Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 127253 |
| ensemblid | ENSG00000162623.16 |
| hgncid | 24757 |
| symbol | TYW3 |
| name | tRNA-yW synthesizing protein 3 homolog |
| refseq_nuc | NM_138467.3 |
| refseq_prot | NP_612476.1 |
| ensembl_nuc | ENST00000370867.8 |
| ensembl_prot | ENSP00000359904.3 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 74733152 |
| end | 74766677 |
| strand | + |
| ver | v1.2 |
| region | chr1:74733152-74766677 |
| region5000 | chr1:74728152-74771677 |
| regionname0 | TYW3_chr1_74733152_74766677 |
| regionname5000 | TYW3_chr1_74728152_74771677 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 259 | 182 | 45 | 46 | 59 | 10 | 21 | 44 | TYW3_chr1_74728152_74771677 | TYW3 | MDRSA others(254): Show |
chr1 | 74728152 | 74771677 |
| a0002 | 0/1 | 259 | 139 | 25 | 22 | 74 | 2 | 15 | 56 | TYW3_chr1_74728152_74771677 | TYW3 | MDRSA others(254): Show |
chr1 | 74728152 | 74771677 |
| a0003 | 0/0 | 259 | 10 | 10 | 0 | 0 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | MDRSA others(254): Show |
chr1 | 74728152 | 74771677 |
| a0004 | 0/0 | 259 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | MDRSA others(254): Show |
chr1 | 74728152 | 74771677 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 777 | 181 | 45 | 45 | 59 | 10 | 21 | TYW3_chr1_74728152_74771677 | TYW3 | ATGGA others(772): Show |
chr1 | 74728152 | 74771677 | ||
| a0001c0005 | 0/0 | 777 | 1 | 0 | 1 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | ATGGA others(772): Show |
chr1 | 74728152 | 74771677 | ||
| a0002c0002 | 0/1 | 777 | 139 | 25 | 22 | 74 | 2 | 15 | TYW3_chr1_74728152_74771677 | TYW3 | ATGGA others(772): Show |
chr1 | 74728152 | 74771677 | ||
| a0003c0003 | 0/0 | 777 | 7 | 7 | 0 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | ATGGA others(772): Show |
chr1 | 74728152 | 74771677 | ||
| a0003c0004 | 0/0 | 777 | 3 | 3 | 0 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | ATGGA others(772): Show |
chr1 | 74728152 | 74771677 | ||
| a0004c0006 | 0/0 | 777 | 1 | 0 | 0 | 1 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | ATGGA others(772): Show |
chr1 | 74728152 | 74771677 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/0 | 3437 | 78 | 12 | 16 | 37 | 2 | 11 | TYW3_chr1_74728152_74771677 | TYW3 | CTTTT others(3432): Show |
chr1 | 74728152 | 74771677 |
| a0001c0001t0003 | 1/0 | 3437 | 40 | 27 | 7 | 0 | 3 | 2 | TYW3_chr1_74728152_74771677 | TYW3 | CTTTT others(3432): Show |
chr1 | 74728152 | 74771677 |
| a0001c0001t0005 | 0/0 | 3437 | 37 | 3 | 21 | 2 | 5 | 6 | TYW3_chr1_74728152_74771677 | TYW3 | CTTTT others(3432): Show |
chr1 | 74728152 | 74771677 |
| a0001c0001t0006 | 0/0 | 3438 | 14 | 0 | 0 | 14 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | CTTTT others(3433): Show |
chr1 | 74728152 | 74771677 |
| a0001c0001t0008 | 0/0 | 3438 | 6 | 0 | 0 | 6 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | CTTTT others(3433): Show |
chr1 | 74728152 | 74771677 |
| a0001c0001t0011 | 0/0 | 3437 | 1 | 0 | 0 | 0 | 0 | 1 | TYW3_chr1_74728152_74771677 | TYW3 | CTTTT others(3432): Show |
chr1 | 74728152 | 74771677 |
| a0001c0001t0012 | 0/0 | 3437 | 1 | 1 | 0 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | CTTTT others(3432): Show |
chr1 | 74728152 | 74771677 |
| a0001c0001t0014 | 0/0 | 3437 | 1 | 1 | 0 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | CTTTT others(3432): Show |
chr1 | 74728152 | 74771677 |
| a0001c0001t0015 | 0/0 | 3437 | 1 | 0 | 0 | 0 | 0 | 1 | TYW3_chr1_74728152_74771677 | TYW3 | CTTTT others(3432): Show |
chr1 | 74728152 | 74771677 |
| a0001c0001t0016 | 0/0 | 3437 | 1 | 1 | 0 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | CTTTT others(3432): Show |
chr1 | 74728152 | 74771677 |
| a0001c0001t0017 | 0/0 | 3437 | 1 | 0 | 1 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | CTTTT others(3432): Show |
chr1 | 74728152 | 74771677 |
| a0001c0005t0013 | 0/0 | 3437 | 1 | 0 | 1 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | CTTTT others(3432): Show |
chr1 | 74728152 | 74771677 |
| a0002c0002t0001 | 0/1 | 3437 | 95 | 17 | 16 | 53 | 1 | 7 | TYW3_chr1_74728152_74771677 | TYW3 | CTTTT others(3432): Show |
chr1 | 74728152 | 74771677 |
| a0002c0002t0004 | 0/0 | 3437 | 40 | 8 | 4 | 19 | 1 | 8 | TYW3_chr1_74728152_74771677 | TYW3 | CTTTT others(3432): Show |
chr1 | 74728152 | 74771677 |
| a0002c0002t0009 | 0/0 | 3437 | 2 | 0 | 2 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | CTTTT others(3432): Show |
chr1 | 74728152 | 74771677 |
| a0002c0002t0010 | 0/0 | 3437 | 2 | 0 | 0 | 2 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | CTTTT others(3432): Show |
chr1 | 74728152 | 74771677 |
| a0003c0003t0007 | 0/0 | 3437 | 7 | 7 | 0 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | CTTTT others(3432): Show |
chr1 | 74728152 | 74771677 |
| a0003c0004t0007 | 0/0 | 3437 | 3 | 3 | 0 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | CTTTT others(3432): Show |
chr1 | 74728152 | 74771677 |
| a0004c0006t0001 | 0/0 | 3437 | 1 | 0 | 0 | 1 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | CTTTT others(3432): Show |
chr1 | 74728152 | 74771677 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0002 | 0/0 | 24 | 5 | 6 | 9 | 1 | 3 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0002g0004 | 0/0 | 8 | 0 | 2 | 4 | 0 | 2 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0002g0011 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0002g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0002g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0002g0023 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0002g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0002g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0002g0041 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0002g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0003g0025 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0003g0027 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0003g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0003g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0003g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0003g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0003g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0003g0052 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0003g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0005g0005 | 0/0 | 10 | 0 | 6 | 0 | 1 | 3 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0005g0015 | 0/0 | 4 | 1 | 1 | 0 | 2 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0005g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0005g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0005g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0005g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0005g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0005g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0005g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0005g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0005g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0005g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0005g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0005g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0005g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0005g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0005g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0005g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0005g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0005g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0005g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0005g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0005g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0006g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0006g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0006g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0006g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0006g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0006g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0006g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0006g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0008g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0008g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0011g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0012g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0014g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0015g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0016g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0001t0017g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0001c0005t0013g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0002c0002t0001g0001 | 0/0 | 33 | 1 | 13 | 14 | 0 | 5 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0002c0002t0001g0006 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0002c0002t0001g0007 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0002c0002t0001g0008 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0002c0002t0001g0012 | 0/0 | 4 | 2 | 1 | 1 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0002c0002t0001g0013 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0002c0002t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0002c0002t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0002c0002t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0002c0002t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0002c0002t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0002c0002t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0002c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0002c0002t0001g0064 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0002c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0002c0002t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0002c0002t0004g0003 | 0/0 | 10 | 0 | 0 | 9 | 0 | 1 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0002c0002t0004g0010 | 0/0 | 5 | 0 | 2 | 1 | 0 | 2 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0002c0002t0004g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0002c0002t0004g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0002c0002t0004g0019 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0002c0002t0004g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0002c0002t0004g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0002c0002t0004g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0002c0002t0004g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0002c0002t0004g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0002c0002t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0002c0002t0004g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0002c0002t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0002c0002t0004g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0002c0002t0004g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0002c0002t0004g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0002c0002t0004g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0002c0002t0009g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0002c0002t0010g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0003c0003t0007g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0003c0003t0007g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0003c0003t0007g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0003c0003t0007g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0003c0003t0007g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0003c0004t0007g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| a0004c0006t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0025 | EUR | GBR | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG00099 | hp2 | a0001 | c0001 | t0005 | g0005 | EUR | GBR | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG00140 | hp1 | a0002 | c0002 | t0004 | g0019 | EUR | GBR | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG00140 | hp2 | a0001 | c0001 | t0005 | g0015 | EUR | GBR | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | FIN | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG00280 | hp2 | a0001 | c0001 | t0005 | g0015 | EUR | FIN | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG00423 | hp1 | a0002 | c0002 | t0010 | g0001 | EAS | CHS | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | CHS | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG00544 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG00597 | hp2 | a0001 | c0001 | t0006 | g0016 | EAS | CHS | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0070 | EAS | CHS | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | CHS | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0110 | AMR | PUR | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0041 | AMR | PUR | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0029 | EAS | CHS | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG00673 | hp2 | a0001 | c0001 | t0005 | g0045 | EAS | CHS | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG00733 | hp1 | a0002 | c0002 | t0001 | g0061 | AMR | PUR | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0025 | AMR | PUR | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0099 | AMR | PUR | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG00735 | hp2 | a0001 | c0001 | t0005 | g0118 | AMR | PUR | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0090 | AMR | PUR | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG00738 | hp2 | a0001 | c0001 | t0005 | g0122 | AMR | PUR | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG00741 | hp2 | a0001 | c0001 | t0005 | g0120 | AMR | PUR | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG01070 | hp1 | a0002 | c0002 | t0009 | g0032 | AMR | PUR | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG01070 | hp2 | a0001 | c0001 | t0005 | g0005 | AMR | PUR | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG01071 | hp1 | a0002 | c0002 | t0009 | g0032 | AMR | PUR | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG01071 | hp2 | a0001 | c0001 | t0005 | g0005 | AMR | PUR | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG01074 | hp1 | a0001 | c0001 | t0005 | g0015 | AMR | PUR | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG01074 | hp2 | a0001 | c0005 | t0013 | g0145 | AMR | PUR | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG01099 | hp2 | a0001 | c0001 | t0005 | g0005 | AMR | PUR | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG01106 | hp2 | a0001 | c0001 | t0005 | g0123 | AMR | PUR | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0149 | AMR | PUR | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG01167 | hp1 | a0002 | c0002 | t0004 | g0010 | AMR | PUR | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0153 | AMR | PUR | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG01168 | hp2 | a0001 | c0001 | t0005 | g0044 | AMR | PUR | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG01169 | hp1 | a0002 | c0002 | t0004 | g0010 | AMR | PUR | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG01169 | hp2 | a0001 | c0001 | t0005 | g0044 | AMR | PUR | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG01175 | hp2 | a0001 | c0001 | t0005 | g0127 | AMR | PUR | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0095 | AMR | PUR | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG01192 | hp2 | a0002 | c0002 | t0001 | g0013 | AMR | PUR | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0154 | AMR | CLM | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG01255 | hp2 | a0001 | c0001 | t0005 | g0121 | AMR | CLM | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG01256 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG01256 | hp2 | a0001 | c0001 | t0017 | g0129 | AMR | CLM | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | CLM | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG01257 | hp2 | a0001 | c0001 | t0005 | g0130 | AMR | CLM | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG01261 | hp1 | a0002 | c0002 | t0004 | g0086 | AMR | CLM | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG01261 | hp2 | a0001 | c0001 | t0005 | g0133 | AMR | CLM | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG01346 | hp1 | a0001 | c0001 | t0005 | g0134 | AMR | CLM | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG01358 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG01358 | hp2 | a0001 | c0001 | t0005 | g0005 | AMR | CLM | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0012 | AMR | CLM | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG01361 | hp2 | a0001 | c0001 | t0005 | g0126 | AMR | CLM | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG01496 | hp2 | a0001 | c0001 | t0005 | g0135 | AMR | CLM | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0107 | EUR | IBS | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG01515 | hp2 | a0001 | c0001 | t0005 | g0119 | EUR | IBS | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0041 | EUR | IBS | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG01516 | hp2 | a0001 | c0001 | t0005 | g0125 | EUR | IBS | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG01884 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | ACB | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0053 | AFR | ACB | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0056 | AFR | ACB | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG01891 | hp2 | a0001 | c0001 | t0014 | g0055 | AFR | ACB | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG01928 | hp1 | a0002 | c0002 | t0004 | g0084 | AMR | PEL | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG01928 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG01934 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG01934 | hp2 | a0001 | c0001 | t0005 | g0128 | AMR | PEL | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0092 | AMR | PEL | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0108 | AMR | PEL | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG01981 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0151 | AMR | PEL | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG01993 | hp2 | a0001 | c0001 | t0005 | g0005 | AMR | PEL | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | KHV | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02015 | hp2 | a0002 | c0002 | t0010 | g0001 | EAS | KHV | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02040 | hp1 | a0001 | c0001 | t0006 | g0141 | EAS | KHV | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0051 | AFR | ACB | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0071 | AFR | ACB | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0068 | EAS | KHV | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02056 | hp2 | a0002 | c0002 | t0004 | g0003 | EAS | KHV | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02074 | hp1 | a0002 | c0002 | t0001 | g0029 | EAS | KHV | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0062 | EAS | KHV | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | KHV | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | KHV | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02083 | hp2 | a0002 | c0002 | t0004 | g0003 | EAS | KHV | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02129 | hp1 | a0004 | c0006 | t0001 | g0001 | EAS | KHV | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | KHV | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | KHV | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02135 | hp2 | a0002 | c0002 | t0004 | g0003 | EAS | KHV | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02148 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | CDX | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0057 | EAS | CDX | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0012 | AFR | ACB | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0115 | AFR | ACB | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0042 | AFR | ACB | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02258 | hp2 | a0002 | c0002 | t0001 | g0007 | AFR | ACB | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02273 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02451 | hp1 | a0001 | c0001 | t0012 | g0136 | AFR | ACB | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02451 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | ACB | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02523 | hp1 | a0002 | c0002 | t0001 | g0087 | EAS | KHV | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0106 | AFR | GWD | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02602 | hp1 | a0001 | c0001 | t0015 | g0004 | SAS | PJL | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0040 | SAS | PJL | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0050 | AFR | GWD | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02615 | hp2 | a0002 | c0002 | t0001 | g0075 | AFR | GWD | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02622 | hp1 | a0001 | c0001 | t0005 | g0117 | AFR | GWD | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0104 | AFR | GWD | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02630 | hp1 | a0002 | c0002 | t0001 | g0033 | AFR | GWD | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0116 | AFR | GWD | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0146 | AFR | GWD | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02647 | hp2 | a0002 | c0002 | t0004 | g0018 | AFR | GWD | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02683 | hp1 | a0002 | c0002 | t0004 | g0003 | SAS | PJL | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0023 | SAS | PJL | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02723 | hp1 | a0002 | c0002 | t0001 | g0013 | AFR | GWD | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02723 | hp2 | a0002 | c0002 | t0004 | g0018 | AFR | GWD | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02735 | hp2 | a0001 | c0001 | t0005 | g0005 | SAS | PJL | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02738 | hp1 | a0001 | c0001 | t0011 | g0004 | SAS | PJL | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02738 | hp2 | a0001 | c0001 | t0005 | g0131 | SAS | PJL | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | GWD | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0048 | AFR | GWD | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02886 | hp2 | a0003 | c0003 | t0007 | g0046 | AFR | GWD | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02895 | hp2 | a0003 | c0003 | t0007 | g0047 | AFR | GWD | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02896 | hp1 | a0002 | c0002 | t0004 | g0020 | AFR | GWD | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0147 | AFR | GWD | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02897 | hp1 | a0003 | c0003 | t0007 | g0047 | AFR | GWD | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02897 | hp2 | a0002 | c0002 | t0004 | g0020 | AFR | GWD | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ESN | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02965 | hp2 | a0002 | c0002 | t0001 | g0007 | AFR | ESN | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0049 | AFR | ESN | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | ESN | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG03017 | hp1 | a0002 | c0002 | t0004 | g0019 | SAS | PJL | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG03017 | hp2 | a0002 | c0002 | t0004 | g0010 | SAS | PJL | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG03041 | hp1 | a0002 | c0002 | t0001 | g0033 | AFR | GWD | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0048 | AFR | GWD | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0112 | AFR | MSL | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG03098 | hp2 | a0002 | c0002 | t0004 | g0018 | AFR | MSL | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG03130 | hp1 | a0002 | c0002 | t0001 | g0013 | AFR | ESN | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG03130 | hp2 | a0002 | c0002 | t0004 | g0079 | AFR | ESN | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG03139 | hp1 | a0002 | c0002 | t0004 | g0020 | AFR | ESN | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0052 | AFR | ESN | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0027 | AFR | ESN | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0053 | AFR | ESN | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | MSL | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG03209 | hp2 | a0002 | c0002 | t0001 | g0007 | AFR | MSL | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG03239 | hp1 | a0002 | c0002 | t0004 | g0085 | SAS | PJL | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0077 | SAS | PJL | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0050 | AFR | MSL | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0043 | AFR | MSL | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG03486 | hp1 | a0002 | c0002 | t0004 | g0082 | AFR | MSL | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0148 | AFR | MSL | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG03492 | hp1 | a0002 | c0002 | t0004 | g0080 | SAS | PJL | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG03492 | hp2 | a0001 | c0001 | t0005 | g0005 | SAS | PJL | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0037 | AFR | ESN | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0042 | AFR | ESN | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG03540 | hp1 | a0003 | c0004 | t0007 | g0026 | AFR | GWD | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0103 | AFR | GWD | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG03579 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | MSL | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0054 | AFR | MSL | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG03654 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0091 | SAS | PJL | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0040 | SAS | PJL | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG03710 | hp2 | a0002 | c0002 | t0004 | g0019 | SAS | PJL | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | BEB | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0025 | SAS | BEB | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0102 | SAS | BEB | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG03834 | hp2 | a0001 | c0001 | t0005 | g0124 | SAS | BEB | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG03927 | hp1 | a0002 | c0002 | t0004 | g0010 | SAS | BEB | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | BEB | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0152 | SAS | BEB | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG04115 | hp1 | a0002 | c0002 | t0004 | g0088 | SAS | STU | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG04115 | hp2 | a0001 | c0001 | t0005 | g0132 | SAS | STU | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | STU | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG04199 | hp2 | a0002 | c0002 | t0001 | g0069 | SAS | STU | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0097 | SAS | STU | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG04204 | hp2 | a0001 | c0001 | t0005 | g0005 | SAS | STU | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA18522 | hp1 | a0002 | c0002 | t0001 | g0012 | AFR | YRI | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA18522 | hp2 | a0003 | c0003 | t0007 | g0144 | AFR | YRI | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHB | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA18612 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | CHB | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA18939 | hp2 | a0002 | c0002 | t0004 | g0014 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA18942 | hp1 | a0002 | c0002 | t0004 | g0003 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA18942 | hp2 | a0001 | c0001 | t0006 | g0009 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA18943 | hp2 | a0002 | c0002 | t0001 | g0059 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA18946 | hp2 | a0001 | c0001 | t0008 | g0017 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA18952 | hp2 | a0002 | c0002 | t0004 | g0003 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA18954 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA18954 | hp2 | a0002 | c0002 | t0004 | g0010 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA18957 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA18959 | hp1 | a0002 | c0002 | t0001 | g0063 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA18959 | hp2 | a0001 | c0001 | t0008 | g0009 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA18960 | hp2 | a0002 | c0002 | t0004 | g0014 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA18961 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA18961 | hp2 | a0001 | c0001 | t0006 | g0009 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA18962 | hp1 | a0001 | c0001 | t0008 | g0009 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA18962 | hp2 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA18964 | hp1 | a0001 | c0001 | t0006 | g0138 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA18964 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA18966 | hp2 | a0001 | c0001 | t0006 | g0139 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA18969 | hp2 | a0001 | c0001 | t0008 | g0017 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA18971 | hp1 | a0002 | c0002 | t0004 | g0003 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA18972 | hp1 | a0001 | c0001 | t0006 | g0016 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA18975 | hp1 | a0001 | c0001 | t0008 | g0017 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA18975 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA18978 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA18984 | hp1 | a0002 | c0002 | t0004 | g0035 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA18984 | hp2 | a0002 | c0002 | t0004 | g0034 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA18985 | hp1 | a0002 | c0002 | t0004 | g0014 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA18986 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA18986 | hp2 | a0002 | c0002 | t0004 | g0081 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA18987 | hp2 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA18990 | hp2 | a0002 | c0002 | t0004 | g0003 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA18991 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA18993 | hp1 | a0002 | c0002 | t0004 | g0003 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA18993 | hp2 | a0002 | c0002 | t0001 | g0074 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA18995 | hp2 | a0001 | c0001 | t0006 | g0140 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA19002 | hp2 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA19003 | hp1 | a0001 | c0001 | t0006 | g0009 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA19003 | hp2 | a0002 | c0002 | t0001 | g0073 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA19005 | hp1 | a0002 | c0002 | t0004 | g0034 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0078 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA19006 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA19009 | hp2 | a0002 | c0002 | t0004 | g0083 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA19010 | hp1 | a0001 | c0001 | t0006 | g0137 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA19011 | hp1 | a0001 | c0001 | t0006 | g0016 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA19011 | hp2 | a0002 | c0002 | t0001 | g0060 