Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1491 |
| ensemblid | ENSG00000116761.12 |
| hgncid | 2501 |
| symbol | CTH |
| name | cystathionine gamma-lyase |
| refseq_nuc | NM_001902.6 |
| refseq_prot | NP_001893.2 |
| ensembl_nuc | ENST00000370938.8 |
| ensembl_prot | ENSP00000359976.3 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 70411268 |
| end | 70439851 |
| strand | + |
| ver | v1.2 |
| region | chr1:70411268-70439851 |
| region5000 | chr1:70406268-70444851 |
| regionname0 | CTH_chr1_70411268_70439851 |
| regionname5000 | CTH_chr1_70406268_70444851 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 405 | 333 | 85 | 46 | 159 | 14 | 28 | 126 | CTH_chr1_70406268_70444851 | CTH | MQEKD others(400): Show |
chr1 | 70406268 | 70444851 |
| a0002 | 0/1 | 405 | 89 | 7 | 28 | 43 | 4 | 6 | 34 | CTH_chr1_70406268_70444851 | CTH | MQEKD others(400): Show |
chr1 | 70406268 | 70444851 |
| a0003 | 0/0 | 405 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | MQEKD others(400): Show |
chr1 | 70406268 | 70444851 |
| a0004 | 0/0 | 405 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | MQEKD others(400): Show |
chr1 | 70406268 | 70444851 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1215 | 328 | 82 | 46 | 158 | 14 | 27 | CTH_chr1_70406268_70444851 | CTH | ATGCA others(1210): Show |
chr1 | 70406268 | 70444851 | ||
| a0001c0003 | 0/0 | 1215 | 3 | 3 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | ATGCA others(1210): Show |
chr1 | 70406268 | 70444851 | ||
| a0001c0004 | 0/0 | 1215 | 1 | 0 | 0 | 0 | 0 | 1 | CTH_chr1_70406268_70444851 | CTH | ATGCA others(1210): Show |
chr1 | 70406268 | 70444851 | ||
| a0001c0005 | 0/0 | 1215 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | ATGCA others(1210): Show |
chr1 | 70406268 | 70444851 | ||
| a0002c0002 | 0/1 | 1215 | 89 | 7 | 28 | 43 | 4 | 6 | CTH_chr1_70406268_70444851 | CTH | ATGCA others(1210): Show |
chr1 | 70406268 | 70444851 | ||
| a0003c0007 | 0/0 | 1215 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | ATGCA others(1210): Show |
chr1 | 70406268 | 70444851 | ||
| a0004c0006 | 0/0 | 1215 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | ATGCA others(1210): Show |
chr1 | 70406268 | 70444851 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2090 | 286 | 62 | 39 | 147 | 12 | 25 | CTH_chr1_70406268_70444851 | CTH | GCCGC others(2085): Show |
chr1 | 70406268 | 70444851 |
| a0001c0001t0002 | 0/0 | 2090 | 3 | 0 | 1 | 0 | 2 | 0 | CTH_chr1_70406268_70444851 | CTH | GCCGC others(2085): Show |
chr1 | 70406268 | 70444851 |
| a0001c0001t0003 | 0/0 | 2090 | 21 | 4 | 5 | 11 | 0 | 1 | CTH_chr1_70406268_70444851 | CTH | GCCGC others(2085): Show |
chr1 | 70406268 | 70444851 |
| a0001c0001t0004 | 0/0 | 2090 | 9 | 8 | 1 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | GCCGC others(2085): Show |
chr1 | 70406268 | 70444851 |
| a0001c0001t0005 | 0/0 | 2090 | 6 | 6 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | GCCGC others(2085): Show |
chr1 | 70406268 | 70444851 |
| a0001c0001t0006 | 0/0 | 2090 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | GCCGC others(2085): Show |
chr1 | 70406268 | 70444851 |
| a0001c0001t0007 | 0/0 | 2090 | 1 | 0 | 0 | 0 | 0 | 1 | CTH_chr1_70406268_70444851 | CTH | GCCGC others(2085): Show |
chr1 | 70406268 | 70444851 |
| a0001c0001t0009 | 0/0 | 2090 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | GCCGC others(2085): Show |
chr1 | 70406268 | 70444851 |
| a0001c0003t0001 | 0/0 | 2090 | 3 | 3 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | GCCGC others(2085): Show |
chr1 | 70406268 | 70444851 |
| a0001c0004t0001 | 0/0 | 2090 | 1 | 0 | 0 | 0 | 0 | 1 | CTH_chr1_70406268_70444851 | CTH | GCCGC others(2085): Show |
chr1 | 70406268 | 70444851 |
| a0001c0005t0001 | 0/0 | 2090 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | GCCGC others(2085): Show |
chr1 | 70406268 | 70444851 |
| a0002c0002t0001 | 0/0 | 2090 | 8 | 5 | 0 | 3 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | GCCGC others(2085): Show |
chr1 | 70406268 | 70444851 |
| a0002c0002t0002 | 0/1 | 2090 | 80 | 2 | 28 | 40 | 4 | 5 | CTH_chr1_70406268_70444851 | CTH | GCCGC others(2085): Show |
chr1 | 70406268 | 70444851 |
| a0002c0002t0008 | 0/0 | 2090 | 1 | 0 | 0 | 0 | 0 | 1 | CTH_chr1_70406268_70444851 | CTH | GCCGC others(2085): Show |
chr1 | 70406268 | 70444851 |
| a0003c0007t0001 | 0/0 | 2090 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | GCCGC others(2085): Show |
chr1 | 70406268 | 70444851 |
| a0004c0006t0001 | 0/0 | 2090 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | GCCGC others(2085): Show |
chr1 | 70406268 | 70444851 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 18 | 0 | 1 | 17 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0002 | 0/0 | 13 | 0 | 0 | 13 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0003 | 0/0 | 12 | 2 | 1 | 2 | 2 | 5 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0005 | 0/0 | 8 | 0 | 0 | 6 | 0 | 2 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0007 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0009 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0010 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0012 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0013 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0032 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0252 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0003g0006 | 0/0 | 7 | 0 | 4 | 3 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0004g0048 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0004g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0004g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0004g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0004g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0004g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0004g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0005g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0005g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0005g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0005g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0005g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0005g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0006g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0007g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0001t0009g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0003t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0003t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0003t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0004t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0001c0005t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0002g0004 | 0/0 | 11 | 0 | 6 | 5 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0002g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0002g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0002g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0002g0023 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0002g0024 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0002g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0002g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0002g0216 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0002c0002t0008g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0003c0007t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| a0004c0006t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0002 | g0023 | EUR | GBR | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0020 | EUR | GBR | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0123 | EUR | GBR | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG00140 | hp2 | a0002 | c0002 | t0002 | g0153 | EUR | GBR | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0114 | EUR | FIN | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG00323 | hp1 | a0002 | c0002 | t0002 | g0023 | EUR | FIN | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0022 | EUR | FIN | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG00408 | hp1 | a0002 | c0002 | t0002 | g0159 | EAS | CHS | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | CHS | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | CHS | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | CHS | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | CHS | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG00558 | hp1 | a0002 | c0002 | t0002 | g0145 | EAS | CHS | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | CHS | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG00642 | hp2 | a0002 | c0002 | t0002 | g0023 | AMR | PUR | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | CHS | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG00733 | hp2 | a0002 | c0002 | t0002 | g0148 | AMR | PUR | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG00738 | hp2 | a0002 | c0002 | t0002 | g0217 | AMR | PUR | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01069 | hp2 | a0002 | c0002 | t0002 | g0034 | AMR | PUR | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01070 | hp1 | a0002 | c0002 | t0002 | g0064 | AMR | PUR | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01071 | hp1 | a0002 | c0002 | t0002 | g0034 | AMR | PUR | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01071 | hp2 | a0002 | c0002 | t0002 | g0017 | AMR | PUR | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01081 | hp1 | a0002 | c0002 | t0002 | g0196 | AMR | PUR | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01081 | hp2 | a0002 | c0002 | t0002 | g0004 | AMR | PUR | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01106 | hp1 | a0002 | c0002 | t0002 | g0152 | AMR | PUR | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0186 | AMR | PUR | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01175 | hp2 | a0002 | c0002 | t0002 | g0006 | AMR | PUR | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | CLM | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01256 | hp2 | a0002 | c0002 | t0002 | g0157 | AMR | CLM | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01257 | hp2 | a0002 | c0002 | t0002 | g0166 | AMR | CLM | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01258 | hp2 | a0002 | c0002 | t0002 | g0110 | AMR | CLM | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01261 | hp1 | a0002 | c0002 | t0002 | g0004 | AMR | CLM | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | CLM | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | CLM | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01496 | hp1 | a0002 | c0002 | t0002 | g0147 | AMR | CLM | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01496 | hp2 | a0002 | c0002 | t0002 | g0006 | AMR | CLM | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0251 | EUR | IBS | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0020 | EUR | IBS | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0195 | EUR | IBS | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0103 | EUR | IBS | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | IBS | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0209 | EUR | IBS | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | ACB | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01891 | hp1 | a0001 | c0003 | t0001 | g0013 | AFR | ACB | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | ACB | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01928 | hp2 | a0002 | c0002 | t0002 | g0105 | AMR | PEL | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01934 | hp2 | a0001 | c0001 | t0004 | g0048 | AMR | PEL | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01952 | hp1 | a0002 | c0002 | t0002 | g0033 | AMR | PEL | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01952 | hp2 | a0002 | c0002 | t0002 | g0004 | AMR | PEL | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01978 | hp1 | a0002 | c0002 | t0002 | g0160 | AMR | PEL | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01978 | hp2 | a0002 | c0002 | t0002 | g0004 | AMR | PEL | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01981 | hp1 | a0002 | c0002 | t0002 | g0151 | AMR | PEL | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01993 | hp1 | a0002 | c0002 | t0002 | g0033 | AMR | PEL | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PEL | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0090 | AMR | PEL | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02027 | hp2 | a0002 | c0002 | t0002 | g0035 | EAS | KHV | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02040 | hp2 | a0002 | c0002 | t0002 | g0111 | EAS | KHV | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02074 | hp1 | a0002 | c0002 | t0002 | g0263 | EAS | KHV | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02074 | hp2 | a0002 | c0002 | t0002 | g0031 | EAS | KHV | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02083 | hp1 | a0002 | c0002 | t0002 | g0237 | EAS | KHV | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02083 | hp2 | a0002 | c0002 | t0002 | g0036 | EAS | KHV | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0178 | EAS | KHV | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | KHV | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | ACB | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02145 | hp2 | a0001 | c0001 | t0006 | g0174 | AFR | ACB | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | CDX | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CDX | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02165 | hp2 | a0002 | c0002 | t0002 | g0262 | EAS | CDX | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | ACB | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02258 | hp2 | a0003 | c0007 | t0001 | g0202 | AFR | ACB | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0049 | AFR | ACB | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02280 | hp2 | a0002 | c0002 | t0002 | g0089 | AFR | ACB | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02293 | hp2 | a0002 | c0002 | t0002 | g0004 | AMR | PEL | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | PEL | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02300 | hp2 | a0002 | c0002 | t0002 | g0173 | AMR | PEL | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | ACB | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02622 | hp1 | a0001 | c0001 | t0005 | g0264 | AFR | GWD | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0182 | AFR | GWD | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | GWD | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0272 | AFR | GWD | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0048 | AFR | GWD | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0266 | AFR | GWD | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0270 | AFR | GWD | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0185 | SAS | PJL | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | GWD | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02818 | hp2 | a0001 | c0003 | t0001 | g0132 | AFR | GWD | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0176 | AFR | GWD | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02895 | hp2 | a0001 | c0001 | t0005 | g0267 | AFR | GWD | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | ESN | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0188 | AFR | ESN | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | ESN | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ESN | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02976 | hp2 | a0004 | c0006 | t0001 | g0039 | AFR | ESN | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | MSL | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG03098 | hp2 | a0002 | c0002 | t0001 | g0230 | AFR | MSL | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ESN | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ESN | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0049 | AFR | ESN | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG03195 | hp2 | a0001 | c0003 | t0001 | g0131 | AFR | ESN | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | MSL | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG03209 | hp2 | a0001 | c0001 | t0005 | g0121 | AFR | MSL | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | MSL | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG03239 | hp2 | a0001 | c0001 | t0007 | g0005 | SAS | PJL | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | MSL | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG03490 | hp2 | a0002 | c0002 | t0002 | g0109 | SAS | PJL | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG03491 | hp1 | a0002 | c0002 | t0002 | g0024 | SAS | PJL | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG03492 | hp1 | a0002 | c0002 | t0002 | g0024 | SAS | PJL | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | ESN | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | GWD | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | MSL | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG03579 | hp2 | a0002 | c0002 | t0001 | g0177 | AFR | MSL | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG03654 | hp1 | a0002 | c0002 | t0002 | g0108 | SAS | PJL | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | BEB | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG03831 | hp2 | a0002 | c0002 | t0008 | g0163 | SAS | BEB | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG03834 | hp1 | a0001 | c0004 | t0001 | g0077 | SAS | BEB | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG03927 | hp1 | a0002 | c0002 | t0002 | g0024 | SAS | BEB | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | BEB | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | BEB | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | STU | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | STU | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | BEB | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | BEB | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | STU | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | STU | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | YRI | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHB | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0269 | AFR | YRI | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18941 | hp2 | a0002 | c0002 | t0002 | g0138 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18944 | hp2 | a0002 | c0002 | t0002 | g0035 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18947 | hp1 | a0002 | c0002 | t0002 | g0135 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18950 | hp1 | a0002 | c0002 | t0002 | g0154 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18951 | hp2 | a0002 | c0002 | t0002 | g0149 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18954 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18957 | hp1 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18959 | hp1 | a0002 | c0002 | t0002 | g0146 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18965 | hp2 | a0002 | c0002 | t0002 | g0014 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18968 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18970 | hp2 | a0002 | c0002 | t0002 | g0014 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18971 | hp2 | a0002 | c0002 | t0002 | g0134 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18972 | hp1 | a0002 | c0002 | t0002 | g0169 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18974 | hp1 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18978 | hp1 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18982 | hp1 | a0002 | c0002 | t0002 | g0156 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18987 | hp1 | a0002 | c0002 | t0002 | g0118 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18990 | hp1 | a0002 | c0002 | t0002 | g0150 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18991 | hp1 | a0002 | c0002 | t0002 | g0162 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18992 | hp1 | a0001 | c0005 | t0001 | g0001 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18994 | hp2 | a0002 | c0002 | t0002 | g0014 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18997 | hp1 | a0001 | c0001 | t0003 | g0223 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19001 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0180 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19007 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19007 | hp2 | a0002 | c0002 | t0002 | g0155 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19009 | hp2 | a0002 | c0002 | t0002 | g0031 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0192 | AFR | LWK | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | LWK | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19043 | hp1 | a0002 | c0002 | t0001 | g0175 | AFR | LWK | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | LWK | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19055 | hp1 | a0002 | c0002 | t0002 | g0142 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19058 | hp1 | a0002 | c0002 | t0002 | g0158 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0225 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19077 | hp1 | a0002 | c0002 | t0002 | g0161 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19078 | hp1 | a0002 | c0002 | t0002 | g0036 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19079 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19080 | hp1 | a0002 | c0002 | t0001 | g0141 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19081 | hp2 | a0002 | c0002 | t0002 | g0014 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19084 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19086 | hp1 | a0002 | c0002 | t0002 | g0170 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19087 | hp2 | a0002 | c0002 | t0002 | g0167 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0224 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0265 | AFR | YRI | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0007 | AFR | YRI | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ASW | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ASW | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0116 | EUR | TSI | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA20805 | hp1 | a0002 | c0002 | t0002 | g0220 | EUR | TSI | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0112 | EUR | TSI | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | GIH | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | GIH | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01123 | hp1 | a0002 | c0002 | t0002 | g0004 | AMR | CLM | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG01123 | hp2 | a0002 | c0002 | t0002 | g0133 | AMR | CLM | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02109 | hp2 | a0002 | c0002 | t0002 | g0168 | AFR | ACB | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0189 | AFR | ACB | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0268 | AFR | ACB | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | ACB | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG02559 | hp2 | a0002 | c0002 | t0001 | g0231 | AFR | ACB | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0271 | AFR | USA | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | USA | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA20300 | hp1 | a0001 | c0001 | t0009 | g0124 | AFR | USA | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | USA | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | LWK | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | LWK | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0002 | g0216 | REF | REF | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0252 | REF | REF | CTH_chr1_70406268_70444851 | CTH | chr1 | 70406268 | 70444851 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:70411557 | A | G | 1 | a0003 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.142A>G | p.Lys48Glu | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 1/12 | 290/2090 | 142/1218 | 48/405 | chr1 | 70411557 | |||
