0001t0004g0110 a0001c0001t0004g0111 a0001c0001t0004g0124 others(3): Show |
6 | HG02258.hp2 HG02572.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.152+415C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108839382 | |||||||
| chr3:108839422 | A | C | 1 | a0001c0001t0001g0180 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.152+455A>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108839422 | |||||||
| chr3:108839492 | A | C | 6 | a0001c0001t0001g0211 a0001c0001t0001g0218 a0001c0001t0004g0009 others(3): Show |
8 | HG00735.hp1 HG02559.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.152+525A>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108839492 | |||||||
| chr3:108839577 | C | T | 1 | a0001c0001t0001g0097 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.152+610C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108839577 | |||||||
| chr3:108839624 | G | A | 10 | a0001c0001t0006g0027 a0001c0001t0006g0125 a0001c0001t0006g0156 others(7): Show |
11 | HG02055.hp2 HG02257.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.152+657G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108839624 | |||||||
| chr3:108839783 | A | G | 93 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(90): Show |
112 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.152+816A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108839783 | |||||||
| chr3:108839845 | T | A | 14 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(11): Show |
15 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.152+878T>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108839845 | |||||||
| chr3:108840110 | T | A | 5 | a0001c0001t0007g0198 a0001c0001t0007g0199 a0001c0001t0007g0202 others(2): Show |
5 | HG01106.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+1143T>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108840110 | |||||||
| chr3:108840110 | T | TA | 10 | a0001c0001t0001g0223 a0001c0001t0006g0027 a0001c0001t0006g0125 others(7): Show |
11 | HG02055.hp2 HG02257.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.152+1150dupA | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 108840110 | ||||||
| chr3:108840418 | G | T | 14 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(11): Show |
15 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.152+1451G>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108840418 | |||||||
| chr3:108840516 | C | T | 1 | a0001c0001t0002g0141 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.152+1549C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108840516 | |||||||
| chr3:108840537 | T | TA | 139 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(136): Show |
193 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.152+1585dupA | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 108840537 | ||||||
| chr3:108840559 | A | C | 10 | a0001c0001t0001g0135 a0001c0001t0002g0025 a0001c0001t0002g0071 others(7): Show |
13 | HG01081.hp1 HG01106.hp1 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.152+1592A>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108840559 | |||||||
| chr3:108840579 | A | G | 1 | a0001c0001t0006g0125 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.152+1612A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108840579 | |||||||
| chr3:108840710 | G | T | 1 | a0001c0001t0007g0239 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.152+1743G>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108840710 | |||||||
| chr3:108840777 | A | G | 16 | a0001c0001t0002g0106 a0001c0001t0002g0141 a0001c0001t0002g0166 others(13): Show |
18 | HG00099.hp1 HG00738.hp2 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.152+1810A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108840777 | |||||||
| chr3:108840816 | G | A | 1 | a0001c0001t0001g0069 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.152+1849G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108840816 | |||||||
| chr3:108840909 | C | T | 2 | a0001c0001t0004g0014 a0001c0001t0004g0066 |
3 | HG01069.hp2 HG01071.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.152+1942C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108840909 | |||||||
| chr3:108840936 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.152+1969C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108840936 | |||||||
| chr3:108841068 | C | T | 5 | a0001c0001t0007g0198 a0001c0001t0007g0199 a0001c0001t0007g0202 others(2): Show |
5 | HG01106.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+2101C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108841068 | |||||||
| chr3:108841071 | T | G | 1 | a0001c0001t0001g0088 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.152+2104T>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108841071 | |||||||
| chr3:108841479 | A | C | 12 | a0001c0001t0001g0026 a0001c0001t0001g0068 a0001c0001t0001g0105 others(9): Show |
19 | HG00597.hp2 HG00642.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.152+2512A>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108841479 | |||||||
| chr3:108841495 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.152+2528A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108841495 | |||||||
| chr3:108841642 | G | A | 1 | a0001c0001t0003g0194 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.152+2675G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108841642 | |||||||
| chr3:108842270 | T | G | 4 | a0001c0001t0002g0126 a0001c0001t0002g0130 a0001c0001t0002g0150 others(1): Show |
4 | HG02451.hp1 HG03130.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.152+3303T>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108842270 | |||||||