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA19012 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA19012 | hp2 | a0001 | c0001 | t0006 | g0009 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA19043 | hp1 | a0001 | c0001 | t0016 | g0113 | AFR | LWK | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA19043 | hp2 | a0003 | c0003 | t0007 | g0143 | AFR | LWK | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA19057 | hp1 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA19063 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA19063 | hp2 | a0001 | c0001 | t0006 | g0150 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA19065 | hp2 | a0002 | c0002 | t0001 | g0066 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA19070 | hp1 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA19070 | hp2 | a0002 | c0002 | t0004 | g0003 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA19074 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA19076 | hp1 | a0001 | c0001 | t0008 | g0017 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA19076 | hp2 | a0002 | c0002 | t0001 | g0072 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA19077 | hp1 | a0002 | c0002 | t0004 | g0035 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA19080 | hp1 | a0001 | c0001 | t0006 | g0016 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA19080 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA19081 | hp2 | a0001 | c0001 | t0005 | g0045 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA19083 | hp2 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA19087 | hp2 | a0002 | c0002 | t0001 | g0067 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA19089 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA19240 | hp1 | a0003 | c0003 | t0007 | g0046 | AFR | YRI | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0007 | AFR | YRI | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA20129 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | ASW | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA20129 | hp2 | a0003 | c0003 | t0007 | g0142 | AFR | ASW | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0065 | EUR | TSI | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0052 | EUR | TSI | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG01123 | hp2 | a0001 | c0001 | t0005 | g0005 | AMR | CLM | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0051 | AFR | ACB | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02109 | hp2 | a0001 | c0001 | t0005 | g0015 | AFR | ACB | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02486 | hp2 | a0003 | c0004 | t0007 | g0026 | AFR | ACB | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0109 | AFR | ACB | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0114 | AFR | ACB | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0111 | AFR | MSL | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0049 | AFR | MSL | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0013 | AFR | USA | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0043 | AFR | USA | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA18955 | hp2 | a0002 | c0002 | t0001 | g0076 | EAS | JPT | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA20300 | hp1 | a0003 | c0004 | t0007 | g0026 | AFR | USA | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0105 | AFR | USA | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0064 | REF | REF | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0027 | REF | REF | TYW3_chr1_74728152_74771677 | TYW3 | chr1 | 74728152 | 74771677 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:74738763 | G | A | 1 | a0003 | 10 | HG02486.hp2 HG02886.hp2 HG02895.hp2 others(7): Show |
missense_variant | MODERATE | c.329G>A | p.Arg110Gln | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/6 | 422/3437 | 329/780 | 110/259 | chr1 | 74738763 | |||
| chr1:74748757 | A | G | 2 | a0002 a0004 |
139 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(136): Show |
missense_variant | MODERATE | c.361A>G | p.Met121Val | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 4/6 | 454/3437 | 361/780 | 121/259 | chr1 | 74748757 | |||
| chr1:74763904 | T | C | 1 | a0004 | 1 | HG02129.hp1 | missense_variant | MODERATE | c.571T>C | p.Cys191Arg | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 6/6 | 664/3437 | 571/780 | 191/259 | chr1 | 74763904 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:74733283 | A | G | 1 | a0003c0004 | 3 | HG02486.hp2 HG03540.hp1 NA20300.hp1 |
synonymous_variant | LOW | c.39A>G | p.Gln13Gln | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 1/6 | 132/3437 | 39/780 | 13/259 | chr1 | 74733283 | |||
| chr1:74752306 | A | T | 3 | a0001c0005 a0003c0003 a0003c0004 |
11 | HG01074.hp2 HG02486.hp2 HG02886.hp2 others(8): Show |
synonymous_variant | LOW | c.441A>T | p.Thr147Thr | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/6 | 534/3437 | 441/780 | 147/259 | chr1 | 74752306 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:74733238 | G | C | 1 | a0001c0001t0011 | 1 | HG02738.hp1 | 5_prime_UTR_variant | MODIFIER | c.-7G>C | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 1/6 | 7 | chr1 | 74733238 | ||||||
| chr1:74764180 | A | G | 1 | a0001c0001t0017 | 1 | HG01256.hp2 | 3_prime_UTR_variant | MODIFIER | c.*67A>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 6/6 | 67 | chr1 | 74764180 | ||||||
| chr1:74764302 | C | T | 1 | a0002c0002t0010 | 2 | HG00423.hp1 HG02015.hp2 |
3_prime_UTR_variant | MODIFIER | c.*189C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 6/6 | 189 | chr1 | 74764302 | ||||||
| chr1:74764376 | G | C | 1 | a0001c0001t0017 | 1 | HG01256.hp2 | 3_prime_UTR_variant | MODIFIER | c.*263G>C | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 6/6 | 263 | chr1 | 74764376 | ||||||
| chr1:74764570 | A | G | 1 | a0001c0001t0016 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*457A>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 6/6 | 457 | chr1 | 74764570 | ||||||
| chr1:74764601 | A | C | 1 | a0001c0001t0008 | 6 | NA18946.hp2 NA18959.hp2 NA18962.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*488A>C | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 6/6 | 488 | chr1 | 74764601 | ||||||
| chr1:74764635 | C | A | 2 | a0001c0001t0006 a0001c0001t0008 |
20 | HG00597.hp2 HG02040.hp1 NA18942.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*522C>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 6/6 | 522 | chr1 | 74764635 | ||||||
| chr1:74764922 | C | T | 3 | a0001c0001t0002 a0001c0001t0011 a0001c0001t0015 |
80 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*809C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 6/6 | 809 | chr1 | 74764922 | ||||||
| chr1:74764945 | A | G | 2 | a0001c0001t0006 a0001c0001t0008 |
20 | HG00597.hp2 HG02040.hp1 NA18942.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*832A>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 6/6 | 832 | chr1 | 74764945 | ||||||
| chr1:74764996 | T | C | 1 | a0001c0001t0012 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*883T>C | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 6/6 | 883 | chr1 | 74764996 | ||||||
| chr1:74765183 | C | T | 1 | a0002c0002t0009 | 2 | HG01070.hp1 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1070C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 6/6 | 1070 | chr1 | 74765183 | ||||||
| chr1:74765220 | AT | A | 2 | a0001c0001t0006 a0001c0001t0008 |
20 | HG00597.hp2 HG02040.hp1 NA18942.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1112delT | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 6/6 | 1112 | INFO_REALIGN_3_PRIME | chr1 | 74765220 | |||||
| chr1:74765301 | T | C | 1 | a0001c0005t0013 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1188T>C | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 6/6 | 1188 | chr1 | 74765301 | ||||||
| chr1:74765396 | G | A | 3 | a0001c0005t0013 a0003c0003t0007 a0003c0004t0007 |
11 | HG01074.hp2 HG02486.hp2 HG02886.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1283G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 6/6 | 1283 | chr1 | 74765396 | ||||||
| chr1:74765879 | T | G | 2 | a0001c0001t0006 a0001c0001t0008 |
20 | HG00597.hp2 HG02040.hp1 NA18942.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1766T>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 6/6 | 1766 | chr1 | 74765879 | ||||||
| chr1:74765897 | T | C | 1 | a0001c0001t0014 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1784T>C | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 6/6 | 1784 | chr1 | 74765897 | ||||||
| chr1:74766000 | T | TAAC | 2 | a0001c0001t0006 a0001c0001t0008 |
20 | HG00597.hp2 HG02040.hp1 NA18942.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1889_*1891dupACA | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 6/6 | 1892 | INFO_REALIGN_3_PRIME | chr1 | 74766000 | |||||
| chr1:74766039 | C | T | 4 | a0002c0002t0001 a0002c0002t0009 a0002c0002t0010 others(1): Show |
99 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*1926C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 6/6 | 1926 | chr1 | 74766039 | ||||||
| chr1:74766301 | A | G | 1 | a0001c0001t0015 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2188A>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 6/6 | 2188 | chr1 | 74766301 | ||||||
| chr1:74766436 | G | A | 3 | a0001c0005t0013 a0003c0003t0007 a0003c0004t0007 |
11 | HG01074.hp2 HG02486.hp2 HG02886.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2323G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 6/6 | 2323 | chr1 | 74766436 | ||||||
| chr1:74766495 | TA | T | 2 | a0001c0001t0006 a0001c0001t0008 |
20 | HG00597.hp2 HG02040.hp1 NA18942.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2390delA | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 6/6 | 2390 | INFO_REALIGN_3_PRIME | chr1 | 74766495 | |||||
| chr1:74766529 | G | A | 2 | a0001c0001t0005 a0001c0001t0017 |
38 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*2416G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 6/6 | 2416 | chr1 | 74766529 | ||||||
| chr1:74766547 | G | T | 5 | a0002c0002t0001 a0002c0002t0004 a0002c0002t0009 others(2): Show |
139 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(136): Show |
3_prime_UTR_variant | MODIFIER | c.*2434G>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 6/6 | 2434 | chr1 | 74766547 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:74733468 | C | T | 158 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0011 others(155): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.174+50C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 1/5 | chr1 | 74733468 | |||||||
| chr1:74733498 | G | C | 1 | a0001c0001t0014g0055 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.174+80G>C | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 1/5 | chr1 | 74733498 | |||||||
| chr1:74733512 | T | C | 1 | a0001c0001t0003g0056 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.174+94T>C | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 1/5 | chr1 | 74733512 | |||||||
| chr1:74733530 | G | A | 54 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0007 others(51): Show |
139 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.174+112G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 1/5 | chr1 | 74733530 | |||||||
| chr1:74733595 | G | A | 54 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0007 others(51): Show |
139 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.174+177G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 1/5 | chr1 | 74733595 | |||||||
| chr1:74733615 | C | G | 112 | a0001c0001t0003g0048 a0001c0001t0003g0049 a0001c0001t0003g0050 others(109): Show |
231 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.174+197C>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 1/5 | chr1 | 74733615 | |||||||
| chr1:74733618 | C | G | 2 | a0001c0001t0003g0043 a0001c0001t0003g0115 |
3 | HG02257.hp2 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.174+200C>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 1/5 | chr1 | 74733618 | |||||||
| chr1:74733800 | G | A | 23 | a0001c0001t0005g0005 a0001c0001t0005g0015 a0001c0001t0005g0044 others(20): Show |
36 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(33): Show |
intron_variant | MODIFIER | c.174+382G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 1/5 | chr1 | 74733800 | |||||||
| chr1:74733922 | T | G | 1 | a0001c0001t0012g0136 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.174+504T>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 1/5 | chr1 | 74733922 | |||||||
| chr1:74733931 | T | C | 54 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0007 others(51): Show |
139 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.174+513T>C | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 1/5 | chr1 | 74733931 | |||||||
| chr1:74733975 | C | CT | 7 | a0001c0001t0003g0052 a0001c0001t0003g0053 a0001c0001t0003g0114 others(4): Show |
9 | HG01167.hp2 HG01255.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.174+567dupT | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 74733975 | ||||||
| chr1:74733975 | CT | C | 54 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0007 others(51): Show |
139 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.174+567delT | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 74733975 | ||||||
| chr1:74733997 | G | T | 1 | a0001c0001t0006g0150 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.174+579G>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 1/5 | chr1 | 74733997 | |||||||
| chr1:74733998 | G | A | 1 | a0001c0001t0006g0150 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.174+580G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 1/5 | chr1 | 74733998 | |||||||
| chr1:74734289 | T | C | 29 | a0001c0001t0003g0052 a0001c0001t0003g0053 a0001c0001t0003g0151 others(26): Show |
44 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(41): Show |
intron_variant | MODIFIER | c.174+871T>C | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 1/5 | chr1 | 74734289 | |||||||
| chr1:74734535 | G | C | 1 | a0003c0004t0007g0026 | 3 | HG02486.hp2 HG03540.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.174+1117G>C | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 1/5 | chr1 | 74734535 | |||||||
| chr1:74734557 | A | G | 7 | a0001c0001t0003g0043 a0001c0001t0003g0109 a0001c0001t0003g0110 others(4): Show |
8 | HG00639.hp1 HG02257.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.174+1139A>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 1/5 | chr1 | 74734557 | |||||||
| chr1:74734559 | T | C | 1 | a0001c0001t0014g0055 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.174+1141T>C | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 1/5 | chr1 | 74734559 | |||||||
| chr1:74734662 | C | T | 1 | a0001c0001t0003g0056 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.174+1244C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 1/5 | chr1 | 74734662 | |||||||
| chr1:74734756 | A | G | 10 | a0001c0001t0003g0025 a0001c0001t0003g0043 a0001c0001t0003g0107 others(7): Show |
13 | HG00099.hp1 HG00639.hp1 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.174+1338A>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 1/5 | chr1 | 74734756 | |||||||
| chr1:74734773 | C | T | 1 | a0001c0001t0014g0055 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.174+1355C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 1/5 | chr1 | 74734773 | |||||||
| chr1:74734802 | G | A | 29 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0011 others(26): Show |
74 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.174+1384G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 1/5 | chr1 | 74734802 | |||||||
| chr1:74734911 | C | G | 11 | a0001c0001t0003g0025 a0001c0001t0003g0043 a0001c0001t0003g0107 others(8): Show |