| chr1:70421629 | G | T | 1 | a0004 | 1 | HG02976.hp2 | missense_variant | MODERATE | c.410G>T | p.Cys137Phe | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 4/12 | 558/2090 | 410/1218 | 137/405 | chr1 | 70421629 | |||
| chr1:70439117 | G | T | 1 | a0002 | 88 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(85): Show |
missense_variant | MODERATE | c.1208G>T | p.Ser403Ile | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 12/12 | 1356/2090 | 1208/1218 | 403/405 | chr1 | 70439117 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:70411544 | G | A | 1 | a0001c0003 | 3 | HG01891.hp1 HG02818.hp2 HG03195.hp2 |
synonymous_variant | LOW | c.129G>A | p.Leu43Leu | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 1/12 | 277/2090 | 129/1218 | 43/405 | chr1 | 70411544 | |||
| chr1:70424383 | C | G | 1 | a0001c0005 | 1 | NA18992.hp1 | synonymous_variant | LOW | c.555C>G | p.Val185Val | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 5/12 | 703/2090 | 555/1218 | 185/405 | chr1 | 70424383 | |||
| chr1:70438796 | G | A | 1 | a0001c0004 | 1 | HG03834.hp1 | synonymous_variant | LOW | c.1161G>A | p.Leu387Leu | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 11/12 | 1309/2090 | 1161/1218 | 387/405 | chr1 | 70438796 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:70411276 | A | T | 2 | a0001c0001t0004 a0001c0001t0005 |
15 | HG01934.hp2 HG02280.hp1 HG02486.hp2 others(12): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-140A>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 1/12 | chr1 | 70411276 | |||||||
| chr1:70439171 | A | G | 1 | a0001c0001t0009 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*44A>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 12/12 | 44 | chr1 | 70439171 | ||||||
| chr1:70439344 | G | T | 1 | a0002c0002t0008 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*217G>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 12/12 | 217 | chr1 | 70439344 | ||||||
| chr1:70439516 | T | C | 2 | a0001c0001t0004 a0001c0001t0006 |
10 | HG01934.hp2 HG02145.hp2 HG02280.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*389T>C | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 12/12 | 389 | chr1 | 70439516 | ||||||
| chr1:70439650 | A | T | 5 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0009 others(2): Show |
67 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*523A>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 12/12 | 523 | chr1 | 70439650 | ||||||
| chr1:70439651 | A | T | 1 | a0001c0001t0007 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*524A>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 12/12 | 524 | chr1 | 70439651 | ||||||
| chr1:70439671 | G | A | 1 | a0001c0001t0003 | 21 | HG01074.hp1 HG01168.hp1 HG01192.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*544G>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 12/12 | 544 | chr1 | 70439671 | ||||||
| chr1:70439719 | C | T | 3 | a0001c0001t0002 a0002c0002t0002 a0002c0002t0008 |
83 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*592C>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 12/12 | 592 | chr1 | 70439719 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:70411654 | C | A | 1 | a0001c0001t0001g0050 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.168+71C>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 1/11 | chr1 | 70411654 | |||||||
| chr1:70411778 | A | G | 2 | a0001c0001t0001g0273 a0001c0001t0001g0274 |
2 | HG02818.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.168+195A>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 1/11 | chr1 | 70411778 | |||||||
| chr1:70411804 | C | G | 11 | a0001c0001t0004g0048 a0001c0001t0004g0049 a0001c0001t0004g0268 others(8): Show |
13 | HG01934.hp2 HG02280.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.168+221C>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 1/11 | chr1 | 70411804 | |||||||
| chr1:70411812 | T | A | 249 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(246): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.168+229T>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 1/11 | chr1 | 70411812 | |||||||
| chr1:70411993 | A | G | 1 | a0002c0002t0002g0237 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.168+410A>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 1/11 | chr1 | 70411993 | |||||||
| chr1:70412060 | T | C | 58 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(55): Show |
92 | HG00558.hp2 HG00597.hp1 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.168+477T>C | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 1/11 | chr1 | 70412060 | |||||||
| chr1:70412096 | G | A | 107 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(104): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.168+513G>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 1/11 | chr1 | 70412096 | |||||||
| chr1:70412114 | A | G | 1 | a0002c0002t0002g0173 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.168+531A>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 1/11 | chr1 | 70412114 | |||||||
| chr1:70412209 | A | G | 2 | a0001c0001t0001g0171 a0001c0001t0001g0172 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.168+626A>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 1/11 | chr1 | 70412209 | |||||||
| chr1:70412281 | G | A | 15 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0029 others(12): Show |
25 | HG00609.hp1 HG01516.hp2 HG01928.hp2 others(22): Show |
intron_variant | MODIFIER | c.168+698G>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 1/11 | chr1 | 70412281 | |||||||
| chr1:70412426 | T | G | 1 | a0001c0001t0006g0174 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.168+843T>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 1/11 | chr1 | 70412426 | |||||||
| chr1:70412544 | G | A | 1 | a0001c0001t0001g0051 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.168+961G>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 1/11 | chr1 | 70412544 | |||||||
| chr1:70412961 | G | A | 4 | a0001c0001t0001g0019 a0001c0001t0001g0029 a0001c0001t0001g0097 others(1): Show |
7 | NA18949.hp1 NA18955.hp1 NA18961.hp1 others(4): Show |
intron_variant | MODIFIER | c.168+1378G>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 1/11 | chr1 | 70412961 | |||||||
| chr1:70413169 | C | G | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(243): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.168+1586C>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 1/11 | chr1 | 70413169 | |||||||
| chr1:70413229 | A | G | 58 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(55): Show |
92 | HG00558.hp2 HG00597.hp1 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.168+1646A>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 1/11 | chr1 | 70413229 | |||||||
| chr1:70413229 | A | T | 1 | a0001c0001t0001g0236 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.168+1646A>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 1/11 | chr1 | 70413229 | |||||||
| chr1:70413259 | C | CT | 6 | a0001c0001t0001g0096 a0001c0001t0001g0232 a0001c0001t0001g0233 others(3): Show |
6 | HG01167.hp1 HG02559.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.168+1692dupT | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 70413259 | ||||||
| chr1:70413259 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.168+1676C>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 1/11 | chr1 | 70413259 | |||||||
| chr1:70413259 | CT | C | 17 | a0001c0001t0001g0052 a0001c0001t0001g0171 a0001c0001t0001g0183 others(14): Show |
24 | HG01074.hp1 HG01168.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.168+1692delT | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 70413259 | ||||||
| chr1:70413265 | T | C | 1 | a0001c0001t0001g0238 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.168+1682T>C | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 1/11 | chr1 | 70413265 | |||||||
| chr1:70413276 | A | T | 9 | a0001c0001t0001g0234 a0001c0001t0004g0048 a0001c0001t0004g0049 others(6): Show |
11 | HG01934.hp2 HG02145.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.168+1693A>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 1/11 | chr1 | 70413276 | |||||||
| chr1:70413455 | G | A | 2 | a0001c0001t0001g0013 a0001c0003t0001g0013 |
4 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.168+1872G>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 1/11 | chr1 | 70413455 | |||||||
| chr1:70413473 | C | T | 48 | a0001c0001t0001g0022 a0001c0001t0001g0037 a0001c0001t0001g0095 others(45): Show |
69 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.168+1890C>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 1/11 | chr1 | 70413473 | |||||||
| chr1:70413541 | G | C | 1 | a0001c0001t0001g0050 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.168+1958G>C | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 1/11 | chr1 | 70413541 | |||||||
| chr1:70413560 | G | T | 9 | a0001c0001t0001g0229 a0001c0001t0004g0048 a0001c0001t0004g0049 others(6): Show |
11 | HG01934.hp2 HG02145.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.168+1977G>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 1/11 | chr1 | 70413560 | |||||||
| chr1:70413739 | C | CT | 81 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(78): Show |
119 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.168+2176dupT | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 70413739 | ||||||
| chr1:70413739 | C | CTT | 47 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0038 others(44): Show |
68 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.168+2175_168+2176d others(4): Show |
CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 70413739 | ||||||
| chr1:70413739 | C | CTTT | 5 | a0001c0001t0001g0044 a0001c0001t0001g0094 a0001c0001t0001g0226 others(2): Show |
6 | HG01192.hp1 HG03491.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.168+2174_168+2176d others(5): Show |
CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 70413739 | ||||||
| chr1:70413739 | CT | C | 20 | a0001c0001t0001g0025 a0001c0001t0001g0045 a0001c0001t0001g0095 others(17): Show |
23 | HG00280.hp1 HG00735.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.168+2176delT | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 70413739 | ||||||
| chr1:70413769 | T | C | 1 | a0001c0001t0001g0245 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.168+2186T>C | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 1/11 | chr1 | 70413769 | |||||||
| chr1:70413822 | T | G | 12 | a0001c0001t0003g0006 a0001c0001t0003g0178 a0001c0001t0003g0179 others(9): Show |
19 | HG01074.hp1 HG01168.hp1 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.169-2134T>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 1/11 | chr1 | 70413822 | |||||||
| chr1:70413892 | C | T | 60 | a0001c0001t0001g0008 a0001c0001t0001g0095 a0001c0001t0001g0139 others(57): Show |
86 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.169-2064C>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 1/11 | chr1 | 70413892 | |||||||
| chr1:70414191 | G | T | 11 | a0001c0001t0001g0032 a0001c0001t0001g0198 a0001c0001t0001g0199 others(8): Show |