| chr3:108842461 | C | G | 261 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(258): Show |
336 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(333): Show |
intron_variant | MODIFIER | c.152+3494C>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108842461 | |||||||
| chr3:108842487 | A | G | 1 | a0001c0001t0002g0187 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.152+3520A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108842487 | |||||||
| chr3:108842562 | C | A | 1 | a0001c0001t0004g0196 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.152+3595C>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108842562 | |||||||
| chr3:108842630 | T | C | 169 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(166): Show |
226 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.152+3663T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108842630 | |||||||
| chr3:108842642 | C | T | 1 | a0001c0001t0013g0120 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.152+3675C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108842642 | |||||||
| chr3:108842848 | A | G | 8 | a0001c0001t0001g0078 a0002c0002t0002g0022 a0002c0002t0002g0040 others(5): Show |
10 | HG02055.hp1 HG02257.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.152+3881A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108842848 | |||||||
| chr3:108843102 | G | C | 1 | a0001c0001t0001g0060 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.153-3966G>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108843102 | |||||||
| chr3:108843121 | T | C | 2 | a0001c0001t0001g0094 a0001c0001t0003g0247 |
2 | HG00544.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.153-3947T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108843121 | |||||||
| chr3:108843173 | C | G | 1 | a0001c0001t0007g0239 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.153-3895C>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108843173 | |||||||
| chr3:108843214 | T | C | 1 | a0001c0001t0004g0107 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.153-3854T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108843214 | |||||||
| chr3:108843269 | C | T | 2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | HG02080.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.153-3799C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108843269 | |||||||
| chr3:108843316 | G | A | 6 | a0001c0001t0001g0201 a0001c0001t0004g0107 a0004c0004t0008g0051 others(3): Show |
6 | HG02055.hp2 HG02145.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.153-3752G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108843316 | |||||||
| chr3:108843330 | G | A | 9 | a0001c0001t0002g0025 a0001c0001t0002g0071 a0001c0001t0002g0072 others(6): Show |
12 | HG01081.hp1 HG01106.hp1 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.153-3738G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108843330 | |||||||
| chr3:108843462 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.153-3606G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108843462 | |||||||
| chr3:108843467 | T | C | 1 | a0001c0001t0001g0057 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.153-3601T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108843467 | |||||||
| chr3:108843545 | A | G | 6 | a0001c0001t0007g0198 a0001c0001t0007g0199 a0001c0001t0007g0202 others(3): Show |
6 | HG01106.hp2 HG01891.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.153-3523A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108843545 | |||||||
| chr3:108843607 | C | A | 7 | a0002c0002t0002g0022 a0002c0002t0002g0040 a0002c0002t0002g0117 others(4): Show |
9 | HG02055.hp1 HG02257.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.153-3461C>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108843607 | |||||||
| chr3:108843609 | C | T | 5 | a0001c0001t0001g0092 a0001c0001t0001g0179 a0001c0001t0001g0180 others(2): Show |
7 | HG00642.hp1 HG01255.hp1 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.153-3459C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108843609 | |||||||
| chr3:108843799 | C | T | 3 | a0001c0001t0002g0152 a0001c0001t0002g0153 a0001c0001t0002g0159 |
3 | HG03098.hp1 HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.153-3269C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108843799 | |||||||
| chr3:108844002 | T | G | 259 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
334 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(331): Show |
intron_variant | MODIFIER | c.153-3066T>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108844002 | |||||||
| chr3:108844083 | G | A | 176 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(173): Show |
234 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.153-2985G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108844083 | |||||||
| chr3:108844224 | A | G | 129 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(126): Show |
180 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.153-2844A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108844224 | |||||||
| chr3:108844299 | G | A | 1 | a0001c0001t0002g0131 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.153-2769G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108844299 | |||||||
| chr3:108844319 | A | AT | 22 | a0001c0001t0001g0087 a0001c0001t0001g0099 a0001c0001t0001g0223 others(19): Show |
26 | HG00735.hp1 HG01081.hp1 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.153-2733dupT | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 108844319 | ||||||