14 | HG00099.hp1 HG00639.hp1 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.174+1493C>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 1/5 | chr1 | 74734911 | |||||||
| chr1:74735011 | C | T | 8 | a0001c0001t0003g0048 a0001c0001t0003g0049 a0001c0001t0003g0050 others(5): Show |
12 | HG01109.hp2 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.175-1531C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 1/5 | chr1 | 74735011 | |||||||
| chr1:74735013 | T | C | 112 | a0001c0001t0003g0048 a0001c0001t0003g0049 a0001c0001t0003g0050 others(109): Show |
231 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.175-1529T>C | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 1/5 | chr1 | 74735013 | |||||||
| chr1:74735101 | C | A | 54 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0007 others(51): Show |
139 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.175-1441C>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 1/5 | chr1 | 74735101 | |||||||
| chr1:74735408 | C | T | 8 | a0001c0001t0003g0048 a0001c0001t0003g0049 a0001c0001t0003g0050 others(5): Show |
12 | HG01109.hp2 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.175-1134C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 1/5 | chr1 | 74735408 | |||||||
| chr1:74735737 | G | A | 1 | a0001c0001t0003g0056 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.175-805G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 1/5 | chr1 | 74735737 | |||||||
| chr1:74736027 | A | G | 1 | a0002c0002t0004g0088 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.175-515A>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 1/5 | chr1 | 74736027 | |||||||
| chr1:74736177 | G | A | 2 | a0001c0001t0003g0048 a0001c0001t0003g0146 |
3 | HG02647.hp1 HG02818.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.175-365G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 1/5 | chr1 | 74736177 | |||||||
| chr1:74736333 | C | G | 7 | a0001c0005t0013g0145 a0003c0003t0007g0046 a0003c0003t0007g0047 others(4): Show |
11 | HG01074.hp2 HG02486.hp2 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.175-209C>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 1/5 | chr1 | 74736333 | |||||||
| chr1:74736463 | C | G | 1 | a0001c0001t0002g0102 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.175-79C>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 1/5 | chr1 | 74736463 | |||||||
| chr1:74736465 | A | G | 2 | a0001c0001t0003g0043 a0001c0001t0003g0115 |
3 | HG02257.hp2 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.175-77A>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 1/5 | chr1 | 74736465 | |||||||
| chr1:74737028 | G | T | 10 | a0001c0001t0003g0025 a0001c0001t0003g0043 a0001c0001t0003g0107 others(7): Show |
13 | HG00099.hp1 HG00639.hp1 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.255+406G>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 2/5 | chr1 | 74737028 | |||||||
| chr1:74737186 | C | T | 11 | a0001c0001t0005g0045 a0001c0001t0006g0009 a0001c0001t0006g0016 others(8): Show |
22 | HG00597.hp2 HG00673.hp2 HG02040.hp1 others(19): Show |
intron_variant | MODIFIER | c.255+564C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 2/5 | chr1 | 74737186 | |||||||
| chr1:74737258 | C | CATCTTT | 6 | a0001c0001t0003g0052 a0001c0001t0003g0053 a0001c0001t0003g0151 others(3): Show |
8 | HG01167.hp2 HG01255.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.255+638_255+643dup others(6): Show |
TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 74737258 | ||||||
| chr1:74737531 | A | G | 7 | a0001c0005t0013g0145 a0003c0003t0007g0046 a0003c0003t0007g0047 others(4): Show |
11 | HG01074.hp2 HG02486.hp2 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.255+909A>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 2/5 | chr1 | 74737531 | |||||||
| chr1:74737694 | C | T | 19 | a0001c0001t0005g0045 a0001c0001t0006g0009 a0001c0001t0006g0016 others(16): Show |
34 | HG00597.hp2 HG00673.hp2 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.256-996C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 2/5 | chr1 | 74737694 | |||||||
| chr1:74737698 | G | A | 23 | a0001c0001t0005g0005 a0001c0001t0005g0015 a0001c0001t0005g0044 others(20): Show |
36 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(33): Show |
intron_variant | MODIFIER | c.256-992G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 2/5 | chr1 | 74737698 | |||||||
| chr1:74737825 | A | G | 1 | a0001c0001t0002g0106 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.256-865A>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 2/5 | chr1 | 74737825 | |||||||
| chr1:74737851 | C | G | 1 | a0002c0002t0001g0087 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.256-839C>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 2/5 | chr1 | 74737851 | |||||||
| chr1:74737977 | A | G | 1 | a0001c0001t0014g0055 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.256-713A>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 2/5 | chr1 | 74737977 | |||||||
| chr1:74738014 | C | T | 1 | a0001c0001t0006g0141 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.256-676C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 2/5 | chr1 | 74738014 | |||||||
| chr1:74738107 | G | GA | 51 | a0001c0001t0003g0052 a0001c0001t0003g0053 a0001c0001t0003g0151 others(48): Show |
126 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.256-574dupA | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 74738107 | ||||||
| chr1:74738114 | A | AC | 18 | a0002c0002t0001g0014 a0002c0002t0004g0003 a0002c0002t0004g0010 others(15): Show |
41 | HG00140.hp1 HG01167.hp1 HG01169.hp1 others(38): Show |
intron_variant | MODIFIER | c.256-576_256-575ins others(1): Show |
TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 2/5 | chr1 | 74738114 | |||||||
| chr1:74738117 | C | A | 102 | a0001c0001t0003g0052 a0001c0001t0003g0053 a0001c0001t0003g0151 others(99): Show |
217 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.256-573C>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 2/5 | chr1 | 74738117 | |||||||
| chr1:74738121 | C | A | 7 | a0002c0002t0001g0008 a0002c0002t0001g0028 a0002c0002t0001g0029 others(4): Show |
14 | HG00621.hp2 HG00673.hp1 HG02074.hp1 others(11): Show |
intron_variant | MODIFIER | c.256-569C>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 2/5 | chr1 | 74738121 | |||||||
| chr1:74738180 | A | G | 1 | a0001c0001t0005g0135 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.256-510A>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 2/5 | chr1 | 74738180 | |||||||
| chr1:74738224 | T | A | 7 | a0001c0001t0005g0044 a0001c0001t0005g0118 a0001c0001t0005g0119 others(4): Show |
8 | HG00735.hp2 HG00738.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.256-466T>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 2/5 | chr1 | 74738224 | |||||||
| chr1:74738290 | G | A | 6 | a0001c0001t0003g0052 a0001c0001t0003g0053 a0001c0001t0003g0151 others(3): Show |
8 | HG01167.hp2 HG01255.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.256-400G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 2/5 | chr1 | 74738290 | |||||||
| chr1:74738346 | T | A | 1 | a0001c0001t0002g0021 | 3 | HG02083.hp1 NA18943.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.256-344T>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 2/5 | chr1 | 74738346 | |||||||
| chr1:74738348 | A | AAAT | 1 | a0001c0001t0002g0021 | 3 | HG02083.hp1 NA18943.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.256-342_256-341ins others(3): Show |
TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 2/5 | chr1 | 74738348 | |||||||
| chr1:74738409 | G | A | 1 | a0003c0003t0007g0046 | 2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.256-281G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 2/5 | chr1 | 74738409 | |||||||
| chr1:74738459 | G | A | 33 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0011 others(30): Show |
81 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.256-231G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 2/5 | chr1 | 74738459 | |||||||
| chr1:74738663 | A | G | 1 | a0001c0001t0014g0055 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.256-27A>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 2/5 | chr1 | 74738663 | |||||||
| chr1:74738841 | A | G | 3 | a0001c0001t0006g0009 a0001c0001t0008g0009 a0001c0001t0008g0017 |
10 | NA18942.hp2 NA18946.hp2 NA18959.hp2 others(7): Show |
intron_variant | MODIFIER | c.354+53A>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74738841 | |||||||
| chr1:74739064 | T | C | 6 | a0003c0003t0007g0046 a0003c0003t0007g0047 a0003c0003t0007g0142 others(3): Show |
10 | HG02486.hp2 HG02886.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.354+276T>C | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74739064 | |||||||
| chr1:74739107 | A | G | 1 | a0001c0001t0005g0123 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.354+319A>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74739107 | |||||||
| chr1:74739130 | T | A | 1 | a0001c0001t0003g0114 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.354+342T>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74739130 | |||||||
| chr1:74739275 | C | G | 6 | a0003c0003t0007g0046 a0003c0003t0007g0047 a0003c0003t0007g0142 others(3): Show |
10 | HG02486.hp2 HG02886.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.354+487C>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74739275 | |||||||
| chr1:74739371 | A | G | 1 | a0001c0001t0005g0122 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.354+583A>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74739371 | |||||||
| chr1:74739446 | C | T | 2 | a0001c0001t0005g0121 a0001c0001t0005g0134 |
2 | HG01255.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.354+658C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74739446 | |||||||
| chr1:74739660 | A | C | 29 | a0001c0001t0003g0052 a0001c0001t0003g0053 a0001c0001t0003g0151 others(26): Show |
44 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(41): Show |
intron_variant | MODIFIER | c.354+872A>C | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74739660 | |||||||
| chr1:74739792 | C | T | 1 | a0002c0002t0001g0077 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.354+1004C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74739792 | |||||||
| chr1:74739797 | T | C | 3 | a0001c0001t0003g0052 a0001c0001t0003g0151 a0001c0001t0003g0152 |
4 | HG01981.hp2 HG03139.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.354+1009T>C | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74739797 | |||||||
| chr1:74739830 | G | T | 36 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0007 others(33): Show |
98 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.354+1042G>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74739830 | |||||||
| chr1:74739831 | T | G | 36 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0007 others(33): Show |
98 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.354+1043T>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74739831 | |||||||
| chr1:74739906 | T | C | 54 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0007 others(51): Show |
139 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.354+1118T>C | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74739906 | |||||||
| chr1:74739999 | G | A | 1 | a0002c0002t0001g0061 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.354+1211G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74739999 | |||||||
| chr1:74740173 | G | A | 1 | a0002c0002t0004g0088 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.354+1385G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74740173 | |||||||
| chr1:74740183 | C | T | 1 | a0001c0001t0003g0114 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.354+1395C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74740183 | |||||||
| chr1:74740190 | G | A | 1 | a0002c0002t0004g0018 | 3 | HG02647.hp2 HG02723.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.354+1402G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74740190 | |||||||
| chr1:74740290 | C | A | 1 | a0001c0001t0005g0124 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.354+1502C>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74740290 | |||||||
| chr1:74740304 | G | C | 36 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0007 others(33): Show |
98 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.354+1516G>C | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74740304 | |||||||
| chr1:74740473 | G | C | 1 | a0001c0001t0003g0114 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.354+1685G>C | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74740473 | |||||||
| chr1:74740499 | GC | G | 6 | a0001c0001t0003g0052 a0001c0001t0003g0053 a0001c0001t0003g0151 others(3): Show |
8 | HG01167.hp2 HG01255.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.354+1715delC | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 74740499 | ||||||
| chr1:74740525 | C | T | 1 | a0001c0001t0005g0133 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.354+1737C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74740525 | |||||||
| chr1:74740564 | C | T | 1 | a0001c0001t0003g0051 | 2 | HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.354+1776C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74740564 | |||||||
| chr1:74740616 | GTTTTTAC others(59): Show |
G | 2 | a0002c0002t0001g0014 a0002c0002t0004g0014 |
4 | NA18939.hp2 NA18960.hp2 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.354+1919_354+1984d others(68): Show |
TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 74740616 | ||||||
| chr1:74740641 | G | A | 30 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0011 others(27): Show |
75 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.354+1853G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74740641 | |||||||
| chr1:74740666 | G | A | 1 | a0001c0001t0002g0004 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.354+1878G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74740666 | |||||||
| chr1:74740735 | CGCTGATT others(18): Show |
C | 1 | a0001c0001t0002g0089 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.354+1964_354+1988d others(27): Show |
TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 74740735 | ||||||
| chr1:74740748 | A | ATTTTTAC others(59): Show |
1 | a0001c0001t0012g0136 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.354+1989_354+2054d others(68): Show |
TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 74740748 | ||||||
| chr1:74740796 | C | T | 2 | a0001c0001t0003g0048 a0001c0001t0003g0146 |
3 | HG02647.hp1 HG02818.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.354+2008C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74740796 | |||||||
| chr1:74740993 | TA | T | 54 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0007 others(51): Show |
139 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.354+2206delA | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74740993 | |||||||
| chr1:74741009 | G | A | 1 | a0001c0001t0002g0042 | 2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.354+2221G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74741009 | |||||||
| chr1:74741053 | G | T | 1 | a0001c0001t0016g0113 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.354+2265G>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74741053 | |||||||
| chr1:74741062 | C | A | 1 | a0002c0002t0001g0087 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.354+2274C>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74741062 | |||||||
| chr1:74741136 | A | G | 102 | a0001c0001t0003g0052 a0001c0001t0003g0053 a0001c0001t0003g0151 others(99): Show |
217 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.354+2348A>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74741136 | |||||||