12 | HG00639.hp2 HG00738.hp1 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.169-1765G>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 1/11 | chr1 | 70414191 | |||||||
| chr1:70414422 | G | C | 1 | a0001c0001t0001g0201 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.169-1534G>C | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 1/11 | chr1 | 70414422 | |||||||
| chr1:70414554 | A | G | 4 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0002c0002t0001g0008 others(1): Show |
8 | HG02135.hp2 NA18954.hp2 NA18962.hp1 others(5): Show |
intron_variant | MODIFIER | c.169-1402A>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 1/11 | chr1 | 70414554 | |||||||
| chr1:70414728 | G | C | 1 | a0001c0001t0001g0055 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.169-1228G>C | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 1/11 | chr1 | 70414728 | |||||||
| chr1:70414823 | A | AT | 72 | a0001c0001t0001g0008 a0001c0001t0001g0095 a0001c0001t0001g0139 others(69): Show |
105 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.169-1122dupT | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 70414823 | ||||||
| chr1:70414834 | T | C | 4 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0203 others(1): Show |
4 | HG02258.hp2 HG02559.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-1122T>C | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 1/11 | chr1 | 70414834 | |||||||
| chr1:70414906 | G | T | 1 | a0001c0001t0001g0088 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.169-1050G>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 1/11 | chr1 | 70414906 | |||||||
| chr1:70414930 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.169-1026C>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 1/11 | chr1 | 70414930 | |||||||
| chr1:70415034 | T | C | 157 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(154): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.169-922T>C | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 1/11 | chr1 | 70415034 | |||||||
| chr1:70415035 | T | C | 9 | a0001c0001t0001g0227 a0001c0001t0004g0048 a0001c0001t0004g0049 others(6): Show |
11 | HG01192.hp1 HG01934.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.169-921T>C | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 1/11 | chr1 | 70415035 | |||||||
| chr1:70415049 | T | G | 1 | a0001c0001t0001g0136 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.169-907T>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 1/11 | chr1 | 70415049 | |||||||
| chr1:70415109 | G | A | 1 | a0001c0001t0003g0178 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.169-847G>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 1/11 | chr1 | 70415109 | |||||||
| chr1:70415188 | G | A | 4 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(1): Show |
4 | HG00280.hp1 HG00735.hp1 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-768G>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 1/11 | chr1 | 70415188 | |||||||
| chr1:70415310 | C | T | 3 | a0001c0001t0001g0261 a0002c0002t0002g0262 a0002c0002t0002g0263 |
3 | HG02074.hp1 HG02165.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.169-646C>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 1/11 | chr1 | 70415310 | |||||||
| chr1:70415404 | T | TA | 11 | a0001c0001t0001g0190 a0001c0001t0001g0227 a0001c0001t0001g0273 others(8): Show |
13 | HG01192.hp1 HG01934.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.169-541dupA | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 70415404 | ||||||
| chr1:70415464 | A | G | 53 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0016 others(50): Show |
83 | HG00558.hp2 HG00597.hp1 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.169-492A>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 1/11 | chr1 | 70415464 | |||||||
| chr1:70415496 | C | T | 1 | a0001c0001t0001g0087 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.169-460C>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 1/11 | chr1 | 70415496 | |||||||
| chr1:70415547 | A | T | 8 | a0001c0001t0001g0032 a0001c0001t0001g0198 a0001c0001t0001g0199 others(5): Show |
9 | HG00639.hp2 HG00738.hp1 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.169-409A>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 1/11 | chr1 | 70415547 | |||||||
| chr1:70415569 | T | C | 223 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(220): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.169-387T>C | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 1/11 | chr1 | 70415569 | |||||||
| chr1:70415656 | C | T | 9 | a0001c0001t0001g0227 a0001c0001t0004g0048 a0001c0001t0004g0049 others(6): Show |
11 | HG01192.hp1 HG01934.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.169-300C>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 1/11 | chr1 | 70415656 | |||||||
| chr1:70415711 | G | T | 3 | a0001c0001t0005g0264 a0001c0001t0005g0265 a0001c0001t0005g0266 |
3 | HG02622.hp1 HG02717.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.169-245G>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 1/11 | chr1 | 70415711 | |||||||
| chr1:70415938 | C | T | 9 | a0001c0001t0001g0227 a0001c0001t0004g0048 a0001c0001t0004g0049 others(6): Show |
11 | HG01192.hp1 HG01934.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.169-18C>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 1/11 | chr1 | 70415938 | |||||||
| chr1:70416050 | C | A | 1 | a0001c0001t0001g0204 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.250+13C>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 2/11 | chr1 | 70416050 | |||||||
| chr1:70416230 | G | A | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(223): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.250+193G>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 2/11 | chr1 | 70416230 | |||||||
| chr1:70416271 | G | A | 1 | a0002c0002t0001g0141 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.250+234G>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 2/11 | chr1 | 70416271 | |||||||
| chr1:70416554 | T | C | 9 | a0001c0001t0001g0227 a0001c0001t0004g0048 a0001c0001t0004g0049 others(6): Show |
11 | HG01192.hp1 HG01934.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.250+517T>C | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 2/11 | chr1 | 70416554 | |||||||
| chr1:70416559 | A | AT | 56 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0019 others(53): Show |
82 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.250+543dupT | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 70416559 | ||||||
| chr1:70416559 | AT | A | 17 | a0001c0001t0001g0038 a0001c0001t0001g0058 a0001c0001t0001g0059 others(14): Show |
18 | HG00544.hp2 HG00558.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.250+543delT | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 70416559 | ||||||
| chr1:70416567 | T | G | 1 | a0001c0001t0001g0116 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.250+530T>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 2/11 | chr1 | 70416567 | |||||||
| chr1:70416784 | C | T | 37 | a0001c0001t0001g0002 a0001c0001t0001g0038 a0001c0001t0001g0039 others(34): Show |
55 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.250+747C>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 2/11 | chr1 | 70416784 | |||||||
| chr1:70416785 | G | A | 16 | a0001c0001t0003g0006 a0001c0001t0003g0178 a0001c0001t0003g0179 others(13): Show |
23 | HG01074.hp1 HG01168.hp1 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.250+748G>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 2/11 | chr1 | 70416785 | |||||||
| chr1:70416809 | G | A | 33 | a0001c0001t0001g0002 a0001c0001t0001g0038 a0001c0001t0001g0039 others(30): Show |
51 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.250+772G>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 2/11 | chr1 | 70416809 | |||||||
| chr1:70416908 | G | C | 33 | a0001c0001t0001g0002 a0001c0001t0001g0038 a0001c0001t0001g0039 others(30): Show |
51 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.250+871G>C | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 2/11 | chr1 | 70416908 | |||||||
| chr1:70417192 | C | A | 1 | a0001c0001t0001g0060 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.251-745C>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 2/11 | chr1 | 70417192 | |||||||
| chr1:70417257 | C | T | 9 | a0001c0001t0001g0227 a0001c0001t0004g0048 a0001c0001t0004g0049 others(6): Show |
11 | HG01192.hp1 HG01934.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.251-680C>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 2/11 | chr1 | 70417257 | |||||||
| chr1:70417292 | CT | C | 9 | a0001c0001t0001g0227 a0001c0001t0004g0048 a0001c0001t0004g0049 others(6): Show |
11 | HG01192.hp1 HG01934.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.251-635delT | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 70417292 | ||||||
| chr1:70417457 | G | A | 1 | a0001c0001t0001g0226 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.251-480G>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 2/11 | chr1 | 70417457 | |||||||
| chr1:70417465 | A | G | 1 | a0001c0001t0001g0234 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.251-472A>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 2/11 | chr1 | 70417465 | |||||||
| chr1:70417472 | A | C | 1 | a0001c0001t0003g0182 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.251-465A>C | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 2/11 | chr1 | 70417472 | |||||||
| chr1:70417580 | T | C | 9 | a0001c0001t0001g0227 a0001c0001t0004g0048 a0001c0001t0004g0049 others(6): Show |
11 | HG01192.hp1 HG01934.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.251-357T>C | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 2/11 | chr1 | 70417580 | |||||||
| chr1:70417702 | G | A | 3 | a0001c0001t0002g0090 a0001c0001t0002g0195 a0001c0001t0002g0209 |
3 | HG01516.hp1 HG01517.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.251-235G>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 2/11 | chr1 | 70417702 | |||||||
| chr1:70417830 | G | A | 1 | a0002c0002t0002g0138 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.251-107G>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 2/11 | chr1 | 70417830 | |||||||
| chr1:70418039 | G | A | 1 | a0001c0001t0001g0238 | 1 | HG03516.hp1 | splice_region_variant&intron_variant | LOW | c.346+7G>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 3/11 | chr1 | 70418039 | |||||||
| chr1:70418157 | A | G | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(223): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.346+125A>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 3/11 | chr1 | 70418157 | |||||||
| chr1:70418230 | T | C | 1 | a0003c0007t0001g0202 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.346+198T>C | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 3/11 | chr1 | 70418230 | |||||||
| chr1:70418312 | C | T | 39 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0012 others(36): Show |
67 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.346+280C>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 3/11 | chr1 | 70418312 | |||||||
| chr1:70418350 | A | G | 1 | a0001c0001t0001g0227 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.346+318A>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 3/11 | chr1 | 70418350 | |||||||
| chr1:70418392 | G | C | 1 | a0001c0001t0001g0061 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.346+360G>C | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 3/11 | chr1 | 70418392 | |||||||
| chr1:70418486 | G | A | 3 | a0001c0001t0005g0264 a0001c0001t0005g0265 a0001c0001t0005g0266 |
3 | HG02622.hp1 HG02717.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.346+454G>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 3/11 | chr1 | 70418486 | |||||||