| chr3:108844398 | T | G | 6 | a0001c0001t0002g0126 a0001c0001t0002g0130 a0001c0001t0002g0150 others(3): Show |
6 | HG02451.hp1 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.153-2670T>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108844398 | |||||||
| chr3:108844456 | T | A | 7 | a0002c0002t0002g0022 a0002c0002t0002g0040 a0002c0002t0002g0117 others(4): Show |
9 | HG02055.hp1 HG02257.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.153-2612T>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108844456 | |||||||
| chr3:108844457 | G | A | 7 | a0002c0002t0002g0022 a0002c0002t0002g0040 a0002c0002t0002g0117 others(4): Show |
9 | HG02055.hp1 HG02257.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.153-2611G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108844457 | |||||||
| chr3:108844458 | G | T | 7 | a0002c0002t0002g0022 a0002c0002t0002g0040 a0002c0002t0002g0117 others(4): Show |
9 | HG02055.hp1 HG02257.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.153-2610G>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108844458 | |||||||
| chr3:108844460 | C | A | 7 | a0002c0002t0002g0022 a0002c0002t0002g0040 a0002c0002t0002g0117 others(4): Show |
9 | HG02055.hp1 HG02257.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.153-2608C>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108844460 | |||||||
| chr3:108844463 | T | A | 7 | a0002c0002t0002g0022 a0002c0002t0002g0040 a0002c0002t0002g0117 others(4): Show |
9 | HG02055.hp1 HG02257.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.153-2605T>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108844463 | |||||||
| chr3:108844464 | G | A | 7 | a0002c0002t0002g0022 a0002c0002t0002g0040 a0002c0002t0002g0117 others(4): Show |
9 | HG02055.hp1 HG02257.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.153-2604G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108844464 | |||||||
| chr3:108844466 | T | TTAATTTA others(27): Show |
7 | a0002c0002t0002g0022 a0002c0002t0002g0040 a0002c0002t0002g0117 others(4): Show |
9 | HG02055.hp1 HG02257.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.153-2602_153-2601i others(36): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108844466 | |||||||
| chr3:108844468 | A | T | 7 | a0002c0002t0002g0022 a0002c0002t0002g0040 a0002c0002t0002g0117 others(4): Show |
9 | HG02055.hp1 HG02257.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.153-2600A>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108844468 | |||||||
| chr3:108844490 | T | A | 4 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(1): Show |
4 | HG01243.hp2 HG02818.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-2578T>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108844490 | |||||||
| chr3:108844499 | G | T | 5 | a0001c0001t0004g0115 a0001c0001t0004g0119 a0001c0001t0004g0121 others(2): Show |
5 | HG01891.hp1 HG02622.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-2569G>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108844499 | |||||||
| chr3:108844502 | C | T | 3 | a0001c0001t0002g0122 a0001c0001t0002g0131 a0001c0001t0005g0260 |
3 | HG02572.hp2 HG03041.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.153-2566C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108844502 | |||||||
| chr3:108844507 | A | G | 7 | a0002c0002t0002g0022 a0002c0002t0002g0040 a0002c0002t0002g0117 others(4): Show |
9 | HG02055.hp1 HG02257.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.153-2561A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108844507 | |||||||
| chr3:108844608 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.153-2460G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108844608 | |||||||
| chr3:108844691 | A | C | 1 | a0001c0001t0001g0201 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.153-2377A>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108844691 | |||||||
| chr3:108844781 | T | G | 1 | a0001c0001t0001g0082 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.153-2287T>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108844781 | |||||||
| chr3:108844842 | T | C | 1 | a0001c0001t0004g0107 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.153-2226T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108844842 | |||||||
| chr3:108844843 | C | CA | 51 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0023 others(48): Show |
62 | HG00099.hp1 HG00323.hp1 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.153-2199dupA | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 108844843 | ||||||
| chr3:108844843 | C | CAA | 24 | a0001c0001t0001g0201 a0001c0001t0002g0031 a0001c0001t0002g0032 others(21): Show |
26 | HG00609.hp1 HG01106.hp2 HG01257.hp1 others(23): Show |
intron_variant | MODIFIER | c.153-2200_153-2199d others(4): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 108844843 | ||||||
| chr3:108844843 | C | CAAA | 12 | a0001c0001t0002g0021 a0001c0001t0004g0009 a0001c0001t0004g0109 others(9): Show |
17 | HG00735.hp1 HG01884.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.153-2201_153-2199d others(5): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 108844843 | ||||||
| chr3:108844843 | C | CAAAA | 8 | a0001c0001t0002g0113 a0001c0001t0004g0107 a0001c0001t0013g0120 others(5): Show |
8 | HG02055.hp1 HG02257.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.153-2202_153-2199d others(6): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 108844843 | ||||||
| chr3:108844843 | C | CAAAAAAA others(6): Show |
1 | a0001c0001t0006g0125 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.153-2211_153-2199d others(15): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 108844843 | ||||||