| chr1:74741165 | A | T | 158 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0011 others(155): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.354+2377A>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74741165 | |||||||
| chr1:74741340 | T | C | 102 | a0001c0001t0003g0052 a0001c0001t0003g0053 a0001c0001t0003g0151 others(99): Show |
217 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.354+2552T>C | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74741340 | |||||||
| chr1:74741345 | C | G | 1 | a0001c0001t0002g0041 | 2 | HG00642.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.354+2557C>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74741345 | |||||||
| chr1:74741346 | G | A | 1 | a0001c0005t0013g0145 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.354+2558G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74741346 | |||||||
| chr1:74741612 | C | T | 33 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0011 others(30): Show |
81 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.354+2824C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74741612 | |||||||
| chr1:74741631 | G | A | 1 | a0001c0001t0003g0151 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.354+2843G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74741631 | |||||||
| chr1:74741636 | G | A | 29 | a0001c0001t0003g0052 a0001c0001t0003g0053 a0001c0001t0003g0151 others(26): Show |
44 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(41): Show |
intron_variant | MODIFIER | c.354+2848G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74741636 | |||||||
| chr1:74741909 | G | A | 6 | a0001c0001t0003g0052 a0001c0001t0003g0053 a0001c0001t0003g0151 others(3): Show |
8 | HG01167.hp2 HG01255.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.354+3121G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74741909 | |||||||
| chr1:74741975 | T | C | 18 | a0001c0001t0005g0045 a0001c0001t0006g0009 a0001c0001t0006g0016 others(15): Show |
33 | HG00597.hp2 HG00673.hp2 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.354+3187T>C | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74741975 | |||||||
| chr1:74742040 | C | A | 1 | a0002c0002t0004g0079 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.354+3252C>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74742040 | |||||||
| chr1:74742072 | A | G | 54 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0007 others(51): Show |
139 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.354+3284A>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74742072 | |||||||
| chr1:74742192 | G | A | 54 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0007 others(51): Show |
139 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.354+3404G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74742192 | |||||||
| chr1:74742335 | C | A | 1 | a0002c0002t0001g0057 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.354+3547C>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74742335 | |||||||
| chr1:74742350 | C | G | 112 | a0001c0001t0003g0048 a0001c0001t0003g0049 a0001c0001t0003g0050 others(109): Show |
231 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.354+3562C>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74742350 | |||||||
| chr1:74742423 | C | T | 1 | a0001c0001t0014g0055 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.354+3635C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74742423 | |||||||
| chr1:74742449 | G | A | 6 | a0001c0001t0003g0052 a0001c0001t0003g0053 a0001c0001t0003g0151 others(3): Show |
8 | HG01167.hp2 HG01255.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.354+3661G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74742449 | |||||||
| chr1:74742471 | G | A | 1 | a0002c0002t0001g0062 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.354+3683G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74742471 | |||||||
| chr1:74742475 | G | A | 1 | a0002c0002t0001g0063 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.354+3687G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74742475 | |||||||
| chr1:74742626 | G | A | 11 | a0001c0001t0005g0045 a0001c0001t0006g0009 a0001c0001t0006g0016 others(8): Show |
22 | HG00597.hp2 HG00673.hp2 HG02040.hp1 others(19): Show |
intron_variant | MODIFIER | c.354+3838G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74742626 | |||||||
| chr1:74742698 | T | G | 23 | a0001c0001t0005g0005 a0001c0001t0005g0015 a0001c0001t0005g0044 others(20): Show |
36 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(33): Show |
intron_variant | MODIFIER | c.354+3910T>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74742698 | |||||||
| chr1:74742848 | A | T | 1 | a0002c0002t0004g0086 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.354+4060A>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74742848 | |||||||
| chr1:74742981 | C | T | 1 | a0001c0001t0002g0101 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.354+4193C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74742981 | |||||||
| chr1:74743047 | G | C | 1 | a0001c0001t0005g0125 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.354+4259G>C | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74743047 | |||||||
| chr1:74743214 | G | A | 1 | a0002c0002t0004g0080 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.354+4426G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74743214 | |||||||
| chr1:74743216 | G | T | 1 | a0001c0001t0003g0105 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.354+4428G>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74743216 | |||||||
| chr1:74743358 | C | T | 2 | a0001c0001t0008g0017 a0002c0002t0001g0076 |
5 | NA18946.hp2 NA18955.hp2 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.354+4570C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74743358 | |||||||
| chr1:74743359 | G | A | 2 | a0001c0001t0003g0104 a0001c0001t0003g0105 |
2 | HG02622.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.354+4571G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74743359 | |||||||
| chr1:74743456 | A | T | 1 | a0001c0001t0002g0040 | 2 | HG02602.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.354+4668A>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74743456 | |||||||
| chr1:74743470 | G | T | 2 | a0002c0002t0001g0033 a0002c0002t0001g0075 |
3 | HG02615.hp2 HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.354+4682G>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74743470 | |||||||
| chr1:74743479 | C | G | 1 | a0001c0001t0002g0100 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.354+4691C>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74743479 | |||||||
| chr1:74743489 | G | A | 1 | a0001c0001t0012g0136 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.354+4701G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74743489 | |||||||
| chr1:74743529 | C | T | 4 | a0002c0002t0001g0008 a0002c0002t0001g0028 a0002c0002t0001g0029 others(1): Show |
12 | HG00621.hp2 HG00673.hp1 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.354+4741C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74743529 | |||||||
| chr1:74743534 | G | A | 1 | a0002c0002t0001g0065 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.354+4746G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74743534 | |||||||
| chr1:74743552 | T | G | 1 | a0001c0001t0002g0036 | 2 | HG02135.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.354+4764T>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74743552 | |||||||
| chr1:74743577 | G | A | 1 | a0001c0001t0005g0015 | 4 | HG00140.hp2 HG00280.hp2 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.354+4789G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74743577 | |||||||
| chr1:74743586 | G | C | 7 | a0001c0001t0003g0043 a0001c0001t0003g0109 a0001c0001t0003g0110 others(4): Show |
8 | HG00639.hp1 HG02257.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.354+4798G>C | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74743586 | |||||||
| chr1:74743605 | T | C | 11 | a0001c0001t0005g0045 a0001c0001t0006g0009 a0001c0001t0006g0016 others(8): Show |
22 | HG00597.hp2 HG00673.hp2 HG02040.hp1 others(19): Show |
intron_variant | MODIFIER | c.354+4817T>C | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74743605 | |||||||
| chr1:74743628 | A | G | 29 | a0001c0001t0003g0052 a0001c0001t0003g0053 a0001c0001t0003g0151 others(26): Show |
44 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(41): Show |
intron_variant | MODIFIER | c.354+4840A>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74743628 | |||||||
| chr1:74743700 | C | A | 1 | a0001c0001t0005g0118 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.354+4912C>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74743700 | |||||||
| chr1:74743783 | A | G | 1 | a0001c0001t0012g0136 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.355-4968A>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74743783 | |||||||
| chr1:74743838 | G | A | 29 | a0001c0001t0003g0052 a0001c0001t0003g0053 a0001c0001t0003g0151 others(26): Show |
44 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(41): Show |
intron_variant | MODIFIER | c.355-4913G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74743838 | |||||||
| chr1:74743954 | G | A | 1 | a0001c0001t0005g0126 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.355-4797G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74743954 | |||||||
| chr1:74744054 | C | T | 1 | a0001c0005t0013g0145 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.355-4697C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74744054 | |||||||
| chr1:74744066 | C | G | 54 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0007 others(51): Show |
139 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.355-4685C>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74744066 | |||||||
| chr1:74744349 | ATCAGAGA others(8): Show |
A | 1 | a0001c0001t0012g0136 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.355-4400_355-4386d others(17): Show |
TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 74744349 | ||||||
| chr1:74744366 | G | A | 1 | a0001c0001t0012g0136 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.355-4385G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74744366 | |||||||
| chr1:74744402 | C | T | 6 | a0001c0001t0003g0049 a0001c0001t0003g0050 a0001c0001t0003g0147 others(3): Show |
8 | HG01109.hp2 HG02615.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.355-4349C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74744402 | |||||||
| chr1:74744422 | C | T | 1 | a0002c0002t0001g0059 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.355-4329C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74744422 | |||||||
| chr1:74744496 | A | G | 3 | a0001c0001t0002g0024 a0001c0001t0002g0042 a0001c0001t0002g0106 |
6 | HG02258.hp1 HG02572.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.355-4255A>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74744496 | |||||||
| chr1:74744504 | G | T | 10 | a0001c0001t0003g0025 a0001c0001t0003g0043 a0001c0001t0003g0107 others(7): Show |
13 | HG00099.hp1 HG00639.hp1 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.355-4247G>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74744504 | |||||||
| chr1:74744514 | C | T | 18 | a0001c0001t0005g0045 a0001c0001t0006g0009 a0001c0001t0006g0016 others(15): Show |
33 | HG00597.hp2 HG00673.hp2 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.355-4237C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74744514 | |||||||
| chr1:74744585 | T | C | 1 | a0002c0002t0001g0066 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.355-4166T>C | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74744585 | |||||||
| chr1:74744631 | C | T | 1 | a0001c0001t0003g0152 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.355-4120C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74744631 | |||||||
| chr1:74744733 | A | G | 1 | a0002c0002t0004g0085 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.355-4018A>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74744733 | |||||||
| chr1:74744768 | C | T | 1 | a0001c0001t0003g0112 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.355-3983C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74744768 | |||||||
| chr1:74744796 | G | A | 1 | a0001c0001t0005g0127 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.355-3955G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74744796 | |||||||
| chr1:74744880 | A | G | 1 | a0002c0002t0001g0013 | 4 | HG01192.hp2 HG02723.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.355-3871A>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74744880 | |||||||
| chr1:74744906 | T | G | 1 | a0002c0002t0001g0059 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.355-3845T>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74744906 | |||||||
| chr1:74744938 | G | A | 6 | a0001c0001t0003g0052 a0001c0001t0003g0053 a0001c0001t0003g0151 others(3): Show |
8 | HG01167.hp2 HG01255.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.355-3813G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74744938 | |||||||
| chr1:74745021 | C | T | 1 | a0002c0002t0001g0074 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.355-3730C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74745021 | |||||||
| chr1:74745131 | C | T | 1 | a0001c0001t0014g0055 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.355-3620C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74745131 | |||||||
| chr1:74745163 | T | A | 1 | a0001c0001t0003g0153 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.355-3588T>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74745163 | |||||||
| chr1:74745163 | T | G | 101 | a0001c0001t0003g0052 a0001c0001t0003g0053 a0001c0001t0003g0151 others(98): Show |
216 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.355-3588T>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74745163 | |||||||
| chr1:74745236 | T | C | 1 | a0001c0001t0003g0105 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.355-3515T>C | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74745236 | |||||||
| chr1:74745262 | C | A | 1 | a0001c0005t0013g0145 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.355-3489C>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74745262 | |||||||
| chr1:74745305 | C | T | 7 | a0001c0001t0003g0043 a0001c0001t0003g0109 a0001c0001t0003g0110 others(4): Show |
8 | HG00639.hp1 HG02257.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.355-3446C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74745305 | |||||||
| chr1:74745306 | G | A | 1 | a0001c0001t0003g0049 | 2 | HG02970.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.355-3445G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74745306 | |||||||
| chr1:74745335 | C | T | 1 | a0001c0001t0002g0099 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.355-3416C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74745335 | |||||||
| chr1:74745400 | T | C | 2 | a0002c0002t0001g0014 a0002c0002t0004g0014 |
4 | NA18939.hp2 NA18960.hp2 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.355-3351T>C | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74745400 | |||||||
| chr1:74745442 | T | A | 1 | a0001c0001t0005g0044 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.355-3309T>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74745442 | |||||||
| chr1:74745486 | G | A | 11 | a0001c0001t0005g0045 a0001c0001t0006g0009 a0001c0001t0006g0016 others(8): Show |
22 | HG00597.hp2 HG00673.hp2 HG02040.hp1 others(19): Show |
intron_variant | MODIFIER | c.355-3265G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74745486 | |||||||