| chr1:70418646 | T | G | 3 | a0002c0002t0001g0175 a0002c0002t0001g0176 a0002c0002t0001g0177 |
3 | HG02886.hp2 HG03579.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.346+614T>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 3/11 | chr1 | 70418646 | |||||||
| chr1:70418883 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.346+851C>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 3/11 | chr1 | 70418883 | |||||||
| chr1:70418973 | C | G | 1 | a0001c0001t0001g0228 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.346+941C>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 3/11 | chr1 | 70418973 | |||||||
| chr1:70418975 | T | C | 1 | a0001c0001t0001g0062 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.346+943T>C | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 3/11 | chr1 | 70418975 | |||||||
| chr1:70419003 | T | C | 56 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0016 others(53): Show |
86 | HG00558.hp2 HG00597.hp1 HG00609.hp2 others(83): Show |
intron_variant | MODIFIER | c.346+971T>C | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 3/11 | chr1 | 70419003 | |||||||
| chr1:70419078 | G | A | 3 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0123 |
7 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(4): Show |
intron_variant | MODIFIER | c.346+1046G>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 3/11 | chr1 | 70419078 | |||||||
| chr1:70419148 | A | G | 9 | a0001c0001t0001g0227 a0001c0001t0004g0048 a0001c0001t0004g0049 others(6): Show |
11 | HG01192.hp1 HG01934.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.346+1116A>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 3/11 | chr1 | 70419148 | |||||||
| chr1:70419153 | C | G | 56 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0016 others(53): Show |
86 | HG00558.hp2 HG00597.hp1 HG00609.hp2 others(83): Show |
intron_variant | MODIFIER | c.346+1121C>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 3/11 | chr1 | 70419153 | |||||||
| chr1:70419311 | T | C | 1 | a0001c0001t0001g0239 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.346+1279T>C | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 3/11 | chr1 | 70419311 | |||||||
| chr1:70419470 | A | T | 9 | a0001c0001t0001g0227 a0001c0001t0004g0048 a0001c0001t0004g0049 others(6): Show |
11 | HG01192.hp1 HG01934.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.346+1438A>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 3/11 | chr1 | 70419470 | |||||||
| chr1:70419596 | C | T | 1 | a0001c0001t0001g0082 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.346+1564C>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 3/11 | chr1 | 70419596 | |||||||
| chr1:70419609 | G | A | 1 | a0001c0001t0001g0097 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.346+1577G>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 3/11 | chr1 | 70419609 | |||||||
| chr1:70419645 | A | G | 1 | a0002c0002t0002g0220 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.346+1613A>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 3/11 | chr1 | 70419645 | |||||||
| chr1:70419700 | T | TA | 9 | a0001c0001t0001g0045 a0001c0001t0001g0112 a0001c0001t0001g0113 others(6): Show |
10 | HG00280.hp1 HG00735.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.346+1676dupA | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 70419700 | ||||||
| chr1:70419700 | TA | T | 57 | a0001c0001t0001g0008 a0001c0001t0001g0095 a0001c0001t0001g0139 others(54): Show |
83 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.346+1676delA | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 70419700 | ||||||
| chr1:70419747 | A | G | 1 | a0001c0001t0003g0189 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.346+1715A>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 3/11 | chr1 | 70419747 | |||||||
| chr1:70419859 | C | G | 9 | a0001c0001t0001g0227 a0001c0001t0004g0048 a0001c0001t0004g0049 others(6): Show |
11 | HG01192.hp1 HG01934.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.347-1707C>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 3/11 | chr1 | 70419859 | |||||||
| chr1:70419994 | G | GT | 19 | a0001c0001t0001g0029 a0001c0001t0001g0080 a0001c0001t0001g0081 others(16): Show |
20 | HG01978.hp1 HG01981.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.347-1555dupT | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 70419994 | ||||||
| chr1:70420061 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.347-1505C>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 3/11 | chr1 | 70420061 | |||||||
| chr1:70420212 | A | C | 57 | a0001c0001t0001g0008 a0001c0001t0001g0095 a0001c0001t0001g0139 others(54): Show |
83 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.347-1354A>C | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 3/11 | chr1 | 70420212 | |||||||
| chr1:70420212 | A | G | 9 | a0001c0001t0001g0227 a0001c0001t0004g0048 a0001c0001t0004g0049 others(6): Show |
11 | HG01192.hp1 HG01934.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.347-1354A>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 3/11 | chr1 | 70420212 | |||||||
| chr1:70420222 | C | T | 56 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0016 others(53): Show |
86 | HG00558.hp2 HG00597.hp1 HG00609.hp2 others(83): Show |
intron_variant | MODIFIER | c.347-1344C>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 3/11 | chr1 | 70420222 | |||||||
| chr1:70420283 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.347-1283G>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 3/11 | chr1 | 70420283 | |||||||
| chr1:70420330 | A | T | 1 | a0001c0001t0003g0185 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.347-1236A>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 3/11 | chr1 | 70420330 | |||||||
| chr1:70420344 | C | T | 9 | a0001c0001t0001g0227 a0001c0001t0004g0048 a0001c0001t0004g0049 others(6): Show |
11 | HG01192.hp1 HG01934.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.347-1222C>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 3/11 | chr1 | 70420344 | |||||||
| chr1:70420505 | T | G | 1 | a0001c0001t0001g0232 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.347-1061T>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 3/11 | chr1 | 70420505 | |||||||
| chr1:70420558 | G | T | 33 | a0001c0001t0001g0002 a0001c0001t0001g0038 a0001c0001t0001g0039 others(30): Show |
51 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.347-1008G>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 3/11 | chr1 | 70420558 | |||||||
| chr1:70420559 | C | T | 9 | a0001c0001t0001g0227 a0001c0001t0004g0048 a0001c0001t0004g0049 others(6): Show |
11 | HG01192.hp1 HG01934.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.347-1007C>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 3/11 | chr1 | 70420559 | |||||||
| chr1:70420642 | T | C | 1 | a0001c0001t0001g0241 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.347-924T>C | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 3/11 | chr1 | 70420642 | |||||||
| chr1:70420646 | A | G | 4 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(1): Show |
4 | HG00280.hp1 HG00735.hp1 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.347-920A>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 3/11 | chr1 | 70420646 | |||||||
| chr1:70420702 | C | T | 56 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0016 others(53): Show |
86 | HG00558.hp2 HG00597.hp1 HG00609.hp2 others(83): Show |
intron_variant | MODIFIER | c.347-864C>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 3/11 | chr1 | 70420702 | |||||||
| chr1:70420793 | T | C | 1 | a0002c0002t0002g0148 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.347-773T>C | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 3/11 | chr1 | 70420793 | |||||||
| chr1:70420972 | T | C | 19 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0020 others(16): Show |
35 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.347-594T>C | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 3/11 | chr1 | 70420972 | |||||||
| chr1:70421085 | T | C | 1 | a0001c0001t0001g0227 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.347-481T>C | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 3/11 | chr1 | 70421085 | |||||||
| chr1:70421101 | T | C | 2 | a0001c0001t0001g0249 a0001c0001t0001g0250 |
2 | HG01346.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.347-465T>C | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 3/11 | chr1 | 70421101 | |||||||
| chr1:70421212 | T | G | 1 | a0001c0001t0005g0267 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.347-354T>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 3/11 | chr1 | 70421212 | |||||||
| chr1:70421234 | G | A | 1 | a0001c0001t0001g0235 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.347-332G>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 3/11 | chr1 | 70421234 | |||||||
| chr1:70421268 | T | C | 1 | a0001c0001t0001g0092 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.347-298T>C | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 3/11 | chr1 | 70421268 | |||||||
| chr1:70421393 | A | T | 16 | a0001c0001t0003g0006 a0001c0001t0003g0178 a0001c0001t0003g0179 others(13): Show |
23 | HG01074.hp1 HG01168.hp1 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.347-173A>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 3/11 | chr1 | 70421393 | |||||||
| chr1:70421416 | A | G | 75 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(72): Show |
121 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.347-150A>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 3/11 | chr1 | 70421416 | |||||||
| chr1:70421494 | T | G | 1 | a0001c0001t0001g0234 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.347-72T>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 3/11 | chr1 | 70421494 | |||||||
| chr1:70421500 | A | C | 15 | a0001c0001t0001g0025 a0001c0001t0001g0045 a0001c0001t0001g0047 others(12): Show |
19 | HG00280.hp1 HG00735.hp1 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.347-66A>C | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 3/11 | chr1 | 70421500 | |||||||
| chr1:70421959 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.456+284G>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 4/11 | chr1 | 70421959 | |||||||
| chr1:70422091 | T | A | 1 | a0001c0001t0001g0058 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.456+416T>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 4/11 | chr1 | 70422091 | |||||||
| chr1:70422117 | T | C | 3 | a0001c0001t0001g0032 a0001c0001t0001g0199 a0001c0001t0001g0200 |
4 | HG00639.hp2 HG00738.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.456+442T>C | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 4/11 | chr1 | 70422117 | |||||||
| chr1:70422232 | T | G | 8 | a0001c0001t0004g0048 a0001c0001t0004g0049 a0001c0001t0004g0268 others(5): Show |
10 | HG01934.hp2 HG02145.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.456+557T>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 4/11 | chr1 | 70422232 | |||||||
| chr1:70422290 | C | T | 2 | a0001c0001t0004g0270 a0001c0001t0004g0271 |
2 | HG02717.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.456+615C>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 4/11 | chr1 | 70422290 | |||||||
| chr1:70422291 | G | A | 1 | a0001c0001t0001g0063 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.456+616G>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 4/11 | chr1 | 70422291 | |||||||
| chr1:70422449 | A | G | 3 | a0002c0002t0002g0196 a0002c0002t0002g0217 a0002c0002t0002g0220 |