| chr3:108844843 | C | CAAAAAAA others(9): Show |
2 | a0001c0001t0006g0027 a0001c0001t0006g0158 |
3 | HG02886.hp2 HG03130.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.153-2214_153-2199d others(18): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 108844843 | ||||||
| chr3:108844843 | C | CAAAAAAA others(10): Show |
1 | a0001c0001t0006g0157 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.153-2215_153-2199d others(19): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 108844843 | ||||||
| chr3:108844843 | C | CAAAAAAA others(14): Show |
1 | a0001c0001t0006g0156 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.153-2219_153-2199d others(23): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 108844843 | ||||||
| chr3:108844859 | A | G | 1 | a0001c0001t0004g0245 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.153-2209A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108844859 | |||||||
| chr3:108844861 | A | AG | 6 | a0001c0001t0001g0058 a0001c0001t0001g0083 a0001c0001t0001g0097 others(3): Show |
7 | HG02630.hp2 HG02738.hp2 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.153-2207_153-2206i others(3): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108844861 | |||||||
| chr3:108844861 | A | G | 122 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(119): Show |
173 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.153-2207A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108844861 | |||||||
| chr3:108844865 | AAAAAG | A | 6 | a0001c0001t0002g0025 a0001c0001t0002g0071 a0001c0001t0002g0072 others(3): Show |
7 | HG01081.hp1 HG01106.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.153-2199_153-2195d others(7): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 108844865 | ||||||
| chr3:108844870 | G | A | 5 | a0001c0001t0006g0027 a0001c0001t0006g0125 a0001c0001t0006g0156 others(2): Show |
6 | HG02717.hp1 HG02886.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.153-2198G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108844870 | |||||||
| chr3:108844874 | T | A | 1 | a0001c0001t0006g0158 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.153-2194T>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108844874 | |||||||
| chr3:108844969 | T | C | 1 | a0001c0001t0001g0136 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.153-2099T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108844969 | |||||||
| chr3:108845042 | A | G | 2 | a0001c0001t0009g0046 a0001c0001t0009g0047 |
2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.153-2026A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108845042 | |||||||
| chr3:108845133 | G | C | 123 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0021 others(120): Show |
145 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(142): Show |
intron_variant | MODIFIER | c.153-1935G>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108845133 | |||||||
| chr3:108845141 | C | T | 2 | a0001c0001t0009g0046 a0001c0001t0009g0047 |
2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.153-1927C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108845141 | |||||||
| chr3:108845144 | A | T | 2 | a0001c0001t0009g0046 a0001c0001t0009g0047 |
2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.153-1924A>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108845144 | |||||||
| chr3:108845251 | G | C | 1 | a0001c0001t0001g0090 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.153-1817G>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108845251 | |||||||
| chr3:108845503 | C | T | 2 | a0001c0001t0001g0077 a0001c0001t0001g0108 |
2 | HG00408.hp1 HG00558.hp2 |
intron_variant | MODIFIER | c.153-1565C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108845503 | |||||||
| chr3:108845710 | T | A | 1 | a0001c0001t0003g0244 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.153-1358T>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108845710 | |||||||
| chr3:108845714 | T | C | 6 | a0001c0001t0007g0198 a0001c0001t0007g0199 a0001c0001t0007g0202 others(3): Show |
6 | HG01106.hp2 HG01891.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.153-1354T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108845714 | |||||||
| chr3:108845774 | G | A | 6 | a0001c0001t0004g0110 a0001c0001t0004g0111 a0001c0001t0004g0124 others(3): Show |
6 | HG02258.hp2 HG02572.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.153-1294G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108845774 | |||||||
| chr3:108845883 | G | A | 88 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0021 others(85): Show |
103 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.153-1185G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108845883 | |||||||
| chr3:108845893 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.153-1175C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108845893 | |||||||
| chr3:108845937 | A | G | 12 | a0001c0001t0001g0005 a0001c0001t0001g0068 a0001c0001t0001g0105 others(9): Show |
21 | HG00597.hp1 HG00597.hp2 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.153-1131A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108845937 | |||||||
| chr3:108845962 | C | T | 1 | a0001c0001t0002g0148 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.153-1106C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108845962 | |||||||
| chr3:108846211 | T | C | 1 | a0001c0001t0003g0243 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.153-857T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108846211 | |||||||
| chr3:108846549 | G | A | 1 | a0001c0001t0002g0181 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.153-519G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108846549 | |||||||