| chr1:74745572 | A | T | 1 | a0001c0001t0002g0103 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.355-3179A>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74745572 | |||||||
| chr1:74745612 | C | T | 1 | a0001c0001t0003g0056 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.355-3139C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74745612 | |||||||
| chr1:74745613 | G | A | 1 | a0003c0003t0007g0142 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.355-3138G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74745613 | |||||||
| chr1:74745878 | G | A | 1 | a0001c0001t0014g0055 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.355-2873G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74745878 | |||||||
| chr1:74745954 | T | A | 54 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0007 others(51): Show |
139 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.355-2797T>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74745954 | |||||||
| chr1:74745967 | C | T | 1 | a0001c0005t0013g0145 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.355-2784C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74745967 | |||||||
| chr1:74746054 | T | C | 29 | a0001c0001t0003g0052 a0001c0001t0003g0053 a0001c0001t0003g0151 others(26): Show |
44 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(41): Show |
intron_variant | MODIFIER | c.355-2697T>C | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74746054 | |||||||
| chr1:74746087 | C | T | 2 | a0001c0001t0003g0107 a0001c0001t0003g0108 |
2 | HG01515.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.355-2664C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74746087 | |||||||
| chr1:74746146 | C | A | 1 | a0001c0001t0014g0055 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.355-2605C>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74746146 | |||||||
| chr1:74746389 | A | G | 1 | a0001c0001t0014g0055 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.355-2362A>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74746389 | |||||||
| chr1:74746446 | A | T | 1 | a0001c0001t0002g0098 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.355-2305A>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74746446 | |||||||
| chr1:74746494 | T | C | 1 | a0001c0001t0016g0113 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.355-2257T>C | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74746494 | |||||||
| chr1:74746654 | A | T | 1 | a0002c0002t0001g0073 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.355-2097A>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74746654 | |||||||
| chr1:74746908 | C | G | 11 | a0001c0001t0005g0045 a0001c0001t0006g0009 a0001c0001t0006g0016 others(8): Show |
22 | HG00597.hp2 HG00673.hp2 HG02040.hp1 others(19): Show |
intron_variant | MODIFIER | c.355-1843C>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74746908 | |||||||
| chr1:74746983 | A | G | 1 | a0001c0001t0003g0056 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.355-1768A>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74746983 | |||||||
| chr1:74747139 | A | G | 1 | a0001c0001t0002g0036 | 2 | HG02135.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.355-1612A>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74747139 | |||||||
| chr1:74747148 | G | C | 18 | a0001c0001t0005g0045 a0001c0001t0006g0009 a0001c0001t0006g0016 others(15): Show |
33 | HG00597.hp2 HG00673.hp2 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.355-1603G>C | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74747148 | |||||||
| chr1:74747162 | A | G | 3 | a0001c0001t0003g0050 a0001c0001t0003g0148 a0001c0001t0003g0149 |
4 | HG01109.hp2 HG02615.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.355-1589A>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74747162 | |||||||
| chr1:74747261 | G | A | 1 | a0002c0002t0004g0019 | 3 | HG00140.hp1 HG03017.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.355-1490G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74747261 | |||||||
| chr1:74747354 | C | T | 2 | a0001c0001t0003g0056 a0001c0001t0014g0055 |
2 | HG01891.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.355-1397C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74747354 | |||||||
| chr1:74747360 | A | G | 102 | a0001c0001t0003g0052 a0001c0001t0003g0053 a0001c0001t0003g0151 others(99): Show |
217 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.355-1391A>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74747360 | |||||||
| chr1:74747363 | C | T | 1 | a0001c0001t0003g0056 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.355-1388C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74747363 | |||||||
| chr1:74747370 | G | A | 8 | a0001c0001t0003g0048 a0001c0001t0003g0049 a0001c0001t0003g0050 others(5): Show |
12 | HG01109.hp2 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.355-1381G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74747370 | |||||||
| chr1:74747404 | G | A | 29 | a0001c0001t0003g0052 a0001c0001t0003g0053 a0001c0001t0003g0151 others(26): Show |
44 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(41): Show |
intron_variant | MODIFIER | c.355-1347G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74747404 | |||||||
| chr1:74747438 | C | T | 1 | a0001c0001t0002g0097 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.355-1313C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74747438 | |||||||
| chr1:74747493 | T | C | 158 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0011 others(155): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.355-1258T>C | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74747493 | |||||||
| chr1:74747505 | C | T | 1 | a0001c0001t0002g0039 | 2 | HG02165.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.355-1246C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74747505 | |||||||
| chr1:74747525 | T | C | 1 | a0001c0005t0013g0145 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.355-1226T>C | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74747525 | |||||||
| chr1:74747620 | G | C | 1 | a0002c0002t0004g0034 | 2 | NA18984.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.355-1131G>C | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74747620 | |||||||
| chr1:74747632 | G | A | 54 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0007 others(51): Show |
139 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.355-1119G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74747632 | |||||||
| chr1:74747636 | C | CA | 6 | a0001c0001t0003g0114 a0001c0001t0006g0137 a0002c0002t0001g0006 others(3): Show |
13 | HG02559.hp2 NA18612.hp2 NA18961.hp1 others(10): Show |
intron_variant | MODIFIER | c.355-1101dupA | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 74747636 | ||||||
| chr1:74747645 | A | G | 1 | a0003c0003t0007g0047 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.355-1106A>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74747645 | |||||||
| chr1:74747661 | A | G | 1 | a0002c0002t0009g0032 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.355-1090A>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74747661 | |||||||
| chr1:74747681 | C | T | 1 | a0001c0001t0014g0055 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.355-1070C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74747681 | |||||||
| chr1:74747703 | A | G | 11 | a0001c0001t0005g0045 a0001c0001t0006g0009 a0001c0001t0006g0016 others(8): Show |
22 | HG00597.hp2 HG00673.hp2 HG02040.hp1 others(19): Show |
intron_variant | MODIFIER | c.355-1048A>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74747703 | |||||||
| chr1:74747744 | CAT | C | 11 | a0002c0002t0001g0014 a0002c0002t0004g0003 a0002c0002t0004g0014 others(8): Show |
26 | HG00140.hp1 HG01261.hp1 HG01928.hp1 others(23): Show |
intron_variant | MODIFIER | c.355-1002_355-1001d others(4): Show |
TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 74747744 | ||||||
| chr1:74747761 | A | G | 2 | a0001c0001t0003g0111 a0002c0002t0004g0018 |
4 | HG02647.hp2 HG02723.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.355-990A>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74747761 | |||||||
| chr1:74747775 | GTA | G | 6 | a0003c0003t0007g0046 a0003c0003t0007g0047 a0003c0003t0007g0142 others(3): Show |
10 | HG02486.hp2 HG02886.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.355-972_355-971del others(2): Show |
TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 74747775 | ||||||
| chr1:74747779 | A | G | 106 | a0001c0001t0003g0048 a0001c0001t0003g0049 a0001c0001t0003g0050 others(103): Show |
221 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.355-972A>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74747779 | |||||||
| chr1:74747819 | G | GTA | 29 | a0001c0001t0003g0052 a0001c0001t0003g0053 a0001c0001t0003g0151 others(26): Show |
44 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(41): Show |
intron_variant | MODIFIER | c.355-924_355-923dup others(2): Show |
TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 74747819 | ||||||
| chr1:74747834 | C | T | 1 | a0001c0001t0002g0096 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.355-917C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74747834 | |||||||
| chr1:74747835 | G | A | 1 | a0002c0002t0001g0068 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.355-916G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74747835 | |||||||
| chr1:74747849 | A | C | 1 | a0001c0001t0014g0055 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.355-902A>C | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74747849 | |||||||
| chr1:74747875 | A | G | 2 | a0001c0001t0003g0049 a0001c0001t0003g0147 |
3 | HG02896.hp2 HG02970.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.355-876A>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74747875 | |||||||
| chr1:74747882 | CAT | C | 29 | a0001c0001t0003g0052 a0001c0001t0003g0053 a0001c0001t0003g0151 others(26): Show |
44 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(41): Show |
intron_variant | MODIFIER | c.355-865_355-864del others(2): Show |
TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 74747882 | ||||||
| chr1:74747890 | CATATACA others(5): Show |
C | 2 | a0001c0001t0003g0109 a0001c0001t0003g0110 |
2 | HG00639.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.355-850_355-839del others(12): Show |
TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 74747890 | ||||||
| chr1:74747900 | C | G | 2 | a0001c0001t0003g0104 a0001c0001t0003g0105 |
2 | HG02622.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.355-851C>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74747900 | |||||||
| chr1:74747935 | G | T | 29 | a0001c0001t0003g0052 a0001c0001t0003g0053 a0001c0001t0003g0151 others(26): Show |
44 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(41): Show |
intron_variant | MODIFIER | c.355-816G>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74747935 | |||||||
| chr1:74747954 | A | T | 1 | a0002c0002t0001g0072 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.355-797A>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74747954 | |||||||
| chr1:74747964 | A | C | 33 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0011 others(30): Show |
81 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.355-787A>C | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74747964 | |||||||
| chr1:74748018 | G | A | 1 | a0001c0001t0003g0051 | 2 | HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.355-733G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74748018 | |||||||
| chr1:74748142 | G | GACAACTT others(1): Show |
112 | a0001c0001t0003g0048 a0001c0001t0003g0049 a0001c0001t0003g0050 others(109): Show |
231 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.355-604_355-603ins others(8): Show |
TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 74748142 | ||||||
| chr1:74748172 | G | T | 1 | a0001c0001t0003g0056 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.355-579G>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74748172 | |||||||
| chr1:74748349 | A | G | 2 | a0001c0001t0003g0104 a0001c0001t0003g0105 |
2 | HG02622.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.355-402A>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74748349 | |||||||
| chr1:74748376 | T | C | 1 | a0001c0001t0002g0022 | 3 | NA18955.hp1 NA18957.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.355-375T>C | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74748376 | |||||||
| chr1:74748509 | G | T | 23 | a0001c0001t0005g0005 a0001c0001t0005g0015 a0001c0001t0005g0044 others(20): Show |
36 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(33): Show |
intron_variant | MODIFIER | c.355-242G>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74748509 | |||||||
| chr1:74748641 | A | T | 1 | a0001c0001t0003g0056 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.355-110A>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74748641 | |||||||
| chr1:74748691 | CCAAA | C | 3 | a0001c0001t0003g0025 a0001c0001t0003g0107 a0001c0001t0003g0108 |
5 | HG00099.hp1 HG00733.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.355-57_355-54delAA others(2): Show |
TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 74748691 | ||||||
| chr1:74748706 | G | C | 29 | a0001c0001t0003g0052 a0001c0001t0003g0053 a0001c0001t0003g0151 others(26): Show |
44 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(41): Show |
intron_variant | MODIFIER | c.355-45G>C | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 3/5 | chr1 | 74748706 | |||||||
| chr1:74749560 | T | C | 6 | a0001c0001t0003g0052 a0001c0001t0003g0053 a0001c0001t0003g0151 others(3): Show |
8 | HG01167.hp2 HG01255.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.426+738T>C | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 4/5 | chr1 | 74749560 | |||||||
| chr1:74749817 | G | A | 35 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0011 others(32): Show |
83 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.426+995G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 4/5 | chr1 | 74749817 | |||||||
| chr1:74750005 | C | T | 16 | a0001c0001t0002g0004 a0001c0001t0002g0021 a0001c0001t0002g0022 others(13): Show |
31 | HG00423.hp2 HG00639.hp2 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.426+1183C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 4/5 | chr1 | 74750005 | |||||||
| chr1:74750044 | A | G | 1 | a0002c0002t0001g0071 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.426+1222A>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 4/5 | chr1 | 74750044 | |||||||
| chr1:74750081 | A | G | 1 | a0001c0001t0012g0136 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.426+1259A>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 4/5 | chr1 | 74750081 | |||||||
| chr1:74750197 | C | T | 1 | a0003c0003t0007g0046 | 2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.426+1375C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 4/5 | chr1 | 74750197 | |||||||
| chr1:74750291 | C | T | 1 | a0002c0002t0001g0068 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.426+1469C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 4/5 | chr1 | 74750291 | |||||||
| chr1:74750405 | A | C | 7 | a0001c0005t0013g0145 a0003c0003t0007g0046 a0003c0003t0007g0047 others(4): Show |
11 | HG01074.hp2 HG02486.hp2 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.426+1583A>C | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 4/5 | chr1 | 74750405 | |||||||
| chr1:74750455 | T | C | 1 | a0001c0001t0014g0055 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.426+1633T>C | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 4/5 | chr1 | 74750455 | |||||||
| chr1:74750643 | A | G | 3 | a0001c0001t0003g0025 a0001c0001t0003g0107 a0001c0001t0003g0108 |