3 | HG00738.hp2 HG01081.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.456+774A>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 4/11 | chr1 | 70422449 | |||||||
| chr1:70422609 | C | CT | 17 | a0001c0001t0001g0079 a0001c0001t0001g0098 a0001c0001t0001g0136 others(14): Show |
19 | HG00408.hp1 HG01175.hp1 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.456+954dupT | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 70422609 | ||||||
| chr1:70422609 | CT | C | 17 | a0001c0001t0001g0028 a0001c0001t0001g0039 a0001c0001t0001g0040 others(14): Show |
19 | HG00140.hp1 HG01070.hp1 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.456+954delT | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 70422609 | ||||||
| chr1:70423204 | A | G | 1 | a0002c0002t0002g0147 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.457-1081A>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 4/11 | chr1 | 70423204 | |||||||
| chr1:70423290 | A | G | 1 | a0001c0001t0001g0215 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.457-995A>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 4/11 | chr1 | 70423290 | |||||||
| chr1:70423307 | C | T | 1 | a0002c0002t0002g0173 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.457-978C>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 4/11 | chr1 | 70423307 | |||||||
| chr1:70423407 | A | T | 13 | a0001c0001t0001g0107 a0001c0001t0001g0193 a0001c0001t0001g0194 others(10): Show |
15 | HG01934.hp2 HG02015.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.457-878A>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 4/11 | chr1 | 70423407 | |||||||
| chr1:70423465 | A | G | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(224): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.457-820A>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 4/11 | chr1 | 70423465 | |||||||
| chr1:70423572 | T | TA | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(211): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.457-701dupA | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 70423572 | ||||||
| chr1:70423572 | T | TAA | 8 | a0001c0001t0001g0227 a0001c0001t0004g0048 a0001c0001t0004g0049 others(5): Show |
10 | HG01192.hp1 HG01934.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.457-702_457-701dup others(2): Show |
CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 70423572 | ||||||
| chr1:70423602 | A | G | 1 | a0001c0001t0001g0137 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.457-683A>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 4/11 | chr1 | 70423602 | |||||||
| chr1:70423793 | T | A | 76 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(73): Show |
122 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.457-492T>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 4/11 | chr1 | 70423793 | |||||||
| chr1:70423798 | G | C | 1 | a0001c0001t0001g0065 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.457-487G>C | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 4/11 | chr1 | 70423798 | |||||||
| chr1:70424027 | C | T | 8 | a0001c0001t0004g0048 a0001c0001t0004g0049 a0001c0001t0004g0268 others(5): Show |
10 | HG01934.hp2 HG02145.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.457-258C>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 4/11 | chr1 | 70424027 | |||||||
| chr1:70424575 | C | T | 2 | a0002c0002t0001g0230 a0002c0002t0001g0231 |
2 | HG02559.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.588+159C>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 5/11 | chr1 | 70424575 | |||||||
| chr1:70424599 | C | G | 1 | a0001c0001t0001g0227 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.588+183C>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 5/11 | chr1 | 70424599 | |||||||
| chr1:70424709 | G | A | 1 | a0002c0002t0002g0149 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.588+293G>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 5/11 | chr1 | 70424709 | |||||||
| chr1:70424746 | G | C | 1 | a0001c0001t0009g0124 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.588+330G>C | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 5/11 | chr1 | 70424746 | |||||||
| chr1:70424795 | G | A | 56 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0016 others(53): Show |
86 | HG00558.hp2 HG00597.hp1 HG00609.hp2 others(83): Show |
intron_variant | MODIFIER | c.588+379G>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 5/11 | chr1 | 70424795 | |||||||
| chr1:70424866 | T | C | 8 | a0002c0002t0002g0004 a0002c0002t0002g0031 a0002c0002t0002g0105 others(5): Show |
19 | HG00558.hp1 HG01081.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.588+450T>C | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 5/11 | chr1 | 70424866 | |||||||
| chr1:70424946 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.588+530G>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 5/11 | chr1 | 70424946 | |||||||
| chr1:70425436 | T | G | 39 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0012 others(36): Show |
67 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.588+1020T>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 5/11 | chr1 | 70425436 | |||||||
| chr1:70425664 | G | T | 1 | a0001c0001t0001g0092 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.588+1248G>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 5/11 | chr1 | 70425664 | |||||||
| chr1:70425706 | G | A | 33 | a0001c0001t0001g0002 a0001c0001t0001g0038 a0001c0001t0001g0039 others(30): Show |
51 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.588+1290G>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 5/11 | chr1 | 70425706 | |||||||
| chr1:70425743 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.588+1327C>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 5/11 | chr1 | 70425743 | |||||||
| chr1:70425897 | A | G | 2 | a0001c0001t0001g0114 a0001c0001t0001g0115 |
2 | HG00280.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.588+1481A>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 5/11 | chr1 | 70425897 | |||||||
| chr1:70425912 | G | A | 1 | a0001c0001t0001g0201 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.588+1496G>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 5/11 | chr1 | 70425912 | |||||||
| chr1:70426575 | T | G | 2 | a0001c0001t0001g0038 a0001c0001t0001g0206 |
3 | NA18953.hp1 NA18964.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.588+2159T>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 5/11 | chr1 | 70426575 | |||||||
| chr1:70426908 | G | A | 4 | a0001c0001t0001g0032 a0001c0001t0001g0198 a0001c0001t0001g0199 others(1): Show |
5 | HG00639.hp2 HG00738.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.588+2492G>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 5/11 | chr1 | 70426908 | |||||||
| chr1:70426959 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.588+2543G>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 5/11 | chr1 | 70426959 | |||||||
| chr1:70427232 | A | T | 8 | a0001c0001t0001g0032 a0001c0001t0001g0198 a0001c0001t0001g0199 others(5): Show |
9 | HG00639.hp2 HG00738.hp1 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.589-2562A>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 5/11 | chr1 | 70427232 | |||||||
| chr1:70427570 | T | C | 1 | a0001c0001t0001g0194 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.589-2224T>C | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 5/11 | chr1 | 70427570 | |||||||
| chr1:70427576 | C | T | 2 | a0002c0002t0002g0110 a0002c0002t0002g0157 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.589-2218C>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 5/11 | chr1 | 70427576 | |||||||
| chr1:70427615 | C | A | 1 | a0001c0001t0001g0104 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.589-2179C>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 5/11 | chr1 | 70427615 | |||||||
| chr1:70427708 | G | T | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(223): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.589-2086G>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 5/11 | chr1 | 70427708 | |||||||
| chr1:70427717 | T | A | 1 | a0001c0001t0001g0066 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.589-2077T>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 5/11 | chr1 | 70427717 | |||||||
| chr1:70427773 | C | T | 3 | a0001c0001t0001g0013 a0001c0001t0005g0121 a0001c0003t0001g0013 |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.589-2021C>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 5/11 | chr1 | 70427773 | |||||||
| chr1:70427798 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.589-1996C>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 5/11 | chr1 | 70427798 | |||||||
| chr1:70427830 | A | G | 3 | a0001c0001t0001g0047 a0001c0001t0001g0140 a0001c0001t0001g0243 |
4 | HG01106.hp2 HG02683.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.589-1964A>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 5/11 | chr1 | 70427830 | |||||||
| chr1:70427870 | C | T | 3 | a0001c0001t0005g0264 a0001c0001t0005g0265 a0001c0001t0005g0266 |
3 | HG02622.hp1 HG02717.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.589-1924C>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 5/11 | chr1 | 70427870 | |||||||
| chr1:70427875 | G | A | 1 | a0001c0001t0001g0257 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.589-1919G>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 5/11 | chr1 | 70427875 | |||||||
| chr1:70427878 | A | G | 1 | a0001c0001t0001g0234 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.589-1916A>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 5/11 | chr1 | 70427878 | |||||||
| chr1:70428079 | A | G | 1 | a0001c0001t0001g0046 | 2 | HG00597.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.589-1715A>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 5/11 | chr1 | 70428079 | |||||||
| chr1:70428194 | G | A | 60 | a0001c0001t0001g0008 a0001c0001t0001g0062 a0001c0001t0001g0065 others(57): Show |
86 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.589-1600G>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 5/11 | chr1 | 70428194 | |||||||
| chr1:70428470 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.589-1324C>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 5/11 | chr1 | 70428470 | |||||||
| chr1:70428512 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.589-1282T>C | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 5/11 | chr1 | 70428512 | |||||||
| chr1:70428537 | A | G | 1 | a0001c0001t0003g0189 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.589-1257A>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 5/11 | chr1 | 70428537 | |||||||
| chr1:70428598 | ATATT | A | 279 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(276): Show |
420 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(417): Show |
intron_variant | MODIFIER | c.589-1170_589-1167d others(6): Show |
CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr1 | 70428598 | ||||||
| chr1:70428603 | T | C | 1 | a0001c0001t0001g0125 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.589-1191T>C | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 5/11 | chr1 | 70428603 | |||||||
| chr1:70428994 | C | T | 1 | a0002c0002t0002g0151 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.589-800C>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 5/11 | chr1 | 70428994 | |||||||
| chr1:70429102 | T | G | 1 | a0001c0001t0001g0021 | 3 | HG01255.hp1 HG01361.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.589-692T>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 5/11 | chr1 | 70429102 | |||||||
| chr1:70429270 | C | A | 8 | a0001c0001t0001g0045 a0001c0001t0001g0112 a0001c0001t0001g0113 others(5): Show |