| chr3:108846560 | T | C | 244 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(241): Show |
314 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(311): Show |
intron_variant | MODIFIER | c.153-508T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108846560 | |||||||
| chr3:108846657 | A | C | 1 | a0001c0001t0001g0068 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.153-411A>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108846657 | |||||||
| chr3:108846708 | T | C | 1 | a0001c0001t0002g0114 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.153-360T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108846708 | |||||||
| chr3:108846783 | G | T | 95 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0021 others(92): Show |
113 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.153-285G>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108846783 | |||||||
| chr3:108846791 | G | A | 239 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(236): Show |
308 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(305): Show |
intron_variant | MODIFIER | c.153-277G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108846791 | |||||||
| chr3:108846866 | T | C | 6 | a0001c0001t0007g0198 a0001c0001t0007g0199 a0001c0001t0007g0202 others(3): Show |
6 | HG01106.hp2 HG01891.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.153-202T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108846866 | |||||||
| chr3:108846968 | T | C | 244 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(241): Show |
314 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(311): Show |
intron_variant | MODIFIER | c.153-100T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108846968 | |||||||
| chr3:108847031 | G | A | 1 | a0001c0001t0003g0250 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.153-37G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108847031 | |||||||
| chr3:108847216 | A | G | 5 | a0001c0001t0004g0115 a0001c0001t0004g0119 a0001c0001t0004g0121 others(2): Show |
5 | HG01891.hp1 HG02622.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.214+87A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 4/5 | chr3 | 108847216 | |||||||
| chr3:108847244 | A | G | 1 | a0001c0001t0001g0088 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.214+115A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 4/5 | chr3 | 108847244 | |||||||
| chr3:108847370 | T | C | 3 | a0001c0001t0002g0152 a0001c0001t0002g0153 a0001c0001t0002g0159 |
3 | HG03098.hp1 HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.214+241T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 4/5 | chr3 | 108847370 | |||||||
| chr3:108847551 | C | T | 163 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(160): Show |
217 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.214+422C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 4/5 | chr3 | 108847551 | |||||||
| chr3:108847591 | G | A | 3 | a0001c0001t0001g0084 a0001c0001t0001g0091 a0001c0001t0001g0162 |
3 | HG00438.hp2 HG00544.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.214+462G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 4/5 | chr3 | 108847591 | |||||||
| chr3:108847651 | G | A | 1 | a0001c0001t0001g0229 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.214+522G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 4/5 | chr3 | 108847651 | |||||||
| chr3:108847956 | G | A | 162 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(159): Show |
216 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.214+827G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 4/5 | chr3 | 108847956 | |||||||
| chr3:108848026 | A | G | 2 | a0001c0001t0002g0172 a0001c0001t0002g0177 |
2 | HG01257.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.214+897A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 4/5 | chr3 | 108848026 | |||||||
| chr3:108848131 | T | C | 1 | a0001c0001t0001g0057 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.214+1002T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 4/5 | chr3 | 108848131 | |||||||
| chr3:108848165 | A | G | 1 | a0001c0001t0001g0224 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.215-1001A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 4/5 | chr3 | 108848165 | |||||||
| chr3:108848188 | G | A | 1 | a0001c0001t0003g0244 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.215-978G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 4/5 | chr3 | 108848188 | |||||||
| chr3:108848302 | T | C | 1 | a0001c0001t0013g0120 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.215-864T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 4/5 | chr3 | 108848302 | |||||||
| chr3:108848368 | T | C | 169 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(166): Show |
225 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.215-798T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 4/5 | chr3 | 108848368 | |||||||
| chr3:108848443 | T | A | 1 | a0001c0001t0004g0107 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.215-723T>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 4/5 | chr3 | 108848443 | |||||||
| chr3:108848517 | G | T | 5 | a0001c0001t0004g0115 a0001c0001t0004g0119 a0001c0001t0004g0121 others(2): Show |
5 | HG01891.hp1 HG02622.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.215-649G>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 4/5 | chr3 | 108848517 | |||||||
| chr3:108848602 | G | C | 168 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(165): Show |