5 | HG00099.hp1 HG00733.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.427-1649A>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 4/5 | chr1 | 74750643 | |||||||
| chr1:74750656 | C | T | 54 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0007 others(51): Show |
139 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.427-1636C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 4/5 | chr1 | 74750656 | |||||||
| chr1:74750704 | G | A | 1 | a0001c0001t0005g0118 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.427-1588G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 4/5 | chr1 | 74750704 | |||||||
| chr1:74750765 | C | T | 29 | a0001c0001t0003g0052 a0001c0001t0003g0053 a0001c0001t0003g0151 others(26): Show |
44 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(41): Show |
intron_variant | MODIFIER | c.427-1527C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 4/5 | chr1 | 74750765 | |||||||
| chr1:74750795 | C | T | 4 | a0002c0002t0001g0007 a0002c0002t0001g0033 a0002c0002t0001g0071 others(1): Show |
11 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.427-1497C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 4/5 | chr1 | 74750795 | |||||||
| chr1:74750800 | C | CT | 19 | a0001c0001t0005g0005 a0001c0001t0005g0015 a0001c0001t0005g0044 others(16): Show |
32 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(29): Show |
intron_variant | MODIFIER | c.427-1468dupT | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 74750800 | ||||||
| chr1:74750800 | C | CTT | 9 | a0001c0001t0003g0052 a0001c0001t0003g0053 a0001c0001t0003g0151 others(6): Show |
11 | HG00735.hp2 HG00741.hp2 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.427-1469_427-1468d others(4): Show |
TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 74750800 | ||||||
| chr1:74750800 | CT | C | 91 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0011 others(88): Show |
225 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.427-1468delT | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 74750800 | ||||||
| chr1:74750800 | CTT | C | 13 | a0001c0001t0002g0090 a0001c0001t0002g0099 a0001c0001t0005g0045 others(10): Show |
24 | HG00597.hp2 HG00673.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.427-1469_427-1468d others(4): Show |
TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 74750800 | ||||||
| chr1:74750800 | CTTTTTTT others(4): Show |
C | 10 | a0001c0001t0003g0048 a0001c0001t0003g0049 a0001c0001t0003g0050 others(7): Show |
14 | HG01109.hp2 HG01891.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.427-1478_427-1468d others(13): Show |
TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 74750800 | ||||||
| chr1:74751022 | G | T | 1 | a0001c0001t0014g0055 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.427-1270G>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 4/5 | chr1 | 74751022 | |||||||
| chr1:74751353 | C | T | 1 | a0001c0001t0003g0153 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.427-939C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 4/5 | chr1 | 74751353 | |||||||
| chr1:74751450 | G | A | 35 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0011 others(32): Show |
83 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.427-842G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 4/5 | chr1 | 74751450 | |||||||
| chr1:74751584 | C | T | 1 | a0001c0001t0003g0114 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.427-708C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 4/5 | chr1 | 74751584 | |||||||
| chr1:74751618 | C | T | 1 | a0002c0002t0004g0020 | 3 | HG02896.hp1 HG02897.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.427-674C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 4/5 | chr1 | 74751618 | |||||||
| chr1:74751730 | C | G | 159 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0011 others(156): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.427-562C>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 4/5 | chr1 | 74751730 | |||||||
| chr1:74751736 | A | G | 29 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0011 others(26): Show |
74 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.427-556A>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 4/5 | chr1 | 74751736 | |||||||
| chr1:74751813 | A | C | 11 | a0001c0001t0003g0025 a0001c0001t0003g0043 a0001c0001t0003g0107 others(8): Show |
14 | HG00099.hp1 HG00639.hp1 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.427-479A>C | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 4/5 | chr1 | 74751813 | |||||||
| chr1:74752068 | C | T | 102 | a0001c0001t0003g0052 a0001c0001t0003g0053 a0001c0001t0003g0151 others(99): Show |
217 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.427-224C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 4/5 | chr1 | 74752068 | |||||||
| chr1:74752150 | C | A | 1 | a0001c0001t0003g0056 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.427-142C>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 4/5 | chr1 | 74752150 | |||||||
| chr1:74752611 | C | T | 1 | a0001c0001t0012g0136 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.560+186C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74752611 | |||||||
| chr1:74752715 | A | G | 1 | a0002c0002t0001g0028 | 2 | NA18939.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.560+290A>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74752715 | |||||||
| chr1:74752928 | GC | G | 30 | a0001c0001t0003g0052 a0001c0001t0003g0053 a0001c0001t0003g0151 others(27): Show |
46 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(43): Show |
intron_variant | MODIFIER | c.560+505delC | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr1 | 74752928 | ||||||
| chr1:74753020 | C | T | 102 | a0001c0001t0003g0052 a0001c0001t0003g0053 a0001c0001t0003g0151 others(99): Show |
217 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.560+595C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74753020 | |||||||
| chr1:74753082 | T | C | 1 | a0001c0001t0003g0112 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.560+657T>C | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74753082 | |||||||
| chr1:74753367 | C | A | 2 | a0001c0001t0003g0104 a0001c0001t0003g0105 |
2 | HG02622.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.560+942C>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74753367 | |||||||
| chr1:74753382 | C | G | 30 | a0001c0001t0003g0052 a0001c0001t0003g0053 a0001c0001t0003g0151 others(27): Show |
46 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(43): Show |
intron_variant | MODIFIER | c.560+957C>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74753382 | |||||||
| chr1:74753441 | T | C | 30 | a0001c0001t0003g0052 a0001c0001t0003g0053 a0001c0001t0003g0151 others(27): Show |
46 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(43): Show |
intron_variant | MODIFIER | c.560+1016T>C | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74753441 | |||||||
| chr1:74753462 | A | G | 54 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0007 others(51): Show |
139 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.560+1037A>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74753462 | |||||||
| chr1:74753621 | C | T | 1 | a0001c0001t0014g0055 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.560+1196C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74753621 | |||||||
| chr1:74753740 | G | A | 10 | a0001c0001t0006g0009 a0001c0001t0006g0016 a0001c0001t0006g0137 others(7): Show |
20 | HG00597.hp2 HG02040.hp1 NA18942.hp2 others(17): Show |
intron_variant | MODIFIER | c.560+1315G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74753740 | |||||||
| chr1:74753867 | A | C | 3 | a0001c0001t0002g0024 a0001c0001t0002g0042 a0001c0001t0002g0106 |
6 | HG02258.hp1 HG02572.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.560+1442A>C | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74753867 | |||||||
| chr1:74754124 | T | C | 2 | a0001c0001t0003g0104 a0001c0001t0003g0105 |
2 | HG02622.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.560+1699T>C | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74754124 | |||||||
| chr1:74754354 | C | T | 6 | a0001c0001t0003g0052 a0001c0001t0003g0053 a0001c0001t0003g0151 others(3): Show |
8 | HG01167.hp2 HG01255.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.560+1929C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74754354 | |||||||
| chr1:74754467 | G | A | 1 | a0002c0002t0001g0077 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.560+2042G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74754467 | |||||||
| chr1:74754720 | G | A | 1 | a0001c0001t0016g0113 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.560+2295G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74754720 | |||||||
| chr1:74754790 | G | T | 1 | a0001c0001t0003g0056 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.560+2365G>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74754790 | |||||||
| chr1:74755138 | G | A | 1 | a0001c0001t0005g0128 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.560+2713G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74755138 | |||||||
| chr1:74755245 | A | G | 30 | a0001c0001t0003g0052 a0001c0001t0003g0053 a0001c0001t0003g0151 others(27): Show |
46 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(43): Show |
intron_variant | MODIFIER | c.560+2820A>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74755245 | |||||||
| chr1:74755464 | T | G | 2 | a0001c0001t0003g0104 a0001c0001t0003g0105 |
2 | HG02622.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.560+3039T>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74755464 | |||||||
| chr1:74755466 | G | A | 33 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0011 others(30): Show |
81 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.560+3041G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74755466 | |||||||
| chr1:74755572 | A | G | 1 | a0001c0001t0003g0056 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.560+3147A>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74755572 | |||||||
| chr1:74756017 | A | G | 10 | a0001c0001t0006g0009 a0001c0001t0006g0016 a0001c0001t0006g0137 others(7): Show |
20 | HG00597.hp2 HG02040.hp1 NA18942.hp2 others(17): Show |
intron_variant | MODIFIER | c.560+3592A>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74756017 | |||||||
| chr1:74756139 | G | A | 18 | a0001c0001t0006g0009 a0001c0001t0006g0016 a0001c0001t0006g0137 others(15): Show |
32 | HG00597.hp2 HG01074.hp2 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.560+3714G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74756139 | |||||||
| chr1:74756216 | G | A | 1 | a0001c0001t0016g0113 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.560+3791G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74756216 | |||||||
| chr1:74756316 | A | G | 3 | a0001c0001t0002g0011 a0001c0001t0002g0092 a0001c0001t0002g0093 |
7 | HG01257.hp1 HG01975.hp1 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.560+3891A>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74756316 | |||||||
| chr1:74756324 | A | C | 1 | a0001c0001t0012g0136 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.560+3899A>C | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74756324 | |||||||
| chr1:74756394 | T | C | 1 | a0001c0001t0002g0094 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.560+3969T>C | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74756394 | |||||||
| chr1:74756448 | C | T | 7 | a0001c0005t0013g0145 a0003c0003t0007g0046 a0003c0003t0007g0047 others(4): Show |
11 | HG01074.hp2 HG02486.hp2 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.560+4023C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74756448 | |||||||
| chr1:74756543 | C | T | 1 | a0001c0001t0014g0055 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.560+4118C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74756543 | |||||||
| chr1:74756650 | A | C | 158 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0011 others(155): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.560+4225A>C | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74756650 | |||||||
| chr1:74756715 | T | C | 1 | a0002c0002t0001g0075 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.560+4290T>C | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74756715 | |||||||
| chr1:74756847 | G | A | 1 | a0002c0002t0001g0070 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.560+4422G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74756847 | |||||||
| chr1:74757114 | G | A | 1 | a0001c0001t0014g0055 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.560+4689G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74757114 | |||||||
| chr1:74757380 | G | T | 7 | a0001c0005t0013g0145 a0003c0003t0007g0046 a0003c0003t0007g0047 others(4): Show |
11 | HG01074.hp2 HG02486.hp2 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.560+4955G>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74757380 | |||||||
| chr1:74757650 | A | G | 18 | a0001c0001t0006g0009 a0001c0001t0006g0016 a0001c0001t0006g0137 others(15): Show |
32 | HG00597.hp2 HG01074.hp2 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.560+5225A>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74757650 | |||||||
| chr1:74758169 | C | T | 10 | a0001c0001t0006g0009 a0001c0001t0006g0016 a0001c0001t0006g0137 others(7): Show |
20 | HG00597.hp2 HG02040.hp1 NA18942.hp2 others(17): Show |
intron_variant | MODIFIER | c.561-5725C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74758169 | |||||||
| chr1:74758332 | C | T | 6 | a0001c0001t0003g0052 a0001c0001t0003g0053 a0001c0001t0003g0151 others(3): Show |
8 | HG01167.hp2 HG01255.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.561-5562C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74758332 | |||||||
| chr1:74758408 | A | ATCATTTA others(69): Show |
1 | a0001c0001t0003g0153 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.561-5449_561-5448i others(78): Show |
TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr1 | 74758408 | ||||||
| chr1:74758408 | A | ATCATTTA others(259): Show |
1 | a0001c0001t0002g0101 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.561-5449_561-5448i others(268): Show |
TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr1 | 74758408 | ||||||
| chr1:74758446 | A | ATCATTTA others(31): Show |
25 | a0001c0001t0003g0056 a0001c0001t0005g0005 a0001c0001t0005g0015 others(22): Show |
39 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(36): Show |
intron_variant | MODIFIER | c.561-5220_561-5183d others(40): Show |
TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr1 | 74758446 | ||||||
| chr1:74758446 | A | ATCATTTA others(69): Show |
23 | a0001c0001t0003g0025 a0001c0001t0003g0043 a0001c0001t0003g0048 others(20): Show |
32 | HG00099.hp1 HG00639.hp1 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.561-5258_561-5183d others(78): Show |
TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr1 | 74758446 | ||||||
| chr1:74758446 | A | ATCATTTA others(107): Show |
16 | a0001c0001t0006g0009 a0001c0001t0006g0016 a0001c0001t0006g0137 others(13): Show |
30 | HG00597.hp2 HG02040.hp1 HG02486.hp2 others(27): Show |
intron_variant | MODIFIER | c.561-5296_561-5183d others(116): Show |
TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr1 | 74758446 | ||||||
| chr1:74758446 | A | ATCATTTA others(259): Show |
2 | a0002c0002t0004g0035 a0002c0002t0004g0083 |
3 | NA18984.hp1 NA19009.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.561-5297_561-5296i others(268): Show |
TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr1 | 74758446 | ||||||
| chr1:74758446 | A | ATCATTTA others(183): Show |
2 | a0001c0005t0013g0145 a0002c0002t0004g0082 |
2 | HG01074.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.561-5372_561-5183d others(192): Show |
TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr1 | 74758446 | ||||||
| chr1:74758446 | A | ATCATTTA others(221): Show |
4 | a0001c0001t0003g0104 a0001c0001t0003g0154 a0002c0002t0001g0067 others(1): Show |
4 | HG01255.hp1 HG02622.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.561-5410_561-5183d others(230): Show |
TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr1 | 74758446 | ||||||
| chr1:74758446 | A | ATCATTTA others(259): Show |
76 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0011 others(73): Show |
204 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(201): Show |
intron_variant | MODIFIER | c.561-5183_561-5182i others(268): Show |
TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr1 | 74758446 | ||||||
| chr1:74758446 | A | ATCATTTA others(297): Show |
2 | a0002c0002t0001g0031 a0002c0002t0001g0087 |
3 | HG02523.hp1 NA18962.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.561-5183_561-5182i others(306): Show |
TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr1 | 74758446 | ||||||
| chr1:74758446 | A | ATCATTTA others(335): Show |
2 | a0001c0001t0003g0105 a0002c0002t0004g0020 |
4 | HG02896.hp1 HG02897.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.561-5183_561-5182i others(344): Show |
TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr1 | 74758446 | ||||||
| chr1:74758446 | A | G | 2 | a0001c0001t0002g0101 a0001c0001t0003g0153 |
2 | HG01167.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.561-5448A>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74758446 | |||||||
| chr1:74758559 | C | CGTCATTT others(31): Show |
1 | a0001c0001t0005g0132 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.561-5298_561-5297i others(40): Show |
TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr1 | 74758559 | ||||||
| chr1:74758560 | G | GTCATTTA others(259): Show |
2 | a0001c0001t0002g0038 a0001c0001t0002g0100 |
3 | HG00423.hp2 HG02015.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.561-5183_561-5182i others(268): Show |
TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr1 | 74758560 | ||||||
| chr1:74758674 | G | GTCATTTA others(259): Show |
1 | a0001c0001t0014g0055 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.561-5183_561-5182i others(268): Show |
TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr1 | 74758674 | ||||||
| chr1:74758712 | A | G | 25 | a0001c0005t0013g0145 a0002c0002t0001g0014 a0002c0002t0004g0003 others(22): Show |
52 | HG00140.hp1 HG01074.hp2 HG01167.hp1 others(49): Show |
intron_variant | MODIFIER | c.561-5182A>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74758712 | |||||||
| chr1:74758758 | A | G | 54 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0007 others(51): Show |
139 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.561-5136A>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74758758 | |||||||
| chr1:74758831 | C | T | 1 | a0001c0001t0003g0147 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.561-5063C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74758831 | |||||||
| chr1:74758876 | A | G | 24 | a0001c0001t0005g0005 a0001c0001t0005g0015 a0001c0001t0005g0044 others(21): Show |
38 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(35): Show |
intron_variant | MODIFIER | c.561-5018A>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74758876 | |||||||
| chr1:74758982 | C | A | 1 | a0001c0001t0005g0130 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.561-4912C>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74758982 | |||||||
| chr1:74759003 | G | T | 1 | a0002c0002t0001g0063 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.561-4891G>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74759003 | |||||||
| chr1:74759040 | G | T | 8 | a0001c0001t0003g0048 a0001c0001t0003g0049 a0001c0001t0003g0050 others(5): Show |
12 | HG01109.hp2 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.561-4854G>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74759040 | |||||||
| chr1:74759128 | T | A | 1 | a0002c0002t0004g0079 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.561-4766T>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74759128 | |||||||
| chr1:74759224 | TGAATGA | T | 11 | a0001c0001t0006g0009 a0001c0001t0006g0016 a0001c0001t0006g0137 others(8): Show |
21 | HG00597.hp2 HG01891.hp2 HG02040.hp1 others(18): Show |
intron_variant | MODIFIER | c.561-4661_561-4656d others(8): Show |
TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr1 | 74759224 | ||||||
| chr1:74759360 | C | G | 1 | a0001c0001t0002g0089 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.561-4534C>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74759360 | |||||||
| chr1:74759374 | C | CT | 6 | a0001c0001t0003g0048 a0001c0001t0003g0146 a0001c0001t0005g0121 others(3): Show |
7 | HG01255.hp2 HG01934.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.561-4505dupT | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr1 | 74759374 | ||||||
| chr1:74759374 | C | CTTT | 10 | a0001c0001t0006g0009 a0001c0001t0006g0016 a0001c0001t0006g0137 others(7): Show |
20 | HG00597.hp2 HG02040.hp1 NA18942.hp2 others(17): Show |
intron_variant | MODIFIER | c.561-4507_561-4505d others(5): Show |
TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr1 | 74759374 | ||||||
| chr1:74759379 | T | C | 1 | a0002c0002t0001g0030 | 2 | NA18987.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.561-4515T>C | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74759379 | |||||||
| chr1:74759506 | C | A | 54 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0007 others(51): Show |
139 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.561-4388C>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74759506 | |||||||
| chr1:74759649 | G | T | 1 | a0002c0002t0001g0062 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.561-4245G>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74759649 | |||||||
| chr1:74759735 | C | T | 1 | a0002c0002t0001g0087 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.561-4159C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74759735 | |||||||
| chr1:74759768 | G | A | 6 | a0001c0001t0003g0052 a0001c0001t0003g0053 a0001c0001t0003g0151 others(3): Show |
8 | HG01167.hp2 HG01255.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.561-4126G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74759768 | |||||||
| chr1:74759941 | G | T | 30 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0011 others(27): Show |
75 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.561-3953G>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74759941 | |||||||
| chr1:74760026 | A | G | 6 | a0003c0003t0007g0046 a0003c0003t0007g0047 a0003c0003t0007g0142 others(3): Show |
10 | HG02486.hp2 HG02886.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.561-3868A>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74760026 | |||||||
| chr1:74760254 | AG | A | 3 | a0001c0001t0002g0024 a0001c0001t0002g0042 a0001c0001t0002g0106 |
6 | HG02258.hp1 HG02572.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.561-3638delG | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr1 | 74760254 | ||||||
| chr1:74760403 | G | T | 1 | a0001c0001t0003g0043 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.561-3491G>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74760403 | |||||||
| chr1:74760541 | A | G | 10 | a0001c0001t0006g0009 a0001c0001t0006g0016 a0001c0001t0006g0137 others(7): Show |
20 | HG00597.hp2 HG02040.hp1 NA18942.hp2 others(17): Show |
intron_variant | MODIFIER | c.561-3353A>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74760541 | |||||||
| chr1:74760568 | A | G | 107 | a0001c0001t0002g0092 a0001c0001t0003g0048 a0001c0001t0003g0049 others(104): Show |
224 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.561-3326A>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74760568 | |||||||
| chr1:74760772 | T | A | 1 | a0001c0001t0003g0104 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.561-3122T>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74760772 | |||||||
| chr1:74760979 | G | A | 1 | a0001c0001t0003g0148 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.561-2915G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74760979 | |||||||
| chr1:74761059 | C | T | 10 | a0001c0001t0003g0025 a0001c0001t0003g0043 a0001c0001t0003g0107 others(7): Show |
13 | HG00099.hp1 HG00639.hp1 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.561-2835C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74761059 | |||||||
| chr1:74761063 | CT | C | 27 | a0001c0001t0003g0048 a0001c0001t0003g0146 a0001c0001t0005g0005 others(24): Show |
42 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(39): Show |
intron_variant | MODIFIER | c.561-2817delT | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr1 | 74761063 | ||||||
| chr1:74761136 | A | G | 10 | a0001c0001t0006g0009 a0001c0001t0006g0016 a0001c0001t0006g0137 others(7): Show |
20 | HG00597.hp2 HG02040.hp1 NA18942.hp2 others(17): Show |
intron_variant | MODIFIER | c.561-2758A>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74761136 | |||||||
| chr1:74761187 | C | T | 158 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0011 others(155): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.561-2707C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74761187 | |||||||
| chr1:74761345 | T | C | 1 | a0001c0001t0003g0146 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.561-2549T>C | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74761345 | |||||||
| chr1:74761429 | C | T | 10 | a0001c0001t0006g0009 a0001c0001t0006g0016 a0001c0001t0006g0137 others(7): Show |
20 | HG00597.hp2 HG02040.hp1 NA18942.hp2 others(17): Show |
intron_variant | MODIFIER | c.561-2465C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74761429 | |||||||
| chr1:74761573 | G | A | 1 | a0001c0001t0003g0153 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.561-2321G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74761573 | |||||||
| chr1:74761634 | C | T | 1 | a0001c0001t0003g0114 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.561-2260C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74761634 | |||||||
| chr1:74761754 | A | T | 3 | a0001c0001t0006g0009 a0001c0001t0008g0009 a0001c0001t0008g0017 |
10 | NA18942.hp2 NA18946.hp2 NA18959.hp2 others(7): Show |
intron_variant | MODIFIER | c.561-2140A>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74761754 | |||||||
| chr1:74761921 | G | A | 1 | a0001c0001t0012g0136 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.561-1973G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74761921 | |||||||
| chr1:74761950 | C | T | 10 | a0001c0001t0006g0009 a0001c0001t0006g0016 a0001c0001t0006g0137 others(7): Show |
20 | HG00597.hp2 HG02040.hp1 NA18942.hp2 others(17): Show |
intron_variant | MODIFIER | c.561-1944C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74761950 | |||||||
| chr1:74761959 | G | A | 10 | a0001c0001t0003g0025 a0001c0001t0003g0043 a0001c0001t0003g0107 others(7): Show |
13 | HG00099.hp1 HG00639.hp1 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.561-1935G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74761959 | |||||||
| chr1:74762001 | G | A | 1 | a0001c0001t0012g0136 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.561-1893G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74762001 | |||||||
| chr1:74762038 | T | G | 3 | a0001c0001t0003g0025 a0001c0001t0003g0107 a0001c0001t0003g0108 |
5 | HG00099.hp1 HG00733.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.561-1856T>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74762038 | |||||||
| chr1:74762100 | G | A | 2 | a0001c0001t0006g0137 a0001c0001t0006g0150 |
2 | NA19010.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.561-1794G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74762100 | |||||||
| chr1:74762234 | T | G | 10 | a0001c0001t0006g0009 a0001c0001t0006g0016 a0001c0001t0006g0137 others(7): Show |
20 | HG00597.hp2 HG02040.hp1 NA18942.hp2 others(17): Show |
intron_variant | MODIFIER | c.561-1660T>G | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74762234 | |||||||
| chr1:74762253 | G | T | 158 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0011 others(155): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.561-1641G>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74762253 | |||||||
| chr1:74762514 | T | A | 7 | a0001c0005t0013g0145 a0003c0003t0007g0046 a0003c0003t0007g0047 others(4): Show |
11 | HG01074.hp2 HG02486.hp2 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.561-1380T>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74762514 | |||||||
| chr1:74762609 | C | T | 10 | a0001c0001t0006g0009 a0001c0001t0006g0016 a0001c0001t0006g0137 others(7): Show |
20 | HG00597.hp2 HG02040.hp1 NA18942.hp2 others(17): Show |
intron_variant | MODIFIER | c.561-1285C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74762609 | |||||||
| chr1:74763056 | C | T | 1 | a0001c0001t0003g0105 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.561-838C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74763056 | |||||||
| chr1:74763059 | TATC | T | 10 | a0001c0001t0006g0009 a0001c0001t0006g0016 a0001c0001t0006g0137 others(7): Show |
20 | HG00597.hp2 HG02040.hp1 NA18942.hp2 others(17): Show |
intron_variant | MODIFIER | c.561-832_561-830del others(3): Show |
TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr1 | 74763059 | ||||||
| chr1:74763106 | T | A | 1 | a0001c0001t0002g0095 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.561-788T>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74763106 | |||||||
| chr1:74763139 | CAGCTATT others(3): Show |
C | 2 | a0001c0001t0002g0041 a0001c0001t0002g0091 |
3 | HG00642.hp2 HG01516.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.561-751_561-742del others(10): Show |
TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr1 | 74763139 | ||||||
| chr1:74763153 | G | A | 1 | a0001c0001t0003g0149 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.561-741G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74763153 | |||||||
| chr1:74763175 | T | TG | 10 | a0001c0001t0006g0009 a0001c0001t0006g0016 a0001c0001t0006g0137 others(7): Show |
20 | HG00597.hp2 HG02040.hp1 NA18942.hp2 others(17): Show |
intron_variant | MODIFIER | c.561-718dupG | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr1 | 74763175 | ||||||
| chr1:74763242 | T | C | 1 | a0001c0001t0003g0109 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.561-652T>C | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74763242 | |||||||
| chr1:74763449 | G | A | 54 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0007 others(51): Show |
139 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.561-445G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74763449 | |||||||
| chr1:74763659 | G | A | 1 | a0001c0001t0014g0055 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.561-235G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74763659 | |||||||
| chr1:74763712 | G | A | 54 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0007 others(51): Show |
139 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.561-182G>A | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74763712 | |||||||
| chr1:74763756 | C | T | 1 | a0002c0002t0009g0032 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.561-138C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74763756 | |||||||
| chr1:74763760 | T | C | 1 | a0001c0001t0003g0056 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.561-134T>C | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74763760 | |||||||
| chr1:74763787 | C | T | 1 | a0001c0001t0005g0117 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.561-107C>T | TYW3 | ENSG00000162623.16 | transcript | ENST00000370867.8 | protein_coding | 5/5 | chr1 | 74763787 |