9 | HG00280.hp1 HG00735.hp1 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.589-524C>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 5/11 | chr1 | 70429270 | |||||||
| chr1:70429353 | G | T | 1 | a0001c0001t0001g0104 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.589-441G>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 5/11 | chr1 | 70429353 | |||||||
| chr1:70429396 | C | G | 1 | a0001c0001t0001g0200 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.589-398C>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 5/11 | chr1 | 70429396 | |||||||
| chr1:70429438 | G | T | 1 | a0001c0001t0001g0128 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.589-356G>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 5/11 | chr1 | 70429438 | |||||||
| chr1:70429443 | A | T | 1 | a0001c0001t0001g0081 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.589-351A>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 5/11 | chr1 | 70429443 | |||||||
| chr1:70429552 | C | T | 2 | a0001c0001t0001g0030 a0001c0001t0001g0127 |
3 | HG01884.hp1 HG02451.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.589-242C>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 5/11 | chr1 | 70429552 | |||||||
| chr1:70429674 | A | T | 1 | a0001c0001t0001g0193 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.589-120A>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 5/11 | chr1 | 70429674 | |||||||
| chr1:70429718 | A | G | 1 | a0001c0001t0001g0038 | 2 | NA18953.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.589-76A>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 5/11 | chr1 | 70429718 | |||||||
| chr1:70429951 | C | T | 6 | a0002c0002t0002g0014 a0002c0002t0002g0036 a0002c0002t0002g0134 others(3): Show |
10 | HG00408.hp1 HG02083.hp2 NA18941.hp2 others(7): Show |
intron_variant | MODIFIER | c.646+100C>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 6/11 | chr1 | 70429951 | |||||||
| chr1:70430023 | A | T | 1 | a0001c0001t0001g0047 | 2 | HG03710.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.646+172A>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 6/11 | chr1 | 70430023 | |||||||
| chr1:70430103 | A | T | 4 | a0001c0001t0001g0032 a0001c0001t0001g0198 a0001c0001t0001g0199 others(1): Show |
5 | HG00639.hp2 HG00738.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.647-214A>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 6/11 | chr1 | 70430103 | |||||||
| chr1:70430180 | T | G | 1 | a0001c0001t0001g0165 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.647-137T>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 6/11 | chr1 | 70430180 | |||||||
| chr1:70430189 | T | C | 1 | a0001c0001t0001g0104 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.647-128T>C | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 6/11 | chr1 | 70430189 | |||||||
| chr1:70430288 | T | C | 5 | a0002c0002t0002g0033 a0002c0002t0002g0147 a0002c0002t0002g0152 others(2): Show |
6 | HG01106.hp1 HG01257.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.647-29T>C | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 6/11 | chr1 | 70430288 | |||||||
| chr1:70430302 | G | C | 1 | a0001c0001t0001g0236 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.647-15G>C | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 6/11 | chr1 | 70430302 | |||||||
| chr1:70430482 | G | A | 57 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0016 others(54): Show |
87 | HG00558.hp2 HG00597.hp1 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.724+88G>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 7/11 | chr1 | 70430482 | |||||||
| chr1:70430548 | A | AT | 57 | a0001c0001t0001g0008 a0001c0001t0001g0095 a0001c0001t0001g0139 others(54): Show |
83 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.724+165dupT | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 70430548 | ||||||
| chr1:70430603 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.724+209G>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 7/11 | chr1 | 70430603 | |||||||
| chr1:70430629 | C | A | 1 | a0001c0001t0001g0104 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.724+235C>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 7/11 | chr1 | 70430629 | |||||||
| chr1:70430636 | G | A | 57 | a0001c0001t0001g0008 a0001c0001t0001g0095 a0001c0001t0001g0139 others(54): Show |
83 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.724+242G>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 7/11 | chr1 | 70430636 | |||||||
| chr1:70430648 | T | A | 1 | a0001c0001t0001g0227 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.724+254T>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 7/11 | chr1 | 70430648 | |||||||
| chr1:70430732 | G | A | 75 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(72): Show |
121 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.724+338G>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 7/11 | chr1 | 70430732 | |||||||
| chr1:70430747 | T | G | 1 | a0001c0001t0001g0104 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.724+353T>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 7/11 | chr1 | 70430747 | |||||||
| chr1:70430757 | G | C | 24 | a0001c0001t0003g0006 a0001c0001t0003g0178 a0001c0001t0003g0179 others(21): Show |
33 | HG01074.hp1 HG01168.hp1 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.724+363G>C | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 7/11 | chr1 | 70430757 | |||||||
| chr1:70430849 | A | T | 4 | a0001c0001t0001g0009 a0001c0001t0001g0060 a0001c0001t0001g0067 others(1): Show |
9 | HG00639.hp1 HG00642.hp1 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.724+455A>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 7/11 | chr1 | 70430849 | |||||||
| chr1:70430913 | A | T | 1 | a0001c0001t0001g0104 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.724+519A>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 7/11 | chr1 | 70430913 | |||||||
| chr1:70430914 | T | G | 1 | a0001c0001t0001g0104 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.724+520T>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 7/11 | chr1 | 70430914 | |||||||
| chr1:70430932 | A | T | 1 | a0001c0001t0001g0104 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.724+538A>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 7/11 | chr1 | 70430932 | |||||||
| chr1:70430933 | T | C | 1 | a0001c0001t0001g0227 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.724+539T>C | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 7/11 | chr1 | 70430933 | |||||||
| chr1:70430950 | G | A | 33 | a0001c0001t0001g0002 a0001c0001t0001g0038 a0001c0001t0001g0039 others(30): Show |
51 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.724+556G>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 7/11 | chr1 | 70430950 | |||||||
| chr1:70430998 | A | T | 1 | a0001c0001t0005g0266 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.724+604A>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 7/11 | chr1 | 70430998 | |||||||
| chr1:70431284 | A | G | 38 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0012 others(35): Show |
66 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.725-799A>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 7/11 | chr1 | 70431284 | |||||||
| chr1:70431448 | C | T | 24 | a0001c0001t0003g0006 a0001c0001t0003g0178 a0001c0001t0003g0179 others(21): Show |
33 | HG01074.hp1 HG01168.hp1 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.725-635C>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 7/11 | chr1 | 70431448 | |||||||
| chr1:70431500 | G | T | 38 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0012 others(35): Show |
66 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.725-583G>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 7/11 | chr1 | 70431500 | |||||||
| chr1:70431516 | C | T | 1 | a0001c0001t0001g0037 | 2 | HG00741.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.725-567C>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 7/11 | chr1 | 70431516 | |||||||
| chr1:70431659 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.725-424G>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 7/11 | chr1 | 70431659 | |||||||
| chr1:70431741 | A | G | 1 | a0001c0001t0001g0053 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.725-342A>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 7/11 | chr1 | 70431741 | |||||||
| chr1:70432054 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.725-29A>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 7/11 | chr1 | 70432054 | |||||||
| chr1:70432445 | G | T | 4 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0203 others(1): Show |
4 | HG02258.hp2 HG02559.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.877+210G>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 8/11 | chr1 | 70432445 | |||||||
| chr1:70432678 | CTCTCT | C | 49 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0016 others(46): Show |
79 | HG00558.hp2 HG00597.hp1 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.877+445_877+449del others(5): Show |
CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 70432678 | ||||||
| chr1:70432682 | CT | C | 105 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(102): Show |
168 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.877+468delT | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 70432682 | ||||||
| chr1:70432682 | CTT | C | 98 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(95): Show |
137 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.877+467_877+468del others(2): Show |
CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 70432682 | ||||||
| chr1:70432833 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.877+598G>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 8/11 | chr1 | 70432833 | |||||||
| chr1:70432963 | C | T | 33 | a0001c0001t0001g0002 a0001c0001t0001g0038 a0001c0001t0001g0039 others(30): Show |
51 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.877+728C>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 8/11 | chr1 | 70432963 | |||||||
| chr1:70432964 | G | A | 38 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0012 others(35): Show |
66 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.877+729G>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 8/11 | chr1 | 70432964 | |||||||
| chr1:70432988 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.877+753G>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 8/11 | chr1 | 70432988 | |||||||
| chr1:70433366 | T | A | 2 | a0001c0001t0003g0188 a0001c0001t0003g0189 |
2 | HG02486.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.878-462T>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 8/11 | chr1 | 70433366 | |||||||
| chr1:70433466 | T | C | 53 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0016 others(50): Show |
83 | HG00558.hp2 HG00597.hp1 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.878-362T>C | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 8/11 | chr1 | 70433466 | |||||||
| chr1:70433720 | G | A | 2 | a0001c0003t0001g0131 a0001c0003t0001g0132 |
2 | HG02818.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.878-108G>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 8/11 | chr1 | 70433720 | |||||||
| chr1:70433720 | G | T | 1 | a0001c0001t0001g0244 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.878-108G>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 8/11 | chr1 | 70433720 | |||||||
| chr1:70433722 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.878-106C>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 8/11 | chr1 | 70433722 | |||||||
| chr1:70433773 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.878-55C>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 8/11 | chr1 | 70433773 | |||||||