223 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(220): Show |
intron_variant | MODIFIER | c.215-564G>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 4/5 | chr3 | 108848602 | |||||||
| chr3:108848678 | C | A | 1 | a0001c0001t0003g0041 | 2 | HG03669.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.215-488C>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 4/5 | chr3 | 108848678 | |||||||
| chr3:108848683 | T | C | 1 | a0001c0001t0001g0212 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.215-483T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 4/5 | chr3 | 108848683 | |||||||
| chr3:108848820 | A | G | 5 | a0001c0001t0004g0115 a0001c0001t0004g0119 a0001c0001t0004g0121 others(2): Show |
5 | HG01891.hp1 HG02622.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.215-346A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 4/5 | chr3 | 108848820 | |||||||
| chr3:108848833 | G | T | 75 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0021 others(72): Show |
90 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.215-333G>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 4/5 | chr3 | 108848833 | |||||||
| chr3:108848859 | A | G | 1 | a0001c0001t0003g0254 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.215-307A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 4/5 | chr3 | 108848859 | |||||||
| chr3:108849002 | C | G | 1 | a0001c0001t0001g0102 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.215-164C>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 4/5 | chr3 | 108849002 | |||||||
| chr3:108849076 | G | A | 169 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(166): Show |
225 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.215-90G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 4/5 | chr3 | 108849076 | |||||||
| chr3:108849352 | A | G | 1 | a0001c0001t0001g0216 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.303+98A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108849352 | |||||||
| chr3:108849416 | C | G | 7 | a0002c0002t0002g0022 a0002c0002t0002g0040 a0002c0002t0002g0117 others(4): Show |
9 | HG02055.hp1 HG02257.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.303+162C>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108849416 | |||||||
| chr3:108849477 | A | G | 169 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(166): Show |
225 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.303+223A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108849477 | |||||||
| chr3:108849479 | G | A | 169 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(166): Show |
225 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.303+225G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108849479 | |||||||
| chr3:108849569 | C | T | 176 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(173): Show |
234 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.303+315C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108849569 | |||||||
| chr3:108849778 | C | G | 169 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(166): Show |
225 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.303+524C>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108849778 | |||||||
| chr3:108849857 | T | G | 1 | a0001c0001t0004g0107 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.303+603T>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108849857 | |||||||
| chr3:108849903 | G | T | 1 | a0001c0001t0001g0201 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.303+649G>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108849903 | |||||||
| chr3:108850029 | T | G | 169 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(166): Show |
225 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.303+775T>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108850029 | |||||||
| chr3:108850063 | T | G | 176 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(173): Show |
234 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.303+809T>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108850063 | |||||||
| chr3:108850123 | T | A | 1 | a0005c0005t0002g0010 | 3 | HG02258.hp1 HG02451.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.303+869T>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108850123 | |||||||
| chr3:108850186 | T | C | 1 | a0001c0001t0002g0153 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.303+932T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108850186 | |||||||
| chr3:108850200 | A | G | 169 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(166): Show |
225 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.303+946A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108850200 | |||||||
| chr3:108850273 | T | C | 2 | a0001c0001t0002g0155 a0001c0001t0002g0161 |
2 | HG00741.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.303+1019T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108850273 | |||||||
| chr3:108850306 | C | CT | 153 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(150): Show |
200 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.303+1066dupT | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 108850306 | ||||||
| chr3:108850306 | C | CTTT | 13 | a0001c0001t0001g0005 a0001c0001t0001g0068 a0001c0001t0001g0105 others(10): Show |
22 | HG00597.hp1 HG00597.hp2 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.303+1064_303+1066d others(5): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 108850306 | ||||||
| chr3:108850333 | T | G | 6 | a0001c0001t0007g0198 a0001c0001t0007g0199 a0001c0001t0007g0202 others(3): Show |
6 | HG01106.hp2 HG01891.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.303+1079T>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108850333 | |||||||
| chr3:108850337 | C | A | 2 | a0001c0001t0004g0054 a0001c0001t0004g0116 |
2 | HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.303+1083C>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108850337 | |||||||
| chr3:108850357 | T | G | 1 | a0001c0001t0004g0196 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.303+1103T>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108850357 | |||||||
| chr3:108850387 | C | T | 169 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(166): Show |
225 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.303+1133C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108850387 | |||||||
| chr3:108850398 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.303+1144G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108850398 | |||||||
| chr3:108850486 | G | A | 1 | a0001c0001t0002g0165 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.303+1232G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108850486 | |||||||
| chr3:108850505 | A | G | 169 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(166): Show |
225 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.303+1251A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108850505 | |||||||
| chr3:108850520 | G | T | 1 | a0001c0001t0001g0201 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.303+1266G>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108850520 | |||||||
| chr3:108850579 | C | T | 1 | a0001c0001t0003g0194 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.303+1325C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108850579 | |||||||
| chr3:108850696 | T | C | 6 | a0001c0001t0007g0198 a0001c0001t0007g0199 a0001c0001t0007g0202 others(3): Show |
6 | HG01106.hp2 HG01891.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.303+1442T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108850696 | |||||||
| chr3:108850703 | T | G | 1 | a0001c0001t0001g0201 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.303+1449T>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108850703 | |||||||
| chr3:108850733 | T | C | 20 | a0001c0001t0004g0009 a0001c0001t0004g0014 a0001c0001t0004g0048 others(17): Show |
23 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.303+1479T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108850733 | |||||||
| chr3:108850859 | T | G | 1 | a0001c0001t0001g0224 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.303+1605T>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108850859 | |||||||
| chr3:108850917 | T | G | 1 | a0001c0001t0013g0120 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.303+1663T>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108850917 | |||||||
| chr3:108851059 | T | C | 170 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(167): Show |
226 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.303+1805T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108851059 | |||||||
| chr3:108851225 | G | A | 169 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(166): Show |
225 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.303+1971G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108851225 | |||||||
| chr3:108851407 | C | T | 1 | a0001c0001t0001g0062 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.303+2153C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108851407 | |||||||
| chr3:108851453 | A | G | 13 | a0001c0001t0001g0005 a0001c0001t0001g0068 a0001c0001t0001g0105 others(10): Show |
22 | HG00597.hp1 HG00597.hp2 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.304-2167A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108851453 | |||||||
| chr3:108851491 | T | C | 3 | a0001c0001t0004g0109 a0001c0001t0009g0046 a0001c0001t0009g0047 |
3 | HG01884.hp2 HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.304-2129T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108851491 | |||||||
| chr3:108851549 | G | A | 169 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(166): Show |
225 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.304-2071G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108851549 | |||||||
| chr3:108851582 | G | T | 1 | a0001c0001t0003g0254 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.304-2038G>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108851582 | |||||||
| chr3:108851628 | TA | T | 7 | a0001c0001t0001g0085 a0001c0001t0001g0230 a0001c0001t0002g0152 others(4): Show |
7 | HG02080.hp2 HG02647.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.304-1978delA | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 108851628 | ||||||
| chr3:108851628 | TAA | T | 159 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(156): Show |
213 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.304-1979_304-1978d others(4): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 108851628 | ||||||
| chr3:108851628 | TAAA | T | 7 | a0001c0001t0001g0201 a0001c0001t0004g0009 a0001c0001t0004g0048 others(4): Show |
9 | HG00735.hp1 HG01081.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.304-1980_304-1978d others(5): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 108851628 | ||||||
| chr3:108851715 | C | A | 1 | a0001c0001t0001g0206 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.304-1905C>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108851715 | |||||||
| chr3:108851764 | T | G | 1 | a0001c0001t0004g0107 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.304-1856T>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108851764 | |||||||