| chr1:70433975 | T | C | 2 | a0001c0001t0001g0117 a0001c0001t0003g0182 |
2 | HG01255.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.999+26T>C | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 9/11 | chr1 | 70433975 | |||||||
| chr1:70434072 | T | C | 1 | a0001c0001t0001g0227 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.999+123T>C | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 9/11 | chr1 | 70434072 | |||||||
| chr1:70434608 | T | C | 1 | a0001c0001t0005g0266 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1000-517T>C | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 9/11 | chr1 | 70434608 | |||||||
| chr1:70434609 | T | C | 3 | a0001c0001t0005g0264 a0001c0001t0005g0265 a0001c0001t0005g0266 |
3 | HG02622.hp1 HG02717.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1000-516T>C | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 9/11 | chr1 | 70434609 | |||||||
| chr1:70434666 | G | C | 1 | a0001c0001t0001g0073 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1000-459G>C | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 9/11 | chr1 | 70434666 | |||||||
| chr1:70434693 | T | G | 3 | a0001c0001t0005g0264 a0001c0001t0005g0265 a0001c0001t0005g0266 |
3 | HG02622.hp1 HG02717.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1000-432T>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 9/11 | chr1 | 70434693 | |||||||
| chr1:70434746 | A | AT | 75 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0027 others(72): Show |
96 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.1000-354dupT | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 70434746 | ||||||
| chr1:70434746 | A | ATT | 4 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0211 others(1): Show |
6 | HG04115.hp1 HG04228.hp2 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.1000-355_1000-354d others(4): Show |
CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 70434746 | ||||||
| chr1:70434746 | AT | A | 10 | a0001c0001t0001g0069 a0001c0001t0001g0074 a0001c0001t0001g0075 others(7): Show |
10 | HG01515.hp1 HG02004.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.1000-354delT | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 70434746 | ||||||
| chr1:70434822 | G | A | 1 | a0002c0002t0002g0155 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1000-303G>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 9/11 | chr1 | 70434822 | |||||||
| chr1:70434824 | C | T | 8 | a0001c0001t0004g0048 a0001c0001t0004g0049 a0001c0001t0004g0268 others(5): Show |
10 | HG01934.hp2 HG02145.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1000-301C>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 9/11 | chr1 | 70434824 | |||||||
| chr1:70434888 | G | A | 1 | a0002c0002t0002g0152 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1000-237G>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 9/11 | chr1 | 70434888 | |||||||
| chr1:70434941 | T | C | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(215): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.1000-184T>C | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 9/11 | chr1 | 70434941 | |||||||
| chr1:70434971 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1000-154C>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 9/11 | chr1 | 70434971 | |||||||
| chr1:70435067 | T | A | 1 | a0001c0001t0001g0190 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1000-58T>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 9/11 | chr1 | 70435067 | |||||||
| chr1:70435178 | G | A | 1 | a0002c0002t0002g0109 | 1 | HG03490.hp2 | splice_donor_variant&intron_variant | HIGH | c.1052+1G>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 10/11 | chr1 | 70435178 | |||||||
| chr1:70435472 | G | A | 4 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0203 others(1): Show |
4 | HG02258.hp2 HG02559.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1052+295G>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 10/11 | chr1 | 70435472 | |||||||
| chr1:70435568 | C | T | 1 | a0002c0002t0002g0158 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1052+391C>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 10/11 | chr1 | 70435568 | |||||||
| chr1:70435652 | G | A | 56 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0016 others(53): Show |
86 | HG00558.hp2 HG00597.hp1 HG00609.hp2 others(83): Show |
intron_variant | MODIFIER | c.1052+475G>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 10/11 | chr1 | 70435652 | |||||||
| chr1:70435785 | A | G | 1 | a0001c0001t0001g0206 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1052+608A>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 10/11 | chr1 | 70435785 | |||||||
| chr1:70435879 | G | GT | 4 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0203 others(1): Show |
4 | HG02258.hp2 HG02559.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1052+703dupT | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 70435879 | ||||||
| chr1:70436148 | TA | T | 39 | a0001c0001t0001g0002 a0001c0001t0001g0038 a0001c0001t0001g0039 others(36): Show |
59 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.1052+985delA | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 70436148 | ||||||
| chr1:70436168 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1052+991C>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 10/11 | chr1 | 70436168 | |||||||
| chr1:70436170 | A | G | 241 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(238): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.1052+993A>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 10/11 | chr1 | 70436170 | |||||||
| chr1:70436206 | G | T | 1 | a0001c0001t0001g0227 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1052+1029G>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 10/11 | chr1 | 70436206 | |||||||
| chr1:70436395 | A | G | 4 | a0001c0001t0001g0032 a0001c0001t0001g0198 a0001c0001t0001g0199 others(1): Show |
5 | HG00639.hp2 HG00738.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1052+1218A>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 10/11 | chr1 | 70436395 | |||||||
| chr1:70436509 | G | A | 3 | a0001c0001t0001g0015 a0001c0001t0001g0046 a0001c0001t0001g0247 |
7 | HG00597.hp2 HG02071.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.1052+1332G>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 10/11 | chr1 | 70436509 | |||||||
| chr1:70436582 | G | A | 33 | a0001c0001t0001g0002 a0001c0001t0001g0038 a0001c0001t0001g0039 others(30): Show |
51 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.1052+1405G>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 10/11 | chr1 | 70436582 | |||||||
| chr1:70436612 | T | C | 1 | a0001c0001t0001g0165 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1052+1435T>C | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 10/11 | chr1 | 70436612 | |||||||
| chr1:70436668 | TA | T | 26 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0020 others(23): Show |
42 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.1052+1505delA | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 70436668 | ||||||
| chr1:70436712 | A | C | 1 | a0002c0002t0002g0089 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1052+1535A>C | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 10/11 | chr1 | 70436712 | |||||||
| chr1:70437041 | G | A | 2 | a0001c0001t0001g0078 a0001c0001t0001g0087 |
2 | NA18964.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.1053-1647G>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 10/11 | chr1 | 70437041 | |||||||
| chr1:70437044 | A | G | 3 | a0001c0001t0001g0019 a0001c0001t0001g0029 a0001c0001t0001g0097 |
6 | NA18949.hp1 NA18955.hp1 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.1053-1644A>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 10/11 | chr1 | 70437044 | |||||||
| chr1:70437161 | A | G | 1 | a0001c0001t0001g0227 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1053-1527A>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 10/11 | chr1 | 70437161 | |||||||
| chr1:70437269 | G | A | 1 | a0001c0001t0004g0270 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1053-1419G>A | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 10/11 | chr1 | 70437269 | |||||||
| chr1:70437701 | A | G | 1 | a0002c0002t0002g0263 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1053-987A>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 10/11 | chr1 | 70437701 | |||||||
| chr1:70437885 | T | C | 2 | a0002c0002t0002g0024 a0002c0002t0002g0153 |
4 | HG00140.hp2 HG03491.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.1053-803T>C | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 10/11 | chr1 | 70437885 | |||||||
| chr1:70438258 | T | C | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(223): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.1053-430T>C | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 10/11 | chr1 | 70438258 | |||||||
| chr1:70438385 | A | G | 72 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(69): Show |
118 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.1053-303A>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 10/11 | chr1 | 70438385 | |||||||
| chr1:70438386 | T | C | 1 | a0001c0001t0001g0076 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1053-302T>C | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 10/11 | chr1 | 70438386 | |||||||
| chr1:70438495 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1053-193C>T | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 10/11 | chr1 | 70438495 | |||||||
| chr1:70438840 | T | TTG | 4 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0005g0267 others(1): Show |
4 | HG02055.hp2 HG02895.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.1191+42_1191+43dup others(2): Show |
CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr1 | 70438840 | ||||||
| chr1:70438840 | T | TTGTG | 130 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(127): Show |
189 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.1191+40_1191+43dup others(4): Show |
CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr1 | 70438840 | ||||||
| chr1:70438840 | T | TTGTGTG | 68 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0012 others(65): Show |
107 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.1191+38_1191+43dup others(6): Show |
CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr1 | 70438840 | ||||||
| chr1:70438840 | T | TTGTGTGT others(1): Show |
35 | a0001c0001t0001g0002 a0001c0001t0001g0038 a0001c0001t0001g0040 others(32): Show |
53 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.1191+36_1191+43dup others(8): Show |
CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr1 | 70438840 | ||||||
| chr1:70438840 | T | TTGTGTGT others(3): Show |
6 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0201 others(3): Show |
6 | HG02155.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1191+34_1191+43dup others(10): Show |
CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr1 | 70438840 | ||||||
| chr1:70438870 | C | G | 2 | a0001c0001t0001g0234 a0001c0001t0001g0242 |
2 | HG02630.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1191+44C>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 11/11 | chr1 | 70438870 | |||||||
| chr1:70438899 | A | G | 2 | a0002c0002t0002g0110 a0002c0002t0002g0157 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1191+73A>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 11/11 | chr1 | 70438899 | |||||||
| chr1:70439003 | T | G | 1 | a0001c0001t0001g0042 | 2 | HG04115.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1192-98T>G | CTH | ENSG00000116761.12 | transcript | ENST00000370938.8 | protein_coding | 11/11 | chr1 | 70439003 |