| chr3:108851821 | G | A | 4 | a0004c0004t0008g0051 a0004c0004t0008g0052 a0004c0004t0008g0065 others(1): Show |
4 | HG02055.hp2 HG02257.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.304-1799G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108851821 | |||||||
| chr3:108851870 | AGTTGACC others(4): Show |
A | 169 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(166): Show |
225 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.304-1741_304-1731d others(13): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 108851870 | ||||||
| chr3:108852014 | C | G | 7 | a0001c0001t0004g0009 a0001c0001t0004g0048 a0001c0001t0004g0054 others(4): Show |
9 | HG00735.hp1 HG01081.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.304-1606C>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108852014 | |||||||
| chr3:108852062 | C | CACA | 6 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0103 others(3): Show |
8 | HG01081.hp1 HG01123.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.304-1532_304-1530d others(5): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 108852062 | ||||||
| chr3:108852062 | CACAACA | C | 7 | a0002c0002t0002g0022 a0002c0002t0002g0040 a0002c0002t0002g0117 others(4): Show |
9 | HG02055.hp1 HG02257.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.304-1535_304-1530d others(8): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 108852062 | ||||||
| chr3:108852202 | G | A | 20 | a0001c0001t0004g0009 a0001c0001t0004g0014 a0001c0001t0004g0048 others(17): Show |
23 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.304-1418G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108852202 | |||||||
| chr3:108852209 | C | T | 129 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(126): Show |
180 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.304-1411C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108852209 | |||||||
| chr3:108852352 | G | T | 1 | a0001c0001t0001g0201 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.304-1268G>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108852352 | |||||||
| chr3:108852369 | G | A | 1 | a0001c0001t0001g0069 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.304-1251G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108852369 | |||||||
| chr3:108852397 | G | GCA | 1 | a0001c0001t0004g0009 | 3 | HG00735.hp1 HG02647.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.304-1198_304-1197d others(4): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 108852397 | ||||||
| chr3:108852397 | GCA | G | 251 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(248): Show |
322 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(319): Show |
intron_variant | MODIFIER | c.304-1198_304-1197d others(4): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 108852397 | ||||||
| chr3:108852495 | A | G | 9 | a0001c0001t0004g0109 a0001c0001t0007g0198 a0001c0001t0007g0199 others(6): Show |
9 | HG01106.hp2 HG01884.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.304-1125A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108852495 | |||||||
| chr3:108852575 | A | G | 3 | a0001c0001t0002g0126 a0001c0001t0005g0238 a0001c0001t0005g0257 |
3 | HG02895.hp1 HG02897.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.304-1045A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108852575 | |||||||
| chr3:108852629 | T | G | 6 | a0001c0001t0007g0198 a0001c0001t0007g0199 a0001c0001t0007g0202 others(3): Show |
6 | HG01106.hp2 HG01891.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.304-991T>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108852629 | |||||||
| chr3:108852692 | T | C | 5 | a0001c0001t0006g0027 a0001c0001t0006g0125 a0001c0001t0006g0156 others(2): Show |
6 | HG02717.hp1 HG02886.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.304-928T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108852692 | |||||||
| chr3:108852740 | C | T | 2 | a0001c0001t0001g0081 a0001c0001t0001g0220 |
2 | NA18993.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.304-880C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108852740 | |||||||
| chr3:108852987 | G | A | 1 | a0001c0001t0002g0197 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.304-633G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108852987 | |||||||
| chr3:108852997 | G | A | 1 | a0001c0001t0003g0043 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.304-623G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108852997 | |||||||
| chr3:108853132 | T | C | 8 | a0001c0001t0002g0025 a0001c0001t0002g0071 a0001c0001t0002g0072 others(5): Show |
11 | HG01081.hp1 HG01106.hp1 HG01981.hp2 others(8): Show |
intron_variant | MODIFIER | c.304-488T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108853132 | |||||||
| chr3:108853134 | C | G | 1 | a0001c0001t0001g0201 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.304-486C>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108853134 | |||||||
| chr3:108853277 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.304-343G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108853277 | |||||||
| chr3:108853393 | A | T | 5 | a0001c0001t0004g0009 a0001c0001t0004g0048 a0001c0001t0004g0054 others(2): Show |
7 | HG00735.hp1 HG01081.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.304-227A>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108853393 | |||||||
| chr3:108853544 | C | T | 5 | a0001c0001t0006g0027 a0001c0001t0006g0125 a0001c0001t0006g0156 others(2): Show |
6 | HG02717.hp1 HG02886.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.304-76C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108853544 |